identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
A2F89FA9BA76504BB64698C78B7A3DA4.text	A2F89FA9BA76504BB64698C78B7A3DA4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Benhamipolynoe antipaticola (Benham 1927)	<div><p>Benhamipolynoe cf. antipaticola (Benham, 1927)</p><p>Figs 2–7</p><p>Lapidasthenia antipaticola Benham, 1927: 7–182, pl. 1–6.</p><p>Description.</p><p>Body brownish, with continuous middorsal longitudinal reddish-brown band, transverse bands from elytra near parapodial bases. Body dorsoventrally flattened, elongate, slender, with nearly parallel sides, tapering posteriorly, subrectangular in cross-section. Seventeen symmetrical pairs of elytra; elytra colorless, transparent with median crescent-shaped dark pigmentation; on elytrophores of segments 2, 4, 5, 7, alternate segments to 29, 32, and 35; elytra continue to middle body, irregularly distributed, may be asymmetrical, with an elytron and cirrus on same segment, or from one to five cirri in succession (Figs 2–3). Elytra lacking fringes, papillae and tubercles, except for some scattered micro-tubercles. Prostomium bilobed, as wide as long, without cephalic peaks; with three antennae and two short, tapering, smooth palps. Ceratophore of median antenna short, cylindrical, inserted in anterior notch of prostomium; lateral antennae inserted terminally or subterminally on anterior part of prostomium, at the same level or slightly ventral to median antenna (without distinct ceratophores); antennae longer than prostomium, tapered, smooth; two pairs of eyes moderate in size; anterior pair on dorsolateral prostomial width, posterior pair near to posterior border. Tentacular segment anterolateral to prostomium, bearing two pairs of long tentacular cirri, upper pairs much longer than lower pairs; basis of tentacular cirri with aciculum, but lacking chaetae. Buccal segment lacking distinct nuchal fold; supporting first pair of dorsal elytra and long ventral buccal cirri (Fig. 4). Parapodia sub-biramous, with small notopodia on anterodorsal lobe; prechaetal lobe quadrangular or subtriangular, postchaetal short and subtriangular, both with acicula. Notopodia short, conical, achaetous acicular lobe. Neuropodia elongate, with a ventral and dorsal deep incision; with subequal, rounded prechaetal and postchaetal lobes (Fig. 5); with 5–11 neurochaetae, rather stout, smooth or with slight indications of spinous rows and falcate tips (Figs 6–7). Ventral cirri short, subulate, extending slightly beyond neuropodial lobe tips. Dorsal cirri with shortcylindrical cirrophores; styles smooth, tapering gradually to filiform tips, extending beyond neurochaetae tips. Nephridial papillae short, starting at chaetiger 6 (Fig. 5). Pygidium short, with one pair of long anal cirri.</p><p>Material examined.</p><p>A complete specimen with 136 chaetigerous segments, with 103 mm in length, and 4 mm wide. MOUFPE-CNI 113; 04 ° 47 ' 50 " S; 036 ° 11 ' 01 " W (Potiguar Basin), 423–461 m depth (1 specimen).</p><p>Distribution.</p><p>Pacific: Off New Zealand, 128 m depth (Benham 1927), Queensland, Australia, 398 m depth (Pettibone 1989), off New Caledonia and adjacent waters, French Polynesia, Wallis and Futuna, Solomon Islands, Indonesia, and Madagascar, from 300–600 m depth (Molodtsova and Budaeva 2007), Malay Archipelago; Atlantic: off Key West, Florida, 237 m depth (Pettibone 1970) and Northeastern Brazil, 423–461 m depth (present study), first report for the Southwestern Atlantic.</p><p>Remarks.</p><p>Benhamipolynoe antipaticola was originally described as Lapidasthenia antipaticola Benham, 1927, from 128 m depth off New Zealand, in association with Stylopathes tenuispina (Silberfeld, 1909) (= Parantipathes tenuispina) (Opresko 2006). The morphological features of the Brazilian specimens agree with the original description, except in the absence of pigmentation in the holotype, according to Pettibone (1989).</p><p>Ecology.</p><p>Found in association with Stylopathes adinocrada Opresko, 2006, a new host for this species. It is also known to live in association with Stylopathes columnaris (Duchassaing, 1870) (Pettibone 1970, Britayev et al. 2014).</p></div>	https://treatment.plazi.org/id/A2F89FA9BA76504BB64698C78B7A3DA4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	De Assis, José Eriberto;de Souza, José Roberto B.;de Lima, Manuela M.;de Lima, Gislaine V.;Cordeiro, Ralf T. S.;Pérez, Carlos D.	De Assis, José Eriberto, de Souza, José Roberto B., de Lima, Manuela M., de Lima, Gislaine V., Cordeiro, Ralf T. S., Pérez, Carlos D. (2019): Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13, DOI: 10.3897/zoologia.36.e28714
