Research Article
Print
Research Article
A new species of Linopherus (Annelida, Amphinomidae) from Beibu Gulf, South China Sea
expand article infoYue Sun§|, Xinzheng Li|
‡ Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China
§ University of Chinese Academy of Sciences, Beijing, China
| Qingdao National Laboratory for Marine Science and Technology, Qingdao, China
Open Access

Abstract

Linopherus beibuwanensis sp. n. is described based on six specimens deposited in the Marine Biological Museum of the Chinese Academy of Sciences, Qingdao, collected from the Beibu Gulf (Tokin Gulf), South China Sea. The new species differs from all other Linopherus species by the shape of prostomium and caruncle. The posterior margin of prostomium is bilobed; the caruncle arises medially and confluently from the posterior margin of the prostomium, joining together with prostomium. A key to distinguish the known species of the genus is provided.

Keywords

Fireworm, new species, polychaete, Pseudeurythoe , systematics, taxonomy

Introduction

Polychaetes belonging to the family Amphinomidae are commonly known as fireworms due to the burning sensation caused by the calcareous harpoon notochaetae (Fauchald, 1977). The amphinomids are globally distributed and common in shallow tropical and subtropical waters (Kudenov 1995): Linopherus abyssalis (Fauchald, 1972a), Linopherus hemuli (Fauchald, 1972b), and Chloeia kudenovi Barroso & Paiva, 2011 are examples of recently reported species from abyssal depths and polar areas (Barroso 2011; Fauchald 1972a, b).

Species of the genus Linopherus Quatrefages, 1865 have been referred as members of Pseudeurythoe Fauvel, 1932. Fauchald (1972a) described a new species from abyssal depths and reviewed the species of Pseudeurythoe. In 1977, he treated Pseudeurythoe as a synonym of Linopherus. Since then Linopherus has been accepted by subsequent authors and in the present work (San Martín 1986; Salazar-Vallejo 1987). Linopherus differs remarkably from the other genera of the family in having species without caruncle or with a reduced caruncle, and branchiae that are limited to the anterior part of the body. The morphology of the prostomium, the development of prostomial appendages, caruncle, parapodia, and the number of branchiae are important in species identification (Kudenov 1995). To date, six species of Linopherus have been reported from the coastal waters of China (Sun, Lei and Zhou 2008): Linopherus ambigua (Monro, 1933), L. paucibranchiata Fauvel, 1932, L. hirsuta (Wesenderg-Lund, 1949), L. oligobranchia (Wu, Shen & Chen, 1975), L. microcephala (Fauvel, 1932), and L. spiralis (Wesenderg-Lund, 1949).

When the authors examined the Amphinomidae archived in the Marine Biological Museum of Chinese Academy of Sciences (MBMCAS), Institute of Oceanology, Chinese Academy of Sciences (IOCAS), six specimens of Linopherus were separated out. Careful examination revealed that these specimens represented a new species. The new species is described here, and a key to worldwide species of Linopherus is provided.

Material and methods

The specimens were collected during the late 1950s to early 1960s from Beibu Gulf (Tonkin Gulf), northern South China Sea. All specimens are deposited in the MBMCAS, preserved in 75% ethanol solution. Microscopy observations and drawings were made using a Zeiss Stemi 2000-C stereomicroscope equipped with an AxioCam MRc 5 digital camera.

Systematics

Family Amphinomidae Lamarck, 1818
Genus Linopherus Quatrefages, 1865

Linopherus beibuwanensis sp. n.

Fig. 1

Material examined

Holotype, MBM010010, Beibu Gulf, 21°15'N, 108°06'E, 91m, sandy mud, coll. Xiutong Ma, 11 Feb 1959. Paratypes, MBM200142, Beibu Gulf, 18°30'N, 107°00'E, 66m, sandy beach, coll. Zhengang Fan, 10 Sep 1960; MBM200143, Beibu Gulf, 18°00'N, 107°45'E, 90m, silty mud, coll. Ruiping Sun, 9 Apr1962; MBM200144, Beibu Gulf, 18°00'N, 108°00'E, 93m, sandy mud, coll. Xiutong Ma, 11 Dec 1959; MBM200145, Beibu Gulf, 18°30'N, 107°00'E, 66m, sandy beach, coll. Xiutong Ma, 9 Dec 1962; MBM200122, Beibu Gulf, 18°00'N, 107°00'E, sandy mud, coll. Zhengang Fan, 14 Feb1960.

