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Research Article
New species of Rissoidae (Mollusca, Gastropoda) from the Archipelago of the Azores (northeast Atlantic) with an updated regional checklist for the family
expand article infoRicardo Cordeiro, Sérgio P. Ávila
‡ University of the Azores, Ponta Delgada, Portugal
Open Access

Abstract

Four new species of shallow-water marine gastropods belonging to the family Rissoidae are described from the Archipelago of the Azores: Setia alexandrae sp. n., S. ermelindoi sp. n., S. netoae sp. n., and Manzonia martinsi sp. n. These novelties increase the regional rissoid fauna to 39 species, of which 29 live in shallow-water habitats. A list of the species of Rissoidae from the Azores is presented based on data from the literature and new material examined.

Keywords

Taxonomy, Caenogastropoda , Rissooidea , Setia , Manzonia , Eastern Atlantic

Introduction

Molluscs are among the best known marine invertebrates in the Archipelago of the Azores. Several publications have addressed this subject in recent decades, resulting in a consistent increase of the mollusc richness for the Azores based on the description and record of species (Amati 1987, Gofas 1989, 1990, Hoenselaar and Goud 1998, Aartsen 2008, Malaquias et al. 2009, Martins et al. 2009, Ávila et al. 2011, Malaquias et al. 2011, Pedro et al. 2011, Ávila and Sigwart 2013, Cordeiro et al. 2013).

The members of the family Rissoidae Gray, 1847 are amongst the most conspicuous, abundant and diverse gastropods inhabiting the continental shelf and upper bathyal region in the Mediterranean Sea and along the Atlantic coasts of Europe (for a review see Ávila et al. 2012). Such gastropods are also very abundant in the northeast Atlantic seamounts (Ávila and Malaquias 2003, Ávila et al. 2004, 2007, Gofas 2007) as well as in the Archipelago of the Azores (Dautzenberg 1889, Aartsen 1982, Amati 1987, Moolenbeek and Faber 1987, Gofas 1989, 1990, Bouchet and Warén 1993, Hoenselaar and Goud 1998, Ávila 2000, Costa and Ávila 2001, Martins et al. 2009), Madeira, Porto Santo and Desertas Islands (Manzoni 1868a, 1868b, Watson 1873, Nobre 1937, Moolenbeek and Faber 1987, Moolenbeek and Hoenselaar 1989, 1998, Hoenselaar and Goud 1998, Segers et al. 2009), Selvagens Islands (Albuquerque et al. 2009), Canary Islands (Rolán 1987, Verduin 1988, Moolenbeek and Hoenselaar 1989, 1992, 1998, Hernández-Otero and García 2003) and Archipelago of Cape Verde (Rolán 1987, Moolenbeek and Rolán 1988, Templado and Rolán 1993, Rolán and Rubio 1999, Rolán and Luque 2000, Rolán 2005, Rolán and Oliveira 2008).

Ávila (2000, 2005) detailed the shallow-water (from the intertidal down to 50 m depth) rissoids of the Azores, identifying a total of 9 genera and 24 species. Ávila et al. (2002, 2010) summarized the palaeontological record for the family in the area. The bathymetrical zonation for the most common rissoid species was described by Ávila (2003) and Ávila et al. (2005).

The genus Setia H. & A. Adams, 1852 is composed of minute gastropods with ovate to ovate-conic shells and convex whorls. The dome-shaped protoconch, having about 1.25 to 1.5 whorls, is smooth or possesses spiral rows of minute gemmae. The teleoconch is smooth or sculptured with weak to moderate spiral threads and axial growth lines. The aperture has a simple peristome.

There are 29 species of Setia in the Atlantic and the Mediterranean Sea (Ávila et al. 2012). With the exception of Setia triangularis (Watson, 1886) reported for the Caribbean and Ascension Island, all are shallow-water species. No species of this genus are reported for the Lusitanian seamounts (Gofas 2007). The Mediterranean Sea contains the largest number of species (18 species; 10 endemic), followed by the Canary Islands (7 species; 1 endemic), mainland Portugal (6 species), Archipelago of Madeira (4 species; 1 endemic), and the Azores (3 species; 2 endemic) (Ávila et al. 2012).

The genus Manzonia Brusina, 1870 is composed of minute gastropods with ovate-conic shells having robust axial sculpture formed by strongly curved to sinuous opisthocline ribs. The protoconch is multispiral (with netted microsculpture) or paucispiral (with gemmate or smooth spiral keels). The distinctive teleoconch microsculpture consists of a pitted surface on the flat spiral cords and very fine spiral threads in the interspaces between primary cords. The aperture is oval and the peristome is duplicated (Ponder 1985, Moolenbeek and Faber 1987).

A total of 24 species of Manzonia is present in the Atlantic and the Mediterranean Sea (Ávila et al. 2012). Of these, 6 are deep-water and 18 are shallow-water species. The deep-water species are restricted to the Lusitanian seamounts (Gofas 2007) and the West African coast (Gofas 2010). Twenty three of the 24 species are distributed in both the eastern Atlantic and the Mediterranean Sea. The remaining species, Manzonia epima (Dall & Simpson, 1901), is restricted to the western Atlantic. The Canary Islands (11 species; 3 endemic), Selvagens Islands (8 species; 1 endemic) and Archipelago of Madeira (7 species; 2 endemic) contain the largest numbers of species. The Archipelago of the Azores contains a single, endemic species (Ávila et al. 2012).

The present study describes three new species of Setia and a new species of Manzonia from the Archipelago of the Azores. A list of the species of Rissoidae from the Azores is presented based on data from the literature and new material examined.

Materials and methods

The specimens used in the present study were obtained from samples collected by about 850 dives and dredges in all islands of the Azores between the years 1967 and 2010. A total of 1,060 lots from the Mollusc Reference Collection of the Department of Biology of the University of the Azores (DBUA) were examined. During the course of examining the material, we found a total of 39,532 specimens of Rissoidae. All specimens were examined under stereomicroscope. The specimens in perfect conditions were selected as type material for the new species and measured with precision of 0.01 mm using a stereomicroscope with a digital camera coupled to a computer.

Living animals were photographed for observation of colour patterns. Shells were sonicated, coated with Au-Pd and then photographed with a Scanning Electron Microscope (SEM) for the study of the protoconch and teleoconch.

