Myrtoessa hyas Radea

Radea, Canella, Parmakelis, Aristeidis & Giokas, Sinos, 2016, Myrtoessahyas, a new valvatiform genus and a new species of the Hydrobiidae (Caenogastropoda, Truncatelloidea) from Greece, ZooKeys 640, pp. 1-18 : 5-9

publication ID

https://dx.doi.org/10.3897/zookeys.640.10674

publication LSID

lsid:zoobank.org:pub:B4EA1C64-7EBB-4B89-B46A-360A9CCB11DB

persistent identifier

https://treatment.plazi.org/id/4811DC7A-037A-4D3A-9F02-36F5F3B2A2BF

taxon LSID

lsid:zoobank.org:act:4811DC7A-037A-4D3A-9F02-36F5F3B2A2BF

treatment provided by

ZooKeys by Pensoft

scientific name

Myrtoessa hyas Radea
status

sp. n.

Myrtoessa hyas Radea sp. n. Figs 2, 3, 4, 5, 6, 7

Type-locality.

Poulithra, Peloponnese, Greece, 36°6.63'N, 22°53.53'E, 70 m a.s.l, stream, 12/IV/2014, C. Radea, G. Tryfonopoulos legs.

Diagnosis.

As for genus.

Etymology.

The specific name (in apposition) derives from the Greek mythology: Hyas, (Υάς in Greek), was one of the seven nymphs Hyades (Υάδες in Greek) bringing humidity and rain, daughters of Atlas and Pleione.

Type material.

Holotype. Ethanol-fixed specimen, ZMUA 4183.

Paratypes. Two ethanol-fixed specimens, ZMUA 4184. Ten ethanol-fixed specimens dissected for anatomical study and four specimens coated for SEM, the remaining in the personal collection of C. Radea deposited in the Department of Ecology & Systematics, UOA.

Other material examined.

Ten specimens, collected from the type locality, Th. Constantinidis, E. Kalpoutzakis legs, 25/IV/2014, in the personal collection of C. Radea deposited in the Department of Ecology & Systematics, UOA.

Description.

Shell (Fig. 2 A–I). Colourless valvatiform shell with up to 3.5 whorls, thin, transparent when fresh, therefore possible to follow the position of rectum; spire more or less depressed; whorls rounded, regularly growing with shallow sutures. Measurements are given in Table 1. Periostracum cream-coloured; aperture adhering to the last whorl, prosocline, roundish to ovate; peristome continuous, thickened at columel lar margin, reflected at columellar margin, the outer margin simple; umbilicus open, deep, wide so that the first whorls can be seen through it, sometimes partially covered by the collumelar margin of aperture (Figs 2F, G, 3B); protoconch microsculpture composed of a dense net of irregularly shaped depressions (Fig. 3A, C, D). The number of protoconch whorls is 1.25. The width of nucleus and protoconch is 102 µm and 262 µm, respectively.

Operculum (Fig. 3E, F). Operculum ovate, thin, corneous, paucispiral, yellowish-orange, darker at the nucleus, with weakly convex inner face without any peg, nucleus sub-central.

Soft body pigmentation (Fig. 2 A–I). Soft body pigmentation of alive specimens extremely variable, the colouration being visible under the transparent shell; many specimens almost totally unpigmented with only a few traces of pigments on walls of visceral sac, several specimens grey pigmented and some others dark grey pigmented; in the last two cases, tentacles with a median grey stripe and snout with grey areas laterally and around eyes; snout longer than wide, parallel-sided with medium distal lobation; eye spots present; tentacles about six times as long as wide (in specimens preserved in ethanol solution 70%).

Nervous system (Fig. 4A). Cerebral ganglia of the same size, white-coloured; supraoesophageal and suboesophageal ganglia of the same size, smaller than cerebral ganglia, white-coloured; supraoesophageal connective about equal to suboesophageal connective; mean RPG ratio 0.39 (three specimens), nervous moderately concentrated.

Ctenidium-Osphradium. Ctenidium with ca 5-7 long lamellae. Osphradium of intermediate width, opposite posterior part of ctenidium.

Radula (Fig. 5). Central tooth trapezoidal, dorsal edge of tooth strongly concave; one pair of medium-sized basal cusps (bc2), basal tongue broadly V-shaped and about equal to lateral margin; median cusp blunt, protruding, broader and longer than laterals, 5 lateral cusps on each side of median cusp, the latter one not well defined (Fig. 5A, B); lateral tooth face taller than wider, basal tongue well developed; outer wing moderately flexed; cutting edge much shorter than outer wing; central cusp longer than lateral cusps, 5 lateral cusps on outer side, 4-5 on inner side (Fig. 5C); inner marginal tooth with ca. 24-28 long almost equal in size cusps; outer marginal tooth with ca. 27 cusps (Fig. 5D).

Digestive system apart from radula (Fig. 6). Style sac smaller than stomach, not protruding to the intestinal loop (Fig. 6A); rectum V-shaped, V being wider in female specimens (Fig. 6B).

Male reproductive system (Fig. 7 A–C). Penis long, tapering, flat, blunt, distal portion being well demarcated from proximal portion, opening through sub-terminal pa pilla on the left, whitish with a median grey stripe at the distal portion (in the grey pigmented specimens), proximal portion bent upon itself and wrinkled near the base; base usually black pigmented ventrally, its attachment area well behind the right eye; penial duct strongly undulating in base and straight distally, near centrally positioned and opening on the left side of penis; prostate like an elongate bean with mean length 0.44 mm (three specimens).

Female reproductive system (Figs 4 B–C, 7 D–E). Pallial oviduct glands, i.e. albumen and capsule glands, very small, total mean length 0.53 mm, total mean width 0.24 mm (three specimens); bursa copulatrix large-sized, pyriform, posteriorly positioned and fully protruding from the posterior end of the albumen gland; bursal duct length a little shorter than or equal to bursa copulatrix length; renal oviduct unpigmented and well-developed, tightly coiled in a shape of lower case ε (Greek); two seminal receptacles lying parallel on the renal oviduct and rather close to each other; distal seminal receptacle (Sr1) very small, globular with very short duct; proximal seminal receptacle (Sr2) larger, usually lying tightly over the renal oviduct and against bursa copulatrix; proximal seminal receptacle (Sr2) with a pink pearl shine. In some specimens, an egg capsule with a single egg was found inside the umbilicus (Fig. 7E).

Distribution and habitat.

So far the distribution of Myrtoessa hyas gen. n. & sp. n., seems to be restricted to the type locality on Parnon Mt., Peloponnisos. At the type locality, the geological substrate is limestone; all the specimens of the new species were found on stones, gravel, mosses and dead leaves of Platanus orientalis L. accumulated on the bottom of a stream. Many Bythinella sp. individuals were found to share the same stream.