Cited by 19Spatial Cognition and NavigationSubterranean biodiversity and taxonomyFish biology, ecology, and behavior

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Extra-Visual Systems in the Spatial Reorientation of Cavefish

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Abstract

Disoriented humans and animals are able to reorient themselves using environmental geometry (“metric properties” and “sense”) and local features, also relating geometric to non-geometric information. Here we investigated the presence of these reorientation spatial skills in two species of blind cavefish (Astyanax mexicanus and Phreatichthys andruzzii), in order to understand the possible role of extra-visual senses in similar spatial tasks. In a rectangular apparatus, with all homogeneous walls (geometric condition) or in presence of a tactilely different wall (feature condition), cavefish were required to reorient themselves after passive disorientation. We provided the first evidence that blind cavefish, using extra-visual systems, were able i) to use geometric cues, provided by the shape of the tank, in order to recognize two geometric equivalent corners on the diagonal, and ii) to integrate the geometric information with the salient cue (wall with a different surface structure), in order to recover a specific corner. These findings suggest the ecological salience of the environmental geometry for spatial orientation in animals and, despite the different niches of adaptation, a potential shared background for spatial navigation. The geometric spatial encoding seems to constitute a common cognitive tool needed when the environment poses similar requirements to living organisms.

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  • A number of studies have demonstrated that teleost fish can rely on the geometry or global shape of the environmental boundaries and surfaces for orientation and navigation.

    “a number of studies have demonstrated also that teleost fish can rely on the geometry or global shape of the environmental boundaries and surfaces for orientation and navigation”

    From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [24]

