Morphology and composition of Goldeye (Hiodontidae; Hiodon alosoides) otoliths.
Osteoglossomorpha
carbonate polymorph
inner ear connection
otoconia
swim bladder
Journal
Journal of morphology
ISSN: 1097-4687
Titre abrégé: J Morphol
Pays: United States
ID NLM: 0406125
Informations de publication
Date de publication:
04 2021
04 2021
Historique:
received:
22
10
2020
revised:
06
01
2021
accepted:
17
01
2021
pubmed:
21
1
2021
medline:
23
6
2021
entrez:
20
1
2021
Statut:
ppublish
Résumé
We provide up-to-date morphological and compositional data on otoliths of the osteoglossomorph Goldeye (Hiodon alosoides). Using computed tomography (CT) X-ray, we documented the location of each of the three pairs of otoliths (lapilli, sagittae, and asterisci) in relation to the swim bladder, which extended forward in close proximity to the sagittae and asterisci. The lappili were the largest otoliths in terms of surface area and volume, but the sagittae were highly modified, appearing spiral in shape when viewed dorsally, with a surface area to volume ratio more than double that of the lapilli. Using scanning electron microscopy, the surface of each otolith was viewable in great detail, and small otoconia (~10.5 μm diameter) were observed on each, but were most numerous on the sagittae. On scanning electron micrographs, the sagittae appeared to be bi-lobed, with asymmetrical lobes each oriented in the same general direction. Using neutron and X-ray diffraction methods, we found three polymorphs of calcium carbonate crystals (aragonite, vaterite, and calcite), sometimes all within the same otolith. However, in general, lapilli and sagittae were composed predominately of aragonite whereas asterisci were composed chiefly of vaterite. With these results, we provide information on a unique species, whose inclusion in future studies would benefit our understanding of fish hearing, fish evolution, and fisheries ecology.
Substances chimiques
Calcium Carbonate
H0G9379FGK
Types de publication
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
511-519Informations de copyright
© 2021 Wiley Periodicals LLC. This article has been contributed to by US Government employees and their work is in the public domain in the USA.
Références
Battle, H. I., & Sprules, W. M. (1960). A description of the semi-buoyant eggs and early development stages of the Goldeye, Hiodon alosoides (Rafinesque). Journal of the Fisheries Research Board of Canada, 17, 245-266.
Betancur-R, R., Wiley, E. O., Arratia, G., Acero, A., Bailly, N., Miya, M., Lecointre, G., & Orti, G. (2017). Phylogenetic classification of bony fishes. BMC Evolutionary Biology, 17, 162. https://doi.org/10.1186/s12862-017-0958-3
Braekevelt, C. R. (1982). Photoreceptor fine structure in the Goldeye (Hiodon alosoides) (teleost). Anatomy and Embryology, 165, 177-192.
Carlström, D. (1963). A crystallographic study of vertebrate otoliths. Biological Bulletin, 125, 441-463.
Chakoumakos, B. C., Pracheil, B. M., Koenigs, R. P., Bruch, R. M., & Feygenson, M. (2016). Empirically testing vaterite structural models using neutron diffraction and thermal analysis. Scientific Reports, 6, 36799.
Coombs, S., & Popper, A. N. (1982). Structure and function of the auditory system in the clown Knifefish, Notopterus chitala. Journal of Experimental Biology, 97, 225-239.
Dehadrai, P. V. (1957). On the swim-bladder and its relation with the internal ear in genus Notopterus (Lacepede). Journal of the Zoological Society of India, 9, 50-61.
Donald, D. B. (1997). Relationship between year-class strength for Goldeyes and selected environmental variables during the first year of life. Transactions of the American Fisheries Society, 126, 361-368.
Donald, D. B., & Kooyman, A. H. (1977). Migration and population dynamics of the Peace-Athabasca delta Goldeye population. Canadian Wildlife Service Occasional Paper 31.
Gauldie, R. W. (1996). Fusion of otoconia: A stage in the development of the otolith in the evolution of fishes. Acta Zoological, 77, 1-23.
Gido, K. B., Dodds, W. K., & Eberle, M. E. (2010). Retrospective analysis of fish community change during a half-century of landuse and streamflow changes. Journal of the North American Benthological Society, 29, 970-987.
Hoover, J. J. (2004). Rare treasure from river bottom: Juvenile Goldeye (Hiodon alosoides) for medium-sized aquaria. American Currents, 30(3), 1-6.
Katechis, C. T., Sakaris, P. C., & Irwin, E. R. (2007). Population demographics of Hiodon tergisus (Mooneye) in the lower Tallapoosa River. Southeastern Naturalist, 6, 461-470.
Kennedy, W. A., & Sprules, W. M. (1967). Goldeye in Canada. Fisheries Research Board of Canada, Bulletin 161, Montreal.
Ladich, F., & Popper, A. N. (2004). Parallel evolution in fish hearing organs. In G. A. Manley, R. R. Fay, & A. N. Popper (Eds.), Evolution of the vertebrate auditory system (pp. 95-127). Springer Science + Business Media.
