Dental structure and tooth attachment modes in the common fangtooth Anoplogaster cornuta (Valenciennes, 1833) (Actinopterygii; Trachichthyiformes; Anoplogastridae)

We studied the structure and attachment modes of the teeth of adult Anoplogaster cornuta using light- and scanning-electron microscopic techniques. All teeth were monocuspid, composed solely of orthodentin, and lacked a covering enameloid cap. Fourteen teeth were present in the oral jaws, with three teeth each on the left and right premaxilla and four teeth each on the left and right dentary. The anteriormost premaxillary and dentary teeth were considerably larger than the more posteriorly located ones. The oral jaw teeth were transparent, non-depressible and firmly ankylosed to their respective dentigerous bone by a largely anosteocytic bone of attachment. No evidence for replacement of the large oral jaw teeth was found in the analyzed adult specimens. The bone of attachment exhibited lower calcium and phosphorus concentrations and a higher Ca/P ratio than the orthodentin. The connection between dentinal tooth shaft and bone of attachment was stabilized by a collar of mineralized collagen fibers. In contrast to the oral jaw teeth, the pharyngeal teeth exhibited a ring-like fibrous attachment to their supporting bones. This mode of attachment provides the teeth with some lateral mobility and allows their depression relative to their supporting bones, which may facilitate intra-pharyngeal prey transport. In contrast, a firm ankylosis was observed in numerous small teeth located on the branchial arches. The function of these teeth is presumably to increase the tightness of the pharyngeal basket and thereby the retention of small prey items in a species living in a habitat with only sparse food supply. Our findings corroborate earlier statements on the tooth attachment modes of the oral jaw teeth of Anoplogaster cornuta, but provide new findings for the attachment modes of pharyngeal teeth in this species.

[1]  C. Martinand-Mari,et al.  Parallel Evolution of Ameloblastic scpp Genes in Bony and Cartilaginous Vertebrates , 2022, Molecular biology and evolution.

[2]  P. Witten,et al.  Cells at the Edge: The Dentin–Bone Interface in Zebrafish Teeth , 2021, Frontiers in Physiology.

[3]  Mark N. Puttick,et al.  Coevolution of enamel, ganoin, enameloid, and their matrix SCPP genes in osteichthyans , 2021, iScience.

[4]  S. Dallas,et al.  Collagen Dynamics During the Process of Osteocyte Embedding and Mineralization , 2019, Front. Cell Dev. Biol..

[5]  Dimitri D. Deheyn,et al.  On the Nature of the Transparent Teeth of the Deep-Sea Dragonfish, Aristostomias scintillans , 2019, Matter.

[6]  U. Kierdorf,et al.  Pig enamel revisited - Incremental markings in enamel of wild boars and domestic pigs. , 2019, Journal of structural biology.

[7]  R. Benson,et al.  The phylogenetic origin and evolution of acellular bone in teleost fishes: insights into osteocyte function in bone metabolism , 2018, Biological reviews of the Cambridge Philosophical Society.

[8]  Moya M. Smith The teeth of non-mammalian vertebrates , 2018, BDJ.

[9]  Nicolas Bailly,et al.  Phylogenetic classification of bony fishes , 2017, BMC Evolutionary Biology.

[10]  V. Buffrénil,et al.  Microstructure and Mineralization of Vertebrate Skeletal Tissues , 2013 .

[11]  M. Glimcher,et al.  Bone mineral: update on chemical composition and structure , 2009, Osteoporosis International.

[12]  B. Mcguire,et al.  Structure, attachment, replacement and growth of teeth in bluefish, Pomatomus saltatrix (Linnaeus, 1776), a teleost with deeply socketed teeth. , 2005, Zoology.

[13]  J. Pasteris,et al.  A mineralogical perspective on the apatite in bone , 2005 .

[14]  J. Trapani Position of Developing Replacement Teeth in Teleosts , 2001, Copeia.

[15]  M. Chardon,et al.  The branchial basket in Teleost feeding. , 2000 .

[16]  P. Fratzl,et al.  Validation of quantitative backscattered electron imaging for the measurement of mineral density distribution in human bone biopsies. , 1998, Bone.

[17]  J. Davenport Ventilation of the gills by the pectoral fins in the fangtooth Anoplogaster cornutum: how to breathe with a full mouth , 1993 .

[18]  K. Bachus,et al.  The meaning of graylevels in backscattered electron images of bone. , 1993, Journal of biomedical materials research.

[19]  D. S. Kim,et al.  A procedure for staining cartilage and bone of whole vertebrate larvae while rendering all other tissues transparent. , 1984, Stain technology.

[20]  W. Fink Ontogeny and phylogeny of tooth attachment modes in actinopterygian fishes , 1981, Journal of morphology.

[21]  R. Shellis,et al.  The structure of the dental hard tissues of the coelacanthid fish Latimeria chalumnae Smith. , 1978, Archives of oral biology.

[22]  G Dingerkus,et al.  Enzyme clearing of alcian blue stained whole small vertebrates for demonstration of cartilage. , 1977, Stain technology.

[23]  B. Berkovitz,et al.  Tooth replacement in the upper jaw of the rainbow trout (Salmo gairdneri). , 1975, The Journal of experimental zoology.

[24]  B. Berkovitz,et al.  A longitudinal study of replacement patterns of teeth on the lower jaw and tongue in the rainbow trout Salmo gairdneri. , 1974, Archives of oral biology.

[25]  G. Cailliet,et al.  Mouth size and predator strategy of midwater fishes , 1974 .

[26]  L. Taverne L'ostéologie d'Elops Linné, C., 1766 (Pisces Elopiformes) et son intérêt phylogénétique , 1974 .

[27]  J. Childress,et al.  Observations on the Feeding Behavior of a Mesopelagic Fish (Anoplogaster cornuta: Beryciformes) , 1973 .

[28]  R. Whitehead Biopsies , 1954, British medical journal.

[29]  V. Tchernavin The feeding mechanisms of a deep sea fish : Chauliodus sloani Schneider , 1953 .

[30]  Feeding Mechanisms in Deep-Sea Fish , 1953, Nature.