Analyze Diet

Teeth out of proportion: Smaller horse and cattle breeds have comparatively larger teeth.

Abstract: There are different descriptions of allometric relationships between important components of the mammalian skull. Craniofacial evolutionary allometry describes a pattern of increasing facial cranium in larger skulls. Another body of literature describes disproportionately larger teeth in smaller species or specimens, matching anecdotal observations with dental problems in dwarf breeds whose teeth appear "too large for their skulls." We test the scaling of tooth row length with body size and skull length in a data set comprising 114 domestic horses (representing 40 breeds) and in another data set of 316 domestic cattle (of >60 breeds). We demonstrate that smaller skulls have a relatively longer tooth row in both horses and cattle; larger specimens have relatively shorter tooth rows. Whereas in horses, larger skulls have a relatively longer diastema, the distance of the mesial maxillary premolar to the premaxilla was proportional to cranium length in cattle. While the reasons for these patterns remain to be detected, they support the hypothesis that tooth size might be less "evolvable," in terms of time required for changes, than body size. The pattern may affect (i) the selective breeding for dwarf breeds by setting minimum constraints for skull size, as described previously for domestic horses with the same data set; (ii) the susceptibility of small breeds for dental problems; and (iii) differences in chewing efficiency between breeds of different sizes. The findings support the existing concept that scaling of tooth to body size across taxa becomes more isometric the longer these taxa are separated in evolutionary time.
Publication Date: 2022-03-14 PubMed ID: 35286773PubMed Central: PMC9790632DOI: 10.1002/jez.b.23128Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article explores the hypothesis that smaller horse and cattle breeds have disproportionately larger teeth, where the tooth size doesn’t reduce in proportion with the overall body size or skull. This idea is explored using samples from 40 horse breeds and over 60 cattle breeds.

Understanding Allometry and Craniofacial Evolution

  • Allometry is a term used in the study of size and shape transformations in organisms. It’s often applied to describe how characteristics of creatures, such as body size or shape, change disproportionately during the growth of an organism.
  • The research refers to a widely recognized pattern in craniofacial evolution, the science investigating how the skull and face of organisms change over time. This pattern shows that larger mammalian skulls tend to have a more extended facial cranium.

Investigating Oversize Teeth in Smaller Breeds

  • There have been anecdotal observations of dental problems in smaller or dwarf breeds which appear to have oversized teeth for their skulls. The researchers sought to scientifically substantiate these observations.
  • The research tested the proportion of tooth row length to body size and skull length using a large sample size of over 100 domestic horses from 40 breeds, and over 300 domestic cattle from more than 60 breeds.

Findings: Disproportionate Tooth Size in Smaller Breeds

  • The researchers found supporting evidence for their hypothesis: smaller skulls in both horses and cattle tend to have more extended tooth rows, while larger specimens presented shorter tooth rows.
  • In horses, the longer the skull size, the larger the diastema, or gap between teeth. However, in cattle, the distance from the mesial maxillary premolar to the premaxilla was proportional to the cranial length.
  • The reasons behind these patterns remain undetermined, but these findings do support the idea that tooth size is less “evolvable,” or slower to change, than body size. The researchers theorize that these patterns could explain issues in breed selection – for instance, there may be a minimum skull size constraint for dwarf breeds – susceptibility to dental issues in smaller breeds, and variations in chewing efficiency amongst breeds of different sizes.

Broader Implications for Evolutionary Taxonomy

  • This study supports the broader concept in evolutionary taxonomy that the ratio of tooth-to-body size tends to become more isometric, or maintains its scale, the longer these taxa are separated in evolutionary time.
  • This means that the longer two species have been separated from a shared ancestor, the more “in proportion” the teeth become to the overall body size.

