Craniella curviclada, Fernandez & Rodriguez & Santos & Pinheiro & Muricy, 2018
publication ID |
https://doi.org/ 10.11646/zootaxa.4429.1.2 |
publication LSID |
lsid:zoobank.org:pub:588CFF51-01DF-4C1C-86D9-D13031F5045B |
DOI |
https://doi.org/10.5281/zenodo.5969278 |
persistent identifier |
https://treatment.plazi.org/id/4B37682E-6643-8201-4DCD-1DC6FCA5FB2B |
treatment provided by |
Plazi |
scientific name |
Craniella curviclada |
status |
sp. nov. |
Craniella curviclada View in CoL sp. nov.
( Figs. 13–14 View FIGURE 13 View FIGURE 14 ; Tab. 4)
Diagnosis. Craniella globular, without a root, with a double-layered cortex; three categories of smooth oxeas, two categories of protriaenes (largest category, slightly anisoclad with bent tips of clads, and smallest category, isoclad and very slender) and one category each of anatriaenes and sigmaspires.
Synonyms. Cinachyra sp. n., Muricy et al. 2006: 115.
Material examined. Holotype. MNRJ 20961 View Materials , REVIZEE Programme sta. Central 2- F20, Espírito Santo State, Southeastern Brazil (19°17’14” S, 37°57’13” W, slope, Espírito Santo Basin, circa 265 km E off Vitória City), dredging, 500 m depth, coll. N.Oc. Astro-Garoupa team, 22 November 1997 GoogleMaps .
Description. The single specimen has been sectioned for study and only half is preserved. Globular sponge without a root ( Figs. 13A–D View FIGURE 13 ); 17 mm in diameter. In cross section, dense concentration of spicules at the center of the body and near the surface ( Fig. 13A View FIGURE 13 ). Surface, even, but rough and slightly hispid. Oscules or pores not visible. Color, in vivo not recorded, and light beige in ethanol. Consistency, firm, but compressible.
Skeleton. Radial, with main bundles of oxeas I from the center to the surface, protruding up to 350 µm above the surface ( Fig. 13E View FIGURE 13 ), up to 250 µm wide and up to 500 µm of distance to each other ( Fig. 13F View FIGURE 13 ). Oxeas II only in the center of body, as a disorganized mass ( Fig. 13F View FIGURE 13 ). Cortex with two layers; outer layer with 930 µm thick and sub-dermal cavities up to 500 µm in diameter, and inner layer with an irregular palisade of cortical oxeas III up to 700 µm high ( Figs. 13E, G View FIGURE 13 ). Protriaenes and anatriaenes in the main spicule bundles; cladomes of protriaenes usually pierce the surface together with the oxeas I ( Fig. 13H View FIGURE 13 ). Sigmaspires scattered in the ectosome and choanosome, and around canals ( Figs. 13I –J View FIGURE 13 ). Choanosome, dense with few canals; approximately 500 µm in diameter.
Spicules. Megascleres ( Tab. 4):
Oxeas I ( Fig. 14A–B View FIGURE 14 ) abundant, anisoactinal (anisoxeas), fusiform, straight to curved, smooth. Extremities, very distinct (one with a typically hastate tip and the opposite end filiform): 1600–3841–5000/28–38–53 µm.
Oxeas II ( Fig. 14C–D View FIGURE 14 ), less abundant than the oxeas I, slightly fusiform, isoactinal, straight or curved, and smooth. Extremities, equal, with hastate to acerate tips: 915–1200–1450/18–26–30 µm.
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Oxeas III ( Fig. 14E–F View FIGURE 14 ), abundant, exclusively cortical (size widely variable), stout, smooth, fusiform and often slightly curved. Extremities equal, with tips acerate: 450–658–900/29–36–49 µm.
Protriaenes I ( Figs. 14G–H View FIGURE 14 ), abundant. Rhabdome, thicker near the cladome, thin after 950 µm in opposite direction to the cladoma, then becoming slightly thicker again and very slender and flexuous up to the opposite extremity: 1360– 1193–2725 /14–20–24 µm. Clads, straight to slightly sinuous, with curved extremities and making an angle of 150º–160º with the rhabdome: 122–165–223/ 12–17–22 µm.
Protriaenes II ( Fig. 14I –K View FIGURE 14 ), less common than the protriaenes I. Rhabdome, straight and becoming thin near the cladome: 301–556–1075/ 7–10–14 µm. Cladome, small, with straight and pointed clads, making an angle of about 135º with the rhabdome: 19–55–115/ 5–7–10 µm.
Anatriaenes ( Fig. 14L–M View FIGURE 14 ), less common than the protriaenes I and II, exclusively choanosomal. Rhabdome, larger than that of both protriaenes, with variable thickness: 2750–3890–6500/22–32–41 µm. Cladome, with clads making an angle of approximately 60º with the rhabdome: 68–135–140/14–22–29 µm.
Microscleres ( Tab. 4):
Sigmaspires ( Fig. 14N View FIGURE 14 ), very abundant, ‘c’ or ‘s’ shaped and entirely microspined (with a few large spines): 14–15–17/0.5–2.0 µm.
Ecology and bathymetric distribution. No macrosymbionts were observed on this sponge. The only specimen was collected from soft seabed with a mix of mud and carbonate sand, at 500 m depth ( Lavrado & Ignacio 2006; Muricy et al. 2006).
