Symplectoscyphus commensalis Vervoort, 1993
publication ID |
https://doi.org/ 10.5852/ejt.2019.562 |
publication LSID |
lsid:zoobank.org:pub:6567F621-7A92-4D1A-8902-A1E76325AF94 |
DOI |
https://doi.org/10.5281/zenodo.3475305 |
persistent identifier |
https://treatment.plazi.org/id/03C0D256-AD61-6112-FE2B-A16D586FFE50 |
treatment provided by |
Plazi |
scientific name |
Symplectoscyphus commensalis Vervoort, 1993 |
status |
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Symplectoscyphus commensalis Vervoort, 1993
Fig. 17 View Fig F–G
Symplectoscyphus commensalis Vervoort, 1993: 247 , figs 56C–F, 57, 58A–E.
Material examined
PACIFIC OCEAN • female colony with stems up to 1 cm high on stem of sertulariid hydroid; off New Caledonia, stn DW4670; 22°58′ S, 167°24′ E; 680– 612 m; 12 Aug. 2016; KANACONO leg.; one stem was used for DNA extraction, DNA 1389; voucher MHNG-INVE- 120850; barcode identifier MK 073103 View Materials ; MNHN-IK-2015-399 GoogleMaps .
Remarks
A small species, with minute hydrothecae resembling those of S. ralphae Vervoort, 1993 through their shape and size (compare Fig. 17F View Fig with Galea 2016: fig 10Q–T). Unlike S. commensalis that forms irregularly-branched colonies (up to 2 nd order branches observed), the latter builds regularly-pinnate colonies. In addition, their respective gonothecae are different [compare Fig. 17G View Fig with Galea 2016: fig. 10U–V).
Distribution
Only known from off New Caledonia ( Vervoort 1993; present study).
? Symplectoscyphus elongatulus Galea , sp. nov.
urn:lsid:zoobank.org:act:E30569B6-8BC4-4B3C-8E84-8EC1A2300839
Figs 16B View Fig , 17 View Fig H–J; Tables 8 View Table 8 , 10 View Table 10
Diagnosis
Sparingly-branched symplectoscyphid forming delicate, coplanar colonies, with erect, monosiphonic stems. Internodes long, slender, distinctly geniculate, each carrying distally a hydrotheca; the latter long, slightly conical, smooth-walled, adnate for ⅓, abaxial wall straight or nearly so, free adaxial wall imperceptibly convex proximally, and distinctly concave below aperture; adaxial cusp produced, slightly everted; eight internal, submarginal projections of perisarc. Gonothecae unknown.
Etymology
From the Latin ‘ ēlongo, -āvi, -āre ’, meaning ‘to lengthen’, with the apposition of the suffix ‘ -ulus, -ula, ulum ’, as a diminutive, to characterize the shape of the internodes of this delicate, straggling species.
Material examined
Holotype
PACIFIC OCEAN • a 5.1 cm high colony without gonothecae; off New Caledonia, stn DW5010; 22°10′ S, 159°03′ E; 290–820 m; 19 Sep. 2017; KANADEEP leg.; MNHN-IK-2015-463. GoogleMaps
Description
Colony erect, 5.1 cm high, arising from creeping hydrorhiza. Stem monosiphonic, flaccid, unable to support itself when out of liquid; basal 1.6 cm ahydrothecate, with smooth perisarc; remainder of stem divided into regular internodes by means of indistinct oblique nodes slanting in alternate directions; internodes distinctly geniculate, long, each bearing distally a hydrotheca; branching sparse, irregular: only two side branches, neither branching further, occur in the present specimen; they are given off laterally and in opposite directions, from below the bases of two distant stem hydrothecae, and are coplanar. Hydrothecae long, slightly conical, adnate for ⅓ or less to their corresponding internodes; abaxial wall straight for most of its length, imperceptibly convex distally; free adaxial wall slightly sigmoid, convex for most of its length, then concave towards aperture; aperture three-cusped, adaxial cusp slightly produced, latero-abaxial cusps less prominent, with rounded tips, separated by wide, shallow embayments; operculum composed of three triangular flaps meeting centrally to form a pyramidal roof; 8 internal, submarginal projections of the perisarc: one minute adaxial, two pairs of latero-adaxial, one large abaxial, and two latero-abaxial. Gonothecae not observed.
Remarks
Only a restricted number of congeners display a combination of long, slender, geniculate internodes and weakly-adnate hydrothecae, namely: S. amphoriferus Allman, 1877 ( Millard 1977; Schuchert 2001), S. bathyalis Vervoort, 1972 (original account, Calder & Vervoort 1998), S. dentiferus (Torrey, 1902) ( Nutting 1904) , S. effusus Vervoort, 1993 (original account, Galea 2016), S. macrocarpus (Billard, 1918) (original account, Billard 1925), S. minutus ( Nutting, 1904) (original account), S. naumovi Blanco, 1969 ( Peña Cantero et al. 2002), S. nesioticus Blanco, 1977 (original account, Peña Cantero et al. 2002), S. paucicatillus Galea, 2016 (original account), S. paulensis Stechow, 1923 ( Vervoort 1993; present report), S. pedunculatus (Billard, 1919) ( Billard 1925; Vervoort 1993) and S. plectilis (Hickson & Gravely, 1907) ( Millard 1977) . However, in any of these the hydrothecae do not adopt the distinctive shape met with in S. elongatulus sp. nov., and none displays submarginal, intrathecal cusps.
Through its Sertularella -like hydrothecae, provided with only three marginal cusps, the present species comes close to? Symplectoscyphus acutustriatus sp. nov. (see above), whose systematic position is discussed in the ‘Molecular study’ section.
Distribution
Only known from off New Caledonia (present study).
MK |
National Museum of Kenya |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Hydroidolina |
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Genus |
Symplectoscyphus commensalis Vervoort, 1993
Galea, Horia R. & Schuchert, Peter 2019 |
Symplectoscyphus commensalis
Vervoort W. 1993: 247 |