Profundiconus puillandrei, Tenorio & Castelin, 2016
publication ID |
https://doi.org/ 10.5852/ejt.2016.173 |
publication LSID |
lsid:zoobank.org:pub:8AA5610F-B490-419D-BBF4-A6D51708350F |
DOI |
https://doi.org/10.5281/zenodo.5640345 |
persistent identifier |
https://treatment.plazi.org/id/55807BF8-D984-42C1-B039-F3EBD8EB2C13 |
taxon LSID |
lsid:zoobank.org:act:55807BF8-D984-42C1-B039-F3EBD8EB2C13 |
treatment provided by |
Plazi |
scientific name |
Profundiconus puillandrei |
status |
sp. nov. |
Profundiconus puillandrei View in CoL sp. nov.
urn:lsid:zoobank.org:act:55807BF8-D984-42C1-B039-F3EBD8EB2C13
Figs 12A–J View Fig.12 , 13A–D View Fig. 13 , 14 View Fig. 14
Conus ikedai View in CoL – Poppe 2008: pl. 615, fig. 1a–b (non C. ikedai Ninomiya, 1987 View in CoL ).
Conus smirna View in CoL – Marshall 1981: 499, fig. 3j (non C. smirna Bartsch & Rehder, 1943 View in CoL ).
Conus View in CoL sp. C – Röckel et al. 1995b: 585, fig. 49.
Profundiconus View in CoL n. sp. g. – Puillandre et al. 2014: Supplementary Material 1 (unfigured).
Etymology
This new species is dedicated to Dr. Nicolas Puillandre, mollusc curator at the MNHN. Dr. Puillandre has a long and outstanding trajectory in the study of the phylogeny of the Conoidea . The naming of the new species after him recognises his important contributions to the taxonomy of Conoidea at the molecular level.
Type material examined
Holotype
NEW CALEDONIA: 43.2 × 18.0 mm, R/V Alis, NORFOLK 1 Expedition, st. DW 1707, Banc Jumeau Est, Norfolk Ridge , 23°43' S, 168°16' E, 381–493 m ( MNHN IM-2000-30771 ; Fig. 12A View Fig.12 ). View Materials GoogleMaps
Paratypes
NEW CALEDONIA: 39.6 × 17.3 mm, R/V Alis, NORFOLK 2 Expedition, st. DW 2072, Banc Aramis, Norfolk Ridge , 25°21' S, 168°57' E, 1000–1006 m ( MNHN IM-2000-30772 ; paratype 1; Fig. 12B View Fig.12 ); View Materials GoogleMaps 40.7 × 16.8 mm, R/V Alis, NORFOLK 2 Expedtion, st. DW 2077, Banc Zorro, Norfolk Ridge, 25°21' S, 168°19' E, 666–1000 m (MNHN IM-2000-30773; paratype 2; Fig. 12C View Fig.12 ); 35.0 × 15.5 mm, R/V Alis, NORFOLK 2 Expedition, st. DW 2068, Banc Porthos, Norfolk Ridge, 25°20' S, 168°57' E, 680–980 m (MNHN IM-2000-30774; paratype 3; Fig. 12D View Fig.12 ); 31.7 × 13.2 mm, R/V Alis, NORFOLK 2 Expedition, st. DW 2066, Banc Athos, Norfolk Ridge, 25°17' S, 168°55' E, 834–870 m (MNHN IM-2000- 30775; paratype 4; Fig. 12E, H View Fig.12 ); 43.6 × 18.1 mm, R/V Alis, NORFOLK 2 Expedition, st. DW 2074, Banc Zorro, Norfolk Ridge, 25°24' S, 168°20' E, 623–691 m ( MNHN IM-2000-30776 ; paratype 5; Fig. 12F View Fig.12 ); 57.3 × 24.6 mm, R/ V Alis, EXBODI Expedition, st. DW 3907, Récifs de l’Astrolabe-Nord Ouest GoogleMaps , 19°50' S, 165°33' E, 608–671 m (MNHN IM-2009-31320; paratype 6; Fig. 12G View Fig.12 ; GenBank accession number (cox1 sequence): KT874752 View Materials ); 45.2 × 18.5 mm, R/V Alis, NORFOLK 2 Expedition, st. DW 2054, Banc Jumeau Est, Norfolk Ridge, 23°40' S, 168°15' E, 736–800 m (MNHN IM-2000- 30778; paratype 7; Fig. 12I View Fig.12 ); 44.8 × 18.2 mm, R/V Alis, BATHUS 3 Expedition, st. DW 776, Loyalty Ridge, 24°44' S, 170°08' E, 770–830 m (MNHN IM-2000-30779; paratype 10); 49.9 × 21.6 mm, R/V Alis, TERRASSES Expedition, st. DW 3045, Mont J, Ride des Loyautés, 23°48' S, 169°46' E, 660– 710 m (MNHN IM-2009-18221; paratype 11; GenBank accession number (cox1 sequence): KJ550484 View Materials ); 37.0 × 17.2 mm, R/V Alis, BATHUS 3 Expedition, st. DW 776, Loyalty Ridge, 24°44' S, 170°08' E, 770–830 m (MNCN 15.05/60171; paratype 12).
