Cladocarpus partitus, Galea, 2020
publication ID |
https://doi.org/ 10.5852/ejt.2020.615 |
publication LSID |
lsid:zoobank.org:pub:637FC87F-13B5-4B32-BC52-11A9B30ECF1D |
DOI |
https://doi.org/10.5281/zenodo.3718315 |
persistent identifier |
https://treatment.plazi.org/id/498492D3-3B64-485D-9414-2BD05CF55103 |
taxon LSID |
lsid:zoobank.org:act:498492D3-3B64-485D-9414-2BD05CF55103 |
treatment provided by |
Plazi |
scientific name |
Cladocarpus partitus |
status |
sp. nov. |
Cladocarpus partitus View in CoL sp. nov.
urn:lsid:zoobank.org:act:498492D3-3B64-485D-9414-2BD05CF55103
Figs 6 View Fig A–B, 7
Diagnosis
Cladocarpus with lightly fascicled, unbranched stems, whose rather long internodes bear a frontal row of 2–3 nematothecae, a lateral apophysis with a basal mamelon, as well as an anterior axillar nematotheca. Cladia relatively spaced from one another. Cormidia elongated, with up to 8 internal septa, 2 abaxial up to 6 adaxial. Hydrotheca deep, mesial nematotheca short, rim with median abaxial cusp, nearly smooth elsewhere; an internal ridge projecting forwards and slightly upwards from the lower fourth of the adaxial wall of hydrotheca, as well as an arched, two-winged septum above, leaving a slit-like, median passage for the hydranth. Phylactocarp borne on stem internode by means of a short apophysis; segmented into moderately-long internodes, each with one frontal, triangular nematotheca; gonothecae on distalmost internodes; tubular, with a main, lateral, subterminal, slit-like aperture, and an inconspicuous, secondary gutter-shaped aperture above.
Etymology
From the Latin ‘ partĭor, -ītus sum, -īri ’, meaning ‘partitioned’, with reference to its hydrothecae that are divided by a transverse, bilobate septum.
Material examined
Holotype
PACIFIC OCEAN • 1 colony, ca 6.5 cm high, hydrorhiza missing; off New Caledonia, stn DW4770 ; 22°58ʹ S, 168°21ʹ E; 455–470 m; 28 Aug. 2016; KANACONO leg.; MNHN-IK-2015-529 . GoogleMaps
Description
Colony erect, feather shaped, delicate, ca 6.5 cm high, hydrorhiza not observed. Stem unbranched although, in the present specimen, the distal part had been partly broken off, but still remained attached, and was consequently displaced laterally by a new, regenerative colony tip that has grown up vertically, giving the impression that the old apex is merely a lateral branch; stem fascicled proximally, grading to monosiphonic distally; every additional auxiliary tube adhering to the dorsal side of the preceding one, not forming a beam around the main tube, but resulting in a laterally-flattened structure ( Fig. 7B View Fig ); division into internodes indistinct, except for 3–4 oblique, deeply-cut nodes towards the proximal part of hydrocaulus, passing through all cauline tubes at a time. Equivalents of internodes 700–1050 µm long, 200–225 µm wide, composed of 2–3 frontal nematothecae in a row, a short lateral cladial apophysis, a reduced nematotheca (with small, rounded aperture) on an inconspicuous mamelon at its base, as well as an axillar, anterior nematotheca rather lateral to it; there is no dorsal axillar nematotheca. Stem nematothecae large, inverted-triangular, with thick perisarc, apertures distal, wide, with inwardly- rolled abaxial wall, giving the impression that two circular apertures are present laterally; apophyses slightly shifted onto the anterior side of the colony, the two rows of hydrocladia forming an obtuse angle. Cladia relatively spaced from one another, up to 1 cm long, unbranched, divided into up to 12 cormidia by means of transverse, though not clearly demarcated nodes (75–95 µm wide), each internode 775–865 µm long, accommodating a hydrotheca and its 3 associated nematothecae: one mesial and a pair of laterals; up to 8 intranodal projections of the perisarc, of which 2 are given off from the abaxial side below the hydrothecal base, and up to 6 arise from the dorsal wall of the hydrotheca and project for a short distance into the lumen of the internode. Hydrotheca elongated, 600–635 µm deep, laterallyflattened, ad- and abaxial walls with slight basal bulges; a septum projecting slightly upwards from the lower portion of the adaxial wall reaches up to the middle of the thecal lumen, and is provided anteriorly with a distal swelling scattered with granular projections; a second, lamellar, two-winged septum is given off upwardly from the lateral sides of the hydrotheca at a rather acute angle, then changes its orientation and slightly plunges downwards, attaching its anterior border to the abaxial wall of the theca, leaving a slit-like, median passage between its two lateral ‘wings’; hydrothecal aperture 225– 230 µm wide, rim with a prominent, central, well-developed, abaxial cusp, nearly smooth elsewhere. Mesial nematothecae elongated, rather broad in frontal view, adnate for most of their length, leaving a short (40–50 µm) portion free from the base of the corresponding hydrotheca; aperture broad, abaxial wall inwardly-rolled, rim crenelate at corners; mesial nematotheca of first cormidium short, guttershaped and not coalescent with the hydrothecal base. Lateral nematothecae 145–155 µm long, broadly cylindrical, reaching the level of the hydrothecal rim; adaxial wall deeply scooped out, abaxial wall crenelate to wavy. Phylactocarp mounted on a short stem apophysis arising laterally, next to a cladial apophysis, on opposite side; divided into several moderately-long (360–485 µm) internodes by means of transverse to slightly oblique nodes, each bearing a frontal nematotheca similar to those of stem, with large apical apertures and inwardly-rolled abaxial walls, giving the impression that the nematothecae are bifid; last couple of internodes additionally provided with a basally concrescent gonotheca; the latter long, tubular (ca 1630 × 400 µm), tapering below, distally with a main, broad, subterminal, slit-like aperture with flimsy, wavy rim, above which a second, short, slender, gutter-shaped aperture is to be found. Sex undeterminable.
Remarks
Although not comprehensively described and/or illustrated, especially upon an apical examination of the hydrothecae, the internal septa of Cladocarpus bicuspis (G.O. Sars, 1874) possibly share morphological affinities with those of the present species. Indeed, a transverse septum, originating from the lateroabaxial hydrothecal walls, projects nearly horizontally midway into the lumen, then plunges down so as to meet the distal, swollen border of the adaxial hydrothecal ridge (G.O. Sars 1874: pl. 2 fig. 9; Kramp 1935: fig. 71b; Cornelius 1995: fig. 47c). Frontal views of the hydrotheca illustrated in the literature ( Broch 1918: fig. 48c; Schuchert 2001: fig. 114b) do not provide sufficient information on the global aspect of the abaxial projection. Besides this possible common feature, the hydrothecae of C. bicuspis are distinctive through the presence of a median, abaxial pair of marginal cusps, separated from a squared to V-shaped gap prolonged downwards, till the level of abaxial ridge, as a perisarcal thickening; additional features related to its gonosome allow a rapid separation from the present new species ( Cornelius 1995).
Also similar seems to be the abaxial septum of Wanglaophenia longicarpa Vervoort & Watson, 2003 , as observed from the illustration in Vervoort & Watson (2003: fig. 81g). This species, however, possesses hydrothecae with a distinct, abaxial, thorn-shaped crest prolonged downwards as a longitudinal ridge, and its phylactocarp has forked costae provided with hydrothecae ( Vervoort & Watson 2003).
Distribution
Known only from its type locality, off New Caledonia (present study).
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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