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Hydroids (Cnidaria, Hydrozoa) of the Danish expedition to

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HYDROIDS OF THE DANISH EXPEDITION TO THE KEI ISLANDS<br />

Sertularella quadridens forma quadridens Ralph, 1961a:<br />

830, fig. 23h.<br />

Sertularella quadridens cornuta. – Vervoort 1993: 232, figs<br />

52b–e, 53a–b.<br />

Material examined:<br />

Normal form<br />

Kei Islands Expedition station 18, several stems, no gono<strong>the</strong>cae.<br />

Morphotype “cornuta”<br />

Kei Islands Expedition stations: 16. – 60. – 63. – 64. – 103.<br />

– 104. – 106. – Kei Island Expedition, Samalon Island near<br />

Ujungpandang, 35 m, 28 Jun 1922.<br />

Morphotype “timorensis”<br />

Kei Islands Expedition station 26, one shoot with gono<strong>the</strong>ca,<br />

much overgrown by Bryozoa and algae.<br />

Description <strong>of</strong> typical form<br />

Colonies erect, pinnate, reaching heights <strong>of</strong> 7 cm.<br />

Stems monosiphonic, unbranched, with alternate<br />

hydrocladia which are more or less in one plane,<br />

divided in<strong>to</strong> internodes in distal regions only,<br />

nodes oblique, sloping alternately <strong>to</strong> left and<br />

right. Each stem internode bearing three hydro<strong>the</strong>cae<br />

in two rows and one hydrocladium, <strong>the</strong><br />

latter rising just below <strong>the</strong> most distal hydro<strong>the</strong>ca.<br />

Hydrocladia straight, unbranched, with distant<br />

nodes and a variable number <strong>of</strong> hydro<strong>the</strong>cae<br />

per internode.<br />

Hydro<strong>the</strong>cae alternate, <strong>the</strong> two rows <strong>of</strong> hydro<strong>the</strong>cae<br />

on <strong>the</strong> hydrocladia in one plane, both<br />

rows well separated, successive hydro<strong>the</strong>cae <strong>of</strong><br />

one row well separated for about somewhat less<br />

than <strong>the</strong> length <strong>of</strong> one hydro<strong>the</strong>ca. Hydro<strong>the</strong>ca<br />

tubular, curved outwards, adnate for 2/3 <strong>to</strong> ¾ <strong>of</strong><br />

its adcauline length, length <strong>of</strong> abcauline side<br />

0.30–0.35 mm, diameter <strong>of</strong> opening 0.20–0.23<br />

mm, length <strong>of</strong> free adcauline side 0.13–0.18 mm,<br />

adcauline side evenly curved, abcauline side<br />

straight in lower part and curved in last fourth,<br />

opening oblique, margin with four cusps; floor<br />

complete, with large pore, lower end <strong>of</strong> adcauline<br />

wall <strong>of</strong>ten with an oblique or vertical process,<br />

sometimes even connected <strong>to</strong> opposite hydro<strong>the</strong>ca<br />

(Fig. 41B), size and form <strong>of</strong> this process<br />

very variable within <strong>the</strong> same shoot (Fig. 41B–<br />

D), many hydro<strong>the</strong>cae even without such a process.<br />

Gono<strong>the</strong>cae <strong>of</strong> this form not observed (see<br />

Watson 2000, Billard 1925b).<br />

187<br />

Variant form “cornuta”<br />

Colony 2–5 cm high, hydro<strong>the</strong>cae slightly larger<br />

(abcauline wall 0.35–0.4 mm), hydro<strong>the</strong>ca more<br />

projecting (adnate for 2/3), process at lower end<br />

<strong>of</strong> adcauline wall absent or represented by a<br />

slight thickening only (Fig. 41E–G). No gono<strong>the</strong>cae<br />

present.<br />

Variant form “timorensis”<br />

Colony 3 cm high, perisarc much thickened, a<br />

large and massive intra<strong>the</strong>cal <strong>to</strong>oth on adcauline<br />

side, <strong>of</strong>ten also smaller on abcauline side, hydro<strong>the</strong>cae<br />

adnate for 2/3 <strong>to</strong> ¾ <strong>of</strong> <strong>the</strong>ir adcauline side,<br />

length abcauline side 0.38–0.40 mm, diameter <strong>of</strong><br />

opening 0.15–0.16 mm. Gono<strong>the</strong>ca on hydrocladia,<br />

about 1.2 mm long, diameter 0.5 mm,<br />

barrel-shaped, with transverse annulation, end<br />

truncate, square, with four sharp corners, operculum<br />

pyramidal and composed <strong>of</strong> four triangular<br />

flaps.<br />

Remarks<br />

Typical Sertularella quadridens have hydro<strong>the</strong>cae<br />

with a characteristic process at <strong>the</strong> lower end<br />

<strong>of</strong> <strong>the</strong> adcauline wall (Fig. 41B–D), which renders<br />

<strong>the</strong>m relatively easy <strong>to</strong> identify, even in <strong>the</strong><br />

absence <strong>of</strong> <strong>the</strong> characteristic gono<strong>the</strong>ca. However,<br />

this process is very variable and can be<br />

absent in quite a number <strong>of</strong> hydro<strong>the</strong>cae. Therefore,<br />

also o<strong>the</strong>rwise closely similar colonies lacking<br />

this process (variant forms) were here also<br />

allocated <strong>to</strong> this species. One <strong>of</strong> <strong>the</strong>se variant<br />

forms likely corresponds <strong>to</strong> <strong>the</strong> form described<br />

by Billard (1925b) as S. quadridens var. cornuta.<br />

Billard (1925b) distinguished this variant from<br />

<strong>the</strong> typical form through <strong>the</strong> more widely spaced<br />

and more projecting hydro<strong>the</strong>cae and smaller<br />

gono<strong>the</strong>ca with longer marginal cusps. The status<br />

<strong>of</strong> this variant is at present unclear. Ritchie (1909,<br />

1910a) suggested it <strong>to</strong> be a variant <strong>of</strong> S. polyzonias,<br />

but Stechow (1923) and Nutting (1927)<br />

recognized it as a full species, an opinion also<br />

favoured by Watson (2000). Billard (1925b) and<br />

Vervoort (1941, 1993) regarded it as a variant <strong>of</strong><br />

S. quadridens. Ano<strong>the</strong>r variant is S. quadridens<br />

var. timorensis, a morphotype originally described<br />

as a separate species by Billard (1919b),<br />

but later demoted <strong>to</strong> a mere variant <strong>of</strong> S. qua-

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