Terminology adopted for shell descriptions follows Ponder (1985). A special focus was placed on protoconch and microsculpture as taxonomic characters at the species level. The suprageneric classification of Gastropoda is based on Bouchet and Rocroi (2005).

The material analysed in this study is deposited in the Mollusc Reference Collection of the Department of Biology of the University of the Azores (DBUA), Portugal. Abbreviations used: sh. – shell; spc. – specimens alive when collected.

Systematics

Class GASTROPODA Cuvier, 1795
Subclass CAENOGASTROPODA Cox, 1960
Order LITTORINIMORPHA Golikov & Starobogatov, 1975
Superfamily RISSOOIDEA Gray, 1847
Family RISSOIDAE Gray, 1847

Setia H. & A. Adams, 1852

Type species

Rissoa pulcherrima Jeffreys, 1848; subsequent designation Kobelt 1878: 128.

Setia alexandrae Ávila & Cordeiro, sp. n.

Figure 1

Setia sp.: Ávila et al. (1998: 496) – DBUA 449, 478, 496, 662.

Setia sp.: Ávila et al. (2000: 147) – DBUA 787.

Setia sp.: Costa and Ávila (2001: 126) – DBUA 898 (as ATA 1).

Setia sp.: Ávila (2003: 32) – DBUA 704/A, 787.

Type material

Holotype, DBUA 1051 (spc., 1.17 × 0.70 mm); paratype 1, DBUA 1070 (spc., 0.99 × 0.65 mm); paratype 2, DBUA 1071 (spc., 1.09 × 0.73 mm); paratype 3, DBUA 1072 (spc., 1.08 × 0.66 mm); paratype 4, DBUA 1073 (spc., 1.04 × 0.65 mm), Graciosa Island (Santa Cruz, intertidal, 01/08/2010); paratype 5, DBUA 1074 (sh., 0.95 × 0.65 mm); paratype 6, DBUA 1075 (sh., 1.02 × 0.61 mm); paratype 7, DBUA 1076 (sh., 1.07 × 0.68 mm), Pico Island (Lajes do Pico, intertidal, 07/1989); paratype 8, DBUA 1077 (spc., 0.91 × 0.62 mm); paratype 9, DBUA 1078 (spc., 1.10 × 0.65 mm), São Miguel Island (Caloura, 5–15 m depth, 21/05/1999).

Type locality

Santa Cruz, Graciosa Island, Azores.

Additional material examined

Graciosa Island: DBUA 35 (Fonte da Areia, intertidal, 3 spc., 10/06/1988); DBUA 37 (Porto Afonso, intertidal, 14 spc., 06/1988); DBUA 40 (Santa Cruz, intertidal, 1 sh., 06/1988); DBUA 48 (Baía da Folga, infralittoral, 1 sh., 06/1988); DBUA 50 (Baía da Folga, 8 m depth, 1 spc., 10/06/1988). Pico Island: DBUA 449 (Lajes do Pico, intertidal, 5 spc., 07/1989); DBUA 468 (Lajes do Pico, intertidal, 11 spc., 07/1989); DBUA 471 (Lajes do Pico, intertidal, 1 spc., 07/1989); DBUA 478 (Lajes do Pico, intertidal, 7 spc., 07/1989), DBUA 496 (Lajes do Pico, intertidal, 31 spc., 28/06/1991); and DBUA 662 (Lajes do Pico, 0–3 m depth, 1 sh., 19/08/1995). São Miguel Island: DBUA 704/A (São Vicente, 12 m depth, 1 spc., 18/07/1996); DBUA 787 (São Vicente, 15.1 m depth, 2 spc., 11/07/1997), DBUA 898 (Atalhada, 11.2 m depth, 4 spc., 10/10/1996), DBUA 901 (Ilhéu de Vila Franca do Campo, 15 m depth, 1 spc., 15/07/1996), DBUA 920 (Caloura, 10 m depth, 1 spc., 12/07/1997), DBUA 963 (Porto de Vila Franca do Campo, 6 m depth, 2 spc., 22/07/1997). Formigas Islets: DBUA 336 (intertidal, 2 spc., 07/1990); and DBUA 355 (15 m depth, 22 spc., 03/07/1991). Santa Maria Island: DBUA 1018 (Ilhéu da Vila, 17 m depth, 6 spc., 5 sh., 26/08/2004); and DBUA 1019 (Ilhéu da Vila, 17 m depth, 2 spc., 26/08/2004).

Etymology

Named after Alexandra Castela, the wife of Sérgio Ávila.

Description

Shell fragile, minute, translucent, oval-conical, up to 1.2 × 0.7 mm (Fig. 1A). Protoconch smooth, dome-shaped (typical of the genus), whorls 1.25, diameter 280 µm, separated from the teleoconch by a clearly visible line (Fig. 1D and E). Teleoconch with 2.5 to 3 inflated, rounded, strongly convex whorls; whorls with regular contour and conspicuous increase in width (Fig. 1B–D). Spire moderately high. Sculpture absent, except for very fine, inconspicuous growth lines (Fig. 1B–D). Suture deep, constricted (Fig. 1B–D). Last whorl large, globose, 70–75% of shell length (Fig. 1B and C). Base large, rounded. Aperture oval, oblique with continuous peristome, adapical angle somewhat acute (Fig. 1B and C). Parietal region thin, very slightly convex (Fig. 1B and C). Outer lip with very thin edge (Fig. 1B and C). Inner lip thin, very slightly recurved over umbilicus (Fig. 1B and C). Umbilicus a very narrow fissure (Fig. 1B and C). Animal light-yellow with dark-brown blotches visible at transparency (Fig. 1A). Operculum simple, thin, nucleus eccentric, yellowish at transparency (Fig. 1A and B).

Figure 1. 

Setia alexandrae sp. n. A Holotype (1.17 × 0.70 mm), DBUA 1051 (shell) B Paratype 3 (1.08 × 0.66 mm), DBUA 1072 (shell) C Paratype 9 (1.10 × 0.65 mm), DBUA 1078 (shell) D Paratype 8, DBUA 1077 (shell, apical view) E Paratype 2, DBUA 1071 (protoconch).

Habitat

On rocky shores covered by algae, from the intertidal down to 20 m depth.

Geographical distribution

Pico, Graciosa, São Miguel and Santa Maria Islands, and Formigas Islets. Probably endemic to the Azores.

