Skip to main content
Log in

Vision in the dimmest habitats on Earth

  • Karl von Frisch Lecture
  • Published:
Journal of Comparative Physiology A Aims and scope Submit manuscript

Abstract

A very large proportion of the world’s animal species are active in dim light, either under the cover of night or in the depths of the sea. The worlds they see can be dim and extended, with light reaching the eyes from all directions at once, or they can be composed of bright point sources, like the multitudes of stars seen in a clear night sky or the rare sparks of bioluminescence that are visible in the deep sea. The eye designs of nocturnal and deep-sea animals have evolved in response to these two very different types of habitats, being optimised for maximum sensitivity to extended scenes, or to point sources, or to both. After describing the many visual adaptations that have evolved across the animal kingdom for maximising sensitivity to extended and point-source scenes, I then use case studies from the recent literature to show how these adaptations have endowed nocturnal animals with excellent vision. Nocturnal animals can see colour and negotiate dimly illuminated obstacles during flight. They can also navigate using learned terrestrial landmarks, the constellations of stars or the dim pattern of polarised light formed around the moon. The conclusion from these studies is clear: nocturnal habitats are just as rich in visual details as diurnal habitats are, and nocturnal animals have evolved visual systems capable of exploiting them. The same is certainly true of deep-sea animals, as future research will no doubt reveal.

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.

Fig. 1a–c
Fig. 2a–c
Fig. 3a–e
Fig. 4a–c
Fig. 5a–c
Fig. 6
Fig. 7a–d
Fig. 8a, b
Fig. 9a–f
Fig. 10
Fig. 11a, b

Similar content being viewed by others

Notes

  1. As recently pointed out by Stavenga (2003), the Land sensitivity equation, despite its great usefulness, does have some limitations, especially for photoreceptors behaving as waveguides and for certain eye designs of lower F-number.

  2. This integral is calculated between two wavelength limits: λ1 and λ2 (Warrant and Nilsson 1998). λ1 is set at 280 nm, the lowest wavelength likely to be seen by any animal (because the relative intensity of daylight below this wavelength is very low, and the internal structures of the eye absorb all wavelengths that are shorter). λ2 is the wavelength at which the spectral sensitivity R(λ) falls to 1% of its maximum at its long wavelength end. R(λ) is given by the rhodopsin template of Stavenga et al. (1993). In this template λ2 = 1.231 λmax, where λ max is the absorbance peak wavelength of the visual pigment.

References

  • Aho A-C, Donner K, Hydén C, Larsen LO, Reuter T (1988) Low retinal noise in animals with low body temperature allows high visual sensitivity. Nature 334:348–350

    Article  CAS  PubMed  Google Scholar 

  • Aho A-C, Donner K, Helenius S, Larsen LO, Reuter T (1993) Visual performance of the toad (Bufo bufo) at low light levels: retinal ganglion cell responses and prey-catching accuracy. J Comp Physiol A 172:671–682

    CAS  PubMed  Google Scholar 

  • Ali MA, Klyne MA (1985) Vision in vertebrates. Plenum Press, New York

    Google Scholar 

  • Arneson L, Wcislo WT (2004) Dominant-subordinate relationships in a facultatively social, nocturnal bee, Megalopta genalis (Hymenoptera: Halictidae). J Kansas Entomol Soc (in press)

    Google Scholar 

  • Autrum H (1981) Light and dark adaptation in invertebrates. In: Autrum H (ed) Handbook of sensory physiology, vol VII/6C. Springer, Berlin Heidelberg New York, pp 1–91

  • Balkenius A, Kelber A (2004) Colour constancy in diurnal and nocturnal hawkmoths. J Exp Biol 207:3307–3316

    Article  PubMed  Google Scholar 

  • Barlow HB (1956) Retinal noise and absolute threshold. J Opt Soc Am 46: 634–639

    CAS  PubMed  Google Scholar 

  • Barlow HB, Levick WR, Yoon M (1971) Responses to single quanta of light in retinal ganglion cells of the cat. Vision Res 11:87–101

