Iberus
Suplemento 6
QL
401
.1123
INVZ
REVISTA DE LA
SOCIEDAD ESPAÑOLA
DE MALACOLOGÍA
Vigo, noviembre 2014
Iberus
Revista de la
Sociedad Española de Malacología
Comité de Redacción (Board of Editors)
Editor de Publicaciones (Editor-iu-Chief)
Serge Gofas Universidad de Málaga, España
Director de Redacción (Executive Editor)
Gonzalo Rodríguez Casero Mieres del Camino, Asturias, España
Editora Ejecutiva (Managing Editor)
Eugenia M° Martínez Cueto-Felgueroso Mieres del Camino, Asturias, España
Editores Adjuntos (Associate editors)
Iberus gualtieranus (Linnaeus, 1758), una especie emblemática de la península Ibérica, que da
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Iberus
REVISTA DE LA
SOCIEDAD ESPAÑOLA
DE MALACOLOGÍA
Suplemento 6
Noviembre 2014
Iberus
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BIOSIS.
Dep. Leg. M- 17439-20 14
ISSN 0212-3010
Diseño y maquetación: Gonzalo Rodríguez
Impresión: Feito S.L. - Vigo
Table of contents
Pistes
1- Map . . .
2- Type species, operculum, radula
3- microsculpture .
4- global comparison 1 .
5- global comparison 2 . .
6~ global comparison 3 . .
7- global comparison 4 .
8“ global comparison 5 . . .
GROUP 1
9 -Anticlimax faviformis spec. nov. New Caledonia ......
10 / 11- Anticlimax simulans spec. nov. Philippines, PNGuinea
12 -Anticlimax umbiliglabra spec. nov. Philippines. ......
GROUP 2
13 / 14“ Anticlimax fecunda spec. nov. New Caled., Vanuatu .
1 5-Anticlimax robusta spec. nov. Philippines .
16 / 17- Anticlimax infaceta spec. nov. Philippines .......
18- Anticlimax bicornis spec. nov. Solomon. . .
19 - Anticlimax singularis spec. nov. Philippines .
20 - Anticlimax puncticulata spec. nov. Philippines .
21 -Anticlimax bicarinata spec. nov. Vanuatu . .
22 / 23- Anticlimax fijiensis spec. nov. Fiji . . .
24 / 25- Anticlimax maranii spec. nov. Philippines .
GROUP 3
26- Anticlimax reinaudi spec. nov. Vanuatu . .
7.7 -Anticlimax serrata spec. nov. Vanuatu . . . .
28 / 29== Anticlimax tamarae spec. nov. Solomon, Philippines .
30 / 31” Anticlimax aitormonzoi spec. nov. Philippines .
32/ 34 -Anticlimax cyclist spec. nov. Philippines, PNGuinea .
35 / 37 -Anticlimax dentata spec. nov. Philippines, PNGuinea.
38 - Anticlimax elata spec. nov. Philippines . .
39 - Aníiclirnax solomonensis spec. nov. Solomon ........
40“ Anticlimax fastigata spec. nov. PNGuinea . .
41 -Anticlimax rhinoceros spec. nov. PNGuinea .
GROUP 4
42-Anticlimax textilis spec. nov. New Caledonia .
43/ 44» Anticlimax vanuatuensis spec. nov. Vanuatu . . . . . .
45- Anticlimax levis spec. nov. Philippines . . .
46- Anticlimax spiralis spec. nov. Vanuatu .
47- Anticlimax simplex spec. nov. Vanuatu ...........
48 - Anticlimax uniformis spec. nov. Philippines . .
49 / 50- Anticlimax maestratii spec. nov. Philippines .
51 / 52 -Anticlimax philippinensis spec. nov. Philippines ....
53- Anticlimax imitatrix spec. nov. Solomon . .
GROUP 5
54 - Anticlimax tentorii spec. nov. Vanuatu . .
55 / 56- Anticlimax discus spec. nov. Philippines, Vanuatu . .
57 / 58- Anticlimax lentiformis spec. nov Fiji, Philippines . . .
59- Anticlimax globulus spec. nov PNGuinea .
S'MWTHSOA Ugfy
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. . 9
. 10
. 11
. 12
. 13
. 14
15
17
17
21
24
26
29
29
32
34
36
39
43
43
46
49
52
56
56
60
63
65
67
67
68
73
74
76
78
81
84
86
88
88
93
Plates pgs.
GROUP 6
60 ¡ 61- Anticlimax boucheti spec. nov. New Caledonia . . 95
62 / 63- Anticlimax philsmithi spec. nov. PNGuinea, Philippines . 98
64- Anticlimax simplicissima spec. nov. PNGuinea . . 98
65- Anticlimax virginiae spec. nov. Vanuatu . . . 102
UNGROUPED SPECIES
66- Anticlimax religiosa spec. nov. Philippines . 104
67 / 68- Anticlimax obesa spec. nov. Philippines, PNGuinea . 104
69 / 71- Anticlimax juanae spec. nov. New Caledonia, Philippines ...... 108
OTHER SPECIES STUDIED
72- Anticlimax cf. rostrata (Hedley, 1900) PNGuinea . 112
73- Anticlimax sp. PNGuinea . . . . . 114
1 4- Anticlimax niasensis (Thiele, 1925) Indonesia, Sumatra . . . . 114
75- Anticlimax padangensis (Thiele, 1925) Indonesia, Sumatra. . 116
76- Vitrinella arifca (Bartsch, 1915) . . 118
© Sociedad Española de Malacología
Iberus, Suplemento 6: 1-126, 2014
The family Tornidae in the tropical Southwest Pacific: the
genus Anticlimax Pilsbry & McGinty, 1946 (Gastropoda,
Truncatelloidea) with the description of 42 new species
La familia Tornidae en el Suroeste del Pacífico Tropical: el género
Anticlimax Pilsbry & McGinty, 1946 (Gastropoda, Truncatelloidea)
con la descripción de 42 especies nuevas
Federico RUBIO* & Emilio ROLÁN**
Recibido el 15-1-2014. Aceptado el 4-X-2014
RESUMEN
Se estudian las especies de la familia Tornidae, género Anticlimax Pilsbry y McGinty,
1 946, del suroeste del Pacífico tropical, recolectadas durante las expediciones Tropical
Deep-Sea Benthos, dirigidas por IRD y MNHN, en Nueva Galedonia, Vanuatu, Fiyi, las
Islas Salomón, Filipinas y Papua-Nueva Guinea. En total han sido estudiadas 44 especies,
tanto de aguas superficiales como profundas, resultando 42 nuevas para la ciencia.
Cada una de las especies se ilustra mediante fotografías al microscopio electrónico de
barrido, discutiendo su variabilidad específica, cuando esto es posible, aportando datos
sobre el hábitat, distribución geográfica y rango batimétrico. Se aportan por vez primera
datos de la rádula y del opérculo en el género, relativos a la especie Anticlimax maranii y
datos anatómicos relativos a la especie Anticlimax cf. cyclist. Se comentan otras especies
relacionadas o próximas a este género. El género Can i marina Aguayo y Borro, 1 946 y el
género Lioprora Laseron, 1958 son considerados sinónimos de Anticlimax. Las especies
Cyclostremiscus (Canimarina) crassilabris Aguayo y Borro, 1946, Anticlimax glabra
Rubio, Rolán y Pelorce, 201 1 y Lioprora rostrata ¡Hedley, 1900), situadas previamente en
el género Canimarina, son transferidas en el presente trabajo al género Anticlimax. Se
ilustran por vez primera Discopsis niasensis Thiele, 1925 y Discopsis padangensis Thile,
1925, se aportan nuevos datos taxonómicos y se transfieren junto con Adeorbis cari na tus
A. Adams, 1 863 al género Anticlimax.
ABSTRACT
This paper reports on the Tornidae of genus Anticlimax Pilsbry & McGinty, 1946 from the
tropical Southwest Pacific, collected during the Tropical Deep-Sea Benthos expeditions con-
ducted by IRD and MNHN in New Celedonia, Vanuatu, Fiji, the Solomon Islands, the
Philippines and Papua New Guinea. Forty four species, from shallow to deep water, have
been studied, with forty two being new for Science. Each species is iliustrated by scanning
electrón microscope phoíographs, discussing its specific variability when this is possible,
and providing information about its habitat, geographical distribution and bathymetric
range. Data regarding the radula and operculum are presented for the first time for the
genus, regarding the species Anticlimax maranii , and so are anatómica! data regarding
* Pintor Ribera 4- 16a, 46930 Quart de Poblet (Valencia), Spain
** Museo de Historia Natural, Universidad de Santiago, Parque Vista Alegre, Campus norte, 15782 Santiago
de Compostela, Spain
1
Iberus , Suplemento 6, 2014
Anticlimax cf. cyclist. Other species similar or related to this genus are studied. The genera
Canimarina Aguayo & Borro, 1946 and Lioprora Laseron, 1958 are considered to be
synonyms of Anticlimax. Cyclostremiscus (Canimarina) crassilabris Aguayo & Borro,
1946, Anticlimax glabra Rubio, Rolán & Pelorce, 201 1 and Lioprora rostrata (Hediey,
1 900), previously placed in genus Canimarina, are here transferred to genus Anticlimax.
Discopsis niasensis Thiele, 1 925 and Discopsis padangensis Thiele, 1 925 are illustrated
for the first time, new taxonomic data are reported and, together with Adeorbis connotas
A. Adams, 1 863 they are transferred to genus Anticlimax.
INTROBUCTXGN
The family Tornidae Sacco, 1896
comprises a very heterogeneous group
of molluscs resulting from the fusión by
synonymy of tornids and vitrinellids
proposed by Bouchet & Rocroi (2005).
Species of tornids and vitrinellids are
very similar in soft anatomy and radula
as was shown in Rolan & Rubio (2002)
in their report on the Tornidae of the
east Atlantic.
Vaught (1989) placed the genus
Anticlimax in Vitrinellidae. Criscione &
Ponder (2013) placed Tornidae in Trun-
catelloidea; after a phylogenetic analysis
of 43 species representing 14 of the 23
families previously included in Ris-
sooidea, and of all the families of Cingu-
lopsoidea, reached the conclusión that
Tornidae, represented by two genera
( Circulus and Pseudoliotia ), is mono-
phyletic, with Nozeba (family Iravadi-
idae) being sister group to the Tornidae.
The operculum is one the characters
which can be employed for distinguí sh~
ing tornids from vitrinellids (Bieler &
Mikkelsen, 1988). Rubio & Rolán
(2011) mention in the remarks on the
taxonomic position of the genus Discop¬
sis , that the operculum of the African
species of Torninae, when it could be
observed, is oval and paucispiral, with a
subcentral nucleus [Tornus subcarinatus
(Montagu, 1803), Tornus leloupi Adams
& Knudsen. 1969, Discopsis apertus
Rolán & Rubio, 2002 and Ponderinella
skeneoides Rolán & Rubio, 2002]. Con-
versely, the known Atlantic species of
Circulinae, Teinostomatinae and Vit-
rinellinae have a circular operculum,
multispiral and with a central nucleus
[Circulus striatus (Philippi, 1836), Teinos-
toma cocolitoris Pilsbry & McGinty, 1945,
Cyclostremiscus calameli (Jousseaume,
1872), Cochliolepis parasítica Stimpson,
1858].
According to Bouchet & Rocroi
(2005), the family Tornidae comprises
four subfamilies: Torninae Sacco, 1896;
Circulinae Fretter & Graham, 1962;
Teinostomatinae Cossmann, 1917; and
Vitrinellinae Bush, 1897. In the subfam-
ily Torninae are included the genera
previously placed in synonymy of
Tornus, the subfamily Circulinae only
ineludes the genus Circulus, the Teinos-
tomatinae only the genus Teinostoma,
and the Vitrinellinae groups together
the other genera formerly included in
the family Vitrinellidae Bush, 1897, here
considered a subfamily. This classifica-
tion will be employed in the present
work.
The genus Anticlimax Pilsbry &
McGinty, 1946 is formed by very small
species which have a characteristic
shape, which is very variable in general
structure and microsculpture.
Rubio, Fernandez-Garcés &
Rolán (2011) studied 101 species of the
family Tornidae in the Caribbean and
neighbouring areas, of which 8 are in
genus Anticlimax and one was a new
species.
The genus exists in the West
Atlantic, where the mentioned 8 Recent
species are known, and in the Pacific
Ocean, where only 4 species were found
in the literature and 2 more were placed
in other genera.
Previously to the present work the 6
species known from the Indian and
Pacific Oceans were collected, 2 in the
West coast of America, ariother 2 in
Sumatra, 1 in Japan and 1 in Australia.
2
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
% (&
Figure 1. Location of cruises in the Tropical Deep-Sea Benthos programme and satellite cruises. 1,
New Caledonia; 2, Vanuatu; 3, Wallis and Futuna; 4, Fiji; 5, Tonga; 6, Solomon Islands; 7, Papua-
New Guinea; 8, Philippines.
Figura . 1. Situación de las expediciones del programa Tropical Deep-Sea Benthos y afines. 1, Nueva
Caledonia; 2, Vanuatu; 3, Wallis y Futuna; 4, Fiyi; 5, Tonga; 6 \ Islas Salomón ; 7, Papua-Nueva
Guinea; 8, Filipinas.
MATERIALS AND METHOD5
In the present work, we studied the
species of tornids of the genus Anticlimax
Pilsbry & McGinty, 1946 from different
oceanographic campaigns carried out by
the Muséum National d'Histoire Naturelle
(hereafter MNHN) in the Tropical South
Pacific (referred in Bouchet, Heros,
Lozouet & Maestrati 2008). These are
detailed as follows:
- MONTROUZIER (1993), a land-
based expedition carried out on the sites
of Touho (East coast of New Caledonia)
and Koumac (West coast), named in
honour of R.R Montrouzier, a pioneer in
the description of the New Caledonian
micromolluscs.
- BATHUS 1-4 (1993-94) on board
R/V Alis around New Caledonia
proper, and on the Norfolk and Loyalty
Ridges.
- MUSORSTOM 8 (1994) on board
R/V Alis , in the Vanuatu Archipelago.
- MUSORSTOM 10 cruise (1998) on
board R/V Alis in the Fijian Archipelago.
- LIFOU (2000) (Biodiversity Work-
shop), a land-based research campaign
at Lifou (Loyalty Islands Province).
- SALOMON 1 (2001) on board R/V
Alis in the central part of the Solomon
Islands, from Guadalcanal to Malaita
and Makira.
- PANGLAO (2004) (Panglao Marine
Biodiversity Project), a land-based expe¬
dition the Central Philippines: Panglao,
Dauis, Cortes, Tagbilaran and Baclayon.
- PANGLAO (2005) on board MV
DA-BFAR explored and researched the
deep-sea fauna of the Bohol and Sulu
Seas.
- SANTO (2006) (Global Biodiversity
Survey) a land-based expedition in the
waters of Espiritu Santo Island in
Vanuatu.
- AURORA (2007) also on board MV
DA-BFAR explored the northeastern
Philippines.
3
Iberus, Suplemento 6, 2014
- PAPUA NIUGINI (2012), a land-
based expedition in the waters of
Madang, Papua New Guinea and on
board R/V Alis.
Materials used in this study were
obtained by the above mentioned
oceanographic expeditions in shallow
and deep water of New Caledonia,
Vanuatu, Fiji, the Solomon and the
Philippine Islands. A map of the
sampled area is presented in Figure 1.
For most of the Tropical Deep-Sea
Benthos cruises, station numbers are pre¬
ceded by a two-letter prefix that refers to
the type of gear used: CC, chalut á crevettes
(shrimp trawl); CH, chalut commercial
(otter trawl); CP, chalut á perche (beam
trawl); DR, drague á roche (rock dredge);
DW, drague Warén (Warén dredge). Since
1985, all stations in the main
MUSORSTOM cruise series are numbered
consecutively (now o ver 3,000), but many
satellite expeditions have used their own
numbering system starting with 1.
On a steep slope, depth intervals for
a single haul can span several hundred
meters. As a consequence, when sum-
marizing the bathymetric range of a
species, we take the inner valúes of the
deepest and shallowest stations, as there
is no evidence that the species occurs
beyond these valúes. For instance, if a
species has been collected at 4 stations
e.g. 582-594 m, 693-811 m, 749-799 m,
283-405 m, and 350-800 m, the combined
confirmed bathymetric range is 405-749
m, the depths between which the
species definitively occurred, not 283-
811 m.
Illustrations for all the studied
species were prepared using a Scanning
Electron Microscope (SEM) Quanta 200.
Measurements of the teleoconch, the
máximum height (H) and máximum
diameter (D) are based on the scale bar
of the SEM micrographs. The proto-
conch was measured by the Verduin
(1976) method in which a nucleus is
considered at the beginning of the spire.
Abbreviations:
AMNH American Museum of Natural
History, New York
AM Australian Museum, Sidney
CACTI Centro de Apoyo Científico y
Tecnológico a la Investigación, Uni-
versity of Vigo
MNHN Museum national d'Histoire
naturelle, París
ZMB Zoologisches Museum, Berlin
D máximum diameter of the shell, mea¬
sured perpendicular to the axis of coiling
H total height of the shell
Stn. station
spm(s) specimen(s). Because most Anti¬
climax shells are not transparent and
animáis can retract deep inside, it is
difficult to ascertain whether there
are soft parts, and no distinction has
been attempted between live-taken
specimens and empty shells.
s clearly empty shells
juv juvenile
fragm fragment
SYSTEM ATIC PART
Superfamily T run c atelloide a Gray, 1840
Family Tornidae Sacco, 1896
Subfamíly Vitrinellinae Bush, 1897
Genus Anticlimax Pilsbry & McGinty, 1946
Climacia Dalí, 1903. Trans. Wag. Free Inst. Sci. 3: 1610 and 1633; pl. LX, figs. 1-3. (Preoccupied:
júnior homonym of Climacia M'Lachlan, 1869 [Neuroptera]; Climacina and Anticlimax are
replacement ñames). Type species: Teinostoma calliglyptum Dalí, 1903 (fossil) (Fig. 2).
Climacina Aguayo & Borro, 1946. Re v. Soc. Malac. " Carlos de la Torre", 4 (1): 11 (Invalid: júnior
homonym of Climacina Gemmellaro, 1878 [Gastropoda]).
Anticlimax Pilsbry & McGinty, 1946 (July). Nautilus 60: 12 (replacement ñame). (Comment:
"Neither the group Climacia or its type species was described by Dalí, both being defined only
by figures, and the size, "diam. 3.0 mm").
4
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Canimarina Aguayo & Borro, 1946 (August). Rev. Soc. Malac. " Carlos de la Torre" , 4(2): 46-47.
(júnior synonym). Type species: Cyclostremiscus (Canimarina) crassilabris Aguayo & Borro, 1946
(by original designation).
Lioprora Laseron, 1958. Rec. Austr. Mus., 24(11): 169 (júnior synonym). Type species: Lioprora ros¬
trata (Hedley, 1900) (by monotypy).
Remarks: Pilsbry & McGinty (1946)
introduced the replacement ñame Anti¬
climax, for the monotypic genus contain-
ing Teinostoma (Climacia) calliglyptum
Dalí, 1903, since the genera Climacia Dalí,
1903 and Climacina Aguayo & Borro,
1946, based on the same type species,
were invalid because of homonymy.
Almost at the same time. Aguayo &
Borro (1946) described Canimarina and
placed it provisionally as a subgenus of
Cyclostremiscus , to accommodate the
new species Cyclostremiscus (Canimarina)
crassilabris. This species, in their
Opinión, had characters which could
ally it to the genera Cyclostremiscus,
Miralabrum, Teinostoma and Climacia, but
could be considered as a new subgenus
due to its own different and unique
characters.
Pilsbry & Olsson (1950) revised the
genus and gave the following descrip-
tion: "The shell is wider than high, with a
dome-shaped or low-conic spire offew (3 or
4) zahoris, carínate periphery and more or
less convex base. The protoconch is smooth,
ofscarcely more than one convex zahori to 1
Ú. Sculpture of cióse, usually punctate,
spiral striation and radial wavelike ribs on
the base, sometimes on the upper surface
also. The aperture is oblicjue, cjuadrangular
or triangular, zaith a thickened peristome,
the outer lip is angular or often extended at
the termination of the keel. Umbilicus bor-
dered by a spirally emerging callous rib, ter-
minating at the colurnella or in the genus
Subclimax it filis the umbilicus".
Pilsbry & Olsson (1950) divided
Anticlimax into two subgenera:
-Subgenus Anticlimax s. str .: charac-
terized by having the umbilicus open,
bordered by a spiral cord whidh. termi-
nates in the colurnella in a small trian¬
gular callus. Type species: Anticlimax
calliglypta (Dalí).
-Subgenus Subclimax : characterized
by having an umbilicus, totally or par-
tially closed by a solid column which
terminates in a callus fused to the col-
umelia. Type species: A. hispaniolensis
Pilsbry & Olsson, 1950.
Faber (2007) considered Canimarina
a valid genus, comparing it only with
Cyclostremiscus, and placing it in Vit-
rinellidae solely on the basis of its
lacking "a clear apertural varix". Also
he considered Solariorbis decipiens
Olsson & McGinty, 1958 a júnior
synonym of Cyclostremiscus (Canimarina)
crassilabris.
In our opinión (see also Rubio et al.,
2011) Canimarina must be considered a
synonym of Anticlimax for the following
reasons:
-Cyclostremiscus (Canimarina) crassi¬
labris shares all the generic characters of
Anticlimax.
-The stated date of publication for
Anticlimax is July and that of Canimarina
is August of the same year, giving the
former priority.
Faber (2012) questioned the syn-
onymy of Canimarina proposed by
Rubio et al. (2011) arguing the presence
of "a sutural to supr asutural keel and near
fíat spire " and "a reticulate sculpture on
the first postnuclear whorl", as sufficient
characters for a generic morphological
differentiation.
At present the genus Anticlimax
groups together species of very different
shape (A. proboscidea, A. decórala, A. cal-
lyglypta, for example), whose keels,
located in different positions, develop
spirally into different apertures accord-
ing to the species.
In our opinión, the presence of retic¬
ular sculpture on the first whorl of the
teleoconch and a sutural to suprasutural
keel, are not sufficient morphological
characters for a generic separation,
above all if we take into account that
this is a genus where only the shells are
known.
Given that Anticlimax was proposed
before Canimarina, and that its descrip-
5
Iberus , Suplemento 6, 2014
tion is sufficient to encompass the difier¬
en! known species, we continué to con-
sider Anticlimax a valid genus and Cam¬
inar ina its júnior synonym. For these
reasons, Canimarina crassilabris, C. glabra
and C. rostrata , should be returned to
genus Anticlimax.
Nothing was known so far about the
animal, radula and operculum of Anti¬
climax. Its generic assignment has been
based only on the distinguishing charac-
ters of the shell, such as overall shape,
the radial folds on the base, the angular
shape of the external lip, and the zigzag-
ging spiral groo ves, among others.
In the Caribbean most of the known
species are fossils from the Miocene and
Plio-Pleistocene. There are few recent
species described, and they occur in
North Carolina, Florida, Cuba, México,
Nicaragua and Belize.
Rubio, Fernández-Garcés &
Rolán (2011), in their revisión of the
family Tornidae in the Caribbean and
neighbouring areas, studied 8 Recent
species (some of them also known as
fossils) of Anticlimax, of which one was
new for Science. Two fossil and poorly
studied species were also recorded:
Anticlimax schumoi (Vanatta, 1913) and
A. athleenae (Pilsbry & McGinty, 1946).
These species are:
- Anticlimax crassilabris (Aguayo &
Borro, 1946)
- Anticlimax glabra Rubio, Rolán &
Pelorce, 2011
- Anticlimax decórala Rolán, Fernán-
dez-Garcés & Rubio, 1997
- Anticlimax probóscide a (Aguayo, 1949)
- Anticlimax pilsbryi (McGinty, 1945)
- Anticlimax locklini Pilsbry & Olsson,
1950
- Anticlimax annae Pilsbry & Olsson,
1950
- Anticlimax hispaniolensis Pilsbry &
Olsson, 1950
- Anticlimax athleenae (Pilsbry &
McGinty, 1946) fossil
- Anticlimax schumoi (Vanatta, 1913)
fossil
Other Recent worldwide species,
most of them also registered in WoRMS
(2013) (except carinata, rostrata, niasensis
and padangensis ) are the following:
Pacific Ocean
Anticlimax occidens Pilsbry & Olsson,
1952. S of Punta Final, San Luis
Gonzaga Bay, Baja California, México
(20 fms).
Anticlimax willetti Hertlein & Strong,
1951. Costa Rica (Keen, 1971: 386). Ft.
Amador Beach, Canal Zone, Panama
(intertidal in hermit crab colony).
Anticlimax carinata (A. Adams, 1863).
Japan: see below in Discussion.
Anticlimax rostrata (Hedley, 1900).
Australia: see below in Discussion.
Indian Ocean
Anticlimax niasensis (Thiele, 1925):
see below in Discussion.
Anticlimax padangensis (Thiele, 1925):
see below in Discussion.
Anticlimax arifca (Bartsch, 1915) is
presented in some lists of this genus but
it is not an Anticlimax : see below in Dis¬
cussion.
Therefore 16 species were known: 10
in the Caribbean and 6 in the Indian and
Pacific Oceans. Here we add 42 new
species from the Tropical South Pacific.
Species studied in this work:
Due to the great diversity of shapes
observed in the tropical species studied
we have considered that the use of sub¬
genera in order to sepárate more easily
the species of this group was not practi-
cal, mainly because we have no infor-
mation on their anatomy, radular and
molecular data; thus, we will place all
species studied in genus Anticlimax.
The generic assignment has been
based only on the distinguishing charac-
ters of the shell. In order to facilítate
study, species were grouped according
to shell morphology. Some of the known
species are also fossil from the Miocene
and Plio-Pleistocene.
Some of the characters mentioned in
the original description of the genus
Anticlimax cannot be considered
absolute and therefore valid for all the
species included in this genus: a smooth
protoconch, for example. In former
times the protoconch was not correctly
examined, employing only low magnifi-
cation, while in SEM photography, the
very minute microsculpture can be
6
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
observed. Also, the number of whorls of
the protoconch mentioned ("... more than
one convex whorl to 1 Vú. ") cannot be con-
sidered as more than a character present
in the few species known at that
rnoment, becoming more variable when
more species have been studied,
Differential characters of Anticli¬
max according to the original descrip-
tiom
1. Shell wider than high;
2. With a dome-shaped or low-conic
spire;
3. Carinate periphery;
4. Sculpture of cióse, usually punc-
tate spiral striation (changed to oval
depressions or zigzag cords and
cordlets) and radial wavelike ribs on the
base, sometimes appearing also on the
upper surface;
5. Aperture oblique, quadr angular or
triangular;
6. Outer lip angular or often
expanded at the termination of the
keels;
7. Umbilicus bordered by a spirally
emerging callous rib; terminating at the
columella or filling the umbilicus.
To these we can add:
8. The protoconch smooth or sculp-
tured by tubercíes, between 1 and 2 Vi
whorls.
9. Teleoconch with spiral zigzag
grooves and cordlets. The microsculp-
ture of the species of the genus Anticli¬
max is not capricious. There is an ontoge-
netic model which is repeated from one
species to another. Even in a single shell
it is possible to recognize several stages
of this process. This succession between
some microsculptures is shown in Fig. 3
(see explanation below).
10. In some species, there may be
areas on the adapical part on which the
sculpture has almost disappeared.
11. The operculum is rounded and
multispiral with a central nucleus (Figs.
2B-C).
12. The radula (Figs. 2D-E) is tae-
nioglossate.
13. Microsculpture: The simplest pat-
tern which frequently appears in the
species of this genus at the beginning of
the teleoconch is that represented in Fig.
3A: on a smooth surface some small
rounded depressions aligned spirally,
appear. In the following state (Fig. 3B),
these small depressions increase in size,
being rounded or oval in form. In Fig. 3C
is represented this state in which there is
an increase of the depressed areas so that
some of them touch each other: the con¬
tad: of the depressed areas (Fig. 3D) is
constant and the areas between depres¬
sions rise into cords with prolongations.
These prolongations may be vertical or a
little oblique. In this case, there are spiral
cords with zigzag borders. Sometimes
these cords are wide, on other occasions
(Fig. 3E), they may change to a narrow
fillet. In Fig. 3F the spiral cord is en-
larged and, in the enlarged areas,
rounded nodules are formed. This usu¬
ally happens in the spiral cords closer to
the suture. In other patterns (Fig. 3G),
the spiral cords present fine prolonga¬
tions which come into contact with other
similar rectangular spaces. This pattern
is frequent in the last part of the last
whorl. On this pattern (Fig. 3H) of rec¬
tangular depressed areas, some fine and
irregular spiral lines appear. The spiral
cords are wider and have a variable bor-
der (Fig. 31). Sometimes, the prolonga¬
tions in the spiral cords are fine and
much more numerous (Fig. 3J). On other
occasions they have scarce undulating
prolongations (Fig. 3K). Finally, on some
occasions they are very irregular and
variable showing microsculpture be¬
tween the cords (Fig. 3L).
Grouping:
Bearing all these characters in mind,
we can group the studied species into
several well defined and differentiated
groups, from 1 to 6, plus another of non-
characteristic grouped species. Due to the
lack of information on soft parts, radula
and DNA, we chose not to introduce dif-
ferent generic or subgeneric ñames, which
would only be justified after more detailed
knowledge of the group.
The description order of the species
will be made presenting them within
the mentioned groups.
7
Iberus , Suplemento 6, 2014
Figure 2. A: Original figures of Teinostoma (Climacia) calliglyptum Dalí, 1903, type species of
genus Anticlimax Pilsbry & McGinty, 1946 (Florida, Pliocene fossil); B-C: Opercula. oí Anticlimax
maranii (600 and 430 pm respectively); D-E: radula of A. maranii. F-G: soft parts oí Anticlimax
cf. cyclist spec. nov.
Figura 2. A: Figuras originales de Teinostoma (Climacia) calliglyptum Dalí, 1903, especie tipo del
género Anticlimax Pilsbry y McGinty, 1946 ( Florida , fósil del Plioceno); B-C: Opérenlos de Anticlimax
maranii (600 y 450 pm respectivamente); D-E: rádula de A. maranii; F-G: partes blandas de Anticli¬
max cf cyclist spec. nov.
8
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 3. Dififerent aspects of the microsculpture of Anticlimax species. See the text.
Figura 3. Diferentes aspectos de la microescultura de las especies de Anticlimax. Véase el texto.
9
Iberus , Suplemento 6, 2014
Figure 4. Synopsis of Anticlimax species. A: A . faviformis spec. nov., holotype, 2.3 mm and paratype,
2.2 mm, New Caledonia. B: A . simulans spec. nov., holotype, 2.2 mm, Philippines. C: A, umbiliglabra spec.
nov., holotype, 1.75 mm, Philippines. D: A. fecunda spec. nov., holotype, 2.24 mm, New Caledonia. E:
A. robusta spec. nov., holotype, 2.46 mm and shell, 2.2 mm, Philippines. F: A. infaceta spec. nov., 2.15
mm, holotype, Philippines. G: A. bicornis spec. nov., holotype, 1.66 mm, Solomon. H: A. singularis
spec. nov., holotype, 1.66 mm, Philippines (MNHN). I: A. puncticulata spec. nov., holotype, 1.29 mm,
Philippines. All shells at MNHN.
Figura 4. Sinopsis de las especies de Anticlimax. A: A. faviformis spec. nov., holotipo, 2,3 mmy paratipo, 2,2 mm,
Nueva Caledonia. B: A. simulans spec. nov., holotipo, 2,2 mm, Filipinas. C: A. umbiliglabra spec. nov.,
holotipo, 1,75 mm, Filipinas. D: A. fecunda spec. nov., holotipo, 2,24 mm, Nueva Caledonia. E: A. robusta
spec. nov., holotipo, 2,46 mmy concha, 2,2 mm, Filipinas. F: A. infaceta spec. nov, 2,15 mm, holotipo,
Filipinas. G: A. bicornis spec. nov, holotipo, 1,66 mm, Salomón . H: A. singularis spec. nov, holotipo, 1,66 mm,
Filipinas. I: A. puncticulata spec. nov, holotipo, 1,29 mm, Filipinas (MNHN). Todas las conchas en MNHN
10
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
mm
Figure 5. Synopsis of Anticlimax species (continued). A: A. bicarinata spec. nov., holotype, 1.3 mm,
Vanuatu. B: A. fijiensis spec. nov., holotype, 1.64 mm, Fiji. C: A. maranii spec. nov., holotype, 1.8
mm, Philippines. D: A. reinaudi spec. nov., holotype, 1.26 mm, Vanuatu. E: A. serrata spec. nov.,
holotype, 2.47 mm, Vanuatu. F: A. tamarae spec. nov., holotype, 1.65 mm, Solomon. G: A. aitor-
monzoi spec. nov., holotype, 2.76 mm, Philippines. H: A. cyclists pee. nov., holotype, 2.68 mm Philip¬
pines (MNHN); I: A. dentata spec. nov., holotype, 2.3 mm, Philippines. All shells at MNHN.
Figura 5. Sinopsis de las especies de Anticlimax ( continuación ). A: A. bicarinata spec. nov., holotipo,
1,3 mm, Vanuatu. B: A. fijiensis spec. nov., holotipo, 1,64 mm, Fiyi. C: A. maranii spec. nov.,
holotipo, 1,8 mm, Filipinas. D: A. reinaudi spec. nov., holotipo, 1,26 mm, Vanuatu. E: A. serrata spec.
nov., holotipo, 2,47 mm, Vanuatu. F: A. tamarae spec. nov., holotipo, 1,65 mm, Salomón. G: A. aitor-
monzoi spec. nov., holotipo, 2,76 mm, Filipinas. H: A. eyelist spec. nov., holotipo, 2,68 mm Filipinas;
I: A. dentata spec . non, holotipo, 2,3 mm, Filipinas. Todas Lis conchas en MNHN.
