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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.