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Stylised drawings. A, B. Ephesiella australiensis. A. Dorsal tubercles of chaetigers 11-14; B. Parapodial papillae and appendages including ventral cirrus, acicular lobe, papillae and nearby macrotubercle; the concentric circles represent the volume of the parapodium (larger ones indicate basal and smaller distal areas) and the red axis its four sides; C, D. Sphaerodoropsis auranticus n. sp.; C. Dorsal tubercles of chaetigers 11-14, and pigmentation pattern; D. Arrangement of parapodial appendages and papillae; E, F. Sphaerodoropsis plurituberculata n. sp.; E. Dorsal tubercles of chaetigers 11-14; F. Arrangement of parapodial appendages and papillae. 

Stylised drawings. A, B. Ephesiella australiensis. A. Dorsal tubercles of chaetigers 11-14; B. Parapodial papillae and appendages including ventral cirrus, acicular lobe, papillae and nearby macrotubercle; the concentric circles represent the volume of the parapodium (larger ones indicate basal and smaller distal areas) and the red axis its four sides; C, D. Sphaerodoropsis auranticus n. sp.; C. Dorsal tubercles of chaetigers 11-14, and pigmentation pattern; D. Arrangement of parapodial appendages and papillae; E, F. Sphaerodoropsis plurituberculata n. sp.; E. Dorsal tubercles of chaetigers 11-14; F. Arrangement of parapodial appendages and papillae. 

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Sphaerodorids are scarce at Lizard Island archipelago and other localities in the Great Barrier Reef, Australia. Intensive collections at a variety of habitats within the Lizard Island archipelago over the last four decades have resulted in a total of just 11 specimens. Nevertheless, they represent two new species and a new record for Lizard Island...

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Context 1
... Ephesiella is a cosmopolitan genus that requires revision. It currently groups 15 species supposedly sharing the presence of only compound chaetae from chaetiger 2. Nevertheless, some species have been described as bearing semi-compound chaetae (e.g., Moore 1909, and description above), a feature half way to members of Sphaerodorum (with only simple chaetae) and Ephesiopsis (with both simple and compound chaetae in all parapodia). Moreover, several species have been described from a single or few specimens (e.g., Desbruyères 1980;Hartmann-Schröder 1982) and consequently, the intraspecific variation has not been addressed. Most specific diagnostic characters rely on the absence or presence of hooks, the number of prostomial appendages, the number and arrangement of parapodial papillae. The types and specimens examined for this study (cited above) all appear to: i) lack hooks and antenniform papillae; ii) have the median antenna distinctly shorter than other prostomial appendages; iii) have three transverse rows of dorsal papillae per chaetiger; iv) number of parapodial papillae range between 4-7; v) bear compound, or semi-compound, chaetae with short blades (2-3 times longer than wide), most of them provided with a distinct spine on the tip of the shaft (not observed in the types, due to their fragile condition for manipulation). Most specimens examined from other Australian localities do share these morphological traits. However, some specimens showed different chaetal morphology (longer blades and/or distal tooth in shaft absent), or different relative position of the macro and microtubercles . Ephesiella australiensis is represented elsewhere in Queensland, but only reported from Townsville ). Sphaerodoropsis Hartman & Fauchald, 1971 Type-species. Sphaerodorum sphaerulifer Moore, 1909 Diagnosis. Body generally short and ellipsoid, some forms slender. Four or more dorsal longitudinal rows of macrotubercles, in one or several transverse rows per segment. Macrotubercles sessile and smooth, without terminal papillae. Microtubercles absent. Papillae over body surface and parapodia. Head appendages short, spherical or digitiform. Parapodia with compound chaetae; hooks absent. Sphaerodoropsis aurantica n. sp. (Figs 2C, D, 3 Diagnosis. Body ellipsoid, with strongly convex dorsum. Nine longitudinal rows of sessile and spherical dorsal macrotubercles, arranged in a single transverse row per segment row and four transverse rows (with up to 38) of spherical papillae per segment. Parapodia with digitiform acicular lobe, shorter ventral cirrus and around 10 spherical papillae. Over 10 compound chaetae per parapodium with thin shafts, long blades (6-8 times longer than its maximum width), with fine and short spinulation along superior edge and a distal recurved ...
