Crella (Pytheas) desventuradae Fernandez, Gastaldi, Zapata-Hernández & Hajdu, 2021
publication ID |
https://doi.org/ 10.11646/zootaxa.5052.3.3 |
publication LSID |
lsid:zoobank.org:pub:FED635BA-B982-400E-B920-1DBA22025EA9 |
DOI |
https://doi.org/10.5281/zenodo.5578596 |
persistent identifier |
https://treatment.plazi.org/id/15003760-FF8D-F673-6591-FBD2FEA7FBAE |
treatment provided by |
Plazi |
scientific name |
Crella (Pytheas) desventuradae Fernandez, Gastaldi, Zapata-Hernández & Hajdu |
status |
sp. nov. |
Crella (Pytheas) desventuradae Fernandez, Gastaldi, Zapata-Hernández & Hajdu View in CoL , sp. nov.
( Table 2 View TABLE 2 ; Figures 4–5 View FIGURE 4 View FIGURE 5 )
Type locality. San Ambrosio Island , SE Pacific .
Material examined. Holotype — MNHNCL POR-15019 , San Ambrosio Island , Desventuradas Archipelago, SE Pacific (- 26.33892500 S, - 79.90749722 W), 10–20 m depth, coll. C.F. Gaymer, 15 th February 2013. Fragment of holotype under MNRJ 19228 View Materials and IZUA-POR 171 . GoogleMaps
Diagnosis. Only Crella (Pytheas) in the Pacific being massive, yellow in life, with tornotes (130–168/2.4–2.6 µm), three categories of acanthostyles (choanosomal, I 90–104/2.5–3.5 µm and II 60–66/2.5–3.5 µm; ectosomal 40–52/2.5–2.8 µm) and arcuate isochelae (11.5–14.5 µm).
Description. Massive to slightly lobate ( Fig. 4A View FIGURE 4 ); holotype in life, 30 (L) x 30 (W) x 4 cm (H) and fragment preserved, 6 (L) x 6 (W) x 4 cm (H). Surface irregular and slightly corrugated, with several subectosomal channels and a thin, strongly adhered membrane ( Figs. 4A–C View FIGURE 4 ). Oscules small, scattered or grouped ( Figs. 4A–B View FIGURE 4 ) and partially covered by a thin membrane ( Fig. 4D View FIGURE 4 ). Pores very small and grouped as pore sieves, with ca. 1 mm in diameter, in preservative ( Figs. 4E–F View FIGURE 4 ). Consistency firm, but compressible. Texture slightly rough. Color yellow in life and beige in preserved specimen.
Skeleton. Plumoreticulate architecture ( Fig. 5A View FIGURE 5 ). Ectosomal region with several tornotes in vertical arrangement and in bouquets, usually protruding up to 50 µm above the surface ( Fig. 5B View FIGURE 5 ). Beneath the surface (subectosomal region) tornotes in paratangential arrangement ( Fig. 5B View FIGURE 5 ) and in slender tracts (ca. 20–50 µm thick), these latter coring spongin fibers ( Fig. 5C View FIGURE 5 ), ca. 50–100 µm thick, throughout the ectosome and choanosome. Acanthostyles (ectosomal category) in tangential to paratangential arrangement at the ectosome and subectosome ( Fig. 5D View FIGURE 5 ). Choanosomal region with a well-developed reticulation of spongin fibers, 50–150 µm thick, making rounded to polygonal meshes, ca. 300–650 µm wide ( Fig. 5E View FIGURE 5 ), echinated by two categories of choanosomal acanthostyles ( Fig. 5F View FIGURE 5 ). Spongin fibers are frequent throughout all skeletal regions; fibers have parts not fully echinated. Some ectosomal and choanosomal acanthostyles occurring into the fibers too ( Fig. 5C, 5F View FIGURE 5 ). All categories of acanthostyles (ectosomal and choanosomal) are distinguished by size (length and width) and patterns of spination. Tornotes, ectosomal and choanossomal acanthostyles and arcuate isochelae occur scattered throughout the choanosomal region. Further, a few arcuate isochelae occur at the ectosomal region and more frequently around choanosomal channels. In spongin there are wide rounded subectosomal (up to 1000 µm longer length) and choanosomal channels (up to 3000 µm longer length).