Cite This Article

APA
Clauss M, Heck L, Veitschegger K, Geiger M. (2022). Teeth out of proportion: Smaller horse and cattle breeds have comparatively larger teeth. J Exp Zool B Mol Dev Evol, 338(8), 561-574. https://doi.org/10.1002/jez.b.23128

Publication

ISSN: 1552-5015
NlmUniqueID: 101168228
Country: United States
Language: English
Volume: 338
Issue: 8
Pages: 561-574

Researcher Affiliations

Clauss, Marcus
  • Clinic for Zoo Animals, Exotic Pets and Wildlife, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
Heck, Laura
  • Palaeontological Institute and Museum, University of Zurich, Zurich, Switzerland.
Veitschegger, Kristof
  • Palaeontological Institute and Museum, University of Zurich, Zurich, Switzerland.
Geiger, Madeleine
  • Palaeontological Institute and Museum, University of Zurich, Zurich, Switzerland.
  • SWILD, Urban Ecology & Wildlife Research, Zurich, Switzerland.
  • Naturmuseum St. Gallen, Rorschacher Strasse 263, 9016, St.Gallen, Switzerland.

MeSH Terms

  • Horses
  • Animals
  • Cattle
  • Tooth
  • Skull
  • Head
  • Biological Evolution
  • Body Size
  • Mammals

