Crinoids are marine animals that make up the class Crinoidea of the echinoderms (phylum Echinodermata). Crinoidea comes from the Greek word krinon, "a lily", and eidos, "form".<ref>Webster's New Universal Unabridged Dictionary. 2nd ed. 1979.</ref> They live both in shallow water and in depths as great as 6,000 meters.Template:Citation needed Sea lilies refer to the crinoids which, in their adult form, are attached to the sea bottom by a stalk.<ref>Template:Cite web</ref> Feather stars<ref>Template:Cite web</ref> or comatulids<ref name=tolweb>Template:Cite web</ref> refer to the unstalked forms.
Crinoids are characterized by a mouth on the top surface that is surrounded by feeding arms. They have a U-shaped gut, and their anus is located next to the mouth. Although the basic echinoderm pattern of fivefold symmetry can be recognized, most crinoids have many more than five arms. Crinoids usually have a stem used to attach themselves to a substrate, but many live attached only as juveniles and become free-swimming as adults.
There are only about 600 extant crinoid species,<ref name=adw>Template:Cite web</ref> but they were much more abundant and diverse in the past. Some thick limestone beds dating to the mid- to late-Paleozoic are almost entirely made up of disarticulated crinoid fragments.
Crinoids comprise three basic sections; the stem, the calyx, and the arms. The stem is composed of highly porous ossicles which are connected by ligamentary tissue. The calyx contains the crinoid's digestive and reproductive organs, and the mouth is located at the top of the dorsal cup, while the anus is located peripheral to it. The arms display pentamerism or pentaradial symmetry and comprise smaller ossicles than the stem and are equipped with cilia which facilitate feeding by moving the organic media down the arm and into the mouth.vestigial stalk. In those deep-sea species that still retain a stalk, it may reach up to Template:Convert in length, although it is usually much smaller. The stalk grows out of the aboral surface, which forms the upper side of the animal in starfish and sea urchins, so that crinoids are effectively upside-down by comparison with most other echinoderms. The base of the stalk consists of a disc-like sucker, which, in some species, has root-like structures that further increase its grip on the underlying surface. The stalk is often lined by small cirri.<ref name=IZ>Template:Cite book</ref>
Like other echinoderms, crinoids have pentaradial symmetry. The aboral surface of the body is studded with plates of calcium carbonate, forming an endoskeleton similar to that in starfish and sea urchins. These make the calyx somewhat cup-shaped, and there are few, if any, ossicles in the oral (upper) surface. The upper surface, or tegmen, is divided into five ambulacral areas, including a deep groove from which the tube feet project, and five interambulacral areas between them. The anus, unusually for echinoderms, is found on the same surface as the mouth, at the edge of the tegmen.<ref name=IZ/>
The ambulacral grooves extend onto the arms, which thus have tube feet along their inner surfaces. Primitively, crinoids had only five arms, but in most living species these are divided into two, giving ten arms in total. In most living species, especially the free-swimming feather stars, the arms branch several times, producing up to two hundred branches in total. The arms are jointed, and lined by smaller feather-like appendages, or pinnules, which also include tube feet.<ref name=IZ/>
Crinoids feed by filtering small particles of food from the sea water with their feather like arms. The tube feet are covered with a sticky mucus that traps any food that floats past. Once they have caught a particle of food, the tube feet can flick it into the ambulacral groove, where the cilia are able to propel the stream of mucus towards the mouth. Generally speaking, crinoids living in environments with relatively little plankton have longer and more highly branched arms than those living in rich environments.<ref name=IZ/>
The mouth descends into a short oesophagus. There is no true stomach, so the oesophagus connects directly to the intestine, which runs in a single loop right around the inside of the calyx. The intestine often includes numerous diverticulae, some of which may be long or branched. The end of the intestine opens into a short muscular rectum. This ascends towards the anus, which projects from a small conical protuberance at the edge of the tegmen.<ref name=IZ/>
Like other echinoderms, crinoids possess a water vascular system that maintains hydraulic pressure in the tube feet. This is not connected to external sea water, as in other echinoderms, but only to the body cavity. The body cavity is itself somewhat restricted, being largely replaced by connective tissue, although it is present as narrow canals within the arms and stalk.<ref name=IZ/>
Crinoids also possess a separate haemal system, consisting of fluid-filled sinuses within the connective tissue. There is a large plexus of sinuses around the oesophagus, with branches extending down to a mass of glandular tissue at the base of the calyx.<ref name=IZ/>
These various fluid-filled spaces, in addition to transporting nutrients around the body, also function as both a respiratory and an excretory system. Oxygen is absorbed primarily through the tube feet, which are the most thin-walled parts of the body, while waste is collected by phagocytic coelomocytes.<ref name=IZ/>
The crinoid nervous system is divided into three parts, with numerous connections between them. The uppermost portion is the only one homologous with the nervous systems of other echinoderms. It consists of a central nerve ring surrounding the mouth, and radial nerves branching into the arms. Below this lies a second nerve ring, giving off two brachial nerves into each arm. Both of these sets of nerves are sensory in nature, with the lower set supplying the pinnules and tube feet.<ref name=IZ/>
