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Notes on some taxa of the Alvania lineata-complex with the
descriptions of three new species from the Mediterranean
Sea (Gastropoda: Rissoidae)
Notas sobre algunos taxones del complejo de Alvania lineata, con la
descripción de tres nuevas especies del Mediterráneo (Gastropoda:
Rissoidae)
Bruno AMATI*1, Massimo APPOLLONI**, Ermanno QUAGGIOTTO***,
Carlo SMRIGLIO**** & Marco OLIVERIO*****
Recibido el 9-X-2018. Aceptado el 28-XII-2018
ABSTRACT
Some taxonomically troublesome nominal taxa of the rissoid genus Alvania Risso, 1826
are examined: Alvania disparilis Monterosato, 1890, A. peloritana (Aradas & Benoit,
1874), A. perversa F. Nordsieck, 1972 and A. dorbignyi (Audouin, 1826). The four
species are here considered as valid, and for the sake of nomenclatural stability lectotypes
of Alvania disparilis, Rissoa peloritana and Alvania perversa are designated. The holo-
type of Alvania dorbignyi is refigured and redescribed, and all Mediterranean records of
this species are reassigned to A. perversa. Alvania schwartziana Brusina, 1866 is
reported for the first time in Italian waters. Three new species are herein described: Alva-
nia bartolinorum n. sp., Alvania unica n. sp. and Alvania zaraensis n. sp.
RESUMEN
Se examinan algunos taxones nominales problemáticos de risóidos del género Alvania
Risso, 1826: Alvania disparilis Monterosato, 1890, A. peloritana (Aradas y Benoit,
1874), A. perversa F. Nordsieck, 1972 y A. dorbignyi (Audouin, 1826). Las cuatro espe-
cies se consideran aquí válidas, y con fines de mantener la estabilidad nomenclatural se
designan lectotipos de Alvania disparilis, Rissoa peloritana y Alvania perversa. El holotipo
de Alvania dorbignyi está figurado de nuevo y redescrito, y todas las citas de esta espe-
cie en el Mediterráneo se reconducen a A. perversa. Alvania schwartziana Brusina, 1866
se cita por primera vez en aguas italianas. Se describen tres nuevas especies: Alvania
bartolinorum n. sp., Alvania unica n. sp. y Alvania zaraensis n. sp.
* Largo Giuseppe Veratti, 37/D, 00146 Rome, Italy; e-mail: bruno_amati@yahoo.it
** Museo Civico di Zoologia, Via Ulisse Aldrovandi, 18, 00197 Rome, Italy; e-mail:
massimo.appolloni@comune.roma.it.
*** Via Secula 13, 36023 Longare, Vicenza, Italy; e-mail: ermanno.quaggiotto@libero.it
**** Department of Science, “Roma Tre” University of Rome, Viale Marconi, 446, 00146 Rome, Italy; e-mail:
csmriglio@alice.it
***** Department of Biology and Biotechnologies “Charles Darwin”, Sapienza University of Rome, Viale
dell’Università 32, I-00185 Rome, Italy; e-mail: marco.oliverio@uniroma1.it
1Corresponding author
© Sociedad Española de Malacología Iberus, 37 (1): 81-112, 2019
81
INTRODUCTION
Rissoidae Gray, 1847 is the most
diverse rissooidean family, with at least
38 recognised genera (Á
VILA
, 2005;
C
RISCIONE
& P
ONDER
, 2013; M
OLLUS
-
CA
B
ASE
, 2018). The genus Alvania Risso,
1826 is currently represented by 314
recognised species of which 263 belong-
ing to the Recent fauna (M
OLLUSCA
B
ASE
,
2018). In the Mediterranean Sea the
genus Alvania is largely represented by
72 Recent species (M
OLLUSCA
B
ASE
,
2018) and includes several species-
complex, e.g. Alvania lineata Risso, 1826,
Alvania dictyophora (Philippi, 1844),
Alvania scabra (Philippi, 1844) and
Alvania subcrenulata (Bucquoy, Dautzen-
berg & Dollfus, 1884). Among them the
Alvania lineata-complex includes some
20 recognised Recent species (Table I),
all with non-planktotrophic develop-
ment, except for Alvania discors (Allan,
1818) which has a planktotrophic larval
stage.
Traditionally, the taxonomy of
Mediterranean rissoids has been based
almost exclusively on shell characters,
whose puzzling variation has often
caused uncertainty about the status of
some of these taxa. Although an inte-
grated approach (teleoconch, proto-
conch, soft parts morphology and
colour pattern, radula, genetics, etc...)
will certainly help in assessing their tax-
onomy, however, in most cases, the
availability of large samples and the
comparative study of type material
provide important data to improve
current taxonomic knowledge. In this
note, we focused on four nominal taxa
of this complex, of uncertain status:
Alvania dorbignyi (Audouin, 1826),
Alvania perversa F. Nordsieck, 1972,
Alvania peloritana (Aradas & Benoit,
1874) and Alvania disparilis Monterosato,
1890, and describe three additional new
species.
Description of the A. lineata group
All the species in the complex have
rather similar shells: thick, of medium-
large size for the genus, with ovate-
conical profile, wide base, and rather
strong teleoconch sculpture, the spiral
usually weaker than the axial; strong
apertural varix in mature specimens,
outer lip usually with denticles on the
inner side (except for Alvania datchaensis
Amati & Oliverio, 1987 and A. claudioi
Buzzurro & Landini, 2007); protoconch
paucispiral indicating a non-plank-
totrophic larval development, except for
Alvania discors (Allan, 1818), rarely
devoid of an apparent sculpture (e.g.
Alvania algeriana (Monterosato, 1877,
Alvania claudioi, Alvania bozcaadensis Tis-
selli & Giunchi, 2013 and Alvania zaraen-
sis n. sp.), usually sculptured by numer-
ous microtubercles randomly arranged
or fused to form parallel minute
threads, or more rarely by flattened
cordlets arranged into an orange skin
pattern (e.g. Alvania lanciae (Calcara,
1845)) or zigzag patterns (e.g. Alvania
datchaensis Amati & Oliverio, 1987).
Shell with usually uniformly coloured
background with or without more or
less fine or interrupted spiral bands. The
external soft parts have been described
for a few species and are conforming to
the general scheme of the genus Alvania
(e.g. B
RUSINA
, 1866: 25 for Alvania
schwartziana Brusina, 1866; P
ONDER
,
1985: 38 for Alvania lineata Risso, 1826;
A
MATI
& N
OFRONI
, 1985: 19; A
LBANO
&
S
ABELLI
, 2009: 56 for Alvania settepassii
Amati & Nofroni, 1985).
MATERIALS AND METHODS
The samples here studied are stored
in public and private collections, as
detailed under each species (see abbre-
viations), and in the Appendix. Pho-
tographs have been taken with a Sony
Cyber-Shot digital camera mounted on
a Kyowa KBS stereomicroscope, edited
with the Combine-Z software (H
ADLEY
,
2006). Most SEM photographs were
taken with a Philips XL30 at the Interde-
partmental Laboratory of Electron
Microscopy (LIME: University “Roma
Tre”, Rome); the SEM photos of the
holotype of Alvania garrafensis are cour-
tesy of Emilio Rolán (Vigo); that of the
type of Alvania dorbignyi is courtesy of
Iberus, 37 (1), 2019
82
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
83
Table I. List of the Mediterranean species of the Alvania lineata Risso, 1826 complex.
Tabla I. Lista de las especies mediterráneas del complejo Alvania lineata Risso, 1826.
Species Figures
Alvania aeoliae Palazzi, 1988 Figure 67
Alvania algeriana (Monterosato, 1877) Figure 72
Alvania aspera (Philippi, 1844) Figure 77
Alvania bartolinorum Amati & Smriglio n. sp. Figures 30-40
Alvania bozcaadensis Tisselli & Giunchi, 2013 Figures 63, 64
Alvania campanii Tisselli & Giunchi, 2013 Figures 65, 66
Alvania claudioi Buzzurro & Landini, 2007 Figure 58
Alvania colossophilus Oberling, 1970 Figure 76
Alvania datchaensis Amati & Oliverio, 1987 Figures 68, 69
Alvania discors (Allan, 1818) Figure 55
Alvania disparilis Monterosato, 1890 Figures 1-11
Alvania dorbignyi (Audouin, 1826) Figures 19-22
Alvania elisae Margelli, 2001 Figures 78, 79
Alvania fractospira Oberling, 1970 Figures 70, 71
Alvania garrafensis Peñas & Rolán, 2008 Figures 73-75
Alvania lanciae (Calcara, 1845) Figures 59-61
Alvania lineata Risso, 1826 Figure 62
Alvania peloritana (Aradas & Benoit, 1874) Figures 12-18
Alvania perversa Nordsieck, 1972 = Alvania dorbignyi AA non (Audouin, 1826) Figures 23-29
Alvania schwartziana Brusina, 1866 Figure 57
Alvania settepassii Amati & Nofroni, 1985 Figure 56
Alvania unica Amati & Quaggiotto n. sp. Figures 41-48
Alvania zaraensis Amati & Appolloni n. sp. Figures 49-54
the MNHN (Paris); those of the types of
Alvania perversa are courtesy of S. Hof
(SRI, Frankfurt am Main). Measure-
ments for the new species were taken
from 25 specimens of Alvania bartolino-
rum n. sp. and 12 specimens of Alvania
zaraensis n. sp. (Tables II-III).
Abbreviations and acronyms
AN: Andrea Nappo collection (Quartu
Sant’Elena, Italy);
AP: Attilio Pagli collection (Vinci, Flo-
rence, Italy);
AR: Alessandro Raveggi collection (Flo-
rence, Italy)
BA: Bruno Amati collection (Rome,
Italy)
CB: Cesare Bogi collection (Livorno,
Italy)
CS-PM: Carlo Smriglio–Paolo Mariottini
collection (Rome, Italy)
EQ: Ermanno Quaggiotto collection
(Longare, Vicenza, Italy)
IN: Italo Nofroni collection (Rome,
Italy)
MBAC: Museum of the Department of
Animal Biology of the University
(Catania, Italy)
CMSN: Museum of Natural History
(Milan, Italy)
MGPUF: Geological Museum and Palae-
ontology of the University (Florence,
Italy)
MCZR: Zoological Museum (Rome,
Italy)
MNHN: National Museum of Natural
History (Paris, France)
MO: Marco Oliverio collection (Rome,
Italy)
RP: Raffaele Petrone (Rome, Italy)
SG: Serge Gofas collection (University of
Malaga)
Iberus, 37 (1), 2019
84
SYSTEMATICS
Class G
ASTROPODA
Cuvier, 1795
Subclass C
AENOGASTROPODA
Cox, 1960
Superfamily R
ISSOOIDEA
Gray, 1847
Family R
ISSOIDAE
Gray, 1847
Genus Alvania Risso, 1826: 140
Type-species: Alvania europea Risso, 1826: 142, pl. IX, fig. 116 = Alvania cimex (Linnaeus, 1758)
(Turbo), by subsequent designation N
EVILL
, 1885: 105
Alvania disparilis Monterosato, 1890 (Figs. 1-11)
Alvania disparilis Monterosato, 1890: 146
Type material: Lectotype (MCZR–M–22155/L, Monterosato coll.) (Figs 1-4), here designated (H 2.95
mm, W 1.75 mm) and 25 paralectotypes (MCZR–M–22155/P, Monterosato coll.) (mostly fragments),
from the type locality, 1 paralectotype (MCZR–M–22155/P, Monterosato coll.) from Sciacca, Sicily.
Other material examined: Sicily. Messina, labelled, “R. Peloritana, subfoss. del Porto di Messina”,
6 sh (of which some broken) (MCZR–M–22150, Monterosato coll.); Messina, labelled “?Duccinella!
Messina!/Alvania peloritana”, 4 sh(MCZR–M–30053, Monterosato coll.); unspecified locality, 5 sh
(MCZR–M–30054, Monterosato coll.).
Type locality: Off Palermo (Sicily, Italy), ‘Funnazzi’, unspecified depth.
SB-MS: Stefano Bartolini-Maria Scape-
rrotta collection, (Florence, Italy)
SEM: scanning electron microscope
SMF: Senckenberg Museum (Frankfurt
am Main, Germany)
Teleoconch=
H: height
W: width
Ha: height of the aperture
H/W: ratio height/width
Nw: number of whorls
Nar: number of axial ribs
Nsc-ab: number of spiral cords above
the aperture
Nsc-ba: number of spiral cords on the base
Protoconch =
h: height
d: diameter of nucleus
Do: diameter of first half whorl
DM: maximum diameter
nw: number of whorls
sh: empty shell(s)
lv: live collected specimen(s) with soft
parts.
Distribution: Central Mediterranean:
off Palermo and Messina (Sicily), at
unspecified depth, possibly ca. 90-180 m
depth (ca. 50-100 ‘braccia’) for off
Palermo. The site name ‘Funnazzi’ indi-
cates an enigmatic fishing area off
Palermo, repeatedly cited by Mon-
terosato and de Gregorio (D
E
G
REGORIO
,
1889a: 248; 1889b: 7, 8); traces of its loca-
tion have been lost even among local
fishermen (see A
PPOLLONI ET AL
., 2018:
table 1).
Description of the lectotype: Shell (Figs
1-4) small, not solid, ovate-conic,
globose, height 2.95 mm, width 1.75
mm, H/W 1.68, aperture 1.45 mm. Pro-
toconch (Figs 3, 4) height 0.375 mm,
globose, paucispiral, of 1.6 whorls,
diameter of nucleus 0.15 mm, diameter
of first half whorl 0.25 mm, maximum
diameter 0.425 mm; sculpture of a
dozen interrupted spiral cordlets,
becoming finer and more numerous
toward the protoconch/teleoconch
boundary. Teleoconch of 3.4 convex
whorls, suture canaliculated. Axial
sculpture on the last whorl of 14 fine
orthocline ribs, half as wide as the inter-
spaces, interrupted at the suprasutural
spiral cordlet. Spiral sculpture starting
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
85
Figures 1-11. Alvania disparilis Monterosato, 1890. 1: lectotype, Palermo (Sicily), H 2.95 mm
(MCZR–M–22155/L); 2, 3: SEM micrograph of the lectotype; 4: detail of the protoconch sculp-
ture of the lectotype; 5: original label; 6: shell from Messina (Sicily) (MCZR–M–22150), H 2.8
mm; 7: original label of the same shell; 8: SEM micrograph of the same shell; 9-11: details of the
protoconch.
Figuras 1-11. Alvania disparilis Monterosato, 1890. 1: lectotipo, Palermo (Sicilia), H 2,95 mm
(MCZR–M–22155/L); 2, 3: micrografía electrónica de barrido del lectotipo; 4: detalle de la escultura
de la protoconcha del lectotipo; 5: etiqueta original; 6: concha de Messina (Sicilia)
(MCZR–M–22150), H 2,8 mm; 7: etiqueta original de la misma concha; 8: micrografía electrónica de
barrido de la misma concha; 9-11: detalles de la protoconcha.
200 µm
20 µm
200 µm
50 µm
100 µm
500 µm
1
2
3
6
54
9
810 11
7
with 2 (II and IV) visible fine spiral
cordlets on early teleoconch; on the last
whorl 9 (4+1+4) cordlets, the four adapi-
cal ones equidistant and twice as wide
as the interspaces, the others slightly
closer at first and then spaced with
increasing distance abapically; minute
tubercles at the intersection of axial ribs
and spirals cordlets, forming a quadran-
gular reticulate pattern. Coloration light
brown, with protoconch and spiral
cordlets slightly darker. Soft parts and
operculum unknown.