Diagnosis

Prostomium globular, posterior margin bilobed, with two pairs of eyes, anterior pair semicircular in shape. Medial caruncle conspicuous, arising from and confluent with posterior prostomial margin, medial lobe projecting above paired lateral lobes. Parapodia biramous, rami widely separated, with single dorsal and single ventral cirrus. Branchiae dendritic, present from chaetiger 3 onwards, with more than 40 pairs.

Description

Holotype (MBM010010) incomplete, lacking posterior part, 17 mm long, 2 mm wide excluding chaeta, with 45 chaetigers. Body elongate, nearly rectangular in cross section, tapering posteriorly. Color in alcohol pale yellow, without color pattern.

Prostomium (Fig. 1A) divided into two parts by transverse groove. Anterior lobe rounded, with pair of cirriform antennae dorsally and similar pair of palps laterally, palps with three distinct articulations. Posterior lobe heart-shaped, bilobed along posterior margin, with median antenna and two pairs of reddish eyes. Anterior pair of eye spots semicircular in shape and large, posterior pair of eye spots rounded and small. Median antenna conical, slightly shorter than paired antennae, located at posterior margin of prostomium. Buccal opening occupying two chaetigers (Fig. 1B).

Figure 1. 

Linopherus beibuwanensis sp. n. A Anterior end in dorsal view B Anterior end in vental view C left parapodia of chaetiger 14 in frontal view D branchiae of chaetiger 28 E harpoon notochaeta F forked neurochaeta G slender capillary chaeta. Scale bars: A–B, 200 μm; C–D, 250 μm; E–F, 50 μm; G, 20 μm.

Caruncle rectangular and conspicuous, medial lobe projecting above paired lateral lobes. Caruncle restrict to chaetiger 1, equal in length to posterior prostomial lobe of prostomium, reaching to anterior margin of chaetiger 2, arising medially and confluently with posterior prostomium (Fig. 1A).

All parapodia biramous, with chaetiger 1 greatly reduced, chaetiger 2 forming first dorsally complete ring. Parapodia with slender cirri (Fig. 1A, C), both notopodia and neuropodia well-developed, chaetal sac forming low rounded lobe. First two parapodia with longer and more conspicuous cirri than other parapodia; ventral cirri of chaetiger 2 longest, each with four articulations (Fig. 1A). Succeeding parapodia with tapering and rather short ventral cirri.

Branchiae present from chaetiger 3, located on posterior face of each notopodia (Fig. 1A), arising as tufts, dendritically branched, decreasing along body and disappearing at approximately chaetiger 42; chaetiger 1 branchiae with five terminal filaments, chaetiger 17 branchiae with 29 or 26 terminal filaments, chaetiger 28 branchiae with 15 filaments (Fig. 1D), chaetiger 42 branchiae with 6 or 7 filaments.

Notochaetae of three types: stout harpoon chaetae, numbering 13–24 per fascicle (Fig. 1E); slender capillary chaetae (Fig. 1G), faintly serrated, without basal spur, many broken; notoacicula, numbering 3–4 per fascicle, hastate (Fig. 1C). Neurochaetae of three kinds: forked chaetae, short limb reduced as spur, with thin shafts and long, distally serrated cutting margins (Fig. 1F); slender, capillary chaetae, smooth; neuroacicula, numbering 2–3 per fascicle, slightly hastate, slender than notoacicula (Fig. 1C).

Variations

All specimens examined are incomplete lacking the posterior part. Specimen size varies from 1.9 to 2.5 mm in maximum width. Branchial chaetiger range varies from 3 to 31–40. The maximum number of branchial filaments varies from 20–29. One female paratype (MBM200143) with eggs in posterior coelomic cavity, ranging in diameter from 71μm to 90 μm.

Etymology

The species is named after Beibuwan, the Chinese name for the Beibu Gulf (Tonkin Gulf), South China Sea.

Distribution

Only known from Beibu Gulf, South China Sea.

