Research Article |
Corresponding author: Canella Radea ( kradea@biol.uoa.gr ) Academic editor: Martin Haase
© 2016 Canella Radea, Aristeidis Parmakelis, Sinos Giokas.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Radea C, Parmakelis A, Giokas S (2016) Myrtoessa hyas, a new valvatiform genus and a new species of the Hydrobiidae (Caenogastropoda, Truncatelloidea) from Greece. ZooKeys 640: 1-18. https://doi.org/10.3897/zookeys.640.10674
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A new to science valvatiform hydrobiid, Myrtoessa hyas Radea, gen. n. & sp. n., from southern Greece, is described and illustrated. The new genus is a tiny gastropod thriving in a stream and is differentiated from the other known European and circum-Mediterranean valvatiform hydrobiid genera by a unique combination of the male and female genitalia features i.e. penis long, flat, blunt, with wide wrinkled proximal part and narrow distal part with a sub-terminal eversible papilla on its left side, bursa copulatrix well-developed, pyriform, fully protruding from the posterior end of the albumen gland and two seminal receptacles respectively. The new monotypic and locally endemic genus is narrowly distributed and its single known population nearby a coastal bustling village is vulnerable to anthropogenic stressors.
Endemicity, freshwater diversity, hydrobiids, taxonomy
The freshwater fauna around the Mediterranean Basin comprises a plethora of valvatiform hydrobiids (
Moreover, during last ten years, several new valvatiform taxa have been described based on shell and diagnostic anatomical characters and, in several cases, their molecular affinities have been investigated (e.g.
In Greece, eight valvatiform-planispiral hydrobiid genera, namely Daphniola Radoman, 1973, Fissuria Boeters, 1981, Graecoarganiella Falniowski & Szarowska, 2011a, Hauffenia Pollonera, 1898, Isimerope Radea & Parmakelis, 2013, Islamia Radoman, 1973, Prespolitorea Radoman, 1983 and Pseudoislamia Radoman, 1979, have been recorded so far (
Herein, a new genus and a new species of a minute valvatiform hydrobiid gastropod collected from Mount Parnon, Arkadia are described, and an identification key provided for the valvatiform hydrobiid genera of Greece based on the character states of male and female genitalia.
Snails in question thrived in a stream at Poulithra village, Parnon Mt., Arkadia (Fig.
Map showing the distribution of the locally endemic Truncatelloidea in Peloponnisos, southern Greek mainland. Abbreviations: B.a. Bythinella atypicos, B.b. Bythinella beckmanni, D.h. Daphniola hadei, H.e. Hauffenia edlingeri, I.a. Iglica alpeus, I.s. Isimerope semele, I.w. Iglica wolfischeri, M.h. Myrtoessa hyas gen. n., sp. n., P.e. Pseudamnicola exilis, R.f. Radomaniola feheri, R.s. R. seminula, R.t. R. tritonum.
General and diagnostic shell characters were studied and four shell measurements (shell height and width, aperture height and width) were taken from 14 specimens using the micrometer of the Stemi 2000-C stereomicroscope. Four ratios were generated from the raw data (Sh/Sw, Ah/Aw, Sh/Ah and Sw/Aw).
Ten specimens were dissected and studied anatomically under the stereomicroscope using very fine pins and pointed watchmaker’s forceps. Prior to dissection, the shell of each specimen was removed by soaking in Pereny solution. The soft body features were documented using the digital camera as described above.
To remove tissue remaining and debris, the shell, the radula and the operculum were immersed in KOH solution (5g/l) at room temperature, rinsed in distilled water and air-dried before being mounted on stubs. The protoconch, the operculum and the radula were studied using scanning electron microscopy (SEM, Jeol JSM–35 operating at 25 kV) after being dried and spray-coated in gold–palladium.
The authority of the family Hydrobiidae was based on
A restricted number of specimens (27 specimens in total) was collected from the sampling locality because the population abundance seemed to be low (no specimen was found during the initial 5 min sampling effort). The collected material was deposited in the Zoological Museum (
Ah aperture height
Aw aperture width
CV* (1+1/4n)*SD/x
coefficient of variation corrected for sample size (
Max maximum
Min minimum
n number of specimens
SD standard deviation
Sh shell height
Sw shell width
x mean
Bc bursa copulatrix
Bd bursal duct
Cg capsule gland
Cm commissure
E eye
Ec egg capsule
Fp faecal pellets
In intestine
Lpg left pleural ganglion
Md mantle
O renal oviduct
Oe oesophagous
Ol oviduct loop
P penis
Pd penial duct
R rectum
Rcg right cerebral ganglion
Sbg suboesophageal ganglion
Sh shell
Sn snout
Sp Sub-terminal penial papilla
Sr1 distal seminal receptacle
Sr2 proximal seminal receptacle
Ss style sac
St stomach
T tentacle
V ventral channel
Myrtoessa hyas sp. n. by original designation.
