Maltzanella godetiana ( KOBELT , 1878) Neubert, 2014

Neubert, Eike, 2014, Revision of Helix LINNAEUS, 1758 in its eastern Mediterranean distribution area, and reassignment of Helix godetiana KOBELT, 1878 to Maltzanella HESSE, 1917 (Gastropoda, Pulmonata, Helicidae), Contributions to Natural History 26, pp. 1-200 : 178-182

publication ID

https://doi.org/ 10.5281/zenodo.13222466

persistent identifier

https://treatment.plazi.org/id/03A48783-57FA-FF00-2887-FC67561DFE0E

treatment provided by

Felipe

scientific name

Maltzanella godetiana ( KOBELT , 1878)
status

comb. nov.

Maltzanella godetiana ( KOBELT, 1878) View in CoL comb. nov. ( Figs 268–273 View Figs 268–271 View Fig View Fig )

1878 Helix (Pomatia) godetiana KOBELT, Jahrbücher der Deutschen Malakozoologischen Gesellschaft 5: 319 [Amorgos, coll. Kobelt ex Godet].

1884 Helix dacoronae LETOURNEUX, Bulletins de la Société malacologique de France, 1: 287 [Santorin "vit sous les rochers entre le couvent Saint-Élie et la colline de Messa Vouno"].

Type material:

godetiana : lectotype SMF 9954 (SD Zilch 1952: 154): H = 39.4; D = 39.5; PH = 29; PD = 21.7; PrD = 8; W = 4.25. dacoronae : syntype MHNG 17941: H = 31.2; D = 33.2; PH = 22.7; PD = 23.1; PrD = 9.5; W = 4.

Specimens examined:

Greek Islands: Kasos: on the way to Agios Georgios, 35.4197 26.9096, 17.04.1982, LIEB (2 subfossil?). Tilos: Western Tilos, from Agios Panteleimonas in direction to Agios Anton, 36.3927 27.3954, 18.06.1996, LIEB (7 subfossil?). Folegandros: Folegandros, 36.6172 24.9162, 12.06.1991, LIEB (2 subfossil?). Amorgos: Island of Amorgos, 36.8401 25.8876, coll. Leutwein ex A. Wild ex J. Thiesse, NMBE 18478/2. Naxos: S of Agiassos, 36.9549 25.4391, 12.12.1979, leg. M. Mylonas, NHMC 50/0982.

Not checked personally (all after Psonis & al. 2014): Astypalea, 36.5393 26.3130; Kounoupoi Islet, 36.538242 26.4677; Pontikousa Islet, 36.5549 26.2286.

Diagnosis: shell large, thin, dark bluish brown with axial yellowish streaks and ribs, protoconch large, dome-shaped, aperture very large, aperture cream coloured, umbilicus closed.

Description: shell of large size, thin, spherical, with a moderately high conical spire; basic shell colour dark bluish brown, usually all five spirals fused, with a bright yellowish spiral in the centre of the last whorl; protoconch large, dome-shaped, its diameter almost reaches 10 mm, smooth, bright corneous to bluish whorls; teleoconch of 3–4 smooth whorls with a dense pattern of relatively fine axial granulated ribs and fine axial yellowish streaks; last whorl descending below the periphery; aperture very large, rounded, palatal shell wall inside aperture dark brown to bluish, apertural rim narrow, labial callus weak, cream coloured, columellar triangle white, relatively small; umbilicus closed in adult shells.

Genital organs ( Fig. 272 View Fig ): penis club-shaped, epiphallus somewhat longer than penis; flagellum short, approximately of the same length as epiphallus+ penis; mrp attaching in a central position on the epiphallus; internally, pp1 smaller than pp2, penial chamber short, with perpendicularly arranged folds, both papillae conical with a central perforation; atrial stimulator a massive rounded knob; female system with a very short vaginal tube, dart sac and glandulae mucosae strongly developed, the glandulae with a short basic stem, multi-branched, only slightly longer than dart sac; pedunculus stem long, with a thick and moderately long diverticulum not exceeding the bursa copulatrix and branching off in the proximal third of pedunculus, bursa copulatrix stem longer than pedunculus stem, vesicle rounded and bent downwards.

Distribution ( Fig. 273 View Fig ): This species is endemic to several islands in the Central southern Aegean Sea. It differs from M. dickhauti ( KOBELT, 1903) ( Fig. 271 View Figs 268–271 ) by the uniformly dark shell colour which is caused by the almost complete fusion of the spiral bands. In M. dickhauti , these are usually narrow and separate, and the cream basic colour of the shell can be seen easily.

Remark: Interestingly, this species has a diverticulum much shorter than the bursa copulatrix (see also Gambetta 1929, who dissected specimens from Stampalia (= Astypalea)). This is similar to many true Helix species and made it difficult to argue against its affiliation to Helix , because in the other two Maltzanella species, the diverticulum is longer and reaches or even surpasses the bursa copulatrix in length ( Schütt 1976: 67, Figs 1–3 View Figs 1–9 ). This observation is interpreted here as convergence, with the reduction of the diverticulum obviously occurring in both genera. It represents the apomorphic character state, because very long diverticula can be found in several genera within the Helicini .

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