Remarks

Setia alexandrae sp. n. is distinguished from the other Azorean congeners by its smooth, transparent to translucent shell, and yellowish animal having light to dark-brown blotches over the entire body. Setia alexandrae sp. n. lacks any colour decoration/pattern on the shell. Colour is a distinctive feature of most of the known Setia (e.g., variably coloured flames, spots or vertical lines, sometimes interrupted medially), which are so abundant on the Azorean Setia subvaricosa Gofas, 1990, S. amabilis (Locard, 1886), S. ambigua (Brugnone, 1873) and S. scillae (Aradas & Benoit, 1876). Setia lacourti (Verduin, 1984) is similar in size (up to 1.2 mm in length) and also lacks any coloured pattern on the shell; this species was reported from the Azores by Segers (2002: 89) as Setia cf. lacourti. Setia alexandrae sp. n. clearly differs from S. lacourti in shell shape (more elongated on the first, flattened on the latter). Setia ambigua was also reported from the Azores (Hoenselaar and Goud in litt. 2002, Ávila et al. 2012), from Terceira Island (Praia da Vitória, 38°43'N, 27°04'W, sandy beach). Setia alexandrae sp. n. differs from S. ambigua by being about 50% smaller and by lacking any coloured decoration on the shell. A very similar specimen to Setia alexandrae sp. n. was recently found in the Pleistocene record of Santa Maria Island, Azores (Prainha outcrop, bed B1 of Ávila et al. (2009a); latitude 36°57'3.05"N, longitude 25°6'44.20"W). This well-preserved juvenile shell is herein reported as Setia cf. alexandrae DBUA-F 137/151-4 (0.61 × 0.40 mm). The protoconch and teleoconch shape and sculpture are identical to Setia alexandrae sp. n., as is the shape of the aperture. However, as it is a juvenile specimen we prefer to treat it as Setia cf. alexandrae until adult material is examined.

Setia ermelindoi Ávila & Cordeiro, sp. n.

Figure 2

Setia cf. lacourti (Verduin, 1984): Segers (2002: 89).

Type material

Holotype, DBUA 1058 (sh., 1.07 × 0.76 mm), São Miguel Island (Caloura, 5–15 m depth, 21/05/1999); paratype 1, DBUA 1079 (spc., 1.08 × 0.80 mm), Pico Island (Lajes do Pico, 1–2 m depth, 24/06/1991); paratype 2, DBUA 1080 (spc., 0.74 × 0.59 mm); paratype 3, DBUA 1081 (spc., 0.92 × 0.76 mm), Pico Island (Lajes do Pico, intertidal, 24/06/1991); paratype 4, DBUA 1082 (spc., 0.94 × 0.70 mm), Flores Island (Santa Cruz, intertidal, 09/07/1989); paratype 5, DBUA 1083 (spc., 0.79 × 0.63 mm); paratype 6, DBUA 1084 (spc., 0.94 × 0.66 mm); paratype 7, DBUA 1085 (spc., 0.78 × 0.62 mm), Flores Island (Santa Cruz, intertidal, 08/08/2010).

Type locality

Caloura, São Miguel Island, Azores.

Additional material examined

Pico Island: DBUA 467 (Lajes do Pico, intertidal, 1 sh., 07/1989). São Miguel Island: DBUA 137 (Ilhéu de Vila Franca do Campo, intertidal, 2 spc., 07/1988); DBUA 689 (São Vicente, 22 m depth, 1 sh., 15/07/1996); DBUA 899 (Faial da Terra, 8.3 m depth, 2 spc., 10/10/1996); DBUA 957 (Pesqueiro, 5.6 m depth, 1 spc., 19/07/1997).

Etymology

Named after Ermelindo Ávila, a writer and historian from Pico Island.

Description

Shell minute, translucent, globose, up to 1.1 × 0.8 mm (Fig. 2A). Protoconch paucispiral, whorls 1.25, diameter 225–235 µm, smooth, with no visible sculpture, except for a few faintly developed axial growth lines, separated from the teleoconch by a clearly visible line (Fig. 1G and H). Teleoconch with 1.75 to 2 inflated, rounded, strongly convex whorls sculptured by faint axial lines (no spiral sculpture present); whorls with regular contour and conspicuous increase in width (Fig. 2B–E). Spire short. Suture deep, constricted (Fig. 2B–E). Last whorl very large, globose, 75–80% of shell length (Fig. 2B–E). Base large, rounded. Aperture oval and oblique with faint posterior angulation (Fig. 2B–E). Parietal region moderately thickened, rather straight to very slightly convex (Fig. 2B–E). Outer lip thin, smooth inner surface (Fig. 2B–D). Inner lip thin, slightly reflected over umbilicus (Fig. 2B–E). Umbilicus a moderately enlarged fissure (Fig. 2B–E). One axial threads always present and running abapically nearby the umbilicus (Fig. 2D). Animal black (Fig. 2A). Foot whitish. Operculum simple, thin, nucleus eccentric, translucent (Fig. 2E and F).

Figure 2. 

Setia ermelindoi sp. n. A Holotype (1.07 × 0.76 mm), DBUA 1058 B Paratype 2 (0.74 × 0.59 mm), DBUA 1080 (shell) C Paratype 5 (0.79 × 0.63 mm), DBUA 1083 (shell) D Paratype 1 (1.08 × 0.80 mm), DBUA 1079 (shell) E Paratype 6 (0.94 × 0.66 mm), DBUA 1084 (shell) F Paratype 6, DBUA 1084 (operculum) G Paratype 7, DBUA 1085 (apical view) H Paratype 7, DBUA 1085 (protoconch).

Habitat

On rocky shores covered by algae, from the intertidal down to 25 m depth.

Geographical distribution

Flores, Pico and São Miguel Islands. Probably endemic to the Azores.

Remarks

This species differs from most of the known Setia species by its globose shell. Setia lacourti (Verduin, 1984) and Setia valvatoides (Milaschewitsch, 1909) also have globose shells, but Setia ermelindoi sp. n. is easily separated from these species by the aperture shape, which is oval in S. ermelindoi sp. n. and rounded in S. lacourti and S. valvatoides. S. ermelindoi sp. n. is also distinguished by the axial thread running abapically near the umbilicus. The shell shape of Setia ermelindoi sp. n. resembles that of some Rissoella species (e.g., R. contrerasi Rolán & Hernández, 2004 and R. inflata (Monterosato, 1880)). However, the animal lacks the typical two pairs of head tentacles found in all Rissoella; instead, it has only one pair typical of Rissoidae. Moreover, Setia ermelindoi sp. n. does not have the pigmented hypobranchial gland (observable through the transparent shell) of several Rissoella (a species-diagnostic character, cf. Rolán and Hernández 2003; e.g., R. contrerasi, R. luteonigra Rolán & Rubio, 2001, R. trigoi Rolán & Hernández, 2004, R. caribaea Rehder, 1943, and R. ornata Simone, 1995).