Context 2
... Male holotype. Body more or less ellipsoid, anterior end bluntly rounded and posterior end tapering (Figs 4A-D, 5A-B), measuring 1.5 mm long, 0.5 mm wide, with 18 chaetigers. Strongly convex dorsum and flat ventrum; segmentation inconspicuous (Figs 4A-D, 5A-B). Live colour transparent with brown gut, milky white coelom; dark brown after preservation. Bright orange subdermal eyes (Fig. 4A-D). Tegument with microscopic oblong granules. Head externally indistinct (Fig. 5A-C). Prostomium with five appendages; a pair of ventral-most palps, digitiform and about three times as long as wide; a pair of lateral antennae similar in shape and size to palp; and a spherical median antenna (Figs 4A-D, 5A). Around 10 small and spherical papillae confined by these appendages. A pair of tentacular cirri, shorter than palps and lateral antennae. Body surface covered in tubercles of two different sizes arranged in more or less 16-18 longitudinal rows in mid-body, four rows per segment, adding a total of around 30 in mid-chaetigers ( Figs 2E, 4A-D, 5B). Microtubercles absent. Ventrum with papillae similar in shape and size to dorsal, arranged in about 10 longitudinal rows, four transverse rows per segment and a total of about 20 papillae per chaetiger in mid-body (Fig. 5A). Ventral papillae containing different type of granules (Fig. 4E). Parapodial sub-conical, increasing in size towards chaetiger 3 and decreasing in last three chaetigers, as long as wide in mid-chaetigers ( Fig. 5A-E, G). Acicular lobe, digitiform, three times longer than wide, similar in shape as size as ventral cirrus (Fig. 5D-E). Parapodia lacking parapodial papillae; but one spherical papilla located close to anterior base of each parapodia (Figs 2F, 5D). Bottle-shaped copulatory organ present in chaetiger 6 ventral to each parapodia, which lack ventral cirri ( Figs 4D, 5A, 6A), suggesting these structures are transformed ventral cirri. Usually six chaetae arranged in a more or less curved transverse line behind the acicular lobe (Fig. 5D-E). Hooks in anterior segments not observed. All chaetae simple (Fig. 5F), appearing semi-compound in some cases, denoting that shaft and blade have probably fused. Distal end enlarged, three times longer than wide, with spinulation in cutting edge and a conspicuous distal projection (Fig. 5F), similar along body and within fascicles. Chaetae showing a thin groove running parallel to edge, in distal end. Pygidium terminal, with inconspicuous spherical single anal cirrus (Fig. 5G). Brown gut seen by transparency, coiled in some parts (Fig. 4A-D) without a distinct muscular ...
Context 3
... Male holotype. Body more or less ellipsoid, anterior end bluntly rounded and posterior end tapering (Figs 4A-D, 5A-B), measuring 1.5 mm long, 0.5 mm wide, with 18 chaetigers. Strongly convex dorsum and flat ventrum; segmentation inconspicuous (Figs 4A-D, 5A-B). Live colour transparent with brown gut, milky white coelom; dark brown after preservation. Bright orange subdermal eyes (Fig. 4A-D). Tegument with microscopic oblong granules. Head externally indistinct (Fig. 5A-C). Prostomium with five appendages; a pair of ventral-most palps, digitiform and about three times as long as wide; a pair of lateral antennae similar in shape and size to palp; and a spherical median antenna (Figs 4A-D, 5A). Around 10 small and spherical papillae confined by these appendages. A pair of tentacular cirri, shorter than palps and lateral antennae. Body surface covered in tubercles of two different sizes arranged in more or less 16-18 longitudinal rows in mid-body, four rows per segment, adding a total of around 30 in mid-chaetigers ( Figs 2E, 4A-D, 5B). Microtubercles absent. Ventrum with papillae similar in shape and size to dorsal, arranged in about 10 longitudinal rows, four transverse rows per segment and a total of about 20 papillae per chaetiger in mid-body (Fig. 5A). Ventral papillae containing different type of granules (Fig. 4E). Parapodial sub-conical, increasing in size towards chaetiger 3 and decreasing in last three chaetigers, as long as wide in mid-chaetigers ( Fig. 5A-E, G). Acicular lobe, digitiform, three times longer than wide, similar in shape as size as ventral cirrus (Fig. 5D-E). Parapodia lacking parapodial papillae; but one spherical papilla located close to anterior base of each parapodia (Figs 2F, 5D). Bottle-shaped copulatory organ present in chaetiger 6 ventral to each parapodia, which lack ventral cirri ( Figs 4D, 5A, 6A), suggesting these structures are transformed ventral cirri. Usually six chaetae arranged in a more or less curved transverse line behind the acicular lobe (Fig. 5D-E). Hooks in anterior segments not observed. All chaetae simple (Fig. 5F), appearing semi-compound in some cases, denoting that shaft and blade have probably fused. Distal end enlarged, three times longer than wide, with spinulation in cutting edge and a conspicuous distal projection (Fig. 5F), similar along body and within fascicles. Chaetae showing a thin groove running parallel to edge, in distal end. Pygidium terminal, with inconspicuous spherical single anal cirrus (Fig. 5G). Brown gut seen by transparency, coiled in some parts (Fig. 4A-D) without a distinct muscular ...