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  1. Cheng, K. A purely geometric module in the rat’s spatial representation. Cognition 23, 149–178 (1986). · DOI
  2. Cheng, K. & Newcomb, N. S. Is there a geometric module for spatial orientation? Squaring theory and evidence. Psychon. Bull. Rev. 12, 1–23 (2005). · DOI
  3. Tommasi, L., Chiandetti, C., Pecchia, T., Sovrano, V. A. & Vallortigara, G. From natural geometry to spatial cognition. Neurosci. Biobehav. Rev. 36, 799–824 (2012). · DOI
  4. Twiman, A. D. & Newcomb, N. S. Five reasons to doubt the existence of a geometric module. Cogn. Sci. 34, 1315–1356 (2010). · DOI
  5. Sovrano, V. A., Bisazza, A. & Vallortigara, G. Modularity and spatial reorientation in a simple mind: Encoding of geometric and nongeometric properties of a spatial environment by fish. Cognition 85, 51–59 (2002). · DOI
  6. Sovrano, V. A., Bisazza, A. & Vallortigara, G. Modularity as a fish views it: Conjoining geometric and nongeometric information for spatial reorientation. J. Exp. Psychol.: Anim. Behav. Process. 29, 199–210 (2003).
  7. Sovrano, V. A., Bisazza, A. & Vallortigara, G. Animal’s use of landmarks and metric information to reorient: Effects of size of experimental space. Cognition 97, 121–133 (2005). · DOI
  8. Sovrano, V. A., Bisazza, A. & Vallortigara, G. How fish do geometry in large and small spaces. Anim. Cogn. 10, 47–54 (2007). · DOI · Paper page
  9. Vargas, J. P., Lopez, J. C., Salas, C. & Thinus-Blanc, C. Encoding of geometric and featural spatial information by Goldfish (Carassius auratus). J. Comp. Psychol. 118, 206–216 (2004). · DOI · Paper page
  10. Lee, S. A., Vallortigara, G., Ruga, V. & Sovrano, V. A. Independent effects of geometry and landmark in a spontaneous reorentation task: A study of two species of fish. Anim. Cogn. 12, 661–870 (2012).
  11. Lee, S. A., Vallortigara, G., Flore, M., Spelke, E. & Sovrano, V. A. Navigation by environmental geometry: The use of zebrafish as a model. J. Exp. Biol. 216, 3693–3699 (2013). · DOI · Paper page
  12. Lee, S. A., Ferrari, A., Vallortigara, G. & Sovrano, V. A. Boundary primacy in spatial mapping: Evidence from zebrafish (Danio rerio). Behav. Process. 119, 116–122 (2015). · DOI
  13. Vallortigara, G., Zanforlin, M. & Pasti, G. Geometric modules in animals’ spatial representations: a test with chicks (Gallus gallus domesticus). J. Comp. Psychol. 104, 248–254 (1990). · DOI
  14. Kelly, D. M., Spetch, M. L. & Heth, C. D. Pigeons’ (Columba livia) encoding of geometric and featural properties of a spatial environment. J. Comp. Psychol. 112, 259–269 (1998). · DOI
  15. Vallortigara, G., Pagni, P. & Sovrano, V. A. Separate geometric and non-geometric modules for spatial reorientation: Evidence from a lopsided animal brain. J. Cogn. Neurosci. 16, 390–400 (2004). · DOI
  16. Sovrano, V. A. & Vallortigara, G. Dissecting the geometric module: A sense linkage for metric and landmark information in animals’ spatial reorientation. Psychol. Sci. 17, 616–621 (2006). · DOI
  17. Chiandetti, C., Regolin, L., Sovrano, V. A. & Vallortigara, G. Spatial reorientation: The effects of space size on the encoding of landmark and geometry information. Anim. Cogn. 10, 159–168 (2007). · DOI
  18. Hermer, L. & Spelke, E. S. A geometric process for spatial reorientation in young children. Nature 370, 57–59 (1994). · DOI
  19. Gouteux, S., Thinus-Blanc, C. & Vauclair, J. Rhesus monkeys use geometry and nongeometric information during a reorientation task. J. Exp. Psychol.: General 130, 505–519 (2001). · DOI
  20. Twiman, A. D., Newcomb, N. S. & Gould, T. J. Of Mice (Mus musculus) and toddlers (Homo sapiens): Evidence for species-general spatial reorientation. J. Comp. Psychol. 123, 342–345 (2009). · DOI
  21. Lee, S. A., Tucci, V., Sovrano, V. A. & Vallortigara, G. Working Memory and Reference Memory Tests of Spatial Navigation in Mice (Mus musculus). J. Comp. Psychol. 129, 189–197 (2015). · DOI
  22. Wystrach, A. & Beugnon, G. Ants learn geometry and features. Curr. Biol. 19, 61–66 (2009). · DOI
  23. Wystrach, A., Cheng, K., Sosa, S. & Beugnon, G. Geometry, features and panoramic views: ants in rectangular arenas. J. Comp. Psychol.: Anim. Behav. Process. 37, 420–35 (2011).
  24. Sovrano, V. A., Rigosi, E. & Vallortigara, G. Reorientation by geometry in bumblebees. Plos One 7, e37449 (2012). · DOI
  25. Sovrano, V. A., Potrich, D. & Vallortigara GLearning of geometry and features in bumblebees (Bombus terrestris). J. Comp. Psychol. 127, 312–318 (2013). · DOI
  26. Chiandetti, C. & Vallortigara, G. Is there an innate geometric module? Effects of experience with angular geometric cues on spatial re-orientation based on the shape of the environment. Anim. Cogn. 11, 139–146 (2008). · DOI
  27. Chiandetti, C. & Vallortigara, G. Experience and geometry: controlled-rearing studies with chicks. Anim. Cogn. 13, 463–470 (2010). · DOI
  28. Chiandetti, C., Spelke, E. S. & Vallortigara, G. Inexperienced newborn chicks use geometry to spontaneously reorient to an artificial social partner. Developmental Sci. 18, 972–978 (2010). · DOI
  29. Brown, A. A., Spetch, M. L. & Hurd, P. L. Growing in circles: Rearing environments alter spatial navigation in fish. Psychol. Sci. 18, 569–573 (2007). · DOI
  30. Sovrano, V. A. & Chiandetti, C. Reorientation ability in redtail splitfin (Xenotoca eiseni): Role of environmental shape, rearing in group and exposure time. Biol. Comm. 62, 51–60 (2017). · DOI
  31. Vallortigara, G., Sovrano, V. A. & Chiandetti, C. Doing Socrates experiment right: controlled rearing studies of geometrical knowledge in animals. Curr. Opin. Neurobiol. 19, 20–26 (2009). · DOI
  32. Cheung, A., Stûrzl, W., Zeil, J. & Cheng, K. The information content of panoramic images II: View-based navigation in nonrectangular experimental arenas. J. Comp. Psychol.: Anim. Behav. Process. 34, 15–30 (2008).
  33. Stûrzl, W., Cheung, A., Zeil, J. & Cheng, K. The information content of panoramic images I: The rotational errors and the similarity of views in rectangular experimental arenas. J. Comp. Psychol.: Anim. Behav. Process. 34, 1–14 (2008).
  34. Pecchia, T. & Vallortigara, G. View-based strategy for reorientation by geometry. J. Exp. Biol. 213, 2987–2996 (2010). · DOI