Setia netoae Ávila & Cordeiro, sp. n.

Figure 3

Type material

Holotype, DBUA 745 (1 spc., 1.57 × 0.90 mm); paratype 1, DBUA 1086 (1 spc., 1.55 × 0.89 mm), São Miguel Island (Baía de Rosto do Cão, low intertidal, 07/1990); paratype 2, DBUA 1087 (1 spc., 1.15 × 0.70 mm); paratype 3, DBUA 1088 (1 spc., 1.17 × 0.71 mm), São Miguel Island (Baía de Belém, São Roque, 8.6 m depth, 04/07/1990); paratype 4, DBUA 1089 (spc., 1.26 × 0.74 mm); paratype 5, DBUA 1090 (spc., 1.12 × 0.68 mm), paratype 6, DBUA 1091 (spc., 1.36 × 0.79 mm), Graciosa Island (Baía da Folga, 8 m depth, 10/06/1988); paratype 7, DBUA 264 (1 sh., 2.09 × 1.07 mm), Flores Island (Lajes das Flores, 6–10 m depth, 27/10/1990).

Type locality

Baía de Rosto do Cão, São Miguel Island, Azores.

Etymology

Named after Ana Neto, an Azorean marine phycologist from the University of the Azores.

Description

Shell minute, cream to translucent in colour, oval-high conical, up to 2.1 × 1.1 mm (Fig. 3A–D and F). Protoconch dome-shaped (typical of the genus), smooth, whorls 1.25, diameter 250 µm, separated from the teleoconch by a clearly visible line (Fig. 3G). Teleoconch with 3.5 to 4 inflated, rounded, strongly convex whorls sculptured with weak axial growth lines; whorls with regular contour and conspicuous increase in width (Fig. 3A–F). Spire moderately high. Suture deep, constricted (Fig. 3E). Last whorl large, globose, 60% of shell length (Fig. 3A–F). Base large, rounded (Fig. 3E). Aperture oval, oblique with continuous and simple peristome (smooth within), and posterior angulation (Fig. 3E). Parietal region thin, rather straight (Fig. 3E). Outer and inner lip with a thin edge (not thickened) (Fig. 3E). Umbilicus a very narrow fissure (Fig. 3E). Animal bright-yellow, with very distinctive single dark-brown patch to inner side of head, readily visible at transparency (Fig. 3A–C and F). Operculum simple, thin, nucleus eccentric, yellowish at transparency (Fig. 3A, B and F).

Figure 3. 

Setia netoae sp. n. A Holotype (1.57 × 0.90 mm mm), DBUA 745 (shell) B Paratype 6 (1.36 × 0.79 mm mm), DBUA 1091 (shell) C Paratype 6, DBUA 1091 (shell, lateral view) D Paratype 7 (2.09 × 1.07 mm), DBUA 264 (shell) E Paratype 1 (1.55 × 0.89 mm), DBUA 1086 (shell) F Paratype 5 (1.12 × 0.68 mm), DBUA 1090 (shell) G Paratype 1, DBUA 1086 (protoconch, apical view).

Habitat

On rocky shores covered by algae, from the intertidal down to 10 m depth.

Geographical distribution

Flores, Graciosa and São Miguel Islands. Probably endemic to the Azores.

Remarks

This species appears to be uncommon on the Azorean shores. It differs from S. subvaricosa by lacking the vertical reddish flames on the shell that characterizes this species. It further differs from S. subvaricosa by the thinner outer lip of the aperture and by the absence of spiral threads on the protoconch. Setia netoae sp. n. differs from S. alexandrae sp. n. in having a more slender shell, 4 instead of 3 whorls on the teleoconch, by the distinctive colour pattern of the animal, and by the proportions of the last whorl/total length of the shell, which are 60% versus 70–75%, respectively. Setia netoae sp. n. differs from other Atlantic congeners (cf. Ávila et al. 2012; and present study) by lacking the usual colourful patterns, such as wavy flames, blotches and lines, observed in the shells of this genus. It also has a more elongate shell than most of the known Setia. The shell resembles that of similar sized Setia antipolitana (van der Linden & Wagner, 1987), but the latter has vertical lines interrupted medially that are not present in S. netoae sp. n.

Manzonia Brusina, 1870

Type species

Turbo costatus J. Adams, 1798, by original designation (=Turbo crassus Kanmacher, 1798; non Turbo costatus von Salis Marschlins, 1793).

Manzonia martinsi Ávila & Cordeiro, sp. n.

Figure 4

Type material

Holotype, DBUA 788 (sh., 1.75 × 1.13 mm); paratype 1, DBUA 1092 (sh., 1.88 × 1.20 mm); paratype 2, DBUA 1093 (sh., 1.76 × 1.14 mm); paratype 3, DBUA 1094 (sh., 1.72 × 1.10 mm); paratype 4, DBUA 1095 (sh., 1.76 × 1.06 mm), São Miguel Island (São Vicente Ferreira, 4.7 m depth, 16/07/1997).

Type locality

São Vicente Ferreira, São Miguel Island, Azores.

Etymology

Named after António M. de Frias Martins, a malacologist from the University of the Azores.

