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92<br />

6.0-6.5 x 4.0-4.5 mm in diameter, Wells' specimen having<br />

larger corallites up to 9 x 7 mm in diameter. Costae evident,<br />

separated by narrow intercostal striae, and covered with fine<br />

granules; epitheca absent. Corallum white. Septa hexamerally<br />

arranged in 4 complete cycles in a Pourtales Plan. Su2 highly<br />

exsert and have smooth (entire) inner sdges that attain the<br />

columella. S3 small; pairs of S4 fuse before their adjacent S3<br />

and extend to columella. Inner edges of S3-4 dentate. Fossa<br />

deep, containing a small, spongy columella.<br />

DISCUSSION.—The specimen reported by Wells (1954) from<br />

the Marshall Islands differs from typical D. florulenta in<br />

several characters and thus its identification is queried. It has<br />

larger corallites; more septa (occasional pairs of S5 in large<br />

corallites); and a smaller, almost lamellar, columella. Comparisons<br />

to the only other sympodially branched Dendrophyllia<br />

from the Japanese region, D. boschmai, are made in the account<br />

of that species.<br />

Van der Horst (1922) described D. florulenta as a new<br />

species apparently unaware that Alcock (1902a) had previously<br />

described the same species under the same name, making Van<br />

der Horst's species both a junior homonym and junior<br />

synonym. Most of Alcock's (1902a,b) brief descriptions of his<br />

new species from the Siboga collection were republished one<br />

month later (Alcock, 1902c), but eight of them were not,<br />

including Dendrophyllia florulenta. I suspect that Alcock's<br />

type specimens were labelled as D. florulenta in the ZMA<br />

collections but not recognized as types, such that when Van der<br />

Horst (1922) later revised the Siboga Dendrophylliidae, he<br />

used what he thought were Alcock's manuscript types as his<br />

type specimens and adopted the name as well.<br />

MATERIAL EXAMINED.—-New Records: TM (KT9015,<br />

CB1-1), 1, USNM 92875; TM (KT9015, CB1-2), 2, USNM<br />

92876; TM (KT9015, CB2-2), 2, USNM 92877; 34°20'N,<br />

\3Q O \QTE (off Okino Shima), 110 m, 18 May 1914, Mortensen's<br />

1914 Pacific Expedition, 1, ZMC. Previous Records:<br />

Specimen from Marshall Islands (Wells, 1954),<br />

USNM 45102.<br />

TYPES.—The holotype of Alcock's D. florulenta is presumed<br />

to be deposited at the ZMA, probably one of the two<br />

syntypes of Van der Horst's D. florulenta, but Alcock (1902a)<br />

did not document the Siboga station from which his specimens<br />

came. Type Locality: Unknown, but undoubtedly from the<br />

Siboga Expedition to Indonesia, probably Siboga-51 or 305.<br />

Two syntypes of Van der Horst's (1922) D. florulenta are<br />

deposited at the ZMA (Coel. 1195, 1256). Type Localities:<br />

Siboga-51, 305: Banda Sea, 69-113 m.<br />

DISTRIBUTION.—Off Japan: Sagami Bay; Eastern Channel,<br />

off Mishima and Okinoshima; north and south of Cheju Do,<br />

South Korea, East China Sea; 70-110 m. Elsewhere: Banda<br />

Sea, Bonin Islands, ?Marshall Islands; 69-243 m.<br />

EnaUopsammia Michelotti, 1871<br />

DIAGNOSIS.—Colonial, arborescent colonies formed by<br />

extratentacular budding. Corallites often, but not always,<br />

SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY<br />

unifacially arranged. Coenosteum dense, synapticulotheca<br />

porous only near calice and on distal branches. Septa arranged<br />

normally. Columella small.<br />

TYPE SPECIES.—Coenopsammia scillae Seguenza, 1864, by<br />

monotypy.<br />

EnaUopsammia rostrata (Pourtales, 1878)<br />

PLATE 39d-f<br />

Amphihelia rostrata Pourtalfcs, 1878:204, pi. 1: figs. 4, 5.<br />

Dendrophyllia amphelioides Alcock, 1902a:l 12-113.<br />

Amphehelia adminicularis Rehberg, 1892:10, pi. 4: fig. 1.<br />

Dendrophyllia amphelioides var. cucullata Vaughan, 1907:157, pi. 47: fig. 3;<br />

pi. 48: figs. 1-4.<br />

Anisopsammia amphelioides.—Eguchi, 1934:368.<br />

EnaUopsammia rostrata.—Zibrowius, 1973:44-45, figs. 14, 15.—Cairns,<br />

1979:186-188, pi. 37: figs. 2, 3, 6; 1982:57-58, pi. 18: figs. 1-4<br />

[synonymy).—Cairns and Parker, 1992:52-53, fig. 18e-i.<br />

EnaUopsammia (Anisopsammia) amphelioides.—Eguchi, 1965:296, 1 fig.<br />

EnaUopsammia amphelioides disticha Eguchi, 1968:C68, pi. C24: figs. 1,6; pi.<br />

C29: figs. 1, 2.—Zibrowius and Grygier, 1985:134.<br />

DESCRIPTION.—Colonies usually planar, having close, dichotomous<br />

branching, which occasionally leads to branch<br />

anastomosis. Corallites occur on only 1 side of colony and are<br />

circular to slightly elliptical in shape: up to 5.6 mm in GCD, but<br />

usually only 4.0-4.5 mm in diameter. Costae better developed<br />

on acalicular face, being about 0.5 mm wide, slightly convex,<br />

and finely granular, separated by narrow, porous intercostal<br />

regions. No septocostal rostra present on Japanese specimens.<br />

Corallum white.<br />

Septa hexamerally arranged in 3 complete cycles (24 septa).<br />

Sj.g equal in size, nonexsert, and quite slender, having vertical,<br />

smooth inner edges. S3 only only half width of an S^_2 and thus<br />

quite slender, usually having a dentate or irregularly shaped<br />

inner edge. Inner edges of pairs of S3 fuse to their adjacent S2<br />

near columella. Fossa quite deep, sometimes slightly curved,<br />

and quite open because of the very narrow septa. Columella<br />

rudimentary, consisting of several small extensions from<br />

lowermost inner edges of Su2.<br />

DISCUSSION.—EnaUopsammia rostrata was first reported<br />

from Japan by Rehberg (1892) based on one specimen, and<br />

later by Eguchi (1965,1968) as E. amphelioides disticha, again<br />

apparently based on one additional specimen. Eguchi's (1968)<br />

reference to a locality record from Enoshima, Sagami Bay is<br />

not documented in his papers. The two lots reported herein are<br />

from the East China Sea southwest of Kyushu, not far from the<br />

type locality off. a. disticha.<br />

All Japanese specimens lack the septocostal rostrum that<br />

characterizes the typical form of this species. But, as earlier<br />

stated (Cairns, 1982:57), the development of a rostrum seems<br />

to be a response to an environmental factor, not a species level<br />

character. The Japanese specimens thus belong to the "amphelioides"<br />

form of this species, i.e., those specimens lacking a<br />

rostrum.<br />

MATERIAL EXAMINED.—New Records: Alb-4891,2 colonies,<br />

USNM 92849, 1 branch, ORI; Alb-4892, 2 colonies,

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