Iberus , Suplemento 6, 2014
Figure 6. Synopsis oí Anticlimax species (continued). A: A. é’Ztfta' spec. nov., holotype, 1 .34 mm, Philip-
pines. B: A. solomonensis spec. nov., holotype, 1.5 mm, Solomon. C: A. fastigata spec. nov., holotype,
2.67 mm, Papua New Guinea. D: A. rhinoceros spec. nov., holotype, 1.65 mm, Papua New Guinea.
E :A. textilis spec. nov., holotype, 2.09 mm, New Caledonia. F :A. vanuatuensis spec. nov., holotype,
1.35 mm, Vanuatu. G: A. levis spec. nov., holotype, 2.0 mm, Philippines. H: A. spiralis spec. nov.,
holotype, 2.44 mm, Vanuatu. I: A. simplex spec. nov., holotype, 2.0 mm, Vanuatu. All shells at MNHN.
Figura 6. Sinopsis de las especies de Anticlimax (continuación). A: A. elata spec. nov., holotipo, 1,34 mm,
Filipinas. B: A. solomonensis spec. nov., holotipo, 1,5 mm, Salomón. C: A. fastigata spec. nov., holotipo,
2.67 mm, Papua Nueva Guinea. D: A. rhinoceros spec. nov., holotipo, 1,65 mm, Papua Nueva Guinea.
E: A. textilis spec. nov., holotipo, 2,09 mm, Nueva Caledonia. F: A. vanuatuensis spec. nov., holotipo,
1.35 mm, Vanuatu. G: A. levis spec. nov., holotipo, 2,0 mm, Filipinas . H: A. spiralis spec. nov., holotipo,
2,44 mm, Vanuatu. I: A. simplex spec. nov., holotipo, 2,0 mm, Vanuatu. Todas las conchas en MNHN.
12
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 7. Synopsis of Anticlimax species (continued). A: A. uniformis spec. nov., holotype, 3.0 mm, Phili-
ppines. B: A. maestratii spec. nov., holotype, 2.6 mm and paratype 2.0 mm, Philippines. C: A, philip-
pinemis spec. nov., holotype, 1.66 mm, Philippines. D: A. imitatrix spec. nov., holotype, 1.3 mm, Solomon
Islands. E: A tentorii spec. nov., holotype, 4.2 mm, Vanuatu. F: A. discus spec. nov., holotype, 1 .78 mm, Philip¬
pines. G: A. lentifonnis spec. nov., holotype, 1 .46 mm, Fiji. H: A gkbulus spec. nov. holotype, 2.6 mm, Papua
New Guinea. I: A. boucheti spec. nov., holotype, 1 .6 mm, New Caledonia. All shells at MNHN.
Figura 7. Sinopsis de las especies de Anticlimax (continuación). A: A. uniformis spec. nov., holotipo, 3,0 mm,
Filipinas. B: A. maestrati spec. nov., holotipo, 2,6 mm and paratype 2.0 mm, Filipinas. C: A. philippinensis
spec. nov., holotipo, 1,66 mm, Filipinas. D: A. imitatrix spec. nov., holotipo, 1,3 mm, Salomón. E: A. ten¬
torii spec. nov., holotipo, 4,2 mm, Vanuatu . F: A. discus spec. nov., holotipo, 1,78 mm, Filipinas. G: A.
lentiformis spec. nov., holotipo, 1,46 mm, Fiyi. H: A. globulus spec. nov. holotype, 2,6 mm. Papua Nueva
Guinea. I: A. boucheti spec. nov., holotipo, 1,6 mm, Nueva Caledonia. Todas las conchas en MNHN
13
Iberus , Suplemento 6, 2014
Figure 8. Synopsis oí Anticlimax species (continued). A: A. philsmithi spec. nov., holotype, 1.5 mm
and paratype, 1.67 mm, Papua New Guinea. B: A. simplicissima spec. nov., holotype, 2.3 mm,
Papua New Guinea. C: A. virginiae spec. nov., holotype, 1.93 mm, Vanuatu. D: A. religiosa spec.
nov., holotype, 1.4 mm, Philippines. E: A . obesa spec. nov., holotype, 5.9 mm, Philippines. F: A.
juanae spec. nov., holotype, 2.55 mm, New Caledonia. All shells at MNHN.
Figura 8. Sinopsis de las especies de Anticlimax ( continuación ). A: A. philsmithi spec. nov., holotipo,
1,5 mm and paratype, 1,7 mm, Papua Nueva Guinea. B: A. simplicissima spec. nov., holotipo, 2,3
mm, Papua Nueva Guinea. C: A. virginiae spec. nov., holotipo, 1,93 mm, Vanuatu. D: A. religiosa
spec. nov., holotipo, 1,4 mm, Filipinas. E: A. obesa spec. nov., holotipo, 5,9 mm, Filipinas. F: A.
juanae spec. nov., holotipo, 2,55 mm, Nueva Caledonia. Todas las conchas en MNHN.
14
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Table I. Differences between species of group 1 .
Tabla I. Diferencias entre las especies del grupo 1.
Group 1
Description : Shell depressed; proto-
conch with numerous fines of Ínter-
ruption -growth, which are like axial
ribs; teleoconch bicarinate, formed by
cells of unequal size aligned in a
spiral direction. Aperture triangular;
external lip expanded laterally
outwards.
It is formed by 3 species: A. favi-
formis, A. simulans and A. umbiliglabra. In
Table I we show the most important dif¬
ferences of the protoconch.
Anticlimax faviformis spec. nov. (Figures 4A, 9A-F)
Type material: Holotype MNHN 27171 (Figs. 4A, 9A) and 4 paratypes MNHN 27172 (Figs. 9B-C).
Material examined: (5 s): Only those of the type locality.
Type locality: New Caledonia, Lagoon of Grand Récif Mengalia, Touho area, 20°44.5'S, 165015.9'E,
8 m [MONTROUZIER: Stn. 1264],
Etymology: The specific ñame derives of the Latin words favus, -i "honeycomb" and formis "form"|
alluding to the sculpture of the shell.
Distribution : Only known from New
Caledonia at 8 rn.
Description : Shell small, formed by
about 3 Va whorls of quick growth, with
a fíat spire and the periphery delimited
by two thick spiral carinae.
Protoconch with only one whorl, 220-
230 jum in diameter and about 60 ¡im across
the nucleus; its surface has two distinct
phases: the first is formed by the nucleus
and Vz whorl and ends in the first slight
thickening; and the second phase, in which
there are about 10 successive thickenings,
forming axial ribs. The teleoconch has 2
Va whorls, with the periphery with the two
mentioned carinae: a basal one, thicker
and prominent, and an adapical one, not
so thick; both forming an angle on the shell.
Profile with a fíat or scarcely concave
periphery and concave base.
Omamentation formed by spiral cords
of unequal size that are crossed by axial
striae forming small cells, which are spi¬
ral ly aligned and ha ve different shape and
size; those at the base, and specially in the
umbilical area, are larger than the others.
Aperture oval, prosocline; parietal area
with a thick callous coating; columella
reflected externally; outer lip thin, with
sharp edge, presenting an extensión in the
area between the two carinae, which gives
it a distinctive profile. Umbilicus narrow
and deep; umbilical margin closes in pro-
gressively and in the area next to the col¬
umella forms a callus of triangular shape,
on whose surface spiral cordlets develop.
Dimensions: the holotype measures
2.3 mm in diameter.
Habitat: Infralittoral species collected
on sandy mud bottom, at 8 m depth.
Remarks: This new species is charac-
terized by its very fíat spire, the thick
peripheral carinae, the rows of cells of
different size and shape spirally aligned
and covering completely the shell; the
convex base and the outer lip with a
prolongation in the periphery. The most
similar species are the other two
included in this first group: see below
the comparison of all three.
15
Iberus , Suplemento 6, 2014
Figure 9A-R Anticlimax faviformis spec. nov. A: holotype, 2.3 mm (MNHN); B-C: paratype, 2.2
(MNHN); D: protoconch of the paratype of figs. B~C; E: protoconch of the holotype; F:
microsculpture. AJI from New Caledonia, Touho area, Lagoon of Grand Récif Mengalia, Stn.
1264, 8 m.
Figura 9A--F Anticlimax faviformis spec . nov. A: holotipo, 2,3 mm (MNHN); B-C: paratipo, 2,2
(MNHN); D: protoconcha del paratipo de las figs. B-C; E: protoconcha del holotipo; F: microescultura.
Todo de Nueva Caledonia, alrededores de Touho, Laguna del Grand Récif Mengalia, Stn. 1264, 8 m.
16
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Anticlimax simulans spec. nov. (Figures 4B, 10A-G, H A F.)
Type material: Holotype MNHN 27173 (Figs. 4B, 10A-C) and one paratype MNHN (27174).
Material examined: (5 s): Philippines, PANGLAO 2004: 1 s, Panglao Island, lagoon off Población,
Stn. Sil, 9°33.6'N, 123°43.6'E, 2 m, fine sand and seagrass; 1 s, Pamilacan Island, Stn. S22, 9°29.4'N,
123°56.0/E, 15-20 m, hard ground covered with seagrass; 2 s, Bohol Island, Cortes, Stn. T18, 9°41.8'N,
123°49.9,E, 80-100 m, muddy bottom with sponges (type material). Papua New Guinea: 1 s, N Sek
Island, PAPUA NIUGINI, Stn. PS47, 05°04.7/S, 145°48.9'E, 8 m, inner slope.
Type locality: Philippines, Cortes, Bohol Island, 9°41.8/N, 123°49.9'E, 80-100 m, muddy bottom
with sponges [PANGLAO 2004: Stn. TI 8].
Etymology: The specific ñame añudes to the similarity with the previous species.
Distribution : Ordy known from the
Philippines, between 2 and 80 m, and
from Papua New Guinea, at 8 m.
Description: Shell small, formed by 3
whorls of quick growth, with a nearly
fíat spire and the periphery delimited by
two strong spiral carinae.
The protoconch has 1 14 whorls,
measures about 290 /im iu diameter and
has two clearly differentiated periods:
the first one smooth with less than Vi
whorl besides the nucleus and the
second, with about 30 thickened ribs.
The teleoconch has 2 !4 whorls, delim¬
ited by two strong peripheral carinae
which angle the shell; the basal one is
wider and more prominent, and the adapi¬
cal one, narrower. Profile with a slightly
concave periphery and base concave.
Ornamentation formed initially by
spiral grooves of similar size which, are
about 12 in number at the beginning of
the teleoconch and which after 3A of whorl
form small cells by Crossing the axial striae;
these are spirally aligned and have dif-
ferent shape and size; on the last whorl 17
lines of cells can be observed on the adapi¬
cal part, 13 on the periphery and 17 on the
base, of which those placed in the umbil¬
ical area are of larger size than the others.
Aperture oval, prosocline; parietal
zone with a strong callous coat; columella
reflected externally; external lip thin, with
a sharp border, presenting a prolongation
in the area included between the two
carinae, which give to the shell a charac-
teristic profile. Umbilicus narrow and
deep. The umbilical margin closes in pro-
gressively and in the area cióse to the col
umella, forms a triangular callus, with
spiral cordlets Crossing the surface.
Dimensions: the holotype measures
2.2 mm in diameter.
Habitat : Infra and circalittoral species
collected from Philippines at 2 m, on a
fine sand and seagrass bottom (Stn. Sil)
and at 15-20 m, on a hard ground
covered with seagrass (Stn. S22). Also
trawled in 80-100 m, on a muddy
bottom with sponges PANGLAO 2004
(Stn. T18). In Papua New Guinea at 8 m,
on the inner slope (Stn. PS47).
Remarks: Anticlimax simulans spec. nov.
is very similar to A. faviformis spec. nov.
from New Caledonia, being differentiated
from the latter by the larger size of the pro¬
toconch and by having more growth lines,
like ribs, in the second period of this. It
also differs by having at the beginning of
the teleoconch, 12 spiral grooves trans-
formed into small cells after 3A of whorl;
by having a smaller number of lines of
cells on the base and by the periphery
being slightly concave.
Anticlimax umbiliglabra spec. nov. (Figures 4C, 12A-D)
Type material: Holotype MNHN 27175 (Figs. 4C, 12A-B).
Material examined: Only from the type locality.
Type locality: Philippines, Panglao Island, lagoon off Población, 9°33.6'N, 123°43.6'E, 2 m, fine sand
and seagrass [PANGLAO 2004: Stn. Sil].
Etymology: The specific ñame is formed by the words "umbilicus", and glabra, "smooth", allud-
ing to the smooth umbilical area which is very different from other species of its group.
17
Iberus, Suplemento 6, 2014
Figure 10A-G. Anticlimax simulans spec. nov. A-C: holotype, 2.2 mm (MNHN); D: protoconch
of the holotype; E-G: microsculpture and detail. Philippines, Panglao Island, Stn. Ti 8, 80-100 m,
in muddy bottom with sponges.
Figura 10A-G . Anticlimax simulans spec . nov. A-C: holotipo, 2,2 mm (MNHN); D: protoconcha del
holotipo; E-G: micro escultura y detalle. Filipinas, Isla de Panglao, Stn. T18, 80-100 m, en fondo de
fango con esponjas.
18
RUBIO & RoláN: The gemís Anticlimax in the tropical Southwest Pacific
Figure 11A-E: Anticlimax simulans spec. nov. A-C: shell, 1.75 mm (MNHN); D: protoconch; E:
microsculpture. N Sek Island, Papua New Guinea, PAPUA MIUGINI: PS47, 8 m.
Figura 11A-E: Anticlimax simulans spec. nov. A-C : concha, 1,75 mm (MNHN); D: protoconcha; E:
microescultura. N de la isla de Sek, Papua Nueva Guinea, PAPUA NIUGINI: PS47, 8 m.
Distribution: Only known from
Panglao Island, its type locality, at 2 m.
Description: Shell small (< 2 mm),
formed by slightly more than 3 whorls
of quick growth, with a nearly fíat spire
and the periphery delimited by two
thick spiral carinae.
The protoconch has only 1 whorl,
measuring 260 jum in diameter and it is
formed by two distinct phases: the first,
rough, has the nucleus and 3A of whorl,
and ends in a slight fhickening; in the
second phase, there are successive axial
thickenings, 8-10 in number, like axial
ribs, but keeping the surface rough. The
teleoconch has less than 2 Vi whorls, and
is delimited by two thick carinae which
angle the shell; the basal carina does not
protrude more than the peripheral.
Profile with the periphery flattened and
base concave.
Ornamentation formed by cells of
different shape and size, spirally
aligned; there are 8=9 spiral fines at the
beginníng of the teleoconch and, on the
last whorl, in apertural view, can be
19
Iberus , Suplemento 6, 2014
Figure 12A-D. Anticlimax umbiliglabra spec. nov. A-B: holotype, 1.75 mm (MNHN); C: proto-
conch of the holotype; D: microsculpture of the protoconch. Philippines, Panglao Island, Stn.
SI 1 , 2 m, in fine sand and seagrass.
Figura 12A-D. Anticlimax umbiliglabra spec. nov. A-B : holotipo , 1,75 mm (MNHN); C: protoconcha
del holotipo ; D: micro escultura de la protoconcha. Filipinas, Isla de Panglao, Stn. Sil, 2 m, en arena
fina y pradera.
observed 15 on the adapical parí, 20 on
the periphery and 20 on the base. Aper-
ture oval, prosocline; parietal callous
area with a thick coating; coíumella
externally reflected; outer lip thin, with
a sharp edge, presenting an extensión in
the area between the two carinae, which
give it a distinctive profile. Umbilicus
wide and deep; in the periumbilical area
there is a wide completely smooth strip,
without rows or cells; the umbilical
margin in the area cióse to the coíumella
forms a callus of triangular shape, on
whose surface run spiral cordlets.
Dimensions: the holotype measures
1.75 mm in diameter.
Habitat : The species was collected at
2 m, on a fine sand and seagrass bottom
(Stn. Sil).
Remarks : Anticlimax umbiliglabra spec.
nov. differs from A. faviformis spec. nov.
and A. simulans spec. nov. by having an
entirely rough protoconch, and 8-10 axial
ribs in the second phase; by having a
flattened periphery; because the basal
carina is not protruding, and because it
has a large smooth area, without cells or
groo ves, on the umbilical wall
20
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Table II. Differences between the species of group 2.
Tabla II. Diferencias entre las especies del grupo 2.
Group 2
Description: Shell wider than high (low
conic spire). Protoconch with 2 or more
phases; F2 with tubercles. Teleoconch:
periphery bicarinate; ornamentation of
spiral grooves in zigzag and wavelike ribs
on the base and the periphery; those of the
base may almost disappear; aperture tri¬
angular; outer lip expanded laterally by
the end of the carinae, of which the upper
one very attenuated at times. Umbilicus
with angled border.
Formed by 9 species: Anticlimax
fecunda, A. robusta, A. infaceta, A. bicornis ,
A. singularis, A. puncticulata , A. bicari-
nata, A. fijiensis, A. maranii. See Table II
for comparison.
Anticlimax fecunda spec nov. (Figures 4D, 13A-F, 14A-F)
Type material: Holotype MNHN 27176 (Figs. 4D, 13A-C).
Material examined: (2 s): New Caledonia: 1 s, Lifou, West-Southwest of Pointe d'Easo, Baie du
Santal, Loyalty Is., LIFOU 2000: Stn. 1430, 2G°47.5'S, 167°07.1,E, 20-25 m (holotype). Vanuatu: 1 s
(Fig. 14), NW Tutuba Island, SANTO 2006: Stn. DS108, 15°33.2'S, 167°16.6'E, 100 m.
Type locality: New Caledonia, Loyalty Is., West-Southwest of Pointe d'Easo, Baie du Santal, 20°47.5'S,
167°07.1,E, 20-25 m [LIFOU 2000: Stn. 1430].
Etymology: The specific ñame is related by the number of spiral cords which are few at the begirt
ning and increase during growth of the spire.
Distribution: Only known from the
type locality in New Caledonia, and
from NW Tutuba Island, Vanuatu.
Between 25 and 100 m.
Description : Shell small, robust,
formed by about 3 Vi whorls of rapid
growth, with a moderately depressed
spire, with two thick carinae angling the
shell; umbilicus broad and deep.
The protoconch is at a higher level
than the rest of the shell, measuring
between 280-310 jum, having 1 Va whorls
21
Iberus , Suplemento 6, 2014
§¡É
mÉMuÉm
wtiraa
Figure 13A-F. Anticlimax fecunda spec. nov. A-C: holotype, 2.24 mm (MNHN); D: apical view
and protoconch of the holotype; E-F: microsculpture, New Caledonia, Loyalty Islands, Baie du
Santal, West-Southwest of Pointe d’Easo, Stn. 1430, 20-25 m, parches (called “patates”) of coral
cióse to a sedimentary passage.
Figura 13A-F. Anticlimax fecunda spec . nov. A-C: holotipo, 2,24 mm (MNHN); D: visión apical y protoconcha
del holotipo; E-F: microescultura, Nueva Caledonia, lies Loyauté, Baie du Santal, Oeste-suroeste de Pointe
dEaso, Stn. 1430, 20-25 m, macizos (denominados “patates”) de coral próximos a un paso sedimentario.
22
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Figure 14A-F. Anticlimax fecunda spec. noy. A-C: shell, 1.93 mm MNHN; D: protoconch; E-F:
microsculpture. Vanuatu, NW Tutuba Island, Stn. DS108, 100 m.
Figura 14A-F. Anticlimax fecunda spec. nov. A-C: concha, 1,93 mm MNHN; D: protoconcha; E-F:
microescultura. Vanuatu, NO de la isla Tutuba, Stn. DS108, 100 m.
23
Iberus , Suplemento 6, 2014
and two distinct phases, the first totally
smooth and the second with some thick
tubercles that are concentrated closer to
the suture; it ends with a clear change of
sculpture. The teleoconch has about 2 Va
whorls, and two carinae, one peripheral
and the other basal, which angle the
shell which is completely covered by
spiral cords, with thick axial ribs on the
periphery and thick axial folds at the
base. In the 1 Va first whorls there are 5
not very prominent spiral cords that
develop in a zigzag pattern forming
rhomboid cells in their interspaces; later
the cords are multiplied, and at each
point of intersection with the axial striae
a small nodule is formed. In the spaces
between cords rnicrotubercles are not to
be observed; instead there is a network
of lines that criss-cross. On the adapical
part, the spiral cords predomínate, and
appear as granular from the first whorl
of the teleoconch due to the interference
with axial striae. More than 25-30 may
be observed on the last whorl. In the
area cióse to the peripheral carina there
are fine axial ribs that predominate on
the spiral cords.
The space between the peripheral
and the basal carinae is slightly concave
and presents 7-10 fine spiral cords Ínter-
sected by marked axial ribs. Base
slightly convex, totally covered with
fine spiral cordlets. There are 20-21 thick
axial folds and a cord that limits and
marks an angle with the umbilicus.
Aperture triangular; parietal area
covered by a thick callus; columella
angled, very thick and reflected towards
the umbilicus; outer lip thick, margin
unchanged by the spiral cords, but mod-
ified by the peripheral carina expanding
it laterally, forming two internal angles
at the point of contact with the carina.
Umbilicus wide and deep, delimited by
2 thick spiral cords; the cord located
inside is definitely thickened near the
inner lip and marks the beginning of the
columella; the more externa! cord,
located on the base, circumscribes the
umbilicus, marks the end of the col¬
umella and is formed by the angulation
of the axial folds. The umbilical wall is
slightly concave and on it, a completely
smooth area in the space between the
cords is observed.
Dimensions: the holotype is 2.24 mm
in diameter; the other shell studied is
l. 93 mm.
Habitat: The holotype was collected
in the infralittoral, living between 20-25
m, on a bottom of rounded coráis (called
"patates") cióse to an area of sediment.
Conversely, the shell from Vanuatu was
collected deeper, in the circalittoral,
dredged at 100 m depth.
Remar ks: The species is characterized
by the lack of complete axial ribs on the
adapical part; the shape of the aperture
and the lateral expansión, due to the
proximity of the peripheral carina; and
the axial, peripheral and basal ribbing.
Anticlimax fecunda spec. nov. may be
differentiated from A. robusta spec. nov.
by the larger size of the protoconch and
by lacking ornamentation on phase 1 of
the protoconch.
From Anticlimax infaceta spec. nov., it
is differentiated by the different orna¬
mentation of phase 2 of the protoconch
and by the lack of spirally aligue d cells
in the teleoconch.
Anticlimax robusta spec. nov. (Figures 4E, 15A-G)
Type material: Holotype MNHN 27179 (Figs. 04E, 15A).
Material examined: (3 s): Philippines. PANGLAO 2004: 1 s, Panglao Island, Napaling, Stn. S5,
9°37.1'N, 123°46.TE, 2-4 m, rock and coral patches, brown algae (Figs. 15B-C); 1 s, Panglao Island,
Pontod Islet, Stn. D4, 9°33.T'N, 123°44.0'E, 0-2 m, soft bottom with seagrass; 1 s, Balicasag Island,
Black Forest, Stn. S3, 9°31.1'N, 123°41.3'E, 6 m, edge of reef platform (type material).
Type locality: Philippines, Balicasag Island, Black Forest, 9°31.TN, 123°41.3'E, 6 m, edge of the reef
platform [PANGLAO 2004: Stn. S3] .
Etymology: The specific ñame is from robustas, - a , -um, "robust" as is shown by the sculpture of
the shell.
24
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 15A-G. Anticlimax robusta spec. noy. A: holotype, 2.46 mm, Philippines, Balicasag Island,
Stn. S3, 6 m (MNHN); B-C: shell, 2.2 mm, Napaling, Panglao Island, Stn. S5, 2-4 m (MNHN);
D: protoconch of the holotype; E: microsculpture of the holotype. F-G: detail of the microsculp-
ture of the protoconch.
Figura 15A-G. Anticlimax robusta spec. nov. A: holotipo, 2,46 mm, Filipinas, Isla de Balicasag, Stn.
S3, 6 m (MNHN); B-C: concha, 2,2 mm, Napaling, Isla de Panglao, Stn. S5, 2-4 m (MNHN); D:
protoconcha del holotipo ; E: microescultura del holotipo. F-G: detalle de la microescultura de la proto-
concha.
25
Iberus , Suplemento 6, 2014
Distribution : Only known from
Panglao and Balicasag Islands, Philip-
pines, between 2 and 6 m.
Description : Shell small (<2.5 mm),
robust in appearance, formed by 3 3á
quickly increasing whorls, with a mod-
erately depressed spire, bicarinate, and
with a wide and deep umbilicus.
The protoconch measures 270 jum,
has 1 Vi whorls with two distinct phases,
the first presenting, on a smooth back-
ground, 2 fine spiral cordlets formed by
microtubercles; the second part has
tubercles of different sizes scattered ran-
domly; it ends with a su d den change of
sculpture. The teleoconch has 2 !4
whorls and is bounded by two carinae,
one peripheral, the other basal; its
surface is completely covered by spiral
cords, with thick axial ribs on the
periphery and thick axial folds at the
base. The spiral cords show their inter-
spaces covered by axial striae and
aligned microtubercles that look like
strands of a lattice, giving the irnpres-
sion of developing in zigzag.
On the adapical part spiral cords pre¬
domínate which, by effect of the axial
striae, appear as granular from the first
whorl of the teleoconch and reaching more
than 30 on the last spiral whorl; in the area
near the peripheral carina fine axial ribs
predominate over the spiral cords. The
space between the peripheral and the basal
carinae is siightly concave and presents 7
fine spiral cords intersected by marked
axial ribs. Base is siightly convex, totally
covered by fine spiral cordlets, there are
17 thick axial folds and a thick cord that
limits and makes an angle with the umbili¬
cus. Aperture oval; parietal area covered
by a thick callus; columella straight, very
thick, not reflected; outer lip thick-walled,
margin remains unchanged by the spiral
cords, but modified by the peripheral
carinae which expand it laterally, forming
two internal angles at the point of contact
with the carinae.
Umbilicus wide and deep, limited
by 2 thick spiral cords; the cord located
inside, is widely thickened near the
inner lip and marks the beginning of the
columella; the more external cord,
located on the base, circumscribes the
umbilicus, marks the end of the col¬
umella and is formed by the angulations
of the axial folds. The umbilical wall is
more or less straight and on it more
weak axial folds and spiral grooves can
be observed.
Dimensions: the holotype is 2.46 mm
in diameter.
Habitat: Infralittoral species dredged
in 0-2 m, soft bottom with seagrass (Stn.
D4); suctioned at 2-4 m, rock and coral
patches, brown algae (Stn. S5) and at 6
m, at the edge of de reef platform (Stn.
S3).
Remarks : Anticlimax robusta spec. nov.
differs from A. fecunda spec. nov. by the
smaller size of its protoconch which has
2 fine spiral cordlets on its first phase.
From Anticlimax infaceta spec. nov. it
differs by the smaller diameter of the
protoconch, the larger size and smaller
number of tubercles of phase 2 and by
presenting heavy axial ribs between the
peripheral and the basal carinae.
Anticlimax infaceta spec. nov. (Figures 4F, 16A-G, 17A-B)
Type material: Holotype MNHN 27177 (Figs. 04F, 16A) and 2 paratypes MNHN 27178 (Figs. 17B- D).
Material examined: (3 s): Only from the type locality.
Type locality: Philippines, Bohol Island, Ubajan, 9°41.5'N, 123°51.0/E, 12 m, muddy bottom
[PANGLAO 2004: Stn. S27].
Etymology: The specific ñame is from the Latin word infacetas , -a, -um, which means "insipid, taste-
less", alluding to the scarce sculpture of the ventral part.
Distribution: Only known from the
type locality at 12 m.
Description: Shell small, robust,
formed by 4 whorls of rapid growth;
two thick carinae angle the shell; umbili¬
cus broad and deep.
The protoconch measures about 310
jum in diameter, has 1 % whorls and two
26
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 16A-G. Anticlimax infaceta spec. nov. A: holotype, 2.15 mm (MNHN); B: paratype, 1.8
mm (MNHN); C-D: paratype, 2.1 mm (MNHN); E: protoconch (holotype); F-G: microsculp-
ture. Philippines, Panglao Island, Stn. S27, 12 m, mud bottom.
Figura 16A-G. Anticlimax infaceta spec. nov. A: holotipo , 2,15 mm (MNHN); B: paratipo, 1,8 mm
(MNHN); C-D: paratipo, 2,1 mm (MNHN); E: protoconcha (holotipo); F-G: microescultura. Filip¬
inas, Isla de Panglao, Stn. S27, 12 m, fondo de fango.
27
Iberus , Suplemento 6, 2014
Figure 17A-C. Protoconchs. A-B: protoconchs of A. infaceta spec. nov. C: protoconch of A. singu-
laris spec. nov.
Figura 17A-C. Protoconchas. A-B: protoconchas de A. infaceta spec. nov. C: protoconcha de A. singu-
laris spec. nov.
distinct phases; the first is completely
smooth and the second has fine small
tubercles scattered over the whole
surface; it ends in a slight thickening.
The teleoconch has two spiral whorls
and is delimited by two carinae, one
being peripheral, the other, basal; orna-
mentation formed by flattened spiral
cords and sinuous axial lines that Ínter-
sect to form in their interspaces lines of
rounded cells covering the adapical part
and the periphery of the shell. On the
adapical part of the last whorl the cords
disappear over a wide strip, which
appears to be almost smooth.
Base convex, observed at the begin-
ning of last whorl, with thick axial ribs
that disappear in some areas from the
first quarter whorl, leaving only fine
growth lines; a thin cord defines and
angles the umbilicus. Aperture triangu¬
lar, oval; parietal area covered by a thin
callous coating; columella arched, very
thick, reflected towards the umbilicus
but not occluding it entírely; outer lip
thick-walled, margin unchanged by the
spiral cords, but modified by the
peripheral carina expanding it laterally,
forming two internal angles at the point
of contact with the carina. Umbilicus
28
RUBIO & RoláN: The genus Antiqñmax in the tropical Southwest Pacific
wíde and deep, with an angled edge
and straight wall, on which there are
fíne spíral cordlets and some axial
folds.
Dímensíonsi the holotype ís 2,15 mm
in máximum díameter.
Habitat Infralittoral species collected
at 12 m, on a muddy bóttom.
Remarles: Ánticlimax infaceta spec.
nov. differs from the remainíng species
of the group by ifs síze and the orna
mentation of the protoconch; by ladáng
axial ribs between the peripheral and
basal carínae and also by lackíng thíck
axial folds at íts base; the outer lip is not
so angled or as thíck as ín other species.
Anticlimax bicomis spec. nov. (Figures 4G, 18A-F)
Type material: Holotype MNHN 27129 (Figs. 04G, 18A-C).
Material examined: Only from the type locality.
Type locality: Solomon Islands, [gó40'S, 160°04'E/ 396-411 m [SALOMON 1: Stn. DW1762],
Etymology: The specifíc ñame alindes to the two horn like prominences in the aperture.
Distribution : Only known from
Solomon Islands, between 396-411 m.
Description: Shell sma.11 (< 2 mm),
robust, bícarinafe, formed by 3 % whorls
separated by a faint suture, with a
rather low spíre and widely umbílicate.
The protoconch is large in relation to
the dimensíons of the shell (about 25%),
with a líttle more than 2 whorls and about
380 jLtm ín díameter; ít has 2 parts, the fírst
(1 U whorls) completely smootli, and the
second (% of whorl) covered by axial
growth lines, more evident along the
suture and with randomly dístributed
tubercles; the termínatíon ís evident by
the change in sculpture of the teleoconch.
Thís has 1 V2 whorls and 2 strong períph-
eral carínae which angle the shell. Adapi¬
cal part convex, covered completely by
spiral cords that develop in zigzag; periph-
ery somewhat concave, covered by spíral
cords also ín zigzag, but without folds or
axial ribs. Base convex delimíted by the
peripheral carina, completely smooth
except cióse to the carina and showíng a
bread umbílícus which aliows the preví-
ous whorls to be seen. Aperture rounded.
prosocline; parietal area callous with a
thíck layer; columella arched, reflected
outward but without formmg callus; outer
lip not modífied by spíral cords, but the
peripheral carina angles and expands it
laterally. Very wide umbilícus, ínsíde
which there are marked growth lines and,
on the deeper umbilical wall area 3-4 spíral
cordlets.
Dimensíons: the holotype ís 1.66 mm
ín díameter.
Habitat: Bathyal species, dredged at
396-411 m depth on the slope.
Remarks : The species ís charaeterízed
by the size and decoration of the proto¬
conch, formed by randomly dístributed
micro-tubercles; the characterístic spíral
cords ín zigzag; the concave periphery
with ribs without axial folds; the base
lackíng spiral cords and a wíde umbílí¬
cus with fine cordlets insí de.
Most of the species of íts group have
peripheral prominences: the most
similar is Ánticlimax singularis spec. nov.,
but thís species has only one promi-
nence on the external lip and the proto¬
conch has a dístínctíve mícrosculpture.
Anticlimax singularis spec. nov. (Figures 41 T 17C, 19A-G)
Type material: Holotype MNHN 27195 (Figs, 4H, 19A-B).
Material examined: Only from the type locality.