Description

Shell minute, white, oval-conical, up to 1.9 × 1.2 mm (Fig. 4A). Protoconch paucispiral, clearly demarcated convex whorls 1.25, diameter 340–365 µm; whorls with a pronounced keel adapically (Fig. 4I) and 5–6 faint spiral cords visible on surface between suture and keel (Fig. 4H and I). Teleoconch with 3 to 3.5 inflated, rounded, strongly convex whorls, angulated at a distance abapically from suture (Fig. 4B–F). Spire moderately high. Suture very deep, strongly constricted (Fig. 4B–F). Last whorl large, globose, 65% of shell length (Fig. 4B–D and F). Base large, rounded (Fig. 4B–D and F). Spiral sculpture consisting of flat cords (5–6 on first teleoconch whorl, 8–9 on penultimate whorl and 9–10 on body whorl) equal to two times broader than the interspaces ornamented with minute pits arranged in spiral lines (Fig. 4G); interspaces with 4 to 6 raised spiral striae (Fig. 4G). Abapical area of body whorl (base) with two strong spiral cords separated by broad spiral depression; third spiral cord located nearer the lip may be present (Fig. 4B and F). Axial sculpture consisting of 10–14 flexuous, opisthocline, moderately broad and strongly elevated ribs (body whorl), fading on base (about 7–8th spiral cord) (Fig. 4B, D and F). Intersection of axial and spiral sculptures raising small knobs (Fig. 4E). Aperture oval, strongly thickened, oblique with continuous peristome (Fig. 4B–D and F). Parietal region slightly convex (Fig. 4B–D and F). Outer lip with very thickened edge (smooth inside) (Fig. 4B–D and F). Inner lip moderately thickened and slightly concave (Fig. 4B–D and F). Umbilicus lacking (Fig. 4B–D and F).

Figure 4. 

Manzonia martinsi sp. n. A Holotype DBUA 788 (1.75 × 1.13 mm) B Paratype 1 (1.88 × 1.20 mm), DBUA 1092 (shell) C Paratype 2 (1.76 × 1.14 mm), DBUA 1093 (shell) D Paratype 3 (1.72 × 1.10 mm), DBUA 1094 (shell) E Paratype 1, DBUA 1092 (shell, apical view) F Paratype 4 (1.76 × 1.06 mm), DBUA 1095 (shell) G Paratype 1, DBUA 1092 (microsculpture of the bodywhorl) H Paratype 1, DBUA 1092 (protoconch, lateral view) I Paratype 1, DBUA 1092 (protoconch, apical view).

Habitat

In the infralittoral on rocks covered by algae.

Geographical distribution

São Miguel Island. Probably endemic to the Azores.

Remarks

Manzonia martinsi sp. n. is similar in shell shape to Manzonia lusitanica Gofas, 2007 and Manzonia crispa (Watson, 1873). It differs from Manzonia lusitanica in having a lower number of spiral cords on the body whorl (9–10 in the new species and 12–13 in M. lusitanica). Manzonia martinsi sp. n. has 9–10 spiral cords on the body whorl and 4–6 raised spiral striae on the interspaces between cords, while M. crispa has 7 spiral cords on the body whorl and 8–10 lower spiral striae between cords. Manzonia martinsi sp. n. differs from M. arata Gofas, 2007 in the number of raised spiral striae on the interspaces as well as on the number of spiral lines with pits on the spiral cords, which are lower 2 to 3 times in the new species (Table 1).

Table 1.

Comparison of the conchological characters of Manzonia arata, M. crispa, M. lusitanica, and M. martinsi sp. n.

Species Number of spiral cords adapical area (body whorl) Number of spiral cords abapical area (body whorl) Number of axial cords (body whorl) Number of raised spiral threads (interspaces) Number of spiral lines with pits (spiral cords) Interspaces and spiral cords
Manzonia arata 8–9 3 12–13 10–12 9–10 Spiral cords narrower than the interspaces.
Manzonia crispa 7 4 10–12 8–10 8–10 Interspaces three times broader than spiral cords.
Manzonia lusitanica 12–13 2 12 3–5 3–6 Spiral cords as broad as interspaces or slightly broader.
Manzonia martinsi sp. n. 9–10 3 10–14 4–6 4–6 Spiral cords equal up to two times broader than interspaces.

Discussion

Biodiversity and endemicity

The published information on the shallow-water rissoids of the Azores was compiled by Ávila (2000, 2005) and subsequently supplemented by Ávila et al. (2012), who analysed a revised and updated checklist with the entire Atlantic and Mediterranean rissoid fauna.

This current work corrects previous misidentifications; and the novelties described herein increase the rissoid fauna of the Azores to 39 species. Twenty-nine rissoid species are known only from the shallow-waters in the Archipelago, 20 of these have also been reported from the late Pleistocene outcrops of Santa Maria Island (Marine Isotope Stage (MIS) 5e, around 120–130 kya), which corresponds to the last interglacial period: Alvania abstersa van der Linden & van Aartsen, 1994, A. angioyi van Aartsen, 1982, A. cancellata (da Costa, 1778), A. cimicoides (Forbes, 1844), A. formicarum Gofas, 1989, A. mediolittoralis Gofas, 1989, A. poucheti Dautzenberg, 1889, A. sleursi (Amati, 1987), A. tarsodes (Watson, 1886), Botryphallus ovummuscae (Gofas, 1990), Cingula trifasciata (J. Adams, 1800), Crisilla postrema (Gofas, 1990), Manzonia unifasciata Dautzenberg, 1889, Merelina tesselata (Schwartz, 1860), Onoba moreleti Dautzenberg, 1889, Pusillina inconspicua (Alder, 1844), Rissoa guernei Dautzenberg, 1889, Setia cf. alexandrae, Setia subvaricosa, and Zebina paivensis (Watson, 1873) (=Z. vitrea) (Ávila et al. 2002, 2009a, 2009b, 2010, and present study) (Table 2).

Table 2.

Checklist of the Rissoidae species reported from the Azores. The records of Crisilla iunoniae [Terceira Island (Praia da Vitória, 38°43'N, 27°04'W, sandy beach)] and Rissoa mirabilis [Santa Maria Island (CANCAP-V expedition, 36°59'N, 25°02'W, 35 and 55 m depth)] are based on Hoenselaar and Goud (in litt., 2002); MIS 5e: Marine Isotope Stage 5e, around 120–130 kya; ?: species not confirmed; *: only fossils known (age not determined); Shallow: intertidal down to 50 m depth; Deep: below 50 m depth; Sh-De: species occurring from shallow to deep-waters.