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 66 references
  1. Andersen H, Plum M. Gestation length and birth weight in cattle and buffaloes: a review.. J Dairy Sci 1965 Sep;48(9):1224-35.
  2. Antonius O. Grundzüge einer Stammesgeschichte der Haustiere. .
  3. Bae DH, Welch JG, Gilman BE. Mastication and rumination in relation to body size of cattle.. J Dairy Sci 1983 Oct;66(10):2137-41.
  4. Bradford GE, Hart R, Quirke JF, Land RB. Genetic control of the duration of gestation in sheep.. J Reprod Fertil 1972 Sep;30(3):459-63.
    pubmed: 5073387doi: 10.1530/jrf.0.0300459google scholar: lookup
  5. Burger J R, George M A, Leadbetter C, Shaikh F. The allometry of brain size in mammals. Journal of Mammalogy 2019;100:276–283.
  6. Cardini A. Craniofacial allometry is a rule in evolutionary radiations of placentals. Evolutionary Biology 2019;46:239–248.
  7. Carranza J, Pérez-Barbería FJ. Sexual selection and senescence: male size-dimorphic ungulates evolved relatively smaller molars than females.. Am Nat 2007 Sep;170(3):370-80.
    pubmed: 17879188doi: 10.1086/519852google scholar: lookup
  8. Clauss M. No evidence for different metabolism in domestic mammals.. Nat Ecol Evol 2019 Mar;3(3):322.
    pubmed: 30778191doi: 10.1038/s41559-019-0817-2google scholar: lookup
  9. Clauss M, Dittmann M T, Müller D W H, Zerbe P, Codron D. Low scaling of a life history variable: Analysing eutherian gestation periods with and without phylogeny‐informed statistics. Mammalian Biology 2014;79:9–16.
  10. Clauss M, Steuer P, Erlinghagen-Lückerath K, Kaandorp J, Fritz J, Südekum KH, Hummel J. Faecal particle size: digestive physiology meets herbivore diversity.. Comp Biochem Physiol A Mol Integr Physiol 2015 Jan;179:182-91.
    pubmed: 25446938doi: 10.1016/j.cbpa.2014.10.006google scholar: lookup
  11. Clauss M, Steuer P, Müller DW, Codron D, Hummel J. Herbivory and body size: allometries of diet quality and gastrointestinal physiology, and implications for herbivore ecology and dinosaur gigantism.. PLoS One 2013;8(10):e68714.
  12. Cochard LR. Postcanine tooth size in female primates.. Am J Phys Anthropol 1987 Sep;74(1):47-54.
    pubmed: 3688209doi: 10.1002/ajpa.1330740105google scholar: lookup
  13. Copes L E, Schwartz G T. The scale of it all: Postcanine tooth size, the taxon‐level effect, and the universality of Gould's scaling law. Palaeobiol 2010;36:188–203.
  14. Davies P, Lister A M. Palaeoloxodon cypriotes, the dwarf elephant of Cyprus: Size and scaling comparisons with P. falconeri (Sicily–Malta) and mainland P. antiquus. In Cavaretta G., Gioia P., Mussi M., & Palombo M. (Eds.), La Terra degli Elefanti—The World of Elephants; Proceedings of the 1st International Congress (pp. 479–480).
  15. Dimitriadis J N. Das Skyrospony: Ein Beitrag zum Studium der Pferde Griechenlands. Zeitschrift für Züchtung Reihe B, Tierzüchtung und Züchtungsbiologie einschließlich Tierernährung 1937;37:343–385.
  16. Dixon P M, Copeland A N. The radiological appearance of mandibular cheek teeth in ponies of different ages. Equine Veterinary Education 1993;5:317–323.
  17. Forsten A. The small caballoid horse of the upper Pleistocene and Holocene. Journal of Animal Breeding and Genetics 1988;105:161–176.
  18. Forsten A. Horse diversity through the ages.. Biol Rev Camb Philos Soc 1989 Nov;64(4):279-304.
  19. Fortelius M. Ungulate cheek teeth: Developmental, functional, and evolutionary interrelations. Acta Zoologica Fennica 1985;180:1–76.
  20. Geist V. The evolution of horn‐like organs. Behaviour 1966;27:175–214.
  21. Gingerich P D. Cranial morphology and adaptations in Eocene Adapidae I. Sexual dimorphism in Adapis magnus and Adapis parisiensis. American Journal of Physical Anthropology 1981;56:217–234.
  22. Gould S J. On the scaling of tooth size in mammals. American Zoologist 1975;15:351–362.
  23. Grandl F, Schwarm A, Ortmann S, Furger M, Kreuzer M, Clauss M. Kinetics of solutes and particles of different size in the digestive tract of cattle of 0.5-10 years of age, and relationships with methane production.. J Anim Physiol Anim Nutr (Berl) 2018 Jun;102(3):639-651.
    pubmed: 29286177doi: 10.1111/jpn.12862google scholar: lookup
  24. Gross J E, Demment M W, Alkon P U, Kotzman M. Feeding and chewing behaviors of Nubian ibex: Compensation for sex‐related differences in body size. Functional Ecology 1995;9:385–393.
  25. Heck L, Clauss M, Sánchez‐Villagra M R. Gestation length variation in domesticated horses and its relation to breed and body size diversity. Mammalian Biology 2017;84:44–51.
  26. Heck L, Sanchez-Villagra MR, Stange M. Why the long face? Comparative shape analysis of miniature, pony, and other horse skulls reveals changes in ontogenetic growth.. PeerJ 2019;7:e7678.
    pmc: PMC6752190pubmed: 31576240doi: 10.7717/peerj.7678google scholar: lookup
  27. Heck L, Wilson LAB, Evin A, Stange M, Sánchez-Villagra MR. Shape variation and modularity of skull and teeth in domesticated horses and wild equids.. Front Zool 2018;15:14.
    pmc: PMC5907714pubmed: 29713365doi: 10.1186/s12983-018-0258-9google scholar: lookup
  28. Hooper AP, Welch JG. Chewing efficiency and body size of kid goats.. J Dairy Sci 1983 Dec;66(12):2551-6.
  29. Hulbert R C. Late Miocene Nannippus (Mammalia: Perissodactyla) from Florida, with a description of the smallest hipparionine horse. Journal of Vertebrate Paleontology 1993;13:350–366.
  30. Hulbert R C, MacFadden B J. Morphological transformation and cladogenesis at the base of the adaptive radiation of Miocene hypsodont horses. American Museum Novitates 1991;3000:1–16.
