Abstract
In the face of the neodarwinian paradigm of selection as an agent exclusively claimed to explain evolutionary processes in recent days, almost countless efforts have been made to prove that selection plays an important role in rudimentation processes in cave animals. Efforts mostly focus on the eye and very often pleiotropy is looked upon as being responsible. For example, eye reduction is claimed to antagonistically drive the improvement of taste or the lateral line sense by pleiotropy. However, this could not be confirmed by crossing analysis or by quantitative trait loci mapping. Energy savings have been suggested as another selection factor. This hypothesis implies that all cave species would have to suffer from food limitation. This attempt ignores the fact that the majority of tropical caves, and even some subtropical ones, abound in energy supply. Nonetheless, the traits, having become functionless in the respective cave species occurring in these habitats, regress. Thus, energy limitation is not able to explain regressive evolution of biologically functionless traits in general, or in particular that of the eye in cave species. In fact, independent inheritance of traits suggests that Astyanax cave fish are subjected to mosaic evolution.
Besides, selection variability plays a central role in Darwin’s concept of evolution. Even in the 1930s, the German evolutionary geneticist Curt Kosswig recognized the importance of the variability exhibited by biologically functionless regressive traits for the interpretation of regressive evolution. According to him, in such traits high phenotypic variability arises and is continuously exhibited for a longer time because a biological function no longer exists. He proposed that this variability was due to the absence of stabilizing selection, because regressive mutations are no longer eliminated and traits become reduced over time merely by their accumulation. Thus, variability and loss are correlated. This so-called “Neutral Mutation Theory” is in accordance with Nei’s “Neutral Theory of Molecular Evolution” which applies to molecular evolution. However, Darwin’s loss without selection is one of two sides of the same coin, the other being “Darwin’s gain”, in which variability is the basis of constructive evolution. However, usually variability does not exhibit an extent as conspicuous as in the case of functionless cave animal traits. There are only a few examples in which variability, for a relatively short period of time, becomes obvious during evolution. This occurs during the initial phase of processes of adaptive radiation, as can be observed in a series of fish species flocks.
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References
Aspiras AC, Rohner N, Martineau B et al (2015) Melanocortin 4 receptor mutations contribute to the adaptation of cavefish to nutrient-poor conditions. Proc Natl Acad Sci U S A 112:9668–9673
Barlow GW (2000) The cichlid fishes. Nature’s grand experiment in evolution. Perseus Publishing, Cambridge
Barr TC (1968) Cave ecology and the evolution of troglobites. In: Dobzhansky T, Hecht MK, Steere WC (eds) Evolutionary biology. Plenum Press, New York, pp 35–101
Barton RA, Harvey PH (2000) Mosaic evolution of brain structure in mammals. Nature 405:1955–1058
Beleza JC, Santos AM, McEvoy B et al (2012) The timing of pigmentation lightening in Europeans. Mol Biol Evol 30(1):24–35. doi:10.1093/molbev/mss207