AD396E924AE65617A0588C6B992EF9C5.text	AD396E924AE65617A0588C6B992EF9C5.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Parahololepidella greeffi (Augener 1918)	<div><p>Parahololepidella cf. greeffi (Augener, 1918)</p><p>Hololepidella greeffi Augener, 1918: 148, pl. 2, figs 22–24, pl. 3, fig. 52, text-fig. 9.</p><p>Hololepidella fagei Rullier, 1964: 132, fig. 4.</p><p>Diagnosis.</p><p>Body dorsoventrally flattened, elongate, with up to 140 segments (Figs 11–12). Elytra very small, leaving middorsum and parapodia uncovered. Fifty or more pairs of elytra on elytrophores of segments 2, 4, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 26, 29, 32, alternating on posterior segments. Prostomium bilobed, with distinct cephalic peaks, and two pairs of large eyes. Ceratophores of median antenna in anterior notch, smooth, tapering, longer than palps. Lateral antennae inserted ventrally to median antenna, smooth, tapering (Fig. 13). Dorsal cirri smooth, withcylindrical long cirrophores (Fig. 15). Parapodia sub-biramous. Notopodia small, digitiform. Neuropodia with longer rounded prechaetal lobe, with subacicular digitiform acicular lobe. Notopodia with reduced number 0–5 notochaetae, unidentate, with faint serration blade (Figs 16–17). Neuropodia with 16–17 notochaetae, unidentate, with faint serration (Fig. 18). Pygidium conical, with two long cirri.</p><p>For complete description, see Britayev et al. (2014).</p><p>Variability.</p><p>Our complete specimens varied in number of segments and elytra after chaetiger 23: specimen 1 (33 mm in length, 72 chaetigers, and 44 pairs of elytra), specimen 2 (44 mm in length, 128 chaetigers, and 70 pairs of elytra), specimen 3 (35 mm in length, 68 chaetigers, and 30 pairs of elytra) and specimen 4 (33 mm in length, 65 chaetigers, and 32 pairs of elytra. Our specimens have elytra on posterior most chaetigers.</p><p>Material examined.</p><p>Two complete specimens, four anterior, and three posterior (i. e., mid-posterior body end) fragments, found on the branches of T. barbadensis . MOUFPE-CNI 351, 04 ° 44 " 31 ' S, 36 ° 26 ' 19 " W, 101–108 m depth (1 specimen from T. tanacetum); MOUFPE-CNI 350, same collection data (2 specimens from T. thamnea). MOUFPE-CNI 349 (same collection data 1 specimens from T. barbadensis).</p><p>Distribution.</p><p>Tropical and Equatorial East Atlantic, Cabo Verde and São Tomé Archipelagos; Western Atlantic Brazil (this paper).</p><p>Remarks.</p><p>Parahololepidella greeffi was originally described as Hololepidella greeffi Augener, 1918, as free-living from shallow waters off São Tomé and Cabo Verde Islands (West Africa). Posteriorly, Pettibone (1969) proposed Parahololepidella to include Hololepidella . The morphological features and cryptic color in preserved specimens from Brazil mostly agree with the currently known descriptions (Augener 1918, Hartman 1959, Pettibone 1969), including the most recent redescription (Britayev et al. 2014), but elytra are present till the end of the body.</p><p>Ecology.</p><p>Parahololepidella cf. greeffi was first reported as a symbiont by Britayev et al. (2014), living in association with Tanacetipathes cf. spinescens (Gray, 1857) (= Antipathes spinescens) (Opresko 2001). Our results confirm the commensal character of the species, which appears to be a polyxenous black coral symbiont as, in addition to T. cf. spinescens it also lives in association T. tanacetum, T. barbadensis and T. thamnea . Tanacetipathes tanacetum has also been found too harbor Antipathipolyeunoa nuttingi Pettibone, 1991 for in North Atlantic Ocean and Caribbean Sea (i. e., Barbados) locations (Pettibone 1991, Molodtsova and Budaeva 2007).</p></div>	https://treatment.plazi.org/id/AD396E924AE65617A0588C6B992EF9C5	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	De Assis, José Eriberto;de Souza, José Roberto B.;de Lima, Manuela M.;de Lima, Gislaine V.;Cordeiro, Ralf T. S.;Pérez, Carlos D.	De Assis, José Eriberto, de Souza, José Roberto B., de Lima, Manuela M., de Lima, Gislaine V., Cordeiro, Ralf T. S., Pérez, Carlos D. (2019): Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13, DOI: 10.3897/zoologia.36.e28714