Context 4
... Holotype 1.8 mm long after fixation, 0.6 mm maximum width; with 20 chaetigers. Body ellipsoid ( Fig. 3A-B); with convex dorsum and flattened ventrum. Tegument with transverse wrinkles, segmentation inconspicuous ( Fig. 3A-B). Head externally indistinct (Fig. 3A-C). Anterior end bluntly rounded (Fig. 3B-C). Prostomium with five appendages, including a pair of palps, in ventral most position, sub-conical and slightly wrinkled; a pair of lateral antennae, similar in shape and size to palps; and a median antenna, shorter (two thirds) and wider than lateral antennae and with a rounded distal end (Fig. 3B-C). Antenniform papillae cannot be unequivocally recognised (Fig. 3C). Around 30 digitiform small papillae confined by prostomial appendages and mouth in frontal view (Fig. 3C). A pair of tentacular cirri, similar in shape and size to lateral antennae and palps, and several scattered papillae similar to prostomial. Macrotubercles, sessile, rounded or provided with an incipient rounded terminal papillae (Fig. 3B, G-H), arranged in longitudinal rows along dorsum, and single transversal rows per segment. First and following chaetigers with nine macrotubercles, decreasing to eight in posterior chaetigers. Macrotubercles with two different sizes, following pattern in Fig. 2C; provided with pores arranged on groups (Fig. 3G-H), some of them with incipient terminal papillae or at least pear-shaped (Fig. 3H). Spherical papillae over dorsum, arranged in four transverse rows per segment; digitiform in anterior-most chaetigers and spherical in following (Fig. 3C-D). Ventral surface with similar spherical papillae, arranged in about 5-6 irregular transverse rows, with a total of around 50 papillae per segment, in mid-body (Fig. 3B). Parapodia sub-conical, increasing in size towards chaetiger 5 and around 1-2 times longer than wide, wrinkled (Fig. 3C-D). Acicular lobe anterior to chaetal fascicle, projecting distally ( Fig. 3D-E, J). Ventral cirri sub-conical to pear-shaped, shorter than acicular lobe ( Fig. 3D-E, J). Mid-body parapodia with around 10 small spherical papillae, slightly different in size: one or two on dorsal surface, three on anterior surface, three on ventral surface and three on posterior surface (Fig. 2D). Compound chaetae present in all chaetigers, arranged in a curved transverse fascicle around acicular lobe and numbering 10-22 per parapodium. Shaft with similar width all along, slightly widened distal end with delicate almost inconspicuous spinulation. Blades similar in length within fascicles (6-8 times longer than its maximum width), with fine and short spinulation along superior edge and a distal recurved tip (Fig. 3J-L). Pygidium terminal, with mid-ventral digitiform anal cirrus and a pair of dorsal anal cirri, similar in shape to macrotubercles (Fig. 3F). Mouth located ventrally near base of palps (Fig. 3C). Gut visible by transparency with muscular pharynx occupying about four segments. Eyes and copulatory organs or gametes not ...
