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      Why do horseflies need polarization vision for host detection? Polarization helps tabanid flies to select sunlit dark host animals from the dark patches of the visual environment

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          Abstract

          Horseflies (Tabanidae) are polarotactic, being attracted to linearly polarized light when searching for water or host animals. Although it is well known that horseflies prefer sunlit dark and strongly polarizing hosts, the reason for this preference is unknown. According to our hypothesis, horseflies use their polarization sensitivity to look for targets with higher degrees of polarization in their optical environment, which as a result facilitates detection of sunlit dark host animals. In this work, we tested this hypothesis. Using imaging polarimetry, we measured the reflection–polarization patterns of a dark host model and a living black cow under various illumination conditions and with different vegetation backgrounds. We focused on the intensity and degree of polarization of light originating from dark patches of vegetation and the dark model/cow. We compared the chances of successful host selection based on either intensity or degree of polarization of the target and the combination of these two parameters. We show that the use of polarization information considerably increases the effectiveness of visual detection of dark host animals even in front of sunny–shady–patchy vegetation. Differentiation between a weakly polarizing, shady (dark) vegetation region and a sunlit, highly polarizing dark host animal increases the efficiency of host search by horseflies.

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          Most cited references43

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          The Biology of Blood-Sucking in Insects

          M Lehane (2005)
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            Visual ecology of biting flies.

            Many of the similarities in visual ecology between the Nematocera and Brachycera and within the Cyclorrhapha may reflect the evolution of blood-feeding in these groups. In Nematocera and Brachycera, blood-feeding is thought to have evolved from predatory or nectar-feeding behavior (138). Only females feed on hosts, and association with hosts generally occurs when hosts are close to the aquatic or semiaquatic habitats of the immatures. Flies feed on nectar, make appetitive flights, disperse, or migrate prior to blood-feeding, and then oviposit in water. Many species are nocturnal or crepuscular. In Cyclorrhapha, flies are closely associated with hosts. They may have arisen from compost-feeding flies that developed a larval dependence on vertebrate-produced microhabitats. Both sexes blood-feed, and mating occurs on or near hosts. Flies generally emerge in the proximity of hosts and maintain close contact with them. These species are diurnal, and their visual systems are well developed. Comparisons between closely related blood-feeding and non-blood-feeding species may provide insight into the visual ecology of blood-feeding species. Despite the different origins of hematophagy, there appears to be a convergence of morphology and behavior that is related to ecology rather than to phylogenetic relationships. This is clearly seen in host-location strategies by tsetse and tabanids. Even within groups such as mosquitoes, species that are active at the same time of day and in the same habitat have more in common than closely related species in different habitats. For this reason, an ecological review would be more cohesive than this phylogenetic discussion. However, because of the disproportionate amount of literature on a small number of groups, the phylogenetic approach is the most practical for this subject. However, this review does point out the great need for research on the less well-studied groups and behaviors.
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              The development of a multipurpose trap (the Nzi) for tsetse and other biting flies.

              S Mihok (2002)
              New trap designs for tsetse (Glossinidae), stable flies (Muscidae: Stomoxyinae), and horse flies (Tabanidae) were tested in Kenya to develop a multipurpose trap for biting flies. Many configurations and colour/fabric combinations were compared to a simplified, blue-black triangular trap to identify features of design and materials that result in equitable catches. New designs were tested against conventional traps, with a focus on Glossina pallidipes Austen and G. longipennis Corti, Stomoxys niger Macquart, and Atylotus agrestis (Wiedemann). A simple design based on minimal blue and black rectangular panels, for attraction and contrast, with a trap body consisting of an innovative configuration of netting, proved best. This 'Nzi' trap (Swahili for fly) caught as many or significantly more tsetse and biting flies than any conventional trap. The Nzi trap represents a major improvement for Stomoxyinae, including the cosmopolitan species S. calcitrans (Linnaeus), with up to eight times the catch for key African Stomoxys spp. relative to the best trap for this group (the Vavoua). Catches of many genera of Tabanidae, including species almost never caught in traps (Philoliche Wiedemann), are excellent, and are similar to those of larger traps designed for this purpose (the Canopy). Improvements in capturing biting flies were achieved without compromising efficiency for the savannah tsetse species G. pallidipes. Catches of fusca tsetse (G. longipennis and G. brevipalpis Newstead) were higher or were the same as catches in good traps for these species (NG2G, Siamese). Altogether, the objective of developing a simple, economical trap with harmonized efficiency was achieved.
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                Author and article information

                Journal
                R Soc Open Sci
                R Soc Open Sci
                RSOS
                royopensci
                Royal Society Open Science
                The Royal Society Publishing
                2054-5703
                November 2017
                8 November 2017
                8 November 2017
                : 4
                : 11
                : 170735
                Affiliations
                [1 ]Environmental Optics Laboratory, Department of Biological Physics, ELTE Eötvös Loránd University , Pázmány sétány 1, Budapest 1117, Hungary
                [2 ]Department of Zoology, Hungarian Natural History Museum, Bird Collection , Ludovika tér 2-6, Budapest 1083, Hungary
                [3 ]Department of Anatomy and Histology, University of Veterinary Medicine , István utca 2, Budapest 1078, Hungary
                [4 ]Department of Cognitive Neurosciences, University of Tübingen , Auf der Morgenstelle 28, Tübingen 72071, Germany
                [5 ]Estrato Research and Development Ltd. , Mártonlak utca 13, Budapest 1121, Hungary
                [6 ]Department of Biology, Centre for Animal Movement Research, Lund University , Ecology Building, Lund 223 62, Sweden
                Author notes
                Author for correspondence: Gábor Horváth e-mail: gh@ 123456arago.elte.hu
                Author information
                http://orcid.org/0000-0002-9008-2411
                http://orcid.org/0000-0001-9039-2180
                Article
                rsos170735
                10.1098/rsos.170735
                5717639
                29291065
                7a60e45d-536b-4db9-8363-291ba3ca0db3
                © 2017 The Authors.

                Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

                History
                : 21 June 2017
                : 5 October 2017
                Funding
                Funded by: Hungarian National Research, Development and Innovation Office;
                Award ID: grant NKFIH K-123930
                Categories
                1001
                202
                60
                1009
                151
                Biology (Whole Organism)
                Research Article
                Custom metadata
                November, 2017

                horseflies,tabanids,polarization vision,parasite–host interaction,visual ecology,imaging polarimetry

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