Remarks: The original material of Al-
vania disparilis Monterosato, 1890
(MCZR–M–22155, Monterosato coll.)
(A
PPOLLONI ET AL
., 2018: 43, pl. 14, figs C,
D), consists of two vials: one contains 26
syntypes, mostly fragments, from ‘Fun-
nazzi’, off Palermo, Sicily, with auto-
graph label by Monterosato reading: “Al.
disparilis, Monts. mss. 1890 Palermo
1886!” (Fig. 5). The best-preserved shell
is here selected as lectotype (Figs 1-4), to
stabilize the name usage. This same shell
was figured by C
AMPANI
, B
ARTOLINI
&
S
PANU
(2012: 89, fig. 7) with erroneous
measurement (H 3.6 mm instead of H
2.95 mm) to compare with A. garrafensis
sensu C
AMPANI
, B
ARTOLINI
& S
PANU
,
2012 (= A. bartolinorum n. sp. this work,
not A. garrafensis Peñas & Rolán, 2008).
The other vial contains a single shell,
from off Sciacca, Sicily, also with auto-
graph label by Monterosato reading:
“Sciacca” (Figs 41-48). This shell is not
conspecific with the specimens from off
Palermo, and represents indisputably an
undescribed species, which will be de-
scribed below (Alvania unica n. sp.). Alva-
nia disparilis Monterosato, 1890 has been
considered as a deep-water form of Alva-
nia lanciae (Calcara, 1845) (K. Nicolay
and G. Schirò in
VAN
A
ARTSEN
, 1982: 4).
Alvania lanciae (Calcara, 1845) (:29, pl.
IV, fig. 12) (Figs 59-61) differs from
Alvania disparilis by its conspicuously
microsculptured teleoconch (lacking in A.
disparilis) and by the protoconch sculp-
ture of irregular pits, with an orange-skin
like pattern, vs. a dozen interrupted
spiral cordlets in A. disparilis. Further-
more, A. lanciae has usually a more robust
shell, with large nodules at the intersec-
tions, slightly elongated along the spirals,
gradually stronger toward the base, vs.
weaker minute tubercles in A. disparilis,
and the spiral sculpture above the aper-
ture is irregularly spaced vs. equidistant
and finer in A. disparilis.
Alvania garrafensis Peñas & Rolán,
2008 (:21, figs 8-13) (Figs 73-75) has a
weaker spiral sculpture, particularly on
the first whorls, slightly stronger only on
the base but not overrunning the axial
one (in Alvania disparilis the spiral sculp-
ture is on the whole teleoconch and the
intersection with the axials forms a
quadrangular reticulation and minute
tubercles); the axials are hardly visible
on the first whorl, are rounded and
orthocline with an evident shoulder (in
Alvania disparilis the axials are fine and
orthocline, lacking any shoulder, and
visible from the first whorl). The outline
and the protoconch sculpture are similar.
Alvania lineata Risso, 1826 (:142, pl.
IX, fig. 120) (Fig. 62) differs from Alvania
disparilis by its more robust shell reach-
ing a larger size, with a more slender
outline, with more marked and nodu-
lose sculpture (axial and spiral), with
axials reaching the base, a robust varix
and a more slender protoconch.
See also remarks under Alvania bar-
tolinorum n. sp., Alvania unica n. sp. and
Alvania zaraensis n. sp. for the differ-
ences with these species.
Iberus, 37 (1), 2019
86
Alvania peloritana (Aradas & Benoit, 1874) [new status] (Figs. 12-18)
Rissoa (Alvania)peloritana Aradas & Benoit, 1874: 205, pl. IV, fig. 16
Type material: lectotype (MCZR–M–22150/L, Monterosato coll. ex Benoit) (Figs 12, 13), here des-
ignated (H 3.35 mm, W 1.88 mm), and 1 paralectotype (MCZR–M–22150/P, Monterosato coll. ex
Benoit) (Fig 16, 17; H 3.0 mm, W 1.62 mm) from the type locality.
Type locality: Messina, Sicily, Italy, unspecified depth.
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
87
Figures 12-18. Alvania peloritana Aradas & Benoit, 1874. 12, 13: lectotype, Messina (Sicily), H
3.35 mm (MCZR–M–22150/L); 14, 15: original labels; 16, 17: paralectotype, Messina, H 3 mm
(MCZR–M–22150/P); 18: original drawings (reproduced from A
RADAS
& B
ENOIT
, 1874: pl. IV,
fig. 16).
Figuras 12-18. Alvania peloritana Aradas y Benoit, 1874. 12, 13: lectotipo, Messina (Sicilia), H 3,35 mm
(MCZR–M–22150/L); 14, 15: etiquetas originales; 16, 17: paralectotipo, Messina, H 3 mm
(MCZR–M–22150/P); 18: dibujos originales (reproducidos de A
RADAS
& B
ENOIT
, 1874: pl. IV, fig. 16).
Distribution: Central Mediterranean
Sea: Messina (Sicily), Italy, unspecified
depth. Aradas and Benoit reported it
from the Messina harbour, sympatric
with Alvania cimex and Alvania montagui.
Description of the lectotype: Shell (Figs
12, 13) small, solid, ovate-conical, rather
slender, height 3.35 mm, width 1.88 mm,
height aperture 1.45 mm, H/W 1.78.
Protoconch paucispiral, of 1.3 slightly
convex whorls with adapical shoulder,
height 0.30 mm, diameter of nucleus
0.14 mm, diameter of first half whorl
0.30 mm, maximum diameter 0.40 mm.
Protoconch sculpture constituted by
small tubercles, often fused, forming
series of spirals cords.
Teleoconch of 4.1 convex whorls,
suture canaliculated. Axial sculpture of 10
orthocline rounded ribs on the last whorl,
as wide as half the interspaces, overrun-
ning the suprasutural spiral cordlet.
Spiral sculpture starting with 2 (II
and IV) visible fine spiral cordlets on
12 13
14
15
16 18
17
early teleoconch. On the last whorl 8
(4+1+3) cordlets, equidistant and as
wide as twice the interspaces, slightly
passing over the axials. Quadrangular
cancellation by the intersection of axials
and spirals. Apertural varix weak. Col-
umellar wall angled medially. Umbilical
chink very narrow. Teleoconch without
visible microsculpture (90X). Coloration
light brown, with whitish axial ribs and
columellar area, white apertural varix,
some spiral and slightly darker cordlets.
Soft parts unknown, typical operculum
of the genus, thin, corneous, with eccen-
tric nucleus.
Remarks: In the lot of Alvania pelori-
tana (Aradas & Benoit, 1874) in the Mon-
terosato collection (MCZR–M–22150, ex
Benoit), one vial contains two specimens
with the soft parts dried inside, (Figs 12,
13; 16, 17) with autograph labels by
Benoit reading: “Riss. Peloritana
Messina” and “Riss. Peloritana Messina
Lazzaretto - Weinkauff la riguarda come
varietà della Montagui” (Figs 14, 15).
Those specimens represent the only
known type material of this taxon. The
type material of A. peloritana has not
been found either in the Aradas collec-
tion in Milano (MCSN) (G. B
UZZURRO
,
pers. comm. 2007), or in Catania
(MBAC) (D. S
CUDERI
, pers. comm. 2014),
where there is other type material of
Aradas (S
CUDERI
, 2007: 125; S
CUDERI
&
A
MATI
, 2013: 511).
The actual identity of Alvania pelori-
tana has long been controversial, the
taxon having been considered either as
a nomen dubium, or as a variety,
synonym or subspecies of either Alvania
discors or Alvania lineata (e.g. M
ON
-
TEROSATO
, 1872: 36; 1875: 27; 1878: 84;
G
RANATA
-G
RILLO
, 1877: 147; F. N
ORD
-
SIECK
, 1972: 195; M
ARÍN
& R
OS
, 1987:
139; P
ALAZZI
, 1997: 36; S
CUDERI
& T
ERL
-
IZZI
, 2012: 50; M
OLLUSCA
B
ASE
, 2018).
The original description and the
iconography, along with the extreme
shell variability in the Alvania lineata-
group, contributed to the uncertainty.
Furthermore, there is an issue raised by
P
ALAZZI
(1997: 35), on the probable
inversion of the figures in the original
work. The available type material of A.
peloritana matches satisfactorily both
the original description and the figures
(A
RADAS
& B
ENOIT
, 1874: 205, pl. IV, fig.
16), with the possible exception of the
simple and acute outer lip (“Il labro è
semplice ed acuto”). The two specimens
(lectotype and paralectotype) have a
weakly developed apertural varix and
the paralectotype shows very weak
internal denticles. These features are
more marked in A. discors and A. li -
neata.
A. peloritana shows intermediate fea-
tures between A. discors and A. lineata,
so that Weinkauff (fide Benoit, see origi-
nal label) (Fig. 14) and P
ALAZZI
(1997:
36) considered it as a synonym of A.
montagui and A. lineata, respectively.
The specimen from Messina (Sicily)
recently figured as A. peloritana by
V
ILLARI
& S
CUDERI
(2017: 197, fig. 21)
does not match the type material of A.
peloritana and rather corresponds to an
unusual form of A. lineata with sculp-
ture of the teleoconch less marked.
Alvania discors (Allan, 1818) (:463, pl.
X, fig. 5) (Fig. 55), differs from Alvania
peloritana in the multispiral protoconch
(vs. paucispiral in A. peloritana), the
larger size, the almost flat whorls (v.
slightly convex in A. peloritana), the
interrupted axials (v. overrunning the
suprasutural cordlet in A. peloritana), the
variable and polychrome coloration (v.
almost monochrome in A. peloritana).
Alvania lineata Risso, 1826 (:142, pl.
IX, fig. 120) (Fig. 62) differs mainly in
the larger size, the spiral and axial
sculpture more marked, the axials
reaching well beyond the periphery, in
the marked tubercles at the intersec-
tions of axial and spiral sculptures, in
the more robust apertural varix, and in
the more protruded apex. The proto-
conch of A. peloritana observed at 90´
magnification, shows a sculpture
similar to that of A. lineata (e.g. P
ONDER
,
1985: 135, fig. 86B; G
OFAS
, M
ORENO
&
S
ALAS
, 2011: 181, unnumbered figure)
but finer.
See also remarks under Alvania bar-
tolinorum n. sp., Alvania unica n. sp. and
Alvania zaraensis n. sp. for the differ-
ences with these species.
Iberus, 37 (1), 2019
88
Distribution: unknown (see below).
Description of the holotype: Shell (Figs
19-22) small, solid, ovate-conical, rather
slender, height 2.45 mm, width 1.35 mm
and height of aperture 1 mm, H/W 1.81.
Protoconch paucispiral (Fig. 22), of
barely convex whorls with an adapical
shoulder. Protoconch sculpture not
visible (apparently smooth).
Teleoconch of 4+ slightly convex
whorls, suture canaliculated and undu-
lated. Axial sculpture of 10 opisthocline
rounded ribs on the last whorl (ortho-
cline and then slightly flexuose on the
first whorls), as wide as the interspaces
(more spaced on the last half whorl),
interrupted immediately below the
suprasutural spiral cordlet. Spiral
sculpture weak; on the last whorl 5 well
spaced spiral cordlets on the base and
one in correspondence with the suture,
the upper part apparently devoid of
spirals. Apertural varix strong, with 8
elongate internal denticles. Columellar
wall angled medially. Coloration light
brown-beige. Soft parts and operculum
unknown.
Remarks: It has not yet been defined
with certainty whether Alvania dor-
bignyi (Audouin, 1826) (Figs 19-22) is a
native Mediterranean species (M
IENIS
,
1985: 652; Ö
ZTÜRK
, B
UZZURRO
& A
VNI
B
ENLI
, 2004: 68; M
IENIS
, 2005: 104), or an
Indo-Pacific immigrant (F. N
ORDSIECK
,
1972b: 230; A
MATI
& N
OFRONI
, 1985: 23;
B
ARASH
& D
ANIN
, 1992: 54; Z
ENETOS
,
G
OFAS
, R
USSO
& T
EMPLADO
, 2004;
Á
VILA
, 2005: 43; D
ELONGUEVILLE
&
S
CAILLET
, 2007: 58). It is thus considered
as cryptogenic (G
OFAS
& Z
ENETOS
,
2003). This issue arises since S
AVIGNY
(1817: pl. III, fig. 22) during Napoleon’s
Egyptian campaign, sampled terrestrial,
freshwater and marine molluscs in both
the Red Sea and the Mediterranean,
and the holotype of Rissoa dorbignyi
Audouin was among that material,
apparently without clear collecting
data. However, the marine samples are
commonly assumed having all been
collected in the Red Sea, based on I
SSEL
(1869: 6) [“Ne risultarono per la parte
malacologica 18 tavole in foglio
mirabilmente eseguite, che rappresen-
tano circa 220 specie marine dell’Eritreo
e più di 30 terrestri e fluviatili dell’E-
gitto.”]. We thus, follow here the
common assumption that Rissoa dor-
bignyi Audouin was collected in the
Red Sea, is/was a Red Sea species, pos-
sibly not extending northward beyond
the Suez area [“Elle est très rare dans
les sables de la baie de Suez.”
(M
OAZZO
, 1939: 185)]. There is a moder-
ately rich rissoid fauna in the Red Sea,
with at least the following genera repre-
sented: Manzonia Brusina, 1870,
Parashiela Laseron, 1856, Rissoa Des-
marest, 1814, Setia H. Adams & A.
Adams, 1852 Voorwindia Ponder, 1985,
Lucidestea Laseron, 1956, Cingula
Fleming, 1818, Ceratia H. Adams & A.
Adams, 1852, Onoba H. Adams & A.
Adams, 1852, Rissoina d’Orbigny, 1840,
Schwartziella G. Nevill, 1881, Stosicia
Brusina, 1870 and Zebina H. Adams &
A. Adams, 1854 (I
SSEL
, 1869: 291;
P
ALLARY
, 1926: 57; H
ORNUNG
&
M
ERMOD
, 1927: 364; M
OAZZO
, 1939: 185;
D
EKKER
& O
RLIN
, 2000: 20; J
ANSSEN
,
Z
USCHIN
& B
AAL
, 2011: 383) Although
the genus Alvania has not been con-
firmed (D
EKKER
& O
RLIN
, 2000: 20) its
presence cannot be completely ruled
out (M
OAZZO
, 1939: 185).
Iconography of shells under the
name “Alvania dorbignyi” in the recent
literature is scanty and we could not
find any ascertained Mediterranean
record of a properly identified spec-
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
89
Alvania dorbignyi (Audouin, 1826) (Figs. 19-22)
Rissoa D’Orbignyi Audouin, 1826:171 [based on S
AVIGNY
, 1817: pl. III, fig. 22]
Type material: holotype (Figs 19-22) H 2.45 mm, W 1.35 mm (type loc.) (MNHN-IM-2000-27705
Paris).
Type locality: unspecified [scope of the publication is Egypt, most of the material from the Red
Sea].
imen. D
ELONGUEVILLE
& S
CAILLET
(2007: 55, fig. 24) figured under A.
dorbignyi a shell of A. perversa; C
AMPANI
(2008: 1, fig. 2) a shell of A. discors; F.
N
ORDSIECK
(1972b: 231, figs 13, 14)
figured A. dorbignyi and Alvania
perversa F. Nordsieck, 1972, respectively,
but his figure 13, showed in fact a
‘dorbignyized’ A. perversa (a sort of
iconographic stretching, certainly not
uncommon in Nordsieck’s works, see
P
ALAZZI
, 1997: 36).