Context 5
... Holotype 1.8 mm long after fixation, 0.6 mm maximum width; with 20 chaetigers. Body ellipsoid ( Fig. 3A-B); with convex dorsum and flattened ventrum. Tegument with transverse wrinkles, segmentation inconspicuous ( Fig. 3A-B). Head externally indistinct (Fig. 3A-C). Anterior end bluntly rounded (Fig. 3B-C). Prostomium with five appendages, including a pair of palps, in ventral most position, sub-conical and slightly wrinkled; a pair of lateral antennae, similar in shape and size to palps; and a median antenna, shorter (two thirds) and wider than lateral antennae and with a rounded distal end (Fig. 3B-C). Antenniform papillae cannot be unequivocally recognised (Fig. 3C). Around 30 digitiform small papillae confined by prostomial appendages and mouth in frontal view (Fig. 3C). A pair of tentacular cirri, similar in shape and size to lateral antennae and palps, and several scattered papillae similar to prostomial. Macrotubercles, sessile, rounded or provided with an incipient rounded terminal papillae (Fig. 3B, G-H), arranged in longitudinal rows along dorsum, and single transversal rows per segment. First and following chaetigers with nine macrotubercles, decreasing to eight in posterior chaetigers. Macrotubercles with two different sizes, following pattern in Fig. 2C; provided with pores arranged on groups (Fig. 3G-H), some of them with incipient terminal papillae or at least pear-shaped (Fig. 3H). Spherical papillae over dorsum, arranged in four transverse rows per segment; digitiform in anterior-most chaetigers and spherical in following (Fig. 3C-D). Ventral surface with similar spherical papillae, arranged in about 5-6 irregular transverse rows, with a total of around 50 papillae per segment, in mid-body (Fig. 3B). Parapodia sub-conical, increasing in size towards chaetiger 5 and around 1-2 times longer than wide, wrinkled (Fig. 3C-D). Acicular lobe anterior to chaetal fascicle, projecting distally ( Fig. 3D-E, J). Ventral cirri sub-conical to pear-shaped, shorter than acicular lobe ( Fig. 3D-E, J). Mid-body parapodia with around 10 small spherical papillae, slightly different in size: one or two on dorsal surface, three on anterior surface, three on ventral surface and three on posterior surface (Fig. 2D). Compound chaetae present in all chaetigers, arranged in a curved transverse fascicle around acicular lobe and numbering 10-22 per parapodium. Shaft with similar width all along, slightly widened distal end with delicate almost inconspicuous spinulation. Blades similar in length within fascicles (6-8 times longer than its maximum width), with fine and short spinulation along superior edge and a distal recurved tip (Fig. 3J-L). Pygidium terminal, with mid-ventral digitiform anal cirrus and a pair of dorsal anal cirri, similar in shape to macrotubercles (Fig. 3F). Mouth located ventrally near base of palps (Fig. 3C). Gut visible by transparency with muscular pharynx occupying about four segments. Eyes and copulatory organs or gametes not ...
Context 6
... plurituberculata n. sp. (Figs 2E, F, 4, 5, ...

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Citations

... In a previous version of the present review (Capa et al. 2014), the family contained 10 genera, delineated based on the number of longitudinal rows of large epithelial tubercles, the number and arrangement of additional smaller epithelial papillae, the chaetal morphology, and the relative length of antennae. After some partial revisions of the group, Sphaerodoridae at present includes 131 species classified in eight genera, one of the them newly erected and three being synonymized (Capa and Bakken 2015, Capa and Rouse 2015, Capa et al. 2016a, b, 2018, 2019. After the currently accepted classification, the most speciose genus is Sphaerephesia Fauchald, 1972, with 36 species;followed by Sphaerodorum Örsted, 1843 andSphaerodoridium Lützen, 1961 (each with 24 species); and Geminofilum Capa et al. 2019 (19 species) Bakken 2015, Capa et al. 2019). ...
... External fertilization (Christie 1984) is thought to be the general reproductive strategy, but "copulatory structures" have recently been described in over 25 species mainly belonging to Euritmia, Clavodorum, Gemonifilum, Sphaerephesia, Sphaerodoropsis, and Sphaerodoridium (Moreira et al. 2004, Böggemann 2009, Reuscher and Fiege 2011, Capa and Bakken 2015, Capa and Rouse 2015, Capa et al. 2019). Males were described as presenting one to four pairs of modified, inflated, and distally opened ventral cirri between parapodia of chaetigers 4-8 (varying between species), whereas females presented one or two pairs of oval, distally opened tuberclelike structures, located ventrolaterally between parapodia generally in the same segments as the "copulatory organs" of the males (Fig. 7.13.14.12D-E) or else modified, inflated ventral cirri with pores (Capa et al. 2019). ...
... Females with oocytes at early stage of maturation have been observed after spawning in at least Sphaerodorum flavum (see Christie 1984). In Sphaerodoropsis plurituberculata Capa & Rouse, 2015 sperm develops in cluster attached to a large central cytophore until elongate heads are about 35 μm long and they develop a flagellum of similar length (Capa and Rouse 2015). Free sperm at various stages of development is dispersed in the coelom, giving adult male coelomic content a whitish appearance. ...