Spicules. Megascleres ( Table 2 View TABLE 2 ). Tornotes ( Figs. 5G, 5H View FIGURE 5 ) straight and smooth, tips usually mucronate; juvenile forms slender: 130– 150.8 (14.4)–168/2.4– 2.5 (0.1)–2.6 µm. Choanosomal acanthostyles I ( Figs. 5G, 5I View FIGURE 5 ), largest category of acanthostyles, straight, not fully spined, blunt bases (no tyle), tips acerate or slightly blunt; spines small (up to 2.5 µm high), straight to slightly bent towards the bases, usually absent on the apical third; juvenile forms slender, with smaller and straighter spines: 90– 98.2 (5.7)–104/2.5– 3.1 (0.4)–3.5 µm. Choanosomal acanthostyles II ( Figs. 5F, 5J View FIGURE 5 ), intermediate category of acanthostyles, as thick as previous, but almost fully spined, spines usually absent from apical fourth, small (up to 3 µm high), straight or slightly bent towards base; juvenile forms slender, with smaller, straight spines: 60– 64.2 (2.7)–66/2.5– 3.2 (0.4)–3.5 µm. Ectosomal acanthostyles ( Figs. 5G, 5K View FIGURE 5 ), the smallest category of acanthostyles, slightly curved to sinuous, isodiametric, fully spined, blunt bases (no tyle), tips conical to acerate; spines small (up to 2.5 µm high), straight, uniformly distributed; juvenile forms, slender with several smaller and thinner spines: 40– 46.6 (4.4)–52/2.5– 2.7 (0.2)–2.8 µm. Acanthoxeas ( Fig. 5L View FIGURE 5 ), rare, pattern of spination (fully spined) closer to the ectosomal acanthostyles: average of 50/2.5 µm (n = 2). Microscleres ( Table 2 View TABLE 2 ). Arcuate isochelae ( Figs. 5G, 5M View FIGURE 5 ) in one size category, axis curved, alae slightly rounded and relatively short; distance between opposite alae, 1/3 (or a bit over) of maximum chelae length; juvenile forms with slender axis and smaller alae (reduced alae): 11.5– 13.6 (1.2)–14.5 µm.
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Ecology. Specimen grew over hard bottom covered by calcareous algae.
Distribution. Provisionally endemic to San Ambrosio island (type locality) in Desventuradas Archipelago (- 26.33333333 S, - 79.88333333 W), ca. 900 km from the Chilean coast ( Fig. 1 View FIGURE 1 ), belonging in the Nazca-Desventuradas Marine Park.
Etymology. The name ‘desventuradae’ is a reference to the Desventuradas Archipelago, where the type locality of the new species is located.
Remarks. The new species constitutes only the second species of sponge reported from San Ambrosio Island, located in the National Nazca-Desventuradas Marine Park. Only Pseudosuberites hyalinuus ( Ridley & Dendy, 1887) was known from there (see van Soest 2002b: 238; Fig. 9D View FIGURE 9 , for a revision of this species as Pseudosuberites hyalina ).
Crella (P.) desventuradae Fernandez, Gastaldi, Zapata-Hernández & Hajdu , sp. nov. is set apart from all known species of Crella (P.) by the smaller dimensions of its spicule set; viz., tornotes up to 168/2.6 µm, acanthostyles (the larger ones) up to 104/3.5 µm, and arcuate isochelae up to 14.5 µm ( Table 2 View TABLE 2 ). A few acanthoxeas occur in C. (P.) desventuradae Fernandez, Gastaldi, Zapata-Hernández & Hajdu , sp. nov. as they do in C. (P.) chiloensis Fernandez, Gastaldi, Pardo & Hajdu , sp. nov. We believe these acanthoxeas to be deformed ectosomal acanthostyles due similar size, pattern of spination and position in the skeleton.
Although distant about 1365 km from each other, the two SE Pacific species are geographically closer to each other than to any of the other known Crella (P.) species ( Table 2 View TABLE 2 ). In addition, spiculation and dimensions of spicules in both are more similar than to those of any other known species of Crella (P.); viz., three categories of acanthostyles and one category each of tornotes and arcuate chelae, with measurements in the table 2. However, both species differ in the yellow vs. reddish orange color in life (Desventuradas vs. Chiloé spp.), relative quantity of spongin fibers in the skeleton (more fibers vs. less fibers, respectively), spination pattern of acanthostyles I (evenly distributed vs. more concentrated at the base, respectively) and dimensions of the acanthostyles (larger vs. smaller, respectively).Among these characters, C. (P.) desventuradae Fernandez, Gastaldi, Zapata-Hernández & Hajdu , sp. nov. can be mainly distinguished of C. (P.) chiloensis Fernandez, Gastaldi, Pardo & Hajdu , sp. nov. by a denser reticulation (making a mesh) of spongin fiber throughout all skeleton and less echinated fibers, while in the latter species, reticulation of spongin fibers (without a mesh) are heavely echinated and more frequent in the choanosome.
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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