Bibliography & Index of the Sirenia & Desmostylia

Bibliography and Index of the Sirenia and Desmostylia

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		Griffith, Edward; et al. (detail)
		1827-34	The animal kingdom arranged in conformity with its organization, by the Baron Cuvier ... with additional descriptions of all the species hitherto named, and of many not before noticed. London, Geo. B. Whittaker: 15 vols. Illus. –No. 751 in J. C. Smith, Georges Cuvier: an annotated bibliography of his published works, Smithsonian Inst. Press, 1993; see also Smith 752. The Mammalia constitute vols. 1-4 (1827). Includes Manatus senegalensis.

		Thomas, Oldfield; et al. (detail)
		1914	Nomina conservanda in Mammalia. Zool. Anz. 44(6): 284-286. –Same in substance as Thomas et al. (1924).

x		Thomas, Oldfield; et al. (detail)
		1924	Nomina conservanda in Mammalia. Proc. Zool. Soc. London 1924(2): 345-348. July 9, 1924 (read Apr. 1, 1924). –Recommends the conservation of the names Manatus and Rhytina in preference to Trichechus and Hydrodamalis, respectively (347).

	D	Yabe, Hisakatsu; et al. (detail)
		1951	Study of Desmostylus (first report). Jour. Geol. Soc. Japan 57(670): 256.

	D	Shikama, Tokio [et al.?] (detail)
		1957b	Palaeontology. Vol. 2. Tokyo, Asakura. –Desmostylia, 552-557.

		Fisher, James; Simon, Noel; Vincent, Jack; et al. (detail)
		1969	Wildlife in danger. New York, Viking Press; London, Collins: 1-368. –Discusses dugong distribution, population trends, uses, and legal protection (97-100).

x		Bradley, Richard, Et Al. (detail)
		1983	The Pre-Columbian exploitation of the manatee in Mesoamerica. Univ. Oklahoma Dept. Anthrop., Papers in Anthrop. 24(1): i + 82. 8 figs. Spring 1983. –Rev.: D. P. Domning, Sirenews No. 1: 14-17, 1984. M.A. thesis by Bradley, with Editor's Introduction by Stephen I. Thompson (3-8) and Comments by Frederick W. Lange, Franklin O. Loveland, Barbara L. Stark, B. L. Turner II, and Charles R. Wicke (61-82). Reviews data on manatee exploitation in the Americas, and speculates that the Olmecs were heavily dependent on manatees for food, raised them in artificial lagoons, portrayed them in their art, and may have used manatee calves in sacrifices.

	D	Inuzuka, Norihisa; et al. (eds.) (detail)
		1984	Desmostylians and their paleoenvironment. Monogr. Assoc. Geol. Collab. in Japan 28: 1-138. May 1984. –In Japanese.

	D	Suzuki, Keiji; et al. (detail)
		1986b	Investigated report on Paleoparadoxia of the Yanagawa Formation. Yanagawa (Japan), Yanagawa Town Educational Committee: 1-22. 7 pls. –In Japanese.

		Zhang, Yongzu; et al. (detail)
		1997	Distribution of mammalian species in China. China Forestry Publishing House: 1-279. –Dugong, 111.

		Heithaus, M.; Dill, L.; Marshall, G. et al. (detail)
		2002

		Kendall, Sarita; et al. (detail)
		2004	Los manatíes del Amazonas. Bogotá, Fundación Omacha: 1-24. Illus. –An attractive paperback booklet giving a gen. acc. of Amazonian manatee natural history, conservation, and folklore. Besides Kendall, 24 other coauthors are credited with contributions to the text.

		Lima, R. P,; Alvite, C. M. C.; Vergara-Parente, J. E.; et al. (detail)
		2005	Reproductive behavior in a captive-released manatee (Trichechus manatus manatus) along the northeastern coast of Brazil and the life history of her first calf born in the wild. Aquat. Mamms. 31: 420-426.