    Article  Google Scholar 

  • Baylor DA, Matthews G, Yau K-W (1980) Two components of electrical dark noise in toad retinal rod outer segments. J Physiol (Lond) 309:591–621

    CAS  PubMed  Google Scholar 

  • Becker L (1958) Untersuchungen über das Heimfindevermögen der Bienen. Z Vergl Physiol 41:1–25

    Google Scholar 

  • Blest AD, Land MF (1977) The physiological optics of Dinopis subrufus: a fish lens in a spider. Proc R Soc London Ser B 196:197–222

    CAS  PubMed  Google Scholar 

  • Byrne M, Dacke M, Nordström P, Scholtz C, Warrant EJ (2003) Visual cues used by ball-rolling dung beetles for orientation. J Comp Physiol A 189:411–418

    Article  Google Scholar 

  • Capaldi EA, Dyer FC (1999) The role of orientation flights on homing performance in honeybees. J Exp Biol 202:1655–1666

    PubMed  Google Scholar 

  • Childs SB, Buchler ER (1981) Perception of simulated stars by Eptesicus fuscus (Vespertilionidae): a potential navigational mechanism. Anim Behav 29:1028–1035

    Google Scholar 

  • Clarke GL, Denton EJ (1962) Light and animal life. In: Hill MN (ed) The sea. Wiley, New York, pp 456–468

    Google Scholar 

  • Collin SP (1999) Behavioural ecology and retinal cell topography. In: Archer SN, Djamgoz MBA, Loew ER, Partridge JC, Vallerga S (eds) Adaptive mechanisms in the ecology of vision. Kluwer, Dordrecht, pp 509–535

    Google Scholar 

  • Collin SP, Partridge JC (1996) Fish vision: retinal specialisations in the eyes of deep-sea teleosts. J Fish Biol 49A:157–174

    Article  Google Scholar 

  • Collin SP, Hoskins RV, Partridge JC (1997) Tubular eyes of deep-sea fishes: a comparative study of retinal topography. Brain Behav Evol 50:335–357

    CAS  PubMed  Google Scholar 

  • Cronin TW, Shashar N (2001) The linearly polarized light field in clear, tropical marine waters: spatial and temporal variation of light intensity, degree of polarization and e-vector angle. J Exp Biol 204:2461–2467

    CAS  PubMed  Google Scholar 

  • Dacke M, Nilsson D-E, Scholtz CH, Byrne M, Warrant EJ (2003a) Insect orientation to polarized moonlight. Nature 424:33

    Article  CAS  Google Scholar 

  • Dacke M, Nordström P, Scholtz CH (2003b) Twilight orientation to polarised light in the crepuscular dung beetle Scarabaeus zambesianus. J Exp Biol 106:1535–1543

    Article  Google Scholar 

  • Dacke M, Byrne M, Scholtz CH, Warrant EJ (2004) Lunar orientation in a beetle. Proc R Soc Lond B 271:361–365

    Article  PubMed  Google Scholar 

  • De Vries H (1943) The quantum character of light and its bearing upon threshold of vision, the differential sensitivity and visual acuity of the eye. Physica 10:553–564

    Google Scholar 

  • Denton EJ (1990) Light and vision at depths greater than 200 metres. In: Herring PJ, Campbell AK, Whitfield M, Maddock L (eds) Light and life in the sea. Cambridge University Press, Cambridge, pp 127–148

    Google Scholar 

  • Donner K (1989) Visual latency and brightness: an interpretation based on the responses of rods and ganglion cells in the frog retina. Vis Neurosci 3:39–51

    CAS  PubMed  Google Scholar 

  • Douglas RH, McGuigan CM (1989) The spectral transmission of freshwater teleost ocular media—an interspecific comparison and a guide to potential ultraviolet sensitivity. Vision Res 29:871–879

    Article  CAS  PubMed  Google Scholar 

  • Doujak FE (1985) Can a shore crab see a star? J Exp Biol 166:385–393

    Google Scholar 

  • Dubs A, Laughlin SB, Srinivasan MV (1981) Single photon signals in fly photoreceptors and first order interneurons at behavioural threshold. J Physiol (Lond) 317:317–334