3535637F3E6B5B07A127D99E348CF9DF.text	3535637F3E6B5B07A127D99E348CF9DF.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Stylopathes adinocrada (Opresko 2006)	<div><p>Stylopathes adinocrada (Opresko, 2006)</p><p>Figs 8–10</p><p>Antipathes columnaris; Opresko, 1974: 101–115 (part).</p><p>Stylopathes adinocrada Opresko, 2006: 123.</p><p>Description.</p><p>Colony highly pinnulated, monopodial, 19.5 cm long, with a central formation of fused pinnules forming a “ worm run " harboring a polychaete (Figs 8–9). Primary pinnules with subpinnulation and a dense pinnulation pattern, arranged in three rows, 10–20 mm long, with ca. 11 secondary pinnules per posterior primary one. Colonies pinnulated to fourth order. Subpinnules slightly more abundant on abpolypar side of posterior primary pinnules; proximal end of primary pinnules with denser pinnulation pattern. Spines small, 0.024 to 0.06 mm long, arranged in ca. 5 rows in lateral view (Fig. 10), separated ca. 0.28 mm each other within same row. Polyps not seen (lost tissue).</p><p>Material examined.</p><p>MOUFPE-CNI 113; 04 ° 47 ' 50 " S; 036 ° 11 ' 01 " W (Potiguar Basin), 423–461 m depth (1 colony).</p><p>Distribution.</p><p>Bahamas, 134–708 m depth (Opresko 2006), Surinam (Opresko 2006) and northeastern Brazil (423–461 m depth, present study). Stylopathes (as S. columnaris) was known to occur in the coast of the state of Pará (Opresko 1974, Castro et al. 2006, Opresko 2006), but this is the first record of S. adinocrada for the Southwestern Atlantic.</p><p>Remarks.</p><p>The studied material resemble the holotype, but was slightly larger, ca. 20 cm versus, ca. 17 cm, respectively. The pinnulation pattern was also similar but the spines were slightly smaller (up to 0.048 mm, rarely 0.06 mm) and more separated within a given row (i. e., up to 0.28 mm versus 0.1–0.2 mm the holotype). The type species of Stylopathes is S. columnaris, but two more species were included within the genus based on two morphotypes erroneously identified as S. columnaris (Opresko 2006) . One of them, S. adinocrada, differs from S. columnaris mainly due to its scattered pinnulation pattern, although in both species the subpinules occur mainly in the distal portion of the primary pinnule, rarely covering the worm run (Opresko 2006).</p></div>	https://treatment.plazi.org/id/3535637F3E6B5B07A127D99E348CF9DF	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	De Assis, José Eriberto;de Souza, José Roberto B.;de Lima, Manuela M.;de Lima, Gislaine V.;Cordeiro, Ralf T. S.;Pérez, Carlos D.	De Assis, José Eriberto, de Souza, José Roberto B., de Lima, Manuela M., de Lima, Gislaine V., Cordeiro, Ralf T. S., Pérez, Carlos D. (2019): Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13, DOI: 10.3897/zoologia.36.e28714
54E65FF28B09576FBB640A2C2A8A7A73.text	54E65FF28B09576FBB640A2C2A8A7A73.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Tanacetipathes barbadensis (Brook 1889)	<div><p>Tanacetipathes barbadensis (Brook, 1889)</p><p>Figs 22–27</p><p>Aphanipathes barbadensis Brook, 1889: 128, pl. II, fig. 10; pl. XI, fig. 4.</p><p>Description.</p><p>Corallum monopodial or branched up to the first order with branches emerging close to base (Fig. 22). Colonies in bottlebrush pattern, with primary pinnules mainly arranged in four rows, reaching up to 6 rows. Secondary pinnules inclined towards distal end of primary posterior pinnule; anterior primary pinnules rarely with subpinnulation. 1–4 (more commonly 2–3) long secondary pinnule per posterior primary, usually at proximal end of primary pinnule (Fig. 23). No more than three tertiary pinnules, when present, near proximal end of secondary pinnule. Posterior primary pinnules 10–26 mm long. Anterior primary pinnules 3–12 mm long. Secondary pinnules 2–12 mm long (more commonly 6 mm). Smooth, conical spines, arranged in 5 to 6 rows visible under optical microscope (Fig. 26). Polypar spines 0.084 –0.216 mm long (more commonly 0.144 mm). Abpolypar spines 0.048 –0.084 mm long. Distance between spines mostly 0.12–0.18 mm, with ca. four spines per mm in each row. Polyps not seen (lost tissue).