		Adimey, N. M.; Abernathy, K.; Gaspard, J. C. III et al. (detail)
		2007	Meeting the manatee challenge: the feasibility of using CRITTERCAM on wild manatees. Mar. Technol. Soc. J. 41: 14-18. https://doi.org/10.4031/002533207787442015

		Castelblanco-Martínez, Delma Nataly; et al. (detail)
		2007	Mamíferos aquáticos. Chap. 14 in: Rapp Py-Daniel L. et al. (eds.), Biodiversidade do Médio Madeira: bases científicas para propostas de conservação. Manaus, Probio/Mma.: 225-238.

		Harvey, J. W.; Harr, K. J.; Murphy, D.; et al. (detail)
		2007	Clinical biochemistry in healthy manatees (Trichechus manatus latirostris). Jour. Zoo Wildlife Med. 38: 269-279.

		Jaffe, J. S.; et al. (detail)
		2007	Measurement of the acoustic reflectivity of Sirenia (Florida manatees) at 171 kHz. Jour. Acoustical Soc. Amer. 121(1): 158-165.

		Okumura, N.; Ichikawa, K,; Akamatsu, T.; et al. (detail)
		2007	Stability of call sequence in dugongs' vocalization. Proc. Oceans 06 Asia Pacific 19: 12-15. 10.1109/OCEANSAP.2006.4393936

		Luna, F,O, Araujo, J.P., Lima, R.,P. et al. (detail)
		2008	Captura e utilizacao do peixe-boi marinho (Trichechus manatus manatus) no litoral norte do Brasil. Biotemas 21: 115-123. https://doi.org/10.5007/2175-7925.2008v21n1p115

		Marsh, H,; Grech , A,; Hodgson A. et al. (detail)
		2008	Distribution and abundance of the dugong in Gulf of Carpentaria waters: a basis for cross-jurisdictional conservation planning and management. Australian Centre for Applied Marine Mammal Science: 57 pp.

		Nakanishi Y.; Adulyanukosol K.; Arai N.; et al. (detail)
		2008	Dugong grazing scars confirmed in Enhalus acoroides meadows. J. Adv. Mar. Sci. and Soc. 14: 1-8.

		Ichikawa, K.; Akamatsu T.; Shinke, T.; et al. (detail)
		2009	Detection probability of vocalizing dugongs during playback of conspecific calls. J. Acoust. Soc. Amer. 126: 1954-1959.

		Satizábal, P.; Mignucci-Giannoni, A. A.; Duchêne, S.; Caicedo-Herrera, D.; Perea-Sicchar, C. M.; García-Dávila, C. R.; et al. (detail)
		2012	Phylogeography and sex-biased dispersal across riverine manatee populations (Trichechus inunguis and Trichechus manatus) in South America. PLoS One 7: e52468. doi: 10.1371/journal.pone.0052468

		Schumann, N,; Gales, N,; Harcourt, R.; et al. (detail)
		2013	Impacts of climate change on Australian marine mammals. Austral. J. Zool. 61: 146-169. 10.1071/ZO12131

		Acevedo-Olvera, G.; Delgado-Estrella, A.; Barreto-Castro, M. R.; et al. (detail)
		2015	Environmental characterization of a fluvial lagoon ecosystem (Pom-Atasta, Campeche, Mexico) as a critical manatee habitat. WIT Trans Built Env.: 168:407-413. 10.2495/SD150351

		D'Souza, E.; Patankar, V.; Arthur, R., et al. (detail)
		2015	Seagrass herbivory levels sustain site-fidelity in a remnant dugong population. PLoS ONE 10:1-18. 10.1371/journal.pone.0141224

		Aven, A. M.; Carmichael, R. H.; Hieb, E. E., et al. (detail)
		2016	West Indian manatee movements reveal novel occupancy and distribution patterns in the northern Gulf of Mexico. PeerJ Preprints. https://doi.org/10.7287/peerj.preprints.2072v1

		Nanayakkara, R. P.; de Mel, R. K.; Cabral, S. J. et al. (detail)
		2016	Dugongs, Dugong dugon (Family: Sirenia) and humans: the fisher's perspective. Asian J. Conserv. Bio. 5: 51-54.

