Published December 31, 2017 | Version v1
Taxonomic treatment Open

Celleporina joannae Almeida, Souza, Menegola & Vieira, 2017, n. sp.

Description

Celleporina joannae n. sp.

(Figs. 74–77; Table 8)

Celleporina costazii: Almeida et al. 2015b: 5.

Material examined. Holotype: UFBA 1664, Camamu Bay, 13°53’S, 38°59’W, 18–20 m, coll. October 2012 (on sponge Spongosorites sp.). Paratypes: UFBA 1665, Camamu Bay, 13°53’S, 38°59’W, 18–20 m, coll. October 2012 (on sponge Spongosorites sp.); UFBA 1671, UFBA 2396–97, Camamu Bay, 13°53’S, 38°59’W, 18–20 m, coll. October 2012 (on sponge Spongosorites sp.).

Type locality. Camamu Bay, Bahia State, NE Brazil.

Etymology. Named after JoAnn Sanner (Smithsonian Institution, National Museum of Natural History), for her contribution to bryozoology.

Description. Colony encrusting, multilaminar, forming small spherical nodules. Autozooids mound-like, globular to sub-erect. Frontal shield heavily calcified, smooth, marginally punctured by 6–8 large widely-spaced pores. Sometimes additional frontal pseudopores are seen surrounding the peristome, often in young zooids with low peristomes that expose the primary orifice. Primary orifice terminal, circular, sunken, with a broadly U-shaped sinus; condyles rounded, thickened and conspicuous. Secondary orifice formed by a deep tubular peristome, margin usually smooth but sometimes somewhat crenulated. Single or paired peristomial avicularia, proximolateral to the orificial border, placed at peristomial lobes; rostrum triangular, with complete cross-bar, margins smooth, oriented upwardly and distolaterally. Additional frontal avicularia absent. Ooecia slightly wider than long, frontal surface in level with peristome; tabula occupying most of the frontal surface, bordered by a single row of 8– 12 distolateral pores; ooecial surface with distinct ribs in later astogeny. Ooecia open into distal part of peristome, just above the operculum; aperture quadrangular, edged by a broad band of smooth ectooecium.

Remarks. Celleporina joannae n. sp. can be distinguished from other species of Celleporina by the combination of a tubular peristome with 1–2 avicularia placed at lobes, a widely U-shaped sinus with strong rounded condyles, no frontal avicularia, and ooecia with a quadrangular aperture and a tabula bordered by a single row of 8–12 distolateral pores.

At least eight species of Celleporina are reported to the Western Atlantic (Vieira et al. 2008; Bock 2016). Three of them are readily distinguished from C. joannae n. sp. in having ooecia with entirely porous tabula, viz. Celleporina diota (Marcus, 1938), Celleporina langei (Marcus, 1939) and Celleporina lucida (Hincks, 1880). Two other species, Celleporina abtrusa Winston & Vieira, 2013 and Celleporina bicostata Hayward, 1980, have smooth ooecial tabula. Celleporina joannae n. sp. most closely resembles Celleporina lacrimula Hayward, 1992 and Celleporinas surcularis (Packard, 1863) in having ooecial pores commonly separated by distinct ribs, and a peristome with lobes. The species are distinct, however, in the primary orifice (drop-shaped in C. lacrimula and almost circular in C. surcularis; with a broadly U-shaped sinus and strong condyles in C. joannae n. sp.) and in their vicarious avicularia (present in C. lacrimula C. lacrimula and C. surcularis; absent in C. joannae n. sp.).

Specimens from the Brazilian coast described by Marcus (1937, 1939, 1949) under the name Celleporina costazii (Audouin, 1826) differ from C. joannae n. sp. in having a median peristomial umbo and vicarious avicularia and ooecia becoming entirely porous.

Species of Celleporina are commonly found encrusting shells, other bryozoans, corals and hydrozoans, worm tubes and algae (e.g., Cook 1985; Marcus 1938, 1939; Hayward & Ryland 1999; Ramalho et al. 2011; Winston & Vieira 2013). Here we found spot-like colonies with 2–3 mm in diameter encrusting the rugose-textured sponge Spongosorites sp. (Fig. 11).

Distribution. Atlantic: Brazil (Bahia).