Distribution. Known only from the type locality, the continental slope off Espírito Santo State, SE Brazil, SW Atlantic ( Fig. 1 View FIGURE 1 ).
Etymology. The name ‘curviclada’ refers to the curved tips of clads of the larger protriaenes (protriaenes I of this study).
Remarks. Unlike Craniella crustocorticata , Craniella curviclada sp. nov. fits well in the diagnosis of Craniella proposed by Carella et al. (2016), due to its globular shape, absence of porocalices, and presence of a distinct two-layered cortex.
Now forty-three species of Craniella are known worldwide; including Craniella curviclada sp. nov., of which 16 occur in the Atlantic Ocean: eight in the western Atlantic, seven in the eastern Atlantic and one occurring in the North, East and West Atlantic ( Tab. 4). The new species is set apart from all species of Craniella from the Atlantic due to either features of habit, surface, spiculation or a combination of these. These differences are described below.
Craniella australis Samaai & Gibbons 2005 View in CoL , Craniella azorica View in CoL , Craniella carteri View in CoL , Craniella metaclada ( Lendenfeld 1907) View in CoL , Craniella monodi ( Burton 1929) View in CoL and Craniella zetlandica ( Carter 1872) View in CoL lack sigmaspires and Craniella disigma Topsent 1904 View in CoL has two categories of sigmaspires. Since one category of sigmaspires is present in Craniella curviclada View in CoL sp. nov., six previous species are set apart from the new species ( Tab. 4). Remarkably, protriaenes of Craniella australis View in CoL have clads with slightly bent tips (Saamai & Gibbons, 2005: 10; Fig.7 View FIGURE 7 ), which are similar to those of Craniella curviclada View in CoL sp. nov., but these protriaenes are longer and bear smaller clads and cladome than those of the new species ( Figs. 14G–H View FIGURE 14 ); viz. Craniella australis View in CoL (rhabd. 819–4000/9–65; ca. 30 µm of distance between clads) and Craniella curviclada View in CoL sp. nov. rhabd. 1360–2725 /14–24; ca. 200 µm of distance between clads).
Craniella cranium ( Müller 1776) View in CoL , Craniella cranium View in CoL f. microspira Lévi 1967 and Craniella schmidtii Sollas 1886 View in CoL have two categories of oxeas instead of three as in the new species. Further, Craniella schmidtii View in CoL has smaller choanosomal oxeas, up to 1600 µm (vs. up to 5000 µm in Craniella curviclada View in CoL sp. nov.).
Craniella gravida sensu Pollock 1998 View in CoL , Craniella insidiosa Schmidt 1870 View in CoL , Craniella lens Schmidt 1870 View in CoL , Craniella tethyoides Schmidt 1870 View in CoL and Craniella zetlandica View in CoL are poorly described and their re-description is beyond the scope of this study. However, Craniella insidiosa View in CoL has a papillose habit (vs. globular habit in Craniella curviclada View in CoL sp. nov.) and Craniella tethyoides View in CoL has anatriaenes bearing smaller clads, 70–90 µm in length (vs. 68 – 140 µm in length in Craniella curviclada View in CoL sp. nov.).
Craniella crustocorticata View in CoL has a root at the base, a strongly conulose surface, oxeas with nearly equal extremities, a single-layered cortex, and sigmaspires with relatively many large spines in comparison to Craniella curviclada View in CoL sp. nov.. The new species differs from Craniella crustocorticata View in CoL by the absence of a root at the base, absence of conules on the surface, presence of two-layered cortex in the skeleton, stout anisoactinal oxeas, and sigmaspires with fewer spines (viz., see results of this study).
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.
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Craniella curviclada
Fernandez, Julio C. C., Rodriguez, Pablo R. D., Santos, George G., Pinheiro, Ulisses & Muricy, Guilherme 2018 |
Craniella curviclada
Fernandez & Rodriguez & Santos & Pinheiro & Muricy 2018 |
Craniella curviclada
Fernandez & Rodriguez & Santos & Pinheiro & Muricy 2018 |
Craniella curviclada
Fernandez & Rodriguez & Santos & Pinheiro & Muricy 2018 |
Craniella curviclada
Fernandez & Rodriguez & Santos & Pinheiro & Muricy 2018 |
Craniella curviclada
Fernandez & Rodriguez & Santos & Pinheiro & Muricy 2018 |
Craniella curviclada
Fernandez & Rodriguez & Santos & Pinheiro & Muricy 2018 |
Craniella curviclada
Fernandez & Rodriguez & Santos & Pinheiro & Muricy 2018 |
Craniella crustocorticata
van Soest 2017 |
Craniella crustocorticata
van Soest 2017 |
Craniella australis
Samaai & Gibbons 2005 |
Craniella australis
Samaai & Gibbons 2005 |
Craniella australis
Samaai & Gibbons 2005 |
Craniella gravida
sensu Pollock 1998 |
Craniella disigma
Topsent 1904 |
Craniella carteri
Sollas Sollas 1886 |
Craniella schmidtii
Sollas 1886 |
Craniella schmidtii
Sollas 1886 |
Craniella insidiosa
Schmidt 1870 |
Craniella lens
Schmidt 1870 |
Craniella tethyoides
Schmidt 1870 |
Craniella insidiosa
Schmidt 1870 |
Craniella tethyoides
Schmidt 1870 |