Parexogone wolfi ( San Martín, 1991 ), San Martin, 1991

Barroso, Rômulo, Paiva, Paulo Cesar De, Nogueira, João Miguel De Matos & Fukuda, Marcelo Veronesi, 2017, Deep sea Syllidae (Annelida, Phyllodocida) from Southwestern Atlantic, Zootaxa 4221 (4), pp. 401-430 : 406-407

publication ID

https://doi.org/10.5281/zenodo.252007

publication LSID

lsid:zoobank.org:pub:F353EEB2-882D-464B-A2CC-F40606B58EDC

DOI

https://doi.org/10.5281/zenodo.3504848

persistent identifier

https://treatment.plazi.org/id/03CD87F5-2B61-FFAD-26F1-F980FF5E85E2

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scientific name

Parexogone wolfi ( San Martín, 1991 )
status

 

Parexogone wolfi ( San Martín, 1991) View in CoL

Figure 3 View FIGURE 3

Exogone (Parexogone) wolfi San Martín, 1991: 726 View in CoL –727, fig. 6; 2003: 243–244, figs. 129–130; 2005: 111–113, fig. 64. Exogone View in CoL sp. A. Uebelacker 1984: 30 –37, fig. 30.

Parexogone wolfi View in CoL . Böggeman & Purschke 2005: 223 –225, fig. 2.

Material examined. Project ' Oceanprof '. 22°04’32.8”S, 39°54’11.4”W, 0–2 cm, 722 m deep: 1 spec. (MNRJP 1153), 30 Jun 2003; 22°04’33.9”S, 39°52’05.1”W, 0–2 cm, 1030 m deep: 1 spec. (MNRJP 1154), 30 Jun 2003; 22°04’43.3”S, 39°49’09.3”W, 0–2 cm, 1299 m deep: 1 spec. (MNRJP 1155), 25 Mar 2006; 22°35’03.7”S, 40°08’52.5”W, 0–2 cm, 1043 m deep: 2 specs (MNRJP 1156), 15 Jun 2003; 22°34’05.0”S, 40°00’12.6”W, 0–2 cm, 1337 m deep: 1 spec. (MNRJP 1157), 15 Jun 2003; 22°26’28.8”S, 39°58’53.3”W, 0–2 cm, 1046 m deep: 2 specs (MNRJP 1158), 20 Jun 2003; 22°30’21.7”S, 39°56’53.7”W, 0–2 cm, 1353 m deep: 1 spec. (MNRJP 1159), 21 Jun 2003. Project ‘ HABITATS ’. 21°42’37”S, 40°8’59”W, 147 m deep: 1 spec., 9 Mar 2009; 22°31’7”S, 40°31’32”W, 139 m deep: 8 specs, 23 Feb 2009; 23°11’29”S, 41°0’49”W, 150 m deep: 5 specs, 21 Feb 2009; 23°13’2”S, 40°57’36”W, 724 m deep: 3 specs, 24 Jun 2008; 23°13’48”S, 40°55’56”W, 986 m deep: 39 specs, 8 May 2009; 23°15’11”S, 40°53’53”W, 1302 m deep: 18 specs, 9 May 2008; 23°36’14”S, 41°21’29”W, 142 m deep: 1 spec., 1 Mar 2009. Project ‘ AMBES ’. 19°54’4”S, 39°22’27”W, 1335 m deep: 6 specs, 27 Jun 2013; 21°4’14”S, 40°14’14”W, 141 m deep: 1 spec., 11 Jul 2013.

Additional material examined. Parexogone wolfi — United States, Florida, off Port Everglades (26°00'54"N, 80°03'24"W), 188 m deep: 1 spec. ( USNM 101326 About USNM , holotype), det. G. San Martín, 1991 GoogleMaps ; France, Bay of Biscay, Capbreton Canion (43°43'25"N, 02°18'17"W) 983–1032 m deep: 3 specs ( MNCN 16.01 About MNCN /2948), coll. Campaña Capbreton 88, 8 Jul 1988, det. G. San Martín, Ceberio & Aguirrezabalaga GoogleMaps .