Ladich, F., & Schulz-Mirbach, T. (2016). Diversity in fish auditory systems: One of the riddles of sensory biology. Frontiers in Ecology and Evolution, 4, 28. https://doi.org/10.3389/fevo.2016.00028
Li, G., & Wilson, M. V. H. (1994). An Eocene species of Hiodon from Montana, its phylogenetic relationships, and the evolution of the postcranial skeleton in the Hiodontidae (Teleostei). Journal of Vertebrate Paleontology, 14, 153-167.
Long, J. M., & Grabowski, T. B. (2017). Otoliths. In M. C. Quist & D. Isermann (Eds.), Age and growth of fishes: principles and techniques (pp. 189-219). American Fisheries Society.
Long, J. M., & Snow, R. A. (2016). Ontogenetic development of otoliths in alligator gar. Transactions of the American Fisheries Society, 145, 537-544.
Long, J. M., & Stewart, D. R. (2010). Verification of otolith identity used by fisheries scientists for aging channel catfish. Transactions of the American Fisheries Society, 139, 1775-1779.
Maisey, J. G. (1987). Notes on the structure and phylogeny of vertebrate otoliths. Copeia, 1987, 495-499.
Martin, M. (1952). Age and growth of the Goldeye Hiodon alosoides (Rafinesque) of Lake Texoma, Oklahoma. Proceedings of the Oklahoma Academy of Science, 33, 37-49.
Moon, D. N., Fisher, S. J., & Willis, D. W. (1998). Goldeye recruitment and growth in two Missouri River backwaters. Proceedings of the South Dakota Academy of Science, 77, 139-144.
Moore, G. A., & McDougal, R. C. (1949). Similarity in the retina of Amphiodon alosoides and Hiodon tergisus. Copeia, 1949, 298.
Nelson, J. S., Grande, T. S., & Wilson, M. V. H. (2016). Fishes of the world (5th ed.). John Wiley & Sons, Inc.
Nolf, D. (1985). Otolithi piscium. In Handboook of paleoichthyology (Vol. 10). Gustav Fischer Verlag.
Nolf, D. (2013). The diversity of fish otoliths, past and present. Royal Belgian Institute of Natural Sciences.
ORS (Object Research Systems, Inc.). (2019). Dragofly 4.1 computer software. Montreal, Canada. Available from http://www.theobjects.com/dragonfly.
Popper, A. N., & Coombs, S. (1980). Auditory mechanisms in teleost fishes: Significant variation in both hearing capabilities and auditory structures are found among species of bony fishes. American Scientist, 68, 429-440.
Popper, A. N., & Coombs, S. (1982). The morphology and evolution of the ear in Actinopterygian fishes. American Zoologist, 22, 311-328.
Popper, A. N., & Lu, Z. (2000). Structure-function relationships in fish otolith organs. Fisheries Research, 146, 15-25.
Popper, A. N., Ramcharitar, J., & Campana, S. E. (2004). Why otoliths? Insights from inner ear physiology and fisheries biology. Marine and Freshwater Research, 56, 497-504.
Pracheil, B. M., Chakoumakos, B. C., Feygenson, M., Whitlege, G. W., Koenig, R. P., & Bruch, R. M. (2017). Sturgeon and Paddlefish (Acipenseridae) saggital otoliths are composed of the calcium carbonate polymorphs vaterite and calcite. Journal of Fish Biology, 90, 549-558.
Pracheil, B. M., George, R., & Chakoumakos, B. C. (2019). Significance of otolith calcium carbonate crystal structure diversity to microchemistry studies. Reviews in Fish Biology and Fisheries, 29, 569-588.
Ramcharitar, J. U., Deng, X., Ketten, D., & Popper, A. N. (2004). Form and function in the unique inner ear of a teleost: The silver perch (Bairdiella chrysoura). The Journal of Comparative Anatomy, 475, 531-539.
Rietveld, H. M. (1969). A profile refinement method for nuclear and magnetic structures. Journal of Applied Crystallography, 2, 65-71.
Schulz-Mirbach, T., Ladich, F., Plath, M., & Heβ, M. (2019). Enigmatic ear stones: What we know about the functional role and evolution of fish otoliths. Biological Reviews, 94, 457-482.
Schulz-Mirbach, T., Metscher, B., & Ladich, F. (2012). Relationship between swim bladder morphology and hear abilities-a case study on Asian and African cichlids. PLoS One, 7(8), e42292. https://doi.org/10.1371/journal.pone.0042292
Shelton, W. L. (1968). Changes in the abundance of Goldeye (Hiodon alosoides; Rafinesque), in Lake Texoma, Oklahoma. Proceedings of the Oklahoma Academy of Science, 49, 184-187.
Toby, B. H., & Von Dreele, R. B. (2013). GSAS-II: The genesis of a modern open-source all-purpose crystallography software package. Journal of Applied Crystallography, 46, 544-549. https://doi.org/10.1107/S0021889813003531
Wang, J., & Becker, U. (2009). Structure and carbonate orientation of vaterite (CaCO3). American Mineralogist, 94, 380-386.