Besharse JC, Brandon RA (1974) Effects of continuous light and darkness on the eyes of the troglobitic salamander Typhlotriton spelaeus. J Morphol 149:527–546
Bibliowicz J, Alié A, Père S et al (2013) Differences in chemosensory response between eyed and eyeless Astyanax mexicanus of the Rio Subterráneo cave. EvoDevo 4:25–31
Bilandžija H, Parkhurst A, Jeffery WR (2013) A potential benefit of albinism in Astyanax cavefish: downregulation of the oca2 gene increases tyrosine and catecholamine levels as an alternative to melanin synthesis. PLoS One 8:1–14
Borowsky RL (2015) Regressive evolution: testing hypotheses of selection and drift. In: Keene AC, Yoshizawa M, McGaugh SE (eds) Biologiy and evolution of the Mexican cavefish. Elsevier, Amsterdam, pp 93–107
Borowsky RL, Cohen D (2013) Genomic consequences of ecological speciation in Astyanax cavefish. PLoS One 8(11):e79903. doi:10.1371/journal.pone.0079903
Calderoni L, Rota-Stabelli O, Frigato E et al (2016) Relaxed selective constraints drove functional modifications in peripheral photoreception of the cavefish P. andruzzii and provide insight into the time of cave colonization. Heredity 117:383–392
Covich A, Stuiver M (1974) Changes in oxygen 18 as a measure of long-term fluctuations in tropical lake levels and molluscan populations. Limnol Oceanogr 19:682–691
Crish SD, Dengler-Crish C, Catania KC (2006) Central visual system of the naked mole-rat (Heterocephalus glaber). Anat Rec A Discov Mol Cell Evol Biol 288(2):205–212
Culver DC (1987) Eye morphometrics of cave and spring populations of Gammarus minus (Amphipoda: Gammaridae). J Crustac Biol 7:136–147
Culver DC, Kane TC, Fong DW (1995) Adaptation and natural selection in caves. Harvard University Press, Cambridge
Davies WL (2011) Adaptive gene loss in vertebrates: photosensitivity as a model case. In: Encyclopedia of life sciences (ELS). Wiley, Chichester. doi:10.1002/9780470015902.a0022890
Deharveng L, Bedos A (2000) The cave fauna of Southeast Asia. Origin, evolution and ecology. In: Wilkens H, Culver DC, Humphreys WF (eds) Ecosystems of the world: subterranean ecosystems, vol 30. Elsevier, Amsterdam, pp 603–632
Dillman CB, Bergstrom DE, Noltie DB et al (2010) Regressive progression, progressive regression or neither? Phylogeny and evolution of the Percopsiformes (Teleostei, Paracanthopterygii). Zool Scr 40:45–60
Dollo L (1893) Les lois de l’évolution. Bull Soc Belge Geol Pal Hydr VII:164–166
Duboué ER, Keene AC, Borowsky RL (2011) Evolutionary convergence on sleep loss in cavefish populations. Curr Biol 21:671–676
Eigenmann CH (1909) Cave vertebrates of America. Carnegie Inst Wash Publ 104:1–241
Elipot Y, Hinaux H, Callebert J et al (2013) Evolutionary shift from fighting to foraging in blind cavefish through changes in the serotonin network. Curr Biol 23:1–10
Ellis R (1996) Deep Atlantic: life, death, and exploration in the abyss. The Lions Press, New York
Emerling CA, Springer MS (2014) Eyes underground: regression of visual protein networks in subterranean mammals. Mol Phylogenet Evol 78:260–270
Espinasa L, Borowsky RL (2000) Eyed cave fish in a karst window. J Cave Karst Stud 62:180–183
Fernandes CS, Batalha MA, Bichuette ME (2016) Does the cave environment reduce functional diversity? PLoS One 11(3):e0151958. doi:10.1371/journal.pone.0151958
Freese E, Yoshida A (1965) The role of mutations in evolution. In: Bryson V, Vogel HJ (eds) Evolving genes and proteins. Academic, New York, pp 341–355
