Phototaxis

Moths are positively phototactic

Phototaxis is a kind of taxis, or locomotory movement, that occurs when a whole organism moves towards or away from stimulus of light.[1] This is advantageous for phototrophic organisms as they can orient themselves most efficiently to receive light for photosynthesis. Phototaxis is called positive if the movement is in the direction of increasing light intensity and negative if the direction is opposite.[2]

Two types of positive phototaxis are observed in prokaryotes. The first is called scotophobotaxis (from the word "scotophobia"), which is observed only under a microscope. This occurs when a bacterium swims by chance out of the area illuminated by the microscope. Entering darkness signals the cell to reverse flagella rotation direction and reenter the light. The second type of phototaxis is true phototaxis, which is a directed movement up a gradient to an increasing amount of light. This is analogous to positive chemotaxis except that the attractant is light rather than a chemical.

Phototactic responses are observed in many organisms such as Serratia marcescens, Tetrahymena, and Euglena. Each organism has its own specific biological cause for a phototactic response, many of which are incidental and serve no end purpose.

Phototaxis in zooplankton

Phototaxis in zooplankton is well studied in the marine annelid Platynereis dumerilii:

Platynereis dumerilii trochophore and metatrochophore larvae are positively phototactic. Phototaxis there is mediated by simple eyespots that consists of a pigment cell and a photoreceptor cell. The photoreceptor cell synapses directly onto ciliated cells, which are used for swimming. The eyespots do not give spatial resolution, therefore the larvae are rotating to scan their environment for the direction where the light is coming from.[5]

Platynereis dumerilii nectochaete larvae can switch between positive and negative phototaxis. Phototaxis there is mediated by two pairs of more complex pigment cup eyes. These eyes contain more photoreceptor cells that are shaded by pigment cells forming a cup. The photoreceptor cells do not synapse directly onto ciliated cells or muscle cells but onto inter-neurons of a processing center. This way the information of all four eye cups can be compared and a low resolution image of four pixels can be created telling the larvae where the light is coming from. This way the larva does not need to scan its environment by rotating.[4] This is an adaption for living on the bottom of the sea the life style of the nectochaete larva while scanning rotation is more suited for living in the open water column, the life style of the trochophore larva. Phototaxis in the Platynereis dumerilii nectochaete larva has a broad spectral range which is at least covered by three opsins that are expressed by the cup eyes:[6] Two rhabdomeric opsins[7] and a Go-opsin.[6]

However, not every behavior that looks like phototaxis is phototaxis: Platynereis dumerilii nechtochate and metatrochophore larvae swim up first when they are stimulated with UV-light from above. But after a while, they change the direction and avoid the UV-light by swimming down. This looks like a change from positive to negative phototaxis (see video left), but the larvae also swim down if UV-light comes non-directionally from the side. And so they do not swim to or away from the light, but swim down,[3] this means to the center of gravity. Thus this is a UV-induced positive gravitaxis. Positive phototaxis (swimming to the light from the surface) and positive gravitaxis (swimming to the center of gravity) are induced by different ranges of wavelengths and cancel out each other at a certain ratio of wavelengths.[3] Since the wavelengths compositions change in water with depth: Short (UV, violet) and long (red) wavelengths are lost first[6], phototaxis and gravitaxis form a ratio-chromatic depth gauge, which allows the larvae to determine their depth by the color of the surrounding water. This has the advantage over a brightness based depth gauge that the color stays almost constant independent of the time of the day or whether it is cloudy.[8][9]

See also

Further reading

  • Madigan, Michael T.; Martinko, John M. (2006). Brock Biology of Microorganisms (11th ed.). Upper Saddle River, N.J.: Pearson/Prentice Hall. ISBN 0131443291.
  • Jékely, G. (31 August 2009). "Evolution of phototaxis". Philosophical Transactions of the Royal Society B: Biological Sciences. 364 (1531): 2795–2808. doi:10.1098/rstb.2009.0072. PMC 2781859. PMID 19720645.
  • Randel, Nadine; Jékely, Gáspár (23 November 2015). "Phototaxis and the origin of visual eyes". Philosophical Transactions of the Royal Society B: Biological Sciences. 371 (1685): 20150042. doi:10.1098/rstb.2015.0042. PMC 4685581. PMID 26598725.

References

  1. ↑ Martin, E.A., ed. (1983), Macmillan Dictionary of Life Sciences (2nd ed.), London: Macmillan Press, p. 362, ISBN 0-333-34867-2
  2. ↑ Menzel, Randolf (1979), "Spectral Sensitivity and Color Vision in Invertebrates", in H. Autrum (editor), Comparative Physiology and Evolution of Vision in Invertebrates- A: Invertebrate Photoreceptors, Handbook of Sensory Physiology, VII/6A, New York: Springer-Verlag, pp. 503–580. See section D: Wavelength-Specific Behavior and Color Vision, ISBN 3-540-08837-7
  3. 1 2 3 Verasztó, Csaba; Gühmann, Martin; Jia, Huiyong; Rajan, Vinoth Babu Veedin; Bezares-Calderón, Luis A.; Piñeiro-Lopez, Cristina; Randel, Nadine; Shahidi, Réza; Michiels, Nico K.; Yokoyama, Shozo; Tessmar-Raible, Kristin; Jékely, Gáspár (29 May 2018). "Ciliary and rhabdomeric photoreceptor-cell circuits form a spectral depth gauge in marine zooplankton". eLife. 7. doi:10.7554/eLife.36440. PMID 29809157.
  4. 1 2 3 Randel, Nadine; Asadulina, Albina; Bezares-Calderón, Luis A; Verasztó, Csaba; Williams, Elizabeth A; Conzelmann, Markus; Shahidi, Réza; Jékely, Gáspár (27 May 2014). "Neuronal connectome of a sensory-motor circuit for visual navigation". eLife. 3. doi:10.7554/eLife.02730.
  5. ↑ Jékely, Gáspár; Colombelli, Julien; Hausen, Harald; Guy, Keren; Stelzer, Ernst; Nédélec, François; Arendt, Detlev (20 November 2008). "Mechanism of phototaxis in marine zooplankton". Nature. 456 (7220): 395–399. doi:10.1038/nature07590.
  6. 1 2 3 Gühmann, Martin; Jia, Huiyong; Randel, Nadine; Verasztó, Csaba; Bezares-Calderón, Luis A.; Michiels, Nico K.; Yokoyama, Shozo; Jékely, Gáspár (August 2015). "Spectral Tuning of Phototaxis by a Go-Opsin in the Rhabdomeric Eyes of Platynereis". Current Biology. 25 (17): 2265–2271. doi:10.1016/j.cub.2015.07.017. PMID 26255845.
  7. ↑ Randel, N.; Bezares-Calderon, L. A.; Gühmann, M.; Shahidi, R.; Jekely, G. (10 May 2013). "Expression Dynamics and Protein Localization of Rhabdomeric Opsins in Platynereis Larvae". Integrative and Comparative Biology. 53 (1): 7–16. doi:10.1093/icb/ict046. PMC 3687135. PMID 23667045.
  8. ↑ Nilsson, Dan-Eric (31 August 2009). "The evolution of eyes and visually guided behavior". Philosophical Transactions of the Royal Society B: Biological Sciences. 364 (1531): 2833–2847. doi:10.1098/rstb.2009.0083. PMC 2781862. PMID 19720648.
  9. ↑ Nilsson, Dan-Eric (12 April 2013). "Eye evolution and its functional basis". Visual Neuroscience. 30 (1–2): 5–20. doi:10.1017/S0952523813000035. PMID 23578808.
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