Type locality: Philíppines, Bohol Island, Cortes, 9°43.3/N, 123°48.8'E, 126-135 m, in mud bottom
[FANGLAO 2004: Stn. T26].
Etymology: The spedfic ñame is due to the very strange sculpture of the protoconch, different from
all other species in the family.
29
Iberus , Suplemento 6, 2014
Figure 18A-F. Anticlimax bicornis spec. nov. A-C: holotype, 1.66 mm (MNHN): D: protoconch of
the holotype; E-F: microsculpture. Solomon Islands, Stn, DW1762, 396-411 m.
Figura 18A-F. Anticlimax bicornis spec. nov. A-C: holotipo, 1.66 mm (MNHN): D: protoconcha del
holotipo; E-F: micro escultura. Islas Salomón, Stn. DW1762, 396-411 m.
30
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Figure 19A-G. Anticlimax singularis spec. noy. A»B: holotype, 1.66 mm (MNHN): C; fragment of
the holotype; D: protoconch of the holotype, same as fig. 17C; E-F: mícrosculpture of the proto-
conch; D: mícrosculpture of the teleoconch. Philippines, Bohol Island, Stn. T26, 126-135 m.
Figura 19A-G. Anticlimax singularis spec, nov. A-B; hoíotipo , 1,66 mm (MNHN); C; fragmento del
holotipo ; D; protoconchá del hoíotipo, la misma de la fig. 17C E-F: microescukura de la pmtoconcha;
D: microescukura de la teleoconcha . Filipinas, Isla de Bohol \ Stn. T26, 126-135 m.
31
Iberus , Suplemento 6, 2014
Distrihution : Only known from the
Philippines, Panglao 2004, between 126-
135 m.
Description : Shell small (<2 mm),
wider than high, formed by 3 Vi whorls
separated by a slightly marked suture,
wíth a low spíre, wídely umbílicate.
The protoconch has a little more
than 2 whorls, measures about 390 jtim
in diameter and has three distínct
phases: the fírst one (nucleus and V2
whorl) is completely smooth; a second
phase of about Vi whorl is also smooth;
the third íncreases a little the diameter
and ís completely covered by oblique,
orderly línes in variable posítion; a few
growth línes at the end, The teleoconch
has just 1 % whorls and 2 carinae, one
peripheral, the other basal; the periph-
eral disappears ín the last quarter and
the basal is the most prominent of the
two.
The ornamentatíon is composed of
flattened spiral cords, ribs and axial
folds; there are rounded ce lis in the
ínterspaces between cords. On the
adapical parí., the spiral cords develop
ín zigzag; 7 cords at the beginning of
the teleoconch, íncreasing to 20-22 in
the last quarter-whorl, can be ob¬
servad between the peripheral carina
and the suture; no nodulose cordlets
are present but in the last quarter-
whorl axial ribs become more evident.
The space between the carinae has 10
spiral cordlets ín zigzag and rounded
cells in the ínterspaces, seen in an
apertural posítion; in the last half
whorl more than 40 fine axial ribs,
most evident over the basal carina, but
not forming folds, can be counted.
Spíre and base convex, the space
between the carinae slightly concave.
Base with evident axial folds that
extend from the basal carina towards
the umbílicus, penetrating insíde; at
the beginning there are some wíde and
flattened spiral cords íntersected by
weak axial folds.
Apertiire triangular; parietal area
covered by a thick callous coatíng; col-
umella arched and reflected towards the
umbílicus; adapical part of outer líp not
modifíed by the terminatíon of spiral
cords; irnique angle on lip whích corre-
sponds to the basal carina and expands
the aperture laterally. Umbílicus wíde
and deep, allowing the previous whorls
to be seen, not limited by a carina;
umbilical wall convex, smooth, wíth
weak axial folds.
Dímensíons: the holotype is 1.66 mm
ín diameter.
Habitat : Bathyal species trawled at
126-135 m, on a muddy bottom (Stn.
T26).
Remarks : The holotype was broken in
two píeces duríng study but there
remains enough to represen! the species
maínly because of the very uncommon
sculpture of the protoconch and so it ís
maíntaíned.
The species ís characterized by: the
decoratíon of the third phase of the pro¬
toconch; the presente of rounded cells
ín the spaces between the cords and the
carinae of the adapical part; the absenté
of nodules on the cords; the triangular
aperture and the presente of a unique
angle insíde the outer líp; the absence of
axial folds between the peripheral and
basal carinae.
The existente of three díííerent
periods or phases ín protoconch devel-
opment ís not common and we have no
explanation for them. In the present
species they seem to be very evident ín
the protoconch scars and sculpture.
Anticlimax puncticulata spec. nov. (Figures 41, 20A-F)
Type material: Holotype MNHN 27224 (Figs. 41, 20A) and 3 paratypes MNHN 27225 (Figs.
20B-D).
Material examined: (4 s): Only from the type locality.
Type locality: Philippínes, Bohol Island, Cortes, 9°41.8'N, 123°49.9/E, 80-100 m, reef slope with silt
[PANGLAO 2004: Stn. T18].
Etymology: The specific ñame alindes to the "micropunctate" aspect of the shell.
32
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Figure 20A-F. Antidimax puncticuíata spec. nov. A: holotype, 1.29 mm Stn A53 (MNHN): B-B:
paratype 1.37, 1.5 mm (MNHN); E-F: protoconchs from the paratypes. Phílippínes, Bohol
Island, Cortes, Stn. T18, 30-100 m.
Figura \20A~F. Antíclímax puncticuíata spec. nov. A: holotipo , 1,29 mm Stn Á53 (MNHN): B-D:
paratipos 137, 1,5 mm (MNHN); E-F: protoconchas de los paratipos. Filipinas, Isla de Bohol, Cortes,
Stn . TI 8, 80-100 m.
33
IberuSy Suplemento 6, 2014
Distribution : Only known from the
Philippines, Bohol Island, Cortes, Stn.
T18, 80=100 m.
Description: Shell very small (<1.5 mm),
wider than high, formed by 3 Vi whorls
separated by a slightly marked suture,
with a low spire, widely umbilicate.
The protoconch has 2 whorls, mea-
suring 340=370 jum in diameter and has
three distinct phases, the first phase and
the second phase, of about a half whorl,
are completely smooth; then appears a
third phase that is covered by small,
regularly distributed, elongated tuber-
cles. The teleoconch has 1 M whorl and 2
carinae; the basal carina is the more
prominen i, while the peripheral, which
develops in the last half whorl, may dis-
appear in some specimens.
The ornamentation is composed of
flattened spiral cords, axial ribs and
rounded cells in the spaces between the
cords. On the adapical part, the spiral
cords develop in zigzag, 4-5 cords can
be observed at the beginning of the
teleoconch and 15-16 on the last quarter-
whorl between the peripheral carina
and the suture; no nodulose cordlets are
apparent, while in the last quarter-
whorl the axial ribs become more
evident. The space between the carinae
has 5-6 spiral cordlets in zigzag and
rounded cells in their interspaces, seen
in an apertural position; in general, the
peripheral carina is scarcely developed:
in some specimens it may be observed
on the last quarter-whorl and in others
it hardly shows at all. Profile with a
convex spire and the space between the
carinae straight or slightly concave. Base
almost fíat, with evident axial ribs that
extend from the basal keel towards the
umbilicus, penetrating inside.
Aperture quadrangular, very wide;
parietal area with a marked angle and a
thin layer of callus that barely covers it;
columella arched, thickened at the base
and reflected towards the umbilicus,
forming thick folds on it; the adapical
part of outer lip not modified by the ter-
mination of spiral cords; the outer lip
shows a single angle which corresponds
to the basal carina and expands the
aperture laterally. The height and width
of the umbilicus allow the previous
whorls to be seen and the umbilical wall
is convex, with strong axial folds.
Dimensions: the holotype is 1.29 mm
in diameter. The largest shell measures
1.50 mm in diameter.
Habitat: Circalittoral species trawled
at 80-100 m, on a muddy bottom with
sponges (Stn. T18).
Remarles: Anticlimax puncticulata spec.
nov. is characterized by the ornamenta¬
tion of the third phase of the protoconch,
intermediate between A. infaceta and A.
singularis ; the presence of rounded cells in
the spaces between the adapical cords and
the periphery; the absence of nodules on
the cords; the presence or absence in the
last quarter of the whorl of a peripheral
carina; the large apertural square with a
unique angle in the inner part of the outer
lip; the absence of marked axial folds
between the peripheral and basal carinae;
the axial costulation on its base and inside
the umbilicus.
As in Anticlimax infaceta , A. singularis ,
A. bicornis, A. bicarinata and A. fijiensis ,
there are three different periods or phases
in the protoconch development of Anti¬
climax puncticulata. This is not a common
situation and we have no explanation for
it. In the present species it is very evident
in the protoconch scars and sculpture.
Anticlimax bicarinata spec. nov. (Figures 3 A, 21A-F)
Type material: Holotype MNHN 27121 (Figs. 5A, 21A-C).
Material examined: Only from the type locality.
Type locality: Vanuatu, 15°40'S, 167°2Q'E, 622-625 m [MUSORSTOM 8: Stn. DW1072].
Etyrnology: The specific ñame alindes to the presence of the two peripheral carinae in the last whorl.
Distribution: Only known from Description: Shell very small (<1.5
Vanuatu, between 622-625 m. mm), depressed, bicarinate and widely
34
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 21A-F. Anticlimax hicarinata spec. nov. A-C: holotype, 1.3 mm MNHN; D: protoconch of
the holotype; E-F: microsculpture. Vanuatu, MUSORSTOM 8: Stn. DW1072, 622-625 m.
Figura 21A-F. Anticlimax bicarinata spec. nov. A-C: holotipo, 1,3 mm MNHN; D: protoconcha del
holotipo; E-F: microescultura. Vanuatu, MUSORSTOM 8: Stn. DW1072, 622-625 m.
35
Iberus , Suplemento 6, 2014
umbilicate; formed by about 3 Va whorls
of rapid growth.
Protoconch large in relation to the
size of the shell, about 400 jum in díame¬
te r, having about 2 whorls; it is a pp ar¬
en tly smooth in the first 1 Vi whorls, and
the remaining granulóse part has very
small tubercles and terminates with a
change when the new sculpture of the
teleoconch begins. Teleoconch with 1 Va
whorls, having two peripheral carinae
located respectively near the adapical
part of the shell and delimiting the base;
straight edge. The whole teleoconch is
covered by spiral cords of regular size,
which develop in zigzag and are crossed
by thick axial growth lines that make up
a ty pical reticule.
Profile with spire and base convex,
periphery fíat. At the base, the spiral
cords are more flattened and less
prominent, disappearing when they
reach the last quarter of whorl. Aper-
ture oval, prosocline; parietal area
covered by a thin callous coating; col-
umella slightly tilted, not thickened or
reflected towards the umbilicus; outer
lip with smooth margin, modified and
expanded laterally by the presence of
carinae, which form two angles inter-
nally. Umbilicus wide, allowing the pre-
vious whorls to be seen, delimited by a
thin carina which angles it; on its inner
wall only fine growth lines can be
observed.
Dimensions: the holotype is 1.3 mm
in diameter.
Habitat : Bathyal species dredged at
622-625 m.
Remarks : Thís species is character-
ized by the large protoconch (>400 jum
diameter) in relation to the diameter of
the shell (31%); the shape and location
of the peripheral carinae; the reticulum
formed by cords in zigzag and axial
growth lines; the umbilicus is wide
and limited by a thin carina.
Anticlimax fijiensis spec. nov. has a
very different profile with two more
prominent carinae (see below).
Anticlimax fijiensis spec. nov. (Figures 5B, 22A-F, 23A-F)
Type material: Holotype MNHN (27122, Figs. 5B, 22A-B) and one paratype MNHN 27123 (Fig.
22C) from the type locality; another paratype MNHN 27124 (Figs. 23A-C) from Stn. DW1334, 251-
257 m.
Material examined: (3 s): Fiji, MUSORSTOM 10: 2 s, Stn. DW1333, 16°5Q'S, 178°12'E, 200-215 m
(type material); 1 s, Stn. DW1334, 16°51'S, 178°14'E, 251-257 m (paratype).
Type locality: Fiji, 16°50.36'S, 178°12.55'E, 200-215 m [MUSORSTOM 10: Stn. DW1333].
Etymology: The specific ñame is that of the archipelago where the species was collected.
Distribution : Only known from Fiji,
its type locality, Stn. DW1334 and
DW1333.
Description: Shell small (<2.0 mm), of
flattened aspect, bicarinate and widely
umbilicate; formed by 4 whorls of quick
growth.
The protoconch has more than 1 Va
whorls (almost 2), placed at a slightly
higher level than the teleoconch, mea-
suring 340 ¡im in diameter and having
two distinct phases; the first is com-
pletely smooth and the second is com-
pletely covered by a grainy surface of
regular size; there is no labial varix.
Teleoconch with just 1 Va whorls, bicari¬
nate with two small keels, one periph¬
eral and the other basal, the latter most
expanding the circumference of the shell.
Ornamentation formed by spiral cords in
zigzag, axial ribs and cells of different
shape in the Ínter spaces between cords.
On the adapical part, initially 5
zigzagging spiral cords can be observed
that cross with axial striae to form
rounded cells in the interspaces between
the cords; on the last whorl the cords,
numbering 23 between suture and
peripheral keel, have small granules
that give a characteristic appearance.
The space between the keels is concave
and on it the spiral cords are crossed by
36
RUBIO & RoláN: The genus Anticlirnax in the tropical Southwest Pacific
Figure 22A-F. Anticlimax fijiensis spec. nov. A-B: holotype, 1.64 mm MNHN; C: paratype5 1.6
mm (MNHN); D: protoconch of the holotype; E-F: microsculpture. Fiji, MUSORSTOM 10:
Stn. DW1333, 200-215 m.
Figura 22A-F. Anticlimax fijiensis spec. nov. A-B: holotipo, 1,64 mm MNHN; C: paratipo, 1,6 mm
(MNHN); D: protoconcha del holotipo; E-F: micro escultura. Fiyi, MUSORSTOM 10: Stn. DW1333,
200-215 m.
37
Iberus , Suplemento 6, 2014
Figure 23A-E Anticlimax fijiensis spec. nov. A-C: paratype, 1.76 mm MNHN; D: protoconch; E-
F: microsculpture. Fiji, MUSORSTOM 10: Stn. DW1334, 251-257 m.
Figura 23A-F. Anticlimax fijiensis spec. nov. A-C: paratipo, 1,76 mm MNHN; D: protoconcha; E-F:
microescultura. Fiyi, MUSORSTOM 10: Stn. DW1334, 251-257 m.
38
RUBIO & RoláN: The gemís Anticlimax in the tropical Southwest Pacific
fine sinuous axial ribs, formíng cells in
the interspaces.
Base convex, with axial ribs that
extend from the basal keel on the edge
of the umbilicus and rounded cells over
its entire surface. Umbilicus wide and
deep, allowing the previous whorls to
be seen; on the umbilical wall there are
some spiral cordlets and marked growth
lines. Aperture triangular, outer lip
expanded laterally, with two internal
angles corresponding to the carinae;
parietal area covered by a thin callous
coating; columella arched, thin edge d.
not reflected.
Dimensions: the holotype measures
1.64 mm in máximum diameter.
Habitat : Bathyal species dredged at
200-257 m.
Remarles: The characters of this
species which allow us to distinguish it
from other species of its group are the
fine granulation of the end of the proto-
conch and the concavity of the space
between the two carinae. From Anticli¬
max reinaudi spec. nov. it also differs in
lacking axial folds on the space between
the carinae. A. bicarinata spec. nov.
differs in having a flatter spire and in
the greater prominence of its carinae.
Anticlimax maranii spec. nov. (Figures 2B-E, 5C, 24A-F, 25A-H)
Type material: Holotype MNHN 27132 (Figs. 5C, 24A-C).
Material examined: (2 spms, 1 s): Philippines, PANGLAO 2004: 1 s, Panglao Island, Napaling, Stn.
B9, 8-10 m, caves in the reef wall (type material); 1 spm, Panglao Island, Doljo Point, Stn. B12,
9°35.6/N, 123°43.2,E, 24-27 m, reef slope; 1 spm, Panglao Island, Napaling, Stn. B21, 9°37.2'N,
123°46.4,E, 20-21 m, reef wall with small caves (Fig. 25).
Type locality: Panglao Island, Napaling, Philippines, 9°33.1'N, 123°44.0'E, 8-10 m, caves in the reef
wall [PANGLAO 2004: Stn. B9].
Etymology: This species is named after Gilberto Marani, informatics technician in the MNHN mala-
cology group, in recognition to his behind-the-scene contribution for maps, tables and graphs in
many malacological papers.
Distribution: Only known from Panglao
Island, Philippines, between 10 and 24 m.
Description: Shell small (<2 mm),
wider than high, formed by 3 Vi whorls
separated by an indistinct suture, with a
low spire, widely umbilicate.
The protoconch has 1 % whorls, mea-
suring about 330 jum in diameter and with
two distinct phases, the first one being
completely smooth while the second phase
is covered by a comma-shaped sculpture;
there is no thickening. The teleoconch has
1 3á whorls and 3 carinae, one peripheral,
one basal and one periumbilical. The oma¬
men (ation is composed of spiral cords,
ribs, axial folds and rounded cells in the
spaces between the cords.
On the adapical part, the spiral cords
cross the axial striae, with 5-6 cords
developed in zigzag on the first spire
whorl; in the last Vi whorl, about 15
nodulose cordlets can be seen.
The space between the carinae has 15
spiral cordlets, viewed in an apertural posi
tion; on the last whorl more than 40 axial
folds can be counted. Dorsum and base
are convex, the spaces between carinae are
concave. Base with a smooth wide area
near the basal carina and 5-6 wide and
narrow spiral cords intersected by weak
axial folds; a third periumbilical carina
angles and limits the umbilicus.
Aperture quadrangular; parietal area
covered by a thick callous coating; col¬
umella arched and reflected towards the
umbilicus; adapical part of the outer lip
is crenulated externally by the termina-
tion of the spiral cords; in the periphery
there are two angles that correspond to
each of the carinae; the larger angle cor-
responds to the basal carina and
expands the aperture laterally. Umbili¬
cus wide and deep, allowing the previ¬
ous whorls to be seen, limited by a
carina which angles it; umbilical wall
convex, smooth, with growth lines.
Dimensions: the holotype is 1.80 mm
in diameter.
39
Iberus , Suplemento 6, 2014
Figure 24A-F. Anticlimax maranii spec. nov. A-C: holotype, 1.8 mm (MNHN): D: protoconch
(holotype); E-F: microsculpture. Philippines, Panglao Island, Napaling, Stn. B9, 8-10 m.
Figura 24A-F Anticlimax maranii spec. nov. A-C: holotipo, 1,8 mm (MNHN): D: protoconcha
(holotipo); E-F: microescultura. Filipinas, Isla de Panglao, Napaling, Stn. B9, 8-10 m.
40
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 25A-H. Anticlimax maranii spec. nov. A-C: shell, 1.6 mm: D: protoconch; E-F: microsculp-
ture; G: microsculpture of the protoconch; H: operculum. Philippines, Panglao Island, Napaling, Stn.
B21, 20-21 m.
Figura 25A-H. Anticlimax maranii spec. nov. A-C: concha, 1,6 mm: D: protoconcha; E-F: microescultura;
G: microescultura de la protoconcha; H: opérculo. Filipinas, Isla de Panglao, Napaling, Stn. B21, 20-21 m.
41
Iberus , Suplemento 6, 2014
Table III. Differences between species of group 3
Tabla III: Diferencias entre las especies del grupo 3 .
Operculum fine, multispiral and
with central nucleus (Figs. 2B-C) charac-
teristic of the species of Vitrinellidae.
Radula (Figs. 2D-E) taenioglossate,
formula 2-1-R-1-2. Central tooth very
wide; cutting edge with a main rounded
central cusp and 3 smaller cusps at each
side; lateral edges expanded and thick-
ened, free from the rest of base for most
of their length; base with a pair of denti-
cles, ventral enlargement with a well
developed U-like shape.
Lateral tooth elongate, similar to
central one, but its base lacks denticles;
cutting edge rather long, with a main
central cusp and 6-7 smaller cusps at
each side.
Marginal teeth long, curved; inner
marginal tooth with 7-8 small cusps on
the upper third of its outer edge; outer
marginal tooth similar in shape and size
to the inner marginal teeth, but lacking
cusps.
Habitat : Infralittoral species collected
by brushing at 8-10 m, inside caves in
the reef wall (Stn. B9); at 24-27 m, on the
reef slope (Stn. B12) and at 20-21 m in a
reef wall with small caves (Stn. B21).
Remarks : The lower prominent carina
with more distinct axial sculpture on its
lower part is very characteristic of this
species, and not present in others of its
group. In some shells this prominence is
attenuated.
The radula of Anticlimax maranii is
typical of Rissooidea or Truncatel-
loidea, and shows a great similarity
with that of Nozeba topaziaca (Hedley)
(in Ponder, 1984: 55, fig. Fl). This cióse
relationship between Tornidae and
Nozeba, has recently been proven by
Criscíone & Ponder (2013) after a
phylogenetic analysis of species of
Circulus, Pseudoliotia and Nozeba,
among others.
Another species which shows a great
similarity in its radula and operculum is
Cyclostremiscus calameli (Jousseaume,
1872), a vitrinellid of the western coast
of Africa (in Rolan & Rubio, 2002).
It is also very similar to the radula of
Tornus subcarinatus (Montagu, 1803),
type species of the genus (in Rolan &
Rubio, 2002), but the operculum of this
species is oval and paucispiral, with a
subcentral nucleus.
42
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Group 3
Description : Low conic spire, shell wider
than high. Protoconch: F2 with tubercles
or fine short threads. Teleoconch: bicari-
nate; usually with strong axial folds
between the peripheral carina and the basal
one; the adapical part covered by cords or
by spiral grooves. Aperture quadrangular.
This group is formed by 10 species:
A. reinaudi, A. serrata , A. tamarae, A.
aitormonzoi, A. cyclist, A. dentata, A. elata,
A. solomonensis, A. fastigata and A. rhi-
naceros.
Table III with their most important
differential characters may be useful.
Anticlimax reinaudi spec. nov. (Figures 5D, 26A-F)
Type material: Holotype MNHN 27120 (Figs. 5D, 26A-C).
Material examined: Only of the type locality.
Type locality: Vanuatu, NE Malo Island, 15°38.5'8, 167°15.1'E, 13 m, sand and dead coráis [SANTO
2006: Stri. DB86].
Etymology: This species is named after Guy Reinaud, Presiden! of Pro-Natura International, co-
organiser with MNHN of the "Our Planet Reviewed" expeditions.
Distribution : Only known from
Vanuatu at 13 m.
Description: Shell very small (<1.5
mm), depressed, formed by 3 whorls of
rapid growth, separated by a scarcely
marked suture; carínate, widely umbili-
cate and with thick axial folds.
Protoconch about 370 jum in diameter
and with 1 3A whorls; the nucleus and the
first % of whorl are smooth, the remain-
ing whorl is covered by coarse granules of
different sizes, randomly distributed; the
end of the protoconch is evident. The teleo-
conch has a little more than 1 whorl; two
marked carinae angle the periphery and
a third one outlines the umbilicus. Spire
convex, periphery and base almost fíat.
Ornamentation formed by spiral cords,
ribs and axial striae. On the adapical part
the cords cross the axial striae forming
little raised nodules; on the periphery, the
number of cords increases, they are finer
and more numerous, but the axial striae
domínate; at the base, which is almost fíat,
there are numerous, fine spiral cords and
axial ribs that increase as they get closer
to the umbilicus, but fade on the last part
and do not form folds.
Aperture quadrangular; on its edge
there are four angulations: one in the
parietal area; another at the intersection
of the columella with the umbilical
carina and two more produced by the
peripheral carinae that modify the outer
lip. Only a slight callous layer covers the
parietal area; the columella is virtually
straight, not reflected or thickened; the
outer lip is not very thick. Umbilicus
large allowing the previous whorls to be
seen, limited by a carina that angles
forming a funiculus; on this wall slight
traces of spiral cords can barely be
observed.
Dimensions: The holotype is 1.26
mm in diameter.
Habitat: Infralittoral species found at
13 m on a sand and dead coral bottom.
Remarks: The most similar species to
Anticlimax reinaudi spec. nov. is Anticli¬
max serrata spec. nov., from which it
differs by the lower number of spiral
cords on the adapical part; its straight
columellar edge; the double angle
observed on the outer lip, formed by the
peripheral carinae, and by having a wide
umbilicus delimited by another carina.
Anticlimax serrata spec. nov. (Figures 5E, 27A-H)
Type material: Holotype MNHN 27125 (Figs. 5E, 27A). Paratypes: 1 s MNHN 27126, (Figs. 27B-D)
from Palikulo Bay, Vanuatu, Stn. DB53, 5 m and 1 s MNHN 27127, from S Aoré Island, Vanuatu,
Stn. DB12, 10-18 m.
43
Iberus , Suplemento 6, 2014
Figure 26A-F. Anticlimax reinaudi spec. nov. A-C: holotype, 1.26 mm (MNF1N); D: apical view
and protoconch (holotype); E-F: microsculpture. Vanuatu, NE Malo Island, Stn. DB86, 13 m.
Figura 26A-E Anticlimax reinaudi spec. nov. A-C: holotipo, 1,26 mm (MNHN); D: vista apical y
protoconcha (holotipo); E-F: microescultura. Vanuatu, NE Isla de Malo, Stn. DB86, 13 m.
44
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Figure 27A--H. Antidimax serrata spec. nov. A: holotype, 2.47 mm5 Vanuatu, S coast of Santo Island,
Belmoul lagoon* Stn. LS2? 3 m (MNHN); B~D: paratype, 2.3 mm3 Palikulo Bay, Vanuatu, Stn.
DB53, 5 m (MNHN); E: apical view and protoconcli (holotype); F-H: microsculpture and detall.
Figura 27A-H. Anticlimax serrata spec. nov. A; hoíotipo , 2,47 mm, Vanuatu , costa sur de la Isla de Santo ,
laguna Belmoul Stn . LS2, 3 m (MNHN); B-D: paratipo , 2.3 mm, Bahía de Palikulo , Vanuatu, Stn .
DB53 , 5 m (MNHN); E: vista apical y protoconcha (hoíotipo); F-H: micnescultura y detalle „
45
Iberus , Suplemento 6, 2014
Material examined: (3 s): Vanuatu, SANTO 2006: 1 s, Belmoul lagoon, S coast of Santo Isl., Stn. LS2,
15°35.5'S, 167°06.2'E/ 3 m (holotype); 1 s, Palikulo Bay, Stn. DB53, 15°28.8'S, 167°15.2,E/ 5 m (paratype);
1 s, S Aoré Island, Stn. DB12, 15°36.6'S, 167°10.1,E/ 10-18 m (paratype).
Type locality: Vanuatu, Belmoul lagoon, S coast of Santo Isl., 15°35.5,S, 167°06.2'E, 3 m [Exp. SANTO
2006: Stn. LS02].
Etymology: The specific ñame alludes to the prominent thick folds of the curved basal area, like a
serration.
Distribution : Only known from
Vanuatu, between 3 and 10 m.
Description: Shell small (<2.5 mm),
wider than high, formed by nearly 4
whorls separated by a hardly marked
suture, with a low spire, narrowly
umbilicate.
Protoconch with about 1 % whorls,
measuring about 310 jum, completely
smooth in its initial part and presenting
thick tubercles of variable size in the
remaining whorl, ending in a scar at the
beginning of the teleoconch.
The teleoconch has almost 2 !4
whorls and 2 peripheral carinae, the
lower one at first bluntly rounded and
becoming more acute towards the end.
The ornamentation is composed of spiral
cords, ribs and axial folds. The spiral
cords, starting at the first whorl, intersect
with the axial striae, developing in
zigzag and also into nodulose cordlets.
On the last whorl, starting from the
peripheral carina, 20 heavy axial ribs run
towards the base. These ribs are proso
cline, continued on the basal peripheral
carina, over which they develop into
thick folds. The base is slightly concave
and on it there are thick axial ribs located
next to the curved basal area and spiral
cordlets in its central area.
Aperture rounded; parietal area
covered by a callous coating, forming an
angle at the junction with the outer lip;
colurnella thick and reflected towards the
umbilicus, occluding it progressively; the
colurnella forms an expanded area at the
intersection with the outer lip, which has
a smooth margin and a strong angle at
the termination of the basal carina.
Umbilicus narrow and deep, not
delimited by a spiral cord; small axial
ribs can be observed inside.
Dimensions: the holotype is 2.47 mm
in diameter.
Habitat : Infralittoral species found
between 3 and 18 m depth.
Remarks : The most evident charac-
ters are the short and prominent axial
ribs at the periphery, not present in any
of the other known species, except A .
elata (see below).
Anticlimax tamarae spec. nov. (Figures 5F, 28A-F, 29A-F)
Type material: Holotype MNHN 27128 (Figs. 5F, 28A-B).
Material examined: (3 s): Solomon Islands: 1 s, SALOMON 1: Stn. CP1858, 9°37.Q'S, 160°42'E, 435-461
m (type material). Philippines: 2 s, PANGLAO 2005: Stn. DW2371, 8°35/N, 123°16'E, 172-175 m.
Type locality: Solomon Islands, 9°37.0/S, 160o42'E, 435-461 m [SALOMON 1: Stn. CP1858].
Etymology: The specific ñame is after Tamara Prieto Hernández, Galician biologist who was study-
ing Bioinformatics in the Autonomous University of Barcelona and Genómica in Xenética in the
University of Vigo.
Distribution : Only known from the
Solomon Islands, between 435-461 m
and the Philippine Islands, between 172-
175 m.
Description : Shell very small (>1.5
mm), depressed, solid, bicarinate, and
widely umbilicate.
Protoconch measuring about 340 jum,
with more than 1 3A whorls and 2 distinct
phases separated by an evident scar line;
the first Vi whorl is completely smooth
and the rest is covered by growth lines,
tubercles of different sizes and small
spiral threads that are grouped in the
suture zone, sometimes obliquely. Teleo¬
conch with 1 3A whorls and two periph¬
eral carinae, one in prolongation of the
suture and the other basal, which angle
46
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 28A-F. Anticlimax tamarae spec. nov. A-B: holotype, 1 .65 mm (MNHN); C: apical view and pro-
toconch of the holotype; D-F: microsculpture and detall. Solomon Islands, Stn. CP 1858, 435-461 m.
Figura 28A-F. Anticlimax tamarae spec. nov. A-B: holotipo, 1,65 mm (MNHN); C: vista apical y pro-
toconcha del holotipo; D-F: micro escultura y detalle. Islas Salomón, Stn. CP 1858, 435-461 m.
the shell The shell is completely covered
by spiral cords of different sizes that
develop in zigzag and cross with the
axial growth Unes forming a reticule. The
adapical part is covered by spiral cords,
wider on the central area and narrower
near the suture and the peripheral areas.
The periphery between the carinae is
completely covered by spiral cords; thick
sinuous axial folds develop between both
carinae, which seen apically give a star-
shaped profile to the shell.
The base is slightly convex and has
very broad and low spiral cords.
47
Iberus , Suplemento 6, 2014
Figure 29A-F. Anticlimax tamarae spec. nov. A-C: shell, 1.7 mm (MNHN); D: protoconch; E-F:
microsculpture. Philippines, PANGLAO 2005, Stn. DW2371, 172-175 m.
Figura 29A-E Anticlimax tamarae spec. nov. A-C: concha , 1,7 mm (MNHN); D: protoconcha; E-F:
microescultura. Filipinas, PANGLAO 2005, Stn. DW2371, 172-175 m.
Umbilicus wide allowing the previous
whorls to be seen, completely covered
inside by spiral cords. Aperture oval,
prosocline; parietal area with a thick
callous coating; columella arched, very
reflected towards the umbilicus; outer
lip modified by the spiral cords but
mainly by the peripheral carinae which
angles it internally and prolong it later-
ally.
48
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Dimensions: the holotype is 1.65 mm
in diameter.
Habitat : Bathyal species dredged at
435-461 m in the Solomon Islands and at
172-175 m in the Philippines.
Remarks : The species is character-
ized by the large size and ornamenta-
tion of its protoconch; the axial folds
that develop between the peripheral
carinae; the spiral cords in zigzag
which are more evident on the peri-
phery; the large umbilicus fully covered
inside by spiral cords. No other species
looks like this.
Anticlimax aitormonzoi spec. nov. (Figures 5G, 30A-F, 31A-G)
Type material: Holotype MNHN 27130 (Figs. 5G, 30A- B) and 8 paratypes M.NHN 27131 (Fig, 30C-D).
Material examined: (34 s): Philippines. PANGLAO 2004: 9 s, Panglao Island, off San Isidro, Sin.
T9, 9°33.5'N- 9°33.9'N, 123°49.5'-123°50.5'E, 97-120 m, fine sand with seagrass (type material); 3 s,
Between Panglao and Pamílacan Island, Stn. T27, 9°33;N, 123°5TE, 106-137 m, fine sand and mud
with echinoderms; 2 s, Bohol Island, Cortes, Stn. T26, 9°43'N, 123°49,E, 123-135 m, mud; 5 s, Panglao
Island, Bolod, Stn. T2, 9°32'N, 123°48'E, 152 m, coarse sand; 1 s, Panglao Island, Pontod Islet, Stn.
D4, , 9°33.TN, 123°44.0'E, 0-2 m, soft bottom with seagrass; 2 s, Bohol Island, west Baclayon, Stn.