  31. Janis C M. Correlation of cranial and dental variables with body size in ungulates and macropodoids. In Damuth J., & MacFadden B. J. (Eds.), Body size and mammalian paleobiology (pp. 255–299).
  32. Kay R F. Molar structure and diet in extant Cercopithecidae. In Butler P. M., & Joysey K. A. (Eds.), Development, function and evolution of teeth (pp. 309–339).
  33. Kirkwood J K. The influence of size on the biology of the dog. Journal of Small Animal Practice 1985;26:97–110.
  34. Larson G, Fuller D Q. The evolution of animal domestication. Annual Review of Ecology, Evolution, and Systematics 2014;45:115–136.
  35. Leche W. Zoologie. In S. Hedin (Ed.), Scientific results of a journey in Central Asia 1899–1902 (Vol. 6, pp. 1–69).
  36. Lister A M. Sea‐levels and the evolution of island endemics: The dwarf red deer of Jersey. Special Publications 1995;96:151–172.
  37. Lister A M. Dwarfing in island elephants and deer: Processes in relation to time of isolation. Symposia of the Zoological Society of London 1996;69:277–292.
  38. Lister A M, Hall C. Variation in body and tooth size with island area in small mammals: A study of Scottish and Faroese house mice (Mus musculus). Annales Zoologici Fennici 2014;51:95–110.
  39. Lundholm B. Abstammung und Domestikation des Hauspferdes. .
  40. MacFadden B J. Fossil horses. .
  41. Maffei M D, Klimstra W D, Wilmers T J. Cranial and mandibular characteristics of the Key deer (Odocoileus virginianus clavium). Journal of Mammalogy 1988;69:403–407.
  42. Maglio VJ. EVOLUTION OF MASTICATION IN THE ELEPHANTIDAE.. Evolution 1972 Dec;26(4):638-658.
  43. Marshall L G, Corruccini R S. Variability, evolutionary rates, and allometry in dwarfing lineages. Palaeobiology 1978;4:101–119.
  44. McKeown M. Craniofacial variability and its relationship to disharmony of the jaws and teeth.. J Anat 1975 Jul;119(Pt 3):579-88.
    pmc: PMC1231645pubmed: 1141055
  45. Poppi D P, Hendricksen R E, Minson D J. The relative resistance to escape of leaf and stem particles from the rumen of cattle and sheep. Journal of Agricultural Science 1985;105:9–14.
  46. Poppi D P, Norton B W, Minson D J, Hendricksen R E. The validity of the critical size theory for particles leaving the rumen. Journal of Agricultural Science 1980;94:275–280.
  47. Prothero D R, Sereno P C. Allometry and paleoecology of medial Miocene dwarf rhinoceroses from the Texas Gulf coastal plain. Palaeobiology 1982;8:16–30.
  48. nR Core Teamn. R: A language and environment for statistical computing. version 3.4.1. 2017.
  49. Radinsky L. Relative brain size: a new measure.. Science 1967 Feb 17;155(3764):836-8.
    pubmed: 4959814doi: 10.1126/science.155.3764.836google scholar: lookup
  50. Radinsky L. ONTOGENY AND PHYLOGENY IN HORSE SKULL EVOLUTION.. Evolution 1984 Jan;38(1):1-15.
  51. Radinsky L B. Approaches in evolutionary morphology: A search for patterns. Annual Review of Ecology, Evolution, and Systematics 1985;16:1–14.
  52. Reiter A M. Pathophysiology of dental disease in the rabbit, guinea pig, and chinchilla. Journal of Exotic Pet Medicine 2008;17:70–77.
  53. Shea BT, Gomez AM. Tooth scaling and evolutionary dwarfism: an investigation of allometry in human pygmies.. Am J Phys Anthropol 1988 Sep;77(1):117-32.
    pubmed: 3189517doi: 10.1002/ajpa.1330770117google scholar: lookup
  54. Shingu Y, Kondo S, Hata H, Okubo M. Digestibility and number of bites and chews on hay at fixed level in Hokkaido native horses and light half‐bred horses. Journal of Equine Veterinary Science 2001;12:145–147.
  55. Shipley L A, Gross J E, Spalinger D E, Hobbs N T, Wunder B A. The scaling of intake rate in mammalian herbivores. American Naturalist 1994;143:1055–1082.
  56. Shoemaker L, Clauset A. Body mass evolution and diversification within horses (family Equidae).. Ecol Lett 2014 Feb;17(2):211-20.
    pubmed: 24304872doi: 10.1111/ele.12221google scholar: lookup
  57. Sieslack J, Farke D, Failing K, Kramer M, Schmidt MJ. Correlation of brachycephaly grade with level of exophthalmos, reduced airway passages and degree of dental malalignment' in Persian cats.. PLoS One 2021;16(7):e0254420.
  58. Spencer L M. Morphological correlates of dietary resource partitioning in the African bovidae. Journal of Mammalogy 1995;76:448–471.
  59. Tamagnini D, Meloro C, Cardini A. Anyone with a long‐face? Craniofacial evolutionary allometry (CREA) in a family of short‐faced mammals, the Felidae. Evolutionary Biology 2017;44:476–495.
  60. Thomason J J. The functional morphology of the manus in the tridactyl equids Merychippus and Mesohippus: Paleontological inferences from neontological models. Journal of Vertebrate Paleontology 1986;6:143–161.
  61. Veitschegger K, Wilson LAB, Nussberger B, Camenisch G, Keller LF, Wroe S, Sánchez-Villagra MR. Resurrecting Darwin's Niata - anatomical, biomechanical, genetic, and morphometric studies of morphological novelty in cattle.. Sci Rep 2018 Jun 14;8(1):9129.
    pmc: PMC6002398pubmed: 29904085doi: 10.1038/s41598-018-27384-3google scholar: lookup
  62. Waddington C. Canalization of development and the inheritance of acquired characters. Nature 1942;150:563–565.
  63. Wagner K. Recente Hunderassen. Eine osteologische Untersuchung. Skriffer Utgitt au det Norske Vidensk‐Akad.
  64. Wayne RK. CRANIAL MORPHOLOGY OF DOMESTIC AND WILD CANIDS: THE INFLUENCE OF DEVELOPMENT ON MORPHOLOGICAL CHANGE.. Evolution 1986 Mar;40(2):243-261.
  65. Weidenreich F. The brain and its role in the phylogenetic transformation of the human skull. Transactions of the American Philosophical Society 1941;31:320–442.
  66. Welch J G. Rumination, particle size and passage from the rumen. Journal of Animal Science 1982;54:885–894.

