
The Crinoidea
includes the most exquisite members of the Echinodermata, far more stunning as
a rule than any plodding urchin or commonplace starfish (just to let you know
at the outset where my allegiance lies). With a family tree rooted in almost
500 million years of history, they are the senior group of living echinoderms.
Their typically echinoderm features include:
·
5-sided adult symmetry derived from a bilateral larva.
·
Water vascular system - a network of coelomic
canals and reservoirs that may serve in respiration, circulation, feeding and
locomotion, and that terminates in external podia, or tube feet.
·
Calcareous endoskeleton consisting of individual plates (ossicles)
with a meshwork fine structure (stereom), each
formed from a single high-magnesium calcite crystal.
·
Mutable collagenous (or catch connective)
tissue that can alter between rigid and flaccid states under neuronal control.
·
Deuterostome, enterocoelous
embryonic development with radial cleavage (Brusca
and Brusca 1990).
Features
that distinguish crinoids from other echinoderms are:
·
Two to four circlets of ossicles (never 4 in living species) fused
together as a cup- or box-like calyx that contains or supports the
viscera.
·
Five flexible, usually branched and featherlike rays—extensions of the body wall supported by
skeletal plates and bearing food-collecting grooves and extensions of
the water-vascular, nervous, haemal and reproductive
systems.
·
The oral surface contains both mouth and anus and orients away from the
substrate.

Most of the several
thousand known fossil crinoids and several dozen modern deep-water species bear
a stalk on the side of the body opposite the mouth (aboral) and are
known as sea lilies. Imagine a feathery starfish on a stick. (Thanks,
Conrad.) Modern stalked crinoids live almost entirely in waters deeper than 200
m, although Metacrinus rotundus
occurs in 100 m off
This website outlines our current understanding of living crinoids: their
phylogeny, distribution and ecology. It also includes a detailed
introduction to morphological features, terms and symbology, a
discussion of practical aspects of working with specimens and the difficulties
associated with species identifications. There's also an artificial key to
the families of living crinoids—artificial because detailed phylogenies have
not yet been worked out (watch this space).
REFERENCES
Ausich, W.I. 1996. Echinodermata.
Pp. 242-261, IN: Feldmann, R. M. (ed.) Fossils of
Ausich, W.I. 1997. Calyx plate
homologies and early evolutionary history of the Crinoidea. Pp. 289-304,
IN: Waters, J. A. & Maples, C. G. (eds.) Geobiology
of Echinoderms. Paleontological Society Papers 3.
Brusca, R.
& Brusca, G.J. 1990. Invertebrates. Sinauer,
Guensburg, T.E.
& Sprinkle, J. 2003. The oldest known crinoids (Early
Ordovician,
Heinzeller, T.
& Welsch, U. 1994. Crinoidea. Pp. 9-148 IN:
Hess, H., Ausich, W.I., Brett, C.E. &
Simms, M.J. 1999. Fossil Crinoids.
Messing,
C.G. 1997. Living Comatulids. Pp. 3-30 IN: Waters,
J.A. & Maples, C.G. (eds.) Geobiology
of Echinoderms. Paleontological Society Papers 3.
Messing, C.G. and Dearborn, J.H. 1990. Marine
Flora and Fauna of the
Meyer,
D.L. and Macurda, D.B., Jr. 1977. Adaptive radiation of the
comatulid crinoids. Paleobiology 3:74-82.
Oji, T.
1986. Skeletal variation related to arm regeneration in Metacrinus
and Saracrinus, Recent stalked crinoids. Lethaia 19:355-360.
Roux, M., Messing, C.G. & Améziane, N. 2002. Artificial
keys to the genera of living stalked crinoids (Echinodermata). Bulletin of
Marine Science 70(3):799-830.