NEW ZEALAND: 38.9 × 17.5 mm, R/V Tangaroa , st. K861, Kermadec Ridge, 30°36.5' S, 178°22.5' W, 1030 m ( NIWA 99587; paratype 8; Fig. 12J View Fig.12 ); 44.9 × 19.5 mm, R/V Tangaroa , st. K831, Kermadec Ridge, 29°51.5' S, 178°10.5' W, 965 m ( NIWA 99588; paratype 9).
Type locality
NEW CALEDONIA: Banc Jumeau Est GoogleMaps , Norfolk Ridge, 381–493 m, 23°43' S, 168°16' E (NORFOLK 1 st. DW1707).
Other material examined
NEW CALEDONIA: 33.2 × 14.8 mm, R/V “Alis”, NORFOLK 2 Expedition, st. DW 2057, Banc Introuvable, Norfolk Ridge, 24°40' S, 168°39' E, 555–565 m ( MNHN IM- 2007-34865; GenBank accession number (cox1 sequence): KJ550262 View Materials ). Note: This specimen, matching the holotype, was photographed (http://coldb.mnhn.fr/catalognumber/mnhn/im/2007-34865) and sequenced, but the shell was destroyed in the process and is no longer available.
Additionally, we examined 31 more specimens from 15 uncataloged MNHN lots collected at several stations in Norfolk Ridge and Loyalty Ridge, New Caledonia, by the R/V “Alis” in the course of several campaigns. Several specimens of shells in private collections collected in Balut Is., Philippines at 100– 150 m, showing the conchological features of Profundiconus puillandrei sp. nov., were also examined.
Description
Morphometric parameters: S L = 29–57 mm; RD = 0.53–0.62; RSH = 0.22–0.29; PMD = 0.81–0.90.
Shell moderately small to medium sized (maximum length 57.0 mm). Shell profile ventricosely conical, with high spire. Spire profile sigmoid to slightly concave. Protoconch multispiral, with 3–3.5 whorls, white to yellow-brown. Last whorl of larval shell shows minute axial ridges. Early teleoconch whorls with nodules which are often indistinct after whorls 5 to 6, but may persist, forming nodulose ridge reaching shoulder on last whorl. Sutural ramp flat to slightly concave, with very fine striae and arcuate threads becoming obsolete in late whorls. Shoulder with distinct ridge, usually smooth, although nodulose or even strongly nodulose in some specimens. Last whorl with convex sides adapically, then almost straight and slightly concave abapically. Last whorl smooth or with very fine striae becoming more evident towards base. Spire and last whorl patternless, white to pale straw-yellow in colour. Columella white. Aperture pale yellow or white. Periostracum yellow, thin and translucent. Operculum with serrations.
Radular tooth examined in holotype ( Fig. 13A View Fig. 13 ), in paratypes 3 ( Fig. 13B–D View Fig. 13 ), 6 and 9, and in an additional non-type specimen. 48 to 62 teeth in radular sac. Radular tooth small for size of shell: its total length relative to shell length S L /T L = 75–105. Anterior portion shorter than posterior section of tooth (T L/AP L = 3.1–3.6). With one barb and pointed blade which covers 50–62% of anterior portion of tooth. External cusp present, extending between 64 and 90% of length of anterior portion of tooth. External cusp laterally widened and serrated, with 4–5 small denticles. Large adapical opening occupying most of anterior portion of tooth (100AO L/AP L = 64–75). Fringe of closely spaced projections pointing towards apex immediately below waist. Shaft fold present. Large and prominent basal spur on top of slanted base of tooth.
Distribution and habitat
New Caledonia (Norfolk Ridge and Loyalty Ridge) and New Zealand (Kermadec Ridge), at depths from 380 to 1100 m ( Fig. 14 View Fig. 14 ). Several empty shells matching P. puillandrei sp. nov. from Balut Is., Mindanao, Philippines, have been examined. The identity of these specimens from the Philippines (allocated in several private collections) could not be confirmed by radular or molecular studies, but the conchological features seem consistent with the identification of these specimens (often labelled as Conus cf. ikedai , or Conus darkini “albinistic”) as P. puillandrei sp. nov. This is a feasible possibility given the multispiral protoconch of this species (suggesting a planktonic larval development), and might represent a significant range extension to the Philippines.
