The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Extra-Visual Systems in the Spatial Reorientation of Cavefish
Open accessAbstract
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
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]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Regressive Evolution in Astyanax Cavefish
Jeffery, W. R. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102108-134216 · Cited by 298
Flagged first, then by citations
Research works printed but not linked: 69
- Cheng, K. A purely geometric module in the rat’s spatial representation. Cognition 23, 149–178 (1986). · DOI
- 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
- 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
- Twiman, A. D. & Newcomb, N. S. Five reasons to doubt the existence of a geometric module. Cogn. Sci. 34, 1315–1356 (2010). · DOI
- 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
- 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).
- 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
- 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
- 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
- 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).
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Hermer, L. & Spelke, E. S. A geometric process for spatial reorientation in young children. Nature 370, 57–59 (1994). · DOI
- 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
- 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
- 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
- Wystrach, A. & Beugnon, G. Ants learn geometry and features. Curr. Biol. 19, 61–66 (2009). · DOI
- 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).
- Sovrano, V. A., Rigosi, E. & Vallortigara, G. Reorientation by geometry in bumblebees. Plos One 7, e37449 (2012). · DOI
- Sovrano, V. A., Potrich, D. & Vallortigara GLearning of geometry and features in bumblebees (Bombus terrestris). J. Comp. Psychol. 127, 312–318 (2013). · DOI
- 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
- Chiandetti, C. & Vallortigara, G. Experience and geometry: controlled-rearing studies with chicks. Anim. Cogn. 13, 463–470 (2010). · DOI
- 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
- 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
- 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
- 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
- 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).
- 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).
- Pecchia, T. & Vallortigara, G. View-based strategy for reorientation by geometry. J. Exp. Biol. 213, 2987–2996 (2010). · DOI
- 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
- Gould, J. L. The local map of honey-bee: Do insects have cognitive maps? Science 232, 861–863 (1986). · DOI
- Trajano, E., Bichuette, M. E., & Kapoor, B. G. Biology of subterranean fishes. (CRC Press, 2010). · DOI
- 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
- 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
- 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).
- 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
- Bleckmann, H. & Zelick, R. Lateral line system of fish. Integr. Zool. 4, 13–25 (2009). · DOI
- 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
- Alunni, A. et al. Developmental mechanisms for retinal degeneration in the blind cavefish Astyanax mexicanus. J. Comp. Neurol. 505, 221–233 (2007). · DOI
- Soares, D. & Niemiller, M. L. Sensory Adaptations of Fishes to Subterranean Environments. BioScience 63, 274–283 (2013). · DOI
- 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
- 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
- Teyke, T. Collision with and avoidance of obstacles by blind cave fish Anoptichthys jordani (Characidae). J. Comp. Physiol. A 157, 837–843 (1985). · DOI
- Teyke, T. Learning and remembering the environment in the blind cave fish Anoptichthys jordani. J. Comp. Physiol. A 164, 655–662 (1989). · DOI
- 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
- 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
- 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
- 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
- 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
- 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
- Borowsky R. Cavefishes. Curr. Biol. 28, R51–R65 (2018). · DOI
- 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
- 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
- Flammang, B. E., Suvarnaraksha, A., Markiewicz, J. & Soares, D. Tetrapod-like pelvic girdle in a walking cavefish. Sci. Rep. 6, 23711 (2016). · DOI
- Holzman, R., Perkol-Finkel, S. & Zilman, G. Mexican blind cavefish use mouth suction to detect obstacles. J. Exp. Biol. 217, 1955–1962 (2014). · DOI
- 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).
- 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
- 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
- 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
- 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
- Cavallari, N. et al. A blind circadian clock in cavefish reveals that opsins mediate peripheral clock photoreception. PLoS Biol. 9, e1001142 (2011). · DOI
- 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
- Sutherland, N. S., & Mackintosh, N. J. Mechanisms of animal discrimination learning. (Academic Press,1971).
- Caro, T. M., Roper, R., Young, M. & Dank, R. Inter-observer reliability. Behaviour 69, 3–4 (1979).
Cited by
Sorted by citations
Spatial Cognition in Teleost Fish: Strategies and Mechanisms
Rodríguez, F., Quintero, B., Amores, L., Madrid, D., Salas-Peña, C., & Salas, C. (2021) · Animals · doi:10.3390/ani11082271 · Cited by 59
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)
- PMC
- PMC6283829
- 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
- gold
- doi.org
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review