    CAS  PubMed  Google Scholar 

  • Dvorak D, Snyder AW (1978) The relationship between visual acuity and illumination in the fly Lucilia sericata. Z Naturforsch C 33:139–143

    CAS  PubMed  Google Scholar 

  • Emlen ST (1970) Celestial rotation: its importance in the development of migratory orientation. Science 170:1198–2011

    Google Scholar 

  • Emlen ST (1975) The stellar-orientation system of a migratory bird. Sci Am 233:102–111

    CAS  PubMed  Google Scholar 

  • Frank TM, Widder EA (1996) UV light in the deep sea: in situ measurements of downwelling irradiance in relation to the visual threshold sensitivity of UV-sensitive crustaceans. Mar Fresh Behav Physiol 27:189–197

    Google Scholar 

  • Frisch K von (1914) Der Farbensinn und Formensinn der Biene. Zoologische Jahrbücher. Abt Allg Zool Physiol Tiere 35:1–188

    Google Scholar 

  • Fritsches KA, Marshall NJ, Warrant EJ (2003) Retinal specialisations in the blue marlin—eyes built for sensitivity to low light levels. Mar Fresh Res 54:1–9

    Article  Google Scholar 

  • Fuortes MGF, Yeandle S (1964) Probability of occurrence of discrete potential waves in the eye of Limulus. J Gen Physiol 47:443–463

    Article  CAS  PubMed  Google Scholar 

  • Gál J, Horváth G, Barta A, Wehner R (2001) Polarization of the moonlit clear night sky measured by full-sky imaging polarimetry at full moon: comparison of the polarization of moonlit and sunlit skies. J Geophys Res 106:22647–22653

    Article  Google Scholar 

  • Greenwood PH (1976) A new and eyeless cobitid fish (Pisces, Cypriniformes) from the Zagros Mountains, Iran. J Zool Soc Lond 180:129–137

    Google Scholar 

  • Greiner B, Ribi WA, Warrant EJ (2004a) Neuronal organisation in the first optic ganglion of the nocturnal bee Megalopta genalis. Cell Tissue Res (in press)

    Article  PubMed  Google Scholar 

  • Greiner B, Ribi WA, Warrant EJ (2004b) Retinal and optical adaptations for nocturnal vision in the halictid bee Megalopta genalis. Cell Tissue Res 316:377–390

    Article  PubMed  Google Scholar 

  • Hardie R (1979) Electrophysiological analysis of fly retina. I: comparative properties of R1–6 and R7 and 8. J Comp Physiol A 129:19–33

    Google Scholar 

  • Hateren JH van (1984) Waveguide theory applied to optically measured angular sensitivities of fly photoreceptors. J Comp Physiol 154:761–771

    Google Scholar 

  • Hateren JH van (1993) Spatiotemporal contrast sensitivity of early vision. Vision Res 33:257–267

    Article  PubMed  Google Scholar 

  • Hecht S, Shlaer S, Pirenne (1942) Energy, quanta and vision. J Gen Physiol 25:819–840

    Article  Google Scholar 

  • Herzmann D, Labhart T (1989) Spectral sensitivity and absolute threshold of polarization vision in crickets: a behavioral study. J Comp Physiol A 165:315–319

    Google Scholar 

  • Höglund G, Hamdorf K, Rosner G (1973) Trichromatic visual system in an insect and its sensitivity control by blue light. J Comp Physiol 86:265–279

    Google Scholar 

  • Horvath G, Varju D (1995) Underwater refraction-polarization patterns of skylight perceived by aquatic animals through Snell’s window of the flat water surface. Vision Res 35:1651–1666

    Article  CAS  PubMed  Google Scholar 

  • Hughes A (1977) The topography of vision in mammals of contrasting life style: comparative optics and retinal organisation. In: Crescitelli F (ed) Handbook of sensory physiology, vol VII/5. Springer, Berlin Heidelberg New York, pp 613–756

  • Janzen DH (1968) Notes on nesting and foraging behavior of Megalopta (Hymenoptera: Halictidae) in Costa Rica. J Kansas Entomol Soc 41:342–350