Description. Body thin, elongate; longest specimen examined 6.0 mm long, 0.2 mm wide, with 67 chaetigers. Palps completely fused, triangular. Prostomium ovate, shorter than palps, with two pairs of eyes in trapezoidal arrangement, anterior and posterior eyes sometimes close to each other, nearly coalescent; antennae inserted slightly separated from each other; lateral antennae inserted slightly anteriorly to median antenna, approximately in front of anterior eyes, ovate to digitiform; median antenna inserted on middle of prostomium or slightly anteriorly, up to 5 times longer than lateral ones, reaching beyond tip of palps or chaetiger 4, if directed posteriorly ( Fig. 3 View FIGURE 3 A, J). Peristomium shorter than subsequent segments; peristomial cirri ovate to papilliform, shorter than lateral antennae ( Fig. 3 View FIGURE 3 A, J). Dorsal cirri on all chaetigers, papilliform, larger than peristomial cirri but shorter than lateral antennae ( Fig. 3 View FIGURE 3 A, J); ventral cirri similar to peristomial cirri. Compound chaetae as spiniger-like and falcigers. Anterior parapodia with up to 3 spiniger-like chaetae each, from midbody onwards 1–2 spiniger-like chaetae per parapodium; shafts of spiniger-like chaetae from anterior and mid-body chaetigers with long and thin distal spines; blades bidentate and spinulate, spines of almost uniform length, except for the distalmost spines, much longer than remaining and directed distally, reaching beyond level of distal tooth ("aristae"); blades 55–35 µm long on anterior parapodia, 80–58 µm long on midbody and 40–10 µm long on posterior parapodia ( Fig. 3 View FIGURE 3 B–D, K). Anterior parapodia with 8–10 falcigers each, midbody with 3–4, posterior parapodia with 2–3 falcigers each; shafts of facigers distally spinulated, spines longer on anterior body; falciger blades bidentate and spinulate, teeth close to each other, distal tooth slightly larger, blades with distally directed aristae reaching beyond level of distal tooth, sometimes absent on posterior body; blades of falcigers 22–11 µm long on anterior parapodia, 28–11 µm on midbody, and 12–8 µm long on posterior parapodia ( Fig. 3 View FIGURE 3 B–D, L). Dorsal simple chaetae present from proventricle level, sigmoid, distally tapering, bidentate and spinulated, aristae reaching beyond level of distal tooth, chaetae progressively stouter and more conspicuously bidentate towards posterior body ( Fig. 3 View FIGURE 3 E–F); ventral simple chaetae only present on posterior body, bidentate, smooth or with short subdistal spines ( Fig. 3 View FIGURE 3 G). Anterior parapodia with up to 3 aciculae each, distally inflated and slightly oblique, with apparently hollow tips ( Fig. 3 View FIGURE 3 H); single acicula per parapodium from midbody onwards, similar in shape to those of anterior body chaetigers, but progressively stouter ( Fig. 3 View FIGURE 3 I). Pygidium with 1 pair of elongate anal cirri as long as median antenna. Pharynx through 3–4 chaetigers, with conical tooth close to anterior border; proventricle extending for ~3 chaetigers, with ~16 rows of muscle cells ( Fig. 3 View FIGURE 3 A).

Remarks. Brazilian specimens have longer blades of spiniger-like chaetae, up to 80 µm long, similar to those of specimens from the Gulf of México and Florida ( San Martín 1991), and Bay of Biscay ( San Martín 2003), while Australian specimens have spiniger-like chaetae with shorter blades, up to 58 µm long ( San Martín 2005). Furthermore, the specimens herein analysed have the proventricle extending through 3 chaetigers, while specimens from other localities have a shorter proventricle, extending through 2 chaetigers ( San Martín 1991, 2005). The wide distribution and bathymetric range of this species, together with the discrepancies between descriptions of specimens from different localities, may indicate that this is in fact a complex of sibling species. Although already informally recorded in Brazil ( Fukuda 2010; Barroso 2011), this is the first formal report of this species to Brazilian waters.