Gnaspini P, Trajano E (2000) Guano communities in tropical caves. In: Wilkens H, Culver DC, Humphreys WF (eds) Ecosystems of the world: subterranean ecosystems, vol 30. Elsevier, Amsterdam, pp 251–268
Gross JM, Perkins BD (2008) Zebrafish mutants as models for congenital ocular disorders in humans. Mol Reprod Dev 75:547–555
Gross JB, Borowsky RL, Tabin CJ (2009) A novel role for Mc1r in the parallel evolution of depigmentation in independent populations of the cave fish, Astyanax mexicanus. PLoS Genet 5:1–14
Hausberg C (1995) Das Aggressionsverhalten von Astyanax fasciatus (Cuvier 1819; Characidae, Teleostei): Ontogenie, Genetik und Evolution bei der epigäischen und hypogäischen Form. Dissertation, University of Hamburg
Hinaux H, Poulain J, Da Silva C et al (2013) De novo sequencing of Astyanax mexicanus surface fish and Pachón cavefish transcriptomes reveals enrichment of mutations in cavefish putative eye genes. PLoS One 8(1):e53553. doi:10.1371/journal.pone.0053553
Hinaux H, Blin M, Fumey J et al (2015) Lens defects in Astyanax mexicanus cavefish: evolution of crystallins and a role for alphaA-crystallin. Dev Neurobiol 75(5):505–521
Hinaux H, Devos L, Blin M et al (2016) Sensory evolution in blind cavefish is driven by early embryonic events during gastrulation and neurulation. Development 143:4521–4532. doi:10.1242/dev.141291
Hoch H (2000) Acoustic communication in darkness. In: Wilkens H, Culver DC, Humphreys WF (eds) Ecosystems of the world: subterranean ecosystems, vol 30. Elsevier, Amsterdam, pp 211–220
Hodell DA, Curtis JH, Brenner M (1995) Possible role of climate in the collapse of classic maya civilization. Nature 375:391–394
Hodell DA, Brenner M, Curtis JH et al (2001) Solar forcing of drought frequency in the Maya lowlands. Science 292:1367–1370
Hoffman S, Hausberg C (1993) The aggressive behavior of the Micos cave population (Astyanax fasciatus, Characidae, Teleostei) after selection for functional eyes in comparison to an epigean one. Mémoires de Biospéléologie 20:101–103
Horstkotte J, Strecker U (2005) Trophic differentiation in the phylogenetically young Cyprinodon species flock (Cyprinodontidae, Teleostei) from Laguna Chichancanab (Mexico). Biol J Linn Soc 85:125–134
Huber R, Staaden MJ van, Kaufman LS et al (1997) Microhabitat use, trophic patterns, and the evolution of brain structure in African cichlids. Brain Behav Evol 50:167–182
Humphries JM (1984) Cyprinodon verecundus n. sp., a fifth species of pupfish from Laguna Chichancanab. Copeia 1984:58–68
Humphries JM, Miller RR (1981) A remarkable species flock of Cyprinodon from Lake Chichancanab, Yukatan, Mexico. Copeia 1981:52–64
Hüppop K (1989) Genetic analysis of oxygen consumption rate in cave and surface fish of Astyanax fasciatus (Characidae, Pisces). Further support for the neutral mutation theory. Mémoires de Biospéléologie 16:163–168
Hüppop K (2000) How do cave animals cope with the food scarcity in caves? In: Wilkens H, Culver DC, Humphreys WF (eds) Ecosystems of the world: subterranean ecosystems, vol 30. Elsevier, Amsterdam, pp 159–188
Hüppop K (2012) Adaptation to low food. In: White WB, Culver DC (eds) Encyclopedia of caves, 2nd edn. Elsevier, Amsterdam, pp 1–9
Hüppop K, Wilkens H (1991) Bigger eggs in subterranean Astyanax fasciatus. Z Zool Syst Evol 29:280–288
Jeffery WR (2005) Adaptive evolution of eye degeneration in the Mexican blind cavefish. J Hered 96:185–196
Jeffery WR, Ma L, Parkhurst A et al (2015) Pigment regression and albinism in Astyanax cavefish. In: Keene AC, Yoshizawa M, McGaugh SE (eds) Biology and evolution of the Mexican cavefish. Elsevier, Amsterdam, pp 155–171