    Google Scholar 

  • Jerlov NG (1976) Marine optics. Elsevier, Amsterdam

    Google Scholar 

  • Kelber A, Hénique U (1999) Trichromatic colour vision in the hummingbird hawkmoth, Macroglossum stellatarum. J Comp Physiol A 184:535–541

    Article  Google Scholar 

  • Kelber A, Warrant EJ (2004) Colour vision in dim light: more common than we think. News Physiol Sci (in press)

    Google Scholar 

  • Kelber A, Balkenius A, Warrant EJ (2002) Scotopic colour vision in nocturnal hawkmoths. Nature 419:922–925

    Article  CAS  PubMed  Google Scholar 

  • Kelber A, Balkenius A, Warrant EJ (2003a) Colour vision in diurnal and nocturnal hawkmoths. Integr Comp Biol 43:571–579

    Google Scholar 

  • Kelber A, Vorobyev M, Osorio D (2003b) Animal colour vision—behavioural tests and physiological concepts. Biol Rev 78:81–118

    Article  PubMed  Google Scholar 

  • Krapp HG, Hengstenberg R (1996) Estimation of self-motion by optic flow processing in single visual neurons. Nature 384:463–466

    Article  CAS  PubMed  Google Scholar 

  • Labhart T, Petzold J, Helbling H (2001) Spatial integration in polarization-sensitive interneurones of crickets: a survey of evidence, mechanisms and benefits. J Exp Biol 204:2423–2430

    CAS  PubMed  Google Scholar 

  • Land MF (1976) Superposition images are formed by reflection in the eyes of some oceanic decapod crustacea. Nature 263:764–765

    CAS  PubMed  Google Scholar 

  • Land MF (1981) Optics and vision in invertebrates. In: Autrum H (ed) Handbook of sensory physiology, vol VII/6B. Springer, Berlin Heidelberg New York, pp 471–592

  • Land MF (1984) Crustacea. In: Ali MA (ed) Photoreception and vision in invertebrates. Plenum, New York, pp 401–438

    Google Scholar 

  • Land MF (1989) The eyes of hyperiid amphipods: relations of optical structure to depth. J Comp Physiol A 164:751–762

    Google Scholar 

  • Land MF (2000) On the functions of double eyes in midwater animals. Philos Trans R Soc London Ser B 355:1147–1150

    Article  CAS  Google Scholar 

  • Land MF, Osorio DC (1990) Waveguide modes and pupil action in the eyes of butterflies. Proc R Soc London Ser B 241:93–100

    Google Scholar 

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

    Google Scholar 

  • Land MF, Gibson G, Horwood J (1997) Mosquito eye design: conical rhabdoms are matched to wide aperture lenses. Proc R Soc London Ser B 264:1183–1187

    Article  Google Scholar 

  • Land MF, Gibson G, Horwood J, Zeil J (1999) Fundamental differences in the optical structure of the eyes of nocturnal and diurnal mosquitoes. J Comp Physiol A 185:91–103

    Article  Google Scholar 

  • Laughlin SB (1981) Neural principles in the peripheral visual systems of invertebrates. In: Autrum H (ed) Handbook of sensory physiology, Vol VII/6B. Springer, Berlin Heidelberg New York, pp 133–280

  • Laughlin SB (1990) Invertebrate vision at low luminances. In: Hess RF, Sharpe LT, Nordby K (eds) Night vision. Cambridge University Press, Cambridge, pp 223–250

    Google Scholar 

  • Laughlin SB, Blest AD, Stowe S (1980) The sensitivity of receptors in the posterior median eye of the nocturnal spider Dinopis. J Comp Physiol 141:53–65

    Google Scholar 

  • Leggett LMW, Stavenga DG (1981) Diurnal changes in angular sensitivity in crab photoreceptors. J Comp Physiol 144:99–109

    Google Scholar 

  • Lehrer M (1996) Small-scale navigation in the honeybee: active acquisition of visual information about the goal. J Exp Biol 199: 253–261

