Terebellides europaea, Lavesque & Hutchings & Daffe & Nygren & Londoño-Mesa, 2019

Lavesque, Nicolas, Hutchings, Pat, Daffe, Gullemine, Nygren, Arne & Londoño-Mesa, Mario H., 2019, A revision of the French Trichobranchidae (Polychaeta), with descriptions of nine new species, Zootaxa 4664 (2), pp. 151-190 : 163-165

publication ID

https://doi.org/ 10.11646/zootaxa.4664.2.1

publication LSID

lsid:zoobank.org:pub:6F0BFDDC-99CA-4CED-9F56-B6DA226CD42D

persistent identifier

https://treatment.plazi.org/id/8B3961A4-2660-49E0-B7C9-9C878A8F1EE8

taxon LSID

lsid:zoobank.org:act:8B3961A4-2660-49E0-B7C9-9C878A8F1EE8

treatment provided by

Plazi

scientific name

Terebellides europaea
status

sp. nov.

Terebellides europaea View in CoL n. sp.

Figures 7–8 View FIGURE 7 View FIGURE 8 , Table 2 View TABLE 2

Type material: Holotype: MNHN-IA-TYPE 1866, complete, Northeast Atlantic Ocean, Brittany, Bay of Brest , ZC, 48°18’55”N, 4°21’54”W, 1.3 m depth, January 2016 GoogleMaps . Paratypes: MNHN-IA-TYPE 1867, complete specimen (posterior part used for molecular analysis), Northeast Atlantic Ocean, Brittany, Bay of Brest , VC, 48°18’59”N, 4°23’28”W, 2.2 m depth, July 2017 GoogleMaps ; MNHN-IA-TYPE 1868, complete (posterior part used for molecular analysis), Northeast Atlantic Ocean, Brittany, Bay of Brest , ZC, 48°18’55”N, 4°21’53”W, 5 m depth, May 2018 GoogleMaps ; MNHN-IA- TYPE 1869, complete (posterior part used for molecular analysis), Northeast Atlantic Ocean, Brittany, Bay of Brest , BK, 48°21’28”N, 4°26’38”W, 7 m depth, May 2018 GoogleMaps , mounted for SEM.

Additional material examined: SMA _BR_10, complete (posterior part used for molecular analysis), Northeast Atlantic Ocean, Brittany, Bay of Brest , VC, 48°18’59”N, 4°23’28”W, 2.2 m depth, July 2017 GoogleMaps . SMA _SP_10, complete, (posterior part used for molecular analysis), Northeast Atlantic Ocean, Spain, Ria de Ferrol , 43°28’N, 8°14’W, 40 m depth, June 2017 GoogleMaps .

Description. Small size species, with holotype 16.9 mm long (15.4 mm) and 2.1 mm (1.5–2.2 mm). Body tapering posteriorly with segments becoming increasingly shorter and more compacted towards pygidium.

Prostomium compact; eyespots absent; large upper lip surrounding mouth with many buccal tentacles ( Figs 7 View FIGURE 7 B–D & 8A). Buccal tentacles of two types, uniformly cylindrical and with expanded tips, spatulate ( Fig. 8A View FIGURE 8 ). Lower lip forming an expanded structure below upper lip ( Figs 7 View FIGURE 7 A–B & 8A). S1 and S2 short, only visible ventrally; following segments with lobes as ventral collars ( Fig. 7 View FIGURE 7 A–B). Lateral lappets on SG 3–6, ( TC 1–5), continuing ven- trally in TC 1–6, largest on TC 1 and 2 and declining in size posteriorly. No conspicuous dorsal rounded projection on anterior chaetigers. Postero-lateral undulating glandular region on TC 3 ( Fig. 7D View FIGURE 7 ).

Branchiae arising as a single structure from TC 1 and reaching TC 6 ( TC 4), consisting of a single elongate and annulated stalk situated mid-dorsally, made up of two pairs of lobes fused on 1/2 of length, lower pair thinner ( Fig. 7C View FIGURE 7 ). Posterior region of upper terminal pointed projections and of lower lobes with long pointed projections ( Fig. 7 View FIGURE 7 B–C). Upper lobes provided with about 50 well packed lamellae, lamellae of different width and size ( Figs 7 View FIGURE 7 B–C & 8A–B). Both sides of branchial lamellae provided with well-marked parallel rows of cilia, no tufts of cilia on outer edge ( Fig. 8 View FIGURE 8 A–B). Presence of rounded papillar projections over the edge of anterior branchial lamellae ( Figs 7 View FIGURE 7 B–C & 8A–B). Anterior branchial projection (5 th lobe) present ( Figs 7 View FIGURE 7 A–B, D & 8A).

