Abstract
Several aspects of the behavior of fossil sirenians can be inferred from their skeletal remains. Their transition from terrestrial walking to obligate swimming is relatively well documented by their postcranial skeletons. The salinity of their aquatic habitats, as well as their diets, is determinable from stable isotopes in their tooth enamel. Deflection and width of the front parts of their skulls, respectively, reflect where in the water column they fed, and how selective they were in feeding. Specializations of tusks and other teeth also offer hints about diet, intraoral food transport, and mastication. Sizes of the infraorbital and mental foramina may reflect the importance of their prehensile and tactile vibrissae. The three Recent sirenian genera have divergently adapted in radically different ways, especially in feeding adaptations, to environmental changes of the last 10 million years. Fossils shed little light on vision, chemical senses, or touch, apart from the facial vibrissae, but future study of their ear bones could reveal much about the evolution of sirenian hearing.
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References
Anderson PK (2002) Habitat, niche, and evolution of sirenian mating systems. J Mamm Evol 9:55–98. https://doi.org/10.1023/A:1021383827946
Bajpai S, Domning DP, Das DP et al (2009) A new middle Eocene sirenian (Mammalia, Protosirenidae) from India. Neues Jahrb Geol Pal Abh 252:257–267. https://doi.org/10.1127/0077-7749/2009/0252-0257
Barboza M, Larkin IV (2020) Gross and microscopic anatomy of the nasal cavity, including olfactory epithelium, of the Florida manatee Trichechus manatus latirostris. Aquat Mamm 46:274–284. https://doi.org/10.1578/AM.46.3.2020.274
Beatty BL, Vitkovski T, Lambert O et al (2012) Osteological associations with unique tooth development in manatees (Trichechidae, Sirenia): a detailed look at modern Trichechus and a review of the fossil record. Anat Rec 295:1504–1512. https://doi.org/10.1002/ar.22525
Benoit J, Adnet S, El Mabrouk E et al (2013) Cranial remain from Tunisia provides new clues for the origin and evolution of Sirenia (Mammalia, Afrotheria) in Africa. PLoS ONE 8:e54307. https://doi.org/10.1371/journal.pone.0054307
de Buffrénil V, Canoville A, D’Anastasio R et al (2010) Evolution of sirenian pachyosteosclerosis, a model-case for the study of bone structure in aquatic tetrapods. J Mamm Evol 17:101–120. https://doi.org/10.1007/s10914-010-9130-1
Clementz MT, Sorbi S, Domning DP (2009) Evidence of Cenozoic environmental and ecological change from stable isotope analysis of sirenian remains from the Tethys-Mediterranean region. Geology 37:307–310. https://doi.org/10.1130/G25533A.1
Diaz-Berenguer E, Badiola A, Moreno-Azanza M et al (2018) First adequately-known quadrupedal sirenian from Eurasia (Eocene, Bay of Biscay, Huesca, northeastern Spain). Nat Sci Rep 8:1–13. https://doi.org/10.1038/s41598-018-23355-w
Domning DP (1978) Sirenian evolution in the North Pacific Ocean. Univ Calif Publ Geol Sci 118:xi + 176
Domning DP (1982) Evolution of manatees: a speculative history. J Paleont 56:599–619
Domning DP (1995) What do we know about the evolution of the dugong? In: Mermaid symposium: first international symposium on Dugong and Manatees. November 15–17, 1995, Toba, Mie, Japan. Abstracts. Toba (Japan), Toba Aquarium, pp 23–24
Domning DP (1997) Sirenia. In: Kay RF, Madden RH, Cifelli RL et al. (eds) Vertebrate paleontology in the Neotropics: the Miocene fauna of La Venta, Colombia. Smithsonian Inst., Washington & London, pp 383–391
Domning DP (2001a) The earliest known fully quadrupedal sirenian. Nature 413:625–627. https://doi.org/10.1038/35098072
Domning DP (2001b) Sirenians, seagrasses, and Cenozoic ecological change in the Caribbean. In: Miller W III, Walker SE (eds) Cenozoic palaeobiology: the last 65 million years of biotic stasis and change. Palaeogeogr Palaeoclimatol Palaeoecol 166(Special Issue):27–50