Jónasson PM (1992) The ecosystem of Thingvallavatn: a synthesis. Oikos 64:405–434
Jónasson PM (1993) Continental rifting-energy pathways of two contrasting rift lakes. Verhandlungen des Internationalen Vereins für Limnologie 25:1–14
Jónasson PM (1998) Continental rifting and habitat formation: Arena for resource polymorphism in Arctic charr. Ambio 27:162–169
Juberthie-Jupeau L (1976) Sur le système neurosécréteur du pédoncule oculaire d’un décapode souterrain microphthalme Typhlatya garciai Chace. Ann Spéléol 31:107–114
Katz PS (2011) Neural mechanisms underlying the evolvability of behavior. Philos Trans R Soc Lond B Biol Sci 366:2086–2090
Katz PS, Lillvis JL (2014) Reconciling the deep homology of neuromodulation with the evolution of behavior. Curr Opin Neurobiol 29:39–47. doi:10.1016/j.conb.2014.05.002
Kim B-M, Kang S, Ahn DH et al (2017) First insights into the subterranean crustacean Bathynellacea transcriptome: transcriptionally reduced opsin repertoire and evidence of conserved homeostasis regulatory mechanisms. PLoS One 12(1):e0170424. doi:10.1371/journal
Kimura M (1968) Evolutionary rate at the molecular level. Nature 217:624–626
King JL, Jukes TH (1969) Non-Darwinian evolution. Science 164:788–797
Kodric-Brown A, Strecker U (2001) Responses of Cyprinodon maya and C. labiosus females to visual and olfactory cues of conspecific and heterospecific males. Biol J Linn Soc 74:541–548
Konec M, Delić T, Trontelj P (2016) DNA barcoding sheds light on hidden subterranean boundary between Adriatic and Danubian drainage basins. Ecohydrology 9:1304–1312. doi:10.1002/eco.1727
Kosswig C (1935) Die Evolution von “Anpassungs”-Merkmalen bei Höhlentieren in genetischer Betrachtung. Zool Anz 112:148–155
Kosswig C (1949) Phänomene der regressiven Evolution im Lichte der Genetik. Communications de la Faculté des Sciences de l’Université d’Ankara 8:110–150
Kosswig C (1960a) Darwin und die degenerative evolution. Abhandlungen und Verhandlungen des Naturwissenschaftlichen Vereins Hamburg NF 4:21–42
Kosswig C (1960b) Zur Phylogenese sogenannter Anpassungsmerkmale bei Höhlentieren. Int Rev Ges Hydrobiol 45:493–512
Kosswig C (1976) Génétique et l‘évolution regressive - Mécanismes de la rudimentation des organes chez les embryons de vertébrés. Colloq Int CNRSN 266:19–29
Kosswig C, Kosswig L (1940) Die Variabilität bei Asellus aquaticus, unter besonderer Berücksichtigung der Variabilität in isolierten unter- und oberirdischen Populationen. Révue de la Faculté des Sciences Istanbul 5:1–55
Kowalko JE, Rohner N, Linden TA et al (2013a) Convergence in feeding posture occurs through different loci in independently evolved cave populations of Astyanax mexicanus. Proc Natl Acad Sci U S A 110:16933–16938
Kowalko JE, Rohner N, Rompani SB et al (2013b) Loss of schooling behavior in cavefish through sight-independent and sight-dependent mechanisms. Curr Biol 23:1874–1883
Krishnan J, Rohner N (2017) Cavefish and the basis for eye loss. Philos Trans R Soc B 372(1713):20150487. doi:10.1098/rstb.2015.0487
Langecker TG (1989) Studies on the light reaction of epigean and cave populations of Astyanax fasciatus (Characidae, Pisces). Mem Biospeleol 16:169–176
Langecker TG (1993) Genetic analysis of the dorsal light reaction in epigean and cave-dwelling Astynnax fasciatus (Teleostei, Characidae). Ethol Ecol Evol 3:357–364
Langecker TG (2000) The effects of continuous darkness on cave ecology and cavernicolous evolution. In: Wilkens H, Culver DC, Humphreys WF (eds) Ecosystems of the world: subterranean ecosystems, vol 30. Elsevier, Amsterdam, pp 135–157
