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Research Article
A new species of the genus Policordia (Bivalvia, Verticordioidea, Lyonsiellidae) from off the coast of southern California
expand article infoLyudmila A. Safonova, Kelvin L. Barwick§
‡ Moscow State University, Moscow, Russia
§ Unaffiliated, Fountain Valley, United States of America
Open Access

Abstract

A new species, Policordia hispida, is described and compared with three similar species: P. densicostata (Locard, 1898); P. pilula (Pelseneer, 1911) and a yet un-described species, Policordia sp. (= P. pilula sensu Ivanova, 1977 not Pelseneer, 1911). This is a first record for the genus in the Californian province.

Keywords

Policordia hispida , Heterodonta , Anomalodesmata , Eastern Pacific, carnivorous bivalves, bathyal

Introduction

Like other lyonsiellids, the genus Policordia Dall, Bartsch & Rehder, 1938 (Bivalvia, Lyonsiellidae) comprises specialized carnivorous bivalves widely distributed in the world’s oceans. Representatives of the genus live in a large range of depths, 138–9380 m (Allen and Turner 1974; Knudsen 1970) but most commonly occur in deep-sea ocean basins and trenches. Policordia is characterized by having a small thin fragile shell with an external sculpture consisting of very fine commarginal growth lines and radial threads. It lacks hinge teeth (Coan et al. 2000). It differs from other genera of the family Lyonsiellidae in that Policordia lacks any granules or spinules on the shell surface (Allen and Turner 1974; Poutiers and Bernard 1995). Anatomical modifications of the digestive and respiratory systems of Policordia are the result of adaptations for a carnivorous way of life. The digestive tract of Policordia includes a muscular stomach with an inner layer of scleroprotein used to crush prey. The stomach is connected to extensive digestive diverticula by one or two ducts. Members of Policordia have a large inhalant siphon surrounded by sensitive tentacles. Ctenidia are present but reduced, varying in their filament numbers and the degree of their muscularization among species (Allen and Turner 1974; Ivanova 1977).

Presently 25 species are assigned to the genus Policordia primarily on the basis of conchological features (Bouchet and Gofas 2013). However, data on anatomical characters show that diversity in the genus is much higher and Policordia may prove to be a paraphyletic group requiring thorough revision (Safonova 2007).

Recently specimens conchologically similar to the type species of the genus (Policordia diomedea Dall, Bartsch & Rehder, 1938) were collected from two separate sites off the coast of southern California. These are the first records of the genus from the Californian Marine Province (Coan et al. 2000). Here we describe it as a new species.

Methods

The new species is represented by preserved, live taken, specimens that were collected using a 0.1 m2 chain-fired Van Veen Grab. Sediment samples were screened with a 1 mm sieve, fixed in a 10% solution of buffered formaldehyde and then transferred to 70% ethanol. Morphological measurements were made with calipers and an ocular micrometer (±0.1 mm). The length (L), height (H) and width (W) of the valves were recorded. Gross anatomy was observed using a dissecting microscope.

Additional material used. RV “Vityaz”, Cruise 45, station 6103, 59.1167°N, 142.1°W; 1500 m, 1 specimen; 11 May 1969 (Policordia sp. = P. pilula of Ivanova, 1977 not Pelseneer, 1911, deposited in IORAS).

Institutional abbreviations:

LACM Museum of Natural History of Los Angeles County

SBMNH Santa Barbara Museum of Natural History

CSD-EMTS City of San Diego Environmental Monitoring Technical Services Laboratory

OCSD Orange County Sanitation District

IBS RAS A.V. Zhirmunsky Institute of Marine Biology, Vladivostok, Russia

IO RAS P. P. Shirshov Institute of Oceanology, Moscow, Russia

Systematic account

Superfamily Verticordioidea Stoliczka, 1870
Family Lyonsiellidae Dall, 1895

Policordia Dall, Bartsch & Rehder, 1938

Type species

By original designation, Policordia diomedea Dall, Bartsch & Rehder, 1938.

Recent

Atlantic, Indian and Pacific Oceans.

Gender

Feminine.

Policordia hispida sp. n.

Type locality

USA, California, Orange County; 33.3688°N; 117.6899°W; 411 m (OCSD B13-9137; 30 July 2013).

