Tylorhaphe wallacei, Herbert, 2024
publication ID |
https://doi.org/ 10.5852/ejt.2024.973.2765 |
publication LSID |
lsid:zoobank.org:pub:524B5B20-A190-4023-AC2B-7B48A725930A |
persistent identifier |
https://treatment.plazi.org/id/714FF54E-372F-321E-FDB1-FCF2FA9AFEF3 |
treatment provided by |
Plazi |
scientific name |
Tylorhaphe wallacei |
status |
gen. et sp. nov. |
Tylorhaphe wallacei gen. et sp. nov.
urn:lsid:zoobank.org:act:1FC6F4A9-1000-4B89-8C68-C22A43FE818D
Figs 65–67 View Fig View Fig View Fig
Diagnosis
Closest to Tylorhaphe luteopicta gen. et sp. nov., but with stronger sculpture, including distinct axial pliculae; periphery less strongly angled; umbilicus narrower, its rim with a strong spiral cord that overhangs the underlying cavity.
Etymology
I take pleasure in naming this remarkably beautiful species in honour of Alfred Russel Wallace (1823– 1913), in recognition of his pioneering contribution to biogeography and evolutionary biology.
Material examined
Holotype ( Fig. 66 View Fig )
PAPUA NEW GUINEA • living specimen; New Ireland, south of Selapiu Island , Stn DW 4473; 02°43′ S, 150°36′ E; depth 93–149 m; 4 Sep. 2014; NO Alis -KAVIENG 2014 leg.; MNHN-IM-2000-38878. GoogleMaps
Paratypes
PAPUA NEW GUINEA – New Ireland • 9 specimens, living; south east of Selapiu Island, Stn DW4467; 02°44′ S, 150°35′ E; depth 213–287 m; 3 Sep. 2014; NO Alis -KAVIENG 2014 leg.; MNHN- IM-2000-38879 GoogleMaps • 1 specimen, living; same data as for holotype; DNA voucher; MNHN-IM-2023-58751 GoogleMaps • 6 specimens, living; same data as for holotype; MNHN-IM-2000-38880 GoogleMaps • 2 specimens, living; south of Selapiu Island , Stn DW 4462; 02°43′ S, 150°36′ E; depth 90–201 m; 3 Sep. 2014; NO Alis -KAVIENG 2014 leg.; DNA vouchers; MNHN-IM-2013-58616 and -58617 GoogleMaps • 1 specimen, living; south of Selapiu Island , Stn DW 4466; 02°43′ S, 150°36′ E; depth 204–272 m; 3 Sep. 2014; NO Alis -KAVIENG 2014 leg.; DNA voucher; MNHN-IM-2023-58916 GoogleMaps • 5 specimens, living; south of Selapiu Island , Stn DW 4474; 02°43′ S, 150°36′ E; depth 90–185 m; 4 Sep. 2014; NO Alis -KAVIENG 2014 leg.; MNHN- IM-2000-38881 GoogleMaps .
Other material PAPUA NEW GUINEA – New Ireland • 37 specimens, living; south of Selapiu Island , Stn DW 4472; 02°43′S, 150°36′ E; depth 87–144 m; 4 Sep. 2014; NO Alis -KAVIENG 2014 leg.; MNHN GoogleMaps • 26 specimens, living; south of Selapiu Island , Stn DW 4465; 02°43′ S, 150°36′ E; depth 90–228 m; 3 Sep. 2014; NO Alis -KAVIENG 2014 leg.; MNHN GoogleMaps • 2 specimens, living; south of Selapiu Island , Stn DW 4462; 02°43′ S ,
150°36′ E; depth 90–201 m; 3 Sep. 2014; NO Alis -KAVIENG 2014 leg.; MNHN • 1 specimen, living; south of Selapiu Island, Stn DW 4466; 02°43′ S, 150°36′ E; depth 204–272 m; 3 Sep. 2014; NO Alis - KAVIENG 2014 leg.; MNHN GoogleMaps • 29 specimens, living; south of Selapiu Island, Stn DW 4474; 02°43′ S, 150°36′ E; depth 90–185 m; 4 Sep. 2014; NO Alis -KAVIENG 2014 leg.; MNHN GoogleMaps .
