Data from: Electroreception in early vertebrates: survey, evidence and new information
Data files
Jan 22, 2019 version files 1.63 GB
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Camuropiscis_Suborbital_SAMP53772.pdf
57.31 MB
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Eastmanosteus_postsuborbital_MVP231104.pdf
170.30 MB
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Eastmanosteus_Postsuborbital_subsection_MVP231104.pdf
168.32 MB
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Kimberleyichthys_Postsuborbital_ANUV1037.pdf
269.32 MB
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Ligulalepis_ANUV3628_sensory pits.pdf
3.08 MB
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Parabuchanosteus_Suborbital_ANUV1686.pdf
199.02 MB
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Speonesydrion_ANU49340_anterior.pdf
9.13 MB
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Speonesydrion_ANU49340_posterior.pdf
27.90 MB
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torosteidsp_Postsuborbital_SAMP50606.pdf
80.09 MB
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Torosteus_Postsuborbital_MVP230808.pdf
136.05 MB
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Torosteus_Suborbital_MVP230808.pdf
394.79 MB
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V244_suborbital.pdf
19.36 MB
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V79_large_model.pdf
23.02 MB
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V79_small_model.pdf
23.90 MB
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V79.ply
49.19 MB
Abstract
Electroreception is widespread in living vertebrates, and is often considered a primitive vertebrate character. However, the early evolution of electroreception remains unclear. A variety of structures in early vertebrate fossils have been put forward as potential electroreceptors, but these need to be reassessed in light of the now substantial literature on electroreceptors in living vertebrates. Here we review the evidence for all putative electroreceptors in early vertebrates, and provide new information from CT scans. In the jawless osteostracans, the pore canal system in the dermal skeleton and the lateral and dorsal fields do not resemble electroreceptors in living species. Nevertheless the presence of a recurrent ramus of the anterior lateral line nerve in osteostracans suggests electroreceptors were present, by comparison with lampreys. In placoderms, cutaneous sense organs on arthrodire cheek plates are possible electroreceptors. CT data shows that the orientation of these pits is anomalous for electroreceptors, and intimately associated with bone growth. A newly identified type of cheek pit, for which the term “Young’s apparatus” is introduced, is known so far only from two arthrodire specimens. It is closely associated with the underlying jaw joint, but its precise function is unknown. In osteichthyans, the “pore-group” clusters of early sarcopterygians may have housed electroreceptors. CT data from Devonian lungfish support this interpretation, showing internal morphology consistent with electroreceptors, and innervation via the rostral tubuli underlying the dermal bone of the snout. The early osteichthyan Ligulalepis has pit structures which may be electroreceptors, and they were possibly innervated by lateral line nerves. Specialised electroreceptor systems, including elaborated “pore-group” pits in Devonian lungfish and rostral organs in the earliest coelacanths, show that electroreception may have had an important role in niche specialisation in early vertebrates. Finally, fossil data does not support the hypothesis that vertebrate hard tissues initially evolved to shield electroreceptors.