Published December 31, 2015 | Version v1
Taxonomic treatment Open

Dipolydora armata Langerhans 1880

Description

Dipolydora armata (Langerhans, 1880)

(Fig. 5)

Polydora armata Langerhans, 1880: 93 –94, pl. 4, fig. 5a–c; Blake & Kudenov 1978: 255 –258, fig. 43a–e. Dipolydora armata.— Blake 1996 (Part.): 196–198, fig. 4.36; Bick 2001: 178 –186, figs. 1–7; Williams 2001: 438 –442, figs 5,

6; Radashevsky & Nogueira 2003: 377–381, figs 1–7; Sato-Okoshi et al. 2008: 495–496, fig. 4. Dipolydora cf. armata.— Radashevsky & Fauchald 2000: fig. 6F.

Material examined. Queensland: AM W.45506, MI QLD 2447 (20); MIMB 28114, MI QLD 2447 (7).

Adult morphology. Up to 2.5 mm long, 0.3 mm wide for 30 chaetigers. Body and palp pigmentation absent. Prostomium incised anteriorly, extending posteriorly to end of chaetiger 2 as a low caruncle. Occipital antenna and eyes absent.

Chaetiger 1 with capillaries and small postchaetal lamellae in both rami. Winged notopodial capillaries gradually becoming longer, thinner and less numerous along midbody chaetigers. Notopodia from chaetigers 18– 24 onwards with up to three thin alimbate capillaries and 15 awl-like spines in a bundle (Fig. 5 E, F).

Chaetiger 5 with up to three dorsal superior winged capillaries, two heavy falcate spines, and four ventral winged capillaries (Fig. 5 A, B). Falcate spines with central main fang, large lateral tooth and apical structure appearing as wide cowling or third tooth on convex side of main fang; numerous fine bristles present on basis of teeth (Fig. 5 B).

Hooks in neuropodia from chaetiger 7, up to three in a series, accompanied by 1–2 inferior capillaries throughout body and 1–3 alternating capillaries in 5–10 posterior chaetigers (Fig. 5 C, D). Hooks bidentate; shaft slightly curved, without constriction (Fig. 5 C, D).

Branchiae from chaetiger 7 to chaetiger 11, fewer in small individuals, flattened, with surfaces oriented parallel to body axis, basally fused to notopodial postchaetal lamellae.

Pygidium small, cup-shaped, with only narrow dorsal gap or bilobed, divided by dorsal gap and ventral incision into two rounded lateral lobes.

Remarks. Dipolydora armata was originally described from Madeira Island by Langerhans (1880) as a borer of calcareous algae and has since been reported world-wide. In Australia, D. armata was reported from Western Australia (Augener 1914; Hartmann-Schröder 1979; Sato-Okoshi et al. 2008), Victoria and South Australia (Blake & Kudenov 1978; Hartmann-Schröder 1987; McDiarmid et al. 2004). Worms from Lizard Island appear identical to D. armata described from California (Hartman 1941; Blake 1996), the Marshall Islands (Woodwick 1964), Mediterranean (Bick 2001), Philippines (Williams 2001), Brazil and other localities (Radashevsky & Nogueira 2003, type material re-examined).

Dipolydora armata has been considered cosmopolitan, widespread in tropical and subtropical waters, and rare in boreal and temperate waters. Such a wide distribution of the same species seems, however, suspicious taking into account small size of adults (usually 3–4 mm long for 30–35 chaetigers), low fecundity (up to 100 eggs per brood), adelphophagy (larvae feeding on the nurse eggs inside egg capsule), low larval production, and very short time that larvae swim in the water (see Lewis 1998 for details of larval development in the species). Molecular investigation is certainly needed to confirm the conspecificity of the remote populations.

Habitat. In this study, adult D. armata were found boring into the shell of a gastropod Turbo sp. at about 14 m depth.

Distribution. Widespread in tropical and subtropical waters. Intertidal to 100 m. The species is herein reported for the first time from Queensland and the Great Barrier Reef.

