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Hydroids (Cnidaria, Hydrozoa) of the Danish expedition to

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174<br />

hydro<strong>the</strong>ca. No such patches were found in D.<br />

disticha. However, not enough well preserved<br />

material could be examined <strong>to</strong> substantiate this<br />

difference.<br />

Both D. moluccana and D. disticha have a<br />

very thin and delicate hydro<strong>the</strong>cal perisarc. It is<br />

<strong>of</strong>ten damaged or dis<strong>to</strong>rted in preserved samples.<br />

Toge<strong>the</strong>r with <strong>the</strong> frequent renovations <strong>the</strong>y can<br />

look deceptively like hydro<strong>the</strong>cae <strong>of</strong> <strong>the</strong> genus<br />

Salacia. A careful search for undamaged hydro<strong>the</strong>cae<br />

will, however, reveal <strong>the</strong> difference (cf.<br />

Medel & Vervoort 1998: 31 and Cornelius 1979:<br />

309, note 21). The flimsy perisarc is actually an<br />

important trait <strong>to</strong> distinguish D. disticha from D.<br />

pumila. A fur<strong>the</strong>r difference is <strong>the</strong> separation <strong>of</strong><br />

<strong>the</strong> hydro<strong>the</strong>cae: <strong>the</strong>y are not contiguous on ei<strong>the</strong>r<br />

side. Dynamena pumila also forms branched<br />

and unbranched forms (see Cornelius 1995b<br />

or Schuchert 2001 for recent descriptions).<br />

Dynamena pumila occurs in cooler waters <strong>of</strong> <strong>the</strong><br />

North Atlantic, while D. disticha is predominantly<br />

known from warmer water.<br />

The material identified by Pictet (1893) as<br />

Sertularia gracilis Hassal, 1848 (MHNG INVE<br />

25032) is clearly a Dynamena species and resembles<br />

somewhat D. moluccana, although it has<br />

simple shoots. But <strong>the</strong> hydro<strong>the</strong>cae are distinctly<br />

smaller (0.2 mm abcauline side) and <strong>the</strong>y are on<br />

long internodes. It could thus belong <strong>to</strong> Dynamena<br />

dalmasi (Versluys, 1899) (see Calder 1991<br />

and Medel & Vervoort 1998 for recent descriptions).<br />

Distribution<br />

Indonesia (Pictet 1893, Billard 1925b), Papua<br />

New Guinea (Thornely 1904), Marshall Islands<br />

(Cooke 1975), Australia (Bale 1884, as S. divergens),<br />

Seychelles (Jarvis 1922 as S. cornicina<br />

var. pinnata), sou<strong>the</strong>rn Africa (Millard 1975),<br />

Japan (Hirohi<strong>to</strong> 1995, as D. exigua). Type locality:<br />

Bay <strong>of</strong> Ambon.<br />

Geminella ceramensis (Billard, 1925)<br />

Fig. 31.<br />

Sertularella ceramensis Billard, 1925a: 649. – Billard<br />

1925b: 170, fig. 30, pl. 7: fig. 20.<br />

Geminella ceramensis. – Vervoort 1993: 109, fig. 3a–e.<br />

Not Geminella ceramensis. – Vannucci Mendes 1946: 570,<br />

pl. 4: figs 40–41.<br />

P. SCHUCHERT<br />

Fig. 31. Geminella ceramensis (Billard, 1925). A. Pair <strong>of</strong><br />

hydro<strong>the</strong>cae. B. Hydro<strong>the</strong>cal opening in oblique view showing<br />

<strong>the</strong> three opercular valves. C. Gono<strong>the</strong>ca. – Scales: A–B<br />

= 0.1 mm; C = 0.2 mm.<br />

Material examined:<br />

Kei Islands Expedition station 57, with gono<strong>the</strong>cae.<br />

Description<br />

Colonies erect, stems irregularly branched, up <strong>to</strong><br />

1 cm in height. S<strong>to</strong>lons tubular, ramified. Stem<br />

and branches with identical structure, regularly<br />

segmented by more or less distinct transverse<br />

nodes. Segments elongate, 0.7–1.1 mm long,<br />

each with a pair <strong>of</strong> opposite <strong>to</strong> subopposite hydro<strong>the</strong>cae<br />

in its middle. Side-branches originate<br />

below a hydro<strong>the</strong>ca, first segment without hydro<strong>the</strong>ca,<br />

about half as long as o<strong>the</strong>r segments.<br />

Hydro<strong>the</strong>ca conical, adcauline side adnate<br />

for half or less <strong>of</strong> length, abcauline side almost

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