Ptilototheca soutpansbergensis, Herbert, 2016
publication ID |
https://doi.org/ 10.5852/ejt.2016.236 |
DOI |
https://doi.org/10.5281/zenodo.3854750 |
persistent identifier |
https://treatment.plazi.org/id/C146B323-FFB7-FFE7-FDC3-9E49FE3BF783 |
treatment provided by |
Valdenar |
scientific name |
Ptilototheca soutpansbergensis |
status |
gen. et sp. nov. |
Ptilototheca soutpansbergensis View in CoL gen. et sp. nov.
urn:lsid:zoobank.org:act:F3F6A7DF-A655-483B-9865-AB0AA56DCCE8
Figs 4–8 View Fig View Fig View Fig View Fig View Fig
Etymology
Named after the Soutpansberg massif, to which the species is endemic.
Material examined
Holotype
SOUTH AFRICA: Limpopo, Soutpansberg, Sibasa area, Phiphidi Falls , 22.9483° S, 30.3950° E, ~ 1000 m, indigenous forest, in leaf-litter, D. Herbert, 20 Nov. 1997, diameter 9.2 mm, height 6.1 mm ( NMSA V5567 About NMSA /T4069, body in ethanol). GoogleMaps
Paratypes (listed west to east)
SOUTH AFRICA: Limpopo, Soutpansberg, Hanglip Forest, picnic site, 22.99951° S, 29.88643° E, 1540m,northern mist-belt forest, in leaf-litter,leg.D.Herbert, L. Davis &M.Cole, stn 14-14, 29 Nov.2014 ( NMSA P0214/T4070, three specimens, body of one in ethanol); Hanglip Forest, 23.017° S, 29.900° E, indigenous forest, J. Swaye, Mar. 2001 ( NMSA V9485/T4071, five dry specimens; ELM D18041/T039, one dry specimen); Goedehoop Forest, 23.067° S, 30.121° E, 1250 m, sorted from leaf-litter, C. Symes, 30 Oct. 1999 ( NMSA V7506/T4066, six dry specimens); Entabeni Forest, 22.99092° S, 30.27829° E, Afromontane forest, in leaf-litter, J. Swaye, L91, L95, Oct.–Nov. 2001 ( NMSA W2259/T4067, nine dry specimens, seven in ethanol); Entabeni Forest, environs of Kliphuis, 22.98589° S, 30.28127° E, 1345 m, northern mist-belt forest, in leaf-litter, D. Herbert, L. Davis & M. Cole, stn 14-17, 30 Nov. 2014 ( NMSA P0183/T4068, 11 specimens, bodies of five in ethanol; NHMUK 20160040, one dry specimen; RMNH.5004144, one dry specimen); Entabeni Forest, environs of Kliphuis, 22.98455° S, 30.28272° E, 1365 m, northern mist-belt forest, in leaf-litter, D. Herbert, L. Davis & M. Cole, stn 14-16, 30 Nov. 2014 ( NMSA P0186/T4063, 10 specimens, bodies of five in ethanol); Thathe Vondo Forest, 22.87705° S, 30.35026° E, Afromontane forest, in leaf-litter, J. Swaye, L41, Oct.–Nov. 2001 ( NMSA W2080/T4064, 18 dry specimens, two in ethanol); Thathe Vondo Forest, near sacred shrine, 22.92649° S, 30.35270° E, 1075 m, northern mist-belt forest, in leaf-litter, D. Herbert, L. Davis & M. Cole, stn 14-18, 1 Dec. 2014 (P0225/T4065, one specimen, body in ethanol; ELM D18049/T040, one dry specimen); Thathe Vondo Forest, near sacred shrine, 22.92173° S, 30.35760° E, 1090 m, northern mist-belt forest, in leaf-litter, D. Herbert, L. Davis & M. Cole, stn 14-19, 1 Dec. 2014 ( NMSA P0304/T4060, two specimens, body of one in ethanol).
Other material (listed west to east, all in NMSA)
SOUTH AFRICA: Limpopo, Soutpansberg, Dundee Forest, 23.017° S, 29.515° E, 1525 m, sorted from leaf-litter, C. Symes, 24 Jul. 1999 (V7516); Hanglip Forest, 23.00002° S, 29.88789° E, 1360 m, mist-belt forest, in leaf-litter, A. Moussalli & D. Stuart-Fox, 16 Dec. 2006 (W5637); Hanglip Forest, 23.017° S, 29.900° E, 1370 m, A.C. & W.H. van Bruggen, Feb. 1965 (A8342); Entabeni Forest, 23.013° S, 30.080° E, 1175 m, sorted from leaf-litter, C. Symes, 16 Jul. 1999 (V7494); Goedehoop Forest, 23.07253° S, 30.11494° E, 1190 m, Afromontane forest, in leaf-litter, J. Swaye, L59, Oct.–Nov. 2001 (W2064); Entabeni Forest, 23.000° S, 30.233° E, indigenous forest, J. Swaye, L19a, Mar. 2001 (V9475); Entabeni, Matiwa Kop, 22.983° S, 30.250° E, 1310 m, in forest, A.C. & W.H. van Bruggen, Feb. 1965 (A8352); Entabeni Forest, 22.983° S, 30.250° E, 1160 m, A.C. & W.H. van Bruggen, Feb. 1965 (A8341); Entabeni Forest, 22.99541° S, 30.28023° E, Afromontane forest, in leaf-litter, J. Swaye, L30, Feb.–Mar. 2001 (W2261); Thathe Vondo Forest, 22.872933° S, 30.338783° E, 1280 m, indigenous Afromontane forest, in leaf-litter, J. Horn, 1 Mar. 2006 (W7717); Thathe Vondo Forest, 22.876° S, 30.349° E, 1430 m, indigenous forest, in leaf-litter, C. Symes, 4 Nov. 1999 (V7639).