The holotype of Rissoa dorbignyi
figured by B
OUCHET
& D
ANRIGAL
(1982:
21, fig. 68) and rephotographed here
(Figs 20-22) seems therefore to be the
only known specimen of that species
and shows diagnostic features with
respect to the native Mediterranean
species of the genus commonly con-
fused under the name A. dorbignyi. The
holotype has a paucispiral protoconch,
as most species of the Alvania lineata-
complex, but more slender; the small
shell (H 2.5 mm) is smaller than the
averages of the other species; the spiral
sculpture is very weak to faint with
only a few evident basal cordlets,
whereas in the other species it is always
present, more or less strong; the axial
ribs are flat, broad and as wide as the
interspaces vs. never flat (acute and/or
rounded) in the other species with the
exception of A. settepassii. Issel (1869:
205) described the figure of Savigny
erroneously including spiral coloured
stripes [“…Alla base di ciascun giro
vedonsi, nella figura, parecchie fasce
scure trasversali.”] whereas he was
quite probably describing the appar-
ently uncoloured spiral cordlets or the
interspaces (Fig. 21). We are providing
here a new series of photographs of the
holotype (courtesy of MNHN) (Figs 20-
22). The new pictures were taken at a
different angle (V
IRGINIE
H
ÉROS
,
MNHN, pers. comm.) with respect to
the previous ones (B
OUCHET
& D
ANRI
-
GAL
, 1982: 21, fig. 68) that showed the
base less angular, the suture less
canaliculate and a slightly lower height,
and may also have been distorted
under the scanning electron micro-
scope. We agree with M
IENIS
(1985: 652)
that the Mediterranean specimens com-
monly identified as A. dorbignyi repre-
sent a distinct species, definitely not
matching the holotype of Rissoa dor-
bignyi (Fig. 19), and here ascribed to
Alvania perversa F. Nordsieck, 1972 (see
below).
Alvania lineata Risso, 1826 (:142, pl.
IX, fig. 120) (Fig. 62) differs from Alvania
dorbignyi (Audouin, 1826), by the spiral
strong sculpture present on the whole
teleoconch, with pointed tubercles at the
intersections of spirals and axials, vs. the
abapical half of the whorls apparently
devoid of spirals with only 5 well
spaced spiral cordlets on the base in A.
dorbignyi; the axials are rounded and
extend to the base vs. flat and inter-
rupted in A. dorbignyi.
Alvania discors (Allan, 1818) (:463, pl.
X, fig. 5) (Fig. 55) differs from Alvania
dorbignyi (Audouin, 1826) in its multi-
spiral protoconch vs. paucispiral in A.
dorbignyi; the almost flat teleoconch
whorls vs. convex in A. dorbignyi; the
suture more neatly canaliculated and
the larger size.
Alvania settepassii Amati & Nofroni,
1985 (:19, 4 unnumbered figs) (Fig. 56)
differs from Alvania dorbignyi (Audouin,
1826) in the flat teleoconch whorls vs.
convex in A. dorbignyi; the suture non-
canaliculated vs. canaliculated in A. dor-
bignyi; the axial ribs rounded, slightly to
neatly prosocline vs. flat, orthocline or
flexuose and slightly opisthocline in A.
dorbignyi.
Alvania schwartziana Brusina, 1866
(:25, fig. 9) (Fig. 57), endemic to the east
Adriatic, differs from Alvania dorbignyi
(Audouin, 1826) in its lower and
globose protoconch vs. slender, less
convex and adapically shouldered in A.
dorbignyi; in the dark-brown mono-
chrome coloration vs. light brown-beige
in A. dorbignyi; in the more marked
spiral sculpture.
See also remarks under Alvania per-
versa F. Nordsieck, 1972, Alvania bartoli-
norum n. sp., Alvania unica n. sp. and
Alvania zaraensis n. sp. for the differ-
ences with these species.
Iberus, 37 (1), 2019
90
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
91
Figures 19-22. Alvania dorbignyi (Audouin, 1827). 19: holotype, ?Red Sea, H 2.45 mm (MNHN,
SEM micrograph reproduced from B
OUCHET
& D
ANRIGAL
, 1982); 20, 21: light photograph of
the same specimen gold-coated for SEM; 22: idem, first whorls. Figures 23-29. Alvania perversa F.
Nordsieck, 1972. 23, 24: lectotype, Haifa (Israel), H 2.8 mm (SMF); 25, 26: Šiqmônah, Haifa,
(Israel), first whorls (BA); 27: paralectotype, Haifa (Israel), H 3.6 mm (SMF); 28, 29: Haifa bay
(Israel), H 4 mm (M. T. Spanu collection, Alghero).
Figuras 19-22. Alvania dorbignyi (Audouin, 1827). 19: holotipo, ?Mar Rojo, H 2,45 mm (MNHN,
micrografía electrónica de barrido reproducida de B
OUCHET
& D
ANRIGAL
, 1982); 20, 21: fotografía
del mismo ejemplar con revestimiento de oro para el MEB; 22: idem, primeras vueltas. Figuras 23-29.
Alvania perversa F. Nordsieck, 1972. 23, 24: lectotipo, Haifa (Israel), H 2,8 mm (SMF); 25, 26:
Šiqmônah, Haifa, (Israel), primeras vueltas (BA); 27: paralectotipo, Haifa (Israel), H 3,6 mm (SMF);
28, 29: bahía de Haifa (Israel), H 4 mm (colección M. T. Spanu, Alghero).
19 20 21
22
23
24
25
26
27 28
29
Iberus, 37 (1), 2019
92
Alvania perversa F. Nordsieck, 1972 [new status] (Figs. 23-29)
Alvania (Alvanolira)dorbignyii perversa F. Nordsieck, 1972a: 193
Alvania (Alvanolira)perversa F. Nordsieck, 1972b: 230, fig. 14
Alvania (Alvanolira) dorbignyii perversa F. Nordsieck, 1982: 107
Alvania dorbignyi AA non Alvania dorbignyi (Audouin, 1826)
Type material: SMF 239358/1 is labelled by A. Zilch as ‘Lectotypus’. “The specimen labelled as
lectotype does not match the figure and is a badly preserved abraded specimen, much poorer than
several of the paratype lot. Moreover, the lectotype designation is invalid because it was never pub-
lished. The majority of the “paratypes” is also badly preserved.” (R. J
ANSSEN
in litt. 07.21.2014);
SMF 239359/25 labelled by A. Zilch as “Paratypen”. Syntype SRI ex SMF 239359, H = 2.8 mm, W
= 1.8 mm (lectotype, here designated) (Figs 23, 24) (type loc.). Paralectotype (type loc.) SRI ex SMF
239359, H = 3.6 mm, W = 2.2 mm (Fig. 27), and other 24 paralectotypes (type loc.) SRI ex SMF 239359.
Other material examined: Israel: Šiqmônah, Haifa, 1-2 m depth, x.1998, 1 sh (BA) (Fig. 25, 26); Haifa
Bay, 0-22 m depth, 32 sh (CB); Haifa, 9 m depth, 2 sh (MO); Ashdod, beach, 6 sh (CB); Soreq, 12 m
depth, 2 sh (CB); Rosh Hanikrà, 3-4 m depth , 16 sh (CB); Shavey, Zion beach, 6 sh (CB); Akko, 8 m
depth, 1 sh (CB); Naharyia, 0-1 m depth, 5 sh (EQ); Turkey: Bozcaada I., 5 m depth, 1 sh (EQ).
Type locality: Haifa, Israel.
Distribution: Eastern Mediterranean:
Israel (this work, and B
OGI
& G
ALIL
,
2006: 16, sub nomine A. dorbignyi),
Turkey (this work), Cyprus (with
unchecked records from B
OGI
, C
IAN
-
FANELLI
& T
ALENTI
, 1988: 194; C
ECALUPO
& Q
UADRI
, 1996: 105, sub nomine A. dor-
bignyi) and Tunisia (C
AMPANI
, 2008: 1,
fig. 2, sub nomine A. dorbignyi). Empty
shells were collected in 0/22 m depth.
Description of the lectotype (Photo: S.
Hof, courtesy of R. Janssen, Sencken-
berg Research Institute Frankfurt a. M.):
Shell (Figs 23, 24) small, solid, ovate-
conical, height 2.8 mm, width 1.8 mm,
height aperture 1.4 mm, H/W 1.55. Pro-
toconch paucispiral, globose, apparently
devoid of sculpture.
Teleoconch of 3.5 convex, almost flat
whorls, suture canaliculated. Axial
sculpture of 12 orthocline or slightly
opisthocline acute ribs on the last whorl,
as wide as twice the interspaces, inter-
rupted immediately below the suprasu-
tural spiral cordlet.
Spiral sculpture on the last whorl of
9 (4+1+4) fine cordlets, equidistant and
as wide as twice the interspaces of equal
strength. Quadrangular cancellation by
the intersection of axials and spirals
sculptures. Apertural varix weak, no
internal denticles. Columellar wall
angled medially. Umbilical chink very
narrow. Coloration light beige, with
darker brown-orange spiral cordlets
(except the last basal one). Soft parts
and operculum unknown.
Remarks: Alvania perversa F. Nord-
sieck, 1972 is the first name available for
the species frequently identified as
Alvania dorbignyi by several authors, not
Alvania dorbignyi (Audouin, 1826), and
which we consider as a distinct valid
species (Figs 23-29). Alvania dorbignyi
perversa F. Nordsieck, 1972 is currently
considered as taxon inquirendum (M
OL
-
LUSCA
B
ASE
, 2018). A. perversa has com-
monly been considered as a small
variety/subspecies of A. dorbignyi, due
to its allegedly smaller size and the
weak apertural varix (F. Nordsieck,
1972b: 230, fig. 14). However, the type
material of A. perversa includes speci-
mens larger than the lectotype (e.g. H =
3.6 mm, W = 2.2 mm, paralectotype)
(Fig. 27). According to the examined
material, A. perversa ranges 2.65-4.5 mm
in height. The lack of denticles on the
inner side of the lip in the lectotype is
due to it being probably immature, since
the examined material showed 7-8
weak, spaced denticles in full grown
specimens. The protoconch sizes are:
nucleus 0.14-0.15 mm, first half whorl
diameter 0.24-0.25 mm, maximum
diameter 0.35-0.40 mm, height 0.250-
0.275 mm and 1.25-1.3 whorls. On the
teleoconch, the fourth suprasutural
spiral cordlet is commonly more promi-
nent than the others. The coloration is
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
93
rather constant: from beige to orange-
brown, and the spirals always darker. It
has been found sympatric with Alvania
discors (Allan, 1818) and Alvania lineata
Risso, 1826 in Tunisia and Israel
(C
AMPANI
, 2008: 1; Cesare Bogi, pers.
comm.).
Alvania discors (Allan, 1818) (:463, pl.
X, fig. 5) (Fig. 55) differs from Alvania
perversa in its multispiral protoconch vs.
paucispiral in A. perversa; the flat whorls
vs. convex in A. perversa; the axials
broader and flatter; the coloration differ-
ent (similar only in the so variety ‘fer-
ruginea’); the larger size.
Alvania settepassii Amati & Nofroni,
1985 (:19, 4 unnumbered figs) (Fig. 56)
differs from Alvania perversa in its col-
oration being monochrome beige-
orange vs. beige to brown-orange, with
darker spirals (except the last basal one);
the weak spirals on the last whorl vs. 9
fine cordlets equidistant and of equal
strength in A. perversa; the suture non
canaliculated vs. canaliculated in A. per-
versa.
Alvania schwartziana Brusina, 1866
(:25, fig. 9) (Fig. 57) differs from Alvania
perversa by the almost flat whorls vs.
convex or slightly convex; by the inner
lip with 8-9 elongate, strong and close
teeth vs. smooth or with 7-8 weak teeth
widely spaced; by its monochrome
dark-brown shell; by the orthocline
axials vs. orthocline or slightly opistho-
cline acute ribs. It is restricted to the
Adriatic Sea whilst A. perversa occurs in
the Levantine Sea (Eastern Mediter-
ranean Sea)
Alvania lineata Risso, 1826 (:142, pl.
IX, fig. 120) (Fig. 62) differs from Alva-
nia perversa F. Nordsieck, 1972 by its
more slender and higher protoconch
(300-350 µm vs. 250-275 µm in A. per-
versa); the more rounded axials, over-
run by the spiral cordlets and the acute
minute tubercles at the intersections.
Along the Israeli coasts the two species
co-occur sympatrically without any in-
termediate.
Alvania algeriana (Monterosato, 1877)
(:34, pl. III, fig. 5) (Fig. 72) differs from
Alvania perversa by its more slender
outline, the deeper and more canalicu-
lated suture, the spiral sculpture present
only on the lower half of the whorls, of
5 robust cords, the different coloration:
brown-reddish background, frequently
with spirally arranged darker blotches
on the spiral cords vs. light beige, with
darker brown-orange spiral cordlets
(except the last basal one) in A. perversa;
the smaller protoconch with more
whorls (d. 0.125 mm, Do 0.20 mm, nw
1.5 vs. d. 0.14-0.15 mm, Do 0.24-0.25
mm, nw 1.25-1.3 in Alvania perversa).
Alvania dorbignyi (Audouin, 1826)
(:171) (Figs 19-22), for what can be
desumed from the type, differs from
Alvania perversa F. Nordsieck, 1972 by its
protoconch more slender, less convex
and with an evident adapical shoulder
(lacking in A. perversa); the axial sculp-
ture on the last whorl of 9 flat, orthocline
(or flexuose and slightly opisthocline)
ribs, as wide as the interspaces, vs. 12
orthocline or slightly opisthocline (never
flexuose) acute ribs, as wide as twice the
interspaces in A. perversa; the spiral
sculpture barely evident, apparently
lacking on the upper part of the whorls,
with 5 well spaced basal cordlets vs. 9
fine and equidistant cordlets on the
whole teleoconch in A. perversa.
See also remarks under Alvania bar-
tolinorum n. sp., Alvania unica n. sp. and
Alvania zaraensis n. sp. for the differ-
ences with these species.
Alvania bartolinorum Amati & Smriglio n. sp. (Figs. 30-40, Table II)
Alvania garrafensis sensu AA (C
AMPANI
, B
ARTOLINI
& S
PANU
, 2012: 85, figs 1-6; S
CAPERROTTA
,
B
ARTOLINI
& B
OGI
, 2012: 48, 5 unnumbered figs) not Alvania garrafensis Peñas & Rolán, 2008.
Type material: holotype (MNHN IM-2000-27706), H 3.58 mm, W 2.16 mm. (Figs 30-32) (legit Stefano
Bartolini, Florence). Paratypes: 3 sh (type loc.) (BA); 2 sh (type loc.) (CS-PM); 20 sh (type loc.) (SB-
MS); 10 sh (type loc.) (AR); 5 sh (type loc.) (EQ).
Other material examined: Krk I., Croatia, 54 m depth, ix.2008, 4 sh (AR), 252 sh (SB-MS), 16 sh
(EQ); Krk I., Giapni Potok, Croatia, 54 m depth, 23 sh (AR).
Type locality: Krk I., Croatia, 54 m depth.
Etymology: Dedicated to Stefano Bartolini and Maria Scaperrotta (Florence), for their kindness in
making the materials from their collection always available for study, and for providing the type
material.
Outer lip with sharp edge, weakly vari-
cose, with 7-9 (7) fine elongate internal
denticles. Colour brown-beige with
pinkish hue, first whorls often darker
brown-orange, aperture often pink-
violet. Rarely monochrome brown or
white. Operculum and soft part
unknown.