The third portion of the nervous system lies below the other two, and is responsible for motor action. This is centred on a mass of neural tissue near the base of the calyx, and provides a single nerve to each arm and a number of nerves to the stalk.<ref name=IZ/>
Reproduction and life cycle
Crinoids are dioecious, with separate male and female individuals. They have no true gonads, producing their gametes from genital canals found inside some of the pinnules. The pinnules eventually rupture to release the sperm and eggs into the surrounding sea water.<ref name=IZ/>
The fertilised eggs hatch to release a free-swimming vitellaria larva. The larva is barrel-shaped with rings of cilia running round the body, and a tuft of sensory hairs at the upper pole. In some cases females have been known to temporarily brood the larvae using chambers within the arms. The larva does not feed, and lasts only for a few days before settling to the bottom and attaching itself to the underlying surface using an adhesive gland on its ventral surface. The larva then metamorphoses into a stalked adult. Even the free-swimming feather stars sometimes go through this stage, with the adult eventually breaking away from the stalk.<ref name=IZ/>
Within 10 to 16 months the crinoid will be able to reproduce.Template:Citation needed
Most modern crinoids are free-swimming and lack a stem. Examples of fossil crinoids that have been interpreted as free-swimming include Marsupitsa, Saccocoma and Uintacrinus.Template:Citation needed
In 2005, a stalked crinoid was recorded pulling itself along the sea floor off the Grand Bahama Island. While it has been known that stalked crinoids move, before this recording the fastest motion of a crinoid was 0.6 meters/hour (2 ft/h). The 2005 recording showed a crinoid moving much faster.<ref>Template:Cite conference</ref>
The earliest known crinoid groups date to the Ordovician. There are two competing hypotheses pertaining to the origin of the group: the traditional viewpoint holds that crinoids evolved from within the blastozoans (the eocrinoids and their derived descendants the cystoids), whereas the most popular alternative suggests that the crinoids split early from among the edrioasteroids.<ref name='Guensburg2010'>Template:Cite doi</ref> The debate is difficult to settle, in part because all three candidate ancestors share many characteristics, including radial symmetry, calcareous plates, and stalked or direct attachment to the substrate.<ref name='Guensburg2010'/>
The crinoids underwent two periods of abrupt adaptive radiation; the first during the Ordovician, the other after they underwent a selective mass extinction at the end of the Permian period.<ref name=Foote1999>Template:Cite journal</ref> This Triassic radiation resulted in forms possessing flexible arms becoming widespread; motility, predominantly a response to predation pressure, also became far more prevalent.<ref name=Baumiller2008>Template:Cite doi</ref> This radiation occurred somewhat earlier than the Mesozoic marine revolution, possibly because it was mainly prompted by increases in benthic predation, specifically of echinoids.<ref name='Baumiller2010'>Template:Cite doi</ref> After the end-Permian extinction, crinoids never regained the morphological diversity they enjoyed in the Paleozoic; they occupied a different region of morphospace, employing different ecological strategies from those that had proven so successful in the Paleozoic.<ref name=Foote1999/>
The long and varied geological history of the crinoids demonstrates how well the echinoderms have adapted to filter-feeding. The fossils of other stalked filter-feeding echinoderms, such as blastoids, are also found in the rocks of the Palaeozoic era. These extinct groups can exceed the crinoids in both numbers and variety in certain horizons. However, none of these others survived the crisis at the end of the Permian period.
Fossils of interest
Some fossil crinoids, such as Pentacrinites, seem to have lived attached to floating driftwood and complete colonies are often found. Sometimes this driftwood would become waterlogged and sink to the bottom, taking the attached crinoids with it. The stem of Pentacrinites can be several metres long. Modern relatives of Pentacrinites live in gentle currents attached to rocks by the end of their stem. The largest fossil crinoid on record had a stem Template:Convert in length.<ref>Template:Cite book</ref>
In 2006, geologists isolated complex organic molecules from 350-million-year-old fossils of crinoids—the oldest such molecules yet found. Christina O'Malley, a doctoral student in earth sciences at The Ohio State University, found orange and yellow organic molecules inside the fossilized remains of several species of crinoids dating back to the Mississippian period.<ref>Oldest Complex Organic Molecules Found in Ancient Fossils Ohio State Research News, Retrieved on March 13, 2011.</ref>
- Fossilised crinoid columnals extracted from limestone quarried on Lindisfarne, or found washed up along the foreshore, which were threaded into necklaces or rosaries, became known as St. Cuthbert's beads.
- In the Midwestern United States, fossilized segments of columnal crinoids are sometimes known as Indian beads.<ref>Template:Cite web</ref>
- Crinoids are the state fossil of Missouri.<ref>Template:Cite web</ref>
Template:Reflist <ref>1</ref> Fossils at a Glance (Second Edition) by Clare Milsom and Sue Rigby <references />
- Tree of Life (source of taxonomic information on this page)
- Article and video of crinoid crawling
- On the Crinoid Genus Scyphocrinus and its Bulbous Root Camarocrinus by Frank Springer. 3 p., 74 p. illus., IX pl. (2 fold.) 33 cm. Washington: Smithsonian Institution, 1917
- American Silurian Crinoids by Frank Springer. iv, 239 p. 33 pl., 2 port. 32 cm. Washington: The Smithsonian Institution, 1926
- Introduction to the Crinoidea: Sea lilies and feather stars... ucmp.berkeley.edu. Retrieved on February 7, 2007.
- A Journey in Crinoid Keeping by Michael Lukaczyn
- Crinoid Species of Cambodia
- Video of red feather staraz:Dəniz lalələri
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