  35. Pecchia, T., Gagliardo, A. & Vallortigara, G. Stable panoramic views facilitate snap-shot like memories for spatial reorientation in homing pigeons. Plos One 6, 1–5 (2011). · DOI
  36. Gould, J. L. The local map of honey-bee: Do insects have cognitive maps? Science 232, 861–863 (1986). · DOI
  37. Trajano, E., Bichuette, M. E., & Kapoor, B. G. Biology of subterranean fishes. (CRC Press, 2010). · DOI
  38. Yoshizawa, M., Yamamoto, Y., O’Quin, K. E. & Jeffery, W. R. Evolution of an adaptive behavior and its sensory receptors promotes eye regression in blind cavefish. BMC Biology 10, 108 (2012). · DOI
  39. Foulkes, N. S., Whitmore, D., Vallone, D. & Bertolucci, C. Studying the evolution of the vertebrate circadian clock: The power of fish as comparative models. In “Genetics, Genomics and Fish Phenomics” (Edited by Nicholas S. Foulkes); Adv. Genet. 95, 1–30 (Elsevier, 2016). · DOI
  40. Bleckmann, H. Reception of hydrodynamic stimuli in aquatic and semiaquatic animals in Progress in Zoology (ed. Rathmayer, W.), vol. 41 pp. 1–115. (Gustav Fischer, 1994).
  41. von der Emde, G. Non-visual environmental imaging and object detection through active electrolocation in weakly electric fish. J. Comp. Physiol. A 192, 601–612 (2006). · DOI
  42. Bleckmann, H. & Zelick, R. Lateral line system of fish. Integr. Zool. 4, 13–25 (2009). · DOI
  43. Stemmer, M., Schuhmacher, L. N., Foulkes, N. S., Bertolucci, C. & Wittbrodt, J. Cavefish eye loss in response to an early block in retinal differentiation progression. Development 142, 743–752 (2015). · DOI
  44. Alunni, A. et al. Developmental mechanisms for retinal degeneration in the blind cavefish Astyanax mexicanus. J. Comp. Neurol. 505, 221–233 (2007). · DOI
  45. Soares, D. & Niemiller, M. L. Sensory Adaptations of Fishes to Subterranean Environments. BioScience 63, 274–283 (2013). · DOI
  46. Montgomery, J. C., Coombs, S. & Baker, C. F. The mechanosensorylateral line system of the hypogean form of Astyanax fasciatus. Environ. Biol. Fishes 62, 87–96 (2001). · DOI
  47. Dezfuli, B. S., Capuano, S., Magosso, S., Giari, L. & Berti, R. The lateral line system in larvae of the blind cyprinid cavefish. Phreatichthys andruzzii. Anat. Rec. (Hoboken) 292, 423–430 (2009). · DOI
  48. Teyke, T. Collision with and avoidance of obstacles by blind cave fish Anoptichthys jordani (Characidae). J. Comp. Physiol. A 157, 837–843 (1985). · DOI
  49. Teyke, T. Learning and remembering the environment in the blind cave fish Anoptichthys jordani. J. Comp. Physiol. A 164, 655–662 (1989). · DOI
  50. Burt de Perera, T. Spatial parameters encoded in the spatial map of the blind Mexican cave fish, Astyanax fasciatus. Anim. Behav. 68, 291–295 (2004). · DOI
  51. Burt de Perera, T., De Vos, A. & Guilford, T. The vertical component of a fish’s spatial map. Anim. Behav. 70, 405–409 (2005). · DOI
  52. Sutherland, L., Holbrook, R. I. & Burt De Perera, T. Sensory system affects orientational strategy in a short-range spatial task in blind and eyed morphs of the fish, Astyanax fasciatus. Ethology 115, 504–510 (2009). · DOI
  53. Holbrook, R. I. & Burt De Perera, T. Separate encoding of vertical and horizontal components of space during orientation in fish. Anim. Behav. 78, 241–245 (2009). · DOI
  54. Sganci, S., Ceccolini, F. & Berti, R. Non visual discrimination of shapes in the blind cave cyprinid Phreatichtys andruzzi Vinciguerra 1924. Ethol. Ecol. Evol. 22, 353–358 (2010). · DOI
  55. Bisazza, A., Tagliapietra, C., Bertolucci, C., Foà, A. & Agrillo, C. Non-visual numerical discrimination in a blind cavefish (Phreatichthys andruzzii). J. Exp. Biol. 217, 1902–1909 (2014). · DOI
  56. Borowsky R. Cavefishes. Curr. Biol. 28, R51–R65 (2018). · DOI
  57. Von der Emde, G. & Bleckmann, H. Finding food: senses involved in foraging for insect larvae in the electric fish Gnathonemus petersii. J. Exp. Biol. 201, 969–980 (1998). · DOI
  58. Windsor, S. P., Norris, S. E., Cameron, S. M., Mallinson, G. D. & Montgomery, J. C. The flow fields involved in hydrodynamic imaging by blind Mexican cave fish (Astyanax fasciatus). Part I: open water and heading towards a wall. J. Exp. Biol. 213, 3819–3831 (2010). · DOI
  59. Flammang, B. E., Suvarnaraksha, A., Markiewicz, J. & Soares, D. Tetrapod-like pelvic girdle in a walking cavefish. Sci. Rep. 6, 23711 (2016). · DOI
  60. Holzman, R., Perkol-Finkel, S. & Zilman, G. Mexican blind cavefish use mouth suction to detect obstacles. J. Exp. Biol. 217, 1955–1962 (2014). · DOI
  61. Pearce, J. M., Good, M. A., Jones, P. M. & McGregor, A. Transfer of spatial behavior between different environments: Implications for theories of spatial learning and for the role of the hippocampus in spatial learning. J. Exp. Psychol.: Anim. Behav. Process. 30, 135–147 (2004).
  62. Schumacher, S., Burt de Perera, T. & von der Emde, G. Electrosensory capture during multisensory discrimination of nearby objects in the weakly electric fish Gnathonemus petersii. Sci. Rep. 7, 43665 (2017). · DOI
  63. Schumacher, S., von der Emde, G. & Burt de Perera, T. Sensory influence on navigation in the weakly electric fish Gnathonemus petersii. Anim. Behav. 132, 1–12 (2017). · DOI
  64. Graff, C., Kaminski, G., Gresty, M. & Ohlmann, T. Fish perform spatial pattern recognition and abstraction by exclusive use of active electrolocation. Curr. Biol. 14, 818–823 (2004). · DOI
  65. Calderoni, L. et al. Relaxed selective constraints drove functional modifications in peripheral photoreception of the cavefish Phreatichthys andruzzii and provide insight into the time of cave colonization. Heredity 117, 383–392 (2016). · DOI
  66. Cavallari, N. et al. A blind circadian clock in cavefish reveals that opsins mediate peripheral clock photoreception. PLoS Biol. 9, e1001142 (2011). · DOI
  67. Coghill, L. M., Hulsey, C. D., Chaves-Campos, J., de Leon, F. J. G. & Johnson, S. G. Next generation phylogeography of cave and surface Astyanax mexicanus. Mol. Phylogenet. Evol. 79, 368–374 (2014). · DOI
  68. Sutherland, N. S., & Mackintosh, N. J. Mechanisms of animal discrimination learning. (Academic Press,1971).
  69. Caro, T. M., Roper, R., Young, M. & Dank, R. Inter-observer reliability. Behaviour 69, 3–4 (1979).