Remarks
Profundiconus puillandrei sp. nov. has been dredged alive from 1030–1180 m off Curtis Island, Kermadec Ridge, New Zealand (identified as Conus smirna ; see Marshall 1981). This observation makes this species one of the deepest-living ones among the known cone snails. P. puillandrei sp. nov. was initially identified as “giant” P. vaubani ( Fig. 1I View Fig. 1 ). Apart from being smaller in size, P. vaubani has a paucispiral protoconch of 1.75 whorls and a ridge at the shoulder with axial costae, which are absent in the case of P. puillandrei sp. nov. The shell pattern of P. vaubani consists of light brown axial streaks from base to spire, whereas the shell of P. puillandrei sp. nov. is patternless. The radular teeth of P. vaubani ( Fig. 2A–C View Fig. 2 ) and P. puillandrei sp. nov. ( Fig. 13 View Fig. 13 ) are superficially similar, but the tooth of P. vaubani has a much larger relative size, with S L/T L = 27–31 compared to 75–105 for P. puillandrei sp. nov. The new species can also be compared with P. profundorum ( Fig. 1A, L View Fig. 1 ) and P. smirnoides ( Fig. 1D View Fig. 1 ). Like P. puillandrei sp. nov, these two species have multispiral protoconchs.There are no significant differences in shell shape among these species: ANCOVA for MD, HMD and SH, using species hypothesis as a factor and S L as covariate, did not yield statistically significant results. However, they differ significantly in average shell length: puillandrei S L 39.82 mm, profundorum S L 96.93 mm (t = 10.28, p = 2.13 × 10-12; U = 0, p = 5.15 × 10-7), smirnoides S L 76.09 mm (t = -10.20, p = 5.25 × 10-10; U = 0, p = 2.5 × 10-5).
The shell of P. puillandrei sp. nov. has a distinct shoulder ridge, usually smooth but some times nodulose, which is absent in P. profundorum and less developed and always smooth in P. smirnoides . The shell of P.puillandrei sp.nov. is patternless, whereas both P.profundorum and P. smirnoides exhibit a characteristic pattern of broad, pale brown spiral bands on each side of centre, often interrupted by creamy white axial streaks in the case of P. smirnoides . The morphology of the radular tooth of P. puillandrei sp. nov. ( Fig. 13 View Fig. 13 ) and of P. smirnoides ( Fig. 9H View Fig. 9 ) is very different. The radular tooth of P. profundorum is unknown, preventing its comparison with the tooth of P. puillandrei sp. nov.
Most of the shells of P. puillandrei sp. nov. examined were not nodulose at the shoulder ridge ( Fig. 12 View Fig.12 ). About 10% of the specimens studied had a nodulose spire and shoulder ridge (i.e., paratype 6, Fig. 12G View Fig.12 ), coming mainly from Loyalty Ridge. These include two of the sequenced individuals, which, however, were genetically similar to the ones with a smooth ridge. Moreover, nodulose and non-nodulose specimens exhibit analogous radular and protoconch morphology. The presence of nodules at the spire and shoulder causes an apparent difference in shape, which is possibly the main source of intraspecific phenotypic variability within this species. Nodulose specimens may resemble a small P. teramachii (e.g., paratype 6, Fig. 12G View Fig.12 ), a distinct but related species as inferred from the tree in Fig. 5 View Fig. 5 . The shell of P. teramachii is also patternless and has a ground colour and protoconch morphology similar to that of P. puillandrei sp. nov. The radular tooth of P. teramachii ( Fig. 2D–F View Fig. 2 ) is also similar to that of P. puillandrei sp. nov. ( Fig. 13 View Fig. 13 ). However, P. teramachii attains a larger size (S L = 55–111 mm), has a lower spire (RSH 0.11–0.22 versus 0.22–0.29 in P. puillandrei sp. nov.) and usually exhibits a broadly carinate shoulder. P. puillandrei sp. nov. is phylogenetically related to P. neotorquatus stat. nov., P. neocaledonicus sp. nov., P.teramachii and P. smirnoides .
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.
Kingdom |
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Phylum |
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Class |
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Order |
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Family |
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Genus |
Profundiconus puillandrei
Tenorio, Manuel J. & Castelin, Magalie 2016 |
Profundiconus
Tenorio & Castelin 2016 |
Conus ikedai
Ninomiya 1987 |
C. ikedai
Ninomiya 1987 |
Conus smirna
Bartsch & Rehder 1943 |
C. smirna
Bartsch & Rehder 1943 |
Conus
Linnaeus 1758 |