Species Recent Fossil record (MIS 5e) Bathymetric zonation Azorean endemic
Alvania abstersa Van der Linden & Van Aartsen, 1994 1 1 Shallow 1
Alvania adiaphorus Bouchet & Warén, 1993 1 Deep
Alvania adinogramma Bouchet & Warén, 1993 1 Deep
Alvania angioyi Van Aartsen, 1982 1 1 Shallow 1
Alvania cancellata (Da Costa, 1778) 1 1 Shallow
Alvania cimicoides (Forbes, 1844) 1 1 Deep
Alvania formicarum Gofas, 1989 1 1 Shallow 1
Alvania internodula Hoenselaar & Goud, 1998 1 Shallow 1
Alvania lamellata Dautzenberg, 1889 1 Deep 1
Alvania mediolittoralis Gofas, 1989 1 1 Shallow
Alvania multiquadrata van der Linden & Wagner, 1989 ? * Shallow
Alvania nonsculpta Hoenselaar & Goud, 1998 1 Deep 1
Alvania platycephala Dautzenberg & Fischer, 1896 1 Deep
Alvania poucheti Dautzenberg, 1889 1 1 Shallow 1
Alvania sleursi (Amati, 1987) 1 1 Shallow
Alvania stenolopha Bouchet & Warén, 1993 1 Deep
Alvania tarsodes (Watson, 1886) 1 1 Shallow 1
Alvania zoderi Hoenselaar & Goud, 1998 1 Deep 1
Amphirissoa cyclostomoides Dautzenberg & Fischer, 1897 1 Deep
Benthonella tenella (Jeffreys, 1869) 1 Deep
Benthonellania fayalensis (Watson, 1886) 1 Deep
Botryphallus ovummuscae (Gofas, 1990) 1 1 Shallow 1
Cingula trifasciata (J. Adams, 1800) 1 1 Shallow
Crisilla iunoniae (Palazzi, 1988) 1 Shallow
Crisilla postrema (Gofas, 1990) 1 1 Shallow
Manzonia martinsi sp. n. 1 Shallow 1
Manzonia unifasciata Dautzenberg, 1889 1 1 Shallow 1
Merelina tesselata (Schwartz, 1860) * Shallow
Obtusella intersecta (S.V. Wood, 1857) 1 Sh-De
Obtusella roseotincta (Dautzenberg, 1889) 1 Deep 1
Onoba moreleti Dautzenberg, 1889 1 1 Shallow 1
Pseudosetia azorica Bouchet & Warén, 1993 1 Deep
Pusillina inconspicua (Alder, 1844) 1 1 Sh-De
Rissoa guernei Dautzenberg, 1889 1 1 Shallow
Rissoa mirabilis (Manzoni, 1868) 1 Shallow
Setia alexandrae sp. n. 1 1 Shallow 1
Setia ambigua (Brugnone, 1873) 1 Shallow
Setia ermelindoi sp. n. 1 Shallow 1
Setia netoae sp. n. 1 Shallow 1
Setia quisquiliarum (Watson, 1886) 1 Shallow 1
Setia subvaricosa Gofas, 1990 1 1 Shallow 1
Zebina paivensis (Watson, 1873) * Shallow
Total 39 20 19

Although Obtusella intersecta (S.V. Wood, 1857) is a deep-water species in the Azores (the shallowest record is from Faial, at 75 m depth – Hoenselaar and Goud in litt. 2002), it is also found in shallow-waters in other sites from its wide geographical range (e.g., 15–34 m depth at Mauritanian shores, CANCAP III; 22–50 m depth at Cape Verde, CANCAP VI; 20–35 m depth, Bonden, Sweden (58°12'N, 11°20'E); all data from Hoenselaar and Goud in litt. 2002) (Table 2).

Hoenselaar and Goud (in litt. 2002) reported Alvania multiquadrata van der Linden & Wagner, 1989 as a living species in the Azores. However, we did not find recent specimens of this taxon in the area. Alvania multiquadrata was only found as fossil shells by the CANCAP expeditions (CANCAP-V, Sta. 5.071, south of São Miguel Island, 37°49'N, 25°25'W, at 220 m depth, on gravel bottoms) (Table 2).

The Rissoidae is the most species-rich molluscan family in the Archipelago of the Azores. It also contains the largest number of endemic marine species in the region: 19 endemics (48.7%), if we consider all rissoids; or 15 (51.7%), if we consider only the 29 shallow-water species. All 19 Azorean endemic rissoids (15 shallow and 4 deep-water species) possess a non-planktotrophic mode of larval development.

The last account on the shallow-water marine molluscs from the Azores reports 423 taxa (Ávila, unpublished data), of which 6 are introduced species (Cardigos et al. 2006) and 34 are pelagic species. If these 40 species are discounted, there are 383 shallow-water benthic molluscs, of which 41 are endemic to the Azores (10.7% of endemisms). We note that the Rissoidae constitutes 36.6% of all endemic shallow-water benthic molluscs from the Azores, which further highlights the contribution of this family to regional biodiversity.

Acknowledgements

The authors are grateful to Jorge Medeiros for assistance with Scaning Electronic Microscope. Thanks are due to Robert Hershler, Silvio Lima and to an anonymous referee for helpful comments and suggestions on an earlier version of the manuscript. R. Cordeiro holds a PhD grant from the “Fundação para a Ciência e a Tecnologia” (FCT, Portugal, SFRH/BD/60366/2009). S.P. Ávila acknowledges his “Ciência” 2008 research contract funded by FCT.