Remarks: Recently, C
AMPANI
, B
AR
-
TOLINI
& S
PANU
(2012: 85) and S
CAPER
-
ROTTA
, B
ARTOLINI
& B
OGI
(2012: 48) have
figured Alvania bartolinorum n. sp. under
the name Alvania garrafensis Peñas &
Rolán, 2008. Alvania garrafensis (Peñas &
Rolán, 2008: 21, figs 8-13) (Figs 70-72)
differs in the smaller shell (H 2.8 mm vs.
H 2.84–3.96 mm of A. bartolinorum), the
more globose outline, the proportionally
smaller aperture, the more globose apex,
the first whorl with a very weak spiral
sculpture and a nearly absent axial one,
the orthocline axials on the other whorls
with evident subsutural shoulder, the
uniform light brown coloration vs.
brown-beige with pinkish hue, with
darker apex and pink-violet aperture in
A. bartolinorum. Empty shells of Alvania
garrafensis are collected deeper (90 m
depth vs. 40-54 m depth of A. bartolino-
rum n. sp.).
Alvania lineata Risso, 1826 (:142, pl.
IX, fig. 120) (Fig. 62) in its most common
morphotype, has a stronger sculpture,
especially the spirals, with marked
nodules at intersections, has a mono-
chrome background with darker spirals,
a thicker varix and the axial ribs reach-
ing the base.
Alvania schwartziana Brusina, 1866
(:25, fig. 9) (Fig. 57) differs from Alvania
bartolinorum n. sp. by its teleoconch with
flat whorls vs. convex or slightly convex,
the aperture ovate-pyriform with the
extern lip flat vs. large aperture, ovate-
squared, often flared anteriorly; first
whorls with obtuse profile vs. more
acute, almost coeloconoid in A. bartolino-
Iberus, 37 (1), 2019
94
Distribution: Basing on the examined
material, it is known with certainty only
from Croatia, northeastern Adriatic Sea
(Krk and Prvic Islands), with empty
shells collected in 40-54 m depth. A
specimen from the southern Adriatic
(off the Apulian coast), 101 m depth,
possibly drifted from shallower habitat,
has been figured (Peter Sossi at
<http://www.naturamediterraneo.com
/forum/topic.asp?TOPIC_ID=39830>,
29.xii.2007, as Alvania garrafensis). Col-
lected in sympatry with A. lineata Risso,
1826 at the type locality.
Description: (between parentheses
data of the holotype). Shell (Figs 30-32)
small, solid, ovate-conic, height
2.84–3.96 mm (3.58 mm), width 1.75-2.28
mm (2.16 mm), H/W 1.54-1.82 (1.66).
Protoconch (Figs 39, 40) paucispiral,
globose, consisting of 1.3-1.6 (1.6)
whorls, sculptured by partly fused and
confused spiral series of granules;
height 0.35-0.44 mm (0.40 mm), nucleus
diameter 0.14-0.21 mm (0.19 mm), diam-
eter of first half whorl 0.25-0.30 mm
(0.275 mm), maximum diameter 0.44-
0.50 mm (0.50) mm. Teleoconch of 3.3-
4.1 (3.8) convex whorls, last whorl
rather convex, suture impressed,
canaliculated. Axial sculpture on the last
whorl with 12-18 (15 + v) ribs narrower
than interspaces, plus the varix, ortho-
cline on the first whorls, opisthocline
and slightly sinuose on last whorl, inter-
rupted at the periphery. Spiral sculpture
starting with 2 (II, IV) cords. Last whorl
with 8-11 (10) spirals non-equidistant, 4-
6 (4) above the aperture, 1 at labial
insertion and 3-5 (5) stronger, on the
base. Spirals on last whorl slightly
weaker than on previous whorls.
Microsculpture on teleoconch of con-
fused spiral microstriae and weak
growth lines (Fig. 39). Umbilical chink
absent or very narrow. Aperture large,
ovate-squared, often flared anteriorly.
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
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Figures 30-40. Alvania bartolinorum n. sp. 30-32: holotype, Krk I. (Croatia), 54 m depth, H 3.58
mm (MNHN IM-2000-27706); 33: paratype, Krk I. (Croatia), 54 m depth, H 3.3 mm (SB-MS);
34: paratype, Giapni Potok (Croatia), 54 m depth H 3.85 mm (BA); 35: paratype, Krk I.,
(Croatia), 54 m depth, H 3.45 mm (SB-MS); 36: paratype, Prvic Krk (Croatia), 54 m depth, H
3.45 mm (BA); 37: paratype, Giapni Potok (Croatia), 54 m depth,H 3.05 mm (BA); 38: paratype,
Krk I. (Croatia), 54 m depth, H 3.05 mm (SB-MS); 39, 40: paratype, Krk I., (Croatia), SEM
micrograph of the protoconch, and detail (CS-PM).
Figuras 30-40. Alvania bartolinorum n. sp. 30-32: holotipo, Isla Krk (Croacia), profundidad 54 m, H
3,58 mm (MNHN IM-2000-27706); 33: paratipo, Isla Krk (Croacia), profundidad 54 m, H 3,3 mm
(SB-MS); 34: paratype, Giapni Potok (Croacia), profundidad 54 m, H 3,85 mm (BA); 35: paratipo,
Isla Krk, profundidad 54 m, H 3,45 mm (SB-MS); 36: paratipo, Prvic Krk (Croacia), profundidad 54
m, H 3,45 mm (BA); 37: paratipo, Giapni Potok, profundidad 54 m, H 3,05 mm (BA); 38: paratipo,
Isla Krk, profundidad 54 m, H 3,05 mm (SB-MS); 39, 40: paratype, Isla Krk, micrografía electrónica
de barrido de la protoconch, y detalle (CS-PM).
30 31 32 33
34
36 37
38 39
40
35
100 µm
50 µm
rum n. sp.; protoconch acute, paucispi-
ral, maximum diameter 0.511 mm,
sculptured by ca. 12 spirals and undu-
lated cords (syntype MCZR) vs. globose,
paucispiral, with maximum diameter of
0.500 mm, sculptured by partly fused
and confused spiral series of granules.
Colour dark-brown monochrome vs.
brown-beige with pinkish hue, first
whorls often darker brown-orange,
aperture often pink-violet. Rarely mono-
chrome brown or white.
Alvania disparilis Monterosato, 1890
(:146) (Figs 1-11) also has a globose
outline, spiral and axial sculptures are
both evident on the first whorls, with
fine axials and spirals and quadrangular
cancellation.
Alvania peloritana (Aradas & Benoit,
1874) (:205, pl IV, Fig. 16) (Figs 12-18)
differs from A. bartolinorum n. sp. by its
stronger spiral sculpture; the aperture
not flared anteriorly as is generally in A.
bartolinorum n. sp.; the smaller proto-
conch (maximum diameter 0.40 mm vs.
0.44-0.50 in A. bartolinorum n. sp.); the
axial sculpture of 10 ribs on the last
whorl vs. 12-18 ribs in A. bartolinorum n.
sp.; the spiral sculpture of 3 spiral cords
on the base vs. 4-6 in A. bartolinorum n.
sp.
Alvania dorbignyi (Audouin, 1827)
(:171) (Figs 19-22) differs from A. bartoli-
norum n. sp. in its smaller size (H 2.45
mm vs. H 2.84-3.96 mm in A. bartolino-
rum n. sp.); the axial ribs more robust
and fewer than 10 vs. 12-18 in A. bartoli-
norum n. sp.; the spiral sculpture weaker
on the adapical part of the whorls vs. of
same strength on the whole surface in
A. bartolinorum n. sp.
Alvania perversa F. Nordsieck, 1972
(:230, fig. 14) (Figs 23-29) differs from A.
bartolinorum n. sp. in the different col-
oration (light beige background, with
darker brown-orange spiral cordlets
(except the last basal one) vs. brown-
beige with pinkish hue, first whorls often
darker brown-orange, aperture often
pink-violet, rarely monochrome brown
or white, in A. bartolinorum n. sp.).
See also remarks under Alvania unica
n. sp. and Alvania zaraensis n. sp. for the
differences with these species.
Iberus, 37 (1), 2019
96
Protoconch 1 2 3 4 5 6 7 8 9 10 11 12
h 0.40 0.35 0.375 0.40 0.35 0.35 0.40 0.40 0.375 0.40 0.375 0.35
d 0.19 0.15 0.17 0.175 0.20 0.21 0.175 0.19 0.20 0.20 0.19 0.20
Do 0.275 0.275 0.25 0.29 0.325 0.29 0.30 0.30 0.30 0.30 0.30 0.30
DM 0.50 0.45 0.50 0.45 0.475 0.50 0.50 0.50 0.45 0.475 0.475 0.45
nw 1.6 1.5 1.5 1.6 1.3 1.4 1.5 1.4 1.4 1.35 1.45 1.5
Teleoconch 1 2 3 4 5 6 7 8 9 10 11 12
H 3.58 3.05 3.3 3.45 3.6 3.2 3.5 3.4 3.4 3.7 3.65 3.15
W 2.16 1.75 2.05 1.9 2.2 1.85 2.2 2.1 2.1 2.2 2.05 1.95
R H/W 1.66 1.74 1.61 1.81 1.66 1.73 1.59 1.62 1.62 1.68 1.78 1.61
Nw 3.8 3.8 3.7 3.8 4 3.7 3.7 3.7 3.9 3.8 4 3.6
Nar+v 15+v 13+v 16+v 14+v 11+v 13+v 15+v 18+v 16+v 14+v 12+v 14+v
Ns 10(5) 8(4) 9(4) 11(6) 10(5) 9(4) 8(4) 10(5) 10(5) 10(6) 9(4) 8(4)
Nd 77no no 97no no 8 no no no
Sts 222222222222
Table II. Measurements of the protoconch and teleoconch of Alvania bartolinorum n. sp., in mm.
Number 1 is the holotype. Abbreviations, h: height; d: diameter of nucleus; Do: diameter of first
half whorl; DM: maximum diameter; nw: number whorls; H: height, W: width; Nw: number
whorls; Nar+v: number axial ribs+ varix; Ns: numbers of spirals on the last whorl (above the aper-
ture); Nd: number of denticles; Sts: starting number of spiral cordlets; RH/W: ratio height/width.
Alvania unica Amati & Quaggiotto n. sp. (Figs. 41-48)
Type material: holotype (MCZR–M–22155/H), H 3.45 mm, W 2.15 mm, [paralectotype of Alvania
disparilis Monterosato, 1890].
Type locality: Sciacca, Sicily, Italy.
Etymology: With reference to the only one specimen known.
rower than interspaces, interrupted at
the periphery. Spiral sculpture starting
with 2 (II, IV) cordlets, last whorl with
11 (5, 1, 5) fine cordlets not equidistant,
the three subsutural closer, those on the
base more spaced and equidistant.
Microsculpture not observed on the
teleoconch. Umbilical chink absent.
Outer lip thickened by a broad and
robust varix, with 10 small internal den-
ticles. Colour tawny, varix and aperture
whitish. Operculum and soft parts
unknown.
Remarks: Although based on a single
specimen, this species is indisputably
diagnosed by the peculiar morphology
of the robust shell, with lanceolate
outline slightly coeloconoid and acute
spire, not corresponding to any known
Recent or fossil northeastern Atlantic
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.: Notes on the Alvania lineata-complex and three new Mediterranean species
97
Tabla II. Medidas de la protoconcha y teleoconcha de Alvania bartolinorum n. sp., en mm. El número 1
corresponde al holotipo. Abreviaturas, h: altura; d: diámetro del núcleo; Do: diámetro de la primera media
vuelta; DM: máximo diámetro; nw: número de vueltas; H: altura, W: anchura; Nw: número de vueltas;
Nar+v: número de costillas axiales + variz; Ns: número de espiras de la última vuelta (sobre la apertura);
Nd: número de dentículos; Sts: número inicial de cordones espirales; RH/W: ratio altura/anchura.
13 14 15 16 17 18 19 20 21 22 23 24 25
0.35 0.42 0.44 0.35 0.40 0.40 0.40 0.352 0.38 0.40 0.40 0.42 0.40
0.17 0.14 0.16 0.15 0.175 0.175 0.152 0.152 0.14 0.152 0.152 0.152 0.152
0.275 0.26 0.28 0.25 0.275 0.275 0.26 0.26 0.28 0.26 0.272 0.28 0.272
0.45 0.46 0.48 0.45 0.475 0.45 0.46 0.46 0.44 0.44 0.44 0.472 0.448
1.4 1.6 1.5 1.5 1.6 — 1.6 1.3 1.35 1.4 1.5 1.6 1.4
13 14 15 16 17 18 19 20 21 22 23 24 25
3.45 2.84 3.96 3.05 3.85 3.0 3.2 3.2 3.32 3.48 3.0 3.32 3.24
2.05 1.8 2.28 1.9 2.25 1.95 2.06 1.88 1.82 2.04 1.94 1.96 2.06
1.68 1.58 1.74 1.60 1.71 1.54 1.55 1.70 1.82 1.70 1.55 1.69 1.57
3.8 3.3 4.1 ———3.7 3.75 3.8 4 3.5 3.7 3.7
15+v 13+v 15+v 15+v 14+v — 14+v 14+v 13+v 14+v 13+v 13+v 13+v
10(5) 9(5) 9(5) 10(5) 8(4) 9(4) 9(5) 9(5) 10(6) 11(6) 9(5) 9(5) 10(5)
no no no no 8 no 99no no 78no
2222222222222
Distribution: Known only from the
holotype, Central Mediterranean:
Sciacca (Sicily), unspecified depth (see
also under A. disparilis). Possible Pleis-
tocene (Würm) material.
Description: Shell (Figs 41-48) small,
solid, ovate-conic, slightly coeloconoid,
height 3.45 mm, width 2.15 mm, H/W
1.60. Protoconch (Figs 44-46, 48) pau-
cispiral, acute, of 1.5 whorls, sculptured
by ca. 10 spiral cordlets frequently inter-
rupted and randomly fused, height
0.375 mm, diameter of nucleus 0.15 mm,
diameter of first half whorl 0.25 mm,
maximum diameter 0.475 mm. Teleo-
conch of 3.8 convex whorls, suture
weakly impressed. Axial sculpture on
the last whorl of 15 robust ribs plus the
varix, orthocline on the first whorls,
slightly sinuose on the last whorl, nar-
species (even considering teratological
specimens). Considering the sediment
deposited inside the aperture, it is possi-
ble that the shell is a fossil.
Alvania disparilis Monterosato, 1890
(:146) (Figs 1-11) has a less robust shell,
smaller (H 2.95 mm vs. H 3.45 mm in A.
unica n. sp.), larger H/W (1.68 vs. 1.60 in
A. unica n. sp.), the aperture is propor-
tionally smaller (1.45 mm vs. 1.6 mm in
A. unica n. sp.), the outline is more
globose with more convex whorls, vs.
the lanceolate/coeloconoid outline and
acute spire in A. unica n. sp.; the proto-
conch is smaller (0.425 mm vs. 0.475 mm
in A. unica n. sp.). The sculpture is also
different: 14 fine axials, as wide as half
the interspaces, and 9 (4+1+4) fine non
equidistant spirals, forming quadrangu-
lar reticulate pattern and small tuber-
cles, vs. 15 robust slightly sinuose axials,
barely narrower than interspaces inter-
rupted at the periphery, and 10 (5+1+4)
fine spirals not equidistant; colour is
with a light brown background and
darker spirals and protoconch vs. tawny
monochrome A. unica n. sp. with varix
and aperture whitish.
Alvania claudioi Buzzurro & Landini,
2007 (:24, figs 1a-c) (Fig. 58) has a
smaller shell (H 2.5-2.63 mm vs. H 3.45
mm of A. unica n. sp.), more convex
whorls, finer and more numerous
spirals, more evident on the base.