    PubMed  Google Scholar 

  • Liebmann P, Entine G (1968) Visual pigments of frog and tadpole (Rana pipens). Vision Res 8:761–775

    Article  PubMed  Google Scholar 

  • Lillywhite PG (1977) Single photon signals and transduction in an insect eye. J Comp Physiol 122:189–200

    Google Scholar 

  • Lillywhite PG, Laughlin SB (1979) Transducer noise in a photoreceptor. Nature 277:569–572

    Google Scholar 

  • Locket NA (1971) Retinal anatomy in some scopelarchid deep-sea fishes. Proc R Soc London Ser B 178:161–184

    CAS  PubMed  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

  • Locket NA (1985) The multiple bank rod foveae of Bajacalifornia drakei, an alepocephalid deep-sea teleost. Proc R Soc London Ser B 224:7–22

    Google Scholar 

  • Loew ER (1994) A third, ultraviolet-sensitive, visual pigment in the tokay gecko (Gekko gekko). Vision Res 34:1427–1431

    Article  CAS  PubMed  Google Scholar 

  • Loew ER, Govardovskii VI, Röhlich P, Szél A (1996) Microspectrophotometric and immunocytochemical identification of ultraviolet photoreceptors in geckos. Vis Neurosci 13:247–256

    CAS  PubMed  Google Scholar 

  • Losey GS, Cronin TW, Goldsmith TH, Hyde D, Marshall NJ, McFarland WN (1999) The UV visual world of fishes: a review. J Fish Biol 54:921–943

    Article  Google Scholar 

  • Lythgoe JN (1979) The ecology of vision. Clarendon Press, Oxford

    Google Scholar 

  • Martin GR (1994) Form and function in the optical structure of bird eyes. In: Davies MNO, Green PR (eds) Perception and motor control in birds: an ecological approach. Springer, Berlin Heidelberg New York, pp 5–34

    Google Scholar 

  • Martin GR, Katzir G (1999) Visual field in short-toed eagles Circaetus gallicus and the function of binocularity in birds. Brain Behav Evol 53:55–66

    Article  CAS  PubMed  Google Scholar 

  • Martin GR, Rojas LM, Ramirez Y, McNeil R (2004) The eyes of oilbirds (Steatornis caripensis): pushing at the limits of sensitivity. Naturwissenschaften 91:26–29

    Article  CAS  PubMed  Google Scholar 

  • McIntyre PD, Caveney S (1998) Superposition optics and the time of flight in onitine dung beetles. J Comp Physiol A 183:45–60

    Article  Google Scholar 

  • Moeller JF, Case JF (1994) Properties of visual interneurons in a deep-sea mysid, Gnathophausia ingens. Mar Biol 119:211–219

    Google Scholar 

  • Moeller JF, Case JF (1995) Temporal adaptations in visual systems of deep-sea crustaceans. Mar Biol 123:47–54

    Google Scholar 

  • Moon P (1940) Proposed standard solar-radiation curves for engineering use. J Franklin Inst 230:583–617

    Article  Google Scholar 

  • Motani R, Rothschild BM, Wahl W (1999) Large eyeballs in diving ichthyosaurs. Nature 402:747

    Article  CAS  Google Scholar 

  • Munk O (1980) Hvirveldyrøjet: Bygning, funktion og tilpasning. Berlingske, Copenhagen

    Google Scholar 

  • Murphy PA (1981) Celestial compass orientation in juvenile American alligators (Alligator mississippiensis). Copeia 3:638–645

    Google Scholar 

  • Murphy CJ, Evans HE, Howland HC (1985) Towards a schematic eye for the great horned owl. Fortschr Zool 30:703–706

    Google Scholar 

  • Nicol JAC (1989) The eyes of fishes. Oxford University Press, Oxford

    Google Scholar 

  • Nilsson D-E (1989) Optics and evolution of the compound eye. In: Stavenga DG, Hardie RC (eds) Facets of vision. Springer, Berlin Heidelberg New York, pp 30–73

    Google Scholar 

  • Nilsson D-E, Nilsson HL (1981) A crustacean compound eye adapted for low light intensities (Isopoda). J Comp Physiol 143:503–510

