Endoxocrinus parrae explained

Endoxocrinus parrae is a species of stalked crinoids of the family Isselicrinidae. It is the most commonly found isocrinine species in west Atlantic Ocean.

Morphology

As members of the order Isocrinida, E. parrae possess a heteromorphic stalk that is made of calcareous nodal columns. Their body is mostly made of porous ossicles, with minimal soft tissue connecting the calcareous structure.[1] The stalks can measure 50.5 cm in some subspecies, but average between 10.2 cm and 23.5 cm. The stalks average between 4–5mm in diameter, and are connected to between 23 and 58 feeding arms that branch off radially around the mouth and anus.[2] While some subspecies of E. parrae possess arms with a smooth dorsal surface, others have been shown to exhibit a serrated dorsal surface, while others have shown morphology that is between the two characteristics, not quiet smooth but not fully serrated.[3] Cirri allow the crinoid to attach itself to the sediment and continue upwards along the stalk.

Distribution and habitat

Endoxocrinus parrae is found in benthic communities between 200–1000m deep in the western Atlantic Ocean, and Indo-West Pacific Ocean[4] though it is most common between 500-600m. It has been found as far north as the Florida strait and as far south as Brazil, and is native to tropical benthic communities.[5] E. parrae has been shown to grown at a more rapid rate in shallower depths due to temperature, but also exhibit less growth in areas without a strong flow of water. As E. parrae are filter feeders, a strong current is required for them to obtain necessary nutrients and energy for growth and survival.[6] They are most commonly found in large groups along areas of good water flow, such as along ridges, boulders, and mounds. E. parrae have also been observed crawling along the sea floor from areas of low flow to higher flow.[7]

Feeding biology and behavior

As filter feeders, Endoxocrinus parrae use their large branching arms to collect food from the water column. About 60% of the gut content of E. parrae has been found to be detritus, suggesting that they mostly feed on marine snow and other particulate matter in the water column. While feeding, E. parrae will selectively feed on small, organic particles, and have been documented waving their arms in response to capturing large, inorganic particles. This waving action flings the particles away from the crinoid's mouth, keeping it clean.[8]

Along the ocean floor, E. parrae is often preyed upon by pencil urchins such as Calocidaris micans.[9] The stomachs of C. mican collected around E. parrae contained large amounts of crinoid stems and soft tissue. In response to this, Endoxocrinus parrae have been observed detaching itself and using its cirri to move across the bottom of the ocean away from the predator. In addition, it is believed that the crinoids offer part of their stem up to the pencil urchin, allowing it time to flee while the urchin feeds.[10] E. parrae have reached speeds of up to 140 m per hour while crawling across the sea floor.[11]

Subspecies

While originally thought to be three separate species- Endoxocrinus parrae, Endoxocrinus prionedes, and Endoxocrinus carolinae, are now recognized as three subspecies of Endoxocrinus parrae. The speciation of E. parrae has been hypothesized to be a result of different environmental conditions.

Notes and References

  1. Book: Ruppert . Edward E. . Fox . Richard S. . Barnes . Robert D. . Invertebrate Zoology, 7th edition. . 2004 . Cengage Learning . 978-81-315-0104-7 . 917–927.
  2. David . Jerome . Roux . Michel . Messing . Charles G. . Ameziane . Nadia . Revision of the pentacrinid stalked crinoids of the genus Endoxocrinus (Echinodermata, Crinoidea), with a study of environmental control of characters and its consequences for taxonomy . Zootaxa . 2006 . 1156 . 1–50 . 10.5281/zenodo.172265.
  3. Oji . Tatsuo . Is Predation Intensity Reduced With Increasing Depth? Evidence from the West Atlantic Stalked Crinoid Endoxocrinus parrae (Gervais) and Implications for the Mesozoic Marine Revolution . Paleobiology . 1996 . 22 . 3 . 339–351 . 10.1017/S0094837300016328.
  4. McClintock . James B. . Baker . Bill J. . Baumiller . Tomasz K. . Messing . Charles G. . Lack of chemical defense in two species of stalked crinoids: support for the predation hypothesis for mesozoic bathymetric restriction . Journal of Experimental Marine Biology and Ecology . 1 January 1999 . 232 . 1 . 7 . 10.1016/s0022-0981(98)00003-3 .
  5. Oji . Tatsuo . Dimorphism and Geographic Distribution of Two Phenotypes of a West Atlantic Stalked Crinoid Endoxocrinus parrae (Gervais) . Japan Paleontology Report and Journal . 159 . 603–606 . 10.14825/prpsj1951.1990.159_603 . 1990 .
  6. Messing . Charles G . David . Jérôme . Roux . Michel . Améziane . Nadia . Baumiller . Tomasz K. . In situ stalk growth rates in tropical western Atlantic sea lilies (Echinodermata: Crinoidea) . Journal of Experimental Marine Biology and Ecology . Dec 28, 2007 . 353 . 2 . 211–220 . 10.1016/j.jembe.2007.08.021.
  7. Barreras . Ruber Rodriguez . Messing . Charles G. . A New List of Cuban Crinoids (Echinodermata: Crinoidea) . Caribbean Journal of Science . June 2013 . 47 . 2–3 . 198–212. 10.18475/cjos.v47i3.a09 .
  8. Young. Craig M.. Emson. Roland H.. 1995. Rapid Arm Movements in Stalked Crinoids. Biological Bulletin. 188. 1. 89–97. 10.2307/1542071. 29281300. 1542071.
  9. Book: O'Hara, Timothy. Byrne, Maria. Australian Echinoderms: Biology, Ecology and Evolution . 2017 . Csiro Publishing . 978-1-4863-0763-0 . 192.
  10. Baumiller. Tomasz K.. Mooi. Rich. Messing. Charles G.. 2008. Urchins in the Meadow: Paleobiological and Evolutionary Implications of Cidaroid Predation on Crinoids. Paleobiology. 34. 1. 22–34. 10.1666/07031.1.
  11. Milius. Susan. October 22, 2005. Great Galloping Crinoids. Science News. 168. 17. 261–262. 10.2307/4016930. 4016930.
  12. Web site: Messing . C. . World List of Crinoidea. Endoxocrinus (Endoxocrinus) parrae (Gervais in Guérin, 1835). . World Register of Marine Species . World Register of Marine Species . 14 April 2019.