Geographic distribution and bathymetric range. Atlantic Ocean—USA, Florida, 188 m deep (type locality) ( San Martín 1991) ; Gulf of México, 34–106 m deep ( Uebelacker 1984) ; Bay of Biscay , 1000 m deep ( San Martín et al. 1996); Angola Basin, 3964–5497 m deep ( Böggemann & Purschke 2005; Böggemann 2009). Indian Ocean— Australia, Western Australia, 8 m deep ( San Martín 2005). Brazilian specimens were collected from 722–1353 m deep.

Barroso, R. (2011) Anelideos poliquetas das familias Amphinomidae, Opheliidae, Syllidae e Paraonidae de oceano profundo da Bacia de Campos, Sudeste do Brasil. PhD thesis. Museu Nacional da Universidade Federal do Rio de Janeiro, Universidade Federal do Rio de Janeiro, Rio de Janeiro, 174 pp.

Boggemann, M. & Purschke, G. (2005) Abyssal benthic Syllidae (Annelida: Polychaeta) from the Angola Basin. Organisms, Diversity & Evolution, 5, 221 - 226.

Boggemann, M. (2009). Polychaetes (Annelida) of the abyssal SE Atlantic. Organisms Diversity & Evolution, 9, 252 - 428.

Fukuda, M. V. (2010) Contribuicao ao conhecimento taxonomico dos silideos Polychaeta: Syllidae) da regiao sudeste-sul do Brasil. PhD thesis, Instituto de Biociencias, Universidade de Sao Paulo, Sao Paulo, 340 pp.

San Martin, G. & Hutchings, P. A. (2006) Eusyllinae (Polychaeta, Syllidae) from Australia with the description of a new genus and fifteen new species. Records of the Australian Museum, 58, 257 - 370.

San Martin, G., Lopez, E. & Aguado, M. T. (2009) Revision of the genus Pionosyllis (Polychaeta: Syllidae: Eusyllinae), with a cladistic analysis, and the description of five new genera and two new species. Journal of the Marine Biological Association of the United Kingdom, 89 (7), 1455 - 1498.

San Martin, G. (2005) Exogoninae (Polychaeta, Syllidae) from Australia with the description of a new genus and twenty-two new species. Records of the Australian Museum, 57, 39 - 152.

San Martin, G. (1991) Grubeosyllis and Exogone (Exogoninae, Syllidae, Polychaeta) from Cuba, the Gulf of Mexico, Florida and Puerto Rico, with a revision of Exogone. Bulletin of Marine Science, 49 (3), 715 - 740.

San Martin, G., Ceberio, A. & Aguirrezabalaga, F. (1996) Exogone species (Polychaeta: Syllidae: Exogoninae) from the Capbreton Canyon (Bay of Biscay, NE Atlantic). Cahiers de Biologie Marine, 37, 249 - 258.

San Martin, G. (2003) Annelida Polychaeta II: Syllidae. In: Ramos, M. A. (Ed.), Fauna Iberica. Lol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 544.

Uebelacker, J. M. (1984) Family Syllidae Grube, 1850. In: Uebelacker, J. M. & Johnson, P. G. (Eds.), Taxonomic Guide to the Polychaetes of the Northern Gulf of Mexico. Lol. IL. Barry A. Vittor & Associates, Metairie, pp. 1 - 151. [pp. 30 - 1 - 30 - 151]

Gallery Image

FIGURE 3. Parexogone wolfi. (A) anterior body, dorsal view; (B – D) compound chaetae, anterior, mid- and posterior body chaetigers, respectively; (E – F) dorsal simple chaetae, anterior and posterior body chaetigers, respectively; (G) ventral simple chaeta; (H – I) aciculae, anterior and posterior body chaetigers, respectively; SEM: (J) anterior end, right lateral view; (K) spiniger-like chaeta, midbody chaetiger; (L) falcigers, midbody chaetiger.

USNM

Smithsonian Institution, National Museum of Natural History

MNCN

Museo Nacional de Ciencias Naturales

Kingdom

Animalia

Phylum

Annelida

Class

Polychaeta

Order

Phyllodocida

Family

Syllidae

SubFamily

Exogoninae

Genus

Parexogone