This group of sea cucumbers was first described by scientists aboard the H.M.S. Challenger during its 1873-1876 voyage.[4] Théel described the genus: "Body more or less depressed, with the anterior part of its brim rather large. Mouth ventral, at a greater distance from the foremost extremity of the body. Anus posterior, dorsal, usually almost terminal. Tentacles (?) twelve to twenty. Pedicels arranged in a single row round the brim of the body and in a double one along the odd ambulacrum. The dorsal surface seldom naked, commonly with a greater or smaller number of retractile or non-retractile, more or less inconsiderable processes, arranged in a single row all along each ambulacrum or in an irregular double row, or scattered over the lateral interambulacrae."[4] Théel also documented the details of species B. typica, B. sanguinolenta, and B. abyssicola.[4]
Anatomy
Among Psychropotidae, Benthodytes (synonym Benthodites) are characterized by "soft retractile tentacles, circum-oral or post-oral papillae and the absence of an unpaired dorsal appendage."[5]
Significance
Several species of Benthodytes are good indicators of the potential impacts of deep-sea mining and have been the subject of multiple studies.[6][7] Identification of distinct species is most often based on photography, since the delicate anatomy of the sea cucumbers is often damaged in the process of sampling.[6] Genome sequencing technology is paving the way for more accurate accounts of the evolution and taxonomy of Benthodytes species, starting with B. rosea and B. typica.[8] Additionally, the mitochondrial genome of B. marianensis has been sequenced and was found to contain a novel gene arrangement among holothurians that could be an adaptation allowing for survival at great depths.[9]
Species
Several species included in the genus Benthodytes have been reclassified using different nomenclature.[10] This list is subject to change as phylogenetic data clarifies the relationships among difficult-to-identify creatures whose soft appendages are often lost in the process of sample collection.[11]
↑ Glover A, Wiklund H, Rabone M, Amon D, Smith C, O'Hara T, Mah C, Dahlgren T (2016) Abyssal fauna of the UK-1 polymetallic nodule exploration claim, Clarion-Clipperton Zone, central Pacific Ocean: Echinodermata. Biodiversity Data Journal 4: e7251. https://doi.org/10.3897/BDJ.4.e7251
↑ Théel, H. (1882). Report on the Holothuroidea dredged by H.M.S. 'Challenger' during the years 1873-76. Part i. Report on the Scientific Results of the Voyage of H.M.S. Challenger during the years 1873–1876. Zoology. 4 (part 13): i-ix, 1-176, pl. 1-46., available online at http://19thcenturyscience.org/HMSC/HMSC-Reports/Zool-13/htm/doc.html
1 2 3 Théel, H. (1882). Report on the Holothuroidea dredged by H.M.S. 'Challenger' during the years 1873-76. Part i. Report on the Scientific Results of the Voyage of H.M.S. Challenger during the years 1873–1876. Zoology. 4 (part 13): i-ix, 1-176, pl. 1-46., available online at http://19thcenturyscience.org/HMSC/HMSC-Reports/Zool-13/htm/doc.htm
↑ Amon D J, Ziegler A F, Kremenetskaia A, Mah C L, Mooi R, O’Hara T, Pawson D L, Roux M, Smith C R. Megafauna of the UKSRL exploration contract area and eastern Clarion-Clipperton Zone in the Pacific Ocean: Echinodermata. Biodiversity Data Journal. May 2017; 5. e11794. 10.3897/BDJ.5.e11794.
↑ Bisol P M, Costa R, Sibuet M. Ecological and genetical survey on two deep-sea holothurians: Benthogone rosea and Benthodytes typica. Marine Ecology Progress Series. December 1983; 15 (3): 275-281. doi:10.3354/meps015275
Felley J D, Vecchione M, Wilson R R. Small-scale distribution of deep-sea demersal nekton and other megafauna in the Charlie-Gibbs Fracture Zone of the Mid-Atlantic Ridge. Deep Sea Research Part II: Topical Studies in Oceanography. January 2008; 55 (1-2): 153-160. https://doi.org/10.1016/j.dsr2.2007.09.021.
Brown A, Hauton C, Stratmann T, Sweetman A, van Oevelen D, Jones D O B. Metabolic rates are significantly lower in abyssal Holothuroidea than in shallow-water Holothuroidea. The Royal Society Open Science. May 2018; 5(5): doi:10.1098/rsos.172162
Murty Hughes S J, Ruhl H A, Hawkins L E, Hauton C, Boorman B, Billett D S M. Deep-Sea echinoderm oxygen consumption rates and an interclass comparison of metabolic rates in Asteroidea, Crinoidea, Echinoidea, Holothuroidea and Ophiuroidea. Journal of Experimental Biology. 2011; 214: 2512-2521. doi:10.1242/jeb.055954
This page is based on this Wikipedia article Text is available under the CC BY-SA 4.0 license; additional terms may apply. Images, videos and audio are available under their respective licenses.