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Metadata

Authors
Sovrano, V. A., Potrich, D., Foà, A., & Bertolucci, C.
Affiliations
  • University of Trento (IT)
  • University of Ferrara (IT)
Corresponding author
Sovrano, Valeria Anna
Venue
Scientific Reports
Published
2018-12-06
Volume
8
Issue
1
Pages
17698-17698
ISSN
2045-2322 (ISSN-L)
OpenAlex
W2902175327
Cited by
19
References
1
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 4 · 2021: 3 · 2020: 4 · 2019: 2
FWCI
1.19
Type
journal article
Language
en
Open access
Locations
  • Scientific Reports (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, other-oa)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Institutional Research Information System (Università degli Studi di Trento) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
  • Institutional Research Information System University of Ferrara (University of Ferrara) (submittedVersion, cc-by)
Funders
Università degli Studi di Ferrara (FAR 2014)
Topics
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
  • Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Subterranean biodiversity and taxonomy
  • Physical Sciences › Environmental Science › Nature and Landscape Conservation › Fish biology, ecology, and behavior
Keywords
spatial reorientation, blind cavefish, Astyanax mexicanus, environmental geometry, geometric cues, tactile cues, disorientation, spatial navigation, animal cognition
MeSH terms
Animals, Cues, Discrimination Learning, Fishes, Orientation, Pattern Recognition, Visual, Space Perception

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