Degrees of polarization of reflected light eliciting polarotaxis in dragonflies (Odonata), mayflies (Ephemeroptera) and tabanid flies (Tabanidae).

With few exceptions insects whose larvae develop in freshwater possess positive polarotaxis, i.e., are attracted to sources of horizontally polarized light, because they detect water by means of the horizontal polarization of light reflected from the water surface. These insects can be deceived by artificial surfaces (e.g. oil lakes, asphalt roads, black plastic sheets, dark-coloured cars, black gravestones, dark glass surfaces, solar panels) reflecting highly and horizontally polarized light. Apart from the surface characteristics, the extent of such a 'polarized light pollution' depends on the illumination conditions, direction of view, and the threshold p* of polarization sensitivity of a given aquatic insect species. p* means the minimum degree of linear polarization p of reflected light that can elicit positive polarotaxis from a given insect species. Earlier there were no quantitative data on p* in aquatic insects. The aim of this work is to provide such data. Using imaging polarimetry in the red, green and blue parts of the spectrum, in multiple-choice field experiments we measured the threshold p* of ventral polarization sensitivity in mayflies, dragonflies and tabanid flies, the positive polarotaxis of which has been shown earlier. In the blue (450nm) spectral range, for example, we obtained the following thresholds: dragonflies: Enallagma cyathigerum (0%<p*< or =17%), Ischnura elegans (17%< or =p*< or =24%). Mayflies: Baetis rhodani (32%< or =p*< or =55%), Ephemera danica, Epeorus silvicola, Rhithrogena semicolorata (55%< or =p*< or =92%). Tabanids: Tabanus bovinus, Tabanus tergestinus (32%< or =p*< or =55%), Tabanus maculicornis (55%< or =p*< or =92%).

[1]  Horváth,et al.  Polarization pattern of freshwater habitats recorded by video polarimetry in red, green and blue spectral ranges and its relevance for water detection by aquatic insects , 1997, The Journal of experimental biology.

[2]  G. Horváth,et al.  Polarized light and oviposition site selection in the yellow fever mosquito: No evidence for positive polarotaxis in Aedes aegypti , 2008, Vision Research.

[3]  R. Schwind,et al.  Polarization vision in water insects and insects living on a moist substrate , 1991, Journal of Comparative Physiology A.

[4]  R. Schwind Spectral regions in which aquatic insects see reflected polarized light , 1995, Journal of Comparative Physiology A.

[5]  Gábor Horváth,et al.  Dragonflies Find Crude Oil Visually More Attractive than Water: Multiple-Choice Experiments on Dragonfly Polarotaxis , 1998, Naturwissenschaften.

[6]  G. Horváth,et al.  How can dragonflies discern bright and dark waters from a distance? The degree of polarisation of reflected light as a possible cue for dragonfly habitat selection , 2002 .

[7]  G. Horváth,et al.  Ecological traps for dragonflies in a cemetery: the attraction of Sympetrum species (Odonata: Libellulidae) by horizontally polarizing black gravestones , 2007 .

[8]  G. Horváth,et al.  Visual ecological impact of "Shiny black anthropogenic products" on aquatic insects: Oil reservoirs and plastic sheets as polarized traps for insects associated with water , 2001 .

[9]  J. Lancaster,et al.  Aquatic Insects: Challenges to Populations , 2008 .

[10]  Rüdiger Wehner,et al.  How bees analyse the polarization patterns in the sky , 1984, Journal of Comparative Physiology A.

[11]  C. Steiner,et al.  Habitat selection in the larvae of two species of Zygoptera (Odonata): biotic interactions and abiotic limitation , 2000, Hydrobiologia.

[12]  J. Zeil,et al.  Kuwait oil lakes as insect traps , 1996, Nature.

[13]  N. Shashar,et al.  Reflected polarization guides chironomid females to oviposition sites , 2008, Journal of Experimental Biology.

[14]  Luc De Meester,et al.  Water turbidity affects predator–prey interactions in a fish–damselfly system , 2005, Oecologia.

[15]  H. Wildermuth Dragonflies Recognize the Water of Rendezvous and Oviposition Sites by Horizontally Polarized Light: A Behavioural Field Test , 1998, Naturwissenschaften.

[16]  G. Horváth,et al.  Why do red and dark-coloured cars lure aquatic insects? The attraction of water insects to car paintwork explained by reflection–polarization signals , 2006, Proceedings of the Royal Society B: Biological Sciences.

[17]  G. Horváth,et al.  Imaging polarimetry of glass buildings: why do vertical glass surfaces attract polarotactic insects? , 2008, Applied optics.

[18]  H. Wildermuth,et al.  Visual deception of a male Libellula depressa by the shiny surface of a parked car (Odonata: Libellulidae) , 2005 .

[19]  G. Horváth,et al.  Why do mayflies lay their eggs en masse on dry asphalt roads? Water-imitating polarized light reflected from asphalt attracts Ephemeroptera. , 1998, The Journal of experimental biology.

[20]  G. Horváth,et al.  Polarization vision in aquatic insects and ecological traps for polarotactic insects , 2008 .

[21]  D. Varjú,et al.  Polarized Light in Animal Vision: Polarization Patterns in Nature , 2004 .

[22]  Labhart,et al.  How polarization-sensitive interneurones of crickets perform at low degrees of polarization , 1996, The Journal of experimental biology.

[23]  Bruce A. Robertson,et al.  Polarized light pollution: a new kind of ecological photopollution , 2009 .

[24]  R. Morse The Dance Language and Orientation of Bees , 1994 .

[25]  Gábor Horváth,et al.  Ventral polarization vision in tabanids: horseflies and deerflies (Diptera: Tabanidae) are attracted to horizontally polarized light , 2008, Naturwissenschaften.

[26]  G. Horváth,et al.  Positive polarotaxis in a mayfly that never leaves the water surface: polarotactic water detection in Palingenia longicauda (Ephemeroptera) , 2007, Naturwissenschaften.

[27]  G. Horváth,et al.  Glass buildings on river banks as “polarized light traps” for mass-swarming polarotactic caddis flies , 2008, Naturwissenschaften.

[28]  G. Horváth,et al.  Why is it worth flying at dusk for aquatic insects? Polarotactic water detection is easiest at low solar elevations , 2004, Journal of Experimental Biology.

[29]  G. Horváth,et al.  A ‘polarisation sun‐dial’ dictates the optimal time of day for dispersal by flying aquatic insects , 2006 .