T7, 9°36.1,N, 123°53.3'E, 61-62 m, muddy fine sand; 2 s, Panglao Island, off San Isidro, Philippines,
Stn. TIO, 9°33.4'N-9°33.8'N, 123°49.6/-123°5 1.5'E, 117-124 m, mud and fine sand; 8 s, Bohol Island,
west of Baclayon, Stn. T6, 9°35.1/N, 123°51.2'E, 34-82 m, coarse muddy sand with large sponges; 1
s, Bohol Island, Cortes, Stn. T18, 9041.8'N, 123°49.9'E, 80-100 m, muddy bottom with sponges; 1 s,
Panglao Island, Biking, Stn. SI, 9°35.3'N, 123°50.5'E, 5 m, reef slope with overhangs.
Type locality: Philippines, Panglao Island, off San Isidro, 9°33.5-33.9'N, 123°49.5-50.5/E, 97-120 m,
fine sand with seagrass [PANGLAO 2004: Stn. T9].
Etymology: The specific ñame is after the grandson of the first author Altor Monzó.
Distribution : Only known from
Panglao and Bohol islands, Philippines,
between 2 and 152 m.
Description: Shell small {<2.7 mm),
formed by 4 14 whorls separated by a
slightly marked suture; the shell is
wider than high, with a low spire and
narro wly umbilicate.
The protoconch has a little more
than 2 whorls, measures about 410 jum
in diameter, is completely smooth on its
initial part and has fine tubercles on the
remaining whorl, without any terminal
thickening. The teleoconch has 2 whorls
and 2 carinae, one peripheral, the other
basal. The ornamentation is composed
of spiral cords, axial folds and rounded
cells in the spaces between the cords. On
the adapical part, the first spire whorl
bears 4-5 spiral cords which develop in
zigzag Crossing the axial striae. Nodu-
lose cordlets appear after the first whorl,
26 on the last Vi whorl; in the area near
the peripheral carina, sinuous axial ribs
predominate over the cords.
The space between carinae has 15
spiral cordlets as seen in apertural posi-
tion. On the last half whorl, 20-22 thick
folds appear on the lower peripheral
carina being more prominent those near
the end of the whorl. Base with short
axial folds, and thin growth lines.
Aperture quadrangular; parietal area
covered by a broad callous layer; col-
umella arched, thick and reflected
towards the umbilicus; the outer lip has
a smooth margin and two angles, the
most prominent is situated at the level
of the basal carina and prolongs the lip
laterally. Umbilicus funnel-shaped,
narrow and deep, not bounded by a
spiral cord, inside there are 2-3 spiral
cordlets.
Dimensions: the holotype is 2.76 mm
in diameter; the larger photographed
paratype is 2.6 mm.
Habitat: Species of wide bathymetric
distribution, found in infra-circalittoral
levels. Dredged at 0-2 m, in soft bottom
with seagrass (Stn. D4) and trawled at
152 m, in coarse sand bottom (Stn. T2);
at 61-62 m, in muddy fine sand bottom
(Stn. T7); at 97-120 m, in fine sand with
seagrass (Stn. T9); at 117-124 m, in mud
49
Iherus , Suplemento 6, 2014
Figure 30A-F. Anticlimax aitormonzoi spec. nov. A-B: holotype, 2.76 mm (MNHN): C-D:
paratypes, 2.6, 2.4 mm (MNHN); E: protoconch of a paratype; F: microsculpture. Philippines,
Panglao Island, ofF San Isidro, Stn. T9, 97-120 m.
Figura 30A-F Anticlimax aitormonzoi spec. nov. A-B: holotipo, 2,76 mm (MNHN): C-D: paratipos,
2,6, 2,4 mm (MNHN); E: protoconcha de un paratipo; F: microescultura. Filipinas, Isla de Panglao,
frente a San Isidro, Stn. T9, 97-120 m.
and fine sand bottom (Stn. TIO); at 123-
135 m, in mud bottom (Stn. T26) and at
106-137 m, in fine sand and mud bottom
with echinoderms (Stn. T27).
Remarles: The differences with the
most similar species are: Anticlimax
bicornis spec. nov. has a wider umbilicus
and its periphery lacks prominences; A.
serrata spec. nov. has prominences all
over the periphery of the last whorl and
its umbilicus is more sculptured; A. rein-
audi spec. nov. has a fíat periphery, an
angled funnel shaped umbilicus and a
more sculptured protoconch.
50
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 31A-G. Anticlimax aitormonzoi spec. nov. A-B: shell, 2.18 mm (MNHN); C: paratype,
2.55 mm; D: protoconch; E-G: microsculpture and detail. Philippines, between Panglao and
Pamilacan Island, PANGLAO 2004, Stn. T27, 106-137 m, fine sand and muddy bottom with
echinoderms.
Figura 31A-G. Anticlímax aitormonzoi spec. nov. A-B: concha, 2,18 mm (MNHN); C: paratipo,
2,55 mm; D: protoconcha; E-G: microescultura y detalle. Filipinas, entre las islas de Panglao y Pami-
lacán, PANGLAO 2004, Stn. T27, 106-137 m, arena fina y fango con equinodermos.
51
IberuSy Suplemento 6, 2014
Anticlimax cyclist spec. nov. (Figures 2F-G, 5H, 32A-G, 33A-F, 34A-F)
Type material: Holotype MNHN 27226 (Figs. 5H, 32A-C) and one paratype MNHN 27227.
Material examined: (4 s): Philippines. PANGLAO 2004: 2 s, Panglao Island, Looc, Stn. S32, 9°35.8'N,
123°44.6'E, 2-3 m, hard platean with sand covering rocks (type material). Papua New Guinea,
PAPUA NIUGINI: Stn PS43, 1 s, S Urembo I., 5°14.7'S, 145°47.4'E/ 14 rn, outer slope; 1 s, Bilbil Island,
Stn. PB29, 5°18'S, 145°46.1'E, 17 m
Type locality: Panglao Island, Looc, 9°35.8'N, 123°44.6'E, 2-3 m, hard platean with sand covering
rocks [PANGLAO 2004: Stn. S32],
Etymology: The specific ñame refers to the bicycle which has a similar toothed wheel.
Distribution: Only known from the
Philippines, between 2-3 m, and Papua
New Guinea, between 14 and 17 m.
Description: Shell small (>2 mm),
wider than high, formed by 3 Vi whorls
separated by a marked suture, with a
low spire, widely umbilicate.
The protoconch has 1 3á whorls,
measuring about 320 jum in diameter
and having two distinct phases; the first
is completely smooth and the second is
covered by thick tubercles. There is no
clear separation with the teleoconch
except by the change of sculpture. The
teleoconch has 2 whorls and 3 carinae,
one perípheral, one basal and one peri-
umbilical. The ornamentation is quite
complex; it is composed of spiral cords,
ribs and axial folds; rounded cells in the
spaces between ribs and a filiform mesh
occupying the cells.
On the adapical part, the spiral cords
cross with axial striae in the first whorl
to form 7 cords that develop in zigzag
and show rounded cells between the
cords; on the last whorl the ribs are
more evident and intersect with the
spiral cordlets to form small nodules;
LJp to 22-24 cords can be seen on the last
half whorl.
The space between carinae (periph-
eral-basal) shows more than 30 fine
spiral cordlets in apertural view; on the
last whorl there are 20-22 thick axial
folds on the the basal carina, which are
projecting further than the periphery.
Spire and base are convex, the space
between the carinae is concave. Base is
completely smooth on the last whorl; in
previous whorls the axial ribs are pre¬
dominan! over spiral cords, with a
groove-like space between the cords,
limited by the axial ribs. A third carina.
periumbilical, angles and limits the
umbilicus.
Aperture quadrangular; parietal area
covered by a thick callous coating, with
an angle at the point of unión of the
outer lip with the previous whorl; col-
umella arched and reflected towards the
umbilicus; adapical part of outer lip
crenulated externally by the the termi-
nation of the spiral cords; on it there are
two angles that correspond to each of
the carinae; the greater angle corre-
sponds to the basal carina and expands
laterally the aperture. Umbilicus height
and width, which allows the previous
whorls to be seen,limited by a cama that
angles it; umbilical wall convex, smooth,
with fine growth lines.
External anatomy: The soft parts (Fig.
2F-G) are here described based on the pho-
tographs of a living individual of Anticli¬
max cf. cyclist spec. nov. from SANTO
[DSCN1661]. The head has a long and
narrow snout, bilobed distally and a little
depressed. Long cephalic tentacles finely
ciliated in their distal half are observed
with an eye on a slight basal bulge. We
could not see any palliai tentacles on the
right side. The anterior end of the foot is
expanded into small lateral projections;
posteriorly the foot is rounded, no metapo-
dial tentacle was observed. Opercular lobe
simple; there are no tentacles associated
with the opercular lobe.
Colour: the buccal mass and an area
behind the eyes are palé red. Head,
snout, foot and cephalic tentacles are
translucent with opaque white flecks.
The early whorls of live specimens
are brown from the digestive gland
showing through the shell.
Dimensions: the holotype is 2.68 mm
in diameter.
52
RUBIO & RoláN: The genu s Anticlimax in the tropical Southwest Pacific
Figure 32A-G. Anticlimax cyclist spec. nov. A-C: holotype, 2.68 mm (MNFiN); D: umbilical view;
E: protoconch of the paratype; F-G: microsculpture. Panglao Island, Baclayon, Philippines, Stn.
S32, hard bottom with sand covering rocks, at 2-3 m.
Figura 32A-G. Anticlimax cyclist spec. nov. A-C: holotipo, 2,68 mm (MNHN); D: vista umbilical; E:
protoconch a del paratipo; F-G: microescultura. Isla de Panglao, Baclayon, Filipinas, Stn. S32, fondo
duro con arena cubriendo las rocas, a 2-3 m.
53
Iherus, Suplemento 6, 2014
Figure 33A-F. Anticlimax cyclist spec. nov. A-C: shell, 3.0 mm; protoconch; E-F: microsculpture
and detail. Papua New Guinea, S Urembo Island, Stn. PS43, 14 m.
Figura 33A-F Anticlimax cyclist spec. nov. A-C: concha , 3,0 mm; protoconcha; E-F: microescultura y
detalle. Papua Nueva Guinea, S de la Isla de Urembo, Stn. PS43, 14 m.
Habitat : Infralittoral species collected
in Philippines by suction on hard
plateau with sand covering rocks, at 2-3
m (Stn. S32). In Papua New Guinea it
has been dredged at 14 m (Stn. PS43)
and 17 m (Stn. PB29).
Remarks: The species is characterized
by the low spire; the spiral cords that
are nodulose on the adapical part; the
filiform ornamentation that mns
through the cells and the completely
smooth base.
The species with which it has more
similarity is Anticlimax maranii spec.
nov. which differs by the adapical nodu¬
lose cords; the greater number of spiral
cordlets and smaller number of axial
folds in the space between the periph-
54
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 34A-F. Anticlimax cyclist spec. nov. A-C: shell, 2.3 mm; D: protoconch; E-F: microsculpture
and detail. Papua New Guinea, Bilbil Island, Stn. PB29, 17 m.
Figura 34A-F. Anticlimax cyclist spec. nov. A-C: concha, 2,3 mm; D: protoconcha; E-F: microescul-
tura y detalle. Papua Nueva Guinea, Isla de Bilbil, Stn. PB29, 17 m.
eral and basal carinae, and in having the
base completely smooth.
From A. dentata spec. nov. it is distin-
guished by its very low spire; the
smaller size of its protoconch; the lack of
ornamentation both on its base and
umbilical wall and the less elevated
aperture.
55
Iberus , Suplemento 6, 2014
Anticlimax dentata spec. nov. (Figures 51, 35A-F, 36A-F, 37A-F)
Type material: Holotype MNHN 27194 (Figs. 51, 35A-B).
Material examined: (9 s): Philippines» PANGLAO 2004: 1 s, Pamilacan Island, Stri. S22, 9°29.4/N,
123°56.0,E, 15-20 m, hard ground covered with sand; 1 s, Panglao Island, Biking, Stn. SI, 9°35.3'N,
123°50.5'E, 5 m, reef slope with overhangs; 1 s, Bohol Island, Ubajan, Stn. S25, 9°41.5'N, 123°51.0'E, 21
m, muddy (type material); 2 s, Bohol Island, Baclayon, Stn. S32, 9°35.8,N, 123°44.6'E, 60-62 m, muddy
sand. Papua New Guinea. PAPUA NIUGINI: 2 s, S Megas Islet, Stn. PS12, 5°05.3'S, 145°48.6'E, 6 m; 1
s, S Yabob L, Stn. PD66, 5°15.5'S, 145°47.3/E, 2-6 m; 1 s, Hargun L, Stn. PS18, 5°01.6'S, 145°48.1,E, 16 m.
Type locality: Philippines, Bohol Island, Ubajan, 9°41.5/N, 123°51.0/E, 21 m, muddy bottom
[PANGLAO 2004: Stn. S22].
Etymology: The specific ñame refers to the peripheral carina with prominences that look like teeth.
Distribution : Only known from the
Philippines, between 5 and 60 m, and
Papua New Guinea, between 6 and 16 m.
Description : Shell small (<3.2 mm),
with a relatively high spire, strongly
bicarinate and widely umbilicate.
The protoconch measures about 450
jum, has 1 34 whorls and 2 distinct
phases; the first is completely smooth
and the second is covered with thick
tubercles scattered randomly. The teleo-
conch has 2 whorls and two carinae
which angle the shell, one situated
peripherally and the other basally. The
ornamentation is composed of spiral
cords, ribs and axial folds and rounded
or quadrangular cells in the spaces
between the cords, that have fine
threads inside.
On the adapical part, the spiral cords
develop in zigzag. At the beginning of
the teleoconch 6 cords can be observed,
which subsequently intersect with the
axial ribs forming nodules; on the last
quarter-whorl, between the peripheral
carina and the suture there are up to 15-
16 cords. The space between the periph¬
eral and the basal carinae is fully
covered by spiral cordlets and axial ribs
which turn into thick folds extending
from the middle area towards the basal
carina. Up to 19 thick axial folds of
similar shape and size may be seen on
the last half whorl. The base is fíat and
completely covered by spiral cordlets
and axial growth-lines.
The umbilicus is wide and deep, lim-
ited by a carina which angles it; in its in¬
terior there are spiral cordlets and marked
growth lines; umbilical wall convex. Aper-
ture quadrangular, prosocline, very high;
parietal area with a thick callus; columel-
la arched, thickened and reflected towards
the umbilicus; outer lip modified by the
basal carina which angles it intemally and
prolongs it laterally; adapical edge of the
outer lip crenulated externally by the ter¬
mina tion of the spiral cords.
Dimensions: the holotype is 2.35 mm
in diameter.
Habitat : Infralittoral species collected
by suction at 15-20 m, on hard substrate
covered with sand (Stn. S22); on a reef
slope with overhangs at 5 m (Stn. SI); on
a muddy bottom at 21 m (Stn. S25) and
on a muddy sand bottom, at 60-62 m
(Stn. S32). In Papua New Guinea it has
been collected between 2 and 16 m.
Remarks : The species is characterized
by its high spire, the very wide proto¬
conch and the ornamentation on phase 2
(of the protoconch); the regularity of the
spiral cords on the adapical part; the
regularity of shape and size of the axial
folds in the space between carinae; the
periumbilical carina, the high aperture
and the presence of one single external
angle on the external lip.
Anticlimax elata spec. nov. (Figures 6A, 38A-E)
Type material: Holotype MNHN 27193 (Figs. 6A, 38A-B).
Material examined: (4 s): Philippines. PANGLAO 2004: 1 s, Bohol Island, Manga, Stn. S21, 9°41.7'N,
123°50.9/E, 4-12 m, reef slope with silt (type material); 1 s, Bohol Island, Ubajan, Stn. S25, 9°41.5'N,
56
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 35A-F. Anticlimax dentata spec. nov. A-B: holotype, 2.35 mm, (MNHN); C: protoconch
(holotype); D-F: microsculpture. Philippines, Bohol Island, Ubajan, Stn. S25, 21 m.
Figura 35A-F Anticlimax dentata spec. nov. A-B : holotipo, 2,35 mm, (MNHN); C: protoconch
(holotipo); D-F: microescultura. Filipinas, Isla de Bohol, Uhajan, Stn. S25, 21 m.
57
Iherus , Suplemento 6, 2014
Figure 36A-F. Anticlimax dentata spec. nov. A-B: shell, 2.3 mm (MNHN): C: protoconch; D-E:
microsculpture. F: microsculpture of the protoconch. Philippines, Pamilacan Island, Stn. S22, 15-20 m.
Figura 36A-F. Anticlimax dentata spec. nov. A-B: concha, 2,3 mm (MNHN): C: protoconcha ; D-E:
micro escultura. F: microescultura de la protoconcha. Filipinas, Isla de Pamilacán, Stn. S22, 15-20 m.
58
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 37A-F. Anticlimax dentata spec. nov. A: shell, 3.1 mm, Stn. PS18; B-C: shells, 2.9, 2.2 mm,
Stn. PS12; D: protoconch; E-F: microsculpture. S Megas Islet, Papua New Guinea, Stn. PS12, 6 m.
Figura 37A-F Anticlimax dentata spec. nov. A: concha, 3,1 mm, Stn. PS18; B-C: conchas, 2,9, 2,2 mm, Stn.
PS12; D: protoconcha; E-F: microescultura. S Islote de Megas, Papua Nueva Guinea, Stn. PS12, 6 m.
59
Iherus, Suplemento 6, 2014
123°51.0'E, 21 m, mud; 2 s, Bohol Island, Cortes, Stn. T18, 9°41.8'N, 123°49.9'E, 80-100 m, muddy
bottom with sponges.
Type locality: Philippines, Bohol Island, Manga, 9°41.7'N, 123°50.9'E, 4-12 m, reef slope with silt.
Etymology: The specific ñame alludes to the high spire, infrequent in the group.
Distribution: Only known from the
Philippines between 12 and 80 m.
Description: Shell small (<2.Q mm),
formed by 3 Vi whorls, with a relatively
high spire, strongly bicarinate and
widely umbilicate.
The protoconch measures about 270
¡urn, has 1 % whorls and 2 distinct
phases; the first is completely smooth
and the second is covered with thick
tubercles scattered randomly. The teleo-
conch has 1 3á whorls and two carinae
which angle the shell, one peripheral
and the other basal. The ornamentation
is composed of spiral cords, ribs and
axial folds with rounded cells in the
spaces between cords.
On the adapical part, the spiral cords
develop in zigzag. Seven cords may be
observed at the beginning of the teleo-
conch, which are subsequently trans-
formed into nodules by the Crossing of the
axial ribs, and become 17 ín the last
quarter-whorl between the peripheral
carina and the suture. The space between
the peripheral and the basal carinae is fully
covered by spiral cordlets, whose number
increases when cióse to the aperture, and
by axial ribs that develop into thick folds
from halfway down and over the basal
carina. There are 14-15 thick axial folds on
the last whorl, which give the shell a star-
like profile in apical view. The base is
concave and completely covered by thick
axial folds and spiral cordlets.
Umbilicus narrow and deep, pro-
gressively occluded by the thickening of
the columella; in its interior there are
spiral cordlets. Aperture quadrangular,
prosocline; parietal area with a thick
callous layer; columella arched, thick-
ened at the base forming a cord that
occludes the umbilicus; outer lip modi-
fied by the carinae which angle it inter-
nally and also prolong it laterally.
Dimensions: the holotype is 1.34 mm
in diameter.
Habitat: Infra-circalittoral species
suctioned at 4-12 m, on reef slope with
silt and mud, at 21 m (Stn. S25); trawled
on muddy bottom with sponges at 80-
100 m (Stn. T18).
Remarles: The species is characterized
by its high spire; the small size of the
protoconch; the regularity of the nodu-
lose cords and the large axial folds; its
quadrangular aperture and the columel-
lar thickening forming a cord that
occludes the umbilicus.
Anticlimax serrata spec. nov. is
extremely similar but is more depressed,
has a slightly larger protoconch, more
axial peripheral ribs and the umbilical
funnel is smaller.
Anticlimax solomonensis spec. nov. (Figures 6B, 39A-F)
Type material: Holotype MNHN 27196 (Figs. 6B, 39A-B).
Material examined: Only from the type locality.
Type locality: Solomon Islands, 8°40'S, 160°04'E, 396-411 m [SALOMON 1: DW1762].
Etymology: The specific ñame is of the archipelago where the holotype was found.
Distribution: Only known from the
Solomon Is. between 396-411 m.
Description: Shell small (<2 mm),
with a relatively high spire, strong,
bicarinate and narrowly umbilicate.
The protoconch measures about 340
jum, has 2 whorls and 2 distinct phases;
the first phase is completely smooth but
the second, seemingly smooth, has thin
growth lines near the suture. The teleo-
conch has just over 1 Vi whorls and two
carinae which angle the shell, one
peripheral and the other basal.
The ornamentation is composed of
spiral nodulose cords, ribs and axial
folds; cells of different shape occur in
60
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 38A-E. Anticlimax data spec. nov. A-B: holotype, 1.34 mm (MNHN): C: protoconch
(holotype); D-E: microsculpture. Philippines, Bohol Island, Manga, Stn. S21, 4-12 m.
Figura 38A-E. Anticlimax data spec. nov. A-B: holotipo , 1,34 mm (MNHN): C: protoconcha
(holotipo); D-E: microescultura. Filipinas , isla de Bohol, Manga, Stn . S21, 4-12 m.
61
Iberus, Suplemento 6, 2014
Figure 39A-F. Anticlimax solomonénsis spec. nov. A-B: hoiotype, 1.5 mm (MNHN): C: protoconch
(holotype); D-F: mícrosculpture. Soloman Islands, SALOMON 1, DW1762, 396-411 m.
Figura 39A-E Antíclimax solomonénsis spec. nov. A~B: hoiotipo , 1,5 mm (MNHN): C: pntoconcha
(holotipo); D-F: micmescultura. Mas Salomón , SALOMON 1, DW1762, 396-411 m.
the spaces between the cords. On the
adapícal part the spíral cords are devel-
oped ín zigzag; three thíck cords may be
observed at the beginníng of the teleo-
conch, which subsequently and by the
effect of the axial ribs become nodulose
and reach 12-14 in number on the last
half whorl between the perípheral
carina and the suture; sínce the nodules
are high, the cells that occupy the spaces
between cords also are so. In the space
between fhe carinae the axial ribs pre¬
domínate over the spiral cords forrmng
rounded cells in the inferspaces.
On the last half whorl, the cords
become finer and more numerous, the axial
ribs are transformed into thíck axial folds
of triangular aspect which extend from
the perípheral to the basal carina and the
cells dísappean The base ís very convex
and bears spíral cordlets together with
axial ribs and cells in the interspaces; in
62
RUBIO & KoláN: The genus Anticlimax in the tropical Southwest Pacific
the last Vz whorl there are axial folds.
Umbílícus narrow and deep, límíted by a
thíck cord whích occludes ít progressively
by the thíckeníng of the base of the col-
umella. Aperture triangular, prosoclíne;
parietal area wíth a thick callous coating;
columella arched, thick and reflected
towards the umbílícus, wíth a thíckening
at the base whích forms the periumbilical
cord; outer lip margín modified only by
the angle corresponding to the basal carina,
whích prolongs ít lateraüy.
Dímensíons: the holotype is 1.5 mm
in diameter.
Habitat: Bathyal species dredged in
396-411 m.
Remarles: The Ipecies ís characterized
by íts hígh spite; the lower number of cords
at the beginning of the teleoconch; the ele-
vated nodul.es of the cords as well as the
deep cells of the spaces beíween cords; the
large axial folds of triangular aspect and
the umbílícus closed by the cord gener-
ated by the thíckening of the columella.
Anticlimax fastígata spec. nov. (Figures 6C, 40A-F)
Type material: Holotype MNHN 27228 (Figs. 6C, 40A-C).
Material examined: Only from the type locality.
Type locality: Papua Nueva Guinea, Lauhamug 1 , 4°59.4Í5, 145°47.6'E, 10 m [PAPUA NIUGINI:
Stn. PS20].
Etymology: The specific ñame alindes to the pointed end of the spire (from the Latín fastigatus, - a ,
-um whích means relévate").
Distribuiion : Only known from
Papua Nueva Guinea, at 10 m.
Description : Shell small (<3 mm),
somewhat hígh, strong, robust, bícari-
nate and umbílícate.
The protoconch mensures 260-290
fim and has a little more than 1 Vz
whorls. There are two distinct phases,
the fírst, approxímately % of whorl, is
completely smooth and the second,
which ís partialiy concealed by the
teleoconch, presents randomly dístríb-
uted thick tuberdes.
The teleoconch has 2 whorls and two
thick carínae, one perípheral and
another basal, that angle the shell
markedly.
Grnamentation formed by cords and
spiral grooves, ríbs and axial folds. The
adapícal part ís fully covered by spiral
cords of different sízes, not nodulose,
developíng in zigzag, wíth 3 cords at the
beginning of the teleoconch whích
become 16 at the end, between the suture
and the perípheral carina; some of these
cords are dívíded into two fíner ones
near the lip; the space between cords, on
the fírst whorl is occupíed by oval cells
that are transformed ínto grooves on the
last whorl; nexf to the lip, 3-4 thick axial
ríbs develop irregularly in shape and
very cióse together, thíckening the outer
lip and projectíng the perípheral carina
outward. The períphery ís delímíted by
two strong carinae which angle the shell;
between both carínae, fine spiral cordlets
are developed, as well as ríbs and thick
undulafíng folds, nuniberíng 9-10 spiral
cordlets, 10 ribs and 12 thick axial folds
on the last whorl.
The base is slightly convex and ís
covered by spiral cords which are
dívíded ínto two as they approach the
lip. Umbílícus narrow and deep, not
Ümited by any carina. Aperture quad-
rangular, prosoclíne, ínner and outer
líps very coarse, expanded outwards;
parietal area covered by a thíck callous
coating forming a marked angle; col¬
umella arched, very reflected towards
the umbílícus and developíng an exten¬
sivo callous area. af the base; outer lip
modified by the two carinae that angle ít
ínternaliy and expand ít outwards.
Dímensíons: the holotype is 2.67 mm
in diameter.
Habitat Infralittoral species dredged
at 10 m depth.
Remarles: No other studíed species
has the morphological characters
observed ín A. fastigata . The species is
characterized by íts robustness; the
63
Iberus , Suplemento 6, 2014
Figure 40A-F. Anticlimax fastigata spec. nov. A-C: holotype, 2.67 mm; D: protoconch (holotype);
E-F: microsculpture. Lauhamug Island, Papua New Guinea, Stn. PS20, 10 m.
Figura 40A-E Anticlimax fastigata spec . nov. A-C: holotipo, 2,67 mm; D: protoconcha (holotipo); E-
F: microescultura. Isla de Lauhamug, Papua Nueva Guinea, Stn. PS20, 10 m.
strength of the carinae; the small size of
its protoconch; the thick axial folds that
develop between the carinae; the axial
folds that develop on the adapical part.
next to the lip, that project the peripheral
carina outwardly; the narrow and deep
umbilicus; the thick quadrangular aper-
ture and the lips projected outwards.
64
RUBIO & ROLÁN: The gemís Anticlimax in the tropical Southwest Pacific
Figure 41A-F. Anticlimax rhinoceros spec. nov. A-C: holotype, 1.65 mm; D: protoconch of the
holotype; E-F: microsculpture. W Wonad Island, Papua New Guinea, Stn. PS32, 19 m.
Figura 41A-F. Anticlimax rhinoceros spec. nov. A-C: holotipo, 1,65 mm; D: protoconcha del holotipo ;
E-F: microescultura. O de la isla de Wonad, Papua Nueva Guinea, Stn. PS32, 19 m.
Anticlimax rhinoceros spec. nov. (Figures 6D, 41A-F)
Type material: Holotype MNHN 27229 (Figs. 6D, 41 A-C)
Material examined: Only from the type locality.
Type locality: Papua New Guinea, West Wonad L, 5°08.rS, 145°49.3'E, 19 m [PAPUA NIUGINI: Stn. PS32].
Etymology: The specific ñame alindes to the profile in apical view, which can recall the outline of
a rhinoceros.
Distribution : Only known from Description: Shell small (<2 mm).
Papua New Guinea, at 19 m. bicarinate, wider than high, formed by 3
65
Iberus , Suplemento 6, 2014
Table IV. Differences between species of group 4.
Tabla TV: Diferencias entre las especies del grupo 4.
Va whorls separated by a shallowly
marked suture, with a low spire, nar¬
ro wly umbilicate.
The teleoconch has a little more than
1 whorl and 2 carinae, one peripheral
and the other basal. The ornamentation
is composed of spiral nodulose cords,
ribs and axial folds; the spiral cords cross
the axial ribs forming in the first half-
whorl very nodulose cords that begin to
develop in zigzag and then disappear.
Both the subsutural and periumbili-
cal spiral cords present characteristic
thick nodules. On the last whorl, from
halfway down the space between
carinae toward the base there are about
14 thick axial folds. These folds become
thicker as the approach the basal carina.
The base is almost fíat and is completely
decorated with thick axial ribs crossed
by fine spiral cordlets.
Aperture triangular; parietal area
covered by a thick callous coating, forming
an angle at the junction with the outer lip;
columella arched, thick and reflected
towards the umbilicus, but without occlud-
ing it; outer lip with smooth, with an
unmodified margin except for a marked
angle near the basal carina which prolongs
it laterally. Umbilicus wide and deep,
allowing the previous whorls to be seen;
umbilical wall straight, with spiral cords.
Dimensions: the holotype is 1.65 mm
in diameter.
Habitat : Infralitoral species dredged
at 19 m depth.
Remarks : Anticlimax rhinoceros is
characterized by the nodulose cords on
the first Vi whorl of the teleoconch; by
the cord of thick nodules that runs next
to the suture; by its fíat base and the
wide folds that limit the basal carina; by
the periumbilical nodulose cord; by the
concentration of thick folds on the basal
carina, next to the outer lip, and by the
great inclination of the aperture.
Other species such as A. niasensis, A.
padangensis have a similar profile; they
differ from A. rhinoceros spec. nov. in A.
padangensis having less folds on the
basal carina and A. niasensis having a
thick subsutural cord of strong tubercles
and another periumbilical cord with
smaller tubercles.
66
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Group 4
Description : Low cónica! spire. Teleo-
conch: A marked and/or prominent
basal carina which angles the external
lip and prolongs it laterally. Adapically
rounded. Ornamentation of fine spiral
grooves in zigzag. Base with light axial
folds. Aperture rounded; columella not
very thick and reflected. Umbilicus
almost closed by a thickening of the col-
umellar callus.
This group is formed by 9 species: A.
textilis, A. vanuatuensis, A. levis, A. spi-
ralis, A. simplex, A. uniformis, A. maes-
tratii, A. philippinensis and A. imifatrix.
Table IV gives a useful summary of
their differences.
Anticlimax textilis spec. nov. (Figures 6E, 42A-F)
Type material: Holotype MNHN 27197 (Figs. 6E, 42A-C).
Material examined: Only from the type locality.
Type locality: New Caledonia, 22°39'S, 167°10'E, 202-227 m [BATHUS 2: Stn. DW715].
Etymology: The specific ñame refers to the similarity of the shell microsculpture to textiles.
Distribution: Only known from New
Caledonia, between 202-227 m.
Description : Shell flattened, solid,
keeled at its base, formed by 3 Vi rapidly
increasing whorls. Protoconch formed
by 2 whorls, placed at a level higher than
the teleoconch, measuring about 360 ¡um
in diameter; it is apparently smooth,
although its distal portion shows a short
section which is rough with irregular
threads, ending with a slight line and the
change of sculpture. The teleoconch has
2 quickly increasing whorls, separated
by a marked suture; a peripheral keel
defines the base where there is no cord
or carina. Adapical part and base of the
shell both convex. At the beginning of
the teleoconch there are a few spiral
zigzag sulci separating a few wide cords.
On the last Vi whorl, at the base, near
the basal keel, a concave area is formed
which modifies the outer lip. Ornamen¬
tation composed of rather low spiral
cords, wider than their interspaces,
which are crossed by fine axial striae.
Aperture oval, prosocline; parietal area
covered by a thick callous coating; col¬
umella arched, thickened and reflected
towards the umbilicus; outer lip
smooth, with a sharp edge, modified by
the basal keel and by a concave sinus in
its basal part, which determines a char-
acteristic angulation. Narro w and deep
umbilicus which does not allow the
earlier whorls to be seen, gradually
closed by the thickening and reflection
of the columella.
Dimensions: the holotype measures
2.09 mm in diameter.
Habitat : Bathyal species dredged at
202-227 m.
Remarks : The obvious characteristic
is the presence of the teleoconch
microsculpture, simple at the beginning
and very fine and complex at the end.
Anticlimax textilis spec. nov. differs
from A. vanuatuensis , A. levis and A. spi-
ralis, by the carinate profile of the shell;
the larger size and different ornamenta¬
tion of the protoconch and the sinus in
the basal part of the outer lip. A. simplex
is distinguished by the different orna¬
mentation of the protoconch and lacking
spiral nodulose cords on the first whorl
of the teleoconch. A. uniformis differs by
having the protoconch smaller and with
a different ornamentation and lacking the
prominent basal keel of the teleoconch.
Anticlimax vanuatuensis spec. nov. (Figures 6F, 43A-E, 44A-E)
Type material: Holotype MNHN 27198 (Figs. 6F, 43A-C). Paratype MNHN 27199 (Figs. 44A-C)
from Segond Channel, vicinity of Maritime College, Stn. LD21, 1-6 m.
