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NUMBER 557 61<br />

Desmophyllum dianthus (Esper, 1794)<br />

ACCOUNT.—See Part 1.<br />

Lophelia Milne Edwards and Haime, 1849<br />

DIAGNOSIS.—See Part 1.<br />

Lophelia pertusa (Linnaeus, 1758)<br />

ACCOUNT.—See Part 1.<br />

Anomocora Studer, 1878<br />

DIAGNOSIS.—Corallum subcylindrical and free, with a<br />

tendency to bud new corallites at random from thecal wall, the<br />

buds subsequently losing their organic connection. Before bud<br />

detachment the corallum is colonial. Wall thin. Columella<br />

trabecular, multiple irregularly shaped paliform lobes usually<br />

present on S^_3. Tabular endothecal dissepiments common and<br />

widely spaced.<br />

TYPE SPECIES.—Coelosmilia fecunda Pourtales, 1871, by<br />

monotypy.<br />

Anomocora sp.<br />

Parasmilia fecunda Yabe and Eguchi, 1932b:443.<br />

Anomocora fecunda.—Eguchi, 1965:290, 2 figs.; 1968:C42, pi. CIO: figs. 1-5;<br />

?pl. C20: figs. 10, 11; ?pl. C23: fig. 3.—Cairns, 199la: 19.<br />

DISCUSSION.—No additional specimens of Anomocora are<br />

reported in the present study and the two specimens of A.<br />

fecunda reported by Eguchi (1968) are not available for study.<br />

Eguchi (1968) did not describe his Japanese specimens, but his<br />

specimen (#701) illustrated on plate CIO does appear to be an<br />

Anomocora; the other specimen (#741) cannot be identified<br />

from the illustrations. Specimen #701, from off Chigasaki,<br />

Sagami Bay (100 m), has relatively large corallites 12-16 mm<br />

in calicular diameter, thin, ridged costae; an incomplete fifth<br />

cycle of septa; prominent paliform lobes; and sparse budding.<br />

I agree with Zibrowius (1980) that the Japanese specimens are<br />

not A. fecunda, which appears to be restricted to the Atlantic<br />

(Caims, 1979). The Japanese specimens have larger corallites,<br />

more septa per corallite, more prominent paliform lobes, and<br />

less frequent budding. Anomocora has been reported several<br />

times in the Indo-West Pacific by: Gardiner and Waugh (1939)<br />

Red Sea; Marenzeller (1904a) off Sumatra; Cairns (1984)<br />

Hawaiian Islands; and Caims (1991a) off the Galapagos.<br />

MATERIAL EXAMINED.—New Records: None. Previous<br />

Records: Reference specimens of A. fecunda from the<br />

western Atlantic (Cairns, 1979).<br />

DISTRIBUTION.—Sagami Bay; 50-100 m.<br />

Coenosmilia Pourtales, 1874<br />

DIAGNOSIS.—Corallum colonial, small bushy colonies<br />

formed by extratentacular budding of ceratoid corallites just<br />

below calice edge or from a commom basal coenosteum.<br />

Corallum firmly attached. Columella a solid fusion of<br />

elements; paliform lobes absent. Tabular endothecal dissepiments<br />

present.<br />

DISCUSSION.—Coenosmilia and Anomocora are quite similar<br />

in morphology and have been synonymized by Zibrowius<br />

(1980). Coenosmilia, however, can be distinguished by having<br />

an attached corallum, more regular budding, a more solid<br />

columella, and the absence of paliform lobes.<br />

TYPE SPECIES.—Coenosmilia arbuscula Pourtales, 1874, by<br />

monotypy.<br />

Coenosmilia sp. cf. C. arbuscula Pourtales, 1874<br />

PLATE 27a,*<br />

DESCRIPTION OF SPECIMENS FROM TM (KT9202, YS2).—A<br />

well-preserved corallum is ceratoid: 7.6 x 6.7 mm in calicular<br />

diameter, 3.1 mm in pedicel diameter, and 24 mm in height,<br />

bearing no buds. A second poorly preserved specimen is only<br />

slightly smaller and has 3 buds equally spaced just below the<br />

caliclar edge. C[_2 low, finely serrate ridges; C3 slightly less<br />

prominent ridges; C4 broad and unridged. Corallum white.<br />

Septa hexamerally arranged in four cycles, but with one pair<br />

of S4 missing (= 46 septa), according to the formula:<br />

S1>S2»S3>S4. S1 little exsert (0.8 mm), and not wide (about<br />

0.8 mm wide), having vertical, slightly sinuous inner edges that<br />

merge with the columella. S2 of same exsertness, less wide (0.6<br />

mm), and have inner edges that also merge with the columella.<br />

S3 less exsert and only about half width of S,_2, their inner<br />

edges not coming close to the columella. S4 rudimentary, each<br />

composed of a row of small spines. Pali and paliform lobes<br />

absent. Fossa deep, containing a large trabecular columella.<br />

Tabular endothecal dissepiments present.<br />

DISCUSSION.—The Japanese specimens are extremely similar<br />

to C. arbuscula, including aspects of their budding pattern,<br />

size, costal shape, and number of septa. The two specimens at<br />

hand differ only in having a deeper fossa and smaller S3 than C.<br />

arbuscula. Coenosmilia arbuscula is known only from the<br />

North Atlantic from 109-622 m (Cairns, 1979; Zibrowius,<br />

1980); before a confident identification can be made, more<br />

North Pacific specimens will need to be examined and<br />

compared.<br />

MATERIAL EXAMINED.—New Records: TM (KT9202,<br />

YS2), 2, USNM 92709. Reference Specimens: Specimens<br />

from Atlantic reported by Cairns (1979) and Zibrowius (1980),<br />

including the syntypes (MCZ).<br />

DISTRIBUTION.—A seamount (Yaku-Shinsone) in the northern<br />

Tokara Retto, Ryukyu Islands; 238-240 m.<br />

Phyllangia Milne Edwards and Haime, 1848c<br />

DIAGNOSIS.—Colonial, extratentacular budding forming<br />

reptoid to plocoid colonies, often basally united by thick<br />

coenosteum. Inner edges of S, smooth, those of higher cycle<br />

septa smooth to finely dentate. Sparse endotheca present.<br />

Columella rudimentary; P2 or P3 sometimes present.

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