Notes

Published as part of Radashevsky, Vasily I., 2015, Spionidae (Annelida) from Lizard Island, Great Barrier Reef, Australia: the genera Aonides, Dipolydora, Polydorella, Prionospio, Pseudopolydora, Rhynchospio, and Tripolydora, pp. 635-694 in Zootaxa 4019 (1) on pages 643-645, DOI: 10.11646/zootaxa.4019.1.22, http://zenodo.org/record/235906

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Linked records

Additional details

Biodiversity

Family
Spionidae
Genus
Dipolydora
Kingdom
Animalia
Order
Spionida
Phylum
Annelida
Scientific name authorship
Langerhans
Species
armata
Taxon rank
species
Taxonomic concept label
Dipolydora armata Langerhans, 1880 sec. Radashevsky, 2015

References

  • Langerhans, P. (1880) Die Wurmfauna von Madeira. III. Zeitschrift fur wissenschaftliche Zoologie, 34, 87 - 143.
  • Blake, J. A. & Kudenov, J. D. (1978) The Spionidae (Polychaeta) from southeastern Australia and adjacent areas with a revision of the genera. Memoirs of the National Museum of Victoria, 39, 171 - 280.
  • Blake, J. A. (1996) Family Spionidae Grube, 1850. Including a review of the genera and species from California and a revision of the genus Polydora Bosc, 1802. In: Blake, J. A., Hilbig, B. & Scott, P. H. (Eds.), Taxonomic Atlas of the Benthic Fauna of the Santa Maria Basin and Western Santa Barbara Channel. Vol. 6. The Annelida Part 3 - Polychaeta: Orbiniidae to Cossuridae. Santa Barbara Museum of Natural History, Santa Barbara, California, pp. 81 - 223.
  • Bick, A. (2001) The morphology and ecology of Dipolydora armata (Polychaeta, Spionidae) from the western Mediterranean Sea. Acta Zoologica, 82, 177 - 187. [Stockholm] http: // dx. doi. org / 10.1046 / j. 1463 - 6395.2001.00078. x
  • Williams, J. D. (2001) Polydora and related genera associated with hermit crabs from the Indo-West Pacific (Polydora: Spionidae), with descriptions of two new species and a second polydorid egg predator of hermit crabs. Pacific Science, 55, 429 - 565. http: // dx. doi. org / 10.1353 / psc. 2001.0037
  • Radashevsky, V. I. & Nogueira, J. M. M. (2003) Life history, morphology and distribution of Dipolydora armata (Polychaeta: Spionidae). Journal of the Marine Biological Association of the United Kingdom, 83, 375 - 384. http: // dx. doi. org / 10.1017 / S 0025315403007227 h
  • Sato-Okoshi, W., Okoshi, K. & Shaw, J. (2008) Polydorid species (Polychaeta: Spionidae) in south-western Australian waters with special reference to Polydora uncinata and Boccardia knoxi. Journal of the Marine Biological Association of the United Kingdom, 88, 491 - 501. http: // dx. doi. org / 10.1017 / S 0025315408000842
  • Radashevsky, V. I. & Fauchald, K. (2000) Chaetal arrangement and homology in spionids (Polychaeta: Spionidae). Bulletin of Marine Science, 67, 13 - 23.
  • Augener, H. (1914) Polychaeta II, Sedentaria. Die Fauna Sudwest-Australiens. Ergebnisse der Hamburger sudwestaustralischen Forschungsreise 1905 herausgegeben von Prof. Dr. W. Michaelsen und Dr. R. Hartmeyer, 5, 1 - 172.
  • Hartmann-Schroder, G. (1979) Teil 2. Die Polychaeten der tropischen Nordwestkuste Australiens (zwischen Derby im Norden und Port Hedland im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 76, 77 - 218.
  • Hartmann-Schroder, G. (1987) Teil 13. Die Polychaeten der antiborealen Kuste von Victoria (Australien) (zwischen Warrnambool im Western und Port Welshpool im Osten). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 84, 27 - 66.
  • McDiarmid, H., Day, R. & Wilson, R. (2004) The ecology of polychaetes that infest abalone shells in Victoria, Australia. Journal of Shellfish Research, 23, 1179 - 1188.
  • Hartman, O. (1941) Some contributions to the biology and life history of Spionidae from California. With keys to species and genera and descriptions of two new forms. Allan Hancock Pacific Expeditions, 7, 289 - 323.
  • Woodwick, K. H. (1964) Polydora and related genera (Annelida, Polychaeta) from Eniwetok, Majuro, and Bikini Atolls, Marshall Islands. Pacific Science, 18, 146 - 159.
  • Lewis, J. B. (1998) Reproduction, larval development and functional relationships of the burrowing, spionid polychaete Dipolydora armata with the calcareous hydrozoan Millepora complanata. Marine Biology, 130, 651 - 662. [Berlin] http: // dx. doi. org / 10.1007 / s 002270050287