    Google Scholar 

  • Ohly KP (1975) The neurons of the first synaptic regions of the optic neuropil of the firefly, Phausius splendidula L. (Coleoptera). Cell Tissue Res 158:89–109

    CAS  PubMed  Google Scholar 

  • Partridge JC, Shand J, Archer SN, Lythgoe JN, Groningen-Luyben WAHM van (1989). Interspecific variation in the visual pigments of deep-sea fishes. J Comp Physiol A 164:513–529

    CAS  PubMed  Google Scholar 

  • Pasternak T, Merigan WH (1981) The luminance dependence of spatial vision in the cat. Vision Res 21:1333–1339

    Article  CAS  PubMed  Google Scholar 

  • Pick B, Buchner E (1979) Visual movement detection under light- and dark-adaptation in the fly, Musca domestica. J Comp Physiol A 134:45–54

    Google Scholar 

  • Ribi WA (1977) Fine structure of the first optic ganglion (lamina) of the cockroach Periplaneta americana. Tissue Cell 9:57–72

    CAS  PubMed  Google Scholar 

  • Rose A (1942) The relative sensitivities of television pickup tubes, photographic film and the human eye. Proc Inst Radio Eng New York 30:293–300

    Google Scholar 

  • Roth LSV, Kelber A (2004) Nocturnal coulour vision in geckos. Proc R Soc London Ser B, in press

  • Rozenberg GV (1966) Twilight: a study in atmospheric optics. Plenum Press, New York

    Google Scholar 

  • Scholes JH, Reichardt W (1969) The quantal content of optomotor stimuli and the electrical responses of receptors in the compound eye of the fly Musca. Kybernetik 6:74–80

    CAS  PubMed  Google Scholar 

  • Schwemer J, Paulsen R (1973) Three visual pigments in Deilephila elpenor (Lepidoptera, Sphingidae). J Comp Physiol 86:215–229

    CAS  Google Scholar 

  • Sinclair S (1985) How animals see. Facts on File Publications, New York

    Google Scholar 

  • Snyder AW (1977) Acuity of compound eyes: physical limitations and design. J Comp Physiol 116:161–182

    Google Scholar 

  • Snyder AW (1979) Physics of vision in compound eyes. In: Autrum H (ed) Handbook of sensory physiology, vol VII/6A. Springer, Berlin Heidelberg New York, pp 225–313

  • Snyder AW, Stavenga DG, Laughlin SB (1977a) Spatial information capacity of compound eyes. J Comp Physiol 116:183–207

    Google Scholar 

  • Snyder AW, Laughlin SB, Stavenga DG (1977b) Information capacity of eyes. Vision Res 17:1163–1175

    Article  CAS  PubMed  Google Scholar 

  • Sotthibandhu S, Baker RR (1979) Celestial orientation by the large yellow underwing moth, Noctua Pronuba L. Anim Behav 27:786–800

    Google Scholar 

  • Srinivasan MV, Bernard GD (1975) The effect of motion on visual acuity of the compound eye: a theoretical analysis. Vision Res 15:515–525

    Article  CAS  PubMed  Google Scholar 

  • Srinivasan MV, Dvorak DR (1980) Spatial processing of visual information in the movement-detecting pathway of the fly. J Comp Physiol 140:1–23

    Google Scholar 

  • Srinivasan MV, Laughlin SB, Dubs A (1982) Predictive coding: a fresh view of inhibition in the retina. Proc R Soc London Ser B 216:427–459

    CAS  PubMed  Google Scholar 

  • Stavenga DG (1976) Fly visual pigments: difference in visual pigments of blowfly and dronefly peripheral retinula cells. J Comp Physiol 111:137–152

    CAS  Google Scholar 

  • Stavenga DG (2003) Angular and spectral sensitivity of fly receptors. II. Dependence on facet lens F-number and rhabdomere type in Drosophila. J Comp Physiol A 189:189–202