Domning DP (2005) Fossil Sirenia of the West Atlantic and Caribbean region. VII. Pleistocene Trichechus manatus Linnaeus, 1758. J Vert Pal 25:685–701. https://doi.org/10.1671/0272-4634(2005)025[0685:FSOTWA]2.0.CO;2
Domning DP, Beatty BL (2007) Use of tusks in feeding by dugongid sirenians: observations and tests of hypotheses. Anat Rec 290:523–538. https://doi.org/10.1002/ar.20540
Domning DP, de Buffrénil V (1991) Hydrostasis in the Sirenia: quantitative data and functional interpretations. Mar Mamm Sci 7:331–368. https://doi.org/10.1111/j.1748-7692.1991.tb00111.x
Domning DP, Furusawa H (1995) Summary of taxa and distribution of Sirenia in the North Pacific Ocean. Island Arc 3:506–512. https://doi.org/10.1111/j.1440-1738.1994.tb00129.x
Domning DP, Gingerich PD (1994) Protosiren smithae, new species (Mammalia, Sirenia), from the late Middle Eocene of Wadi Hitan Egypt. Contr Mus Pal Univ Michigan 29:69–87
Domning DP, Hayek LC (1984) Horizontal tooth replacement in the Amazonian manatee (Trichechus inunguis). Mammalia (Paris) 48:105–127. https://doi.org/10.1515/mamm.1984.48.1.105
Domning DP, Hayek LC (1986) Interspecific and intraspecific morphological variation in manatees (Sirenia: Trichechus). Mar Mamm Sci 2:87–144. https://doi.org/10.1111/j.1748-7692.1986.tb00034.x
Edinger T (1933) Über Gehirne tertiärer Sirenia Ägyptens und Mitteleuropas sowie der rezenten Seekühe. Abh Bayer Akad Wiss, math-natw Abt (n.s.) 20:5–36
Edinger T (1975) Paleoneurology 1804–1966: an annotated bibliography. Adv Anat Embryol Cell Biol 49:1–258
Gaspard JC III, Bauer GB, Mann DA et al (2017) Detection of hydrodynamic stimuli by the postcranial body of Florida manatees (Trichechus manatus latirostris). J Comp Physiol A 203:111–120. https://doi.org/10.1007/s00359-016-1142-8
Gheerbrant E, Domning DP, Tassy P (2005) Paenungulata (Sirenia, Proboscidea, Hyracoidea, and relatives). In: Rose KD, Archibald JD (eds) The rise of placental mammals: origins and relationships of the major extant clades. Johns Hopkins, Baltimore, pp 84–105
Hautier L, Sarr R, Tabuce R et al (2012) First prorastomid sirenian from Senegal (western Africa) and the old world origin of sea cows. J Vertebr Paleontol 32:1218–1222. https://doi.org/10.1080/02724634.2012.687421
Janis C, Ehrhardt D (1988) Correlation of relative muzzle width and relative incisor width with dietary preferences in ungulates. Zool J Linnean Soc 92:267–284. https://doi.org/10.1111/j.1096-3642.1988.tb01513.x
Kerber L, Moraes MH (2021) Endocranial morphology of an early/middle Miocene South American dugong and the neurosensorial evolution of sirenians. J Mamm Evol. https://doi.org/10.1007/s10914-021-09555-8
Kleinschmidt A (1951) Über ein Skelet und eine Rekonstruktion des äusseren Habitus der Riesenseekuh, Rhytina gigas Zimmermann 1780. Zool Anz 146:292–314
Kojeszewski T, Fish FE (2007) Swimming kinematics of the Florida manatee (Trichechus manatus latirostris): hydrodynamic analysis of an undulatory mammalian swimmer. J Exp Biol 210:2411–2418. https://doi.org/10.1242/jeb.02790
Lanyon JM, Sanson GD (2006a) Degenerate dentition of the dugong (Dugong dugon), or why a grazer does not need teeth: morphology, occlusion and wear of mouthparts. J Zool 268:133–152. https://doi.org/10.1111/j.1469-7998.2005.00004
Lanyon JM, Sanson GD (2006b) Mechanical disruption of seagrass in the digestive tract of the dugong. J Zool 270:277–289. https://doi.org/10.1111/j.1469-7998.2006.00135.x
Lanyon JM, Athousis C, Sneath HL et al (2021) Body scarring as an indicator of social function of dugong (Dugong dugon) tusks. Mar Mamm Sci 37:1–12. https://doi.org/10.1111/mms.12788
Lyman CP (1939) A vestigial lower incisor in the dugong. J Mammal 20:229–231
Mackay-Sim A, Duvall D, Graves BM (1985) The West Indian manatee (Trichechus manatus) lacks a vomeronasal organ. Brain Behav Evol 27:186–194. https://doi.org/10.1159/000118729