67
Iberus , Suplemento 6, 2014
Material examined: (2 s): Vanuatu, SANTO 2006: 1 s, W Tangoa Island, Stn. LD39, 15°35.4'S,
166°58.7,E/ 6-9 m, fine brownish mineral sand (holotype); 1 s, Segond Channel, vicinity of Maritime
College, Stn. LD21, 15031.3'S, 167°09.9'E, 1-6 m, grey mineral sand (paratype).
Type locality: Vanuatu, W Tangoa Island, 15°35.4,S, 166°58.7'E, 6-9 m, fine brownish mineral sand
[SANTO 2006: Stn. LD39].
Etymology: The specific ñame refers to that of the island where the species was collected.
Distribution : Only known from
Vanuatu Island ai 6 m.
Description: Shell very small (<1.5
mm), solid, with a rounded periphery,
umbilicus small and deep, almos!
occluded by a columeilar thickening;
outer lip very prolonged laterally.
Protoconch of about 310 jum in diam
eter and almost 2 whorls, the first is
almost smooth, and the second has thick
tubercles and fragments of cords over its
surface; it ends at the beginning of the
sculpture of the teleoconch. This has 1 Vi
whorls of rapid growth; thick spiral
cords, becoming smaller at the end and
attenuated in the adapical part, develop
in zigzag and cover all the shell; at the
middle of the base, which is strongly
convex, thick cords and axial ribs arise,
ending at the umbilical edge.
The periphery is rounded and there
is no carina until the last half whorl,
where a moderately thick one develops,
sufficient to produce a thickening and
angulation of the outer lip. In the
peripheral basal zone cióse to the outer
lip, the spiral cords disappear, leaving
only fine ramified lines.
Aperture rounded, forming 3 char-
acteristic angles: one at the unión of the
parietal area with the outer lip; a
second, at the base, formed by the col-
umellar thickening and subsequent
reflection towards the umbilicus and
finally, the basal peripheral angle,
which expands the aperture laterally.
Umbilicus narrow and deep, almost
completely occluded by the columeilar
callus.
Dimensions: the holotype is 1.35 mm
in diameter.
Habitat : Infralittoral species dredged
at 6-9 m in fine brownish mineral sand
bottom (Stn. LD39) and at 1-6 m in grey
mineral sand bottom (Stn. LD21).
Remarks: Its rounded periphery, the
lack of thick carinae which angle the shell
and the angle that expands the outer lip
laterally, characterize the species.
The most similar species to Anticli¬
max vanuatuensis spec. nov. is A. levis,
which differs by the ornamentation of
the protoconch and teleoconch and by
having axial folds on the base.
From A. textilis spec. nov. it differs in
the smaller size of its protoconch; by
lacking the sinus on the basal part of the
outer lip and by a different ornamenta¬
tion of the teleoconch; and because A.
vanatuensis lacks a peripheral keel.
A. spiralis, A. simplex and A. uniformis
are distinguished by the different orna¬
mentation of the second phase of the
protoconch.
A. textilis and A. uniformis by the
lack of a basal keel. A. simplex for
lacking spiral nodulose cords on the
first whorl of the teleoconch.
A. niasensis (Thiele, 1925) has a
median peripheral carina on the entire
last whorl.
A. padangensis (Thiele, 1925) has a
strong spiral sculpture on the adapical
part.
Anticlimax levis spec. nov. (Figures 6G, 45A-D)
Type material: Holotype MNHN 27200 (Figs. 6G, 45A-B).
Material examined: Only from the type locality.
Type locality: Philippines, Bohol island, west of Baclayon, 9°35.1/N, 123°51.2'E, 34-82 m, coarse
muddy sand with large sponges [PANGLAO 2004: Stn. T6].
Etymology: The specific ñame is from the Latin adjective levis -e, which means "smooth, polished",
alluding to the smooth adapical part of the greater part of the shell.
68
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 42A-F. Anticlimax textilis spec. nov. A-C: holotype, 2.09 mm (MNHN); D: apical view and
protoconch (holotype); E-F: detall of the microsculpture. New Caledonia, BATHUS 2, Stn.
DW715, 202-227 m.
Figura 42A-F. Anticlimax textilis spec. nov. A-C: holotipo, 2,09 mm (MNHN); D: vista apical y pro -
toconcha (holotipo); E-F: detalle de la microescultura. Nueva Caledonia, BATHUS 2, Stn. DW715,
202-227 m.
69
Iherus , Suplemento 6, 2014
view and protoconch (holotype); E-F: microsculpture. Vanuatu, W Tangoa Island, Stn. LD39, 6-9
m, muddy sand bottom.
Figura 43A-F Anticlimax vanuatuensis spec. nov. A-C: holotipo , 1,35 mm (MNHN); D: vista apical
y protoconcha (holotipo); E-F: microescultura. Vanuatu, O de la isla Tangoa, Stn. LD39, 6-9 m, fondo
arenoso y fangoso.
70
RUBIO & Rolan: The genus Anticlimax in the tropical Southwest Pacific
Figure 44A-E. Anticlimax vanuatuensis spec. nov. A-C: paratype, 1.4 mm (MNHN); D: proto-
conch of the same paratype; E: microsculpture. Vanuatu, Segond Channel, vicinity of Maritime
College, Stn. LD21, 1-6 m, sandy bottom.
Figura 44A-E. Anticlimax vanuatuensis spec. nov. A-C: paratipo, 1,4 mm (MNHN); D: proto concha
del mismo paratipo; E: microescultura. Vanuatu, Canal Segond, cerca del Maritime College, Stn.
LD21, 1-6 m, fondo arenoso.
71
Iberus , Suplemento 6, 2014
Figure 45A-D. Anticlimax levis spec. nov. A-B: holotype, 2.0 mm (MNHN); C: protoconch of the
holotype; D: detail of the microsculpture. Philippines, Bohol Island, west of Baclayon, Stn. T 6,
34-82 m, coarse muddy sand with large sponges.
Figura 45A-D. Anticlimax levis spec. nov. A-B: holotipo, 2,0 mm (MNHN); C: protoconcha del
holotipo; D: detalle de la microescultura. Filipinas, isla de Bohol, Oeste de Baclayon, Stn. T6, 34-82 m,
arena gruesa fangosa con grandes esponjas.
Distribution: Only known from the
Philippines, its type locality between 34-
82 m.
Description: Shell small (about 2.00
mm), solid, formed by 4 lA whorls of rapid
growth, suture barely visible, carinate
basally, with a low spire and narrowly
umbilicate. The protoconch is located at a
higher level than the teleoconch, measures
320 jum, has 1 3á whorls and 2 distinct
phases; the first is completely smooth and
the second bears well-marked growth
lines. The teleoconch has about 2 whorls
and shows a single carina in a basal posi-
tion, that develops on the last half whorl.
Adapical part and base very convex,
periphery rounded.
On the adapical part of the first
spiral whorl, 4 thick zigzagging spiral
cords can be observed; the spaces
between the cords are initially occupied
by rhomboidal cells that change into
grooves from the first quarter-whorl and
disappear after the first whorl, appear-
ing again near the aperture; more than
30 spiral cords can be counted, distrib-
uted between the suture and the basal
carina. Base convex, not limited by the
basal carina until the last Vi whorl; deco-
rated with spiral cords in zigzag and
rhomboid cells in the spaces between
the cords, as well as marked growth-
lines, which do not form ribs; on the last
half whorl, the ornamentation of the
72
RUBIO & RoláN: The genus Anticíirnax in the tropical Southwest Pacific
base disappears, leaving only the
growth lines.
Aperture triangular, prosocline; pari¬
etal area covered by a thin callous coating;
columella arched, very thick and reflected
towards the umbilicus, forming in addi-
tion a very thick columellar callus which
tends to cióse the umbilicus progressively.
Outer lip thin, with smooth margin, only
modified by the basal keel that angles and
expands it considerably laterally. Umbili¬
cus very narrow and deep, reduced to a
narrow fissure that is almost occluded by
the columellar callus.
Dimensions: the holotype is 2.00 mm
in diameter.
Habitat: Infra-circalittoral species
trawled between 34-82 m in coarse
muddy sand with large sponges.
Remarks : The species with which A.
levis spec. nov. has most similarity is A.
vanuatuensis, distinguished by the differ-
ent ornamentation of the second phase of
the protoconch; by the different and less
distinctive ornamentation of the adapical
part and the base of the teleoconch and
by the lack of axial folds on the base.
From Anticlimax maestratii spec. nov.
it is distinguished by the smaller size of
the protoconch and the lack of grooves
in its second phase; because the spiral
cords disappear from the first whorl of
the teleoconch and on the adapical part ,
appearing again cióse to the outer lip;
finally, by the not so rounded aperture
and a much larger columellar callus.
From Anticlimax philippinensis spec.
nov. it diífers by lacking tubercles in phase
two of the protoconch; by the less open
umbilicus and the much more developed
columellar callus and because the spiral
cords disappear from the first whorl of the
teleoconch and on the adapical part ,
appearing again near the outer lip.
From A. textilis spec. nov. and A. uni-
formis spec. nov. it may be distinguished
by the distinct shape of the outer lip. From
A. simplex by lacking spiral nodulose cords
on the first whorl of the teleoconch.
A. niasensis (Thiele, 1925) has a
peripheral carina in the middle over the
entire last whorl. A. padangensis (Thiele,
1925) has a strong spiral sculpture on
the adapical part.
Anticlimax spiralis spec. nov. (Figures 6FF, 46A-F)
Type material: Holotype MNHN 27201 (Figs. 6H, 46A-C)
Material examined: Only from the type locality.
Type locality: Vanuatu, Coolidge wreck, Segond Channel, 15°31.4'S, 167°14.1,E, 20-31 m [SANTO
2006: Stn. FS54].
Etymology: The specific ñame refers to the faint spiral microsculpture existent on the teleoconch.
Distribution : Only known from
Vanuatu, between 20-31 m.
Description: Shell small (<2.5 mm),
depressed, with about 4 whorls of rapid
growth, separated by a thin suture; with
a low spire, and the umbilicus very
narrow and deep.
Protoconch with 1 Vz apparently
smooth whorls, measuring about 250
jum, and showing two phases: the first is
completely smooth and the second pre-
sents granules of different sizes scat-
tered randomly. The end is very evident
by the change to the sculpture of the
teleoconch. This has 2 Vz whorls; on the
first whorl there are thick zigzagging
spiral cords, wider than their inter-
spaces; on subsequent whorls these
cords disappear completely from the
adapical part and the base, remaining
only at the periphery; marked growth
lines can be observed. The adapical part,
the periphery and the base are convex.
There are no carinae or peripheral
keels; only on the last quarter whorl, two
slight peripheral angulations which
modify the aperture appear, one adapical
and the other basal. Aperture quadran-
gular, prosocline. The parietal area is
covered by a thick callous coating and
forms an angle with the outer lip; col¬
umella very thick, widened at the base
and reflected towards the umbilicus,
forming a callus which occludes it pro-
73
Iherus , Suplemento 6, 2014
gressively; outer lip with a smooth margin,
modified by two angles corresponding to
the peripheral carinae. Umbilicus narro w
and deep, progressively occluded by the
thickened eolurneilar callus; there is no
períumbilical cord, only marked growth
lines that penétrate inside and that together
form rough and irregular umbilical folds.
Dimensions: the holotype is 2.44 mm
in diameter.
Habitat: Infralittoral species found in
sediments collected between 20-31 m.
Remarks : The species is characterized
by the lack of spiral cords on the adapical
part and the base of the last 1 Vi whorls;
the lack of obvious peripheral carinae; the
angles on the outer lip that correspond to
these carinae and the eolurneilar callus
that gradually occludes the umbilicus,
very similar to the species of Solariorbis.
Anticlimax sp ir alis spec. nov. differs
from the remaining species of the group
by the smaller size of its protoconch. A .
textilis, A. simplex, A. uniformis and A.
philippinensis differ by lack of evident
peripheral or basal keels. A. vanuatuen-
sis, A. levis and A. maestratii have 2
angles inside the outer lip.
Anticlimax simplex spec. nov. (Figures 61, 47A-E)
Type material: Holotype MNHN 27202 (Figs. 61, 47A-C).
Material examined: Only from the type locality.
Type locality: Vanuatu, 16°16'S, 167°21'E, 360-419 m [MUSORSTOM 8: Stn. DW1065].
Etymology: The specific ñame alindes to the scarce number of remarkable details of the shell.
Distribution : Only known from Vanua¬
tu, its type locality, between 360-419 m.
Description : Shell small (about 2
mm), solid, formed by 3 Vi whorls of
rapid growth, suture barely visible, carí¬
nate basally; with a low spire and nar¬
ro wly umbilicate.
Protoconch with about 2 whorls and
measuring about 380 jum; the first 1 lA
whorls are completely smooth, the rest
shows axial growth lines, more visible near
the suture and numerous granules that are
arranged at the periphery; the protoconch
ends with an evident change of the sculp-
ture. Teleoconch with a little less than 2
whorls; at the end of the spire 2 periph¬
eral carinae can be seen, one in prolonga-
tion of the suture and the other basal; the
former one disappears over the last 3A
whorl, leaving the basal more prominent,
like a small keel. On the adapical part of
the first whorl there are thick zigzagging
spiral cords forming thick nodules; over
the last half whorl they gradually fade
until almost disappearing from the whorl,
with the spiral cords remaining only on
the periphery of the shell.
Base convex, periphery initially fíat,
later convex; in its first XA whorls there are
spiral cordlets which disappear completely
covered by a thin callous layer. Aperture
oval, prosocline; parietal area covered by
a thick callous coating; columella arched,
thickened and reflected towards the
umbilicus, forming a eolurneilar callus
which tends to progressively cióse the
umbilicus. Outer lip thin, smooth, single
margin modified by the peripheral carina
which angles and expands it laterally.
Umbilicus very narrow and deep, partially
occluded by the eolurneilar callus.
Dimensions: the holotype is 2.00 mm
in diameter.
Habitat: Bathyal species dredged on
the slope in deep bottom between 360-
419 m.
Remarks: This species may be distin-
guished from other congeners by the nodu-
lose cords in zigzag from the first whorl
of the teleoconch; the presence over 3A of
the last whorl of a basal keel; the very
narrow umbilicus, almost occluded by the
eolurneilar callus; the shape of the outer
lip expanded externally.
Anticlimax simplex spec. nov. may be
distinguished from A. vanuatuensis , A.
levis , A . spiralis, A. textilis, A. philippinen¬
sis and A . uniformis by the spiral nodu-
lose cords on the first whorl of the teleo¬
conch. From A. maestratii by lacking the
fine spiral grooves on phase two of the
protoconch.
74
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Figure 46A-F. Anticlimax spiralis spec. nov. A-C: holotype, 2.44 mm (MNHN); D: protoconch
(holotype); E-F: microsculpture. Vanuatu, Segond Channel, Coolidge wreck, Stn. FS54, 20-31 m.
Figura 46A-F. Anticlimax spiralis spec. nov. A-C : holotipo, 2,44 mm (MNHN); D: protoconcha
(holotipo); E-F: micro escultura. Vanuatu, Canal Segond, pecio del Coolidge, Stn. FS54, 20-31 m.
75
Iberus , Suplemento 6, 2014
Figure 47A-E. Anticlimax simplex spec. noy. A-C: holotype, 2.0 mm MNHN; D: protoconch
(holotype); E: microsculpture. Vanuatu, MUSORSTOM 8, Stn. DW1Q65, 360-419 m.
Figura 47A-E. Anticlimax simplex spec. nov. A-C: holotipo, 2,0 mm MNHN; D: protoconcha
(holotipo); E: microescultura. Vanuatu , MUSORSTOM 8, Stn. DW1065, 360-419 m.
Anticlimax uniformis spec. nov. (Figures 7 A, 48A-G)
Type material: Holotype MNHN 27203 (Figs. 7 A, 48A-B) and 13 paratypes MNHN 27204 (Fig.
48C).
Material examined: (21 s): Philippines. PANGLAO 2004: 14 s, between Panglao and Pamilacan
Islands, Stn. T27, 9°33'N, 123°51,E/ 106-137 m, fine sand and mud with echinoderms (type mater¬
ial); 3 s, Panglao Island, Bolod, Stn. T2, 9°32.4'N, 123°47.8'E, 152 rn, coarse sand; 2 s, Panglao Island,
off San Isidro, Stn. TIO, 9°33.4-33.8'N, 123°49.5-50.5'E, 117-124 m, mud and fine sand; 2 s, Bohol
Island, west of Baclayon, Stn. T5, 9°35.3'N, 123°52.2'E, 84-87 m, coarse muddy sand.
76
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 48A-G. Anticlimax uniformis spec. nov. A-B: holotype, 3.0 mm (MNHN); C: paratype, 3.2
mm (MNHN); D: protoconch of the holotype; E: protoconch of the paratype; F-G: microsculp-
ture and detail. Philippines, between Panglao and Pamilacan Islands, Stn. T27, 106-137 m.
Figura 48A-G. Anticlimax uniformis spec. nov. A-B: holotipo, 3,0 mm (MNHN); C: paratipo, 3,2
mm (MNHN); D: protoconcha del holotipo; E: protoconcha del paratipo; F-G: micro escultura y detalle.
Filipinas, entre las islas de Panglao y Pamilacán, Stn. T27, 106-137 m.
77
Iberus, Suplemento 6, 2014
Type locality: The Philippines, between Panglao and Pamilacan Islands, 9°33.4'N, 123°51.0'E, 106-
137 m, fine sand and mud with echinoderms [PANGLAO 2004: Stn. T27].
Etymology: The specific ñame makes reference to the uniformity of the sculpture on the dorsum
of the last whorl, in opposition to other species of the group which have smooth areas.
Distribution : Only known from the
Philippines, between 87 and 152 m.
Description : Shell small (about 3
mm), solid, formed by 3 Vi whorls of
rapid growth with a suture barely
visible; carinate basally; with a low spire
and narrowly umbilicate.
The protoconch measures about 400
jum and has 2 Vs whorls of spire and 2
distinct phases; the first is completely
smooth while on the second, there are
axial growth-lines, more visible next to
the suture and numerous micro gran¬
ules that are arranged near the periph-
ery. The teleoconch has about 2 whorls;
it shows a single, very prominent basal
carina, and a small keel, on which there
are small oblique incisions. Adapical
area and base are convex. On the adapi¬
cal part of the first whorl of the spire, 4-
5 thick zigzagging spiral cords can be
seen, as well as spaces between cords
occupied initially by rounded cells and,
after the first Vi whorl, by groo ves; on
the last whorl the cords are much finer
and more numerous, with more than 40
cords between the suture and the basal
carina on the last quarter.
Base convex, totally smooth, without
ornamentation except for fine growth
lines. Aperture triangular, prosocline;
parietal callous area covered by a thin
layer; columella arched, thickened and
reflected towards the umbilicus,
forming a columellar callus which tends
progressively to cióse the umbilicus.
Outer lip thin, margin smooth, only
modified by a basal keel that angles and
expands it laterally. Umbilicus very
narrow and deep, partially occluded by
the columellar callus.
Dimensions: the holotype is 3.00 mm
in diameter.
Habitat: Circalittoral species trawled
at 152 m in coarse sand bottom (Stn. T2);
at 84-87 m in coarse muddy sand
bottom (Stn. T5); at 117-124 m in fine
muddy sand bottom (Stn. TIO) and at
106-152 m in fine sand and mud with
echinoderms (Stn. T27).
Remarks: Characteristics of the species
are the non-nodulose spiral cords seen on
the adapical part of the shell and a com¬
pletely smooth base, without ornamenta¬
tion except for fine growth lines.
Anticlimax uniformis spec. nov.
differs from A. vanuatuensis , A. levis, A.
spiralis, A. textilis and A. philippinensis,
by the larger size of its protoconch; from
A. simplex because it lacks spiral nodu-
lose cords on the first whorl of the teleo¬
conch. From A. maestratii spec. nov. it
differs in having a prominent basal keel
and small tubercles rather than fine
spiral grooves on phase two of the pro¬
toconch.
Anticlimax maestratii spec. nov. (Figures 7B, 49A-E, 50A-E)
Type material: Holotype MNHN 27205 (Figs. 7B, 49A) and 18 paratypes (MNHN 27206) (Fig. 49B-C).
Material examined: (34 s): Philippines. PANGLAO 2004: 1 s, between Panglao and Pamilacan
Islands, Stn. T27, 9°33'N, 123°51'E, 106-137 m, fine sand and mud with echinoderms (Fig. 50); 1 s,
Panglao Island, Bolod, Stn. T4, 9°33.0'N, 123°48,5'E, 82 m, many large sponges; 4 s, Bohol Island,
west of Baclayon, Stn. T7, 9°36.1'N, 123°53.3,E, 61-62 m, fine muddy sand; 8 s, Bohol Island, west
of Baclayon, Stn. T5, 9°35.3'N, 123°52.2'E, 84-87 m, coarse muddy sand; 19 s, Panglao Island, off
San Isidro, Stn. T9, 9°33.5,N-9°33.9'N, 123°49.5,-123°50.5,E, 97-120 m, fine sand with seagrass
(type material); 1 s, Bohol Island, Cortes, Stn. T18, 9°41.8,N, 123°49.9'E, 80-100 m, muddy bottom
with sponges.
Type locality: The Philippines, Panglao Island, off San Isidro, Exp. 9°33.5-33.9'N, 123°49.5-50.5'E,
97-120 m [PANGLAO 2004: Stn. T9] .
Etymology: The species ñame is after Philippe Maestrati, member of the Malacology staff of the
MNHN, for his cooperation in the selection of material.
78
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 49A-E. Anticlimax maestratii spec. nov. A: holotype, 2.6 mm (MNHN); B-C: paratypes,
2.7, 2.0 mm; D: protoconch (holotype); E: microsculpture. Philippines, Panglao Island, off San
Isidro, Stn. T9, 97-120 m.
Figura 49A-E. Anticlimax maestratii spec. nov. A: holotipo, 2,6 mm (MNHN); B-C: paratipos, 2,7,
2,0 mm; D: protoconcha (holotipo); E: micro escultura. Filipinas, Isla de Panglao, frente a San Isidro,
Stn . T9, 97-120 m.
Distribution : Only known from the
Philippines, between 62 and 106 m.
Description : Shell small (<3.00 mm),
solid, formed by 4 Va whorls of rapid
growth, suture barely visible, carinate
basally; with a low spire and narrowly
umbilicate. The protoconch is located at
a higher level than the teleoconch, mea»
sures about 390 jum, and has little more
than 2 whorls and 2 distinct phases; the
first is completely smooth and the
second shows 3-4 very light spiral
grooves, small scattered granules which
are situated cióse to the suture and
growth lines. The teleoconch has about
2 whorls and shows a single carina, in a
basal position, that is more developed
over the last quarter whorl. Adapical
79
Iberus , Suplemento 6, 2014
Figure 50A-E. Anticlimax maestratii spec. nov. A-C: shell, 1.9 mm (MNHN); D: protoconch,
from the shell figs. A-C; E: microsculpture. Philippines, between Panglao and Pamilacan Islands,
Stn. T27, 106-137 m, fine sand and mud with echinoderms.
Figura 50A-E. Anticlimax maestratii spec. nov. A-C: concha, 1,9 mm (MNHN); D: protoconcha, de
la concha de la fig. A-C; E: microescultura. Filipinas, entre las islas Panglao y Pamilacdn, Stn. T27,
106-137 m, en arena fina y fango con equinodermos.
part and base very convex, rounded at
the periphery.
On the adapical part of the first
whorl, 3-4 thick zigzagging spiral cords
can be seen; the spaces between cords
are occupied initially by rhomboidal
cells, changed into grooves after the first
Vz whorl; on the last Vi whorl the cords
are much finer and more numerous,
with a space appearing near the suture
where both cords and grooves disap-
pear. Base convex, ornamented with
80
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
spiral cords in zigzag and rhomboid
cells in the spaces between the cords, as
well as marked growth lines, not
forming ribs; on the last half whorl, the
ornamentation of the base disappears,
leaving only the growth lines which
penétrate into the umbilicus.
Aperture triangular, very convex,
prosocline; parietal area covered by a
thin callous coating; columella arched,
very thick and reflected towards the
umbilicus forming in addition a thick
columellar callus which tends progres-
sively to cióse the umbilicus. Outer lip
thin, with smooth margin, only modi-
fied by the basal keel which angles and
expands it laterally. Umbilicus very
narrow and deep, reduced to a narrow
fissure that is almost occluded by the
columellar callus.
Dimensions: the holotype is 2.60 mm
in diameter.
Habitat : Circalittoral species, trawled
at 82 m on bottom with many large
sponges (Stn. T4); at 84-87 m in coarse
muddy sand bottom (Stn. T5); at 61-62
m in fine muddy sand bottom (Stn. T 7);
at 97-120 m on fine sand with seagrass
bottom; at 80-100 m, muddy bottom
with sponges (Stn. T18) and at 106-137
m in fine sand and mud bottom with
echinoderms (Stn. T27).
Remarks : Anticlimax maestratii spec.
nov. is very similar in shape to A. levis
spec. nov. from which it differs by the
srnaller size of its protoconch; by
showing small tubercles and several
spiral grooves in phase two of the proto¬
conch; and by having the whole adapi¬
cal part of the teleoconch covered by
spiral cords and having a much more
oblong aperture.
From A. philippinensis spec. nov. it is
distinguished by the larger size of its
protoconch; by having the same number
of whorls with spiral grooves in phase
two of the protoconch; and because its
basal carina develops only on the last Vi
whorl.
Anticlimax maestratii spec. nov may
be distinguished from A. textilis, A. van-
uatuensis, A. levis and A. spiralis by the
larger size of its protoconch and by
having fine spiral grooves in its second
phase. A. simplex differs by lacking
spiral nodulose cords on the first whorl
of the teleoconch. A. uniformis differs by
lacking a prominent basal carina.
Anticlimax philippinensis spec. nov. (Figures 7C, 51A-E, 52A-F)
Type material: Holotype MNHN 27207 (Figs. 7C, 51A-B) and 1 paratype MNHN 27208 (Fig. 51C).
Material examined: (17 s): Philippines. PANGLAO 2004: 10 s, Bohol Island, west of Baclayon,
9°35.1'N, 123°51.2,E, 34-82 m, coarse muddy sand with large sponges; 1 s, Bohol Island,
Baclayon, Stn. T33, 9°36.0'N, 123°53.7'E, 67-74 m, sand with sponges (Fig. 52); 3 s, Bohol Island,
Cortes, Stn. T18, 9°41.8'N, 123°49.9'E, 80-100 m, muddy bottom with sponges. PANGLAO 2005:
2 s, Balicasag Island, Dipolog Bay, Stn. CP2378, 8°38.8'N, 123°20.TE, 63-65 m, muddy sand
bottom with sponges (type material); 1 s, Panglao Island, Bolod, Stn. TI, 9°32'N, 123°47'E, 83-102
m, mud and many sponges.
Type locality: The Philippines, Balicasag Island, Dipolog Bay, 8°38.8'N, 123°20.TE, 65 m, muddy
sand bottom with sponges [PANGLAO 2004: CP2378].
Etymology: The specific ñame is after the archipelago where the species was found.
Distributiva: Only known from the
Philippines, between 34 and 83 m.
Description : Shell small (<2.00 mm),
solid, formed by 3 Vi whorls growing
rapidly, with a barely visible suture; carí¬
nate basally, with a low spire and nar¬
ro wly umbilicate. The protoconch is
located at a higher level than the teleo¬
conch, measures 320-350 jum, and has a
little more than 2 whorls and 2 distinct
phases; the first is completely smooth
and in the second, there are small scat-
tered granules which are situated cióse to
the suture, as well as growth lines. The
teleoconch is approximately 1 Vi whorls;
it shows only a single carina, in a basal
position, that develops on the last whorl.
Adapical area and base very convex.
81
Iberus , Suplemento 6, 2014
Figure 51A-E. Anticlimax philippinensis spec. nov. A-B: holotype, 1.65 mm (MÑHÑ); C:
paratype, 1.33 mm (MNHN); D: protoconch of the holotype; E: detail of the microsculpture.
Philippines, Balicasag Xsland, PANGLAO 2005, Stn. CP2378, 65 m, sand and muddy bottom
with sponges.
Figura 51A-E. Anticlimax philippinensis spec. nov. A-B : holotipo, 1, 65 mm (MNHN); C: paratipo ,
1,33 mm (MNHN); D: protoconcha del holotipo; E: detalle de la microescultura. Filipinas, Isla de Bal¬
icasag, PANGLAO 2005, Stn. CP2378, 65 m, fondo de arena y fango con esponjas.
On the adapical part of the first
spiral whorl 3 thick, zigzagging, spiral
cords can be observed; the spaces
between the cords, occupied initially by
rhomboidal cells and, after the first half
whorl, by grooves; in the last Vz whorl,
the cords are more numerous, with
more than 20 between the suture and
the basal carina. Base convex; in an
apertural view, 10-11 spiral cords and
quadrangular cells can be seen in the
interspaces of the first quarter of the last
whorl; the rest is completely smooth
except for marked growth lines.
82
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 52A-F. Anticlimax philippinensis spec. nov. A-C: shell, 1.47 mm; D: protoconch (shell of
Figs. A-C); E-F: microsculpture. Philippines, Bohol Island, Baclayon, PANGLAO 2004, Stn. T33,
67-74 m3 sand with sponges.
Figura 52A-F. Anticlimax philippinensis spec. nov. A-C: concha , 1,47 mm; D: protoconcha (de la
concha de las Figs. A-C)); E-F : microescultura. Filipinas, Isla de Bohol, Baclayon, PANGLAO 2004,
Stn. T33, 67-74 m, arena con esponjas.
83
Iberus , Suplemento 6, 2014
Aperture triangular, prosocline; pari¬
etal area covered by a thin callous
coating; columella arched, very thick
and reflected towards the umbilicus,
forming in addition a thick columellar
callus which tends to cióse progres-
sively the umbilicus. Outer lip thin,
with a smooth margin, only modified by
the basal keel which angles and expands
it laterally. Umbilicus very narrow and
deep, reduced to a fissure that is almost
occluded by the columellar callus.
Dimensions: the holotype is 1.65 mm
in diameter.
Habitat : Circalittoral species trawled
at 67-74 m in sand with sponges bottom
(Stn. T33) and at 63-65 m in muddy sand
bottom with sponges; at 34-82 m, in
coarse muddy sand with large sponges
(Stn. T6); at 83-102 m, mud and many
sponges (Stn. TI); at 80-100 m, muddy
bottom with sponges (Stn. T18).
Remarks: From Anticlimax maestratii
spec. nov., A. philippinensis may be dis-
tinguished by the smaller size of the
protoconch and by the lack of spiral
grooves on its phase two; also because
the basal carina is developed on the last
whorl and by having a wider umbilicus.
A. levis spec. nov. differs by having
the adapical part of the teleoconch fully
covered by spiral cords; because the
basal carina is developed on the last
whorl; by having a less prominent col¬
umellar callus and a more open umbili¬
cus.
Anticlimax imitatrix spec. nov. (Figures 7D, 53A-D)
Type material: Holotype MNHN 27230 (Figs. 7D, 53A-B).
Material examined: Only the type material.
Type locality: Solomon Islands, 9°37'S, 160°42,E, 435-461 m [SALOMON 1: Stn. CP1858].
Etymology: The specific ñame alindes to the similarity with the morphology of other species.
Distribution: Only known from the
Solomon Islands, its type locality,
between 435-461 m.
Description : Shell very small (<1.5
mm), strong, bicarinate; with a relatively
high spire and narro wly umbilicate. The
protoconch measures about 330 jum,
with a little more than 2 whorls and 2
distinct phases; the first is completely
smooth and the second apparently
smooth, but bears fine growth lines near
the suture and tiny scattered tubercles.
The teleoconch has 1 Vi whorls and two
carinae which angle the shell, one
peripheral and the other basal. The
peripheral carina is attenuated near the
outer lip and does not modify or angle it.
The ornamentation is composed of
spiral cords, axial folds and cells of dif-
ferent shape in the spaces between the
cords. On the adapical part, the spiral
cords are wide and zigzagging on the
first half whorl, becoming flattened
nodules on the following Vi whorl, to
become smooth again on the last half
whorl. At the beginning of the teleo¬
conch 3 thick cords can be seen; 15 in
the last half whorl between the periph¬
eral carina and the suture. In the space
between the carinae there are 8-9 spiral
cordlets and small axial folds that disap-
pear on the last whorl, keeling the basal
carina and anglirig the outer lip.
The base is convex and on it spiral
cordlets, axial ribs and cells in the inter-
space can be seen.
Umbilicus narrow and deep, limited
by a large cord caused by the thickening
of the base of the columella, occluding it
progressively. Aperture triangular,
prosocline; parietal area callous with a
thick layer; columella arched, thick and
reflected towards the umbilicus, with, at
its base, a cord-like thickening that
occludes that umbilicus; outer lip
margin modified only by the angle cor-
responding to the basal carina, which
prolongs it laterally.
Dimensions: the holotype is 1.3 mm
in diameter.
Habitat: Bathyal species dredged at
435-461 m.
Remarks: The species is characterized
by its small size in comparison with the
84
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 53A-D. Anticlimax imitatrix spec. nov. A--6: holotype, 1.3 mm (MNHN); C: protoconch
(holotype); D: microsculpture. Solomon Islands, Stn. CP1858, 435-461 m.
