Desmacella stylostrongyla, Nascimento & Pinheiro, 2022

Nascimento, Elielton & Pinheiro, Ulisses, 2022, A new species of Desmacella Schmidt, 1870 (Porifera, Demospongiae, Desmacellidae) from the Northeast region of Brazil, Zootaxa 5190 (1), pp. 143-146 : 143-145

publication ID

https://doi.org/ 10.11646/zootaxa.5190.1.7

publication LSID

lsid:zoobank.org:pub:88F90182-58DC-4130-92DA-83E1DAC49B98

DOI

https://doi.org/10.5281/zenodo.7126155

persistent identifier

https://treatment.plazi.org/id/E34CC35E-0158-FFC0-98A8-FAB4FEA1DA53

treatment provided by

Plazi

scientific name

Desmacella stylostrongyla
status

sp. nov.

Desmacella stylostrongyla View in CoL sp. nov.

( Figures 1A–H View FIGURE 1 )

Type locality. Brazil, Bahia State ( Mata de São João City ) .

Type material. Holotype — UFBA 3774 , off Mata de São João City (12°26’56.3”S 37°55’31.0”W) Bahia State, Brazil, 28 m depth, coll. Andrade, Walter (II.2004). GoogleMaps

Diagnosis. Desmacella with styles, two categories of sigma and raphides.

External morphology ( Fig. 1A View FIGURE 1 ). Massive sponge, 10 x 6 cm (length x width). Hispid and worn surface, with distinct oscules (3–6 mm in diameter), compressible consistency, but fragile and easy to tear. Colour light brown (fixed in ethanol 80%).

Skeleton ( Fig. 1B View FIGURE 1 ). Ectosomal skeleton without distinct spicule brushes, although individual spicules may pierce the dermal membrane heavily charged with sigmas. Choanosomal skeleton formed by large styles arranged in a halichondroid reticulation. Abundant sigmas randomly distributed. Raphides are dispersed in the choanosome and trichodragmas were observed in the secondary bundles ( Fig 1H View FIGURE 1 ).

Spicules ( Figs. 1C–G; I View FIGURE 1 ). Styles I (170– 353.6 –460/5– 6.7 –10 µm, length/width, average in italic): straight to slightly curved. ranging from strongyloid, acerate, rounded and mucronate tips. Styles II (270– 365 –470/ 1.2– 2.4 –3.7 µm): slender, slightly curved to slightly sinuous. Sigmas I (45– 65 –90 µm, length): larger, thin, C- or S-shaped, abundant and with smooth ends. Sigmas II (12– 18.4 –30 µm): thin, C-or S-shaped and with smooth ends. Raphides (51– 72.2 –112.2 µm, length) in trichodragmas.

Distribution. Only type locality: off Mata de São João City (Bahia State, the Northeast region of Brazil).

Etymology. The species name is given due to the presence of styles varying to strongyles.

Remarks. Desmacella stylostrongyla sp. nov. belongs to the genus Desmacella by the possession of styles and sigmas, and a skeleton consisting of plumose bundles of styles ( Ridley & Dendy 1886). It differs from Desmacella species present in the Atlantic Ocean by combining stylote megascleres (varying to strongyles), two categories of sigmas and raphides.

The new species differs from D. microsigmata Cavalcanti, Santos & Pinheiro, 2015 , D. tylovariabilis Cavalcanti, Santos & Pinheiro, 2015 , D. annexa Schmidt, 1870 , D. digitata ( Lévi, 1960) , D. grimaldii ( Topsent, 1890) , D. informis ( Stephens, 1916) , D. infundibuliformis ( Vosmaer, 1885) , D. inornata ( Bowerbank, 1866) , D. jania Verrill, 1907 , D. meliorata Wiedenmayer, 1977 , D. peachi Ferrer-Hernandez, 1914 , D. pumilio Schmidt, 1870 , D. suberitoides ( Burton, 1932) , D. topsenti (Burton, 1930) , D. vagabunda Schmidt, 1870 , D. vestibularis ( Wilson, 1904) and D. vicina Schmidt, 1870 by the presence of styles instead of tylostyles. Additionally, D. microsigmata , D. tylovariabilis . D. digitata , D. grimaldii , D. informis , D. infundibuliformis , D. inornata , D. jania , D. meliorata , D. pumilio , D. suberitoides , D. topsenti , D. vagabunda , D. vestibularis and D. vicina don’t have raphides, which are observed in the new species. Desmacella polysigmata Van Soest, 1984 that occurs in the Caribbean Sea ( Belize) is the most similar species to Desmacella stylostrongyla sp. nov., because it has stylote megascleres varying to strongyles and two categories of sigma ( Van Soest 1984). However, D. polysigmata has larger and robust styles (10– 15.2 –19 µm versus 5– 6.7 –10 µm in D. stylostrongyla sp. nov.), and sigmas I and II with half of the length (30– 37.3 –42 µm and 10– 11.6 –15 µm versus 45– 65 –90 µm and 12– 18.4 –30 µm) ( Cavalcanti et al. 2015: 367–368). Additionally, toxiform microxeas are absent in D. polysigmata ( Van Soest 1984) .

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