Citations

This article has been cited 7 times.
  1. Geiger M, Sánchez-Villagra MR, Sherratt E. Cranial shape variation in domestication: A pilot study on the case of rabbits. J Exp Zool B Mol Dev Evol 2022 Dec;338(8):532-541.
    doi: 10.1002/jez.b.23171pubmed: 35934897google scholar: lookup
  2. Gomes Rodrigues H, Chabot J, Cucchi T, Billet G. Accommodation of Dental Variations During Jaw Growth in Ungulate Mammals. J Exp Zool B Mol Dev Evol 2025 Dec;344(8):487-504.
    doi: 10.1002/jez.b.23321pubmed: 40761128google scholar: lookup
  3. Ming KM, Le Verger K, Geiger M, Schmelzle T, Georgalis GL, Shimbo G, Sasaki M, Ohdachi SD, Sánchez-Villagra MR. Insular dwarfism in horses from the Aegean Sea and the Japanese archipelago. Mamm Biol 2024;104(4):345-361.
    doi: 10.1007/s42991-024-00408-4pubmed: 39070961google scholar: lookup
  4. Tinsley T, Fogle C, Means E, Robertston J. The prevalence and risk factors of dental disease found in 100 miniature horses. Front Vet Sci 2023;10:1239809.
    doi: 10.3389/fvets.2023.1239809pubmed: 38098989google scholar: lookup
  5. Saliari K, Trebsche P. Cattle Make the Difference: Variations and Developments of Animal Husbandry in the Central European La Tène Culture. Animals (Basel) 2023 Jun 1;13(11).
    doi: 10.3390/ani13111847pubmed: 37889794google scholar: lookup
  6. Avedik A, Clauss M. Chewing, dentition and tooth wear in Hippopotamidae (Hippopotamus amphibius and Choeropsis liberiensis). PLoS One 2023;18(10):e0291825.
    doi: 10.1371/journal.pone.0291825pubmed: 37792716google scholar: lookup
  7. Christensen MM, Hallikas O, Das Roy R, Väänänen V, Stenberg OE, Häkkinen TJ, François JC, Asher RJ, Klein OD, Holzenberger M, Jernvall J. The developmental basis for scaling of mammalian tooth size. Proc Natl Acad Sci U S A 2023 Jun 20;120(25):e2300374120.
    doi: 10.1073/pnas.2300374120pubmed: 37307487google scholar: lookup