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Brower, James C. (1992) Hybocrinid and disparid crinoids from the Middle Ordovician (Galena Group, Dunleith Formation) of northern Iowa and southern Minnesota. Journal of Paleontology, 66 (6) 973-993 doi:10.1017/s0022336000021053

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Reference TypeJournal (article/letter/editorial)
TitleHybocrinid and disparid crinoids from the Middle Ordovician (Galena Group, Dunleith Formation) of northern Iowa and southern Minnesota
JournalJournal of Paleontology
AuthorsBrower, James C.Author
Year1992 (November)Volume66
Issue6
PublisherCambridge University Press (CUP)
DOIdoi:10.1017/s0022336000021053Search in ResearchGate
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Mindat Ref. ID415752Long-form Identifiermindat:1:5:415752:0
GUID0
Full ReferenceBrower, James C. (1992) Hybocrinid and disparid crinoids from the Middle Ordovician (Galena Group, Dunleith Formation) of northern Iowa and southern Minnesota. Journal of Paleontology, 66 (6) 973-993 doi:10.1017/s0022336000021053
Plain TextBrower, James C. (1992) Hybocrinid and disparid crinoids from the Middle Ordovician (Galena Group, Dunleith Formation) of northern Iowa and southern Minnesota. Journal of Paleontology, 66 (6) 973-993 doi:10.1017/s0022336000021053
In(1992, November) Journal of Paleontology Vol. 66 (6) Cambridge University Press (CUP)
Abstract/NotesFour hybocrinid and disparid crinoids from the Middle Ordovician Dunleith Formation (Galena Group) of northern Iowa and southern Minnesota are described: Hybocrinus conicus Billings, Ohiocrinus levorsoni n. sp., Caleidocrinus (Huxleyocrinus) gerki n. sp., and Ectenocrinus simplex (Hall). The first three taxa are rare. Ectenocrinus simplex is an abundant and protean form ranging from the Shermanian to the Maysville and from the Appalachians to the Midcontinent. One Middle Ordovician specimen from the Dunleith is a complete small adult with stem and a lichenocrinid holdfast. The column was largely upright with the crown located about 25 cm above the seafloor. The Middle Ordovician crinoids differ somewhat from the later Cincinnatian material where only young E. simplex exhibit lichenocrinid holdfasts. Older crinoids became detached and were eleutherozoic well before the column was 25 cm long. Thus, the Cincinnatian individuals lost the attachment device earlier during ontogeny than their ancestors in the Middle Ordovician. Unlike most associated crinoids, E. simplex formed a roughly conical filtration net. The arms of E. simplex are extensively branched. Ten main arms bear unbranched ramules on alternate brachials, and the arm structure converges on the pinnulate pattern. Narrow food grooves and short covering plates are present. Analogies with living crinoids indicate that small food particles were caught by small and close-spaced tube-feet. The formation of new plates and ramules at the arm tips increases the size of the food-gathering system throughout ontogeny. The food-gathering capacity comprises the number of food-catching tube-feet times the width of the food grooves, and it measures the number and size of food particles that can be caught. Both size and capacity of the food-gathering system are positively allometric compared to crown volume and the amount of tissue that must be nourished. This is mainly caused by the addition of new ramules at the arm tips, which generates an exponentially increasing plate supply rate. Examination of numerous specimens from various geographic and stratigraphic horizons with multivariate statistics shows that the species was homogeneous throughout its range aside from the differences in living habits mentioned above.


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