Type material

Holotype:LACM 3322, valves separated, with soft parts in 70% ethanol, length 4.8 mm, height 4.3 mm, width 1.8 mm. Paratype: SBMNH 462739, USA, California, San Diego County; 32.7993°N; 117.4055°W; 449 m (CSD-EMTS 8338, 23 July 2014); valves separated, with soft parts in 70% ethanol, length 3.8 mm, height 3.4 mm, width 1.4 mm.

Diagnosis

Shell subquadrate, longer than high with broadly rounded posterodorsal margin; 30–32 radial periostracal lamellae present; umbones prominent. Each mantle margin with approximately 30 mantle glands lacking long cylindrical portion. Inhalant siphon with 18–19 papillated tentacles and 2 pairs of smooth tentacles. Exhalant siphon with 5 conical tentacles. Byssal thread present.

Description

Shell. The translucent fragile shell is subquadrate (Figs 1, 3) with the length greater than the height (Table 1); inequivalve, with the right valve overlapping the left. The beaks are prosogyrate, delimited from the posterior angle by compressions. The posterodorsal margin is straight and is directed obliquely downwards from umbo; the posteroventral margin is slightly rounded and forms extended and slightly compressed angle with the posterodorsal margin. The anteroventral margin is rounded on the left valve and nearly straight on the right valve. Shell with irregular fine commarginal growth checks, covered with a colorless periostracum, which in turn forms a series of regularly spaced, radial lamellae (30–32) extending from the umbo, of the total, 13–14 are secondary (incomplete). Adhering to some radial lamellae are bunches of fine fibers giving the shell a slightly hirsute appearance externally. Shell nearly completely covered with fragile thick-silt coating (not shown, removed prior to examination). Hinge margin thin, edentate, with relatively large lithodesma inserted posterior to umbo along posterodorsal margin. Lithodesma has small posterior sinus, about ¼ of length, right posterior branch less than the left (Fig. 1).

Figure 1. 

Policordia hispida sp. n. Shell of holotype, external view and lithodesma; lv left valve rv right valve ld lithodesma.

Table 1.

Measurement of right valve (mm).

Measurement L H W H/L W/L
Holotype (LACM 3322) 4.8 4.3 1.8 0.9 0.4
Paratype (SBMNH 462739) 3.8 3.4 1.4 0.9 0.4

Anatomy. Mantle of the holotype has about 30 flask-shaped mantle glands located along the mantle edge. Mantle glands consist of short ducts formed by a few cells and oval structure above them, similar to glands of P. atlantica (Allen and Turner 1974). There is one row of papillated tentacles surrounding the inhalant siphon, 10 tentacles on the right side and 9 on the left (Figs 2, 3). Each tentacle carries 6–8 short papillated extensions (Figs 2, 4). Additionally, slightly outside the row of papillated tentacles, there are two, left and right, pairs of simple conical tentacles (Fig. 4). The first pair (counting from anterior to posterior) is between the fifth and sixth papillated tentacles; the second pair is between the seventh and eighth papillated tentacles. The exhalant siphon is surrounded by a total of five conical tentacles, one located dorsally and two pairs laterally (Figs 2, 3).

Figure 2. 

Policordia hispida sp. n. Body structure, medial section through the body (views from left and right respectively); aam anterior adductor muscle est exhalant siphon tentacles f foot g gills hg hindgut ist inhalant siphon tentacles ld lithodesma of oral funnel ov ovaries pam posterior adductor muscle pc pericardium pg pedal ganglion sh shell st stomach t testis vg visceral ganglion.

Figure 3. 

Policordia hispida sp. n. Holotype, wet specimens in 70% ethanol; left and right valve respectively; scale bar = 1 mm.

Figure 4. 

Policordia hispida sp. n. The fifth and sixth papillated tentacles of the inhalant siphon with a simple conical tentacle between them; ist inhalant siphon tentacles at conical tentacle.

The foot has a heel; byssus present (Figs 2, 3).

Gills comparably wide, elongated, longer than base of foot. They consist of inner and outer demibranchs (Fig. 5); attached by outer demibranch margin laterally to mantle wall and posteriorly to junction between siphons. Outer demibranch without inter-filamentary junctions, inner demibranch with a single inter-filamentary connection.