Langecker TG, Neumann B, Hausberg C et al (1995) Evolution of the optical releasers for aggressive behavior in cave-dwelling Astyanax fasciatus (Teleostei, Characidae). Behav Process 34:161–168
Langecker TG, Wilkens H, Parzefall J (1996) Studies of the trophic structure of an energy-rich Mexican cave (Cueva de las Sardinas) containing sulfurous water. Mém Biospéléol 23:121–125
Lao O, de Gruijter JM, Duijn K v et al (2007) Signatures of positive selection in genes associated with human skin pigmentation as revealed from analyses of single nucleotide polymorphisms. Ann Hum Genet 71:354–369
Menuet A, Alunni A, Joly JS et al (2007) Expanded expression of Sonic Hedgehog in Astyanax cavefish: multiple consequences on forebrain development and evolution. Development 134:845–855. doi:10.1242/dev.02780
Meyer-Rochow VB, Juberthie-Jupeau L (1987) An electron microscope study of the eye of the cave mysid Heteromysoides cotti from the island of Lanzarote (Canary Islands). Stygologia 3:24–33
Mitchell RW, Russell WH, Elliott WR (1977) Mexican eyeless characin fishes, genus Astyanax: environment, distribution, and evolution. Special publications of the Museum Texas Tech University 12:1–89
Moran D, Softley R, Warrant EJ (2015) The energetic cost of vision and the evolution of eyeless Mexican cavefish. Sci Adv 1(8):e1500363. doi:10.1126/sciadv.1500363
Muller HJ (1949) The Darwinian and modern conceptions of natural selection. Proc Am Philos Soc 93:459–470
Nei M (2013) Mutation-driven evolution. Oxford University Press, Oxford
Nei M, Suzuki Y, Nozawa M (2010) The neutral theory of molecular evolution in the genomic era. Annu Rev Genomics Hum Genet 11:265–289
Niemiller ML, Fitzpatrick BM, Shah P et al (2012) Evidence for repeated loss of selective constraint in rhodopsin of amblyopsid cavefishes (Teleostei: Amblyopsidae). Evolution 67:732–748
Niven JE, Anderson JC, Laughlin SB (2007) Fly photoreceptors demonstrate energy-information trade-offs in neural coding. PLoS Biol 5:828–840
Orr HA (1998) Testing natural selection vs. genetic drift in phenotypic evolution using quantitative trait loci. Genetics 149:2099–2104
Palacios M, Voelker G, Rodriguez LA et al (2016) Phylogenetic analyses of the subgenus Mollienesia (Poecilia, Poeciliidae, Teleostei) reveal taxonomic inconsistencies, cryptic biodiversity, and spatio-temporal aspects of diversification in Middle America. Mol Phylogenet Evol 103:230–244
Parzefall J (1993) Schooling behaviour in population-hybrids of Astyanax fasciatus and Poecilia mexicana (Pisces, Characidae and Poeciliidae). In: Schröder JH, Bauer J (eds) Trends in ichthyology: an international perspective. Blackwell Scientific, Oxford, pp 297–303
Parzefall J (2001) A review of morphological and behavioural changes in the cave molly, Poecilia mexicana, from Tabasco, Mexico. Environ Biol Fishes 62:263–275
Pennisi E (2016) Blind cave fish may provide insights into human health. Science 352(6293):1502–1503. doi:10.1126/science.352.6293.1502
Peters N, Peters G (1968) Zur genetischen interpretation morphologischer Gesetzmäßigkeiten der degenerativen evolution. Zeitschrift Morphologie der Tiere 62:211–244
Peters N, Peters G (1973) Genetic problems in the regressive evolution of cavernicolous fish. In: Schröder JH (ed) Genetics and mutagenesis of fish. Springer, Berlin, pp 187–201