		Zeh, D. R., Heupel, M. R., Hamann, M. et al. (detail)
		2016	Quick fix GPS technology highlights risk to dugongs moving between protected areas. Endangered Species Res. 30: 37-44. 10.3354/esr00725

		Balensiefer, D. C.; Attademo, F. L. N.; Sousa, G. P.; Freire, A. C. D. B.; da Cunha, F. A. G. C.; Alencar, A. E. B.; et al. (detail)
		2017	Three decades of Antillean manatee (Trichechus manatus manatus) stranding along the Brazilian Coast. Trop. Conserv. Sci. 10: 1-9. doi: 10.1177/1940082917728375

		Delisle, A,; Kim, M. K,; Stoeckl, N. et al. (detail)
		2017	The socio-cultural benefits and costs of the traditional hunting of dugongs Dugong dugon and green turtles Chelonia mydas in Torres Strait, Australia. Oryx 52: 250?261. https://doi.org/10.1017/S0030605317001466

		Puc-Carrasco, G,; Morales-Vela, B.; Olivera-Gomez, L. D.; et al. (detail)
		2017	First field-based estimate of Antillean manatee abundance in the San Pedro River system suggests large errors in current estimates for Mexico. Cienc. Mar. 43:285-299. 10.7773/cm.v43i4.2704

		Shawky, A. M.; Sallam, W. S.; Alwany, M. A.; et al. (detail)
		2017	Photo identification of dugongs in Marsa Alam and Wadi El Gemal National Park, Egyptian coast of the Red Sea. Al Azhar Bull. Sci. 28:1-10.

		Hagihara, R.; Jones, R. E, Sobtzick, S.; et al. (detail)
		2018	Compensating for geographic variation in detection probability with water depth improves abundance estimates of coastal marine megafauna. PloS One 13:e0191476. https://doi.org/10.1371/journal.pone.0191476

		O'Shea, T. J.; Takeuchi, N.; Weijs, L. et al. (detail)
		2018	Ecotoxicology of the Sirenia in the twenty-first century. In: Panti, C. & Fossi, C. (eds) Marine mammal ecotoxicology: Impacts of multiple stressors on population health. pp. 429-456. 10.1016/B978-0-12-812144-3.00016-4

		Attademo, F. L. N.; Gomes, G. L.; Silva Flavio, J. L., et al. (detail)
		2020	Comportamento de peixes-boi - guia ilustrado. Brasilia, Instituto Chico Mendes de Conservacao da Biodiversidade

		Bassett, B.L.; Hostetler, J. A.; Leone, E.; et al. (detail)
		2020	Quantifying sublethal Florida manatee-watercraft interactions by examining scars on manatee carcasses. Endangered Species Research 43:395-408. https://doi.org/10.3354/esr01075

		Brady, B.; Hedwig, D.; Trygonis, V.; et al. (detail)
		2020	Classification of Florida manatee (Trichechus manatus latirostris) vocalizations. J. Acoust. Soc. Amer. 147: 1597--1606. 10.1121/10.0000849

		Cowart, J. R.; Collins, D. M.; Mignucci-Giannoni, A. A.; Alejandro-Zayas, T., Rivera-Guzman, A. L.; et al. (detail)
		2020	Manual collection and semen characterization in a West Indian manatee (Trichechus manatus). Frontiers in Veterinary Science 7: 810. –Abstract, copied here from Sirenews No. 72, p. 52: "Limited information is available regarding male reproductive physiology in West Indian manatees (Trichechus manatus). Currently, no reports evaluating any seminal characteristics exists in this species. To fill an apparent gap in knowledge, ejaculate samples were collected and characterized from a single, adult West Indian manatee. Samples were analyzed for the following semen parameters: volume, agglutination, pH, osmolality, viscosity, concentration, total sperm number, motility and kinematic parameters, morphology, plasma membrane integrity, acrosome integrity, chromatin maturation, and chromatin condensation. These results are the first of their kind for this species and suggest high semen quality, based on multiple ejaculates, in this male West Indian manatee."

