Encyclopedia of Animal Cognition and Behavior

Living Edition
| Editors: Jennifer Vonk, Todd Shackelford

Caudata Cognition

  • Savannah M. BerryEmail author
  • Joseph R. MendelsonIII
Living reference work entry
DOI: https://doi.org/10.1007/978-3-319-47829-6_1011-1

Synonyms

Definition

Mental processing of environmental and social information and sensory input in salamanders.

Introduction

There are approximately 8,000 species of known amphibians, about 500 of which are salamanders (Frost 2019). Amphibians arose about 360 million years ago with the oldest salamander fossil dating to the Miocene (Petranka 1998). Members of the class Amphibia are ectothermic tetrapods, lack scales, and have heavily glandular skin. Salamanders are unique from frogs and caecilians, most obviously, by always having a tail and forelimbs; a few salamander species lack hind limbs. Many species have biphasic life cycles where they spend the first portion of their lives in water and their adult life on land; however, there are some species that are solely terrestrial and solely aquatic (Petranka 1998). Modes of respiration include gills, lungs, and gas exchange through the skin (i.e., cutaneous...

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References

  1. Agrillo, C. (2014). Numerical and arithmetic abilities in non-primate species. Oxford: Oxford University Press.Google Scholar
  2. Anthony, C. D., Wicknick, J. A., & Jaeger, R. G. (1997). Social interactions in two sympatric salamanders: Effectiveness of a highly aggressive strategy. Behaviour, 134, 71–88.CrossRefGoogle Scholar
  3. David, R. S., & Jaeger, R. G. (1981). Prey location through chemical cues by a terrestrial salamander. Copeia, 1981, 435–440.CrossRefGoogle Scholar
  4. Dawley, E. M., Fingerlin, A., Hwang, D., John, S. S., & Stankiewicz, C. A. (2000). Seasonal cell proliferation in the chemosensory epithelium and brain of red-backed salamanders, Plethodon cinereus. Brain, Behavior and Evolution, 56, 1–13.CrossRefGoogle Scholar
  5. Ducey, P. K. (1989). Agonistic behavior and biting during intraspecific encounters in Ambystoma salamanders. Herpetologica, 1989, 155–160.Google Scholar
  6. Frost, D. R. (2019). Amphibian species of the world: An online reference. Version 6.0. New York: American Museum of Natural History. Retrieved from http://research.amnh.org/herpetology/amphibia/index.html.Google Scholar
  7. Gabor, C. R., & Jaeger, R. G. (1995). Resource quality affects the agonistic behaviour of territorial salamanders. Animal Behaviour, 49, 71–79.CrossRefGoogle Scholar
  8. Gibbons, M. E., Ferguson, A. M., Lee, D. R., & Jaeger, R. G. (2003). Mother-offspring discrimination in the red-backed salamander may be context dependent. Herpetologica, 59, 322–333.CrossRefGoogle Scholar
  9. Gillette, J. R. (2003). Population ecology, Social behavior, and intersexual differences in a natural population of red-backed salamanders: A long-term field study. Unpublished doctoral dissertation. University of Louisiana at Lafayette, LafayetteGoogle Scholar
  10. Gillette, J. R., Kolb, S. E., Smith, J. A., & Jaeger, R. G. (2000). Pheromonal attractions to particular males by female redback salamanders (Plethodon cinereus). In R. Bruce, R. Jaeger, & L. Houck (Eds.), The Biology of plethodontid salamanders (pp. 431–440). New York: Springer Science and Business Media.CrossRefGoogle Scholar
  11. Herrick, C. J. (1948). The brain of the tiger salamander, Ambystoma tigrinum. Chicago: University of Chicago Press.CrossRefGoogle Scholar
  12. Hill, R. L., Mendelson, J. R., III, & Stabile, J. L. (2015). Direct observation and review of herbivory in Sirenidae (Amphibia: Caudata). Southeastern Naturalist, 14, N5–N9.CrossRefGoogle Scholar