Peters N, Scholl A, Wilkens H (1975) Der Micos-Fisch, Höhlenfisch in statu nascendi oder Bastard ? Ein Beitrag zur Evolution der Höhlentiere. J Zool Syst Evol Res 13:110–124
Peters N, Schacht V, Schmidt W et al (1993) Gehirnproportionen und Ausprägungsgrad der Sinnesorgane von Astyanax mexicanus (Pisces, Characinidae). Z Zool Syst Evol 31:144–159
Poulson TL, White WB (1969) The cave environment: limestone caves provide unique natural laboratc for studying biological and geological processes. Science 165:971–981
Protas M, Conrad M, Gross JB et al (2007) Regressive evolution in the Mexican Cave Tetra, Astyanax mexicanus. Curr Biol 17:452–454. doi:10.1016/j.cub.2007.01.051
Protas ME, Trontelj P, Patela NH (2011) Genetic basis of eye and pigment loss in the cave crustacean, Asellus aquaticus. Proc Natl Acad Sci U S A 108:5702–5707. doi:10.1073/pnas.1013850108
Rétaux S, Casane D (2013) Evolution of eye development in the darkness of caves: adaptation, drift, or both? EvoDevo 4(1):1–12
Rétaux S, Pottin K, Alunni A (2008) Shh and forebrain evolution in the blind cavefish Astyanax mexicanus. Biol Cell 100:139–147
Rodrigues FR (2013) Comparison of brain and cranial nerve morphology between eyed surface fish and blind cave fish of the species Astyanax mexicanus. Dissertation, Universidade de Lisboa
Rohner N, Jarosz DF, Kowalko JE et al (2013) Cryptic variation in morphological evolution: HSP90 as a capacitor for loss of eyes in cavefish. Science 342:1372–1375
Schemmel C (1967) Vergleichende Untersuchungen an den Hautsinnesorganen ober- und unterirdisch lebender Astyanax-Formen. Zeitschrift Morphologie der Tiere 61:255–316
Schemmel C (1980) Studies on the genetics of feeding behavior in the cave fish Astyanax mexicanus f. Anopthichthys. An example of apparent monofactorial inheritance by polygenes. Z Tierpsychol 53:9–22
Schluter D (1996) Ecological speciation in postglacial fishes. Philos Trans Biol Sci 351:807–814
Schön I, Martens K (2004) Adaptive, pre-adaptive and non-adaptive components of radiations in ancient lakes: a review. Organ Divers Evol 4:137–156
Stevenson MM (1992) Food habits within the Laguna Chichancanab Cyprinodon (Pisces: Cyprinodontidae) species flock. Southwest Nat 37:337–343
Strecker U (1996) Molekulargenetische und ethologische Untersuchungen zur Speziation eines Artenschwarmes der Gattung Cyprinodon (Cyprinodontidae, Teleostei). Universität, Hamburg
Strecker U (2002) Cyprinodon esconditus, a new pupfish from Laguna Chichancanab, Yucatan, Mexico (Cyprinodontidae). Cybium 26:301–307
Strecker U (2006) Genetic differentiation and reproductive isolation in a Cyprinodon fish species flock from Laguna Chichancanab, Mexico. Mol Phylogenet Evol 39:865–872
Strecker U, Kodric-Brown A (2000) Mating preferences in a species flock of Mexican pupfishes (Cyprinodon, Teleostei). Biol J Linn Soc 71:677–687
Strecker U, Meyer CG, Sturmbauer C et al (1996) Genetic divergence and speciation in an extremely young species flock in Mexico formed by the genus Cyprinodon (Cyprinodontidae, Teleostei). Mol Phylogenet Evol 6:143–149
Strecker U, Hausdorf B, Wilkens H (2012) Parallel speciation in Astyanax cave fish (Teleostei) in Northern Mexico. Mol Phylogenet Evol 62:62–70
Strickler AG, Yamamoto Y, Jeffery WB (2007) The lens controls cell survival in the retina: evidence from the blind cavefish Astyanax. Dev Biol 311:512–523
Turgeon J, Estoup A, Bernatchez L (1999) Species flock in the North American Great Lakes: molecular ecology of Lake Nipigon ciscoes (Teleostei, Coregonidae: Coregonus). Evolution 53:1857–1871