    CAS  Google Scholar 

  • Stavenga DG (2004a) Angular and spectral sensitivity of fly receptors. III. Dependence on the pupil mechanism in the blowfly Calliphora. J Comp Physiol A 190:115–129

    Article  CAS  Google Scholar 

  • Stavenga DG (2004b) Visual acuity of fly photoreceptors in natural conditions—dependence on UV sensitizing pigment and light-controlling pupil. J Exp Biol 207:1703–1713

    Article  PubMed  Google Scholar 

  • Stavenga DG, Smits RP, Hoenders BJ (1993) Simple exponential functions describing the absorbance bands of visual pigment spectra. Vision Res 33:1011–1017

    Article  CAS  PubMed  Google Scholar 

  • Strausfeld NJ, Blest AD (1970) Golgi studies on insects. I. The optic lobes of Lepidoptera. Philos Trans R Soc London Ser B 258:81–134

    Google Scholar 

  • Tyler JE, Smith RC (1970) Measurement of spectral irradiance underwater. Gordon and Breach, New York

    Google Scholar 

  • Wagner H-J, Fröhlich E, Negishi K, Collin SP (1998) The eyes of deep sea fish II. Functional morphology of the retina. Prog Ret Eye Res 17:637–685

    Article  CAS  Google Scholar 

  • Walls GL (1942) The Vertebrate eye and its adaptive radiation. The Cranbrook Press, Bloomfield Hills

    Google Scholar 

  • Warrant EJ (1999) Seeing better at night: life style, eye design and the optimum strategy of spatial and temporal summation. Vision Res 39:1611–1630

    Article  CAS  PubMed  Google Scholar 

  • Warrant EJ (2000) The eyes of deep-sea fish and the changing nature of visual scenes with depth. Philos Trans R Soc London Ser B 355:1155–1159

    Article  CAS  Google Scholar 

  • Warrant EJ (2001) The design of compound eyes and the illumination of natural habitats. In: Barth FG, Schmid A (eds) Ecology of sensing. Springer, Berlin Heidelberg New York, pp 187–213

    Google Scholar 

  • Warrant EJ, Locket NA (2004) Vision in the deep sea. Biol Rev 79:671–712

    Article  PubMed  Google Scholar 

  • Warrant EJ, McIntyre PD (1990) Limitations to resolution in superposition eyes. J Comp Physiol A 167:785–803

    Google Scholar 

  • Warrant EJ, McIntyre PD (1991) Strategies for retinal design in arthropod eyes of low F-number. J Comp Physiol A 168:499–512

    Google Scholar 

  • Warrant EJ, McIntyre PD (1992) The trade-off between resolution and sensitivity in compound eyes. In: Pinter RB, Nabet B (eds) Nonlinear vision: determination of neural receptive fields, function, and networks. CRC Press, Boca Raton, pp 391–421

    Google Scholar 

  • Warrant EJ, McIntyre PD (1993) Arthropod eye design and the physical limits to spatial resolving power. Prog Neurobiol 40:413–461

    Article  CAS  PubMed  Google Scholar 

  • Warrant EJ, Nilsson D-E (1998) Absorption of white light in photoreceptors. Vision Res 38:195–207

    Article  CAS  PubMed  Google Scholar 

  • Warrant EJ, Porombka T, Kirchner WH (1996) Neural image enhancement allows honeybees to see at night. Proc R Soc London Ser B 263:1521–1526

    Google Scholar 

  • Warrant EJ, Collin SP, Locket NA (2003) Eye design and vision in deep-sea fishes. In: Collin SP, Marshall NJ (eds) Sensory processing of the aquatic environment. Springer, Berlin Heidelberg New York, pp 303–322

    Google Scholar 

  • Warrant EJ, Kelber A, Gislén A, Greiner B, Ribi W, Wcislo WT (2004) Nocturnal vision and landmark orientation in a tropical halictid bee. Curr Biol 14:1309–1318

    Article  CAS  PubMed  Google Scholar 

  • Waterman TH (1954) Polarisation patterns in submarine illumination. Science 120:927–932