Remarks

Linopherus beibuwanensis sp. n. is referred to Linopherus because of the arrangement of branchiae and the reduced but characteristic caruncle. Linopherus beibuwanensis sp. n. is unique in this genus for the combined shape of its prostomium and the caruncle. While the posterior prostomial margin is straight (not bilobed) in most Linopherus species, their caruncles are also either absent or reduced. In the latter case, species with reduced caruncles typically exhibit a transverse groove that appears to isolate the caruncle from the prostomium, which is usually partly or completely concealed by the second chaetiger (see Langerhans 1881; Fauvel 1932; Monro 1933, 1937; Treadwell 1941; Wesenberg-Lund 1949; Knox 1960; Fauchald 1972a, b; Kudenov 1975; Wu et al. 1975; Kudenov and Blake 1985; San Martín 1986; Salazar-Vallejo 1987).

Linopherus beibuwanensis sp. n. is similar to L. abyssalis in having the posterior prostomial margin bilobed. The new species can be distinguished from the latter by the presence of eyes and arrangement of branchiae; the former has two pairs of eyes and more than 40 pairs of branchiae, while the latter has no externally detectable eyes and only 5-6 pairs of branchiae.

Caruncle morphology appears to be an essential character which can be used to distinguish the species of Linopherus. However, Linopherus species are small in size, and so their caruncle morphology is imperfectly known since it is usually concealed by constriction of the anterior chaetigers. Clearly, further research on this taxon is necessary.

Key to species of Linopherus (modified from Fauchald 1972 and Salazar-Vallejo 1987)

1 Branchiae present from chaetiger 2 continuing to end of body L. reducta (Kudenov & Blake, 1985)
Branchiae present from chaetiger 3 or 4 2
2 Branchiae present from chaetiger 3 3
Branchiae present from chaetiger 4 15
3 Eyes absent 4
Eyes present, one or two pairs 5
4 Several pairs of branchiae until end of body L. tripunctata (Kudenov, 1975)
Only six pairs of branchiae L. oligobranchia (Wu, Shen & Chen, 1975)
5 First pair of eyes semicircular 6
First pair of eyes rounded 8
6 Posterior margin of prostomium bilobed, more than 40 pairs of branchiae L. beibuwanensis sp. n.
Posterior margin of prostomium not bilobed, less than 40 pairs of branchiae 7
7 Six pairs of branchiae, caruncle absent L. fauchaldi San Martín, 1986
About 23 pairs of branchiae, caruncle present, small and rounded L. microcephala (Fauvel, 1932)
8 Anterior lobe of prostomium conical, not expanded anteriorly L. kristiani Salazar-Vallejo, 1987
Anterior lobe of prostomium rounded, anteriorly expanded 9
9 One pair eyes 10
Two pairs of eyes 11
10 Caruncle present, cirri of second chaetiger longer than others L. paucibranchia (Fauvel, 1932)
Caruncle absent, cirri of second chaetiger as long as others L. hirsuta (Wesenberg-Lund, 1949)
11 More than 20 pairs of branchiae present 12
Maximally 16 pairs of branchiae present 14
12 Branchiae present only on anterior chaetigers, eyes indistinct L. ambigua (Monro, 1933)
Branchiae present in all but first two and last few chaetigers, eyes distinct 13
13 Caruncle absent, eyes inconspicuous L. spiralis (Wesenberg-Lund, 1949)
Caruncle present, eyes conspicuous L. oculata (Treadwell, 1941)
14 13-16 pairs of branchiae present, caruncle present L. annulata (Hartmann-Schröder, 1965)
Maximally seven pairs of branchiae present, caruncle absent L. canariensis Langerhans, 1881
15 More than 40 pairs of branchiae present, eyes distinct, caruncle absent L. acarunculata (Monro, 1937)
Less than 10 pairs of branchiae, eyes absent, caruncle present 16
16 Seven pairs of branchiae present, subdistally inflated (hastate) acicular chaetae absent L. minuta (Knox, 1960)
Less than 7 pairs of branchiae present, subdistally inflated (hastate) acicular chaetae present 17
17 Five or six pairs of branchiae present, dorsal cirri absent in branchial chaetigers, caruncle in deep pocket at posterior margin of prostomium, small and rounded L. abyssalis (Fauchald, 1972)
Five pairs of branchiae present, dorsal cirri absent in branchial chaetigers, caruncle button-shaped L. hemuli (Fauchald, 1972b)

