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note
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The character set is a modification of that used for Paleozoic crinoids (10). Included are 11 characters of the stem, 32 cup characters, 22 brachial characters, and 4 tegminal characters. Morphological differences between Paleozoic and post-Paleozoic crinoids mean that a modified character set is more informative, although Paleozoic and post-Paleozoic crinoids could be accommodated by the same character set.
-
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27
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10544241017
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note
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Data and sources are available from the author on request. Genera not sampled are those too poorly preserved to allow reliable character coding.
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30
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personal communication
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10544248034
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note
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Sampling is irregular after the Eocene, and so measures of disparity are not presented here; however, the available character data suggest no post-Eocene increase in disparity.
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34
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The cited work (10) excluded the Middle Cambrian Echmatocrinus, a possible crinoid [J. Sprinkle, Morphology and Evolution of Blastozoan Echinoderms (Museum of Comparative Zoology, Harvard University, Cambridge, MA, 1973); _ and D. Collins, Geol. Soc. Am. Abstr. Progr. 27, A113 (1995)] whose affinities have been questioned [S. Conway Morris, Nature 361, 219 (1993); W. I. Ausich and L. E. Babcock, in Sixth North American Paleontological Convention Abstracts of Papers, J. E. Repetski, Ed. (Paleontological Society, Washington, DC, 1996), p. 16].
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Ausich, W.I.1
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Data were reanalyzed with each of the recognized orders (Bourgueticrinida, Comatulida, Cyrtocrinida, Encrinida, Isocrinida, Millericrinida, Roveacrinida, and Uintacrinida) omitted in turn [according to methods in M. Foote, Paleobiology 19, 403 (1993)]. Except for Cyrtocrinida, omitting a single order leaves Neocomian and Late Triassic disparity subequal. When Cyrtocrinida are omitted, disparity through the first two Cretaceous intervals is reduced to the Jurassic level. When Cyrtocrinida and Roveacrinida are omitted, disparity is nearly constant throughout the Jurassic and Cretaceous.
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10544235966
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note
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Because of incomplete preservation, most species have at least some missing character data. In this analysis I used the species in each genus with the fewest missing characters.
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42
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0000071395
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Because unordered characters cannot be averaged, I first ordinated species using principal-coordinates analysis [J. C. Gower, Biometrika 53, 325 (1966)] on the between-species morphological distance matrix (10). Twenty principal coordinates were used because interspecies distances based on this number of coordinates correlate well with distances based on the raw character data. Similar results are obtained if other numbers of principal coordinates are used.
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note
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I thank B. Chernoff and D. Jablonski for advice and discussions; B. Chernoff, D. Jablonski, and A. I. Miller for reviews; J. J. Sepkoski Jr. for unpublished data on crinoid genera and families; and T. K. Baumiller, D. Jablonski, and the staff of the John Crerar Library for help in obtaining literature. This research was supported by NSF (grants DEB-9207577, DEB-9496348, and EAR-9506568).
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