Caulleriella fucata, Blake, 2018

Blake, James A., 2018, Bitentaculate Cirratulidae (Annelida, Polychaeta) collected chiefly during cruises of the R / V Anton Bruun, USNS Eltanin, USCG Glacier, R / V Hero, RVIB Nathaniel B. Palmer, and R / V Polarstern from the Southern Ocean, Antarctica, and off Western South America, Zootaxa 4537 (1), pp. 1-130 : 48-51

publication ID

https://doi.org/ 10.11646/zootaxa.4537.1.1

publication LSID

lsid:zoobank.org:pub:169CBE5C-3A6E-438B-8A81-0491CBFBAC85

DOI

https://doi.org/10.5281/zenodo.3798608

persistent identifier

https://treatment.plazi.org/id/03A2CB16-FFDA-A278-FF36-F955FD3FFB87

treatment provided by

Plazi

scientific name

Caulleriella fucata
status

sp. nov.

Caulleriella fucata View in CoL new species

Figure 24 View FIGURE 24

Material Examined. Antarctic Peninsula, Palmer Archipelago, Anvers Island, Arthur Harbor, dock at Palmer Station, R / V Hero Sta. 721-5446, 29 Mar 1972, 64.775°S, 64.0683°W, 11m, holotype ( USNM 1013891 View Materials and 4 paratypes ( USNM 1013892 View Materials ); Sta. 731-1751, 16 Feb 1973, 64.775°S, 64.0683°W, 12 m, (1, USNM 1013941 View Materials ). GoogleMaps

Description. A moderate-sized species, holotype 6.4 mm long, 0.5 mm wide across thickest part of middle body for 85 setigerous segments. Body generally thick throughout, with segments wider than long; posterior end sometimes expanded, but never narrower than middle body segments. Venter flattened, with shallow groove. Dorsal surface rounded or domed throughout. Entire body rust-colored, with dusky pigment on each segment; darker pigment on pygidium.

Prostomium short, triangular, bluntly rounded on anterior margin ( Fig. 24 View FIGURE 24 A–B); eyespots absent; nuchal organs elongate slits on posterior border with peristomium ( Fig. 24A View FIGURE 24 ). Peristomium about as wide as long, tapering, merging anteriorly with prostomium to form conical pre-setigerous region or head; divided into two large rings by horizontal groove in middle ( Fig. 24 View FIGURE 24 A–B); dorsal crest absent. Peristomium followed by an achaetous segment ( Fig. 24 View FIGURE 24 A–B). Dorsal tentacles widely spaced, in groove on anterior edge of achaetous segment and posterior border of peristomium. First pair of branchiae immediately posterior to dorsal tentacles on posterior border of achaetous segment ( Fig. 24B View FIGURE 24 ); subsequent branchiae in similar position dorsal to notosetae.

Noto- and neuropodia well developed, widely separated as typical of Caulleriella species ( Fig. 24A View FIGURE 24 ). Notopodia set off from domed dorsal surface by grooves ( Fig 24B View FIGURE 24 ); neuropodia with setae directed toward midventral groove. Notosetae all long capillaries, 8–10 per fascicle in anterior setigers, reduced to 3–5 in middle and posterior setigers; neurosetae of setigers 1–4(6) capillaries similar to those of notopodia, completely replaced by 8–10 short, curved bidentate hooks from setiger 5–7; hooks with blunt, thick main fang and thinner, more pointed apical tooth ( Fig. 24D View FIGURE 24 ); hood or sheath not apparent.

Pygidium with 2–3 papillae on dorsal side of anus, and broad lobe ventrally ( Fig. 24C View FIGURE 24 ).

Methyl Green stain. No stain retained.

Etymology. The specific name, fucata , is derived from the Latin fuco, for color, in reference to the pigmentation found on these worms.

Remarks. Caulleriella fucata n. sp. should not be mistaken for any other cirratulid species in Antarctic seas owing to its widely separated noto- and neuropodia, bidentate hooks, and darkly pigmented body. The species is most closely related to C. eltaninae n. sp. (see above) in having bidentate hooks limited to the neuropodia and by having the dorsal tentacles arising from a distinct achaetous segment. The two species differ in that the neuropodial hooks of C. fucata n. sp. begin on setigers 5–7 instead of 20–21 and the branchiae of C. fucata n. sp. begin on an achaetous segment instead of setiger 1. On a global basis, C. fucata n. sp. approaches C. zetlandica described by McIntosh (1911) in lacking dorsal hooks, but this species, recently redescribed by Woodham & Chambers (1994) does not have widely separated parapodial rami. This fact, plus the much-reduced nature of the teeth on the hooks and the lack of cinctures on the posterior end suggests that C. zetlandica should be referred to Tharyx .

Distribution. Antarctic Peninsula, 11– 12 m.

R

Departamento de Geologia, Universidad de Chile

V

Royal British Columbia Museum - Herbarium

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