Shell minute (maximum height 1.05 mm, maximum width 1.30 mm), valvatiform with more or less depressed spire; operculum without peg; central tooth with one basal cusp on each side; ctenidium and osphradium present; penis long, flat, blunt, with wide wrinkled proximal part and narrow distal part with a sub-terminal eversible papilla; female genitalia with large pyriform bursa copulatrix, renal oviduct non-pigmented, coiled in an ε (Greek)- shape; two seminal receptacles lying parallel on the renal oviduct and rather close to each other, a small distal receptacle (Sr1) and a larger proximal one (Sr2).
The generic name derives from the Greek mythology: Myrtoessa (Μυρτώεσσα in Greek) was a naiad nymph in Arkadia. Gender feminine.
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.
As for genus.
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.
Holotype. Ethanol-fixed specimen,
Paratypes. Two ethanol-fixed specimens,
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,
Shell (Fig.
Shell morphometry of Myrtoessa hyas gen. n., sp. n. Measurements are in mm. Abbreviations are given in the materials and methods.
Type locality | Sh | Sw | Ah | Aw | Sh/Sw | Ah/Aw | Sh/Ah | Sw/Aw | |
---|---|---|---|---|---|---|---|---|---|
Poulithra | Min | 0.60 | 1.20 | 0.60 | 0.60 | 0.46 | 0.92 | 1.00 | 0.92 |
N = 14 | Max | 1.05 | 1.40 | 0.70 | 0.70 | 0.77 | 1.17 | 1.67 | 1.17 |
x | 0.88 | 1.31 | 0.63 | 0.63 | 0.67 | 1.02 | 1.40 | 1.02 | |
SD | 0.12 | 0.09 | 0.04 | 0.05 | 0.08 | 0.08 | 0.19 | 0.08 | |
CV* | 0.14 | 0.07 | 0.06 | 0.09 | 0.12 | 0.08 | 0.14 | 0.08 |
Operculum (Fig.
Soft body pigmentation (Fig.
Nervous system (Fig.
Ctenidium-Osphradium. Ctenidium with ca 5–7 long lamellae. Osphradium of intermediate width, opposite posterior part of ctenidium.
Radula (Fig.
Digestive system apart from radula (Fig.
Male reproductive system (Fig.
Female reproductive system (Figs
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.
Twelve locally endemic truncatelloidean species (see
Myrtoessa hyas gen. n. & sp. n. differs from all the known valvatiform hydrobiids in having a unique combination of shell and anatomical characters that according to the standard hydrobiid taxonomy, does not allow its inclusion in any other known genus of the Hydrobiidae family. Consequently, a new monotypic genus is necessary to accommodate it.
The combination of the features of male and female genitalia followed by
Myrtoessa gen. n. compared morphologically with other valvatiform genera distributed in the Balkan Peninsula and in the Mediterranean Basin: eleven morphological characters and character-state scores for thirty-four genera are given (based on Radea et al. 2013).
Distribution | Bursa copulatrix | Seminal receptacle (s) | Penis | Penial lobe(s) | Penial papilla | Penial stylet | Ctenidium | Eyes | Operculum | Umbilicus | Rectum | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Arganiella | Italy, Spain, Montenegro | 1 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 2 | (U) or (S) |
Boetersiella | Spain | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 2 | (U) |
Bracenica | Montenegro | 1 | 3 | 1 | 2 | 0 | 0 | - | 0 | 1 | 3 | - |
Chondrobasis | Spain | 1 | 1 | 1 | 1 | 0 | 0 | 0 | 1 | 0 | 2 | (U) |
Corbellaria | Spain | 1 | 3 | 1 | 2 | 0 | 0 | 0 | - | 0 | 2 | (SS) |
Dabriana | Bosnia | 1 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | - | 1 | - |
Daphniola | Greece | 1 | 3 | 1 | 2 | 0 | 0 | 1 | 1 | 0 | 0 | - |
Fissuria | Greece, Italy, France | 1 | 3 | 3 | 1+3 | 1 | 0 | 1 | 0 | 0 | 0,1,2,3 | (S) |
Gocea | FYROM | 1 | 3 | 1* | 4* | 0 | 0 | - | 1 | 1 | 2 | - |
Graecoarganiella | Greece | 1 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | - | 2 | (S) |
Hauffenia | Italy, Greece | 1 | 2 | 0,1 | 0,4 | 0 | 1 | 1, 0 | 0 | 1ª | 2 | (Z) or (?) |
Heraultiella | France | 1 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 2 | (U) or (V) |
Horatia | Croatia, FYROM | 1 | 3 | 1,2 | 3 | 0 | 0 | 1 | 1 | 0 | 1 | (0) |
Iberhoratia | Spain | 1 | 3 | 1 | 2 | 0 | 0 | 1 | 1 | 0 | 2 | (U) or (S) |