Material examined. Holotype: UFBA 1185, Camamu Bay, 13°53’S, 38°59’W, 18–20 m, coll. October 2012 (on sponge Haliclona (Soestella) melana). Paratypes: UFBA 1667, Camamu Bay, 13°53’S, 38°59’W, 18–20 m, coll. October 2012 (on sponge Haliclona (Soestella) melana); UFBA 2398, Camamu Bay, 13°53’S, 38°59’W, 18–20 m, coll. October 2012 (on sponge Haliclona (Soestella) melana).

Type locality. Camamu Bay, Bahia State, NE Brazil.

Etymology. Honorific for Iara Coelho Sousa, Ana C.S. Almeida’s mother.

Description. Colony encrusting, multilaminar, nodular. Autozooids semi-erect, hexagonal, limited by distinct grooves. Frontal shield heavily calcified, smooth to slightly rugose, convex, raised distally, imperforate centrally, marginally punctured by 5–20 large pseudopores. Primary orifice small relative to frontal shield, sunken, with arcuate distal edge and broad concave proximal sinus, with two triangular condyles placed at proximal third of the orifice. Secondary orifice oval to orbicular, often obscuring primary orifice and forming a smooth tubular peristome, particularly in ovicelled zooids. Avicularia absent. Ooecia globular, partially framed by the tubular peristome, punctured by 10–25 pseudopores, opening into distal part of peristome, just above the operculum.

Remarks. Turbicellepora iarae n. sp. is the only species of the genus that lacks any type of avicularium. However, its colony form, frontal calcification, primary and secondary orifices, and distinct porose ooecia fully agrees with the definition of the genus. Other species reported from Brazilian waters are Turbicellepora brasiliensis Winston, Vieira & Woollacott, 2014, Turbicellepora pourtalesi Winston, 2005 and Turbicellepora winstonae Vieira, Gordon, Souza & Haddad, 2010. Besides the absence of avicularia, T. iarae n. sp. can be also distinguished from T. brasiliensis by the peristome (tubular in T. iarae n. sp.; broad and flat-rimmed in T. brasiliensis), and primary orifice (without sinus in T. iarae n. sp.; with shallower U-shaped sinus in T. brasiliensis). Other differences between T. iarae n. sp. and T. pourtalesi include the bluntly pointed frontal mucro, primary orifice with a median U-shaped sinus, sinuate peristome and avicularia of T. pourtalesi, all absent in T. iarae n. sp. Turbicellepora winstonae is distinct from T. iarae n. sp. in having an orificial sinus, oral avicularia and a short peristome (the peristome of T. iarae n. sp. is well-developed and tubular).

Turbicellepora species are frequently found on hard substrata such as calcareous nodules but also encrusting algae, worm tubes, bryozoans and hydrozoans (e.g., Hayward 1978; Winston 2005; Vieira et al. 2010). Colonies studied here were attached to the smooth-textured sponge Haliclona (Soestella) melana (Fig. 15). Distribution. Atlantic: Brazil (Bahia).

Notes

Published as part of Almeida, Ana C. S., Souza, Facelucia B. C., Menegola, Carla & Vieira, Leandro M., 2017, Diversity of marine bryozoans inhabiting demosponges in northeastern Brazil, pp. 281-323 in Zootaxa 4290 (2) on pages 308-311, DOI: 10.11646/zootaxa.4290.2.3, http://zenodo.org/record/892719

Files

Files (8.0 kB)

Name Size Download all
md5:1885bc8c73939a50f3f9ca0f89e74569
8.0 kB Download

System files (55.7 kB)

Name Size Download all
md5:ad014cc81fcb81d155118bcbb6304b59
55.7 kB Download

Linked records

Additional details

Biodiversity

Collection code
UFBA
Family
Celleporidae
Genus
Celleporina
Kingdom
Animalia
Material sample ID
UFBA 1185 , UFBA 1664 , UFBA 1665 , UFBA 1667 , UFBA 1671, UFBA 2396-97 , UFBA 2398
Order
Cheilostomatida
Phylum
Bryozoa
Species
joannae
Taxonomic status
sp. nov.
Taxon rank
species
Type status
holotype , paratype
Taxonomic concept label
Celleporina joannae Almeida, Souza, Menegola & Vieira, 2017