Verovnik R, Prevorčnik S, Jugovic J (2009) Description of a neotype for Asellus aquaticus Linné, 1758 (Crustacea: Isopoda: Asellidae), with description of a new subterranean Asellus species from Europe. Zool Anz - J Comp Zool 248(2):101–118
Villwock W (1986) Speciation and adaptive radiation in Andean Orestias fishes. In: Vuilleumier F, Monasterio MM (eds) High altitude tropical biogeography. University Press, Oxford, pp 387–403
Wilkens H (1971) Genetic interpretation of regressive evolutionary processes: studies on hybrid eyes of two Astyanax cave populations (Characidae, Pisces). Evolution 25:530–544
Wilkens H (1976) Genotypic and phenotypic variability in cave animals. Studies on a phylogenetically young cave population of Astyanax mexicanus (Fillippi). Annales de Spéléologie 3:137–148
Wilkens H (1988) Evolution and genetics of epigean and cave Astyanax fasciatus (Characidae, Pisces). Support for the Neutral Mutation Theory. In: Hecht MK, Wallace B (eds) Evolutionary biology, vol 23. Plenum, New York, pp 271–367
Wilkens H (2001) Convergent adaptations to cave life in the Rhamdia laticauda catfish group (Pimelodidae, Teleostei). Environ Biol Fishes 62:251–261
Wilkens H (2010) Genes, modules and the evolution of cave fish. Heredity 105:413–422
Wilkens H (2016) Genetics and hybridization in surface and cave Astyanax (Teleostei): a comparison of regressive and constructive traits. Biol J Linn Soc 118:911–928
Wilkens H, Strecker U (2003) Convergent evolution of the cave fish Astyanax (Characidae, Teleostei): genetic evidence from reduced eye size and pigmentation. Biol J Linn Soc 80:545–554
Wilkens H, Peters N, Schemmel C (1979) Gesetzmäßigkeiten der regressiven Evolution. Verh Dtsch Zool Ges 1979:123–140
Wilkens H, Strecker U, Yager J (1989) Eye reduction and phylogenetic age in ophidiiform cave fish. Z Zool Syst Evol 27:126–134
Yamamoto Y, Stock DW, Jeffery WR (2004) Hedgehog signalling controls eye degeneration in blind cavefish. Nature 431:844–847
Yamamoto Y, Byerly MS, Jackman WR et al (2009) Pleiotropic functions of embryonic sonic hedgehog expression link jaw and taste bud amplification with eye loss during cavefish evolution. Dev Biol 330:200–211
Yang X-L, Tornquist K, Dowling JE (1988a) Modulation of cone horizontal cell activity in the teleost fish retina. I. Effects of prolonged darkness and background illumination on light responsiveness. J Neurosci 8:2259–2268
Yang X-L, Tornquist K, Dowling JE (1988b) Modulation of cone horizontal cell activity in the teleost fish retina. II. Role of interplexifoem cells and dopamine in regulating light responsiveness. J Neurosci 8:2269–2278
Yoshizawa M, Yamamoto Y, O’Quin KE et al (2012) Evolution of an adaptive behavior and its sensory receptors promotes eye regression in blind cavefish. BMC Biol 10:108–123
Yoshizawa M, Robinson BG, Duboué ER (2015) Distinct genetic architecture underlies the emergence of sleep loss and prey-seeking behavior in the Mexican cavefish. BMC Biol 13:15–27
Zeutzius I, Probst W, Rahmann H (1984) Influence of dark-rearing on the ontogenetic development of Sarotherodon mossambicus (Cichlidae, Teleostei): II. Effects on allometric growth relations and differentiation of the optic tectum. Exp Biol 43:87–96
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Wilkens, H., Strecker, U. (2017). Mechanisms of Regressive Evolution. In: Evolution in the Dark. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-54512-6_7
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