Isimerope | Greece | 1 | 0 | 1 | 3 | 1 | 0 | 0 | 1 | 0 | 1 | (U) |
Islamia | Greece, France, Italy, Spain, Turkey, Israel | 0 | 3 | 1 | 4 | 0 | 0 | 1 | 1 | 0 | 0 | (U) |
Josefus | Spain | 0 | 3 | 1 | 4 | 0 | 0 | 0 | 1 | 0 | 1 | (U) |
Karevia | FYROM | 1 | 3 | 1 | 3 | 0 | 0 | - | 1 | 0* | 3 | - |
Kerkia | Slovenia | 1 | 1 | 1 | 3 | 0 | 0 | 1 | 0 | 1 | 2 | (S) |
Lyhnidia | FYROM | 1 | 2 | 1* | 4* | 0 | 0 | - | 1 | 0 | 0 | - |
Milesiana | Spain | 0 | 3 | 1 | 2 | 0 | 0 | 1 | 1 | 0 | 2 | (U) |
Myrtoessa | Greece | 1 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | 0 | 2 | (V) |
Ohridohauffenia | FYROM | 1 | 3 | 1 | 3 | 0 | 0 | - | 1 | 0 | 1 | - |
Ohrigocea | FYROM | 1 | 3 | 1 | 3 | 0 | 0 | - | 1 | 0 | 2 | - |
Pezzolia | Italy | 0,1 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | (S) |
Prespolitorea | Greece, FYROM | 1 | 3 | 1 | 3 | 0 | 0 | - | 1 | 0* | 1 | - |
Pseudohoratia | FYROM | 1 | 2 | 1 | 3 | 0 | 0 | 1 | 1 | 1 | 0,1,2 | (0) |
Pseudoislamia | Greece | 1 | 3 | 1 | 4 | 0 | 0 | - | 1 | 0 | 2 | - |
Sardohoratia | Italy | 1 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | (S) |
Sheitanok | Turkey | 1 | 1 | 0 | 0 | 0 | 0 | 1** | 1 | 0* | 3 | - |
Spathogyna | Spain | 1 | 3 | 1 | 2 | 0 | 0 | 1 | 1 | 0* | 2 | (V) |
Strugia | FYROM | 1 | 2 | 1 | 3 | 0 | 0 | - | 1 | 0 | 2 | - |
Tarraconia | Spain | 1 | 0 | 1 | 2 | 0 | 0 | 1 | 1 | 0 | 3 | (U) |
Zaumia | FYROM | 1 | 2 | 1* | 4* | 0 | 0 | - | 0 | 0 | 1 | - |
The opening of penial duct through a sub-terminal papilla is a novel character recorded for the first time in the valvatiform hydrobiids of Europe and Mediterranean Basin since, up to now, only a terminal papilla has been recorded (Table
The new genus inhabits a stream with cold and clear fast running water. The rest known valvatiform genera of Greece thrive in various freshwater systems: Islamia and Pseudoslamia in lakes, springs and streams, Isimerope in springs and rivers, Fissuria in subterranean waters, Daphniola, Hauffenia and Graecoarganiella in springs and Prespolittorea in lakes (
The single population of Myrtoessa hyas gen. n. & sp. n. nearby a coastal touristic village is vulnerable to anthropogenic stressors, in particular during the summer period, due to the numerous tourists, visitors, and hikers as well as to the increased demands for water supply and irrigation.
In last three years, one new locally endemic monotypic truncatelloidean genus, i.e. Isimerope (Radea et al. 2013), and seven new locally endemic species i.e. Radomaniola feheri Georgiev, 2013 (
1 | Bursa copulatrix present | 2 |
– | Bursa copulatrix absent | Islamia |
2 | Seminal receptacle(s) present | 3 |
– | Seminal receptacle(s) absent | Isimerope |
3 | Both proximal (Sr2) and distal (Sr1) receptacles present | 4 |
– | Only proximal (Sr2) receptacle present | Hauffenia |
4 | Proximal seminal receptacle (Sr2) well developed, much larger than the distal one (Sr1) | Prespolitorea |
– | Not as above | 5 |
5 | Penis with papilla | 6 |
– | Penis without papilla | 8 |
6 | Penis with terminal papilla | 7 |
– | Penis with sub-terminal papilla, without lobe(s), distal portion of penis well demarcated from proximal portion | Myrtoessa |
7 | Penis pigmented black, long, tapering, cylindrical with one double lobe on its proximal portion | Graecoarganiella |
– | Penis unpigmented, rather short, parallel-sided, flat with more than one glandular lobes on distal, occasionally on proximal portion too | Fissuria |
8 | Penis with a wide lobe on its distal portion | Pseudoislamia |
– | Penis with a narrow lobe on its proximal portion | Daphniola |
We wish to thank A. Economou-Amilli for the scanning electron micrographs, Th. Constantinidis, E. Kalpoutzakis for collecting additional material, G. Tryfonopulos and the staff of Management Body of Mount Parnon and Moustos wetlands for their help in the field. The fieldwork was done under a collection permit (ref. no. 111704/1686) issued by the Greek Ministry of Environment, Energy and Climate Change. The manuscript was improved by the useful comments and suggestions of Subject Editor M. Haase and two anonymous reviewers.