Mouth is wide, funnel-liked, followed by a rigid oesophagus. Stomach covered with digestive diverticula; hindgut passes through pericardium (Fig. 2).

Figure 5. 

Policordia hispida sp. n. Left gill, ventral view; ga gill axis id inner demibranch if interfilamentar partition od outer demibranch.

The holotype is a hermaphrodite with both testes covering anterior upper quarter of digestive diverticula and the ovaries located posteriorly (Figs 2, 3).

Variation

The shell of the paratype is slightly smaller in absolute dimensions but retains the same ratios of width to length and height to length (Table 1). Like the holotype, the translucent fragile shell is subquadrate; inequivalved with the right valve overlapping the left. In keeping with its smaller size (Allen and Turner 1974), the shell surface has both fewer radial periostracal lamellae (27–29) and secondary lamellae (8–10). The hinge margin is thin and edentate, with a lithodesma that matches the holotype in size and proportions. No silt covering observed.

The mantle of the paratype, as with that of the holotype, has flask-shaped mantle glands. The inhalant siphon is surrounded by 17 papillated tentacles. As in the holotype, there are two left and right pairs of conical tentacles located slightly outside of the row of papillated tentacles. The first pair is located between the second and third papillated tentacles; the second pair is between fifth and sixth (counting from anterior to posterior). The exhalant siphon is surrounded by a total of five conical tentacles; one dorsal and two pairs of laterals. As in the holotype, the foot has a single byssal thread attached.

Etymology

The new species name is derived from the Latin adjective hispida due to the somewhat ‘shaggy’ appearance of the shell.

Distribution

Known only from the type material: Eastern Pacific, southern California, 411–449 m.

Habitat

Type specimens found in silt and fine sand.

Discussion

The new species was assigned to the genus Policordia on the basis of conchological features. The shell surface is smooth, wihtout granules and hinge teeth are absent (Dall et al. 1938; Allen and Turner 1974). Anatomical details of the type species of the genus, Policordia diomedea, are not known. Conchologically, the new species differs from the P. diomedea in that the length is greater than the height and the posterodorsal margin is straighter and longer. P. diomedea is taller; more rounded with a shorter posterodorsal margin (Dall et al. 1938).

Policordia hispida sp. n. most closely resembles P. densicostata (Locard, 1898); P. pilula (Pelseneer, 1911) and an undescribed species, Policordia sp. (= P. pilula sensu Ivanova, 1977 not Pelseneer, 1911) (L. Safonova pers. obs. 2016).

Policordia densicostata, an Atlantic species whose anatomical features were described by Allen and Turner (1974), has a taller shell with more prominent umbones. Policordia densicostata lacks simple conical inhalant tentacles of P. hispida sp. n. Unlike P. densicostata, the new species lacks long cylindrical portion of the mantle glands (Table 2).

Table 2.

Some characters of selected species of Policordia including geographical distributions.

P. hispida sp. n. P. densicostata (Locard, 1898) P. pilula (Pelseneer, 1911)§ Policordia sp. (un–described)|
Length (mm) 4.8 18 5.8 7.0
Length:Height L > H L < H L < H L = H
Inhalant siphon tentacles 18–19, thick, flattened, with 6–8 papillated extensions; 4 outer, smaller, simple conical tentacles 22, all merged at base, each with 3–7 papillated lobes Unknown 23, thick, flattened, with 7 extensions; 4 outer, smaller, simple conical tentacles
Exhalant siphon tentacles Conical, 1 dorsal, 4 lateral (left and right pairs) Conical, blunt with dense covering of papillae, 1 dorsal, 4 lateral (left and right pairs) Unknown Conical, 1 dorsal, 4 lateral (left and right pairs)
Byssus Present Present Unknown Absent
Mantle glands ~ 30; flask shaped without long cylindrical portion ~ 30; flask shaped with long cylindrical portion Unknown 36–34 flask shaped without long cylindrical portion
Shell sculpture 30–32 radial periostracal lamellae (holotype) 30–37 radiating lines of slightly raised ridges ~ 30 radial hair like lines ~ 30 radial lines
Distribution Eastern Pacific, Southern Californian Bight; 411–449 m Atlantic; 1007–2503 m West Pacific; 1301 m Northeastern Pacific, Gulf of Alaska; 1230–2980 m

Policordia pilula has a more vertically extended shell with a more rounded posterodorsal margin (Prashad 1932). The general anatomical characters of this species were described by Pelseneer (1911), but he did not provide any details about the siphon and siphonal tentacles (Table 2).

