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. 2022 Mar 17;17(3):e0265237.
doi: 10.1371/journal.pone.0265237. eCollection 2022.

Species-specific enamel differences in hardness and abrasion resistance between the permanent incisors of cattle (Bos primigenius taurus) and the ever-growing incisors of nutria (Myocastor coypus)

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Species-specific enamel differences in hardness and abrasion resistance between the permanent incisors of cattle (Bos primigenius taurus) and the ever-growing incisors of nutria (Myocastor coypus)

Valentin L Fischer et al. PLoS One. .

Abstract

Hypselodont (ever-growing) teeth of lagomorphs or rodents have higher wear rates (of a magnitude of mm/week), with compensating growth rates, compared to the non-ever-growing teeth of ungulates (with a magnitude of mm/year). Whether this is due to a fundamental difference in enamel hardness has not been investigated so far. We prepared enamel samples (n = 120 per species) from incisors of cattle (Bos primigenius taurus) and nutria (Myocastor coypus, hypselodont incisors) taken at slaughterhouses, and submitted them to indentation hardness testing. Subsequently, samples were split into 4 groups per species (n = 24 per species and group) that were assessed for abrasion susceptibility by a standardized brush test with a control (no added abrasives) and three treatment groups (using fine silt at 4 ±1 μm particle size, volcanic ash at 96 ±9 μm, or fine sand at 166 ±15 μm as abrasives), in which enamel abrasion was quantified as height loss by before-and-after profilometry. The difference in enamel hardness between the species was highly significant, with nutria enamel achieving 78% of the hardness of cattle enamel. In the control and the fine sand group, no enamel height loss was evident, which was attributed to the in vitro system in the latter group, where the sand particles were brushed out of the test slurry by the brushes' bristles. For fine silt and volcanic ash, nutria enamel significantly lost 3.65 and 3.52 times more height than cattle. These results suggest a relationship between enamel hardness and susceptibility to abrasion. However, neither the pattern within the species nor across the species indicated a monotonous relationship between hardness and height loss; rather, the difference was due to qualitative step related to species. Hence, additional factors not measured in this study must be responsible for the differences in the enamel's susceptibility to abrasion. While the in vitro brush system cannot be used to rank abrasive test substances in terms of their abrasiveness, it can differentiate abrasion susceptibility in dental tissue of different animal species. The results caution against considering enamel wear as a similar process across mammals.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Schematic representation of potential results of this study depending on different combinations of whether species differ in enamel hardness (columns), and whether different abrasives lead to different tissue loss irrespective of, or in proportion to, hardness.
Fig 2
Fig 2
Relationship of enamel hardness and enamel height loss in cattle (Bos primigenius taurus, black data) and nutria (Myocastor coypus, grey data) in (a) samples exposed to fine silt or volcanic ash; (b) samples of the control group and samples exposed to fine sand. For statistics, see Table 3. Note the log-log-scale in (a) and the trendlines that are generally not significant but only added to emphasize the data pattern.

References

    1. DeSantis L, Fortelius M, Grine FE, Janis C, Kaiser TM, Merceron G, et al.. The phylogenetic signal in tooth wear: What does it mean? Ecology and Evolution. 2018;8:11359–11362. doi: 10.1002/ece3.4541 - DOI - PMC - PubMed
    1. Clauss M. Phylogenetic signal in tooth wear? A question that can be answered–by testing. Ecology and Evolution. 2019;9:6170–6171. doi: 10.1002/ece3.5214 - DOI - PMC - PubMed
    1. Fraser D, Haupt RJ, Barr WA. Phylogenetic signal in tooth wear dietary niche proxies. Ecology and Evolution. 2018;8:5355–5368. doi: 10.1002/ece3.4052 - DOI - PMC - PubMed
    1. Fraser D, Haupt RJ, Barr WA. Phylogenetic signal in tooth wear dietary niche proxies: What it means for those in the field. Ecology and Evolution. 2018;8:11363–11367. doi: 10.1002/ece3.4540 - DOI - PMC - PubMed
    1. Ackermans NL, Winkler DE, Kaiser TM, Martin LF, Schulz-Kornas E, Hatt J-M, et al.. Correlation of dietary wear proxies in a long term feeding experiment with sheep (Ovis aries). Journal of the Royal Society Interface. 2021;18:20210139. - PMC - PubMed

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