</p><p>Material examined.</p><p>MOUFPE-CNI 349, 04 ° 44 ' 31 " S; 36 ° 26 ' 19 " W, 101–108 m (Potiguar Basin).</p><p>Distribution.</p><p>Barbados (Brook 1889); Ship Mouth, NW Trinidad (Warner 1981); Gulf of México (Opresko 2009), Brazilian coast, from Potiguar Basin, RN (present study) to the Abrolhos Bank (Loiola and Castro 2005), 30 to 108 m depth.</p><p>Remarks.</p><p>Tanacetipathes barbadensis ressembles T. tanacetum (Pourtalès, 1880), but differs in having three or less secondary pinnules per subsequent primary pinnule (instead of 3–7 in T. tanacetum). Our specimens show posterior pinnules smaller than those previously reported for the species, up to 30 mm long versus 60 mm in Opresko and Sanchez (2005), while agreeing with those described by Brook (1889) and Loiola and Castro (2005). The latter, also from the Brazilian continental shelf, presented posterior primary pinnules up to 45 mm long. Therefore, we suggest that the presence of small sized pinnules may be an intraspecific variation typical of Brazilian populations.</p></div>	https://treatment.plazi.org/id/54E65FF28B09576FBB640A2C2A8A7A73	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	De Assis, José Eriberto;de Souza, José Roberto B.;de Lima, Manuela M.;de Lima, Gislaine V.;Cordeiro, Ralf T. S.;Pérez, Carlos D.	De Assis, José Eriberto, de Souza, José Roberto B., de Lima, Manuela M., de Lima, Gislaine V., Cordeiro, Ralf T. S., Pérez, Carlos D. (2019): Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13, DOI: 10.3897/zoologia.36.e28714
78CB17BC368E50ECAAFC50229ADDB4DB.text	78CB17BC368E50ECAAFC50229ADDB4DB.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Tanacetipathes tanacetum (Pourtales 1880)	<div><p>Tanacetipathes tanacetum (Pourtalès, 1880)</p><p>Figs 19–21</p><p>Antipathes tanacetum Pourtalès, 1880: 116, pl. 3, fig. 13.</p><p>Description.</p><p>Corallum monopodial, with branches rarely up to 2 nd order, in bottlebrush pattern, and primary pinnules usually in 4 main rows (Fig. 19). Primary posterior pinnules larger than primary anterior pinnules, 6–20 mm long, varying according to colony size. Anterior primary pinnules 5–7 mm long, cycle separated by ca. 1 mm. Angle between posterior and anterior primary pinnules (polypolar and abpolypar sides, respectively) of ca. 45 °. Angle between two anterior or two posterior primary pinnules (polypar / polypar sides or abpolypar / abpolypar, respectively) of ca. 160 °. Secondary pinnules scarce, 3 – 7 (more common 4 – 5), usually near proximal end of posterior primary pinnules (Fig. 20). Tertiary pinnule rarely present, usually 1 or 2 per secondary pinnule when present. Spines with few ornaments, conical (Fig. 21). Polypar spines 0.048–0.1 mm long, separated by 0.12–0.18 mm. Abpolypar spines 0.036–0.06 mm long. Polyps not seen (lost tissue).</p><p>Material examined.</p><p>MOUFPE-CNI 351, 04 ° 44 ' 31 @ S; 36 ° 26 ' 19 " W, 101–108 m (Potiguar Basin).</p><p>Distribution.</p><p>Bermuda (Cairns et al. 1986), Gulf of Mexico, Potiguar Basin (present study) and southern coast of Brazil (Pérez et al. 2005, Opresko 2009) 50 to 108 m. This is the first record for the Potiguar Basin, northeast Brazil.</p><p>Remarks.</p><p>The lectotype of T. tanacetum designated by Pérez et al. (2005) has posterior primary pinnules 1.2 cm long versus the 2 cm of the Potiguar Basin material, which also lack the characteristic curved back pinnules of the lectotype. Nevertheless, not all specimens have these pinnules (Pérez et al. 2005). Our specimens resemble those from off Bahia, northeastern Brazil, which had polypar spines 0.04–0.27 mm long (Loiola and Castro 2005), in agreement with the 0.13 to 0.3 mm reported by Opresko and Sanchez (2005). In contrast, our colonies showed polypar spines 0.048–0.1 mm long, similar to those of the specimens from Bahia (Loiola and Castro 2005). The original description emphasizes the presence of a “ parasitic worm " similar to that occurring in S. columnaris, but which did not produced changes in host growth (Pourtalès 1880). The symbiotic worm was described as Antipathipolyeunoa nuttingi Pettibone, 1991 in a paper that also provided an identification key based primarily on the associated species of black corals.