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ECHINODERMATA - KU ScholarWorks - University of Kansas

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108 THE UNIVERSITY OF KANSAS PALEONTOLOGICAL CONTRIBUTIONS<br />

exposed, probably were derived from Troosticrinus, a<br />

Silurian genus. These families are here recognized as<br />

Pentremitidae D ' ORBIGNY, 1852; Troosticrinidae BASS-<br />

LER, 1938; Granatocrinidae FAY, n. fam.; Schizoblastidae<br />

FAY, H. fam.; and Nucleocrinidae BATHER, 1899,<br />

respectively.<br />

The family Pentremitidae, D ' ORBIGNY, 1852, includes<br />

ten genera, <strong>of</strong> which all have five spiracles<br />

and probably were derived from Hyperoblastus by<br />

complete closure <strong>of</strong> the sinus. The genus Cordyloblastus<br />

, with four anal deltoids, simple gaps between<br />

side plates, and lancet covered by side plates, was probably<br />

derived from Hyperoblastus. Petaloblastus probably<br />

was derived from Cordyloblastus by outward migration<br />

<strong>of</strong> the lancet plate and downward migration<br />

<strong>of</strong> the deltoids, visible in side view, with concurrent<br />

fusion <strong>of</strong> the cryptodeltoids and superdeltoid into an<br />

epideltoid plate. Another trend from Hyperoblastus<br />

is one toward Devonoblasttts, in which the deltoids<br />

migrate downward, become visible in side view, and<br />

the sinuses are completely closed. This trend leads to<br />

Pentremites in which the lancet moves outward and<br />

one anal deltoid is formed, culminating in Ambolostoma<br />

where five large orals are formed from many<br />

small ones, and to Rho paloblastus, in which the anal<br />

opening moves aborally. A distinct side trend from<br />

Hyperoblastus is one toward Eleutherocrintts, in<br />

which the (D) ambulacrum is shortened and the deltoids<br />

move slightly downward, visible in side view.<br />

Another trend is toward Globo blastus, which probably<br />

was derived from a Devonoblastus that developed a<br />

hydrospire plate and two pores to each side plate as<br />

result <strong>of</strong> infolds <strong>of</strong> the ambulacral margins, with reduction<br />

<strong>of</strong> the hydrospire folds on each side <strong>of</strong> an<br />

ambulacrum to two. Globoblastus probably gave rise<br />

to Ellipticoblastus by reduction <strong>of</strong> the hydrospire folds<br />

to a single one on each side <strong>of</strong> an ambulacrum, and<br />

Ellipticoblastus probably gave rise to Orbitremites by<br />

downward migration <strong>of</strong> the deltoids over the radials.<br />

From this it can be seen that the hydrospire plate is<br />

probably <strong>of</strong> little importance in classification and may<br />

develop independently in diverse families. Also, foreshortening<br />

<strong>of</strong> an ambulacrum has littel value in<br />

higher classification <strong>of</strong> blastoids.<br />

The family Troosticrinidae BASSLER, 1938 includes<br />

five genera, four <strong>of</strong> which are closely related. Troosticrinus<br />

is here considered to be a primitive genus that<br />

probably gave rise to other members <strong>of</strong> this family<br />

by downward migration <strong>of</strong> the deltoids (Schizotremites),<br />

or to forms oval in shape (Pentremitella), or<br />

conical, with long pelvis and four or five hydrospire<br />

folds (Metablastus), reduced to three, with flaring<br />

pelvis (Tricoelocrinus), or from which came globular<br />

forms with hydrospires reduced to two folds on each<br />

side <strong>of</strong> an ambulacrum (Diploblastus).<br />

The family Nucleocrinidae BATHER, 1899, was probably<br />

an aberrant <strong>of</strong>f-shoot from Troosticrinus in which<br />

the cryptodeltoids moved outward and downward.<br />

Elaeacrinus, with many oral plates, is inferred to be a<br />

primitive genus from which came Nucleocrinus with<br />

five simple orals, and Placoblastus with six or seven<br />

orals. It is possible that Placoblastus may be an intermediate<br />

genus with the superdeltoid plate exposed,<br />

and Nucleocrinus an advanced genus with the superdeltoid<br />

suppressed. These genera probably did not<br />

give rise to other known genera.<br />

The Schizoblastidae FAY, n. fam. (herein distinguished)<br />

include forms probably derived from a<br />

form similar to Schizotremites, in which the five<br />

paired spiracles form ten spiracles, with anus separate<br />

EXPLANATION OF PLATE 37<br />

FIGURE PAGE<br />

1-3,10. Monadoblastus granulosus FAY, n.gen., n.sp., holotype<br />

(figs. 1-3), paratype (fig. 10), E14,750, Reimann coll.,<br />

Buffalo Soc. Nat. Sci.; Lower Mississippian, Lake Valley<br />

Formation ( ?Nunn member), Lake Valley, N.Mex.; 1-3,<br />

oral, "D" ambulacral, aboral views (all X11); 10, aboral<br />

view <strong>of</strong> polished cross section with "B" ambulacrum downward<br />

( X9.6) 83<br />

4-6. Tanaoblastus bellatulus (PECK), "hypotype" on label (but<br />

presumed to be holotype), 3,293, Peck coll., Univ. Missouri;<br />

Lower Mississippian, Chouteau Limestone, 9 miles<br />

northeast <strong>of</strong> Osceola, Mo.; oral, "D" ambulacral, aboral<br />

views <strong>of</strong> specimen figured by Peck (1938, pl. 26, figs.<br />

1-3) (all X13.1) 102<br />

7-9. Tanaoblastus haynesi (T. H. CLARK), holotype, 347, Harvard<br />

Mus. Comp. Zoology, Mississippian, Madison Limestone,<br />

Squaw Creek, Mont.; oral; "D" ambulacral, aboral<br />

views showing two hydrospire folds on each side <strong>of</strong> an<br />

ambulacrum and nine spiracular openings around oral<br />

opening (all X6.7) 104<br />

11,12. Carpenteroblastus magnibasis (RowLEy), rnetatype, RX-<br />

22, Robert R. Rowley coll., Univ. Illinois; Lower Mississippian,<br />

Upper Burlington Limestone, Louisiana, Mo.;<br />

//, aboral view <strong>of</strong> internal mold <strong>of</strong> specimen figured by<br />

ROWLEY (1901, pl. 28, figs. 22-23) ( X3.9); 12, oral view<br />

<strong>of</strong> same showing remnant <strong>of</strong> circumesophagael ring and<br />

pores in deltoids ( X8) 52

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