Alvania lanciae (Calcara, 1845) (:29,
pl. IV, fig. 12) (Figs 59-61) has a globose
protoconch vs. acute in A. unica n. sp.; h
0.25-0.30 mm vs. 0.375 mm; d 0.16-0.22
mm vs. 0.15 mm; Do 0.20-0.25 mm vs.
0.25 mm; DM 0.35-0.40 mm vs. 0.475
mm; of 1.25-1.3 whorls vs. 1.5 whorls,
with an orange-skin like microsculpture
of irregular pits, vs. ca. 10 cordlets fre-
quently interrupted and randomly
fused in A. unica n. sp. Teleoconch with
evident microsculpture, absent in A.
unica n. sp.
Alvania varia Tabanelli, Bongiardino
& Perugia, 2011 (:46, pl. 5, figs 25-29)
from the Piacenzian stage of Romagna
(Pliocene), has a shorter protoconch (1.2
whorls vs. 1.5 in A. unica n. sp.), a
smaller maximum diameter (0.30 mm
vs. 0.475 mm in A. unica n. sp.). In A.
unica n. sp. the outline is slightly coelo-
conoid and the axial ribs are interrupted
at the periphery; in A. varia the axial ribs
are interrupted beyond the periphery,
reaching the spirals of the base. A. varia
differs by the lack of internal denticles
on the outer lip, the smaller size (H 2.2
mm vs. H 3.45 mm in A. unica n. sp.)
and the teleoconch microsculpture,
absent in A. unica n. sp.
The specimens from the Pleistocene
of Rhodes I. (Calabrian stage) figured as
Alvania lanciae by C
HIRLI
& L
INSE
(2011:
61, pl 22, figs 2a-e), probably belong to a
distinct species, diagnosed by a differ-
ent apical sculpture (micro tubercles
arranged in spirals vs. orange-skin
microsculpture of irregular pits in A.
lanciae); a different teleoconch sculpture,
with spirals equidistant and of equal
strength (vs. not equidistant and of
varying strength in A. lanciae). These
specimens differ from A. unica n. sp. in
their prosocline lip with weak varix (vs.
orthocline lip with robust varix in the
new species), in the number of spiral
cordlets on the last whorl (4+1+4 and
equidistant vs. 5+1+5 and not equidis-
tant in A. unica n. sp.), and in the fewer
axial ribs on the last whorl (11 vs. 15 in
A. unica n. sp.).
Alvania rugulosa (Aradas, 1847) (orig-
inal combination: Rissoa rugulosa
Aradas, 1847:76) [(not Rissoa rugulosa
Hutton, 1873 = Rissoina chathamensis
(Hutton, 1873)] fossil from Gravitelli
(Messina: Plio-Pleistocene?) is the nomi-
nal taxon morphologically closest to A.
unica n. sp. based on the original de-
scription. A
RADAS
(1847: 76) added that
the teleoconch had 14-15 axials and 11
spirals on the last whorl, 5 on the sec-
ond last, 4 on the third last. It was com-
pared to A. montagui by which it would
differ by being smaller, less tumid and
more elongate. We have not found any
type material of this taxon at either
CMSN, MCZR, MBAC or MGPUF, nor
have we found any topotypical shells
fitting the description. We consider Ris-
soa rugulosa Aradas, 1847 as a nomen
dubium. It has been synonymized with
either A. lineata Risso, 1826 (M
ON
-
TEROSATO
, 1884: 59; B
ELLINI
, 1929: 46) or
Iberus, 37 (1), 2019
98
A
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.: Notes on the Alvania lineata-complex and three new Mediterranean species
99
Figures 41-48. Alvania unica n. sp. 41, 42: holotype, Sciacca (Sicily), H 3.45 mm
(MCZR–M–22155/H); 43: SEM micrograph of the holotype; 44-47: details of the protoconch;
48: original label.
Figuras 41-48. Alvania unica n. sp. 41, 42: holotipo, Sciacca (Sicilia), H 3,45 mm
(MCZR–M–22155/H); 43: micrografía electrónica de barrido del holotipo; 44-47: detalles de la proto-
concha; 48: etiqueta original.
with A. montagui (Payraudeau, 1826) (G.
S
EGUENZA
fide L. S
EGUENZA
, 1903: 44).
A. bartolinorum n. sp. (Figs 30-40)
differs from A. unica n. sp. has a non-
lanceolate outline with a less acute apex,
a less robust and less broad varix, a
more canalized sutures, less rounded
axial ribs, wider basal cords and an
anteriorly flared aperture (vs. more
rounded in A. unica n. sp.).
Alvania garrafensis Peñas & Rolán,
2008 (:21, figs 8-13) (Figs 73-75) differs in
the smaller shell (H 2.8 mm vs. H 3.45
mm of A. unica n. sp.); the more globose
outline; the first whorl with a very weak
spiral sculpture and an almost absent
axial one vs. both sculptures always well
evident on all the whorls in A. unica n.
sp.; the orthocline axial ribs on the last
whorl vs. slightly opisthocline and sinu-
ose in A. unica n. sp.; the round-ovate
aperture vs. round-ovate elongated in A.
unica n. sp.; presence of microsculpture
vs. absence of microsculpture in A. unica
n. sp.; the smaller diameter of proto-
conch, DM 0.410 mm vs. DM 0.475 in A.
unica n. sp., with more delicate sculp-
ture and with more spiral cords, 12 vs.
10 in A. unica n. sp.
Alvania peloritana (Aradas & Benoit,
1874) (:205, pl. IV, fig. 16) (Figs 12-18)
differs from A. unica n. sp. in its non-
lanceolate outline with a less acute apex,
the fewer axials on the last whorl (10 vs.
15), the fewer but stronger spirals on the
last whorl [8 (4+1+3) vs. 11 (5+1+5)].
Alvania dorbignyi (Audouin, 1827) (:
171) (Figs 19-22) differs from A. unica n.
sp. in its smaller size (H 2.45 mm vs. H
3.45 mm), the higher H/W ratio (1.81 vs.
41 42 43
44
45
46 47
48
50 µm
50 µm
200 µm
100 µm
1.60), the fewer axials on the last whorl
(10 vs. 15), the weaker spiral sculpture
(on the last whorl 5 well spaced spiral
cordlets on the base and one more
prominent suprasutural, the upper part
of the whorl apparently devoid of
spirals vs. 11 spiral cordlets on the last
whorls in A. unica n. sp.).
Alvania perversa Nordsieck F., 1972 (:
230, fig. 14) (Figs 23-29) differs from A.
unica n. sp. by the less convex whorls
and the more canaliculated suture, the
fewer axials on the last whorl (12 vs. 15),
and fewer spirals on the last whorl [9
(4+1+4) equidistant vs. 11 (5+1+5) non-
equidistant], the different chromatic
pattern (light beige background, with
darker brown-orange spiral cordlets
(except the last basal one) vs. tawny
background, with whitish varix and
aperture in A. unica n. sp.).
See also remarks under Alvania
zaraensis n. sp. for the differences with
this species.
Iberus, 37 (1), 2019
100
Alvania zaraensis Amati & Appolloni n. sp. (Figs. 49-54, Table III)
Type material: holotype (MCZR–M–22152/H), (H 2.6 mm, W 1.6 mm) and 14 paratypes
(MCZR–M–22152/P), (type loc.).
Type locality: Zara [now Zadar], Croatia.
Etymology: From the type locality, Zara.
Figures 49-54. Alvania zaraensis n. sp. 49, 50: holotype, Zara (now Zadar, Croatia), H 2.6 mm
(MCZR–M–22152/H); 51: original label; 52: SEM micrograph of the holotype; 53, 54: details of
the protoconch and first teleoconch whorl.
Figuras 49-54. Alvania zaraensis n. sp. 49, 50: holotipo, Zara (ahora Zadar, Croacia), H 2,6 mm
(MCZR–M–22152/H); 51: etiqueta original; 52: micrografía electrónica de barrido del holotipo; 53,
54: detalles de la protoconcha y primera vuelta de teleoconcha.
49 50
51
52
53 54 200 µm
200 µm
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.: Notes on the Alvania lineata-complex and three new Mediterranean species
101
Distribution: Mediterranean: Adriatic
Sea, Zara [now Zadar] (Croatia),
unspecified depth; habitat unknown, it
is presumed alive in algal facies.
Description: (between parentheses
data of the holotype). Shell (Figs 49-54)
small, solid, ovate-conic, height
2.10–2.95 mm (2.6 mm), width 1.45-1.9
mm (1.6 mm), H/W 1.45-1.66 (1.62).
Protoconch (Figs 53, 54) paucispiral,
slightly globose, shiny, without appar-
ent sculpture under SEM due to the
worn condition of the specimen, of 1.25-
1.4 (1.25) whorls, height 0.25-0.35 mm
(0.30 mm), diameter of nucleus 0.125-
0.175 mm (0.137 mm), diameter of first
half whorl 0.20-0.275 mm (0.237),
maximum diameter 0.325-0.375 mm
(0.356 mm). Teleoconch of 3.7-4.8 (4)
barely convex whorls, suture deep and
canaliculated. Axial sculpture of 9-12+v
(9+v) strong orthocline ribs, as wide as
the interspaces, interrupted at the
periphery, in correspondence with the
sutural cordlet. Spiral sculpture starting
with 2 (II, IV) weak cordlets. Last whorl
with 8-10 (9) spirals; the adapical 4
above the aperture, equidistant and as
wide as the interspaces, the basal 4-6 (5)
(including the sutural one) finer and
more spaced; fourth adapical cordlet
more pronounced. Rounded tubercles at
the intersections. Microsculpture absent.
Umbilical chink barely visible. Outer lip
thickened by a broad and robust varix,
with 7-8 (7) internal elongate denticles.
Colour monochrome light beige-orange,
rarely light brown with whitish supra-
sutural band. Varix whitish with weak
orange lines in correspondence with the
Table III. Measurements of the protoconch and teleoconch of Alvania zaraensis n. sp., in mm.
Number 1 is the holotype. Abbreviations, h: height; d: diameter of nucleus; Do: diameter of first
half whorl; DM: maximum diameter; nw: number worls; H: height, W: width; RH/W: ratio
height/width; Nw: number of teleoconch whorls; Nar+v: number axial ribs+ varix; Ns: number of
spirals on the last whorl (above the aperture); Nd: number of denticles; Sts: starting number of
spiral cordlets.
Tabla III. Medidas de la protoconcha y teleoconcha de Alvania zaraensis n. sp., en mm. El número 1 corre-
sponde al holotipo. Abreviaturas, h: altura; d: diámetro del núcleo; Do: diámetro de la primera media
vuelta; DM: máximo diámetro; nw: número de vueltas; H: altura, W: anchura; RH/W: ratio
altura/anchura; Nw: número de vueltas de la teleoconcha; Nar+v: número de costillas axiales + variz; Ns:
número de espiras de la última vuelta (sobre la apertura); Nd: número de dentículos; Sts: número inicial de
cordones espirales.
Protoconch 1 2 3 4 5 6 7 8 9 10 11 12
h 0.30 0.35 0.25 —- 0.30 —- 0.30 —- 0.30 0.31 0.30 0.31
d 0.137 0.14 0.14 —- 0.175 0.14 0.125 —- 0.15 0.145 0.14 0.125
Do 0.237 0.225 0.225 —- 0.225 0.225 0.20 —- 0.275 0.245 0.26 0.225
DM 0.356 0.35 0.34 —- 0.365 —- 0.325 —- 0.36 0.365 0.375 0.35
nw 1.25 1.35 1.3 —- 1.35 —- 1.3 —- 1.35 1.35 1.4 1.3
Teleoconch 1 2 3 4 5 6 7 8 9 10 11 12
H 2.6 2.6 2.9 2.95 2.75 2.7 2.75 2.5 2.9 2.75 2.75 2.1
W 1.6 1.65 1.8 1.9 1.77 1.8 1.7 1.57 1.75 1.77 1.75 1.45
RH/W 1.62 1.57 1.61 1.55 1.55 1.50 1.62 1.59 1.66 1.55 1.57 1.45
Nw 444.8 4.8 4.6 4.6 4.6 4 4.8 4.6 4.6 3.7
Nar+v 9+v 11+v 10+v 10+v 9+v 10+v 11+v 12+v 10+v 11+v 9+v 10+v
Ns 9(4) 8(4) 9(4) 9(4) 9(4) 9(4) 10(4) 9(4) 10(4) 10(4) 8(4) 9(4)
Nd 7 no 888no 788887
Sts 222222222222
Iberus, 37 (1), 2019
102
(Right page) Figures 55-70. Alvania spp. 55: Alvania discors (Allan, 1818), Sant’Agostino, Civi-
tavecchia (Italy), H 5 mm (BA); 56: Alvania settepassii Amati & Nofroni, 1985, paratype, Torreval-
daliga, Civitavecchia (Italy), 25-30 m depth, H 4.3 mm (BA); 57: Alvania schwartziana Brusina,
1866, Pago (now Pag, Croatia), H 3.6 mm (BA); 58: Alvania claudioi Buzzurro & Landini, 2007,
Zannone I. (Italy), H 2.5 mm, (BA); 59: Alvania lanciae (Calcara, 1845), Cala Gonone (Sardinia),
0.5 m depth, H 3.25 mm, (BA); 60: Alvania lanciae (Calcara, 1845), Bastia, Corsica (France), H
3.45 mm (MCZR–M–22161); 61: Alvania lanciae (Calcara, 1845), Elba I. (Italy), H 3.58 mm
(AN); 62: Alvania lineata Risso, 1826, Salina I. (Sicily), H 3.65 mm (BA); 63, 64: Alvania boz-
caadensis Tisselli & Giunchi, 2013, Aydincik (Turkey), H 2.15 mm (BA); 65, 66: Alvania cam-
panii Tisselli & Giunchi, 2013, Bozcaada (Turkey), 8 m depth H 2.55 mm (BA); 67: Alvania
aeoliae Palazzi, 1988, Salina I. (Sicily), H 2.3 mm (BA); 68, 69: Alvania datchaensis Amati & Oliv-
erio, 1987, Aydincik (Turkey), H 2.4 mm (BA); 70, 71: Alvania fractospira Oberling, 1970, Trogyr
(Croatia), H 2.55 mm (BA); 72: Alvania algeriana (Monterosato, 1877) Algiers (Algeria), H 2.95
mm (MCZR–M–22182).
(Página derecha) Figuras 55-70. Alvania spp. 55: Alvania discors (Allan, 1818), Sant’Agostino, Civi-
tavecchia (Italia), H 5 mm (BA); 56: Alvania settepassii Amati y Nofroni, 1985, paratipo, Torrevalda-
liga, Civitavecchia (Italia), profundidad 25-30 m, H 4,3 mm (BA); 57: Alvania schwartziana
Brusina, 1866, Pago, (now Pag, Croacia), H 3,6 mm (BA); 58: Alvania claudioi Buzzurro &
Landini, 2007, Zannone I. (Italia), H 2,5 mm, (BA); 59: Alvania lanciae (Calcara, 1845), Cala
Gonone (Cerdeña), profundidad 0,5 m , H 3,25 mm, (BA); 60: Alvania lanciae, Bastia, Córcega
(Francia), H 3,45 mm (MCZR–M–22161); 61: Alvania lanciae, Elba I. (Italia), H 3,58 mm (AN);
62: Alvania lineata Risso, 1826, Salina I. (Sicilia), H 3,65 mm (BA); 63, 64: Alvania bozcaadensis
Tisselli & Giunchi, 2013, Aydincik (Turquía), H 2,15 mm (BA); 65, 66: Alvania campanii Tisselli &
Giunchi, 2013, Bozcaada (Turquía), profundidad 8 m, H 2,55 mm (BA); 67: Alvania aeoliae
Palazzi, 1988, Salina I. (Sicilia), H 2,3 mm (BA); 68, 69: Alvania datchaensis Amati & Oliverio,
1987, Aydincik (Turquía), H 2,4 mm (BA); 70, 71: Alvania fractospira Oberling, 1970, Trogyr
(Croacia), H 2,55 mm (BA); 72: Alvania algeriana (Monterosato, 1877) Argel (Argelia), H 2,95 mm
(MCZR–M–22182).
spirals. Operculum and soft parts
unknown.