</p></div>	https://treatment.plazi.org/id/78CB17BC368E50ECAAFC50229ADDB4DB	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	De Assis, José Eriberto;de Souza, José Roberto B.;de Lima, Manuela M.;de Lima, Gislaine V.;Cordeiro, Ralf T. S.;Pérez, Carlos D.	De Assis, José Eriberto, de Souza, José Roberto B., de Lima, Manuela M., de Lima, Gislaine V., Cordeiro, Ralf T. S., Pérez, Carlos D. (2019): Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13, DOI: 10.3897/zoologia.36.e28714
0F3C484645085639AD1BD4D0228748CF.text	0F3C484645085639AD1BD4D0228748CF.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Tanacetipathes thamnea (Warner 1981)	<div><p>Tanacetipathes thamnea (Warner, 1981)</p><p>Figs 25–27</p><p>Antipathes thamnea Warner, 1981: 148–151, figs. 2–4.</p><p>Tanacetipathes paula Perez, Costa and Opresko, 2005: 8–12, figs 5–8.</p><p>Description.</p><p>Colonies 8–25 cm long, in bottlebrush pattern, monopodial, with branches absent or branching to second order, near colony base (Fig. 25). Primary pinnules usually arranged in four rows. Primary posterior pinnules 10–18 mm long (more common 14–16 mm), larger than the anterior ones (3–12 mm long, varying in juvenile colonies). Secondary pinnules tipping toward distal end of primary pinnule. 7–20 (more commonly 10–15) secondary pinnules per posterior primary pinnule (Fig. 26), 2–12 mm long. Tertiary pinnules scarce, usually more abundant on abpolipar side of posterior primary pinnule, 1–4 per posterior secondary pinnule. Angle between posterior and anterior primary pinnule (polypar and abpolypar sides, respectively) 55 º – 70 °. Angle between two anterior or two posterior primary pinnules (polypar / polypar sides or abpolypar / abpolypar, respectively) 115–130 °. Abpolypar side of posterior primary pinnules with more secondary pinnules than polypar side. Spines smooth, with few ornaments, slightly inclined toward distal end of pinnule or branch (Fig. 27). Distance between spines mainly 0.12–0.18 mm. Polypar spines 0.1–0.2 mm long; Abpolypar spines 0.036 –0.084 mm long. Polyps not seen (lost tissue).</p><p>Material examined.</p><p>MOUFPE-CNI 350, 04 ° 44 ' 31 " S; 36 ° 26 ' 19 " W, 101–108 m (Potiguar Basin).</p><p>Distribution.</p><p>Boca de Navios, NW Trinidad (Warner 1981), Gulf of México (Opresko 2009), and Brazilian coast (Loiola and Castro 2005, present study), 30 to 108 m depth. This is the first record of the species for the Potiguar Basin, Brazil.</p><p>Remarks.</p><p>Our specimens differ from the syntype described by Warner (1981) in some characters. They were slightly shorter (up to 25 cm long versus 20–40 cm long). Some colonies had posterior primary pinnules more elongated and with more secondary pinnules than that described by Loiola and Castro (2005). Warner (1981) also noted that there may be 5–10 secondary pinnules per posterior primary in a 10 mm primary pinnule, considering that a pinnule may reach up to 25 mm. Moreover, Loiola and Castro (2005) found 1–2 tertiary posterior pinnules per posterior secondary whereas our specimens had 1–4. Also, Warner (1981) mentioned a few distally inclined tertiary pinnules. Outnumber primary pinnules may occur especially in the more distal regions of the colonies as well as in larger colonies. Warner (1981) mentioned the presence of errant polychaetes in almost all colonies, living in a kind of tube formed by pinnules on the side of the colony turned toward the sea current.</p></div>	https://treatment.plazi.org/id/0F3C484645085639AD1BD4D0228748CF	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	De Assis, José Eriberto;de Souza, José Roberto B.;de Lima, Manuela M.;de Lima, Gislaine V.;Cordeiro, Ralf T. S.;Pérez, Carlos D.	De Assis, José Eriberto, de Souza, José Roberto B., de Lima, Manuela M., de Lima, Gislaine V., Cordeiro, Ralf T. S., Pérez, Carlos D. (2019): Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13, DOI: 10.3897/zoologia.36.e28714