Type locality
SOUTH AFRICA: Limpopo, Soutpansberg, Sibasa area, Phiphidi Falls, 22.9483° S, 30.3950° E, ~ 1000 m.
Identification
Easily identified on account of the fact that it is the only heliciform urocyclid occurring in the Soutpansberg that has a spirally punctate protoconch. Additional distinctive anatomical characters are given in the generic diagnosis above.
Description
SHELL ( Fig. 4 View Fig ). Small, globose-lenticular, largest specimen with diameter 10.0 mm, height 4.9 mm; H:D 0.62–0.71; periphery below mid-whorl, evenly rounded; suture indented, but not strongly so, inserting above periphery; very thin and delicate. Protoconch diameter 1.1–1.4 mm; junction with teleoconch weakly marked; nucleus more or less smooth, but protoconch thereafter with numerous microscopic punctations arranged in close-set spiral lines ( Fig. 4 View Fig E–F), also with some collabral alignment; in last quarter whorl punctations coalesce to form fine incised spiral lines. Teleoconch of up to 2.5 whorls; whorl expansion moderate; sculptured with fine, close-set, microscopic spiral striae, relatively weak on first whorl but strengthening and relatively distinct from start of second whorl onward; teleoconch otherwise only with weak, uneven growth irregularities. Columella concave, adapical region whitish and reflected over umbilical region and fused to adjacent part of base, forming a distinct umbilical channel; aperture obliquely lunate. Translucent, more or less uniformly yellowish-brown; apical and basal surfaces both glossy.
EXTERNAL FEATURES ( Fig. 5 View Fig ). Head and neck usually dark grey dorsally, pale greyish-white ventrally; grey pigmentation associated with skin granules and thus appearing as dense spotting; pigmentation weaker in some specimens; tentacles brownish-grey, yellowish-brown in pale individuals; posterior of foot more uniformly grey, caudal appendage somewhat darker. Body lobes of mantle edge grey; right and left shell lobes elongate-trigonal to spathulate when extended over shell, pale and translucent; posterior of foot and mantle lobes with scattered, minute, bluish-grey pigment granules. Pulmonary lining behind mantle edge variously bordered with cream and black pigmentation, often as collabral bands; additional dark blotches and lines posterior to this, with a very prominent and well-defined black band overlying primary ureter, to the right of pale tissues of kidney, sometimes with a further well-defined line of cream pigment to the right of (i.e., dorsal to) black band ( Fig. 5B View Fig ). Spire viscera dark brown with irregularly branching, cream venation, usually sparse and sometimes virtually absent. Caudal pit and appendage well developed.
RADULA ( Fig. 6 View Fig ). Formula R+9+(1–2)+(70–80); rachidian tricuspid, laterals essentially bicuspid with a mesocone and strong basal ectocone, but also with a minute endocone on side of mesocone; laterals followed by 1–2 intermediary teeth and then a long series of marginals; marginals curved and terminally bicuspid, but with a series of smaller cusps or serrations on concave outer edge, these proportionately stronger on smaller teeth toward radula margin.
DISTAL GENITALIA ( Fig. 7 View Fig ). Penis cylindrical, tapering toward apex, surrounded in a thin sheath, occasionally slightly kinked in mid region; penis divided into two portions, a thick muscular apical region (~¾ of penis length) ending at a conical penial verge, and a basal thinner-walled preputial region lined internally by coarse rounded papillae ( Fig. 7B View Fig ). Epiphallus extremely short, with a small caecum arising close to penis-epiphallus junction; retractor muscle attached to penis apex, close to base of caecum. Flagellum very short and squat, divided into F1 and F2, but not sharply so ( Fig. 7C View Fig ); F1 broad basally, twisted into approximately one revolution, internal diverticulae poorly delineated; F2 a small papilla-like structure at tip of F1, internal diverticulae more visible. Vas deferens long, thick and much convoluted in proximal portion between base of spermoviduct and penis base; inserts at junction of epiphallus and flagellum without evidence of chalky internal material. Genital atrium simple; vagina short; gametolytic sac capacious, its duct of moderate length; base of free oviduct somewhat swollen, pale apricot; spermoviduct divided into distinct prostatic and oviductal portions. Spermatophore elbowed ( Fig. 7D View Fig ), with a relatively slender capsule; most of tail with well-developed, fan-like spines with multiple branches (often in clumps), the tips finely pointed and recurved; tail initially relatively slender, but broader and more robust in mid-region; unbranched tip of tail very short.
Distribution ( Fig. 8 View Fig )
A narrow-range endemic, known only from the Soutpansberg massif, Limpopo, South Africa; at altitudes between 1000 and 1525 m above sea level.
Habitat
Northern mist-belt forest ( Mucina & Rutherford 2006); all material collected to date has been found in forest floor leaf-litter.
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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