Specimens identified as P. pilula by Ivanova (1977) from the Gulf of Alaska differ from the original description by Pelseneer (1911) and the subsequent description by Prashad (1932). It is an undescribed species (L. Safonova, pers. obs. 2016). The shell shape of P. hispida sp. n. is very similar to P. pilula sensu Ivanova (1977), but differs in the number of radial ribs and mantle glands, the smaller number of tentacles of the inhalant siphon and the presence of a byssus (Table 2).

Acknowledgements

Gennady M. Kamenev (IBS RAS) helped to bring the material to Moscow for study. Elena M. Krylova (IO RAS) critically read the manuscript. Thanks to Paul Valentich-Scott (SBMNH) for his support and encouragement. We are grateful to P. Valentich-Scott, Eugene Coan, and Richard C. Willan for their constructive comments and reviews that significantly improved the manuscript. The publication of this article was funded, in part, by a grant from the Southern California Association of Marine Inverteabrate Taxonomists (SCAMIT Publication Support Fund, Grant 2016-01).

References

  • Allen JA, Morgan RE (1981) The functional morphology of Atlantic deep water species of the families Cuspidariidae and Poromyidae (Bivalvia): An analysis of the evolution of the septibranch condition. Philosophical Transactions of the Royal Society B Biological Sciences 294: 413–546. doi: 10.1098/rstb.1981.0117
  • Allen JA, Turner JF (1974) On the functional morphology of the family Verticordiidae (Bivalvia) with descriptions of new species from the abyssal Atlantic. Philosophical Transactions of the Royal Society B Biological Sciences 268: 401–536. doi: 10.1098/rstb.1974.0038
  • Coan EV, Scott PV, Bernard FR (2000) Bivalve seashells of western North America. Santa Barbara Museum of Natural History, Santa Barbara, 764 pp.
  • Dall WH, Bartsch P, Rehder HA (1938) A manual of the recent and fossil marine pelecypod mollusks of the Hawaiian islands. Bernice P. Bishop Museum Bulletin 153: 1–233.
  • Ivanova VL (1977) New data on the composition and distribution of the bivalve mollusk genus Policordia Dall, Bartsch & Rehder 1939. Akademia Nauk SSSR, Institut Okeanologii, Trudy 108: 173–197.
  • Knudsen J (1970) The systematics and biology of abyssal and hadal Bivalvia. Galathea Report 11. Danish Science Press, Copenhagen, 241 pp.
  • Locard A (1898) Mollusques testacés. Tome 2. Expéditions scientifiques du Travailleur et du Talisman pendant les années 1880, 1881, 1882, 1883. Libraires de L’académie de Médecine, Paris, 515 pp.
  • Pelseneer P (1911) Les Lamellibranches de l’Expedition du Siboga, partie anatomique. Siboga Expeditie 53a: 1–125.
  • Poutiers JM, Bernard FR (1995) Carnivorous bivalve molluscs (Anomalodesmata) from the tropical western Pacific Ocean with a proposed classification and a cataloque of recent species. In: Bouchet P (Ed.) Resultats des Campagnes Musorstom, Volume 14.Memoirs du Museum d’Histoire Naturelle 167: 107–187.
  • Prashad B (1932) The Lamellibranchia of the Siboga Expedition. Systematic part II (exclusive of the Pectinidae). Siboga Expeditie 53c: 1–351.
  • Safonova L (2007) Taxonomical composition and morphological diversity of the genus Policordia (Bivalvia).Jordaens K, Van Houtte N, Van Goethem J, Backeljau T (Eds) World Congress of Malacology, Antwerp (Belgium), July 2007, 191.
  • Salas C (1996) Marine bivalves from off the Southern Iberian Peninsula collected by the Balgim and Fauna I expeditions. Haliotis 25: 33–100.
  • Soot-Ryen T (1966) Revision of the pelecypods from the Michael Sars North Atlantic deep–sea expedition 1910. With notes on the family Verticordiidae and other interesting species. Sarsia 24: 1–32. doi: 10.1080/00364827.1966.10409564
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