References

  • Aartsen JJ (1982) Synoptic tables of Mediterranean and European conchology (Gen. Alvania) (Tav. XVIII). La Conchiglia 14(158–159): 4–5.
  • Aartsen JJ (2008) The Assimineidae of the Atlantic-Mediterranean seashores. Basteria 72: 165–181.
  • Albuquerque M, Borges JP, Calado G (2009) Moluscos Marinhos – Atlas das Ilhas Selvagens. Direcção Regional do Ambiente, Funchal, 309 pp.
  • Amati B (1987) Manzonia (Alvinia) sleursi sp. n. (Gastropoda, Prosobranchia). Notiziário CISMA 10: 25–30.
  • Ávila SP (2000) The shallow-water Rissoidae (Mollusca, Gastropoda) of the Azores and some aspects of their ecology. Iberus 18(2): 51–76.
  • Ávila SP (2003) The littoral molluscs (Gastropoda, Bivalvia and Polyplacophora) of São Vicente, Capelas (São Miguel Island, Azores): ecology and biological associations to algae. Iberus 21(1): 11–33.
  • Ávila SP (2005) Processos e Padrões de Dispersão e Colonização nos Rissoidae (Mollusca: Gastropoda) dos Açores. PhD Thesis, Universidade dos Açores, Ponta Delgada, Portugal.
  • Ávila SP (2013) Unraveling the patterns and processes of evolution of marine life in oceanic islands: a global framework. In: Fernánez-Palacios JM, Nascimento L, Hernández JC, Clemente S, González A, Díaz-González JP (Eds) Climate Change perspectives from the Atlantic: past, present and future. Universidad de La Laguna, Tenerife, 95–125.
  • Ávila SP, Malaquias MAE (2003) Biogeographical relationships of the molluscan fauna of the Ormonde Seamount (Gorringe Bank, Northeast Atlantic Ocean). Journal of Molluscan Studies 69(2): 145–150. doi: 10.1093/mollus/69.2.145
  • Ávila SP, Sigwart J (2013) New records for the shallow-water chiton fauna (Mollusca, Polyplacophora) of the Azores (NE Atlantic). ZooKeys 312: 23–38. doi: 10.3897/zookeys.312.4768
  • Ávila SP, Amen R, Azevedo JMN, Cachão M, García-Talavera F (2002) Checklist of the Pleistocene marine molluscs of Prainha and Lagoinhas (Santa Maria Island, Azores). Açoreana 9(4): 343–370.
  • Ávila SP, Azevedo JMN, Gonçalves JM, Fontes J, Cardigos F (1998) Checklist of the shallow-water marine molluscs of the Azores: 1 – Pico, Faial, Flores and Corvo islands. Açoreana 8(4): 487–523.
  • Ávila SP, Azevedo JMN, Gonçalves JM, Fontes J, Cardigos F (2000) Checklist of the shallow-water marine molluscs of the Azores: 2 – São Miguel island. Açoreana 9(2): 139–173.
  • Ávila SP, Borges JP, Martins AMF (2011) The littoral Trochoidea (Mollusca: Gastropoda) of the Azores. Journal of Conchology 40: 408–427.
  • Ávila SP, Cardigos F, Santos RS (2004) D. João de Castro bank, a shallow-water hydrothermal-vent in the Azores: checklist of the marine mollusks. Arquipélago – Life and Marine Sciences 21A: 75–80.
  • Ávila SP, Cardigos F, Santos RS (2007) Comparison of the community structure of the marine molluscs of the “Banco D. João de Castro” seamount (Azores, Portugal) with that of typical inshore habitats on the Azores archipelago. Helgoland Marine Research 61: 43–53. doi: 10.1007/s10152-006-0052-5
  • Ávila SP, Goud J, Martins AMF (2012) Patterns of diversity of the Rissoidae (Mollusca: Gastropoda) in the Atlantic and the Mediterranean Region. The Scientific World Journal 2012: 164890. doi: 10.1100/2012/164890
  • Ávila SP, Madeira P, Mendes N, Rebelo A, Medeiros A, Gomes C, García-Talavera F, Silva CM, Cachão M, Hillaire-Marcel C, Martins AMF (2008a) Mass extinctions in the Azores during the last glaciation: fact or myth? Journal of Biogeography 35: 1123–1129. doi: 10.1111/j.1365-2699.2008.01881.x
  • Ávila SP, Madeira P, Silva CM, Cachão M, Landau B, Quartau R, Martins AMF (2008b) Local disappearance of bivalves in the Azores during the last glaciation. Journal of Quaternary Science 23: 777–785. doi: 10.1002/jqs.1165
  • Ávila SP, Melo PJ, Lima A, Amaral A, Martins AMF, Rodrigues A (2008c) The reproductive cycle of the rissoid Alvania mediolittoralis Gofas, 1989 (Mollusca, Gastropoda) at São Miguel Island (Azores, Portugal). Invertebrate Reproduction and Development 52: 31–40. doi: 10.1080/07924259.2008.9652269
  • Ávila SP, Madeira P, Zazo C, Kroh A, Kirby M, Silva CM, Cachão M, Martins AMF (2009a) Palaeocology of the Pleistocene (MIS 5.5) outcrops of Santa Maria Island (Azores) in a complex oceanic tectonic setting. Palaeogeography, Palaeoclimatology, Palaeoecology 274: 18–31. doi: 10.1016/j.palaeo.2008.12.014
  • Ávila SP, Silva CM, Schiebel R, Cecca F, Backeljau T, Martins AMF (2009b) How did they get here? Palaeobiogeography of the Pleistocene marine molluscs of the Azores. Bulletin of the Geological Society of France 180: 295–307. doi: 10.2113/gssgfbull.180.4.295
  • Ávila SP, Rebelo A, Medeiros A, Melo C, Gomes C, Bagaço L, Madeira P, Borges PA, Monteiro P, Cordeiro R, Meireles R, Ramalho R (2010) Os fósseis de Santa Maria (Açores). 1. A jazida da Prainha. OVGA – Observatório Vulcanológico e Geotérmico dos Açores, Lagoa, 103 pp.
  • Ávila SP, Santos AC, Penteado AM, Rodrigues AM, Quintino I, Machado MI (2005) The molluscs of the intertidal algal turf in the Azores. Iberus 23(1): 67–76.
  • Bouchet P, Rocroi J-P (2005) Classification and nomenclator of gastropod families. Malacologia 47(1–2): 1–397. doi: 10.4002/040.052.0201
  • Bouchet P, Warén A (1993) Revision of the Northeast Atlantic bathyal and abyssal Mesogastropoda. Bolletino Malacologico Supplemento 3: 579–840.
  • Cardigos F, Tempera F, Ávila SP, Gonçalves J, Colaço A, Santos RS (2006) Non-indigenous marine species of the Azores. Helgoland Marine Research 60(2): 160–169. doi: 10.1007/s10152-006-0034-7
  • Cordeiro R, Malaquias MAE, Mas G, Figueroa I, Borges JP, Ávila SP (2013) New records for the opisthobranch fauna of the Archipelago of the Azores (north-east Atlantic Ocean). Marine Biodiversity Records 6: e28. doi: 10.1017/S1755267213000110