... The family currently includes 131 species classified in eight genera [6,446,447,[450][451][452][453]. As currently delineated, the most speciose genus is Sphaerephesia Fauchald, 1972 [138] (36 species), followed by Sphaerodorum Örsted, 1843 [71] (24), Sphaerodoridium Lützen, 1961 [454] (24), and Geminofilum Capa et al. 2019 [453] (19). ...
... In fact, they are exclusively benthic marine organisms, and are present in all oceans and at all depths. They are often reported from deep-sea sediments, but also occur in shallow waters, including hard substrates and algae (as epibionts) [447,452,453,455,458,[468][469][470], where they are often considered as members of the meiofauna [471,472]. ...
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... The family currently includes 131 species classified in eight genera [6,446,447,[450][451][452][453]. As currently delineated, the most speciose genus is Sphaerephesia Fauchald, 1972 [138] (36 species), followed by Sphaerodorum Örsted, 1843 [71] (24), Sphaerodoridium Lützen, 1961 [454] (24), and Geminofilum Capa et al. 2019 [453] (19). ...
... In fact, they are exclusively benthic marine organisms, and are present in all oceans and at all depths. They are often reported from deep-sea sediments, but also occur in shallow waters, including hard substrates and algae (as epibionts) [447,452,453,455,458,[468][469][470], where they are often considered as members of the meiofauna [471,472]. ...
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Phyllodocida is a clade of errantiate annelids characterized by having ventral sensory palps, anterior enlarged cirri, axial muscular proboscis, compound chaetae (if present) with a single ligament, and of lacking dorsolateral folds. Members of most families date back to the Carboniferous, although the earliest fossil was dated from the Devonian. Phyllodocida holds 27 well-established and morphologically homogenous clades ranked as families, gathering more than 4600 currently accepted nominal species. Among them, Syllidae and Polynoidae are the most specious polychaete groups. Species of Phyllodocida are mainly found in the marine benthos, although a few inhabit freshwater, terrestrial and planktonic environments, and occur from intertidal to deep waters in all oceans. In this review, we (1) explore the current knowledge on species diversity trends (based on traditional species concept and molecular data), phylogeny, ecology, and geographic distribution for the whole group, (2) try to identify the main knowledge gaps, and (3) focus on selected families: Alciopidae, Goniadidae, Glyceridae, Iospilidae, Lopadorrhynchidae, Polynoidae, Pontodoridae, Nephtyidae, Sphaerodoridae, Syllidae, Tomopteridae, Typhloscolecidae, and Yndolaciidae. The highest species richness is concentrated in European, North American, and Australian continental shelves (reflecting a strong sampling bias). While most data come from shallow coastal and surface environments most world oceans are clearly under-studied. The overall trends indicate that new descriptions are constantly added through time and that less than 10% of the known species have molecular barcode information available. Citation: Martin, D.; Aguado, M.T.; Fernández Álamo, M.A.; Britayev, T.A.; Böggemann, M.; Capa, M.; Faulwetter, S.; Fukuda, M.V.; Helm, C.; Petti, M.A.V.; et al. On the Diversity of Phyllodocida (Annelida: Errantia), with a Focus on Glyceridae, Goniadidae, Nephtyi-dae, Polynoidae, Sphaerodoridae, Syllidae and the Holoplanktonic Families. Diversity 2021, 13, 131.
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... Type locality: Off Phi Phi Island, Andaman Sea, Thailand, 29 m. Sphaerodoridium auranticum (Capa & Rouse, 2015), comb. n. ...
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Detailed morphological study of more than 2600 North East Atlantic (NEA) sphaerodorids (Sphaerodoridae, Annelida) and phylogenetic analyses of DNA sequences of representatives of several identified morphospecies enforced changing the current systematic classification within the family, allowed the discovery of new species, provided new information about the morphological and genetic characterisation of members of this group, and increased the species occurrence data to better infer their geographic and bathymetric distribution ranges. Phylogenetic analyses of nuclear (18S rRNA and 28S rRNA) and mitochondrial sequences (COI and 16S rRNA) of NEA short-bodied sphaerodorids revealed outstanding results including paraphyly of the genera Sphaerodoropsis, Sphaerodoridium, and Sphaerephesia. The number of longitudinal and transverse rows of dorsal macrotubercles is proposed as potential synapomorphies for the main clades, and are consequently herein used for the genera delimitation. The new classification proposed here implies nomenclatural changes and the erection of a new genus, Geminofilum gen. n., to accommodate the species previously considered as Sphaerodoropsis with two transverse rows of dorsal macrotubercles per segment. Four species are being described herein: Euritmia nordica Capa & Bakken, sp. n., Sphaerephesia multichaeta Capa, Moreira & Parapar, sp. n., Sphaerephesia ponsi Capa, Parapar & Moreira, sp. n., and Sphaerodoridium celiae Moreira, Capa & Parapar, sp. n. Characterisation of the other 21 species, including updated iconography, and an identification key to all NEA short-bodied sphaerodorids are provided.