Figura 53A-D. Anticlimax imitatrix spec. nov. A-B: holotipo, 1,3 mm (MNHN); C: protoconcha
(holotipo); D: microescultura. Islas Salomón, Stn. CP1858, 435-461 m.
dimensions of the protoconch; the wide
spiral cords that become nodulose on
the adapical part of the Vi last whorl; the
presence of small axial folds that disap-
pear, keeling the basal carina; the trian¬
gular shape of the outer lip, its angle
and the lateral extensión, the thickening
and reflection of the columella.
In its general appearance it is very
similar to A. solomomensis spec. nov., but
may be separated by the presence on the
external lip of a single angle instead of
two; by a srnaller number and different
size of the axial folds on the last whorl;
by the greater number of spiral cords on
the adapical part and by these being
almost smooth.
From A. maestratii spec. nov. it is dis-
tinguished by the srnaller size of the
protoconch and the lack of spiral
grooves. From A. philippinensis and A.
uniformis spec. nov. by the teleoconch
being bicarinate and the srnaller size of
the protoconch.
85
Iberus , Suplemento 6, 2014
Table V. Differences between species of group 5.
Vf Diferencias entre especies del grupo 5.
Group 5
Description : The species of this
group, in spite of their different
shapes, can be grouped together by:
being dome-shaped; having a teleo-
conch with a prominent basal carina
which angles and expands the external
Hp.
It is made up of 4 species: A. tentorii,
A. discus, A. lentiformis and A. globulus.
Their differences are shown in Table V.
Anticlimax tentorii spec. nov. (Figures 7E, 54A-E)
Type material: Holotype in MNHN 27209 (Figs. TE, 54A) and 1 paratype (MNHN 27210) (Fig. 54B).
Material examined: (2 s): Only from the type locality.
Type locality: Vanuatu, SW coast of Aoré Island, Segond Channel, 15°35.1'S, 167°07.6'E, 36 m,
coarse sand rubble [SANTO 2006: Stn. ZS25].
Etymology: The specific ñame derives from the Latin word tentorium, -ii, which means "tent" allud-
ing to the shape of the shell
Distribution : Only known from Aoré
Island, Vanuatu, its type locality at 36 m.
Description : Shell of médium size
for the genus (<4.5 mm), very solid,
strongly convex, dome-shaped, with a
marked basal keel; consisting of 4
whorls of rapid growth. Protoconch
with a little more than one whorl,
measuring about 300 jum and being
seemingly smooth, although this could
not be verified due to abrasión of the
specimen. Teleoconch with 3 whorls; a
thin callous sutural coating extends
from the suture and partially covers
the previous whorl and a strong keel
delimits the base. The ornamentation is
formed by spiral cords wider than
their interspaces, which zigzag and
cover the whole shell. Aperture trian¬
gular; very thick parietal callus;
columella slightly arched, very thick
and reflected towards the umbilicus;
outer lip smooth at its margin, not
modified except for the contact area
with the basal keel that widens and
expands it laterally. Umbilicus not very
wide or deep, concealing the earlier
whorls, not limited by any carina and
with only some axial growth lines
inside.
Dimensions: the holotype is 4.2 mm
in diameter.
Habitat : Infralittoral species collected
in coarse sand and rubble bottom at 36
m in depth.
Remarles: The most significarit char-
acteristics of the present species are: its
large size in comparison to other species
of the genus; the convex form (dome-
shaped); the prominent keel which
amplifies the periphery; the thick col-
umellar callus which closes the umbili¬
cus and the angled shape of the outer
lip. With these characteristics this
species is different from all others
known within the genus.
86
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 54A-E. Anticlimax tentorii spec. nov. A: holotype, 4.2 mm (MNHN); B: paratype, 4.05
mm (MNHN); C: protoconch (holotype); D-E: microsculpture and detail. Vanuatu, Segond
Channel, SW coast of Aoré Island, Stn. ZS25, 36 m.
Figura 54A-E. Anticlimax tentorii spec. nov. A: holotipo, 4,2 mm (MNHN); B: paratipo, 4,05 mm
(MNHN); C: protoconcha (holotipo); D-E: microescultura y detalle. Vanuatu, Canal Segond, costa SO
de la isla Aoré, Stn. ZS25, 36 m.
87
Iberus, Suplemento 6, 2014
Anticlimax discus spec. nov. (Figures 7F, 55A-F, 56A-E)
Type material: Holotype MNHN 27211 (Figs. 7F, 55A-B).
Material examined: (2 s): Philippines, PANGLAO 2004: 1 s, Bohol Island, Cortes, Stn. T18, 9°41.2,N,
123°49.9'E, 80-100 m, muddy bottom with sponges (type material). V anua tu: 1 s, MUSORSTOM 8:
Stn. DW1101, 15°03'S, 167°08'E, 205-210 m (Fig. 56).
Type locality: Philippines, Bohol Island, Cortes, 9°41.8'N, 123°49.9,E, 80-100 m [PANGLAO 2004:
Stn. T18].
Etymology: The specific ñame alindes to the discoidal shape of the sheli of this species.
Distribution: Only known from the
Philippines between 80 and 100 m and
from Vanuatu, between 205 and 210 m.
Description: Shell small (<2.5 mm),
very solid, dome-shaped, not umbilicate.
The species has the particularity that
the protoconch is almost completely
covered by the following whorls of the
spire, making it very difficult to specify
size, number of whorls or ornamenta-
tion; however, from what we have been
able to see with SEM, the protoconch
should have a minimum dimensión of
about 220 jum, o ver 1 Vi whorls and a
slightly rough surface of the embryonic
stage.
The teleoconch has 2 whorls and a
thick basal carina. Each whorl covers the
previous one almost completely and its
entire surface shows zigzagging spiral
cords and grooves in the interspaces,
including the surface of the carina. On
the adapical part and for the last half
whorl, there are 26-28 spiral cords all
them reaching the adapical margin of
the outer lip. On the basal carina 4-7
spiral cords can be seen. The base is
convex and is raised in the central part
surrounding the umbilical area; there
are 20 spiral cords, of which 12 are dis-
tributed between the basal carina and
the elevation and 8, wider ones, from
the elevation to the umbilical callus.
Aperture triangular, prosocline; a
thick parietal callus develops on the
base of the sheli; columella arched, very
thick and reflected towards the umbili-
cus, forming a large columellar callus
which occludes it completely; both pari¬
etal and columellar callus are covered
by spiral cords in zigzag, like the rest of
the sheli. Outer lip with a smooth
margin, expanded laterally by the effect
of the basal carina, which angles it inter-
nally. Umbilicus completely covered by
the expansión of the columellar callus.
Dimensions: the holotype is 1.78 mm
in diameter. A sheli from Vanuatu
reaches 2.37 mm.
Habitat: Circalittoral species trawled
at 80-100 m on muddy bottom with
sponges from Philippines, Panglao 2004,
Stn. T18. Bathyal species dredged at 205-
210 m from Vanuatu, MUSORSTOM 8,
Stn. DW1101.
Remarles: The species is characterized
by its shape (dome-shaped), its orna-
mentation formed by cordlets and
zigzagging spiral grooves which cover
all the sheli, including the parietal and
columellar calluses; the wide basal
carina, the thick columellar callus and
the basal elevation that limits the umbil¬
ical area.
Although initially we believed that
due to the different bathymetry and
long distance the materials collected in
the Philippines and Vanuatu were dif¬
ferent species, once all morphological
characters were verified, we have con-
cluded that they are both the same
species.
Anticlimax lentiformis spec. nov. (Figures 7G, 57A-E, 58A-E)
Type material: Holotype MNHN 27212 (Figs. 7G, 57A-C).
Material examined: (3 s): Fiji: 1 s, MUSORSTOM 10: DW1345, 17°15'S, 178°30'E, 660-663 m (type
material). Philippines: 2 s, Bohol Island, Cortes, PANGLAO 2004: Stn. T18, 9°41.2'N, 123°49.9'E, 80-
100 m, muddy bottom with sponges (Fig. 58).
88
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 55A-F. Anticlimax discus spec. nov. A-B: holotype, 1.78 mm (MNHN); C: protoconch
of the holotype; D-F: microsculpture and detail. Philippines, Bohol Island, Cortes, Stn. TI 8,
80-100 m.
Figura 55A-F. Anticlimax discus spec. nov. A-B: holotipo , 1,78 mm (MNHN); C: protoconcha del
holotipo; D-F: micro es cultura y detalle. Filipinas, Isla de Bohol, Cortes, Stn. T18, 80-100 m.
89
Iherus , Suplemento 6, 2014
Figure 56A-E. Anticlimax discus spec. nov. A-C: shell, 2.37 mm; D-E: microsculpture. Vanuatu,
MUSORSTOM 8, Stn. DW1101, 205-210 m.
Figura 56A-E. Anticlimax discus spec. nov. A-C: concha , 2,37 mm; D-E: microescultura. Vanuatu,
MUSORSTOM 8, Stn. DWllOi, 205-210 m.
Type locality: Fiji, 17°15'S, 178°30'E, 660-663 m [MUSORSTOM 10: Stn. DW1345].
Etymology: The specific ñame derives from the Latín word leus, -tis, "lentis" alluding to the shape
of the shell.
Distrihution : Only knowrt from Fiji,
between 660 and 663, and the Philip-
pines between 80 and 100 m.
Description : Shell very small (<1.5
mm), discoid, robust, strongly carínate,
wider than high and umbilicate. The
90
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 57A-E. Anticlimax lentiformis spec. nov. A-C: holotype, 1.46 mm (MNHN); D: proto-
conch of the holotype; E: detall of the sculpture. Fiji, MUSORSTOM 10, DW1345, 660-663 m.
Figura 57A-E. Anticlimax lentiformis spec. nov. A-C: holotipo, 1,46 mm (MNHN); D: protoconch a
del holotipo; E: detalle de la escultura. Fiyi, MUSORSTOM 10, DW1345, 660-663 m.
protoconch has 2 Vi whorls, measures
about 330 jum, and may vary in regard
to the portion covered by the first teleo-
conch whorl. It has two distinct phases;
the first is completely smooth and the
second is covered by growth lines, more
evident along the suture; the first whorl
of the teleoconch partially covers the
protoconch. The teleoconch has about 1
Vi whorls; a thick peripheral carina sur
rounds it; each whorl partially covers
the previous one. Adapical area and
base are convex. Ornamentation formed
by fíat spiral cords, of different sizes,
separated by marked spiral grooves; in
the vicinity of the outer lip and from the
suture to the peripheral carina there are
up to 26-28 smooth cords.
Base with 8 fíat spiral cords of differ¬
ent size and grooves in the interspaces,
cióse to the peripheral carina; there are
fine axial folds that extend from halfway
91
Iberus , Suplemento 6, 2014
Figure 58A-E. Anticlimax lentiformis spec. nov. A-C: shell, 1.3 mm; D: protoconch; E: detail of the
sculpture. Philippines, Bohol Island, Cortes, Stn. TI 8, 80-100 m, in muddy bottom with sponges.
Figura 58A-E. Anticlimax lentiformis spec. nov. A-C: concha, 1,3 mm; D: protoconcha; E: detalle de
la escultura. Filipinas, Isla de Bohol, Cortes, Stn. T18, 80-100 m, en fondo fangoso con esponjas.
along the base to the umbilicus and
marked growth lines that penétrate
inside.
Apertura triangular, prosocline; pari¬
etal area covered by a thick callous
coating; columella arched, very thick
and reflected towards the umbilicus,
forming a callus which tends to occlude
it; adapical part of the outer lip crenu-
lated externally by the termination of
the spiral cords and centrally notched
by the peripheral carina, which expands
it laterally. Height and width of the
umbilicus allow the previous whorls to
be seen. It is progressively occluded by
the thickening and reflection of the col¬
umella, which does not form a thick
spiral eord
92
Rubio & Rolan: The genus Anticlimax In the tropical Southwest Pacific
Dímensions: the holotype measures
1.46 mm ín máximum diameter.
Habitat: In Piji it is a bathyal species,
dredged between 660-663 m deep; in the
Phílippínes/ it ís a circalíttorai species,
trawled between 80-100 m on a muddy
bottom with sponges.
Remarles : The profile of Anticlimax
lentiformis spec. nov. ís similar to the
spedes of its group.
Anticlimax lentiformis spec. nov. is
characteiized by its discoid shape; aíso
by the first whorl of the teleoeonch cov-
ering partially the protoconch, its thíck
perípheral carina, its triangular aperture
and the thickness of the columellar
callus reflected towards the umbilícus.
The differences are: A. tentorii spec.
nov. ís higher, has a wider umbilícus
and a more prómínent end of the spíre
as a confínuation of the keel. A. discus
spec. nov. has an umbilícus totally
closed by a callus expanded from the
columella.
Anticlimax globulus spec. nov. (Figures 7H, 59A-F)
Type material: Holotype MNHN 27231 (Figs. 7H, 59A-C).
Material examíned: Only the type material, i
Type locality: Papua New Guinea, Hargun L, 5°01.6'S, 145°48.1/E, 16 m [PAPUA NIUGINI: Stn.
PS18].
Etymology: The spedfic ñame alludes to the similarity of this spedes with the morphology of a
knob or button.
Distribution : Only known from
Papua New Guinea, at 16 m.
Descriftion : Shell small (<3 mm),
composéd of 4 rapidly increasing
whorls, dome-shaped, basally carínate;
with a low spire and narrowly umbíií-
cate.
The protoconch is placed higher
than the teleoeonch, measures about 430
íim, has more than 2 !4 whorls, is com-
pletely smooth and shows several
phases of development. The teleoeonch
has 1 Vi whorls, a prómínent basa!
carina and is fully decorated with cords
and spíral grooves and marked growth
lines. At the begínning of the teleo-
conchi, there are 4 cords, wider than
their ínterspaces, on the adapícal part
and 8-9 more cords between the suture
and the basal carina, which beeome
thícker on approaching the lip and
modífy its m.argín.
In the fírst half spíral whorl, the
spaces between the cords are occupíed
by quadrangular ceíls which subse-
quentiy disappear, giving way to more
or less wide grooves with munerous
axial stríae ínside. There ís no peripheral
carina; between the adapícal part and
the basal carina there ís a space occu¬
píed by fíat spíral cords. Base slightly
convex on which there are 10 thíck
spiral cords, dístríbuted between the
basal carina and the umbilícus; 2 smalier
cords penétrate ínto the umbilícus; the
spaces between the cords are occupíed
by grooves insíde which there are
munerous growth lines. Aperture trian¬
gular; parietal area covered by a fhick
callus; thíck columella, arched and
reflected towards the umbilícus, but
wíthouf occludíng ít; adapícal part of
outer lip crenulated externally by the
terminatíon of the spíral cords, formíng
a. scalloped margin, basal carina formíng
a narrow angle which prolongs the lip
late rally. Umbilícus narrow and deep
not limited by a cord or keel, with two
cords that penétrate insíde.
Dímensions: the holotype is 2.67 mm
in diameter.
Habitat: Infralíttoral spedes dredged
at 16 m ín depth.
Remarles: A. globulus spec. nov. ís
characferized by the large size of its pro¬
toconch; by its domed shape; by the
wide cords on the adapícal part which,
when they reach the lip, raíse and
modífy ít formíng a scalloped margin;
by the prómínent basal carina which
angles the outer lip and prolongs ít lat-
erally and by its narrow and deep nave!.
93
Iberus , Suplemento 6, 2014
Figure 59A-F. Anticlimax globulus spec. nov. A-C: holotype, 2.67 mm (MNHN); D: protoconch
(holotype); E-F: microsculpture, Hargun L, Papua New Guinea, Stn. PS18, 16 m.
Figura 59A-R Anticlimax globulus spec. nov. A-C: holotipo, 2,67 mm (MNHN); D: protoconcha
(holotipo); E-F: microescultura , isla de Hargun, Papua Nueva Guinea, Stn . PS18, 16 m.
94
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Table VI. Differences between species of group 6.
Tabla VI. Diferencias entre especies del grupo 6.
Group 6
This group is formed by species which
have no very typical shape or much sim-
ilarity but they are discoid, depressed, fine-
ly microsculptured and lack evident
prominences or protuberant carinae.
Títere are 4 species: Anticlimax
boucheti, A virginiae, A. obesa and A. juanae
spec. nov.
Table VI illustrates the differences
between species.
Anticlimax boucheti spec. nov. (Figures 71, 60A-G, 61A-F)
Type material: Holotype MNHN 27213 (Figs. 71, 60A-C). Paratype MNHN 27214, s (Fig. 61A-C)
from West-Southwest of the Pointe d'Easo, Baie du Santal, New Caledonia, Stn. 1430, 20-25 m.
Material examined: (2 s): New Caledonia. MONTROUZIER: 1 s, Stn. 1331, Grand Récif de Koumac,
Koumac area, 20°40'S-20°40.6'S, 164°U.2,E-164°12.1,E, 55-57 m, outer slope (holotype); LIFOU 2000:
Stn. 1430, West-Southwest of Pointe d'Easo, Baie du Santal, 20°47.5'S, 167°07.TE, 20-25 m (paratype).
Type locality: New Caledonia, Grand Récif de Koumac, Koumac area, 20°40'S-20°40.6'S, 1 64° 11,2' E-
164°12.1/E, 55-57 m, [MONTROUZIER: Stn. 1331].
Etymology: The specific ñame is after Dr. Philippe Bouchet of the MNHN the driving forcé behind
the exploration campaigns of the Tropical South Pacific.
Distribution : Only known from New
Caledonia between 25 and 55 m.
Description : Shell small (<2 mm),
formed by less than 4 rapidly increasing
whorls, with a very low spire.
Protoconch protruding, large in reía-
tion to the size of the shell, measuring
about 350 pm in diameter, and having
almost 2 Va whorls; the nucleus is smooth
and the first whorl has a smooth surface
with granules of different shape and size,
randomly distributed; on the following
whorl marked sinuous axial ribs appear.
Teleoconch with 1 Vi whorls developed
on the same plañe. There are 3 carinae
which angle the shell: 2 peripheral and
one lower. Of the two peíipheral carinae,
the adapical one fades and disappears in
the last Vi whorl, while the lower one limits
the base and modifies the outer lip. The
basal carina separates two areas: one
concave, bordering the peripheral carina
and another, convex, which surrounds the
umbilicus. Ornamentation formed by
spiral cords and axial ribs, the latter undu-
lating at the periphery. At the Crossing
point with the cords, the ribs form a char-
acteristic type of cell reticle and also a small
tubercle at the point of intersection.
Aperture rounded; parietal area
covered by a thin callous coating; col-
umella arched, externally reflected, with
a thin edge modified by the spiral cords
of the umbilicus; outer lip with a sharp
margin modified by the spiral cords,
forming a characteristic angle caused by
the peripheral basal carina and its own
basal one.
Very wide umbilicus, that allows the
previous whorls to be seen, delimited by
a basal carina, and bearing larger cells
than the reticule of the shell.
Dimensions: the holotype measures
1.6 mm in diameter.
95
Iherus, Suplemento 6, 2014
Figure 60A-G. Anticlimax boucheti spec. nov. A-C: holotype, 1.6 mm (MNHN); D: apical view
and protoconch (holotype); E-G: microsculpture and detail of the teleoconch. New Caledonia,
Koumac area, Grand Récif de Koumac, Stn. 1331, 55-57 m.
Figura 60A-G. Anticlimax boucheti spec. nov. A-C: bolo tipo, 1,6 mm (MNHN); D: vista apical y
protoconcha (holotipo); E-G: microescultura y detalle de la teleoconcha. Nueva Caledonia, alrededores
de Koumac, Grand Récif de Koumac, Stn. 1331, 55-57 m.
96
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 61A-F. Anticlimax houcheti spec. nov. A-C: paratype, 1 .39 mm (MNHN); D: apical view
and protoconch; E: microsculpture of the protoconch; F: microsculpture of the teleoconch. New
Caledonia, Loyalty Is., Santal Bay, West-Southwest of Easo Point, Stn. 1430, 20-25 m.
Figura 61A-F. Anticlimax houcheti spec. nov. A-C: paratipo, 1,39 mm (MNHN); D: vista apical y
protoconcha; E: microescultura de la protoconcha; F: micro escultura de la teleoconcha. Nueva Caledo¬
nia, Isla de Loyauté, Bahía de Santal, Oeste-Suroeste de Punta Easo, Stn. 1430, 20-25 m.
97
Iberus , Suplemento 6» 2014
Habitat: Circalíttoral species, lívíng
on the external slope of the reef .
Remarles: The clearest characterístics
of Anticlimax boucheti spec. nov. is the
large size (350 |/m) of its protoconch
ornamenfed with granules on the fírst
whorl and followed by unduiating
axial ribs; its teleoconch with three
peripheral carínae/ whídi is decorated
with spíral cords and axial ribs, undu-
lating along the períphery, and its wide
umbilicus.
Anticlimax philsmithi spec. nov. (Figures 8A, 62A-F, 63Á-F)
Type material: Holotype MNHN 27232 (Figs. 8Á, 62Á-F) and 5 paratypes MNHN 27233.
Material examined: (12 s): Papua New Guinea. PAPUA NIUGINI: 6 s, N Kabanam Point, Stn. PS17,
5°Q6.0'8, 145°48.2"B (type material), 2m;5s, N Kíwo, Stn. PS4ó, 5°08.7/S/ 145048.2'E, 2 m, mangrove
and seagrass. Phílippínes» PANGLAO 2004: 1 s, Panglao Island, Pontod Islet, Stn. D5, 9°33.6'N,
123°43.5'E, 0-3 m, soft bottom with seagrass.
Type locaüty: Papua New Guinea, Kabanam Point, 5°0ó.fTS, 145048.2'E, 2 m [PAPUA NIUGINI: Stn. PS17],
Etymology: Thís species is named after Father Phil Smith, Vice-President of the Divine Word Uní-
versity, Madang, whích hosted the Papua Niuguíni 2012 expedítion.
Distribution: Papua New Guinea at 2
m and the Philíppines between 0 and 3 m.
Descripíion: Shell solid in appear-
anee, forrned by 3 3A fast-growing
whorls, basally carinate; with a nearly
fíat spíre and with a narro w umbilicus.
The protoconch has 2 Vi whorls, mea
suríng about 510 ¿um in diameter and
although seemingly smooth, very fine
tuberdes may be seen cióse to the suture
under high magnification; ít ís possible to
see up to 3 phases in its development. The
teleoconch has just 1 !4 whorls and ís
entírely decorated with spiral cords of
similar size, narrower than their ínter-
spaces, between whích diere are rectan¬
gular cells. Amarked carina limits the base,
and there is no other peripheral keel. The
adapical part ís convex and the base ís fíat.
Between the suture and the basal
carina, there are 18 spíral cords; between
the basal carina and the umbilicus there
are 11-12. On the base, thé space between
the first and second spíral cord is a broad
groove, larger than the others, occupied
by fine axial striae ínstead of the cells.
Umbilicus narrow and deep, not limíted
by any carina or occluded by a callus.
Aperture rounded, prosoclíne; parietal
area callous covered by a thíck layer; col-
umella curved, slíghtly reflected towards
the umbilicus; outer lip with a smooth
margín; basal carina angles it intemally.
Dimensions: the holotype measures
1.5 mm ín diameter. The largest shell
studíed measures 1.80 mm.
Habitat: Infralittoral species collected
at -2 m in mangrove and seagrass
bottom (Stn. PS46 in Papua New
Guinea); 0-3 m, soft bottom with sea¬
grass (Stn. D5 ín Philíppines). Bathymet-
ric range between 0-3 m ín depth.
Remarles: Anticlimax philsmithi spec. nov.
ís characterízed by its wide protoconch in
relation to the total diameter of the shell;
by its basal carina and striae that occupy
the spaces between the cords; by its narrow
umbilicus and aperture slightly angled by
a basal carina. A single spedmen from the
Phílippínes has heen studíed and despíte
the general resemblance, its protoconch
has a diameter of 450 |im, sígníficantly less
than the studíed sampíes from Papua New
Guinea.
Anticlimax simplicissima spec. nov. (Figures 8B, 64A-F)
Type material: Holotype MNHN 27234 (Figs. 8B, 64A-F).
Material examined: Only the type material.
Type locaüty: Papua New Guinea, Alexishafen, 5°05.3/S, 145048.TE, 1-6 m [PAPUA NIUGINI: Stn. PD31].
Etymology: The specific ñame alindes to its shape that lacks prominences and has a spíral simple
sculpture.
98
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 62A-F. Anticlimax philsmithi spec. nov. A: holotype, 1.5 mm (MNHN); B: paratype, 1.67
mm (MNHN); C: paratype, 1.7 mm (MNHN); D: protoconch (paratype); E-F: microsculpture.
N Kabanam Point, Papua New Guinea, Stn. PS17, 2 m.
Figura 62A-F. Anticlimax philsmithi spec. nov. A: holotipo, 1,5 mm (MNHN); B: paratipo, 1,67 mm
(MNHN); C: paratipo, 1,7 mm (MNHN); D: protoconcha (paratipo); E-F : microescultura. N de
Punta Kabanam, Papua Nueva Guinea, Stn. PS17, 2 m.
Distrihution : Only known from its
type locality between 1 and 6 m.
Description: Shell small, sturdy, with
a rounded periphery, formed by 3 M
whorls, umbilicate.
The protoconch is deeply sunken,
has 1 Va whorls, measures 200 jum, is
smooth and shows 2 phases in its devel-
opment. The teleoconch has about 2
whorls. The omamentation is formed by
99
Iberus, Suplemento 6, 2014
Figure 63A-F. Anticlimax philsmithi spec. nov. A-C: shell, 1.8 mm; D: protoconch; E-F:
microsculpture. Philippines, Panglao Island, Pontod Islet, 0-3 m.
Figura 63A-F. Anticlimax philsmithi spec. nov : A-C: concha, 1,8 mm; D: protoconcha; E-F: microes-
cultura. Filipinas, Isla de Panglao, Islote de Pontod, 0-3 m.
cords and spiral grooves, covering all
the shell. The subsutural cord is smooth
and very thick; a thick cord decorated
with axial striae borders the umbilicus;
between the subsutural and the periuni-
bilical cords, zigzagging spiral grooves
are distributed. Two not very pro-
nounced carinae are observed at the
100
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 64A-F. Anticlimax simplicissima spec. nov. A-C: holotype, 2.3 mm (MNHN); D: proto-
conch (holotype); E-F: microsculpture. Alexishafen, Papua New Guinea, Stn. PD31, 1-6 m.
Figura 64A-F. Anticlimax simplicissima spec. nov. A-C: holotipo, 2,3 mm (MNHN); D: protoconcha
(holotipo); E-F: microescultura. Alexishafen, Papua Nueva Guinea, Stn. PD31, 1-6 m.
101
Iberus , Suplemento 6, 2014
begirming of the last whorl, one periph-
eral and the other one basal; both disap-
pear in the last quarter whorl.
The spire and the space between the
carinae is convex; the base is slightly
convex in its central area and concave in
the area bordering the basal carina.
Umbilicus funnel shaped, limited by a
thick spiral cord with axial ridges on its
surface; umbilical wall smooth. Aper-
ture rounded, prosocline; parietal area
covered by a thick callus that extends
into the interior of the umbilicus,
occluding it; columella arched, thick,
not reflected; outer lip thickened,
smooth at its margin, only modified by
a slight internal angle caused by the
basal carina.
Dimensions: the holotype measures
2.3 mm in diameter.
Habitat: Infralittoral species collected
between 1-6 m in depth.
Remarks: A. simplicissima is very dif-
ferent from all other species studied and
known, The species is characterized by
the protoconch, which stands at a level
lower than the whorls of the teleoconch;
the thick subsutural cord and the thick
and striated periumbilical cord; the reg-
ularity of the zigzagging in cords and
spiral grooves; the weak carinae; the
parietal callus that penetrates inside the
umbilicus and the particular funnel
shaped umbilicus.
Its ornamentation in zigzag is very
similar to that of other species such as
A. discus ; the fact that the protoconch is
partially covered by the first whorl of
the teleoconch, approximates it to A.
lentiformis , A. discus and A. religiosa.
Anticlimax virginiae spec. nov. (Figures 8C, 65A-G)
Type material: Holotype MNHN 27215 (Figs. 8C, 65A-C).
Material examined: Only from the type locality.
Type locality: Vanuatu, Malparavu Island, 15°22.2,S, 167°11.3'E, 2-3 m [SANTO 2006: Stn. LD09].
Etymology: The specific ñame is after Virginie Héros, Assistant curator of Molluscs, an importan!
person in the malacological studies in the MNHN.
Distribuí-ion: Only known from the
type material between 2 and 3 m.
Description: Shell small (<2 mm),
robust, wider than high, formed by
about 4 whorls, narrowly umbilicate.
Protoconch with 2 V* whorls, measuring
420 jtun. Although it is seemingly
smooth, under magnification it is com-
pletely covered by microgranules; the
end is evident with the microsculpture
of the teleoconch. Teleoconch with 2
whorls showing 2 thick peripheral
carinae which angle the shell, one
located on the adapical part and the
other in the middle of the periphery;
shell markedly convex from the second
carina to the umbilicus. The whole
teleoconch is covered by spiral cords,
narrower than their interspaces, within
which are distributed fine axial striae
and microtubercles.
Aperture oval, very thick; parietal
area with a thick callus forming an
angle; columella very thick, inclined and
reflected towards the umbilicus,
forming a thick callus which occludes it
completely; outer lip very thick, not
modified by spiral cords ñor expanded
laterally by the peripheral carina. There
is a broadened triangular area at the
junction with the columella. Umbilicus
completely occluded by the thickening
and reflection of the columella.
Operculum multispiral with a
central nucleus.
Dimensions: the holotype measures
1.93 mm in diameter.
Habitat: Infralittoral species found in
sediments collected at 2-3 m in depth.
Remarks: The general shape of the shell
comes closer to genus Panastoma Pilsbry
& Olsson, 1952. The lack of zigzagging
cordlets, the thick columellar callus that
occludes the umbilicus by the reflection
of the columella itself and the outer lip not
prolonged by the spiral cords, are char-
acters which leave no doubt about its posi-
tion in the genus Anticlimax.
102
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 65A-G. Anticlimax virginiae spec. nov. A~C: holotype, 1.93 mm (MNHN); D: apical view
and protoconch (holotype); E: detail of the microsculpture of the protoconch; F-G: microsculp-
ture and detail. Vanuatu, Malparavu Island, Stn. LD09, 2-3 m.
Figura 65A-G. Anticlimax virginiae spec. nov. A-C: holotipo, 1,93 mm (MNHN); D: visión apical y
protoconch a (paratipo); E: detalle de la microescultura de la protoconcha; F-G: micro escultura y detalle.
Vanuatu, Isla de Malparavu, Stn. LD09, 2-3 m.
103
Iberus , Suplemento 6, 2014
Ungrouped species
Species included here are very dif™ not need to mention differential cha-
ferent to any other in the genus and do racters.
Anticlimax religiosa spec. nov. (Figures 8D, 66A-E)
Type material: Holotype MNHN 27216 (Figs. 8D, 66A-C).
Material examined: Only from the type locality.
Type locality: Philippines, Pamilacan Island, 9°29.4'N, 123°56.0'E, 15-20 m, hard ground covered
with sand [PANGLAO 2004: Stn. S22].
Etymology: The specific ñame is referred to the similarity of the shell with a religious borrnet.
Distribution : Only known from its
type locality between 15 and 20 m.
Description: Shell very small (<1.50
mm), wider than high, formed by 3 whorls
profusely decorated, not umbilicate. The
protoconch measures at least 245 jum in di-
ameter and has approximately 1 Vi whorls,
is apparently smooth and has 2 distinct
phases; it is partially concealed by the sub-
sequent whorl. The teleoconch has 1 Vi
whorls, is bícarinate, with a peripheral
and a basal carina. Ornamentation formed
by zigzagging cords and grooves covering
all the shell, including the umbilical cal¬
los; 18 cords between the suture and the
peripheral carina can be observed from
the last Vi whorl, 9 between the peripher¬
al carina and the basal one, 10-11 on the
base and 9 on the umbilical callos. Each
whorl tends to cover largely the previous
one. Adapical part and the space between
carinae are slightly concave; base fíat.
Umbilicus narrow and deep, almost
completely covered by the umbilical
callus. Aperture triangular, parietal area
with a thick callus; columella arched,
thickened and reflected towards the
umbilicus, forming a large callus which
occludes it almost completely; outer lip
modified by the carinae which expand it
laterally.
Dimensions: the holotype size is 1.40
mm in diameter and 0.64 mm in heigth.
Habitat : Infralittoral species suc-
tioned at 15-20 m on hard ground
covered with sand bottom.
Remarks : The shell resembles a
bonnet in shape (a religious cap). The
species is characterized by its shape; by
the regular ornamentation of cords and
grooves in zigzag which are distributed
by the whole shell; for the flattened
space between carinae; the shape of the
outer lip, modified by the two carinae
and the umbilical callus which is
covered by cords and spiral grooves in
zigzag and covering the umbilicus to
leave it reduced to a small fissure.
Anticlimax obesa spec. nov. (Figures 8E, 67A-F, 68A-F)
Type material: Holotype MNHN 27217 (Figs. 8E, 67A-C).
Material examined: (2 s): Philippines. AURORA 2007: 1 s, Stn. DW2739, 16°Q5'N, 121°58'E, 96 m
(type material). Papua New Guinea. PAPUA NIUGINI: 1 s, Yomba I., Beach, Stn. PD74, 5°14.7,S,
145°47.4'E, 1-3 m.
Type locality: Philippines, NO "Da-Bfar", 16°05'N, 121°58/E, 96 m [AURORA 2007: Stn. DW2739],
Etymology: The specific ñame refers to the portly aspect of the shell.