Acknowledgments

We appreciate the assistance of Dr. Sergio I. Salazar -Vallejo (EI Colegio de la Frontera Sur, Chetumal, Mexico) and Dr. Beatriz Yáñez-Rivera (Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Unidad Académica Mazatlán, Mexico) for their kind help with our taxonomic research and for providing us with important references. We are grateful to Dr. Paulo Paiva and Dr. Jerry D. Kudenov for their comments and suggestions improving the manuscript. We are also grateful to the managers of the MBMCAS for their assistance in sorting the specimens. This study was supported by the funds of the Ocean Public Welfare Scientific Research Project (No. 201505004-1), the National Natural Science Foundation of China (No. 41406157), and the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA11020303).

References

  • Barroso R, Paiva PC (2011) A new deep-sea species of Chloeia (Polychaeta: Amphinomidae) from southern Brazil[J]. Journal of the Marine Biological Association of the United Kingdom 91(02): 419–423. https://doi.org/10.1017/S0025315410001499
  • Fauchald K (1972a) Benthic polychaetous annelids from deep water off western Mexico and adjacent areas in the eastern Pacific Ocean[J]. Allan Hancock Monographs in Marine Biology 7: 1–575.
  • Fauchald K (1977) The polychaete worms; definitions and keys to the orders, families and genera [J]. Natural History Museum of Los Angeles County: Los Angeles 28: 1–188.
  • Fauvel P (1932) AnnelidaPolychaeta of the Indian Museum, Calcutta. Memoirs of the Indian Museum 12(1): 1–262, 9 pls.
  • Kudenov JD, Blake JA (1985) A New Species of Pseudeurythoe (Polychaeta: Amphinomidae) from Central California[J]. Bulletin of the Southern California Academy of Sciences 84(1): 38–40.
  • Kudenov JD (1995) Family Amphinomidae Lamarck, 1818[J]. Taxonomic atlas of the benthic fauna of the Santa Maria Basin and Western Santa Barbara Channel 5: 207–215.
  • Langerhans P (1881) Ueber einige canarische Anneliden. Nova Acta der Kaiserlichen Leopold-Carolin Deutschen Akademie der Naturforscher, Halle 42(3): 95–124.
  • Monro CCA (1933) The Polychæta Errantia collected by Dr. C. Crossland at Colón, in the Panama Region, and the Galapagos Islands during the Expedition of the SY ‘St. George’[C]. Proceedings of the Zoological Society of London 103(1): 1–96. https://doi.org/10.1111/j.1096-3642.1933.tb01578.x
  • Monro CCA (1937) Polychaeta. The John Murray Expedition 1933-1934 Scientific Reports 4(8): 243–321.
  • Salazar-Vallejo SI (1987) A new amphinomid polychaete (Annelida: Polychaeta) from western Mexico[J]. Revista de Biologia Tropical 3(1): 77–82.
  • San Martin G (1986) Anelidos Poliquetos Procedentes de la I Expedicion Cubano-Espanola a la Isla de la Juventud y Archipielago de los Canarreos. II. Familias Chrysopetalidae y Amphinomidae. Revista de Investigaciones Marinas 7(1): 17–30.
  • Sun RP, Lei YL, Zhou J (2008) Polychaeta. In: Liu R (Eds) Checklist of Marine Biota of China Sea. Science Press, Beijing, 405–452. [In Chinese]
  • Treadwell AL (1941) Eastern Pacific expeditions of the New York Zoological Society. 23. Polychaetous annelids from the west coast of Mexico and Central America[J]. Zoologica 26: 17–24.
  • Wesenberg-Lund E (1949) Polychaetes of the Iranian gulf[J]. Danish Scientific Investigations in Iran 4: 265–271.
  • Wu BL, Shen SP, Chen M (1975) Preliminary report of polychaetous annelids from Xisha Islands, Guangdong Province, China[J]. Studia Marina Sinica 10: 65–104. [In Chinese]
login to comment