Paradiopatra spinosa, Paxton, Hannelore & Budaeva, Nataliya, 2013
publication ID |
https://doi.org/ 10.11646/zootaxa.3686.2.2 |
publication LSID |
lsid:zoobank.org:pub:3039889E-9CA4-4460-A118-06170AA1D0A6 |
DOI |
https://doi.org/10.5281/zenodo.6145082 |
persistent identifier |
https://treatment.plazi.org/id/F91F87C4-FFEF-FFFE-CB86-8FB4DFAA2FF3 |
treatment provided by |
Plazi |
scientific name |
Paradiopatra spinosa |
status |
sp. nov. |
Paradiopatra spinosa View in CoL n. sp.
Figures 10 View FIGURE 10 , 11 View FIGURE 11 ; Table 2
Material examined. Type material—Holotype (AM W36461) Bass Canyon, 38.573ºS 148.659ºE, RV Southern Surveyor, coll. D. Cummings and S. Holmes, 13 Oct 2009, 1600 m, beam trawl; SLOPE 17: 1 paratype (MV F189437); SLOPE 27: 1 paratype (MV F189438); SLOPE 55: 2 paratypes (MV F189439); 1 paratype (AM W43547); SLOPE 69: 1 paratype mounted for SEM (AM W43553.001).
Type locality. Pacific Ocean, off eastern Australia, Bass Canyon, 38.573ºS, 148.659ºE, 1600 m.
Diagnosis. Ovoid frontal lips; ceratophores without lateral projections; peristomial cirri present; first 2–3 pairs of parapodia with pseudocompound, tridentate falcigers with moderately long pointed hoods, with almost smooth shafts and appendages; very long, spinose aciculae, extending as far as falcigers; subacicular hooks equal, starting from chaetiger 12–13; branchiae absent; delicate protomandibles.
Description. All examined specimens lacking posterior ends. Length of holotype 43 mm in length, partially in tube; anterior 31 mm of worm (41 chaetigers) free of tube, median 9 mm in tube, posterior 3 mm exposed, width 1.6 mm (at chaetiger 10, excluding parapodia); paratypes ranging from 19–60 mm long (34–84 chaetigers), 0.9–1.1 mm wide. Alcohol stored specimens cream-coloured, lacking colour pattern.
Prostomium anteriorly rounded, wider than long, with paired ovoid frontal lips, separated by gap ( Fig. 10 View FIGURE 10 A– C). All palps, antennae and cirri ending in very fine tips. Palps of holotype reaching chaetiger 1; lateral antennae reaching chaetiger 3; median antenna reaching chaetiger 2; palps and antennae of most paratypes in poor condition with some antennostyles overly extended or missing, giving distorted values, thus palps reaching chaetiger 1–2, lateral antennae reaching chaetiger 1–6, median antenna reaching chaetiger 1–5. Palpostyles much thicker than antennostyles ( Fig. 10 View FIGURE 10 B, C). Ceratophores lacking lateral projections; lateral antennae of holotype with five rings, median with four, distal ring about twice as long as proximal ones. Ceratophores of most paratypes ranging from almost smooth to indistinctly ringed, with 3–5 rings for lateral and 3 rings for median antenna. Nuchal grooves short but wide, slightly curved. Eyes absent. Peristomium slightly shorter than first chaetiger. Peristomial cirri slender, about 2/3 length of peristomium, inserted subdistally.
First 2–3 pairs of parapodia modified, projecting anterolaterally, directed slightly ventrally. Prechaetal lobes rounded on all parapodia; postchaetal lobes long and subulate in first four chaetigers, decreasing rapidly in size, absent from chaetiger 11 (10–11). Dorsal cirri subulate and very long on anterior three chaetigers ( Fig. 11 View FIGURE 11 A–C), becoming gradually shorter, present as tiny subulate structures until end of fragments. Ventral cirri subulate on first 3 (3–4) chaetigers, then shorter with blunt end on next chaetiger, before changing to ovoid ventral glandular pads ( Fig. 10 View FIGURE 10 C).
Parapodia supported by 3–4 long spinose aciculae, projecting from prechaetal lobe as far as falcigers and limbate chaetae ( Fig. 11 View FIGURE 11 A–C). First two pairs of parapodia with dorsal fascicle of 1–2 simple spinose limbate chaetae and ventral fascicle of 3–5 tridentate pseudocompound falcigers with moderately long pointed hoods; shafts and appendages of falcigers almost smooth ( Fig. 10 View FIGURE 10 D, E). Tip of falcigers with knob-like terminal tooth and two subterminal teeth ( Fig. 11 View FIGURE 11 D, E); in some cases subterminal teeth are closely spaced ( Fig. 11 View FIGURE 11 F) resembling a single larger tooth, giving bidentate appearance ( Figs 10 View FIGURE 10 E, 11G). Two fascicles of simple limbate chaetae starting from chaetiger 3; chaetiger 3 of holotype and most paratypes with one tridentate falciger ( Fig. 11 View FIGURE 11 C), one paratype with a falciger present on left side only, and one paratype lacking falcigers on chaetiger 3 completely. From chaetiger 4 falcigers absent in all specimens. Ventral fascicle of limbate chaetae replaced by paired bidentate subacicular hooks from chaetiger 12 (12–13), hooks about equal in length and thickness ( Fig. 11 View FIGURE 11 H). Pectinate chaetae slightly oblique with 17–20 teeth. Branchiae absent. Posterior end unknown. Tube cylindrical, with inner soft secreted layer and outer layer of grey mud particles.
Mandibles ( Fig. 11 View FIGURE 11 I) slender, moderately sized protomandibles; paratype examined lacking calcified cutting plate. Maxillae ( Fig. 11 View FIGURE 11 J) lightly sclerotized, with very slender MI. Maxillary formula (based on one paratype): MI = 1 + 1; MII = 9 + 12; MIII = 10 + 0; MIV = 6 + 6; MV = 1 + 1.
Remarks. The similarities of P. s p i n o s a to other species with two or two to three pairs of parapodia with falcigers have been discussed in the Remarks on P. longicappa . Furthermore, P. s p i n o s a can be distinguished from that and all other species in the genus by its unusually long and spinose aciculae. In most species of Paradiopatra the aciculae of the modified parapodia extend slightly or to about half the length of the falcigers from the presetal lobe. In P. spinosa , however, they extend as far as the falcigers and limbate chaetae ( Figs 10 View FIGURE 10 D, 11A–C).
Etymology. The name spinosa refers to the spinose aciculae and limbate chaetae, particularly those of the modified parapodia.
Distribution. Paradiopatra spinosa n. sp., was collected in two transects: south of Sydney, NSW and off eastern Victoria in Bass Strait, in 1500–2250 m, as well as Bass Canyon, during more recent sampling, in 1600 m.
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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