Distribution : Only known from the
Philippines at 96 rn and from Papua
New Guinea between 1 and 3 m.
Description : Shell small (size >5.00
mm); very strong and robust, wider
than high, with a very low spire, carí¬
nate and widely umbilicate. The proto¬
conch has 1 lA whorls, measuring about
330 jum and being apparently smooth or
slightly rough. The first whorl of the
104
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 66A-F. Anticlimax religiosa spec. nov. A-C: holotype, 1.4 mm (MNHN); D: protoconch of
the holotype; E-F: sculpture and detail. Philippines, Pamilacan Island, PANGLAO 2004, Stn.
S22, 1 5-20 m on hard ground covered with sand bottom.
Figura 66A-F. Anticlimax religiosa spec. nov. A-C: holotipo, 1,4 mm (MNHN); D: protoconcha del
holotipo; E-F: escultura y detalle. Filipinas, Isla de Pamilacán, PANGLAO 2004, Stn. S22, 15-20 m,
fondo duro con arena.
teíeoconch tends to cover partially the
protoconch.
The teíeoconch has 3 whorls, is bicar-
inate, with one peripheral and another
periumbilical carinae; omamentation com¬
pasee! of spiral cords, grooves or round-
ed cells in the interspaces between the
cords, ribs and axial folds. On the adapi¬
cal part at the beginning of the teíeoconch
4-5 thick cords are observed, which are
105
Iberus , Suplemento 6, 2014
Figure 67A-F. Anticlimax obesa spec. nov. A-C: holotype, 5.9 mm (MNHN); D: protoconch of the
holotype; E-F: microsculpture. Philippines, AURORA 2007, Stn. DW2739, 96 m.
Figura 67A-F. Anticlimax obesa spec. nov. A-C: holotipo, 5,9 mm (MNHN); D: protoconcha del
holotipo; E-F: microescultura. Filipinas, AURORA 2007, Stn. DW2739, 96 m.
106
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 68A-F. Anticlimax obesa spec. nov. A-B: shell, 5.25 mm; C: protoconch; D-F: microsculp-
ture. Papua New Guinea, Yomba Island, Stn. PD74, 1-3 m.
Figura 68A-F. Anticlimax obesa spec. nov. A-B: concha, 5,25 mm; C; protoconcha; D-F: microescul-
tura. Papua Nueva Guinea, isla de Yomba, Stn. PD74, 1-3 m.
107
Iberus , Suplemento 6, 2014
crossed by fine axial ribs, forming small
nodules at the intersections and with deep
cells of rounded aspect in the spaces be-
tween the cords.
After the first whorl, thick axial folds
appear, which elevate the spire in rela-
tion to the peripheral carina; the nodules
of the cords disappear and the cells are
transformed into continuous grooves.
On the last whorl, on the adapical part,
about 20 strong axial folds and 12-13 spi-
ral cords can be seen. There is no basal
carina. From the peripheral to the peri-
umbilical carinae, there are spiral cords
and quadrangular cells in the inter-
spaces; near the base and down to the
periumbilical carina 19 large axial folds
are present. Umbilicus wide and deep,
externally delimited by a carina which
angles it; a very large cord originates
from the thickening of the columella and
continúes internally; umbilical wall
smooth, with only growth lines.
Aperture quadrangular, slightly
prosocline; parietal area covered by a
very thick callus; columella arched, very
thick and reflected towards the umbili¬
cus, forming a thick callus which also
constitutes the cord inside the umbili¬
cus. External lip with an edge not modi-
fied by the spiral cords, with an internal
angle formed by the peripheral carina,
which does not expand the lip laterally.
Dimensions: holotype measures 5.9
mm in diameter and 3.1 mm in height.
Habitat : Species of the infra- and cir-
calittoral. In the Philippines dredged at
96 m in depth; in Papua New Guinea
collected between 1 and 3 m in depth.
Remarks : Anticlimax obesa spec. nov.
is characterized by the relatively largest
size (5.0 mm) and the robustness of the
shell; by the position of the peripheral
carina; by the thick periumbilical cord;
by many folds that thrust from the base
and by its quadrangular aperture.
Anticlimax juanae spec. nov. (Figures 8F, 69A-G, 70A-F, 71 A-E)
Type material: Holotype MNHN 27218 (Figs. 8F, 69A-C).
Material examined: (9 s): New Caledonia, LIFOU 2000: 1 s, Stn. 1426, Huneté, Baie du Santal, Loyalty
Is., 20°45.9'S, 167°06.2'E, 4-7 m (type material). Philippines. PANGLAO 2004: 1 s, Stn. B41, Bali-
casag Island, 9°30.9,N, 123°40.8/E, 17-19 m, floor of large cave; 1 s, Bohol Island, Maribohoc Bay,
Stn. T14, 9°42'N, 123°49'E, 101-110 m, mud with shells; 1 s, Doljo Point, Panglao Island, Stn. M5,
9°35.5'N, 123°43.3,-123°44.3,E, 0-2 m, mixed intertidal platform, fringe mangrove, seagrass; 2 s,
Baclayon, Bohol Island, Stn. S2, 9°37.4'N, 123°54.5'E, 4-5 m, hard bottom with small sediment
patches; 1 s, Stn. B21, 9°37.2'N, 123°46.4'E, 20-21 m, reef wall with small caves; 1 s, Bohol Island,
Ubajan, Stn. S25, 9°41.5'N, 123°51.0'E, 21 m, mud; 1 s, Panglao Island, Napaling, Stn. B8, 9°37.PN,
123°46.1'E, 3 m, subtidal reef platform.
Type locality: New Caledonia, Huneté, Baie du Santal, Loyalty Is., 20°45.9'S, 167°06.2'E, 4-7 m
[LIFOU 2000: Stn. 1426].
Etymology: The specific ñame is after luana Maria Lijó Ageitos, from Valencia, Spain, a good friend
of the first author.
Distribution : Loyalty Is., in New
Caledonia between 4-7 m and the
Philippines between 2 and 101 m.
Description: Shell small (>2.00 mm),
very strong, robust, bicarinate, densely
ornamented and narrowly umbilicate;
formed by 3 3á whorls; last whorl cover-
ing most of the previous whorls. The pro-
toconch is situated on a lower level and is
partially covered by the first whorl of the
teleoconch. It has 1 lA whorls, measuring
220 jum, is slightly rough and comprises 2
phases separated by a lip thickening. The
teleoconch has 2 Vi whorls and shows two
thick carinae, one basal and the other peri¬
umbilical, developed in zigzag.
Ornamentation formed by thick axial
ribs that begin at the suture zone and end
at the basal carina; by other shorter thick
ribs that unite the basal and periumbili¬
cal carinae; also by spiral cordlets sepa¬
rated by deep grooves, in which fine axial
striae can be seen. These cordlets are
extended in zigzag and are distributed
108
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 69A-G. Anticlimax juanae spec. nov. A-C: holotype, 2.55 mm (MNHN); D: protoconch
(holotype); E-F: microsculpture; G: detail. New Caledonia, Loyalty Is., Santal Bay, in front of
Huneté, Stn. 1426, 4-7 m, bottom of small rocks in sandy areas.
Figura 69A-G. Anticlimax juanae spec. nov. A-C: holotipo, 2,55 mm (MNHN); D: protoconcha
(holotipo); E-F: microescultura; G: detalle. Nueva Caledonia, Islas de Loyauté, Bahía de Santal, frente
a Huneté, Stn. 1426, 4-7 m, fondo de pequeñas rocas en áreas arenosas .
109
IberuSy Suplemento 6, 2014
Figure 70A-F. Anticlimax juanae spec. noy. A-B: shell, 1.9 mm, Philippines, Doljo Point, Panglao
Island, Stn. M5, 0 -2 m; C-D: shell, 2.0 mm, Philippines, Napaling, Panglao Island, Stn. B8, 3 m;
E: protoconch; F: microsculpture.
Figura 70A-F Anticlimax juanae spec . nov. A-B: concha, 1,9 mm, Filipinas, Punta Doljo, Isla de
Panglao, Stn. M5, 0-2 m; C-D: concha, 2,0 mm, Filipinas, Napaling, Isla de Panglao, Stn . B8, 3 m;
E: protoconcha; F: microescultura.
over all the teleoconch; 28 cords can be
observed along the outer lip, from the
suture to the basal carina, 11-12 cords from
the basal to the periumbilical carinae and
15-16 inside the umbilical area.
Aperture triangular; parietal area
with a thick callus; columella curved,
thick, reflected towards the umbilicus;
both the umbilical and the parietal callus
are covered by zigzagging spiral cords;
110
Rubio & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Figure 71A-E. Anticlimax juanae spec. nov. A-B: juvenile shell, 1.4 mm; C: protoconch; D-E:
microsculpture. Philippines, Bohol Island, Maribohoc Bay, Stn. Ti 4, 101-110 m.
Figura 71A-E. Anticlimax juanae spec. nov. A-B: concha juvenil, 1,4 mm; C: protoconcha; D-E:
microescultura. Filipinas, Isla de Bohol, Bahía de Maribohoc, Stn. T14, 101-110 m.
IberuSy Suplemento 6, 2014
outer lip thick, modified by the basal
carina which prolongs it laterally. Umbili-
cus small and deep, almost occluded by
the thickening of the columellar callus;
umbilical area funnel-shaped, with very
weak axial ribs inside.
Dimensions: the holotype is 2.55 mm
in diameter.
Habitat: Infralittoral-circalittoral species
found on a bottom of small stones with
patches of sediment at 4-7 m in depth from
Loyalty Is., New Caledonia. The speci-
mens from the Philippines were collected
at 3 m, brushing on a subtidal reef plat-
form (Stn. B8); at 20-21 m, brushing on reef
wall with small caves (Stn. B21); at 17-19
m, brushing on the floor of large caves
(Stn. B41); at 0-2 m in mixed intertidal plat-
form, fringe mangove, seagrass (Stn. M5);
at 4-5 m, on a hard bottom with patches
of sediment (Stn. S2) and at 101-110 m,
trawled in mud with shells (Stn. T14).
Remarks : This is one of the species with
the most densely ornamented shell among
all the studied material; the carinae and
zigzagging cordlets plus the thick axial
ribs are characters which differentiate this
species from its congeners.
Only two bands, one near the basal
carina and another between the basal
and periumbilical carinae appear
without spiral cords or grooves in the
studied specimen, from Loyalty Is., Baie
du Santal (Fig. 69). This specimen also
has a protoconch that is somewhat larger
in diameter (245 jum), as well as a lower
number of axial folds between the basal
and the periumbilical carinae. All these
differences are not enough for specific
differentiation, so we group all studied
specimens from both Loyalty Is. and the
Philippines within the same species.
The 10 samples from Philippines
studied, have the same ornamentation,
without smooth bands, contrary to what
happens in the single specimen from
Loyalty Islands; only in the case of finding
new specimens exhibiting such smooth
zones could we think of a specific sepa-
ration.
OTHER SPECIES STUDIED
Anticlimax rostrata (Hedley, 1900) (Figures 72A-C)
Anticlimax cf. rostrata (Figure 72E-F)
Liotia rostrata Hedley, 1900 (original combination). Proc. Linn. Soc . N.S.W. 24(3): 502, pl. 26, figs.
4-7. [Type locality: off Cape York, Torres Strait].
Lioprora rostrata (Hedley, 1900): Laseron (1958). Records ofthe Austr alian Museum 24(11): 169, figs. 25-27.
Canimarina rostrata (Hedley, 1900): Faber (2012). Miscellanea Malacologica 5(5): 94.
Type material: Holotype deposited in the Australian Museum (c. 8100), examined by photographs
(Figs. 72A-C).
Other material studied: 1 s. Papua New Guinea, S Urembo L, outer slope, PAPUA NIUGINI: Stn
PS43, 05°15.9/S, 145°47.1,E, 14 m (Figs. 72E-F), in this paper as Anticlimax cf. rostrata.
Remarks : Originally, Hedley (1900)
placed the species in the genus Liotia,
but with doubts. Laseron (1958) created
the genus Lioprora and places Liotia ros¬
trata as the type species, mentioning:
"The rostíate aperture of Lioprora should
alone be sufficient to establish its generic
identity".
Faber (2012) discusses the syn-
onymy of Canimarina with Anticlimax
made by Rubio et al. (2011); he consid-
ers Canimarina a valid genus and
ineludes in it Anticlimax crassilabris, A.
glaber and Lioprora rostrata.
As we have stated previously
(Rubio et al. 2011), we continué to
consider Canimarina a júnior synonym
of Anticlimax, and therefore Lioprora
Laseron, 1958 must be considered a
synonym of Anticlimax and Lioprora
rostrata Hedley, 1900 should be placed
in the genus Anticlimax, changing its
ñame to Anticlimax rostrata (Hedley,
1900).
112
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 72A-E. Anticlimax rostrata (Hedley, 1900). A-B: holotype, 2.8 mm (Australian Museum,
c.8100); C: protoconch of the holotype; D: original figures. E-F: Anticlimax cf. rostrata, 2.55 mm
and protoconch, S Urembo Island, Papua New Guinea, Stn PS43, 14 m.
Figura 72A-E. Anticlimax rostrata (Hedley, 1900). A-B: holotipo, 2,8 mm (Australian Museum,
c.8100); C: protoconcha del holotipo; D: figura original. E-F : Anticlimax cf. rostrata, 2,55 mm y pro-
toconcha, S Isla de Urembo, Papua Nueva Guinea, Stn PS43, 14 m.
This species is characterized by its
spire which is developed almost on the
same plañe, its particular ornamentation
and the broad funnel shaped umbilicus.
The specimen studied and identified
as Anticlimax cf. rostrata presents mor-
phological characters that we can identify
in the holotype as a flattened spire and
113
Iherus , Suplemento 6, 2014
the axial costulation seen on the adapical
part; however, it has no axial ribs on the
periphery and the base. This specimen is
apparently not an adult and therefore has
not fully developed either the aperture or
the characteristic angulation of the outer
lip that expands the aperture laterally.
The protoconch apparently has less
whorls, measuring about 335 iim and has
developed two phases; the first shows a
rough surface and the second has thick
tubercles, that sometimes appear aligned
or, at other times, dispersed; the lip thick-
ening separates it from the teleoconch.
Anticlimax sp. (Figures 73A-E)
Material studied: 1 s. Papua New Guinea, S Urembo I., PAPUA NIUGINI, Stn PS41, 05°15.9'S -
145°47.1,E, 10 m, outer slope.
Description: The protoconch has 1 Vi
whorls measuring about 340 jum in
diameter and there are 2 phases in its
development; the first is situated on a
tilted plañe with respect to the axis of
the shell and is slightly rough; the
second phase shows some very small
and scattered tubercles. The teleoconch
has at least two whorls, is dorsally
slightly convex and basally very convex
and it has a thick peripheral carina.
Ornamentation formed by spiral cords
and axial ribs which intersect forming
cells of different shapes and size. On the
adapical part there are 6 spiral cords at
the beginning of the teleoconch and 15“
16 flatter ones at the end, between the
suture and the peripheral carina.
The base is also completely covered
by spiral cords intersected by axial ribs
that starting from the umbilical margin
go up to the peripheral carina. Umbilicus
wide and deep, with smooth walls, not
occluded by any callus, but limited by a
carina formed by the thickening of the
base of the columella. The aperture is
quadr angular; the columella is thick and
arched; the outer lip is angled centrally
by the effect of the peripheral carina.
Dimensions: the studied shell mea-
sures 2.7 mm in diameter.
Remarles: Anticlimax sp. shows
unique morphological characters that
make it very different from A. rostrata
and A. cf. rostrata, but the fact of having
a single shell, it not being completely
adult or if it is adult, having a broken
aperture, makes it difficult for us to dif-
ferentiate it specifically from congeneric
species.
Other species in this genus
During the study of the tropical
South Pacific species, it was necessary to
make a comparison with other taxa pre-
viously known. Those from the
Caribbean have been recently sampled
and commented by Rubio, Fernández-
Garcés & Rolán (2011). For the
Caribbean species we refer the reader to
that work.
Other species in the Pacific area are:
Anticlimax niasensis (Thiele, 1925) (Figures 74A-F)
Discopsis niasensis Thiele, 1925. Wissenschaftliche Ergebnisse der deutschen Tiefsee-Expedition aufdem
Dampfer " Valdivia " 1898-1899. 17 (2): 76, pl. 5, figs. 34-6. [Type locality: Indian Ocean, Stat. 193:
off Sumatra, S of Mas, (0°30.2/N, 97°59.07'W)].
Type material: Examined: Two dried shells (syntypes): one entire shell, 2 mm; the other syntype
is a fragment deposited in Museum für Naturkunde, Berlin - Malakologie. (ZMB/Moll - 109214).
Type locality: Indian Ocean, Stat. 193: off Sumatra, S of Nias, (0°30.2'N, 97°59.07'W).
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 73A-E. Anticlimax sp. A-C: shell, 2.7 mm; D: protoconch; E: microsculpture. S Urembo L,
Papua New Guinea, Stn. PS41, 10 m.
Figura 73A-E. Anticlimax sp. A-C: concha. , 2,7 mm; D: protoconcha; E: microescultura. S de Isla de
Urembo, Papua Nueva Guinea, Stn. PS41, 10 m.
Description: See Tríele (1925). The
protoconch has a little more than 2
whorls with 280 pm in diameter and, in
spite of its poor condition, some strong
tubercles can be seen on its second whorl.
The last half whorl of the protoconch is
partially covered by the first whorl of the
teleoconch; this makes the protoconch
appear to be deflected in relation to the
axis of the shell (Fig. 74E). The teleo-
conch, on the adapical part, appears
covered by spiral cords with rounded
cells in their interspaces; basaily the shell
is apparently smooth. A strong callus is
developed behind the columella and
occludes the umbilicus progressively.
Remarks: A. niasensis may be distin-
guished from A. padangensis by having a
scarcely ornamented teleoconch, a more
closed umbilicus and by the slight
carina being situated in the middle of
the periphery.
1 15
IheruSy Suplemento 6, 2014
Anticlimax padangensis (Thiele, 1925) (Figures 75A-F)
Discopsis padangensis Thiele, 1925. Wissenschaftliche Ergebnisse der deutschen T iefsee-Expedition auf
dem Dampfer " Valdivia " 1898-1899. 17 (2):76, pl. 5, figs. 40-2. [Holotype - Type locality: Indone¬
sia, Sumatra, Padang].
Type material: Holotype (ZMB / Moll-1 08506); one shell labelled as syntype (ZMB/Moll-109213)
off Sumatra, S of Nias, Q°30'2"N, 97°59/7"Wi Deutsche Tiefsee-Expedition
Type locality: Padang, Sumatra, Indonesia.
Description : See Thiele (1925). The
protoconch has 2 whorls, with a diameter
of about 300 jum and because of its poor
condition we cannot see any ornamenta-
tion. Shell bicarinate: a peripheral and
another basal carinae. The peripheral, is
weakened towards the outer lip avoiding
the forming of an angle; the basal carina
expands the lip laterally and forms a
strong projection of the outer lip. The
space between the carinae is concave.
The teleoconch is covered by spiral cords
on the adapical part; basally the axial ribs
are predominant. Umbilicus large allow-
ing the previous whorls to be seen.
Remarks : For separation from A.
niasensis see above in the remarks on
this species.
Anticlimax carinata (A. Adams, 1863)
Adeorbis carinatus A. Adams, 1863. Proc. Sci. Meet. Zool. Soc. London, pp. 75 [Type locality: Seto-
Uchi; Akasi (Akasi, Hyógo prefecture. Seto inland sea].
Vitrinella carinata (A. Adams, 1863): Okutani (2000). Marine Mollusks in japan, pp. 173, pl. 86, fig. 2.
Type material: Syntype deposited in BMNH (1874.5.19.49) figured in Higo, Callomon & Goto
(1999: G1010).
Description : Original description in
A. Adams (1863): "A. testa ovato-orbicu-
lari , obliqua, depresso-conoidali, subdi -
aphana , alba, late umbilicata ; anfractibus
convexius culis , transversim tenuiter stri-
atis, rapide accrescentibus, ultimo antice
dilatato , ad peripheriam acute carinato;
apertura subtrigonali, antice angulata et
producía, umbilico margine acuto".
Habitat : Known only from shallow
waters in the Seto Inland Sea (Okutani,
2000).
Remarks : A. Adams (1863: 75)
comments: "The keel at the periphery
is marked and prominent, forming an
acute ledge around the last whorl. The
only other species at all resembling it
is A. subcarinata, found in the British
seas".
Okutani (2000: 173) described the
species as: " Shell depressed conical,
translucent white. Body whorl [f] lange
(sic )large with sharply angulate periphery
and fíat base. Suture canaliculated on the
body whorl. Outer lip of the aperture with a
strong projection at its base".
Anticlimax carinatus does not look at
all like Adeorbis subcarinatus Montagu,
1803 ( Tornus subcarinatus ) but it has a
great resemblance to the new described
species Anticlimax vanuatuensis and A.
levis, and the already described A.
niasensis , mainly in the basal keel which
is increased on the last whorl of the
teleoconch and which gives it a charac-
teristic shape. Although we could not
examine the holotype despite having
requested it to the NHMLJK, we con-
sider that it is a different species from A.
vanuatuensis, A. levis and A. niasensis
fundamentally due to its known distrib-
ution area.
Adeorbis carinatus A. Adams, 1863
must be placed in genus Anticlimax,
changing its ñame to Anticlimax carina¬
tus (A. Adams, 1863).
116
RUBIO & ROLÁN: The genus Anticlimax in the tropical Southwest Pacific
Figure 74A-F. Anticlimax niasensis (Thiele, 1925). A-E: syntype, 2 rnm (ZMB, 109214). F: proto-
conch (syntype).
Figura 74A-F. Anticlimax niasensis (Thiele, 1925). A-E: sintipo, 2 mm (ZMB, 109214). F: protocon-
cha (sintipo).
117
Iberus , Suplemento 6, 2014
Figure 7SA-E. Anticlimax padangensis (TMelel 1925). A-C: holotype, 2 mm (ZMB, molí 108506). D-
E: fragment, 1.2 mm, labeíled as syntype, Sumatra (ZMB molí 109213); F; protoconch of this last
fragment.
Figura 75A-E. Anticlimax padangensis (Tbiek, 1925), A-G hobtipo, 2 mm (ZMB, molí 108506). D-E: frag¬
mento, 1,2 mm, etiquetado como sintipo, Sumatra (ZMB moü 109213); F: pmtoconcha de este último fragmento.
SPECIES NOT IN THE GENU8 ANTICLIMAX
Vitrinella arifca Bartsdi, 1915 (Figure 76)
Vitrinella ( Docomphala ) arifca Bartsch, 1915. [Type locality: Fort Alfred, South África].
Type material: Holotype and one paratype deposited in USNM (250554), come from Fort Alfred
(ColL Num. 1427).
118
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Figure 76. Vitrinella ( Docomphala ) arifca Bartsch, 1915. Original figuration in Bull. USNM, 91,
PL 32, figs. 7-9.
Figura 76. Vitrinella (Docomphala) arifca Bartsch, 1915. Representación original en Bull. USNM,
91, PL 32, figs. 7-9.
Description : Original descríption in
Barstch (1915: 168):" Shell minute, rather
thick, semitranslucent, bluish white. Nuclear
whorls one and one-half, well rounded, pol-
ished, smooth. Postnuclear turns one and
one-fourth, strongly rounded, marked by two
slender spiral cords at the summit and mi¬
croscopio spiral striations on the rest of the
surface. In addition to the spiral sculpture
the turns are marked by fine Unes ofgrowih.
On the outer edge of the aperture a number
of strongly incised spiral scratches make
their appearance. Sutures well impressed.
Periphery of the last whorl well rounded.
Base well rounded, strongly umbilicated. The
umbilicus is limited exteriorly by a strong,
slightly tuberculated, spiral cord. Three addi -
tional, strongly tuberculated, spiral cords,
which decrease in strength from the outer
edge inward, mark the inner wall of the um¬
bilicus. The posterior portion of the base, be-
tween the limiting spiral cord of the umbili¬
cus and the periphery, is smooth, while the
other half adjoining the spiral cord is marked
by decidedly retractively slanting, oblique,
slender, axial ribs which anastomose with the
spiral cord limiting the umbilicus. Aperture
circular; outer lip very thick; inner lip very
strong and reflected, strongly curved within,
the outer edge oblique and straight. The pos¬
terior angle of the aperture is filled by a
strong callus. The type measures: altitude
0.6 mm; greater diameter 1.1 mrn".
Remarks: In World Register of Marine
Species (WORMS) Sartori (2013) places
Vitrinella (Docomphala) arifca Bartsch,
1915 in genus Anticlimax, but consider-
ing it as " Species Inquirenda".
In our opinión, on the basis of the
description and original figuration, it is
not an Anticlimax, and probably it is a
Leucorhynchia or a Cirsonella.
119
Iberus , Suplemento 6, 2014
CONCLUSIONS AND COMMENTS
¿fet,
In the present paper, out of 44
species studied, only one could be
assigned, with doubts, to a known taxon
(A. rostrata ); one more is presented as
sp., due to the fact that it is either a juve-
nile or has a broken outer lip; the other
42 have been described as being consid-
ered new. The lack of knowledge about
this group is probably due to the small
size of most species and because the
area has traditionally been scarcely
sampled in a little known Pacific Ocean.
Two more taxa, previously known, were
placed in other genera and now are con¬
si de red in the genus Anticlimax.
Precisely due to their small size and
being collecting in sediments, nothing
was known about the soft parts and we
present here some data on the external
anatomy and on the radula.
The species here studied and
described were collected in the follow-
ing countries:
-Philippines 22 species
-Papua New Guinea 11 species
-Vanuatu 10 species
-New Caledonia 5 species
-Solomon Is. 4 species
-Fiji 2 species.
Due to the scarce material available
for most species, information on overall
range cannot be considered sufficient. In
fact, it is probable that some species
have a larger distribution than a single
archipelago. There are species with a
short protoconch (1 Vi whorls) that are
probably endemic to one archipelago,
but there are quite a few others with
two whorls of protoconch or a little
more indicating a planktotrophic
period, which probably may live in
several archipelagos.
The rarity of the material collected is
highlighted when one realizes that only
in 4 species the number of shells col-
lected was higher than 10; in 2 cases, the
number was between 5-10; on 5 occa-
sions, the shells were 4-5; in 7 cases,
they were 3; in 6, only 2; and in 20 cases,
only one shell was available. Fortu-
nately, the genus is very rich in morpho-
logical details and microsculpture, and
so, conclusions could be reached based
on so few specimens.
In some few cases a particular
species has been collected in more than
one country: five species (A. simulans, A.
cyclist, A. dentata, A. philsmithi and A.
obesa ) were collected in the Philippines
and Papua New Guinea; one species {A.
fecunda ) was collected in New Caledonia
and Vanuatu; another (A. tamarae ) was
collected in the Solomon Islands and the
Philippines; yet another (A. discus) in
Vanuatu and the Philippines; a further
one (A. juanae ) in New Caledonia and
the Philippines; and finally the last {A.
lentiformis ) in Fiji and the Philippines.
The Philippines seems to be the
country with more species, presenting
the greatest diversification of this group;
this is followed by Papua New Guinea
with 11 species and Vanuatu with 10.
Regarding the sculpture, there are
only two patterns common to all the
species: either a smooth surface (some-
times partially), or with spirally aligned
circular or oval depressions (Fig. 3A-C);
these depressions become confluent
when they increase in size (Fig. 3D),
fusing together and forming a space
between cords that has a zigzag profile.
The studied species are mostly from
shallow water. Those collected in very
deep water are few:
Between 0 and 10 m, 15 species were
collected, but exclusively between these
limits only 9 of them; they were 4 in
Papua New Guinea, 2 in the Philip¬
pines, 2 in Vanuatu and 1 in New Cale¬
donia.
Between 10 and 100 m, 26 species
were collected: 15 in the Philippines, 5
in Papua New Guinea, 2 in New Cale¬
donia and 6 in Vanuatu.
Between 100 and 200 m, 9 species in
the Philippines.
Between 200 and 300 m, 3 species: 1
in New Caledonia, 1 in Vanuatu and 1
in Fiji.
In more than 300 m, 3 species: 2 in
the Solomons and 1 in Vanuatu.
In more than 400 m, 6 species: 4 in
the Solomons, 1 in Vanuatu and 1 in Fiji.
120
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Deeper that 600 m, 2 species: 1 in Fiji
and 1 in Vanuatu.
There are some inconsistencies in the
vertical deep collecting in some species:
for example, A. lentiformis was collected
between 80-100 m in the Philippines
while in Fiji it was between 660-663 m.
However, with such limited quantities
of material, the information may be
changed accidentally.
So far, nothing is known about the
habitat of species of Anticlimax. From all
the localities studied, the Philippines is
the geographical area with the largest
number of described species (22), which
are distributed between the infralittoral,
circalittoral and bathyal floors. Infralit-
toral species have been found predomi-
nantly on hard ground bottom covered
with sand or seagrass; or on soft bottom
(fine sand, mud) with seagrass. Circalit¬
toral species have been found in coarse
sand, fine muddy sand, mud and fine
sand or muddy bottoms with sponges.
The bathyal species come from fine sand
and mud bottom with echinoderms or
mud bottom with shells,
There were two species collected
alive: A. maranii found in caves in the
reef wali; in reef slope or in reef wall
with small caves. The study of its radula
show its affinity with species of Nozeba
such as Nozeba topaziaca (Hedley), as
well as with other species belonging to
the genera included in Vitrinellinae as
Cyclostremiscus calameli (Jousseaume,
1872) or Torninae as Tornus subcarinatus
(Montagu, 1803). Anticlimax cf cyclist
from SANTO [DSCN1661] could be
photographed alive and the animal
showed characters of Vitrinellidae
(cephalic tentacles finely ciliate; snout
distally bilobed; foot expanded anteo-
orly with small lateral projections.)
The radular pattern and the multi-
spiral operculum with a central nucleus
BXBLIOGRAFHY
Adams A. 1863. On the Genera and Species of
Liotiinae found injapan. Proceedings ofthe Sci-
entific Meetings ofthe Zoological Society of hon¬
dón, pp. 71-76.
in Anticlimax maranii spec. nov. as well
as the anatomical characters of A. cf
cyclist confirm the systematic position of
Anticlimax in Tornídae, subfamily Vit¬
rinellinae, based so far on the morpho-
logical characters of the shell.
ACKNOWLEDGEMENTS
The material in this paper is based on
the numerous expeditions to the Pacific
Ocean conducted by MNPíN and IRD
o ver the last 25 years. The deep-sea expe¬
ditions are presented by Bouchet et al.
(2008), and the acknowledgements in their
paper are also relevant here. The inde-
fatigable energy of Bertrand Richer de
Forges, sénior scientist on many of these
deep-sea cruises, is specially acknowl-
edged here. The Santo 2006 Global Biodi-
versity Survey and the Papua Niuguini
2012 expedition were made possible
thanks to generous grants from the Total,
Stavros Niarchos and Prince Albert II of
Monaco Foundations to the MNHN "Our
Planet Reviewed" programme. Philippe
Maestrati has coordinated the family-level
sorting of the material studied here. We
also acknowledge the editorial input by
Virginie Heros.
We thank Dr. María Isabel Fraga,
director of the Museo de Historia
Natural of the University of Santiago de
Compostela for the support in obtaining
numerous SEM photographs necessary
for this and other works. This pho-
tographing work was made in coopera-
tion with Jesús Méndez and Inés Pazos
of the CACTI of the University of Vigo.
Also we thank to Javier Conde his
hard work making corrections to the
English text and also to the editor of
Iberus, Serge Gofas, by his constant
effort making corrections and improv-
ing the text with his suggestions.
Aguayo C. & Borro P. 1946. Nuevos molus¬
cos del Terciario Superior de Cuba. Revista
de la Sociedad Malacológica "Carlos de la Torre"
4(1): 9-12, pl. 1.
121
Iberus , Suplemento 6, 2014
Bartsch P. 1915. Report on the Turton collection
of South African marine mollusks, with addi-
tional notes on other South African shells con -
tained in the United State National Museum.
xii + 305 pp. + 54 pls. 8vo, cloth bound.
Bieler R, & Mikkelsen P.M. 1988. Anatomy and
reproductive biology of two western Atlantic
species of Vitrinellidae, with a case of protan-
drous hermaphrodítism in the Rissoaeea. The
Nautilus , 102(1): 1=29.
Bouchet P., Heros V. Lozquet P. & Maes-
trati P. 2008. A quarter-century of deep-sea
malacoiogícal exploration in the South and
West Pacific: Where do we stand? How far
to go? Tropical Deep-Sea Benthos, Volunte
25. Mémoires du Muséum National d'Histoire
Naturelle , 196: 9=40.
Bouchet P. & Rocroi J.P. (Ed.); Fryda ]., Haus-
dorf B., Ponder W., Valdés Á. & Warén A.
2005. Classification and nomenclátor of gas-
tropod families. Malacologia, 47(1=2): 397 pp.
ConchBooks, Hackenheim, Germany.
Criscione F. & Ponder W.F. 2013. A phyloge-
netic analysis of rissooidean and cingulop-
soidean families (Gastropoda: Gaenogas-
tropoda). Molecular Phylogenetics and Rvolu-
tion, 66: 1075-1082.
Faber M.J. 2007. Marine gastropods from the
ABC Isiands and other localitíes 20. Solariorbis
semipunctus Moore, 1965 (Gastropoda: Vit-
rinellídae), first records for Florida, USA and
Curasao. Miscellanea Malacologica, 2(4): 84.
Fígs. 1-3.