  13. Jaeger, R. G. (1981). Dear enemy recognition and the costs of aggression between salamanders. The American Naturalist, 117, 962–974.CrossRefGoogle Scholar
  14. Jaeger, R. G., & Forester, D. C. (1983). Duration of the brooding period in the mountain dusky salamander (Desmognathus ochrophaeus) and its influence on aggression toward conspecifics. Copeia, 1983, 1098–1101.CrossRefGoogle Scholar
  15. Jaeger, R. G., & Gergits, W. F. (1979). Intra-and interspecific communication in salamanders through chemical signals on the substrate. Animal Behaviour, 27, 150–156.CrossRefGoogle Scholar
  16. Jaeger, R. G., Wicknick, J. A., Griffis, M. R., & Anthony, C. D. (1995). Socioecology of a terrestrial salamander: Juveniles enter adult territories during stressful foraging periods. Ecology, 76, 533–543.CrossRefGoogle Scholar
  17. Karuzas, J. M., Maerz, J. C., & Madison, D. M. (2004). An alternative hypothesis for the primary function of a proposed mate assessment behaviour in red-backed salamanders. Animal Behaviour, 68, 489–494.CrossRefGoogle Scholar
  18. Kohn, N. R., Jaeger, R. G., & Franchebois, J. (2005). Effects of intruder number and sex on territorial behavior of female red-backed salamanders (Plethodon cinereus: Plethodontidae). Journal of Herpetology, 39, 645–648.CrossRefGoogle Scholar
  19. Krusche, P., Uller, C., & Dicke, U. (2010). Quantity discrimination in salamanders. The Journal of Experimental Biology, 213, 1822–1828.CrossRefGoogle Scholar
  20. Kundey, S. M., Millar, R., McPherson, J., Gonzalez, M., Fitz, A., & Allen, C. (2016). Tiger salamanders’ (Ambystoma tigrinum) response learning and usage of visual cues. Animal Cognition, 19, 533–541.CrossRefGoogle Scholar
  21. Lang, C., & Jaeger, R. G. (2000). Defense of territories by male-female pairs in the red-backed salamander (Plethodon cinereus). Copeia, 2000, 169–177.CrossRefGoogle Scholar
  22. Mathis, A. (1990). Territoriality in a terrestrial salamander: The influence of resource quality and body size. Behaviour, 112, 162–175.CrossRefGoogle Scholar
  23. McGavin, M. (1978). Recognition of conspecific odors by the salamander Plethodon cinereus. Copeia, 1978, 356–358.CrossRefGoogle Scholar
  24. Nunes, V. d. S., & Jaeger, R. G. (1989). Salamander aggressiveness increases with length of territorial ownership. Copeia, 1989, 712–718.CrossRefGoogle Scholar
  25. Petranka, J. W. (1998). Salamanders of the US and Canada. Washington, DC: Smithsonian Institution Press.Google Scholar
  26. Prosen, E. D., Jaeger, R. G., & Lee, D. R. (2004). Sexual coercion in a territorial salamander: Females punish socially polygynous male partners. Animal Behaviour, 67, 85–92.CrossRefGoogle Scholar
  27. Roth, G. (1987). Studies in brain function: Visual behavior in salamanders. Berlin: Springer-Verlag.CrossRefGoogle Scholar
  28. Semlitsch, R. D. (2008). Differentiating migration and dispersal processes for pond-breeding amphibians. Journal of Wildlife Management, 72, 260–267.CrossRefGoogle Scholar
  29. Twitty, V., Grant, D., & Anderson, O. (1964). Long distance homing in the newt Taricha rivularis. Proceedings of the National Academy of Sciences, 51, 51–58.CrossRefGoogle Scholar
  30. Uller, C., Jaeger, R., Guidry, G., & Martin, C. (2003). Salamanders (Plethodon cinereus) go for more: Rudiments of number in an amphibian. Animal Cognition, 6, 105–112.CrossRefGoogle Scholar

Copyright information

© Springer Nature Switzerland AG 2019

Authors and Affiliations

  1. 1.School of Biological SciencesGeorgia Institute of TechnologyAtlantaUSA
  2. 2.Department of ResearchZoo AtlantaAtlantaUSA

Section editors and affiliations

  • Joseph Boomer
    • 1
  1. 1.University at BuffaloBuffaloUSA