ECHINODERMATA - KU ScholarWorks - University of Kansas
ECHINODERMATA - KU ScholarWorks - University of Kansas
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