    Google Scholar 

  • Waterman TH (1981) Polarization sensitivity. In: Autrum H (ed) Handbook of sensory physiology, vol VII 6B. Springer, Berlin Heidelberg New York, pp 281–469

  • Wcislo WT, Arneson L, Roesch K, Gonzalez V, Smith A, Fernandez H (2004) The evolution of nocturnal behaviour in sweat bees, Megalopta genalis and M. ecuadoria (Hymenoptera: Halictidae): an escape from competitors and enemies? Biol J Linnean Soc (in press)

    Google Scholar 

  • Wehner R (1981) Spatial vision in arthropods. In: Autrum H (ed) Handbook of sensory physiology, vol VII 6C. Springer, Berlin Heidelberg New York, pp 287–616

  • Wehner R (2001) Polarization vision—a uniform sensory capacity? J Exp Biol 204:2589–2596

    CAS  PubMed  Google Scholar 

  • Wikler KC, Rakic P (1990) Distribution of photoreceptor subtypes in the retina of diurnal and nocturnal primates. J Neurosci 10:3390–3401

    Google Scholar 

  • Williams DS (1982) Ommatidial structure in relation to turnover of photoreceptor membrane in the locust. Cell Tissue Res 225:595–617

    CAS  PubMed  Google Scholar 

  • Williams DS (1983) Changes of photoreceptor performance associated with the daily turnover of photoreceptor membrane in the locust. J Comp Physiol 150:509–519

    Google Scholar 

  • Wiltschko W, Daum P, Fergenbauer-Kimmel A, Wiltschko R (1987) The development of the star compass in Garden Warblers, Sylvia borin. Ethology 74:285–292

    Google Scholar 

  • Yeandle S (1958) Evidence of quantized slow potentials in the eye of Limulus. Am J Ophthalmol 46:82–87

    Google Scholar 

  • Zeil J, Kelber A, Voss R (1996) Structure and function of learning flights in bees and wasps. J Exp Biol 199:245–252

    PubMed  Google Scholar 

Download references

Acknowledgements

Much of the work presented in this review would not have been possible without the intelligence, generosity and friendship of so many students and colleagues with whom I have been privileged to collaborate, both in Lund and abroad. It is impossible to name them all, but in Lund it is equally impossible to omit naming seven: Marie Dacke, Almut Kelber, Dan-Eric Nilsson, and our past and present students Anna Balkenius, Rikard Frederiksen, Anna Gislén, and Birgit Greiner. With their laughter, genius and friendship, they have made the work outlined in this review a sheer pleasure to be involved in. I am also greatly indebted to the generosity of Professor Friedrich Barth and the Austrian Academy of Sciences who graciously invited me to deliver the Karl von Frisch Lecture upon which this review is based, and for promoting research undertaken on whole organisms. I am also very grateful to Mike Land and Doekele Stavenga for carefully reviewing the manuscript and suggesting many improvements. As always, I am very grateful to the many institutions that have supported our work over the years, including the Swedish Research Council, the Royal Physiographic Society of Lund, the Crafoord Foundation, the Wenner-Gren Foundation, the Swedish International Development Agency (SIDA) and the University of Lund. And finally, I wish to express my sincerest thanks to the man for whom this review is dedicated, Professor Rüdiger Wehner. Apart from his astonishing achievements in unravelling the secrets of polarised light navigation in animals—the scientific thrill from this alone is worth a standing ovation of thanks—Rüdiger Wehner has been an inexhaustible source of inspiration and support, not only for myself personally, but for the entire Vision Group in Lund. It is difficult to believe that such a youthful and vital man is nearing his retirement. I daresay it will pass as casually as any other date—the cataglyphid ants of the world have not divulged all of their secrets quite yet.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Eric Warrant.

Additional information

Dedicated with gratitude to Professor Rüdiger Wehner, whose life and work has inspired a generation of organismic biologists

Rights and permissions

Reprints and permissions

About this article

Cite this article

Warrant, E. Vision in the dimmest habitats on Earth. J Comp Physiol A 190, 765–789 (2004). https://doi.org/10.1007/s00359-004-0546-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00359-004-0546-z

Keywords

Navigation