... Recently, a less developed bulbous pharyngeal region was also described in the long-bodied sphaerodorids (Helm & Capa, 2015). The structures referred to as copulatory organs, found in some species of Sphaerodoridium Lützen, 1961, Sphaerodoropsis Hartman & Fauchald, 1971 and Sphaerephesia Fauchald, 1972(Moreira, Cacabelos & Troncoso, 2004Moreira & Parapar, 2012;Capa & Bakken, 2015;Capa & Rouse, 2015), have never been reported in members of the long-bodied genera. ...
... Members of Sphaerodorum are dioicous and the sperm of Sphaerodorum flavum is of the 'primitive type' probably indicating external fertilization Franzen, 1956;Franzen, 1958;Capa, Bakken & Purschke, 2014). Other members of the family, the short-bodied forms, have shown pseudocopulation and internal fertilization (Capa & Rouse, 2015). Dispersal capability is therefore assumed limited at these in short bodied sphaerodorids (Capa, Aguado & Bakken, 2016). ...
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Background Long-bodied sphaerodorids (Annelida, Sphaerodoridae) is the common name for members of the three closely and morphologically homogenous currently accepted genera of benthic marine bristle worms: Ephesiella , Ephesiopsis and Sphaerodorum . Members of this group share the presence of two dorsal and longitudinal rows of macrotubercles with terminal papillae, and two longitudinal rows of microtubercles, features that are unique among sphaerodorids. Genera are distinguished by the chaetae morphology. Members of Ephesiella are characterised by having compound chaetae (except, sometimes, simple chaetae in the first chaetigers), Sphaerodorum bear only simple chaetae, and Ephesiopsis have both compound and simple chaetae in all parapodia. Methods Mitochondrial (partial COI and 16S rDNA) and nuclear (partial 18S rDNA and 28S rDNA) sequence data of long-bodied sphaerodorids with compound and simple chaetae, and an outgroup of additional seven sphaerodorid species were analysed separately and in combination using Bayesian inference (BA), and Maximum Likelihood (ML) methods. Long-bodied sphaerodorids from around the world (including type specimens) were examined under a range of optical equipment in order to evaluate putative generic and specific diagnostic features, in addition to intraspecific variability. Results Phylogenetic analyses of mitochondrial and nuclear DNA sequences of specimens identified as Ephesiella and Sphaerodorum, based on chaeta morphology, were performed. Sphaerodorum and Ephesiella were recovered as paraphyletic and nested within each other. Revision of current nominal species diagnostic features are performed and discussed. Discussion Results contradict current generic definitions. Recovery of paraphyletic compound and simple chaetae clades urge the synonymization of these two genera of long-bodied sphaerodorids. Morphological data also suggest the synonymization of Ephesiopsis .
... The large oocytes normally found in sphaerodorids (130-250 µm; Mileikovsky, 1967;Christie, 1984;Capa and Rouse, 2015) and in the present species (144-154 µm) suggest that larval development is lecithotrophic (see also Mileikovsky, 1967;Christie, 1984). ...
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A new polychaete species, Sphaerodoropsis kitazatoi (Annelida: Phyllodocida: Sphaerodoridae), is described from the abyssal Southwest Atlantic Ocean at the base of São Paulo Ridge (4204 m depth). This species was found in sediments impacted by a whale carcass. The new species has four longitudinal rows of macrotubercles and one transversal row per chaetiger and shares several characters with S. anae Aguado & Rouse, 2006 that is also associated with chemosynthetic environments. They can be clearly distinguished from S. anae and other Sphaerodoropsis species by the arrangement and the number of prostomial, body and parapodial papillae.