Description ( Fig. 66 View Fig )
SHELL. Small (diameter up to 6.7 mm), depressed-trochiform (H/D 0.57– 0.6); teleoconch of up to 5.0 whorls; periphery roundly angled, situated just below mid-whorl; suture slightly above periphery; base umbilicate, somewhat flattened. First teleoconch whorl rounded with circa three indistinct spiral cords; shoulder develops and strengthens during second and third whorl; two strong cords arise near end of third whorl, one subsutural the other supraperipheral; subsutural cord initially beaded by prosocline subsutural pliculae, but beading progressively stronger with growth and last whorl with strong nodules on subsutural cord; supraperipheral cord remaining more finely beaded, beads aligned with axial pliculae; interval between subsutural and supraperipheral cords a broad, bevelled slope, almost flat, sculptured with finer secondary cords and further intermediaries, initially few but becoming more numerous and more close-set with growth, up to 10 on last whorl; bevelled slope with distinct, close-set, strongly prosocline pliculae which become finer and even more close-set on last whorl; interaction of spiral and axial element producing a finely beaded reticulation; circa three peripheral spiral cords at start of last whorl. Base with similar, but finer cords, all with pliculate intervals; spiral sculpture usually weaker in mid-region of base (not always), but strengthens considerably toward umbilicus with 2–4 strong cords, innermost of which is largest and forms umbilical rim; all peri-umbilical cords rendered nodular by strong axial pliculae radiating from umbilicus. Umbilicus relatively narrow (± 0.22 of maximum shell diameter), steep-sided and deep; its walls retaining traces of spiral and axial sculpture, and overhung by cord at umbilical rim; funicle lacking. Aperture roundly quadrate; peristome interrupted in parietal region; columella pillar thick with a slight basal swelling and micropustular surface; parietal lip thickened with callus and extending outward as a rounded lobe above insertion of columella; surface of lobe microshagreened sometimes with indistinct in-running ridges in the most mature individuals; edge of lobe slightly thickened and with a step-like drop to underside of preceding whorl; outer lip descending steeply immediately prior to its insertion, its interior somewhat thickened and with traces of in-running ridges; interior otherwise smooth and nacreous with external sculpture evident through transparency; outer lip with shallow subperipheral concavity in mature specimens; thickening of outer lip also evident externally as a slight subterminal swelling.
COLOUR. Shell glossy throughout; colour pattern comprising bold bright yellowish subsutural blotches; bevelled slope with alternating yellowish and opaque white axial lines; bolder blotches in similar colours at periphery and extending onto base in a radiating pattern; peri-umbilical region white; apical whorls translucent whitish to pale yellowish-grey, first whorl with a row of opaque white dots at shoulder; apical bulb of protoconch opaque white; yellow colour may turn a pale apricot-brown post mortem in some individuals.
DIMENSIONS. Holotype, height 3.8 mm, diameter 6.5 mm; largest specimen, diameter 6.7 mm.
PROTOCONCH ( Fig. 67B View Fig ). As in Tylorhaphe luteopicta gen. et sp. nov., but slightly larger, diameter 220– 230 µm.
OPERCULUM ( Fig. 67C–D View Fig ). Corneous; multispiral; peripheral fringe radially striate; radial striations remaining where whorls overlap; surface with distinct spiral microsculpture.
RADULA ( Fig. 67E–F View Fig ). Very similar to that of Tylorhaphe luteopicta gen. et sp. nov.; cusp of transitionary innermost marginal trigonal with three small pointed denticles; second marginal clearly the largest tooth, its cusp with a strong triangular central denticle bearing smaller lateral denticles at its base on both sides.
EXTERNAL ANATOMY (from rehydrated specimens, condition poor). Head with distinct forehead between cephalic tentacles; snout moderately long, cylindrical, distal third bearing long slender papillae; cephalic lappets not evident; cephalic tentacles long and slender, micropapillate, eyestalks long, their tips conspicuously expanded and containing large black eyes; left neck-lobe small, digitate; right neck-lobe rolled to form exhalant siphon; details of epipodial structure not clear; foot evidently broad with lateral propodial lobes on each side, tapering posteriorly. Head-foot translucent cream-white with some opaque white pigmentation on snout, eyestalks, right neck-lobe, sides of foot, and metapodium.
Habitat
Dredged on muddy sand; at depths of 144–213 m (living specimens the same).
Distribution ( Fig. 65 View Fig )
Known only from off the southern coast of Selapiu Island, New Ireland, Papua New Guinea [Bismarck Sea]. Although dredging at similar depths was undertaken at other localities off north-western New Ireland, this species was only collected in this very limited area. Nevertheless, at this locality the species appears moderately abundant.
Remarks
A highly distinctive, sculpturally ornate species. Most similar to Tylorhaphe luteopicta gen. et sp. nov.
MNHN |
Museum National d'Histoire Naturelle |
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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