  • Costa AC, Ávila SP (2001) Macrobenthic mollusc fauna inhabiting Halopteris spp. subtidal fronds in São Miguel island, Azores. Scientia Marina 65(2): 117–126. doi: 10.3989/scimar.2001.65n2117
  • Dautzenberg P (1889) Contribution à la faune malacologique des Iles Açores. Résultats des dragages effectués par le yacht l’Hirondelle pendant sa campagne scientifique de 1887. Révision des mollusques marins des Açores. Résultats des Campagnes Scientifiques du Prince de Monaco 1: 1–112. doi: 10.5962/bhl.title.13198
  • Gofas S (1989) Two new species of Alvania (Rissoidae) from the Azores. Publicações Ocasionais da Sociedade Portuguesa de Malacologia 14: 39–42.
  • Gofas S (1990) The littoral Rissoidae and Anabathridae of São Miguel, Azores. Açoreana Suplemento 2: 97–134.
  • Gofas S (2007) Rissoidae (Mollusca: Gastropoda) from northeast Atlantic seamounts. Journal of Natural History 41: 779–885. doi: 10.1080/00222930701298085
  • Gofas S (2010) A new Manzonia (Gastropoda: Rissoidae) from nothwestern Morocco. Iberus 28(1): 91–96.
  • Hernández-Otero JM, García MH (2003) Rissoidae. In: Moro L, Martín JL, Garrido MJ, Izquierdo I (Eds) Lista de especies marinas de Canarias (algas, hongos, plantas y animales). Consejería de Política Territorial y Medio Ambiente del Gobierno de Canarias, La Laguna, 89–90.
  • Hoenselaar HJ, Goud J (1998) The Rissoidae of the CANCAP expeditions, I: the genus Alvania Risso, 1826 (GastropodaProsobranchia). Basteria 62: 69–115.
  • Malaquias MAE, Calado GP, Padula V, Villani G, Cervera JL (2009) Molluscan diversity in the North Atlantic Ocean: new records of opisthobranch gastropods from the Archipelago of the Azores. Marine Biodiversity Records 2: e28. doi: 10.1017/S175526720800016X
  • Malaquias MAE, Calado GP, Cruz JF, Jensen KR (2011) On the occurrence of the Caribbean sea slug Thuridilla mazda in the eastern Atlantic Ocean. Marine Biodiversity Records 5: e50. doi: 10.1017/S1755267211001023
  • Manzoni A (1868a) Nouvelles espèces de Rissoa recueillies aux îles Canaries et à Madère par M. Mac-Andrew, en 1852. Journal of Conchology 16: 164–168.
  • Manzoni A (1868b) Sur les Rissoa des îles Canaries et de Madère par M. Mac-Andrew en 1852. Journal of Conchology 16: 236–256.
  • Martins AMF, Borges JP, Ávila SP, Costa AC, Madeira P, Morton B (2009) Illustrated checklist of the infralittoral molluscs off Vila Franca do Campo. Açoreana Suplemento 6: 15–103.
  • Moolenbeek RG, Faber MJ (1987) The Macaronesian species of the genus Manzonia (Gastropoda: Rissoidae), part II. De Kreukel 2–3: 23–31.
  • Moolenbeek RG, Hoenselaar HJ (1989) The genus Alvania on the Canary Islands and Madeira (Mollusca: Gastropoda) – Part 1. Bulletin Zoölogisch Museum 11(27): 215–228.
  • Moolenbeek RG, Hoenselaar HJ (1992) New additions to the Manzonia fauna of the Canary Islands (Gastropoda: Rissoidae). Publicacões Ocasionais da Sociedade Portuguesa de Malacologia 16: 13–16.
  • Moolenbeek RG, Hoenselaar HJ (1998) The genus Alvania on the Canary Islands and Madeira (Mollusca: Gastropoda) – Part 2. Bulletin Zoölogisch Museum 16(8): 53–64.
  • Moolenbeek RG, Rolán E (1988) New species of Rissoidae from the Cape Verde Islands (Mollusca: Gastropoda) – Part 1. Bulletin Zoölogisch Museum 11(14): 121–126.
  • Nobre A (1937) Moluscos testáceos marinhos do arquipélago da Madeira. Separata de “Memórias e Estudos do Museu Zoológico da Universidade de Coimbra”, Série I, n.° 98. Coimbra Editora, Coimbra, 101 pp.
  • Pedro NC, Malaquias MAE, Costa AC, Ávila SP (2011) Crimora papillata (Nudibranchia: Triophinae), a new record for the shallow marine molluscs of the Azores. Marine Biodiversity Records 4: e37. doi: 10.1017/S1755267211000364
  • Ponder WF (1985) A review of the Genera of the Rissoidae (Mollusca: Mesogastropoda: Rissoacea). Records of the Australian MuseumSupplement4: 1–221. doi: 10.3853/j.0812-7387.4.1985.100
  • Rolán E (1987) Aportaciones al estudio de los Risoaceos de las Islas Canarias – I. Description de tres especies nuevas. Publicacões Ocasionais da Sociedade Portuguesa de Malacologia 8: 1–4.
  • Rolán E (2005) Malacological fauna from the Cape Verde Archipelago. Part 1, Polyplacophora and Gastropoda. ConchBooks, Hackenheim, 455 pp.
  • Rolán E, Hernández JM (2003) Dos nuevas especies de Rissoella (Mollusca: Rissoellidae) de las Islas Canarias y Senegal. Revista de la Academia Canaria de Ciencias 15(3–4): 229–235
  • Rolán E, Luque ÁA (2000) The subfamily Rissoininae (Mollusca: Gastropoda: Rissoidae) in the Cape Verde Archipelago (West Africa). Iberus 18(1): 21–94.
  • Rolán E, Oliveira Á (2008) A new species of Rissoa (Prosobranchia, Rissoidae) from Cape Verde Archipelago. Gloria Maris 47(4): 73–77.
  • Rolán E, Rubio F (1999) New information on the malacological fauna (Mollusca: Gastropoda) of the Cape Verde Archipelago, with the description of five new species. Apex 14(1): 1–10.
  • Segers W (2002) On some shallow–water marine molluscs of the Azores. Gloria Maris 41(4–5): 84–104.
  • Segers W, Swinnen F, Prins R (2009) Marine molluscs of Madeira. Snoeck Publishers, Heule, 612 pp.
  • Templado J, Rolán E (1993) Las especies del género Crisilla y afines (Gastropoda: Prosobranchia: Rissoidae) en el archipiélago de Cabo Verde. Iberus 11(2): 1–25.
  • Verduin A (1988) On the taxonomy of some Rissoacean species from Europe, Madeira and the Canary Islands (Gastropoda, Prosobranchia). Basteria 52: 9–35.
  • Watson RB (1873) On some marine Mollusca from Madeira including a new genus of the Muricidae, a new Eulima, and the whole of the Rissoidae of the group of islands. Proceedings of the Zoological Society of London 2: 361–391.
  • Watson RB (1886) Report on the Scaphopoda and Gasteropoda collected by H.M.S. “Challenger” during the years 1873–1876. Reports on the Scientific Results of the “Challenger” Expedition 1873–76. Zoology 15(42): 1–756.
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