Marriott S, Cowan E, Cohen J (2013) Somatosensation, echolocation, and underwater sniffing: adaptations allow mammals without traditional olfactory capabilities to forage for food underwater. Zool Sci 30:69–75. https://doi.org/10.2108/zsj.30.69
Marsh H (1980) Age determination of the dugong (Dugong dugon (Müller)) in northern Australia and its biological implications. In: Perrin WF Myrick, AC Jr (eds) Age determination of toothed whales and sirenians. Reports International Whaling Commission 3(Special Issue):181–201
Marsh H, O’Shea TJ, Reynolds JE III (2011) Ecology and conservation of the Sirenia: dugongs and manatees. Cambridge University, Cambridge (U.K.) (Conservation Biology Series No. 18):xvi + 521
Marsh H, Grech A, McMahon K (2018) Dugongs: Seagrass Community Specialists. In: Larkum A, Kendrick G, Ralph P. (eds) Seagrasses of Australia. Springer, Cham. https://doi.org/10.1007/978-3-319-71354-0_19
Owen R (1875) On fossil evidences of a sirenian mammal (Eotherium aegyptiacum, Owen) from the Nummulitic Eocene of the Mokattam Cliffs, near Cairo. Q J Geol Soc London 31:100–105. https://doi.org/10.1144/GSL.JGS.1875.031.01-04.05
Perini FA, Nascimento ER, Cozzuol MA (2020) New species of Trichechus Linnaeus, 1758 (Sirenia, Trichechidae), from the upper Pleistocene of southwestern Amazonia, and the evolution of Amazonian manatees. J Vertebr Paleontol 39:e1697882. https://doi.org/10.1080/02724634.2019.1697882
Promus J (1937) Netting dugong. Walkabout 3:40–41
Reep RL, Stoll ML, Marshall CD et al (2001) Microanatomy of facial vibrissae in the Florida manatee: the basis for specialized sensory function and oripulation. Brain Behav Evol 58:1–14. https://doi.org/10.1159/000047257
Reep RL, Marshall CD, Stoll ML (2002) Tactile hairs on the postcranial body in Florida manatees: a mammalian lateral line? Brain Behav Evol 59:141–154. https://doi.org/10.1159/000064161
Savage RJG, Domning DP, Thewissen JGM (1994) Fossil Sirenia of the West Atlantic and Caribbean region. V. The most primitive known sirenian, Prorastomus sirenoides Owen, 1855. J Vertebr Paleontol 14:427–449. https://doi.org/10.1080/02724634.1994.10011569
Sickenberg O (1934) Beiträge zur Kenntnis tertiärer Sirenen. I. Die eozänen Sirenen des Mittelmeergebietes. II. Die Sirenen des belgischen Tertiärs. Mém Mus Roy Hist Nat Belgique 63:1–352
Sorbi S, Domning DP, Vaiani SC et al (2012) Metaxytherium subapenninum (Bruno, 1839) (Mammalia, Dugongidae), the latest sirenian of the Mediterranean basin. J Vertebr Paleontol 32:686–707. https://doi.org/10.1080/02724634.2012.659100
Steller GW (1751) De bestiis marinis. Novi Comm Acad Sci Petropolitanae 2:289–398
Sunter GH (1937) Adventures of a trepang fisher. London, Hurst & Blackett Ltd., pp 1–288
Takahashi S, Domning DP, Saito T (1986) Dusisiren dewana, n. sp. (Mammalia: Sirenia), a new ancestor of Steller’s sea cow from the Upper Miocene of Yamagata Prefecture, northeastern Japan. Trans Proc Pal Soc Japan (n.s.) 141:296–321. https://doi.org/10.14825/prpsj1951.1986.141_296
York PH, Carter AB, Chartrand K et al (2015) Dynamics of a deep-water seagrass population on the Great Barrier Reef: annual occurrence and response to a major dredging program. Sci Rep 5:13167. https://doi.org/10.1038/srep13167
Zalmout IS, Gingerich PD (2012) Late Eocene sea cows (Mammalia, Sirenia) from Wadi Al Hitan in the Western Desert of Fayum, Egypt. University of Michigan Papers on Paleontology 37:xiii + 158
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Domning, D.P. (2022). What Can We Infer About the Behavior of Extinct Sirenians?. In: Marsh, H. (eds) Ethology and Behavioral Ecology of Sirenia. Ethology and Behavioral Ecology of Marine Mammals. Springer, Cham. https://doi.org/10.1007/978-3-030-90742-6_1
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