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ECHINODERMATA - KU ScholarWorks - University of Kansas

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BLASTOID STUDIES 7<br />

ISp —inner side plate.<br />

—lancet plate.<br />

Lu —lumen.<br />

0 —oral opening (stippled) or oral plate.<br />

OSp —outer side plate.<br />

— pore.<br />

Pf —pore furrow.<br />

—radial plate.<br />

Rp —radial limb.<br />

RI —radial lip.<br />

S —spiracle.<br />

SB —subbasal.<br />

SFg —side food groove.<br />

Sp —side plate(s).<br />

Ss —spiracular slit.<br />

Su —superdeltoid plate.<br />

Sub —subdeltoid plate.<br />

Z —azygous basal, in A-B position when in lower right position.<br />

—arrow marks position <strong>of</strong> main food groove, pointing toward<br />

mouth (in figures showing side plates).<br />

MORPHOLOGY OF BLASTOIDS<br />

INTRODUCTION<br />

Large detailed drawings which show adequately<br />

the detailed morphology <strong>of</strong> the blastoids do not exist,<br />

and therefore many small features <strong>of</strong> skeletal structures<br />

have never been clearly illustrated. Consequently<br />

I decided to draw enlarged portions <strong>of</strong> anal areas,<br />

oral areas, ambulacra, basal plates, stems, hydrospires,<br />

and pores, from the available specimens. A genotype,<br />

holotype, syntype, paratype, neotype, or metatype was<br />

used for this study wherever possible but otherwise it<br />

was necessary to use plesiotypes or hypotypes or unfigured<br />

specimens. Portions <strong>of</strong> this work were initiated<br />

in 1954 at the <strong>University</strong> <strong>of</strong> <strong>Kansas</strong> and carried on<br />

subsequently at the <strong>University</strong> <strong>of</strong> Oklahoma.<br />

TECHNIQUES<br />

Much <strong>of</strong> the work done at the <strong>University</strong> <strong>of</strong> <strong>Kansas</strong><br />

is not incorporated in this study and has been or<br />

is being published separately. However, certain techniques<br />

were used in these early studies and are here<br />

mentioned. The serial peel-section technique, along<br />

with the camera lucida, was used for most detailed<br />

work.<br />

In this procedure parallel sections were ground at<br />

selected regularly spaced small intervals using a Cr<strong>of</strong>t<br />

Parallel Grinding Instrument, which is a well-constructed<br />

micrometer mounted on a flat metal table,<br />

capable <strong>of</strong> being rotated on ball bearings. The micrometer<br />

mount permits determination <strong>of</strong> the exact amount<br />

<strong>of</strong> section to be ground and the ball bearings insure<br />

that each section is parallel with preceding and succeeding<br />

ones. After attaining the desired level, the<br />

section was polished and etched with 5-percent hydrochloric<br />

acid and allowed to dry. Camera lucida drawings<br />

were made <strong>of</strong> the section itself, and for additional<br />

record, peel sections were prepared by immersing the<br />

slightly etched surface in acetone and pressing the<br />

fossil against an acetate sheet. Some acetate should be<br />

dissolved in the acetone for best results. The peel<br />

section, which shows microscopic details <strong>of</strong> the surface<br />

in manner corresponding closely to a thin section,<br />

then was placed in a photographic enlarger so that by<br />

transmitted light features <strong>of</strong> the section could be recorded<br />

on photographic paper. From these photos,<br />

with camera lucida drawings as guide, all information<br />

was transferred onto paper by making direct overlays<br />

in ink. From the inked drawings 3-dimensional<br />

models in glass were built up, and from the models,<br />

3-dimensional drawings were prepared.<br />

Upon examination <strong>of</strong> each specimen, it gradually<br />

became obvious that most genera, in a broad sense,<br />

exhibit the same type <strong>of</strong> basic internal morphology.<br />

Therefore, with later studies, diagrams were drawn<br />

directly from the sections or specimens.<br />

A universal stage was used to determine the optical<br />

character <strong>of</strong> the calyx plates and it was found that<br />

each plate has its own individual orientation.<br />

For later studies at the <strong>University</strong> <strong>of</strong> Oklahoma,<br />

the camera lucida was used in recording features <strong>of</strong><br />

thin sections, polished sections, and details <strong>of</strong> externally<br />

visible morphologic parts. The following data<br />

are presented to show the results <strong>of</strong> morphologic<br />

studies.<br />

GROSS MORPHOLOGY<br />

It is assumed that the reader has some basic knowledge<br />

<strong>of</strong> the Blastoidea. Nevertheless, the following<br />

definitions may be useful for them, though unnecessary<br />

for specialists.<br />

A blastoid may be defined as a stemmed echinoderm<br />

with a body (termed calyx) that bears internal<br />

folded structures called hydrospires, which are located<br />

in the upper half (in direction away from the stem<br />

attachment) <strong>of</strong> the calyx. As a rule, the calyx is composed<br />

<strong>of</strong> 18 to 21 plates arranged in 4 definite cycles.<br />

Normally three plates occur next to the stem at the<br />

base <strong>of</strong> the calyx; these are termed basais, the smallest

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