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Hydroids (Cnidaria, Hydrozoa) of the Danish expedition to

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190<br />

spicuous lateral cusps, median adcauline cusp<br />

not observed, operculum composed <strong>of</strong> two<br />

valves, upper only slightly smaller than lower<br />

one. Bot<strong>to</strong>m <strong>of</strong> hydro<strong>the</strong>ca oblique, adcauline<br />

wall elongated in<strong>to</strong> tapering process. There is no<br />

intra<strong>the</strong>cal ridge. Hydranth with abcauline caecum.<br />

Gono<strong>the</strong>ca arising perpendicular <strong>to</strong> stem between<br />

lowest pair <strong>of</strong> hydro<strong>the</strong>cae, ovoid, 1.2 mm<br />

long, diameter 0.8 mm, with flat truncated end,<br />

wall with sharp, projecting spiral sculpture in 7–<br />

8 loops.<br />

Remarks<br />

There is no doubt that <strong>the</strong> present material is<br />

identical <strong>to</strong> S. borneensis as described and depicted<br />

in Billard (1925b) and Vervoort & Vasseur<br />

(1977). The fertile colony was also found on<br />

<strong>the</strong> same host as <strong>the</strong> type material and in nearly<br />

<strong>the</strong> same water depth.<br />

Vervoort & Vasseur (1977) – who also examined<br />

<strong>the</strong> type material <strong>of</strong> S. borneensis – synonymized<br />

this species with S. turbinata, although<br />

<strong>the</strong>ir material lacked an intra<strong>the</strong>cal ridge (see Fig.<br />

43). They explained its absence by <strong>the</strong> juvenile<br />

state <strong>of</strong> <strong>the</strong>ir material. This explanation appears<br />

now invalid, as also fertile material examined in<br />

this study lacked <strong>the</strong> ridge. Calder (1991) regarded<br />

S. borneensis as distinct from S. turbinata,<br />

but following Leloup (1960) he synonymized<br />

it with <strong>the</strong> Caribbean S. tumida Allman,<br />

1877. Sertularia borneenis is here kept separate<br />

from both S. turbinata and S. tumida. Similar<br />

conclusions were reached by Gibbons & Ryland<br />

(1989), who also regarded S. borneensis as valid.<br />

One sample from a nearby locality (station<br />

68), and thus sympatric with <strong>the</strong> o<strong>the</strong>r specimens<br />

<strong>of</strong> S. borneesis, contained a sertularid clearly<br />

referable <strong>to</strong> S. turbinata (see below, Fig. 44).<br />

Although I acknowledge <strong>the</strong> possibility that both<br />

could be only variants belonging <strong>to</strong> <strong>the</strong> same<br />

biological species, <strong>the</strong>y are preferably kept separate<br />

because no intermediate forms are known so<br />

far. Indonesian morphotypes referable <strong>to</strong> ei<strong>the</strong>r<br />

Sertularia borneensis or S. turbinata differ in <strong>the</strong><br />

following details: Sertularia borneensis lacks an<br />

intra<strong>the</strong>cal ridge, has smaller hydro<strong>the</strong>cae (cf.<br />

Figs 43 and 44), <strong>the</strong> majority <strong>of</strong> <strong>the</strong> hydro<strong>the</strong>cal<br />

pairs are not contiguous, <strong>the</strong> bot<strong>to</strong>m <strong>of</strong> <strong>the</strong> hy-<br />

P. SCHUCHERT<br />

dro<strong>the</strong>ca is more oblique, <strong>the</strong> ahydro<strong>the</strong>cate part<br />

below <strong>the</strong> hinge joint is longer.<br />

Sertularia tumida, a species originally described<br />

from <strong>the</strong> tropical western Atlantic is insufficiently<br />

known because <strong>the</strong> gono<strong>the</strong>cae have<br />

never been described from <strong>the</strong> original region.<br />

Sertularia borneensis is <strong>the</strong>refore preferably<br />

kept separate from S. tumida (or its synonym<br />

S. westindica) as long as <strong>the</strong> gono<strong>the</strong>cae <strong>of</strong><br />

S. tumida remain unknown from waters <strong>of</strong> <strong>the</strong><br />

tropical Atlantic. Perhaps <strong>the</strong> gono<strong>the</strong>cae show<br />

significant differences and <strong>the</strong>y might resemble<br />

more <strong>the</strong> South African S. longa, which has<br />

smooth gono<strong>the</strong>acae but is o<strong>the</strong>rwise hardly distinguishable.<br />

Mammen (1965, as S. west-indica)<br />

provides <strong>the</strong> only description and figure <strong>of</strong> <strong>the</strong><br />

gono<strong>the</strong>ca for material attributed <strong>to</strong> <strong>the</strong> nominal<br />

species S. tumida, but for biogeographic reasons<br />

and also morphological differences Mammen’s<br />

material is better referred <strong>to</strong> S. borneenis or S.<br />

maldivensis.<br />

Sertularia borneensis differs from Atlantic S.<br />

tumida in <strong>the</strong> following details (cf. Calder 1991):<br />

it apparently lacks <strong>the</strong> small median <strong>to</strong>oth on<br />

<strong>the</strong> adcauline rim <strong>of</strong> <strong>the</strong> hydro<strong>the</strong>ca, it is never<br />

branched, and <strong>the</strong> hydro<strong>the</strong>cal bot<strong>to</strong>m is more<br />

oblique. These are admittedly characters prone <strong>to</strong><br />

variation and <strong>of</strong> very limited taxonomic value. If<br />

Atlantic S. tumida should prove <strong>to</strong> have <strong>the</strong> same<br />

gono<strong>the</strong>cae as found here for S. borneensis, both<br />

nominal species would be indistinguishable. Biogeographic<br />

arguments might <strong>the</strong>n never<strong>the</strong>less<br />

be put forward <strong>to</strong> regard both species as distinct.<br />

Sertularia maldivensis Borradaile, 1905, an<br />

inadequately known species, appears conspecific<br />

with S. borneensis. Billard (1925b) did not discuss<br />

why he considered <strong>the</strong>m distinct. Type material<br />

<strong>of</strong> Sertularia maldivensis must be examined<br />

before reliable conclusions can be drawn.<br />

Distribution<br />

Indonesia, Polynesia, perhaps also Maldives.<br />

Type locality: Indonesia, 2°25’S, 117°43’E, 34<br />

m, on Macrorhynchia phoenicea.<br />

Sertularia turbinata (Lamouroux, 1816)<br />

Fig. 44<br />

Dynamena turbinata Lamouroux, 1816: 180.<br />

Desmoscyphus brevicyathus Versluys, 1899: 40, figs 9–10.

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