... Moreover, a group of species to date considered belonging to Sphaerodoropsis (Group 4, according to Borowski 1994) also show these features, although the chaetae, instead of being simple, could be considered as pseudocompound. These are Sphaerodoropsis multipapillata (Hartmann-Schröder, 1974), Sphaerodoropsis heteropapillata Hartmann-Schröder, 1987, and Sphaerodoropsis plurituberculata Capa & Rouse, 2015. Commensodorum commensalis (Lützen, 1961) shares the type of chaetae with Euritmia, being typically simple. ...
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Sphaerodoridae (Annelida) is a seeming uncommon and minimally diverse group of polychaetes in the northwestern Atlantic, with only seven species reported from the United States, and none from the eastern coast of Canada, before the present study. Review of the large Smithsonian collection (National Museum of Natural History, Washington) revealed the presence of two morphologically extraordinary undescribed species and added a new record to the north-western Atlantic region. Euritmia carolensis sp. n. is characterised by bearing approximately 20 sessile spherical papillae arranged in three transverse rows per segment, ventrum with 4–6 larger papillae near the parapodial bases and parapodia without papillae; bearing 4–5 simple chaetae that are enlarged subdistally. Sphaerephesia amphorata sp. n. is distinguished from other congeners in the presence of four longitudinal rows of sessile, bottle-shaped macrotubercles with exceptionally long digitiform terminal papilla, and parapodia with four rounded and small papillae, bearing 4–7 compound chaetae, with blades 7–11 times as long as wide. Other encountered species are also herein re-described, including intraspecific variation and updated iconography. Comparison of material also allowed some systematic changes in the group, including the synonymisation of the genus Amacrodorum with Euritmia, and the transfer of Ephesiopsis shivae to Ephesiella. A key to the species reported from the Northwestern Atlantic is provided.
... Sister group relationships to Syllidae, Phyllodocidae and Goniadidae-Glyceridae have been suggested without reaching a consensus Pleijel and Dahlgren, 1998;Worsaae et al., 2005;Aguado and Rouse, 2006;Zrzav y et al., 2009). The family is distributed worldwide, reported from intertidal to abyssal depths and mainly associated with sed-iments but also with algae (Fauchald, 1974;Hartmann-Schr€ oder, 1981;Sard a-Borrroy, 1987;Moreira, 2012;Capa and Bakken, 2015) or coral reefs (Hartmann-Schr€ oder, 1974, 1979Capa and Rouse, 2015). ...
... Removal of non-sphaerodorid terminals, with the exception of a goniadid left as the outgroup, did not affect the Sphaerodoridae topology, and clade support did not vary significantly (data not shown). Removal of Sphaerodoropsis aurantica Capa and Rouse, 2015, with unstable position between mitochondrial and nuclear partitions, did not affect either the overall topology or clade support. Due to ambiguous position and also based on morphological grounds, this terminal is considered different from Clade 9. ...
... Dispersal capacity of sphaerodorids is unknown. The recent finding of spermatophores in one species (Capa and Rouse, 2015) indicates pseudocopulation and the production of large eggs filled with high levels of lipids and yolk suggests that development in at least some species is direct, non-pelagic and lecithotrophic (Fauvel, 1911;Mileikovskii, 1967;Christie, 1984). Consequently, a restricted geographical distribution of the species would be expected (Mileikovskii, 1960). ...
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Sphaerodoridae is a small, morphologically well-defined group of annelids, with remarkable spherical tubercles covering their body surface. They have generally been considered as part of Phyllodocida, but there is no consensus about its sister group relationships. Monophyly and internal phylogenetic relationships have never been tested. We present the first phylogenetic analysis of the family, including 33 individuals of 19 species in five genera of Sphaerodoridae, and a wide representation of other Phyllodocida, based on molecular data from nuclear 18S rDNA (2240 bp), mitochondrial 16S rDNA (614 bp), and cytochrome c oxidase subunit I (657 bp). Mitochondrial and nuclear loci were analysed separately and in combination using maximum parsimony, maximum likelihood and Bayesian inference. Results show maximum support for the monophyly of Sphaerodoridae, but sister group relationships remain unclear. The genera Sphaerodoropsis and Sphaerodoridium are found to be paraphyletic. Monophyly of Clavodorum, Ephesiella and Sphaerodorum could not be tested because only one species was included for each of these genera. At least six of the morphotypes included in the study do not fit within current species descriptions, suggesting undescribed species. Finally, the transfer of Sphaerodoropsis minuta back to Sphaerodoridium is proposed.