References

  • Almeida, A. C. S., Alves, O., Peso-Aguiar, M., Dominguez, J. & Souza, F. (2015 b) Gymnolaemata bryozoans of Bahia State, Brazil. Marine Biodiversity Records, 8, e 120.
  • Vieira, L. M., Migotto, A. E. & Winston, J. E. (2008) Synopsis and annotated checklist of Recent marine Bryozoa from Brazil. Zootaxa, 1810, 1 - 39.
  • Bock, P. (2016) World List of Bryozoa in World Register of Marine Species. Available from: http: // marinespecies. org / aphia. php? p = taxdetails & id = 1795 (accessed 28 January 2016)
  • Marcus, E. (1938) Bryozoarios marinhos brasileiros II. Boletim da Faculdade de filosofia, ciencias e letras, Universidade de Sao Paulo, Zoologia, 2, 1 - 137.
  • Marcus, E. (1939) Bryozoarios Marinhos Brasileiros, 3. Boletim da Faculdade de Filosofia, Ciencias e Letras da Universidade de Sao Paulo, Zoologia, 3, 111 - 353.
  • Hincks, T. (1880) A history of the British Marine Polyzoa. 2 Vols. Van Voorst, London, cxli + 601 pp. & 83 pls. https: // doi. org / 10.5962 / bhl. title. 3978
  • Hayward, P. J. (1980) Cheilostomata (Bryozoa) from the South Atlantic. Journal of Natural History, 14, 701 - 722. https: // doi. org / 10.1080 / 00222938000770591
  • Hayward, P. J. (1992) Some Antarctic and sub-Antarctic species of Celleporidae (Bryozoa, Cheilostomata). Journal of Zoology, 226, 283 - 310.
  • Packard, A. S. (1863) A list of animals dredged near Caribou Island, Southern Labrador, during July and August 1860. Polyzoa. The Canadian naturalist and geologist, 8, 401 - 429.
  • Marcus, E. (1937) Bryozoarios marinhos brasileiros I. Boletim da Faculdade de filosofia, ciencias e letras, Universidade de Sao Paulo, Zoologia, 1, 5 - 224.
  • Marcus, E. (1949) Some Bryozoa from the Brazilian coast. Comunicaciones Zoologicas Del Museo de Historia Natural de Montevideo, 3, 1 - 33.
  • Audouin, J. V. (1826) Explication sommaire des planches de Polypes de l'Egypte et de la Syrie, publiees par Jules-Cesar Savigny. In: Panckoucke, C. L. F. (Ed.), Description de l'Egypte ou receuil des observations et des recherches qui ont ete faites en Egyptes pendant l'Expedition de l'Armee francaise ... Histoire naturelle. Imprimerie Imperiale, Paris, pp. 225 - 244.
  • Cook, P. L. (1985) Bryozoa from Ghana. Zoologische Wetenschappen, Sciences Zoologiques, 238, 1 - 310.
  • Hayward, P. J. & Ryland, J. S. (1999) Cheilostomatous Bryozoa. Part 2. Hippothoidea - Celleporoidea. In: Barnes, R. S. K & Crothers, J. H. (Eds.), Synopses of the British Fauna. New Series. 14. Field Studies Council, Shrewsbury, pp. 1 - 416.
  • Ramalho, L. V., Muricy, G. & Taylor, P. D. (2011) Taxonomic revision of some lepraliomorph cheilostome bryozoans (Bryozoa: Lepraliomorpha) from Rio de Janeiro State, Brazil. Journal of Natural History, 45, 767 - 798. https: // doi. org / 10.1080 / 00222933.2010.535917
  • Winston, J. E., Vieira, L. M. & Woollacott, R. M. (2014) Scientific results of the Hassler expedition. Bryozoa. No. 2. Brazil. Bulletin of the Museum of Comparative Zoology, 161 (5), 139 - 239.
  • Winston, J. E. (2005) Redescription and revision of Smitt's " Floridan Bryozoa " in the Collection of the Museum of Comparative Zoology, Harvard University. Virginia Museum of Natural History Memoir, 7, 1 - 150.
  • Vieira, L. M., Gordon, D. P., Souza, F. B. C. & Haddad, M. A. (2010) New and little-known cheilostomatous Bryozoa from the south and southeastern Brazilian continental shelf and slope. Zootaxa, 2722, 1 - 30.
  • Hayward, P. J. (1978) Systematic and morphological studies on some european species of Turbicellepora (Bryozoa, Cheilostomata). Journal of Natural History, 12, 551 - 590.