		Favero, I.; Favero, G; Choi-Lima, K; et al. (detail)
		2020	Effects of freshwater limitation on distribution patterns and habitat use of the West Indian manatee, Trichechus manatus, in the northern Brazilian coast. Aquat. Conserv. 30: 1665?1673. https://doi.org/10.1002/aqc.3363.

		Srinivas, Y,; Pande, A,; Gole, S.; et al. (detail)
		2020	Mitochondrial phylogeography reveals high haplotype diversity and unique genetic lineage in Indian dugongs (Dugong dugon). Aquat Cons Mar Fresh Ecosys 31: 818-829. https://doi.org/10.1002/aqc.3490

		Edwards, H. H.; Hostetler, J. A.; Stith, B. M.; et al. (detail)
		2021	Monitoring abundance of aggregated animals (Florida manatees) using an unmanned aerial system (UAS). Sci. Repts. 11: 12920. https://doi.org/10.1038/s41598-021-92437-z

		Grace et al. (detail)
		2021	Testing a global standard for measuring species recovery and assessing conservation success. Conservation Biology 2021: 1-17. DOI: 10.1111/cobi.13756

		Landeo-Yauri, S.,S,; Castelblanco-Martinez, D., N,; Henaut, Y., et al. (detail)
		2021	Behavioural and physiological responses of captive Antillean manatees to small aerial drones. Wildl. Res. https://doi.org/: 10.1071/WR20159

		Lazensky, R.; Silva-Sanchez, C.; Kroll, K. J.; et al. (detail)
		2021	Investigating an increase in Florida manatee mortalities using a proteomic approach. Sci. Repts. 11: 4282. https://doi.org/10.1038/s41598-021-83687-y

		Medeiros, I.; Rebelo, V,; Santos, S; et al. (detail)
		2021	Spatiotemporal dynamics of mangrove forest and association with strandings of Antillean manatee (Trichechus manatus) calves in Paraiba, Brazil. J. Mar. Biolog. Assoc. UK 1-8. doi:10.1017/S002531542100045X

		Castelblanco-Martínez, Delma Nataly; Slone, D. H.; Landeo-Yauri, S. S.; Ramos, E.; Alvarez-Aleman, A.; et al. (detail)
		2021b	Analysis of body condition indices reveals different ecotypes of the Antillean manatee. Sci. Repts. 11(19451): 6 tabs. 6 figs. https://doi.org/10.1038/s41598-021-98890-0 Sept. 30, 2021. –ABSTRACT: Assessing the body condition of wild animals is necessary to monitor the health of the population and is critical to defining a framework for conservation actions. Body condition indices (BCIs) are a non-invasive and relatively simple means to assess the health of individual animals, useful for addressing a wide variety of ecological, behavioral, and management questions. The Antillean manatee (Trichechus manatus manatus) is an endangered subspecies of the West Indian manatee, facing a wide variety of threats from mostly human-related origins. Our objective was to define specific BCIs for the subspecies that, coupled with additional health, genetic and demographic information, can be valuable to guide management decisions. Biometric measurements of 380 wild Antillean manatees captured in seven different locations within their range of distribution were obtained. From this information, we developed three BCIs (BCI1?=?UG/SL, BCI2?=?W/SL3, BCI3?=?W/(SL*UG2)). Linear models and two-way ANCOVA tests showed significant differences of the BCIs among sexes and locations. Although our three BCIs are suitable for Antillean manatees, BCI1 is more practical as it does not require information about weight, which can be a metric logistically difficult to collect under particular circumstances. BCI1 was significantly different among environments, revealing that the phenotypic plasticity of the subspecies have originated at least two ecotypes -- coastal marine and riverine -- of Antillean manatees.

Daryl P. Domning, Research Associate, Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, D.C. 20560, and Laboratory of Evolutionary Biology, Department of Anatomy, College of Medicine, Howard University, Washington, D.C. 20059.

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Bibliography and Index of the Sirenia and Desmostylia

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