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Hydroids (Cnidaria, Hydrozoa) of the Danish expedition to

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244<br />

mary tube and a bundle <strong>of</strong> auxiliary tubes. Primary<br />

tube <strong>of</strong> side-branches originate from primary<br />

tube <strong>of</strong> stem, branching points <strong>of</strong> primary<br />

tubes <strong>of</strong>ten overgrown by few auxiliary tube.<br />

Primary tubes segmented in terminal parts, each<br />

segment with an apophysis for hydrocladium and<br />

two nema<strong>to</strong><strong>the</strong>cae at side <strong>of</strong> apophysis. Primary<br />

tubes usually with hydrocladia, but <strong>the</strong>se may be<br />

broken <strong>of</strong>f in proximal part <strong>of</strong> stem. S<strong>to</strong>lons<br />

tangled, creeping, anchoring colony on solid<br />

substrata. Inside <strong>of</strong> periderm <strong>of</strong> whole colony<br />

densely covered by a lining <strong>of</strong> spherical zooxan<strong>the</strong>llae,<br />

size 7–9 µm.<br />

Hydrocladia alternate, thick and bristly, making<br />

colony resemble a fir twig, hydrocladia 3–5<br />

mm, 6–11 hydro<strong>the</strong>cae, length within one colony<br />

similar, flattened laterally, rear side keeled, regularly<br />

segmented by transverse nodes, each segment<br />

with one hydro<strong>the</strong>ca, with two strong internal<br />

ribs (ridges, thickenings) at <strong>the</strong> level <strong>of</strong> <strong>the</strong><br />

hydro<strong>the</strong>ca, <strong>the</strong>se ribs irregularly curved, fused<br />

<strong>to</strong> a longitudinal ridge running along rear side,<br />

rear wall o<strong>the</strong>rwise remarkably thin.<br />

Hydro<strong>the</strong>ca relatively narrow, depth 0.25–<br />

0.28 mm, diameter 0.13–0.15 mm, campanulate,<br />

not curved, adcauline side completely adnate,<br />

opening slightly inclined <strong>to</strong>wards below (approx.<br />

30°), lateral margin slightly undulated or with a<br />

distinct antero-lateral cusp, hydropore at base <strong>of</strong><br />

rear wall, above hydropore a very short adcauline<br />

shelf which is continued as a transverse internal<br />

ridge, presence variable.<br />

Median inferior nema<strong>to</strong><strong>the</strong>ca very s<strong>to</strong>ut,<br />

breadth in lateral view 2/3 or more <strong>of</strong> hydro<strong>the</strong>cal<br />

diameter, completely adnate, reaching <strong>to</strong> <strong>the</strong><br />

level <strong>of</strong> hydro<strong>the</strong>ca, margin with two broad lateral<br />

cusps (or free end gutter-shaped), on inside<br />

near upper third an oblique septum with a pore on<br />

adcauline side; no foramen in<strong>to</strong> hydro<strong>the</strong>ca. Lateral<br />

nema<strong>to</strong><strong>the</strong>ca over<strong>to</strong>p hydro<strong>the</strong>ca, ovoid <strong>to</strong><br />

cup shaped, about half as high as hydro<strong>the</strong>ca,<br />

opening directed <strong>to</strong>wards above or inclined <strong>to</strong>wards<br />

rear.<br />

Gono<strong>the</strong>cae in closed corbula which replaces<br />

a hydrocladium. Corbula 1.7–2.5 mm long, tubular,<br />

first segment like in ordinary hydrocladia,<br />

<strong>the</strong>n with leaf-like costae, 5–8 per side, fused <strong>to</strong><br />

form a cylinder but with slit-like lateral openings,<br />

costae with one row <strong>of</strong> nema<strong>to</strong><strong>the</strong>cae, basal 2–3<br />

may be on a raised lobe.<br />

P. SCHUCHERT<br />

Remarks<br />

The samples from 1 m and 10 m water depth<br />

showed very obvious differences that are very<br />

likely attributable <strong>to</strong> <strong>the</strong>ir different environment<br />

(cf. Fig. 81A–C and 81D–F). The colonies from<br />

10 m depth were dark brown, while those from<br />

1 m were bright amber coloured. Fur<strong>the</strong>rmore,<br />

<strong>the</strong> colonies from 10 m were more branched,<br />

more flexible, less bristly, had longer and thinner<br />

hydrocladia. There was also a difference in <strong>the</strong><br />

corbulae. This difference, however, could be ei<strong>the</strong>r<br />

due <strong>to</strong> depth or sexual dimorphism. The<br />

limited number <strong>of</strong> independent colonies did not<br />

make it possible <strong>to</strong> draw a reliable conclusion.<br />

The difference was mainly confined <strong>to</strong> <strong>the</strong> presence<br />

or absence <strong>of</strong> a raised lobe near <strong>the</strong> base <strong>of</strong><br />

each costa. This lobe had 2–3 nema<strong>to</strong><strong>the</strong>cae. The<br />

opening behind this lobe was also larger than <strong>the</strong><br />

usual slits. In <strong>the</strong> examined material this type <strong>of</strong><br />

corbula contained gono<strong>the</strong>cae with eggs, while<br />

<strong>the</strong> o<strong>the</strong>r type <strong>of</strong> corbula was quite certainly<br />

male. Both type <strong>of</strong> corbulae have been described<br />

by o<strong>the</strong>r authors. Billard (1913) depicts <strong>the</strong> form<br />

without lobe, while Millard & Bouillon (1974)<br />

depict a corbula with a basal lobe. Bale (1915)<br />

also described such a lobe and he also thought <strong>of</strong><br />

a possible sexual dimorphism.<br />

Aglaophenia cupressina is a very characteristic<br />

species and especially <strong>the</strong> microscopic structure<br />

make its identification easy (see Fig. 81B<br />

and 81E). The colonies <strong>of</strong>ten occur in very shallow<br />

waters and are thus easily encountered. They<br />

are very no<strong>to</strong>rious for <strong>the</strong>ir painful stings.<br />

Naumov (1969, as Corbulifera macgillivrayi)<br />

reported this o<strong>the</strong>rwise tropical shallow water<br />

species from <strong>the</strong> arctic sea <strong>of</strong> Okhotsk and from<br />

deep waters near <strong>the</strong> Kuriles. His material was<br />

sterile. For biogeographic reasons I doubt somewhat<br />

that Naumov’s specimen belonged <strong>to</strong> A.<br />

cupressina, although his figures look identical <strong>to</strong><br />

<strong>the</strong> present material. Although A. cupressina is<br />

widespread in <strong>the</strong> tropical Indo-Pacific, interestingly,<br />

it is not known <strong>to</strong> occur on smaller islands<br />

<strong>of</strong> <strong>the</strong> tropical Pacific (Polynesia).<br />

Distribution<br />

From Zanzibar and Mozambique <strong>to</strong> Great Barrier<br />

Reef, Indonesia, New Guinea, Philippines, Japan.<br />

?Sea <strong>of</strong> Okhotsk. Occurs even in very shal-

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