Remarks: A vial in the Monterosato
collection (MCZR–M–22152) contains 32
shells from Zara (now Zadar, Croatia),
labelled (Fig. 51) “Alvania montagui
xxxxx [unreadable] di Zara”, of which 7
Alvania lineata Risso, 1826, 10 Alvania
lanciae (Calcara, 1845) and 15 Alvania
zaraensis n. sp. Actually, the new species
resembles a dwarf form of Alvania
discors (Allan, 1818) (:463, pl X, fig. 5)
(Fig. 55), but the latter has a multispiral
protoconch of 1.7-1.8 whorls vs. 1.25-1.4
of A. zaraensis n. sp., with the diameter
of nucleus 0.85-0.112 mm vs. 0.125–0.175
in A. zaraensis n. sp.; the shell is then
larger (> 5 mm vs. < 3 mm in A. zaraensis
n. sp.) and more brightly coloured and
more polychrome.
Alvania bozcaadensis Tisselli &
Giunchi, 2013 (:164, figs 1-8, 9-11, 28-29)
(Figs 61, 62) is probably the morpholog-
ically closest species, differing by the
more slender outline, the more globose
apex, the more numerous and finer
axial ribs on last whorl (13-16 vs. 9-12 in
A. zaraensis n. sp.), as wide as half the
interspaces vs. larger than interspaces
in A. zaraensis n. sp., the more globose
apex, often with lower number of
whorls (1.25 vs. 1.25-1.40 in A. zaraensis
n. sp.), and a smaller nucleus (0.100 mm
vs. 0.125-0.175 mm in A. zaraensis n.
sp.).
Alvania lanciae (Calcara, 1845) (:29,
pl. IV, fig. 12) (Figs 59-61) is similar to
the new species in particular with some
of its Central Mediterranean morphs
(A
MATI
, 2012: 118-119 pls 1-2, figs A-G;
A-F) with robust shell and almost flat
whorls; it differs by the evident teleo-
conch and protoconch microsculptures,
absent in A. zaraensis n. sp., and for the
more globose protoconch. (A
MATI
&
O
LIVERIO
, 1987: 51, 52, pl. II, fig. 5 and
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
103
55
56
57
58
59
61
62
63 64 65 66
67
68 69 70 71 72
60
Iberus, 37 (1), 2019
104
Figures 73-82. Alvania spp. 73: Alvania garrafensis Peñas & Rolán, 2008: SEM micrograph of the
holotype, Mar de Cubelles, Garraf (Spain), H 2.8 mm (MNCN); 74: Detail of the protoconch;
75: Detail of the teleoconch; 76: Alvania colossophilus Oberling, 1970, Capo Greco Protaras,
Cyprus, H 3.75 mm (BA); 77: Alvania aspera (Philippi, 1844), Portoroz (Slovenia), H 3 mm (BA);
78: Alvania elisae Margelli, 2001, paratype, Capraia I. (Italy), H 3.75 mm (CS-PM); 79: Alvania
elisae Margelli, 2001, Capri I. (Italy), H 3.6 mm (MCZR-M-30060), intermediate specimen,
tending to species A. settepassii; 80: Alvania dorbignyi (Audouin, 1827), reproduced from S
AVIGNY
,
1817: pl. 3, 22; 81: Alvania dorbignyi (Audouin, 1827), reproduced from N
ORDSIECK
, 1972: 230,
13; 82: Alvania perversa F. Nordsieck, 1972, reproduced from N
ORDSIECK
, 1972: 230, 14.
Figuras 73-82. Alvania spp. 73: Alvania garrafensis Peñas & Rolán, 2008: micrografía electrónica de
barrido del holotipo, Mar de Cubelles, Garraf (España), H 2,8 mm (MNCN); 74: Detalle de la proto-
concha; 75: Detalle de la teleoconcha; 76: Alvania colossophilus Oberling, 1970, Capo Greco Protaras,
Chipre, H 3,75 mm (BA); 77: Alvania aspera (Philippi, 1844), Portoroz (Eslovenia), H 3 mm (BA);
78: Alvania elisae Margelli, 2001, paratipo, isla de Capraia (Italia), H 3,75 mm (CS-PM); 79:
Alvania elisae Margelli, 2001, isla de Capri (Italia), H 3,6 mm (MCZR-M-30060), ejemplar inter-
medio, que tiende hacia la especie A. settepassii; 80: Alvania dorbignyi (Audouin, 1827), reproducido
de S
AVIGNY
, 1817: pl. 3, 22; 81: Alvania dorbignyi (Audouin, 1827), reproducido de N
ORDSIECK
,
1972: 230, 13; 82: Alvania perversa F. Nordsieck, 1972, reproducido de N
ORDSIECK
, 1972: 230, 14.
73
74 75
76
77
78 79
80
81 82
500 µm
100 µm
1 mm
1 mm
1 mm
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
105
Figures 83-88. Alvania montagui (Payraudeau, 1826). 83, 84: syntype in apertural and dorsal view,
Corsica, H 4.2 mm (MNHN-IM-2000-27921): 85: syntype in apertural view, Corsica, H 3.95
mm (MNHN-IM-2000-27921); 86, 87: SEM micrograph of the same syntype as 83, 84, in aper-
tural view (86) and detail of the first whorls (87); 88: original figure (reproduced from
P
AYRAUDEAU
, 1826: pl. V, fig 13; drawing tipped).
Figuras 83-88. Alvania montagui (Payraudeau, 1826). 83, 84: sintipo en vista apertural y dorsal,
Córcega, H 4,2 mm (MNHN-IM-2000-27921); 85: sintipo en vista apertural, Córcega, H 3,95 mm
(MNHN-IM-2000-27921); 86, 87: micrografía electrónica de barrido del mismo sintipo que el 83,
84, en vista apertural (86) y detalle de las primeras vueltas (87); 88: figura original (reproducida de
P
AYRAUDEAU
, 1826: pl. V, fig. 13; dibujo volcado).
pl. III, figs 6,7; A
MATI
, 2012: 120, fig. 3,
A, B; T
ISSELLI
& G
IUNCHI
, 2013: 169, pl.
2, figs 12-14).
Alvania campanii Tisselli & Giunchi,
2013 (:165, figs 15-21, 26-27, 31-32, 36)
(Figs 63, 64) has finer axials as wide as
half the interspaces vs. robust barely
larger than interspaces ribs in A. zaraen-
sis n. sp.; its varix is less robust; the pro-
toconch is more globose, and sculptured
by granules set in series of 12-14 slightly
wavy spiral threads vs. smooth in A.
zaraensis n. sp.
Alvania elisae Margelli, 2001 (:43, figs
1-11, 16-19, pls 1-3) (Figs 78, 79) differs
in the larger shell (H 3.5-4 mm vs. H
2.1-2.95 mm in A. zaraensis n. sp.), the
protoconch has an evident microsculp-
tures vs. absent in A. zaraensis n. sp.; a
greater number of axial ribs on the last
whorl 15-16 vs. 9-12 in A. zaraensis n.
sp.
83 84 85
87 86 88
200 µm
Alvania disparilis Monterosato, 1890
(:146) (Figs 1-11) has a less robust shell
with more convex whorls, finer and
more numerous axial ribs (14-15 vs. 9-12
in A. zaraensis n. sp.).
Alvania peloritana (Aradas & Benoit,
1874) (:205, pl. IV, fig. 16) (Figs 12-18)
has more convex whorls vs. almost flat
in A. zaraensis n. sp.; less incise suture
vs. deeply canaliculate in A. zaraensis n.
sp.; axial ribs extending beyond the
periphery vs. interrupted at the
periphery in A. zaraensis n. sp.; larger
size (3.0-3.35 vs. 2.1-2.95 in A. zaraensis
n. sp.).
Alvania dorbignyi (Audouin, 1827)
(:171) (Figs 19-22) has a higher H/W
ratio (1.81 vs. 1.45-1.66 in A. zaraensis n.
sp.); opisthocline flexuose axials vs.
orthocline in A. zaraensis n. sp.
Alvania perversa F. Nordsieck, 1972
(:230, fig. 14) (Figs 23-29) differs in its
weaker sculpture (both axial and spiral),
with axials less elevate.
Alvania bartolinorum n. sp. (Figs 30-
40) differs in its shell less robust and
thick, with weaker sculpture (both axial
and spiral), especially the spiral one,
and in the maximum diameter of the
protoconch (0.44-0.50 mm vs. 0.325-0.375
mm A. zaraensis n. sp.).
Alvania unica n. sp. (Figs 41-48) dif-
fers in the larger size (height 3.45 mm vs.
2.10–2.95 mm in A. zaraensis n. sp.), the
finer and more numerous axials (15 vs. 9-
12 in A. zaraensis n. sp.), the suture less
canaliculate, the more numerous inner
denticles on the outer lip (10 vs. 7-8 in A.
zaraensis n. sp.), the higher protoconch,
with more whorls and wider diameter
(nw 1.5, h 0.375 mm, DM 0.475 mm vs.
nw 1.25-1.4, h 0.25-0.35 mm, DM 0.325-
0.375 mm in A. zaraensis n. sp.), the pro-
toconch sculpture of c. 10 spiral cordlets,
apparently lacking in A. zaraensis n. sp.
Specimens from some localities of
the eastern Mediterranean – Greece:
Crete, beached bioclastic sand, 2 sh (RP);
Saronikos, 1 sh (EQ); Turkey: Taşucu, 5
sh (EQ); Iskenderum Gulf, 2 sh (EQ);
Bozcaada I. 3 sh (EQ) – are very similar
to typical A. zaraensis n. sp. The shells
are often larger at the same number of
whorls, the height/width ratio is higher,
the tubercles at the intersections are
more rounded; the colour is yellowish
with two white suprasutural cords, and
the basal cords are dashed with darker
colour and the columella is darker. We
consider this material worthy of a
deeper insight for these potentially
diagnostic characters.
Iberus, 37 (1), 2019
106
ACKNOWLEDGEMENTS
Virginie Héros and Philippe Maes-
trati (MNHN, Paris) and Monica
Leonardi (CMSN, Milan) are thanked
for their very kind collaboration with
type material searches; Manuel Caballer
(project e-Recolnat; MNHN, Paris) for
the pictures of the holotype of Alvania
dorbignyi and of the syntypes of Alvania
montagui; Ronald Janssen and S. Hof
(SRI, Frankfurt am Main) for the pic-
tures of the type material of Alvania per-
versa; Paul Mazza (MGPU, Florence) for
his assistance during our visits to
examine Seguenza’s material; Emilio
Rolán (Vigo) for the pictures (SEM) of
the holotype of Alvania garrafensis;
Andrea Nappo (Quartu Sant’Elena) for
the photo of Fig. 61. A sincere thank to
Andrea Di Giulio (Dipartimento di
Scienze, “Roma Tre” University, Rome)
for the SEM photos, carried out at LIME
(Interdepartmental Laboratory of Elec-
tron Microscopy, “Roma Tre” University,
Rome); Danilo Scuderi (Catania), Italo
Nofroni (Rome), Cesare Bogi (Livorno),
Stefano Bartolini and Maria Scaperrotta
(Florence), Alessandro Raveggi (Flo-
rence) Raffaele Petrone (Rome) and
Attilio Pagli (Vinci, Florence) for their
friendly help with discussions and
materials. The authors are grateful to
Serge Gofas (Departamento de Biología
Animal, Universidad de Málaga, Spain)
and to an anonymous reviewer, for the
useful comments that helped to improve
this article.
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
107
BIBLIOGRAPHY
A
ARTSEN VAN
J.J.1982. Tavole sinottiche di con-
chiologia Mediterranea ed Europea (Gen. Al-
vania). La Conchiglia, 16 (158–159): 4–5.
A
LBANO
P. G. & S
ABELLI
B. 2009. I Molluschi delle
Secche di Tor Paterno. Collana: Gli Studi e le
Guide di RomaNatura. 2. Ente Regionale Ro-
maNatura, Roma, 95 pp.
A
LLAN
T. 1818. Sketch of the Geology of the En-
virons of Nice. Transactions of the Royal Soci-
ety of Edimburgh, 8: 427–464.
A
MATI
B. 2012. Alvania consociellaMonterosato,
1884 junior synonym of Alvania lanciae (Cal-
cara, 1845) (Prosobranchia, Rissoidae). Bol-
lettino Malacologico, 48: 116–121.
A
MATI
B. & N
OFRONI
I. 1985. Alvania settepassii
sp. n. (Gastropoda: Prosobranchia). Notiziario
del C.I.S.Ma., 6 (1–2): 19–27 [1984].
A
MATI
B. & O
LIVERIO
M. 1987. Alvania datchaen-
sis sp. n. (Gastropoda; Prosobranchia). No-
tiziario del C.I.S.Ma., 9 (10): 46–53.
A
PPOLLONI
M., S
MRIGLIO
C., A
MATI
B., L
UGLIÈ
L., N
OFRONI
I., T
RINGALI
L. P., M
ARIOTTINI
P.
& O
LIVERIO
M.2018. Catalogue of the primary
types of marine molluscan taxa described by
Tommaso Allery Di Maria, Marquis of Mon-
terosato, deposited in the Museo Civico di Zo-
ologia, Roma. Zootaxa, 4477 (1): 1–138
A
RADAS
A. 1847. Descrizione delle conchiglie
fossili di Gravitelli presso Messina. Atti del-
l’Accademia Gioenia di Scienze Naturali. Ser.
II, 3: 57–88.
A
RADAS
A. & B
ENOIT
L. 1872–1876. Conchigli-
ologia vivente marina della Sicilia e delle
isole che la circondano 1–3. Atti dell’Accade-
mia Gioenia di Scienze Naturali, 8: 113–226, pls
3–4 (1874).
A
UDOUIN
J.V. 1826. Explication sommaire des
planches de Mollusques de l’Egypte et de la
Syrie publiés par J.C. Savigny. In Savigny
J.C. Description de l’Egypte ou recueil des ob-
servations et des recherches qui ont été faites
en Egypte pendant l’expédition de l’armée
française, publié par C.L.F. Panckoucke. Sec-
onde edition, Histoire Naturelle Zoologie An-
imaux Invertébrés, 22: 117–212
Á
VILA
C.M. S.P. 2005. Processos e padrões de dis-
persão e colonização nos Rissoidae (Mollusca:
Gastropoda) dos Açores. Tese de Doutoramento,
Universidade dos Açores, Ponta Delgada.
329 pp.
Á
VILA
C.M. S.P., G
OUD
J. & F
RIAS
M
ARTINS
(
DE
)
A.M. 2012. Patterns of Diversity of the Ris-
soidae (Mollusca: Gastropoda) in the Atlantic
and the Mediterranean Region. The Scientific
World Journal, 2012, Article ID 164890, 30 pp,
2012. doi:10.1100/2012/164890.
B
ARASH
A. & D
ANIN
Z. 1992. Annotated list of
Mediterranean Molluscs of Israel and Sinai.
Fauna Palestina. Mollusca I. The Israeli Acad-
emy of sciences and Humanities. 405 pp, 372
figs.