Eighteen pairs of thoracic notopodia ( SG 3–20; TC 1–18). Notopodia present from TC 1 well–developed; notochaetae of TC 1 slightly longer in length than following notochaetae. All notochaetae simple capillaries, arranged in two rows. Neuropodia present as sessile pinnules from TC 6 ( SG 8) to pygidium, with uncini arranged in a single row from TC 7. First thoracic neuropodia ( TC 6) provided with four (3–5) sharply bent acute tipped to almost straight, geniculate chaetae. All subsequent thoracic neuropodia with about 10–17 uncini per torus arranged in one irregular row. Uncini as shafted denticulate hooks provided with long, thin and pointed main fang, straight terminally. Three or four teeth above the main fang, surmounted by a row of five to six short denticles and an upper crest of several minute denticles ( Fig. 8C View FIGURE 8 ). Abdomen with 33 neuropodia as erect pinnules paddle—shaped with entire margin provided with about 30 uncini; each with four pointed teeth above main fang, surmounted by a row of three to five short pointed teeth and an upper crest of minute teeth ( Fig. 8D View FIGURE 8 ).

Two pairs of elongated nephridial papillae, located latero-posteriorly to base of each notopodium of TC 4 and TC 5. Pygidium blunt.

Methyl green staining pattern. Solid from TC 1 to TC 9, with distinct stripes from TC 10 to about TC 12, distinct white antero-ventral lines from TC 5 to TC 9; white glandular region on TC 3, with central line more intensive stained and lateral deep ridges ( Fig. 7D View FIGURE 7 ).

Etymology. Species name refers to the wide distribution of the species in Europe from the south of the Bay of Biscay ( Spain) to North of Norway.

Habitat. Coastal maerl (rhodolith) beds, 2–11 m depth (this study), from mud to gravels, 8–102 m depth ( Nygren et al 2018).

Type locality. Bay of Brest , Brittany, France .

Distribution. Bay of Biscay (Bay of Brest, Trévignon, Ria of Ferrol) (this study), Kattegat, Skagerrak, North Sea, Irish Sea, Celtic Sea and Norwegian coast and shelf ( Nygren et al. 2018)

Remarks. Except T. stroemii from Adriatic Sea ( Parapar et al. 2013) (see T. lilasae n. sp. Remarks), T erebellides europaea n. sp. differs from other previously known European species by the presence of papillar projections pointing over the edge of the branchial lamellae. In this character, T. europaea n. sp. is also similar to T. bonifi n. sp., T. gentili n. sp., T. lilasae n. sp. and T. resomari n. sp. Among these species, only T. gentili n. sp., shares the same undulating glandular region on TC 3. However, these two species differ in the shape of papillar projection (widely spaced, small and elongated for T. gentili n. sp., rounded and only present on anterior lamellae for T. europaea n. sp.), by the size (<16 mm for T. europaea n. sp.,> 30 mm for T. gentili n. sp.) and the presence of terminal filaments on the lower lobes for T. europaea n. sp., (pointed projections only for T. gentili n. sp.) ( Table 2 View TABLE 2 ).

Based on 16S and COI sequences, T. europaea n. sp. is identical to clade 6 from Nygren et al. (2018, Fig. 10 View FIGURE 10 ). In this study, authors suggested that this clade could be T. stroemii . However, based on our observations, we are now confident that T. europaea n. sp. is different from T. stroemii which should not be associated with clade 6. Indeed, T. europaea n. sp. differs from T. stroemii by the presence of papillar projections over the edge of anterior branchial lamellae (absence for T. stroemii ), the shape of glandular region on TC 3 (undulating with lateral ridges for T. europaea n. sp., oval for T. stroemii ), the absence of both “eagle-shaped’ thoracic uncini and rounded dorsal projection on TC 1–5 (presence for T. stroemii ) ( Table 2 View TABLE 2 ). Next step will be to define which clade corresponds to the true T. stroemii . This is complicated by the fact that Sars did not designate a holotype and the exact locality is fairly vague and we know from Nygren et al. (2018) that more than one species can occur in the same location.

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