Faber M.J. 2012. Marine gastropods from the
ABC-islands and other localities 37. Further
notes on the status of Canimarina Aguayo &
Borro, 1946 (Gastropoda: Vitrinellidae). Mis¬
cellanea Malacologica 5(5): 94.
Hedley C. 1900. Studies on Austr alian Mol-
lusca. No. 2. Proceedings of the Linnean Soci-
ety N.S.W. 24(3): 495-513.
Higo S., Callomon P. & Goto, Y. 1999. Cata¬
logue and hihliography of the marine shell-bear -
ing Mollusca ofjapan. Elle Scientific Publica-
tions, Osaka, pp. 749.
Keen A.M. 1960. In R. C.Moore (ed.), Treatise
on Invertebrate Paleontology, Part 1, Mollusca 1.
Mollusca - general features, Scaphopoda , Am-
phineura, Monoplacophora , Gastropoda - gen¬
eral features, Archaeogastropoda , mainly Paleo-
zoic Caenogastmpoda and Opisthobranchia. Ge¬
ológica! Society of America & Unív. Kansas
Press, Boulder, CO and Lawrence KS, xxiii
+ pp. 1-351.
Laseron C.F. 1958. Liotidae and ailied mol-
luscs from the Dampierian Zoogeographí-
cal Province. Records of the Australian Mu¬
seum 24(11): 165-182.
OB1S Indo-Pacific Molluscan DataBase.
http:/ / clade.ansp.org/obis/ find_mol-
lusk.html
Okutani T. 2000. Marine Mollusks in Japan.
Tokai University Press, Tokyo, Japan, 1173
pp.
Pilsbry H.A. & McGimty T.L. 1946. Vitrinelli¬
dae of Florida. Part4. The Nautilus, 60(1): 12-
18, pl. 2.
Pilsbry H.A. & Olsson A.A. 1945. Vitrinellidae
and similar gastropods of the Panamic
Province. Part I. Proceedings ofthe Academy of
Natural Sciences ofPhiladelphia, 97: 249-273, pls.
22-30.
Pilsbry H.A. & Olsson A.A. 1950. Vitrinellidae
of Florida: Part 5. The Nautilus , 63(3): 85-87,
pl 5.
Pilsbry H.A. & Olsson A. A. 1952. Vitrinellidae
of the Panamic Province: II. Proceedings ofthe
Academy Philadelphia , 104: 35-88, pls. 2-13.
Rolan E., Fernamdez-Garcés R. & Rubio F.
1997. Una nueva especie de Anticlimax (Gas¬
tropoda: Vitrinellidae) de Cuba. Iberus, 15: 31-
34.
Rolan E. & Rubio F. 2002. The family Torrádae
(Gastropoda, Rissooidea) in the East Atlantic.
Supl Reseñas Malacologicas, SEM: 1-93.
Rubio F. & Rolán E. 2011. Posición taxonómica
del género Discopsis (Prosobranchia,
Tomidae). Noticiario SEM , 55: 33-35.
Rubio F.,. Fernández-Garcés R. & Rolán E.
2011. The family Tomidae (Gastropoda, Rís-
sooídea) in the Caribbean and neíghboring
areas. Iberus, 29(2): 1-240.
Thiele J. 1925. Gastropoda der deutschen Tief-
see-Expedítion, Theil 2. Wissenschaftliche
Ergebnisse der deutschen Tiefsee-Expedition auf
dem Dampfer " Valdivia " 1898-1899. 17(2): 1-
348, pl 1-34.
Vaught K.C. 1989. A classification ofthe living
Mollusca. Melbourne, Florida, 139 pp.
Verduin A. 1976. On the systematíc of recent
Ríssoa of the subgenus Turbadla Cray, 1847,
from the Mediterranean and European At¬
lantic coasts. Basteria , 40: 21-73.
WoRMS Editorial Board, 2013. World Reg-
ister of Marine Species. Available from
http: / / www.marinespedes.org at VLIZ. Ac-
cessed 2013-October-26.
122
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
Alphabetial Index
Adeorhis carinata . . . . . . . . . 116
aitormonzoi Anticlimax . . . 11, 49, 50
annae Anticlimax . 6
Anticlimax aitormonzoi . . . 11, 49, 50
Anticlimax annae ................................ 6
Anticlimax arifca . . . . 6, 118, 119
Anticlimax athleenae . . .6
Anticlimax bicarinata . . . 11, 34, 35
Anticlimax bicornis . . 10, 29, 30
Anticlimax boucheti . . . 13, 95, 96
Anticlimax callyglypta . . 5
Anticlimax carinata . . . . . . . 6, 116
Anticlimax crassilabris . 6
Anticlimax cyclist . . . . . 11, 52, 53
Anticlimax decórala . . . . . 5, 6
Anticlimax dentata . 11, 56, 57
Anticlimax discus . . . . . 13, 88, 89
Anticlimax elata . . 12, 56, 61
Anticlimax fastigata . . . 12, 63, 64
Anticlimax faviformis . . 10, 15, 16
Anticlimax fecunda . . . 10, 21, 22
Anticlimax fijiensis . . . 11, 36, 37
Anticlimax glabra . 6
Anticlimax globulus . . . . 13, 93, 94
Anticlimax hispaniolensis . 6
Anticlimax imitatrix . 13, 84, 85
Anticlimax infaceta ........................... 10, 26, 27
Anticlimax juanae . 14, 108, 109
Anticlimax lentiformis . . . . . 13, 88, 91
Anticlimax levis . . . . . 12, 68, 72
Anticlimax locklini . . . 6
Anticlimax maestratii . 13, 78, 79
Anticlimax maranii . . . 11, 39, 40
Anticlimax niasensis . . . . . 6, 114, 117
Anticlimax obesa . . . . 14, 104, 106
Anticlimax occidens . 6
Anticlimax padangensis . . . 6, 114, 118
Anticlimax philippinensis . . . 13, 81, 82
Anticlimax philsmithi . . . 14, 98, 99
Anticlimax pilsbryi . 6
Anticlimax proboscidea . . 5, 6
Anticlimax puncticulata . . . 10, 32, 33
Anticlimax reinaudi . . . . . . . 11, 43, 44
Anticlimax religiosa . . . 14, 104, 105
Anticlimax rhinoceros . . . 12, 65
Anticlimax robusta . . . 10, 24, 25
Anticlimax rostrata . . . . 6, 112, 113, 120
Anticlimax schumoi . .6
Anticlimax serrata ........................... 11, 43, 45
Anticlimax simplex . 12, 74, 76
Anticlimax simplicissima . . . 14, 98, 101
Anticlimax simulans .......................... 10, 17, 18
123
Iberus , Suplemento 6, 2014
Anticlimax singularis . .
Anticlimax solomonensis .
Anticlimax sp ......
Anticlimax spiralis ....
Anticlimax tamarae ....
Anticlimax tentorii ....
Anticlimax textilis ....
Anticlimax umbiliglabra .
Anticlimax uniformis . . .
Anticlimax vanuatuensis .
Anticlimax virginiae . . . ,
Anticlimax willetti . . . .
Anticlimax ........
apertus Discopsis . ... .
arifca Anticlimax . ... .
athleenae Anticlimax . . .
bicarinata Anticlimax . . .
bicornis Anticlimax ....
boucheti Anticlimax . . .
calameli Cydostremiscus .
calliglyptum Teinostoma .
Canimañna ........
Canimarina crassilabris . .
Canimarina glabra . ... .
Canimarina rostrata . . .
carinata Adeorbis . ... .
carinata Anticlimax . . .
carinata Vitrinella .....
Circulus striatus ......
Climacia .........
Climacina .........
Circulus .........
Cochliolepis parasítica . . .
cocolitoris Teinostoma . . .
crassilabris Anticlimax . .
crassilabris Canimarina . .
crassilabris Cydostremiscus
cyclist Anticlimax ....
Cydostremiscus calameli .
Cydostremiscus crassilabris
decipiens Solariorbis . . . .
decórala Antidimax ....
dentata Antidimax ....
Discopsis apertus .....
Discopsis niasensis . ... .
Discopsis padangensis . . ,
discus Antidimax ....
elata Antidimax .....
fastigata Antidimax . . .
faviformis Anticlimax . .
fecunda Antidimax ....
fijiensis Antidimax ....
glabra Antidimax . ... .
glabra Canimarina .....
. .10,29,31
. . 12, 60, 62
. . 114, 115
. . 12, 73, 75
. .11,46,47
. . 13, 86, 87
. .12,67,69
. .10,17,20
. .13,76, 77
. . 12, 67, 70
14, 102, 103
. .... .6
. . . . .4,5
. .... .2
. 6, 118, 119
. .6
. . 11, 34, 35
. .10,29,30
. .13,95,96
. . .2,121
. ... .5,8
. .... .5
. .... .6
. .... .6
. . . .6, 112
. ... .116
... .6,116
. ... .116
. .... .2
...... 4
. .... .4
.... .42
. .... .2
. .... .2
. .... .6
. .... .6
. .... .5
. . 11, 52, 53
. . . 2, 121
. .... .5
. .... .5
. ... .5,6
. .11,56,57
. .... .2
. .114,117
. . 114, 118
. 13, 88, 89
. 12, 56, 61
. 12, 63, 64
. 10, 15, 16
. 10, 21, 22
, . 11, 36, 37
. .... .6
. .... .6
124
RUBIO & RoláN: The genus Anticlimax in the tropical Southwest Pacific
globulus Antidimax . . . 13, 93, 94
hispaniolensis Antidimax . . . 6
imitatrix Antidimax . . . . . 13, 84, 85
infaceta Antidimax . . . 10, 26, 27
juanae Antidimax . . . . 14, 108, 109
leloupi Tornus . . 2
lentiformis Antidimax . . . . . . 13, 88, 91
levis Antidimax . . . . . . 12, 68, 72
Lioprora . . 5
Lioprora rostrata . . . . . . 112
Liotia rostrata . . 112
locklini Antidimax . . 6
maestratii Antidimax . . 13, 78, 79
maranii Antidimax . 11, 39, 40
Miralabrum . . . . . . .5
niasensis Antidimax . . . 6, 114, 117
niasensis Discopsis . . . . 114, 117
Nozeba topaziaca . . . 42, 121
obesa Antidimax . . . . 14, 104, 106
occidens Antidimax . 6
padangensis Antidimax . . . . 6, 114, 118
padangensis Discopsis . . . 114, 118
parasítica Cochliolepis . 2
philippinensis Anticlimax . . . . . 13, 81, 82
philsmithi Anticlimax . . . . . . . 14, 98, 99
pilsbryi Anticlimax . .6
Ponderinella skeneoides . 2
proboscidea Antidimax . . . . 5, 6
Pseudoliotia . 42
puncticulata Anticlimax . . . . . . 10, 32, 33
reinaudi Anticlimax . . . . . 11, 43, 44
religiosa Anticlimax . . . . . . 14, 104, 105
rhinoceros Anticlimax . . . . . 12, 65
robusta Anticlimax . . . 10, 24, 25
rostrata Anticlimax . . . . . 6, 112, 113, 120
rostrata Canimarina . . . 6, 112
rostrata Lioprora . 112
rostrata Liotia . . . . 112
schumoi Anticlimax . . .6
serrata Anticlimax . . . 11, 43, 45
simplex Anticlimax . . . 12, 74, 76
simplicissima Antidimax ....................... 14, 98, 101
simulans Anticlimax . . . 10, 17, 18
singularis Anticlimax . . . 10, 29, 31
skeneoides Ponderinella . . 2
Solariorbis decipiens . 5
solomonensis Anticlimax . . . . . 12, 60, 62
spiralis Anticlimax . . . . . 2, 73, 75
striatus Circulus . 2
subcarinatus Tornus . . . . . . 2, 42, 121
Subclimax . . .5
tamarae Anticlimax . . . 11, 46, 47
Teinostoma calliglyptum . 5, 8
Teinostoma cocolitoris . . 2
125
Iberus , Suplemento 6, 2014
tentorii Anticlimax . 13, 86, 87
textilis Anticlimax . 12, 67, 69
topaziaca Nozeba . . 42, 121
Tornidae . .4
Tornus leloupi . . 2
Tornus subcarinatus . . . 2, 42, 121
Truncatelloidea . . .4
umbiliglabra Anticlimax . . 10, 17, 20
uniformis Anticlimax . . . 13, 76, 77
vanuatuensis Anticlimax . 12, 67, 70
virginiae Anticlimax . . 14, 102, 103
Vitrinella carinata ............................... 116
Vitrinellinae . 4
willetti Anticlimax . 6
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texto, incluidas láminas, gráficos y tablas. Las notas son trabajos de menor extensión. Las monografías son tra¬
bajos sobre un tema único, de extensión superior a las 50 páginas de la revista y que serán publicadas, si
procede, como un suplemento de Iberus. Los autores interesados en publicar monografías deberán ponerse
previamente en contacto con el Editor de Publicaciones. Se entiende que el contenido de los manuscritos no ha
sido publicado, ni enviado simultáneamente a otra revista para su consideración.
• Los manuscritos, así como toda la correspondencia relacionada con los mismos, deberán ser remitidos a:
Serge Gofas, Editor de Publicaciones, Departamento de Biología Animal, Universidad de Málaga, Campus de
Teatinos, s/n, 29071, Málaga, España y /o al correo electrónico <sgofas@uma.es>.
• El texto del trabajo podrá estar redactado en español, inglés, italiano, francés o portugués.
• Los artículos, notas y monografías deberán presentarse sobre DIN A-4, por una sola cara a doble espacio
(incluyendo referencias, pies de figura y tablas), con al menos 3 centímetros de margen por cada lado. Los tra¬
bajos se entregarán por triplicado (original y dos copias) y se incluirá una versión en un CD, o bien remitida
por correo electrónico, utilizando procesadores de texto en sus versiones de corrientes de Windows o Macin¬
tosh. En caso de autoría compartida, uno de los autores deberá hacerse responsable de toda la corresponden¬
cia.
• Junto con el trabajo debe incluirse una lista de al menos 4 posibles revisores del mismo, sin perjuicio de los
que el propio Editor considere oportunos.
• Los manuscritos se presentarán de acuerdo al siguiente esquema:
Primera página. Deberá incluir un título conciso, pero sugerente del contenido del trabajo, así como una traduc¬
ción al inglés del mismo (si el artículo no está escrito en inglés). Cuando sea preciso, deberá incluir referencia a
familia o taxones superiores. A continuación figurarán, por este orden, el nombre y apellidos completos del
autor o autores, las direcciones completas de los mismos, y un resumen del trabajo y su traducción al inglés.
Dicho resumen deberá sintetizar, en conjunción con el título, tanto los resultados como las conclusiones del
artículo; se sugiere una extensión de 100 a 200 palabras.
Páginas siguientes. Incluirán el resto del artículo, que debe dividirse en secciones precedidas por breves encabe¬
zamientos. Siempre que sea posible, se recomienda seguir el siguiente esquema: Introducción, Material y
métodos. Resultados, Discusión, Conclusiones, Agradecimientos y Bibliografía. Si se emplean abreviaturas no
habituales en el texto, deberán indicarse tras el apartado de Material y Métodos.
• Las notas breves deberán presentarse de la misma forma, pero sin resumen.
• Deberán evitarse notas a pie de página y referencias cruzadas. Deberán respetarse estrictamente los Códigos
Internacionales de Nomenclatura Zoológica y Botánica (últimas ediciones). Cuando un taxón aparezca por
primera vez deberá citarse su autor y fecha de su descripción. En el caso de artículos sistemáticos, cuando se
den las sinonimias de los taxones, éstas deberán citarse COMPLETAS, incluyendo en forma abreviada la
publicación donde fueron descritas, y la localidad tipo si es conocida entre corchetes, según el siguiente
esquema (préstese especial cuidado a la puntuación):
Dendrodoris limbata (Cuvier, 1804)
Sinonimias
Doris limbata Cuvier, 1804, Ann. Mus. Hist. Nat. París, 4 (24): 468-469 [Localidad tipo: Marsella].
Doris nigricans Otto, 1823, Nov. Act. Ac. Caes. Leop.-Car., 10: 275.
Dichas referencias no deberán incluirse en la lista de Bibliografía si es la única vez que se nombran en el texto.
Si se incluyen una lista completa de referencias de un taxón inmediatamente tras éste, deberá seguirse el
mismo esquema (sin incluir en Bibliografía las referencias que no se mencionen en otro lugar del texto).
• Sólo los nombres en latín y los de taxones genéricos y específicos deberán llevar subrayado sencillo o prefe¬
rentemente ir en cursiva. En ningún caso deberá escribirse una palabra totalmente en letras mayúsculas, ni
siquiera el Título. Las unidades a utilizar deberán pertenecer al Sistema Métrico Decimal, junto con sus correc¬
tas abreviaturas. En artículos escritos en castellano, en los números decimales sepárese la parte entera de la
decimal por una coma inferior (,), NUNCA por un punto (.) o coma superior (')•
• Las referencias bibliográficas irán en el texto con minúsculas o versalitas: Fretter y Graham (1962) o Fretter
y Graham (1962). Si son más de dos autores se deberán citar todos la primera vez que aparecen en el texto
[Smith, Jones y Brown (1970)] empleándose et al. las siguientes veces [Srnith et al. (1970)]. Si un autor ha publi¬
cado más de un trabajo en un año se citarán con letras: (Davis 1989a; Davis 1989b). No deberá emplearse op.
cit. La lista de referencias deberá incluir todas las citas del texto y sólo éstas, ordenadas alfabéticamente. Se
citarán los nombres de todos los autores de cada referencia, sea cual sea su número. Los nombres de los
autores deberán escribirse, en letras minúsculas o Versalitas. No deberán incluirse referencias a autores
cuando éstos aparezcan en el texto exclusivamente como autoridades de un taxón. Los nombres de las publica-
ciones periódicas deberán aparecer COMPLETOS, no abreviados. Cuando se citen libros, dése el título, editor,
lugar de publicación, n° de edición si no es la primera y número total de páginas. Deberán evitarse referencias
a Tesis Doctorales u otros documentos inéditos de difícil consulta. Síganse los siguientes ejemplos (préstese
atención a la puntuación):
Fretter V. y Graham A. 1962. British Prosobranch Molluscs. Ray Society, London, 765 pp.
Ponder W.F. 1988. The T runcatelloidean (= Rissoacean) radiation - a preliminary phylogeny. En Ponder, W.F.
(Ed.): Prosobranch Phylogeny. Malacological Review, suppl. 4: 129-166.
Ros J. 1976. Catálogo provisional de los Opistobranquios (Gastropoda: Euthyneura) de las costas ibéricas. Mis¬
celánea Zoológica, 3 (5): 21-51.
• Las gráficas e ilustraciones deberán ser originales y presentarse preferentemente en formato electrónico al
formato de caja de la revista o proporcional a éste. Este formato es de 57 mm (una columna) o 121 mm (dos) de
anchura y hasta 196 mm de altura, si bien se recomienda utilizar el formato a dos columnas. Es importante que
todas las figuras sean remitidas en su formato original (por ejemplo, las fotografías en .jpg de alta calidad o .tif,
las gráficas en hojas de cálculo Excel o documentos de CorelDraw), puesto que las ilustraciones insertadas en
el manuscrito WORD son inservibles en la fase de imprenta. Las imágenes digitales deben ser formateadas en
su tamaño de impresión con una resolución mínima de 300 ppp para imágenes en color o escala de grises y de
600 ppp para las de blanco y negro. Considérese la reducción que será necesaria a la hora de decidir el tamaño
de las escalas o letras en las figuras, que no deberán bajar de los 2 mm. En figuras compuestas, cada parte
deberá etiquetarse con letras mayúsculas, el resto de las letras deberán ser minúsculas. Las escalas de dibujos y
fotografías deberán ser gráficas, utilizando unidades del sistema métrico decimal; no deberán hacerse referen¬
cias a los aumentos de una determinada ilustración, ya que éstos cambian con la reducción. En su caso, se
recomienda la utilización de mapas con proyección UTM. Cada figura, gráfica o ilustración deberá presentarse
en hojas separadas y con numeración arábiga (1, 2, 3,...), sin separar "Figuras" y "Láminas". Los pies de
figura, en una hoja aparte, deberán acompañarse de su traducción al inglés (o español si el inglés es la lengua
del trabajo). Utilícese el esquema siguiente:
Figura 1. Neodoris carvi. A: animal desplazándose; B: detalle de un rinóforo; C: branquia.
Las abreviaturas empleadas en las ilustraciones deberán incluirse en los pies de figura.
Los autores interesados en incluir láminas en color deberán consultar con el editor y sufragar el sobrecoste con
una contribución de 30 € por página. Por lo demás, deberán ajustarse a los mismos requisitos indicados para
las figuras.
Si se pretende enviar gráficas o ilustraciones en impresión de papel es imprescindible presentar originales de
buena calidad. Las imágenes en semitonos deben estar bien contrastadas y ajustarse al tamaño definitivo de
impresión; al componer fotografías sobre una hoja, procúrese que los espacios entre ellas sean regulares y que
estén debidamente alineadas. Téngase en cuenta que incluir fotografías de distinto contraste en una misma
página conlleva una pobre reproducción final. Las gráficas de ordenador deberán imprimirse con impresora
láser sobre papel de buena calidad.
• Las Tablas se presentarán en hojas separadas, siempre con numeración romana (I, II, III,...). Las leyendas se
incluirán en una hoja aparte acompañándose de una traducción al inglés. Deberán evitarse las tablas particu¬
larmente complejas. Se recomienda reducir el número y extensión de ilustraciones, láminas o tablas al mínimo
necesario.
• Los artículos que no se ajusten a las normas de publicación serán devueltos al autor con las indicaciones de
los cambios necesarios.
• El Comité Editorial comunicará al autor responsable del trabajo la fecha de recepción del trabajo y la fecha
de envío a revisión. Cada original recibido será sometido a revisión por al menos dos investigadores. El
Comité Editorial, a la vista de los informes de los revisores decidirá sobre la aceptación o no de cada manus¬
crito. El autor recibirá en cada caso copia de los comentarios de los revisores sobre su artículo. En caso de
aceptación, el mismo Comité Editorial, si lo considera conveniente, podrá solicitar a los autores otras modifica¬
ciones que considere oportunas. Si el trabajo es aceptado, el autor deberá enviar una copia impresa del mismo
corregida, acompañada por una versión en un CD, utilizando procesadores de texto en sus versiones corrien¬
tes de Windows (pero no el formato .docx generado por Word 2007, el habitual de Windows Vista) o Macin¬
tosh. La fecha de aceptación figurará en el artículo publicado.
• Las pruebas de imprenta serán enviadas por correo electrónico al autor responsable, exclusivamente para la
corrección de erratas, y deberán ser devueltas en un plazo máximo de una semana. Se recomienda prestar
especial atención en la corrección de las pruebas.
• De cada trabajo se entregarán gratuitamente 50 separatas, además de una versión electrónica en formato pdf.
Aquellos autores que deseen un número mayor, deberán hacerlo constar al devolver las pruebas de imprenta,
y nunca posteriormente. El coste de las separatas adicionales será cargado al autor. Los autores podrán hacer
uso de sus separatas en formato electrónico en una web personal o institucional, siempre que se trate de un
sitio sin ánimo de lucro.
INSTRUCTIONS TO AUTHORS
• Iberus publishes research papers, notes and monographs devoted to the various aspects of Malacology.
Papers are manuscripts of more than 5 typed pages, including figures and tables. Notes are shorter papers.
Monographs should exceed 50 pages of the final periódica!, and may be published as Supplemenfs. Authors
wishing to publish monographs should contact the Editor. Manuscripts are considered on the understanding
that their contents have not been published or simultaneously submitted for publication elsewhere.
• Manuscripts and correspondence regarding editorial matters must be sent to: Serge Gofas, Editor de Publica¬
ciones, Departamento de Biología Animal, Universidad de Málaga, Campus de Teatinos, s/n, 29071, Málaga,
Spain and/or to the e-mail <sgofas@uma.es>.
• Manuscripts may be written in Spanish, English, Italian, French or Portuguese.
• Manuscripts must be typed double spaced (including the references, figure captions and tables) on one side
on A-4 (297x210 mm) with margins of at least 3 cm. An original and two copies must be submitted, together
with a CD or e-mail remittance containing the article written with a current Windows or Macintosh word
processor. When a paper has joint authorship, one author must accept responsibility for all correspondence.
• The authors must inelude a list of at least 4 possible referees; the Editor can choose any others if appropriate.
• Papers should conform the following layout:
First page. This must inelude a concise but informative title, with mention of family of higher taxon when
appropriate, and its Spanish translation. It will be followed by all authors' ñames and surnames, their full
address(es), an abstract (and its Spanish translation) not exceeding 200 words which summarizes not only con¬
tents but results and conclusions.
Following pages. These should content the rest of the paper, divided into sections under short headings. When-
ever possible the text should be arranged as follows: Introduction, Material and methods, Results, Discussion,
Conclusions, Acknowledgements and References. Unusual abbreviations used in the text must be grouped in
one alphabetic sequence after the Material and methods section.
• Notes should follow the same layout, without the abstract.
• Footnotes and cross-references must be avoided. The International Codes of Zoological and Botanical
Nomenclature must be strictly followed. The first mention in the text of any taxon must be followed by its
authority including the year. In systematic papers, when synonyms of a taxon are given, they must be cited IN
FULL, including the periodical, in an abbreviate form, where they were described, and the type localities in
square brackeís when known. Follow this example (please note the punctuation):
Dendrodoris limbata (Cuvier, 1804)
Synonyms
Doris limbata Cuvier, 1804, Ann. Mus. Hist. Nat. París, 4 (24): 468-469 [Type locality: Marseille].
Doris nigricans Otto, 1823, Nov. Act. Ac. Caes. Leop.-Car., 10: 275.
These references must not be included in the Bibliography list, except if referred to elsewhere in the text. If a
full list of references of the taxon is to be given immediately below it, the same layout should be followed (also
excluding from the Bibliography list those which are not cited elsewhere).
Only Latín words and ñames of genera and species should be underlined once or be given in italics. No word
must be written in UPPER CASE LETTERS. SI units are to be used, together with their appropriate symbols. In
Spanish manuscripts, decimal numbers must be separated with a comma (,), NEVER with a point (.) or upper
comma (').
• References in the text should be written in small letters or Small capitals: Fretter and Graham (1962) or
Fretter and Graham (1962). The first mention in the text of a paper with more than two authors must
inelude all of them [Smith, Jones and Brown (1970)], thereafter use et al. [Smith et al. (1970)]. If an author has
published more than one paper per year, refer to them with letters: (Davis 1989a; Davis 1989b). Avoid op. cit.
The references in the reference list should be in alphabetical order and inelude all the publications cited in the
text but only these. ALL the authors of a paper must be included. These should be written in small letters or
Small capitals. The references need not be cited when the author and date are given only as authority for a tax-
onomic ñame. Tifies of periodicals must be given IN FULL, not abbreviated. For books, give the title, ñame of
publisher, place of publication, indication of edition if not the first and total number of pages. Keep references
to doctoral theses or any other unpublished documents to an absolute minimum. See the following examples
(please note the punctuation):
Fretter V. and Graham A. 1962. British Prosobranch Molluscs. Ray Society, London, 765 pp.
Pender W.F. 1988. The Truncatelloidean (= Rissoacean) radiation - a preliminary phylogeny. In Ponder W.F.
(Ed.): Prosobranch Phylogeny. Malacological Review, suppl. 4: 129-166.
Ros J. 1976. Catálogo provisional de los Opistobranquios (Gastropoda: Euthyneura) de las costas ibéricas. Mis¬
celánea Zoológica, 3 (5): 21-51.
• Figures must be original and provided preferably in electronic format and adjusted to page format and
column size. These should be one column (57 mm) or two columns (121 mm) wide and up 196 mm high, or be
proportional to these sizes. Two columns format is recommended. It is essential that all figures be supplied in
their original format (e.g. photographs as high-grade .jpg or as .tif files, graphs as Excel spreadsheets or Corel-
Draw files), as the files inserted into WORD documents cannot be used for printing. Digital images must be
given their final printing size with a resolution at least 300 dpi for colour and halftones, and at least 600 dpi for
black/white.
Take into account possible reduction in lettering drawings; final lettering must be at least 2 mm high. In com-
posite drawings, each figure should be given a capital letter; additional lettering should be in lower-case
letters. A scale line, labelled with SI units, must be used to indicate size; magnification ratio must be avoided
as it may be changed during printing. UTM maps are to be used if necessary. Figures must be submitted on
sepárate sheets, and numbered with consecutive Arabic numbers (1, 2, 3,...), without separating 'Plates' and
'Figures'. Legends for Figures must be typed in numerical order on a sepárate sheet, and a Spanish translation
must be included. Follow this example (please note the punctuation):
Figure 1. Neodoris carvi. A: animal crawling; B: rhinophore; C: gills.
If abbreviations are to be used in illustrations, they should be included in the figure captions.
Authors wishing to publish illustrations in colour should consult with the editor and will be charged a contri-
bution of 30 € per page. They should otherwise follow the same standards as black and white prints.
If the authors want to send Figures in printed format, it is essential to supply good quality origináis. Half-tone
images must be of good contrast, and should be submitted in the final printing size. When mounting pho¬
tographs in a block, ensure spacers are of uniform width. Remember that grouping photographs of varied con¬
trast results in poor reproduction. Computer graphics must be printed on high quality white paper with a
láser printer.
• Tables must be numbered with Román numbers (I, II, III,...) and each typed on a sepárate sheet. Headings
should be typed on a sepárate sheet, together with their English translation. Complex tables should be
avoided. As a general rule, keep the number and extensión of illustrations and tables as reduced as possible.
• Manuscripts that do not conform to these instructions will be returned for correction before reviewing.
• Authors submitting manuscripts will receive an acknowledgement of receipt, including receipt date, and the
date the manuscript was sent for reviewing. Each manuscript will be critically evaluated by at least two refer¬
ees. Based of these evaluations, the Editorial Board will decide on acceptance or rejection. Anyway, authors
will receive a copy of the referees' comments. If a manuscript is accepted, the Editorial Board may indicate
additional changes if desirable. Acceptable manuscripts will be returned to the author for consideration of
comments and criticism; a finalized manuscript must then be returned to the Editor, together with a CD con-
taining the article written with current Windows (but not a .docx format generated by Word 2007, mainly used
under Windows Vista) or Macintosh word processor. Dates of reception and acceptance of the manuscript will
appear in all published articles.
• Proofs will be e-mailed to the author for correcting errors and must be returned corrected within one week.
At this stage no stylistic changes will be accepted. Pay special attention to references and their dates in the text
and the Bibliography section, and also to numbers of Figures and Tables appearing in the text.
• Fifty reprints per article and a pdf file will be supplied free of charge. Additional reprints must be ordered
when the page proofs are returned, and will be charged at cost. NO LATER orders will be accepted. Authors
may post a pdf file of their papers on a personal or institutional webpage, with the condition that it should be
a non-profit website.
1
.
La Sociedad Española de Malacología
Junta Directiva desde el 11 de julio de 2011
Presidente
Vicepresidente
Secretario
Tesorero
Editor de Publicaciones
Bibliotecario
Vocales
Jesús S. Troncoso
Gonzalo Giribet
Ramón Álvarez Halcón
Luis Murillo Guillen
Serge Gofas
Rafael Araujo Armero
José Templado González
Carmen Salas Casanova
Alberto Martínez Ortí
José Ramón Arrébola Burgos
Benjamín Gómez Moliner
La Sociedad Española de Malacología se fundó el 21 de agosto de 1980. La sociedad se registró como una aso¬
ciación sin ánimo de lucro en Madrid (Registro N° 4053) con unos estatutos que fueron aprobados el 12 de
diciembre de 1980. Esta sociedad se constituye con el fin de fomentar y difundir los estudios malacológicos
mediante reuniones y publicaciones. A esta sociedad puede pertenecer cualquier persona o institución interesada
en el estudio de los moluscos.
Sede SOCIAL: Museo Nacional de Ciencias Naturales, d José Gutiérrez Abascal 2, 28006 Madrid, España.
Cuotas para 2014:
DESDE ABRIL
INSCRIPCIÓN: 6 euros, además de la cuota correspondiente.
A los socios residentes en España se les aconseja domiciliar su cuota. Todos los abonos deberán enviarse al
Tesorero (dirección reseñada anteriormente) el 1 de enero de cada año. Los abonos se harán sin recargos para la
sociedad y en favor de la Sociedad Española de Malacología y no de ninguna persona de la junta directiva. Aque¬
llos socios que no abonen su cuota anual dejarán de recibir las publicaciones de la Sociedad. Los bonos de ins¬
cripción se enviarán junto con el abono de una cuota anual al Tesorero.
A los residentes en el extranjero se les ruega que abonen su cuota mediante giro postal en euros (internatio-
nal postal money orders in euros sent to the Treasurer). Members living in foreing countries can deduce 6 euros
if paid before 15 April.
Cada socio tiene derecho a recibir anualmente los números de Iberas, Reseñas Malacológicas y Noticiarios que
se publiquen.
SMITHSONIAN l IRRapifc
3 9088 02025 9602
Iberus
ÍNDICE
Suplemento 6
Rubio F. & ROLÁN E. The family Tornidae in the tropical Southwest Pacific: the genus Anticlimax
Pilsbry & McGinty, 1946 (Gastropoda, Truncatelloidea) with the description of 42 new
species
La familia Tornidae en el Suroeste del Pacífico Tropical: el género Anticlimax Pilsbry & McGinty,
1946 (Gastropoda, Truncatelloidea) con la descripción de 42 especies nuevas . 1-126
ISSN 0212-3010