B
ELLINI
R. 1929. I molluschi del golfo di Napoli
(Studi precedenti, l’ambiente, enumerazione
e sininimia). Annuario del Museo della R. Uni-
versità di Napoli (N. Ser.) 6 (2): 87 pp.
B
OGI
C. & G
ALIL
B. S.2006. Nuovi ritrovamenti
lungo le coste Israeliane. Notiziario S.I.M. 24
(5–8): 16–18.
B
OGI
C., C
IANFANELLI
S. & T
ALENTI
E. 1988.
Contributo alla conoscenza della malaco-
fauna dell’isola di Cipro. In (Nofroni I. ed.)
Atti della prima giornata di studi malacologici del
C.I.S.Ma. pp 187–214.
B
OUCHET
P. & D
ANRIGAL
F. 1982. Napoleon’s
Egyptian campaign (1798–1801) and the Sav-
igny collection of shells. The Nautilus. 96 (1):
9–24.
B
RUSINA
S. 1866. Contribuzione pella fauna dei
Molluschi dalmati. Edito per cura dell’Imperi-
ale e Reale Società Zoologico-Botanica di Vienna,
134 pp.
B
UZZURRO
G. & L
ANDINI
F. 2007. Descrizione
di una nuova specie di Rissoidae (Gas-
tropoda: Prosobranchia) per le coste laziali
(Mar Tirreno). Bollettino Malacologico, 42
(1–4):24–26.
C
ALCARA
P. 1845. Cenno sui Molluschi viventi e
fossili della Sicilia da servire di supplimento ed
insieme di critiche osservazioni all’opera di R. A.
Philippi. Reale Stamperia e Libreria, Palermo,
pp. 1–65, [1–2], pls I–IV.
C
AMPANI
E. 2008. An odd finding of Alvania dor-
bignyi (Gastropoda: Rissoidae). Marine Bio-
di vers ity Reco rds, 2:E3 1.
doi:10.1017/S1755267208000353
C
AMPANI
E., B
ARTOLINI
S. & S
PANU
M.T. 2012.
Alvania garrafensis Penas & Rolan, 2008 (Gas-
tropoda: Rissoidae) from Croatian water.
Iberus, 30 (1): 85–89.
C
ECALUPO
A. & Q
UADRI
P. 1996. Contributo
alla conoscenza malacologica per il Nord
dell’isola di Cipro (Parte II). Bollettino Mala-
cologico, 30 (10–12): 269–276.
C
HIRLI
C. & L
INSE
U. 2011. The Pleistocene Ma-
rine Gastropods of the Rhodes Island (Greece).
Grafiche PDB, Tavarnelle V.P. (Firenze), 447
pp.
C
RISCIONE
F. & P
ONDER
W.F. 2013. A phyloge-
netic analysis of rissooidean and cingulop-
soidean families (Gastropoda: Caenogas-
tropoa). Molecular Phylogenetics and Evolu-
tion, 66: 1075– 1082.
C
RISCIONE
F., P
ONDER
W.F., K
OHLER
F., T
AKANO
T. & K
ANO
Y. 2016. A molecular phylogeny
of Rissoidae (Caenogastropoda: Rissooidea)
allows testing the diagnostic utility of mor-
phological traits. Zoological Journal of the Lin-
nean Society, 179: 23–40.
D
E
G
REGORIO
A. 1889a. Esami di taluni Mol-
luschi viventi e terziari del Bacino Mediter-
raneo. Il Naturalista Siciliano 8 (10–11):
248–256.
D
E
G
REGORIO
A. 1889b. Iconografia conchio-
logica mediterranea vivente e terziaria. I.
Studi sul genere Scalaria: 1–10, Tav. I. An-
nales de Géologie et de Paléontologie. Palermo,
Libreria internazionale L. Pedone Lauriel di
Carlo Clausen.
D
EKKER
H. & O
RLIN
Z. 2000. Check list of Red
Sea Mollusca. Spirula, 47 (supplement), 1–46.
D
ELONGUEVILLE
C. & S
CAILLET
R. 2007. Les es-
pèces invasives de mollusques en Méditer-
ranée. Novapex, 8 (2): 47–70.
G
OFAS
S. & Z
ENETOS
A. 2003. Exotic molluscs
in the Mediterranean basin: current status
and perspectives. Oceanography and Marine Bi-
ology: an Annual Review, 41: 237–277.
G
OFAS
S., M
ORENO
D. & S
ALAS
C. 2011. Mollu-
cos marinos de Andalucìa. Universidad de
Malaga servicio de Publicaciones e Inter-
cambio Cientìfico. Malaga, Vol.1, 342 pp.
G
RANATA
-G
RILLO
G. 1877. Contribuzione pella
Fauna dei Molluschi del Mediterraneo. Cat-
alogo delle Conchiglie di Messina e dintorni.
Il Barth, 4: 143–147.
G
RAY
J.E. 1847. A list of the genera of Recent
Mollusca, their synonyma and types. Pro-
ceedings of the Zoological Society of London 1847:
129–242.
H
ADLEY
A. 2006. Combine ZP public domain
image processing software. Available from
https://web.archive.org/web/201602210321
41/http://www.hadleyweb.pwp.blueyon-
der.co.uk/
H
ORNUNG
A. & M
ERMOD
G. 1927. Mollusques
de la Mer Rouge recueillis par A. Issel faisant
partie des collections du Musée Civique
d’Histoire Naturelle de Gênes. Quatrième
partie, Rissoidés. Annali del Museo Civico di
Storia Naturale Giacomo Doria, Genova, 52 (IV
parte): 363–372.
ICZN [International Commission on Zoologi-
cal Nomenclature] 1999. International code
of zoological nomenclature, Fourth edition.
London: International Trust for Zoological
Nomenclature. London, xxix + 306 pp.
I
SSEL
A. 1869. Malacologia del Mar Rosso ricerche
zoologiche e paleontologiche. Memoria letta al
congresso dei Naturalisti Italiani in Vicenza nel
1868. Pisa, Editori della biblioteca malaco-
logica. 387 pp.
J
ANSSEN
R., Z
USCHIN
M. & B
AAL
C. 2011. Gas-
tropods and their habitats from the northern
Red Sea (Egypt: Safaga) Part 2: Caenogas-
tropoda: Sorbeoconcha and Littorinimorpha.
Annalen des Naturhistorischen Museums in
Wien, Serie A, 113: 373–509, Wien.
M
ARGELLI
A. 2001. A new species from Capraia
Is. (Tuscan Archipelago): Alvania elisae sp.
nov.. La Conchiglia 300: 43–50.
M
ARÍN
A. & R
OS
J. 1987. Catalogo preliminar
de los gasteropodos marinos del sudeste es-
pañol. Iberus, 7(1): 137–145.
M
IENIS
H.K. 1985. Is Alvania dorbignyi (Au-
douin, 1826) a Lessepsian migrant? Levantina,
59, 652–654.
M
IENIS
H.K. 2005. Mariene mollusken uit het
oostelijk deel van de middellandse zee 25. De
CIESM-atlas van exotische mollusken in de
Middellandse Zee en nogmaals iets over de
status van Alvania dorbigny. Spirula, 345:
104–105.
M
OAZZO
P.G. 1939. Mollusques testacés marins du
Canal de Suez. Mémoires de l’Institut d’Egypte,
38, 1–287.
M
OLLUSCA
B
ASE
2018. Alvania dorbignyi perversa
No rdsi eck, 197 2 †. A ccesse d at:
http://www.molluscabase.org/aphia.php?p
=taxdetails&id=873410 on 2018-04-30).
M
ONTEROSATO
T.A. 1872. Notizie intorno alle
conchiglie Mediterranee. Ufficio Tipografico M.
Amenta, Palermo, p. 15–61.
M
ONTEROSATO
T.A. 1875. Nuova rivista delle
conchiglie mediterranee. Atti dell’Accademia
di Scienze e Lettere, Palermo, 2: 1–50.
M
ONTEROS ATO
T.A. 1878. Enumerazione e
sinonimia delle conchiglie mediterranee.
Giorn al e Scienz e Naturali ed Ec on omiche,
Palermo, 13: 61–115.
M
ONTEROSATO
T.A. 1884. Nomenclatura gener-
ica e specifica di alcune conchiglie mediterranee.
Stabilimento Tipografico Virzi. Palermo. 152
pp.
M
ONTEROSATO
T.A. 1890. Conchiglie della pro-
fondità del mare di Palermo. Naturalista Si-
ciliano, 9 (6): 140–151; 9 (7): 157–166; 9 (8):
181–191.
N
EVILL
G. 1885. Hand lists of Mollusca in the In-
di an Mu s eum , Cal c utt a , Pa r t II . GAS -
TRO PODA. Prosobranc hia-Neu robranc hia
(contd.). Calcutta: Printed by order of the
trustees. pp. 306.
N
EWTON
R.S. & S
TEFANON
A. 1975. The “Teg-
nue de Ciosa” area: patch reefs in the north-
er n Adri atic Sea. Ma rin e Geo logy , 19:
M27–M33.
N
ORDSIECK
F. 1972a. Die europäischen Meeress-
chnecken (Opisthobranchia mit Pyramidellidae;
Rissoacea). Vom Eismeer bis Kapverden, Mit-
telmeer und Schwarzes Meer. Gustav Fischer,
Stuttgart XIII + 327 pp.
Iberus, 37 (1), 2019
108
N
ORDSIECK
F. 1972b. Marine Gastropoden aus
der Shiqmona-Bucht in Israël.Archiv für Mol-
luskenkunde 102(4–6): 227–245.
N
ORDSIECK
F. 1982. Die Europäischen Meeres-
Gehäuseschnecken (Prosobranchia). Vom Eis-
meer bis Kapverden, Mittelmeer und Schwarzes
Meer. 2., Völlig Neubearbeitete und Erweiterte
Auflage. Gustav Fischer Verlag, Stuttgart, xii
+ 539 pp.
O
BERLING
J.J. 1970. Quelques espèces nouvelles
de Gastéropodes du basin Méditerranéen.
Kleine Mitteilungen, Naturhistorisches Museum
Bern, 1: 1–7.
Ö
ZTÜRK
B., B
UZZURRO
G. & A
VNI
B
ENLI
H. 2004.
Marine molluscs from Cyprus: new data and
checklist. Bollettino Malacologico, 39 (5–8):
49–78.
P
ALAZZI
S. 1997. Un problema ancora… spin-
oso. I Rissoidi del Mediterraneo. La Conchiglia,
Roma. 29 (285): 35–40.
P
ALLARY
P. 1926. Explication des planches de
J. C. Savigny. Mémoires de l’Institut d’Egypte,
11: I– VII, 1–138.
P
AYRAUDEAU
B.C. 1826. Catalogue descriptif et
méthodique des annélides et des mollusques de l’Ile
de Corse, 218 pp, 8 pls. Paris.
P
EÑAS
A., R
OLÁN
E. & B
ALLESTEROS
M. 2008. Se-
gunda adición a la fauna malacológica del
litoral del Garraf (NE de la Península Ibérica).
Iberus, 26 (2): 15–42.
P
ONDER
W.F. 1985. A Review of the Genera of the
Rissoidae (Mollusca: Mesogastropoda: Rissoacea).
Records of the Australian Museum. Suple-
ment 4: 1–221 [1984].
R
ISSO
A. 1826. Histoire naturelle des principales pro-
ductions l’Europe Méridionale et particulière-
ment de celles des environs de Nice et des Alpes
Maritimes. Paris, Levrault, libraire 4: 439 pp.
S
AVIGNY
J.C. 1817. Description de l’Egypte, ou
recueil des observations et des recherches
qui ont été faites en Egypte pendant l’expé-
dition de l’armée française, publié par ordre
du Gouv erneme nt. His toi re Na t ure l le,
Planches, Vol II. Paris: de l’Imprimerie Royale.
S
CAPERROTTA
M., B
ARTOLINI
S. & B
OGI
C. 2012.
Accrescimenti. Stadi di accrescimento dei mol-
luschi marini del Mediterraneo. Volume IV, 184
pp.
S
CUDERI
D. 2007.The recent discovery of a new
section of the malacological collection of An-
drea Aradas. IV International Congress of
the European Malacological Societies, Octo-
ber 10–14, 2005 - Naples (Italy). Bollettino
Malacologico, 43: 125–129.
S
CUDERI
D. & A
MATI
B. 2012. Rediscovery and
re-evaluation of a “ghost” taxon: the case of
Rissoa galvagni Aradas et Maggiore, 1844
(Caenogastropoda Rissoidae). Biodiversity
Journal, 3 (4): 511–520.
S
CUDERI
D. & T
ERLIZZI
A. 2012. Manuale di Mala-
cologia dell’Alto Jonio. Grifo Ed., 188 pp.
S
EGUENZA
L. 1903. Rissoidi Neogenici della
provincia di Messina. Palaeontographia Italica,
9: 36–60 [reprint paginated 1–26].
T
ABANELLI
C., B
ONGIARDINO
C. & P
ERUGIA
I.
2011. Cingulopsidae e Rissoidae pliocenici
provenienti dallo “spungone” (Pedeappen-
nino romagnolo) e loro eventuale significato
paleoambientale (Gastropoda Caenogas-
tropoda Cingulopsidae, Rissoidae).Quaderno
di Studi e Notizie di Storia Naturale della Ro-
magna, 32: 27–76.
T
ISSELLI
M. & G
IUNCHI
L. 2013. Due nuove
specie di Alvania (Gastropoda: Rissoidae) dal
nord- ovest della Turchia. (Gastropoda
Caenogastropoda Rissoidae). Quaderno di
Studi e Notizie di Storia Naturale della Romagna,
37: 163–174.
V
ILLARI
A. & S
CUDERI
D. 2017. Taxonomical
notes on some poorly known mollusca
species from the Strait of Messina (Italy). Bio-
diversity Journal, 8 (1): 193–204.
Z
ENETOS
A., G
OFAS
S., R
USSO
G. & T
EMPLADO
J. 2004. CIESM Atlas of exotic species in the
Mediterranean. Vol. 3. Molluscs (ed. F. Briand).
Monaco: CIESM.
A
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.: Notes on the Alvania lineata-complex and three new Mediterranean species
109
Iberus, 37 (1), 2019
110
APPENDIX. LIST OF MATERIAL EXAMINED
Alvania bartolinorum n. sp. (See under species heading);
Alvania unica n. sp. (See under species heading);
Alvania zaraensis n. sp. (See under species heading);
Alvania disparilis Monterosato, 1890 (See under species heading);
Alvania peloritana (Aradas & Benoit, 1874) (See under species heading);
Alvania aeoliae Palazzi, 1988: Italy: Cannizzaro, Catania, Sicily 43 m depth, 16 sh
(BA), 30 m depth, 5 sh (BA); Salina I., Sicily, 35 m depth, vii.2002, >500 sh (BA);
Alvania algeriana (Monterosato, 1877): Algeria: Algiers, 6 syntypes
(MCZR–M–22182 Monterosato coll. ex Joly); Algiers, 5 sh (MCZR–M–22182 Mon-
terosato coll. ex Joly);
Alvania aspera (Philippi, 1844): Slovenia: Portoroz, beached, 1980, 8 sh (BA);
Greece: Zakynthos I. under stones 2-3 m depth viii.1990, 1 sh (BA);
Alvania schwartziana Brusina, 1866: Croatia: Zara (now Zadar), 4 syntypes
(MCZR–M–22326, Monterosato coll. ex Brusina); Pago (now Pag, near Zadar), 8 sh
(BA); Starigrad Paklenica, Zadar, 6 m depth, 29 sh (EQ); Italy: “Tegnùe” [reefs built by
coralline algae, bryozoans, sponges and cnidarians, with hardened sediments, typical
of shallow waters in the Gulf of Venice between 8 and 40 meters depth; the local fish-
ermen word, meaning ‘withhold’, refers to the fishing nets frequently remaining
entangled: see e.g. N
EWTON
& S
TEFANON
, 1975], Chioggia, Venice, 20 m depth, 2 sh
(EQ) (first record for Italy);
Alvania garrafensis Peñas & Rolán, 2008: only photographs of the holotype (MNCN
15.05/47516);
Alvania settepassii Amati & Nofroni, 1985: Italy: holotype (MCZR–M–TYPE00004/H)
and 42 paratypes Secche di Tor Paterno, 45 m depth (BA); Civitavecchia, 25-30 m depth,
69 paratypes (BA); Secche di Torre Flavia, Ladispoli 26 m depth 1986, 3 sh (BA); Giglio I.,
27-30 m depth, 16 sh (BA); S. Stefano I., 40 m depth, 1 sh (BA); Torre Astura, beached, 3
sh (BA); Nettuno, beached, 1982, 1 sh (BA); Torvaldaliga, Civitavecchia, 20-22 m depth,
250 sh (CS-PM); Sicily: Vendicari I., 28 m depth, 1 sh (BA); Croatia: Lastovo I. 38 m
depth, 21 sh (BA); Greece: Crete, 960 m depth, 3 sh (AP);
Alvania bozcaadensis Tisselli & Giunchi, 2013: Turkey: Bozcaada I., 12 m depth, 2
paratypes (EQ); Bozcaada I., 8-12 m depth, 23 sh (EQ); Aydincik, 4 sh (BA); Greece:
Leros I., amidst fishing nets residuals, 1985, 5 sh (CS-PM); Analipsi, Astypalea 5-6 m
depth, beached bioclastic sand, 2013, 3 sh (MO);
Alvania perversa F. Nordsieck, 1972: (See under species heading);
Alvania dorbignyi (Audouin, 1826): (See under species heading);
Alvania claudioi Buzzurro & Landini, 2007: Italy: Zannone I. 18 m depth, x.2004, 1
sh (BA); Zannone I., Approdo Romano, 35 m depth, xiv.2008, 11 sh (7 juv.) (EQ);
Alvania campanii Tisselli & Giunchi, 2013: Turkey: Bozcaada I., 12 m depth, 2
paratypes (EQ), Bozcaada I., 8 m depth, 2 sh (BA), 2 sh (CS-PM); Bozcaada I., 8-12 m
depth, 12 sh (EQ);
Alvania colossophilus Oberling, 1970: 1 syntype (NMBE); Croatia: Lastovo I. 38 m
depth, 31 sh (BA); Turkey: Kash, 26.v.1992, 50 m depth, 20 sh (BA); Aydincik, 10 m
depth ix.1990 41 sh (BA); Cyprus: Cape Greco, Protaras, xi.2011, 7 sh (BA); Macronis-
sos, beached xii.1988, 2 sh (BA);
Alvania datchaensis Amati & Oliverio, 1987: holotype and paratypes: MCZR, BA,
MO; Cyprus, Cape Greco, Protaras, ix.2011, 11 sh (BA); Turkey: Aydincik 9-10 m depth
1990 86 sh (BA);
Alvania discors (Allan, 1818): Italy: Trieste, 1980, 1 sh (BA); Sant’Agostino, Civi-
tavecchia, Rome, 0.50 m depth on Posidonia oceanica 1980, 26 sh (BA); Torre Astura,
Rome 1976-77, 64 sh (BA); Porto Cesareo, 55 sh (BA); Sicily: Palermo, 166 sh
(MCZR–M–22145); Ognina, 19 sh (MCZR–M– 22306); Porto Palo di Capopassero, 6 sh
(BA); Lampedusa I., Cala Calandra, 30 m depth, iv.1981, 29 sh (BA); Vendicari I., 28 m
A
MATI ET AL
.: Notes on the Alvania lineata-complex and three new Mediterranean species
111
depth, 7 sh (BA); Capo Asparano, 13 sh (BA); Canizzaro, 30 m depth, 1 sh (BA);
Magnisi (SR), beached bioclastic sand, legit J.J. Oberling (13.iii.1970), 30 sh (BA); Pan-
telleria I., Scauri, 13 m depth, 45 sh (BA); Sardinia: unspecified locality, viii.1981, 14 sh
(BA); Santa Caterina, 1978, 8 sh (BA); Calasetta S. Antioco, 10 sh (BA); Maddalena I., 1
sh (BA); Croatia: Trogyr viii.1989 5-6 m depth, 58 sh (BA); San Lorenzo, 6 m depth, 25
sh (BA); Umag, 1980, 200 sh (BA); France: Verghia, Ajaccio, Corsica, 3 m depth, 4 sh
(BA); Greece: unspecified locality, 15 sh (BA); Zakinthos I., 2-3 m depth, 24 sh (BA);
Turkey: Aydincik, 15 sh. (BA); Malta: undefined locality, 81 sh (BA); undefined local-
ity, 8 sh (BA); Algeria: Oran, viii.1977, 4 sh (BA); Tunisia: Gulf of Gabès, Kerkennah,
beach, 1974, 25 sh (BA); Gulf of Gabès, Kerkennah, loc. Sidi Youssef, 49 sh (BA); Gulf
of Gabès, Kerkennah, beach, 32 sh (BA); Gulf of Gabès, Kerkennah, loc. Sidi Youssef,
vii.2015, 350 sh (BA);
Alvania montagui (Payraudeau, 1826): photographs of the 2 syntypes, Corsica
(MNHN-IM-2000-27921);
Alvania lanciae (Calcara, 1845): lectotype (Amati, 2012) and numerous (>200) para-
lectotypes, Pantelleria I. (MZP–1935); lectotype (Amati, 2012) and 7 paralectotypes of
Alvania consociella Monterosato, 1884, Corsica (MCZR–M–22159), 7 paralectotypes,
Villefranche (Villefranche-sur-Mer) (MCZR–M–30126 cabinet of type material);
France: St. Raphael 49 sh (MCZR–M–22183), original labels reading “Alvania arguta
(ex Locard coll.)” and “A. locardi Monts. mss (ex Caziot coll.)”; Verghia, Ajaccio,
Corsica, 3 m depth, viii.1988, 4 sh (BA); Suasset les Pins, v.1982, 2 sh (IN); Spain:
Palamos, 1978-79, 2 sh (BA); undefined locality, 2 sh (IN); Sardinia: Cala Gonone,
Dorgali, viii.2010, 40°16’58.34”N, 9°38’15.30”E, 0.50 m depth, 42 lv on brown algae,
273 lv and sh on Posidonia oceanica (BA); undefined locality, 30 sh (Fra Piero legit, 1863,
Monterosato coll., MCZR–M–30056); undefined locality, 7 m depth, 7.viii.1981, 6 sh
(BA); Carloforte, Calasapone, 1 m depth, bioclastic sand, viii.2009, 7 sh (BA); Calasetta
S. Antioco, 1977, 22 sh (BA); ‘Punta Cavallo’ (=Capo Coda Cavallo), 30 sh (Fra Piero
legit, 1903, Monterosato coll., MCZR–M–30057); S. Pietro I., 8 sh (IN); S. Pietro I., local-
ity Punta, 1-4 m depth, ix.1986, 17 sh (BA); Gulf of Aranci, viii.1977, 42 sh (IN); Porto
Ferro, Sassari, viii.1980, 20 sh (IN); Maddalena I., Punta Marginetto, 41°15’14.70”N,
9°24’49.26”E, iii.1980, 25 sh (BA); Costa Serena, 1.5 m depth, vii.1991, 5 sh (BA);
Stintino, viii.1977, 110 sh (IN); Isola Piana, Cagliari, vii.1984, 35 sh (IN); Golfo Aranci,
1985, 154 sh (BA); Capo Pecora, Cagliari, 1-2 m depth, vii.1984, 56 sh (IN); Bocche di
Bonifacio 100-200 m depth, 1977, 1 sh (IN); Sicily: Magnisi, 130 sh (MCZR–M–22168);
Magnisi, beached bioclastic sand, legit Oberling (13.iii.1970), 10 sh (BA); Ognina, Sira-
cusa, 10.x.1982, beached bioclastic sand, 16 sh (BA); Punta Asparano, Siracusa, ix.1985,
14 sh (BA); north of Trapani, xii.1981, 12 sh (IN); S. Giuliano, Trapani, iv.1983, 12 sh
(IN); Siracusa, iv.1982, 7 sh (IN); Lampedusa I., viii.1984, 8 sh (IN); Pantelleria I., local-
ity Scauri, 12 vi.1991, 13 m depth, 3 sh (BA); Italy: Porto Maurizio, Imperia, 22 sh (Sul-
liotti legit, Monterosato coll., MCZR–M–30117); Sanremo, Imperia, 6 sh (IN); 4 km
NW of Capraia I., 140 m depth, 1978, 1 sh (MCZR–M ex Mauro Pizzini coll.); Baratti
Gulf, Livorno 10 m depth, viii.1983, 4 sh (IN); Antignano, Livorno, 1.5 m depth Posido-
nia oceanica meadow on muddy bottom, viii.1978, 1 lv (BA); Giannutri I., 18 m depth,
vi.1983, 1 sh (IN); Giannutri I., Grosseto 47 m depth, vi.1982, 1sh (IN); Sant’Agostino,
Civitavecchia, Rome, 1977, beached bioclastic sand, 250 sh (IN); Marina di San-
t’Agostino, Civitavecchia, Rome, 1978, 5 sh (BA); Santa Marinella, Rome, beached bio-
clastic sand, 1977, 13 sh (BA); Torre Astura, Nettuno, Rome, 1977, beached bioclastic
sand, 10 sh (BA); Torre Astura, Nettuno, Rome, 1977, 4 sh (IN); Marina di S. Nicola,
Rome, 23.ii.1978, 4 sh (MCZR–M ex Mauro Pizzini coll.); Gulf of Napoli, bioclastic
sand, iii.1979, 1 sh (BA); Procida I., Napoli, 4.vi.1978, 1 sh (BA); Procida I., Napoli,
ix.1981, 5 m depth, 39 sh, (IN); Scilla, Reggio Calabria, xii.1987, 1 m depth amidst
algae on the pier, 5 lv (IN); Santa Trada, Reggio Calabria, 1987, 1 m depth, 4 sh (IN);
Scilla, Reggio Calabria, viii1987, 7 m depth, 4 sh (IN); Taranto, 2 sh (Monterosato coll.,
MCZR–M–30058); Croatia: Punte Bianche (Velirat ‘Veli Rat’, Dugi Otok) 83 sh
Iberus, 37 (1), 2019
112
(MCZR–M–22168); Trogyr, viii.1989, 6 m depth in Posidonia oceanica meadow, 7 lv
(BA); Salvore 1 sh, (BA); Salvore 40-60 m depth, 2 sh (IN); Umag, iii.1980, 82 sh (BA);
Slovenija: Portoroz, 1977, beached bioclastic sand, 5 sh, (BA); Greece: undefined local-
ity in the Jonian Sea, beached bioclastic sand, 18 sh (BA); Lagonissi, Athens, vi.1982,
25 sh (IN); Astypalea, 25 m depth, 5 sh (CS-PM); Mediterranean Sea, undefined locali-
ties, 6 sh (Monterosato coll., MCZR–M–30128).
Alvania fractospira Oberling, 1970: 1 syntype (NMBE); Croatia: Trogir, 6 m depth
Posidonia oceanica meadow ix.1989, 2 sh (BA); Greece: undefined localities of the Ionian
Sea, beached, 5 sh (BA).
Alvania lineata Risso, 1826: Spain: Fuengirola, 30 m depth, viii.1985, 45 sh (BA);
Malaga, 5-10 m depth 11.xi.2009, 30 sh (BA); Tunisia: Gulf of Gabès, Kerkennah, 1974,
24 sh (BA); Gulf of Gabès, Kerkennah, loc. Sidi Youssef, vii.2015, 200 sh (BA); Sardinia:
San Teodoro, 1 sh (BA); Cala Gonone, Dorgali, Sardinia 1 m depth, viii.2010, 25 lv
(BA); Maddalena I., Sardinia 1989 24 m depth, 1 sh (BA); Gulf Aranci, Sardinia, 1985, 3
sh (BA); Oristano, Sardinia, viii.1978, 4 sh (BA); Cala Gonone, Dorgali, Sardinia 2-4 m
depth, viii.2010, 61 sh (BA); Sicily: Salina I., 35 m depth, vii.2002, 500 sh (BA); Levanzo
I., Punta Altarella 31 m depth, 3.vi.1991, 6 sh (BA); Marettimo I., Egadi, Sicily, 19 sh
(BA); Ognina, Siracusa, Sicily, 13 sh (BA); Magnisi, Eastern Sicily, Beached, legit Ober-
ling (13.iii.1970), 35 sh, (BA); Portopalo di Capo Passero, Sicily, 1 sh (BA); Lampedusa
I., Capo Grecale, vii.2009 50 m depth 10 sh (BA); Cannizzaro, Catania, Sicily, 35/43 m
depth, 61 sh (BA); Ognina, Siracusa, Sicily 1984, washing algae, 24 lv (BA); Lampe-
dusa I., 30 m depth, 53 sh (BA); Lampedusa I., Cala Calandra 30 m depth, 30.iv.1991,
46 sh (BA); Vendicari I., 28 m depth, 23 sh (BA); Ragusa, Secca of Roventa, Sicily 27 m
depth, vi.1989, 8 sh (BA); Marettimo I., Egadi I., 10 sh (BA); Malta: Malta I., beached
bioclastic sand, 1 sh (BA); Italy: Giglio I. 27-36 m depth, 45 sh (BA); Capraia I. 200-280
m depth, 1979, 1 sh (BA); Torre Astura, Rome, 1977, 1 sh (BA); San Felice Circeo,
Latina, 30 m depth, 10 sh (BA); Pozzano Reggio Calabria, 40 m depth, viii.1986, 1 sh
(BA); Secche of Tor Paterno, Rome, 30 m depth, 1.x.1988, 4 sh (BA); Secche of Tor
Paterno, Rome, 45 m depth, 18 sh (BA); Santo Stefano I., Ventotene I. 40 m depth, 14
sh (BA);Ventotene I., 1979, 25 sh (BA); Capraia I., Livorno 140-180 m depth, 1978, 16 sh
(BA); Secca di Torre Flavia 26 m depth, 1986, 64 sh (BA); Scilla (RC), 41 m depth,
16.xii.2006 legit Marconcini, 48 sh (IN); Croatia: Umag, beached bioclastic sand, 73 sh
(BA); Umag, 1978, 7 sh (BA); San Lorenzo, 5 sh (BA); Slovenija: Portoroz, beached bio-
clastic sand, 1 sh (BA); Greece: undefined locality, 29 sh (BA); Crete, 34 sh
(MCZR–M–30127); Crete, beached bioclastic sand, 5 sh (BA); Mediterranean Sea,
undefined localities, 75 sh (MCZR–M–22149);
Alvania elisae Margelli, 2001: Italy: 1 paratype, Capraia I., 2-15 m depth (CS-PM, ex
M. A. Fontana Angioy coll., Rome); Capri I., unspecified depth, 7 sh
(MCZR–M–30060); Elba I., Capo di Fonza, 25 m depth, 80 sh (EQ), 7 sh (BA); Elba I.,
Capo di Stella, 20 m depth, 13 sh (EQ); Elba I., 3 sh (MO).