Placospongia cristata Boury-Esnault, 1973
publication ID |
https://doi.org/ 10.11646/zootaxa.5405.4.2 |
publication LSID |
lsid:zoobank.org:pub:3080C791-0BF8-45E0-940E-CDC796EAAEFD |
DOI |
https://doi.org/10.5281/zenodo.10619627 |
persistent identifier |
https://treatment.plazi.org/id/2C3EA33A-BE45-FF8D-5FA9-69D1FD1C899C |
treatment provided by |
Plazi |
scientific name |
Placospongia cristata Boury-Esnault, 1973 |
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Placospongia cristata Boury-Esnault, 1973 View in CoL
( Figs. 4–6 View FIGURE 4 View FIGURE 5 View FIGURE 6 ; Tables 2–4 View TABLE 2 View TABLE 3 View TABLE 4 and 7 View TABLE 7 )
Synonyms
Placospongia cristata Boury-Esnault, 1973: 276 View in CoL ; Hechtel 1976: 253; Bispo et al. 2006: 24; David-Colón et al. 2023: 507 View Cited Treatment ; Bettcher et al. 2023: 465 View Cited Treatment .
Placospongia melobesioides sensu Arndt 1927: 142 View in CoL ; Hechtel 1969: 32 (non Placospongia melobesioides Gray, 1867 View in CoL ).
Placospongia sp. 1 sensu David-Colón & Marín-Casa 2020.
Placospongia ruetzleri sensu Bettcher et al. 2023: 450 View in CoL (in part) (non Placospongia ruetzleri van Soest, 2017 View in CoL ).
? Placospongia melobesioides sensu Schmidt 1870: 72 View in CoL ; de Laubenfels 1936: 153; de Laubenfels 1953: 540; Collin et al. 2005: 658.
Material examined. Holotype of Placospongia cristata Boury-Esnault, 1973 : MNHN-IP-2015-740, formerly MNHN. LBIM.D.NBE 960 (fragment deposited in UFRJPOR 3382), R / V Calypso sta. 29, off Porto de Galinhas, Pernambuco State, Brazil (8º28’S, 34º55’W), 25 m depth, leg. R / V Calypso; MNRJ 29661, Coroa Alta reef, Santa Cruz Cabrália city, Bahia State, Brazil (16º13.200’S, 38º57.038’W), intertidal, colls. Aline Fioravanso & Marianela Gastaldi, 22 April 2019 (= Placospongia ruetzleri sensu Bettcher et al. 2023 ).
Description ( Fig. 5a View FIGURE 5 ). Shape thinly encrusting, 10 x 5 x 1 mm (length x width x thickness), attached to a carbonate fragment. The surface has smooth cortical plates separated by pore-bearing grooves. The consistency is hard, but fragile. The color is whitish beige in ethanol ( Fig. 5a View FIGURE 5 ).
Skeleton ( Fig. 5b–d View FIGURE 5 ). The cortex is 250–400 µm thick, distinct from the choanosome ( Fig. 5b View FIGURE 5 ). The inner layer of the cortex is densely packed with selenasters and the outer layer consists of randomly distributed spherasters and micro-spheroxyasters ( Figs. 5c– d View FIGURE 5 ). The choanosomal skeleton is formed by sparse tylostyles tracts 90–150 µm thick which run obliquely from the substrate to the cortex ( Fig. 5b View FIGURE 5 ). The micro-spheroxyasters occur abundantly in the choanosome, often in clusters, lining the choanosomal cavities. Immature selenasters and spherasters are scattered throughout the choanosome.
Megascleres ( Fig. 6a–d View FIGURE 6 ; Tab. 4 View TABLE 4 ). Two categories of tylostyles, both of them straight, with blunt ends and rounded tyle ( Figs. 6b and 6d View FIGURE 6 ). Tylostyles I are large and choanosomal: 430–668–910 / 6–10–13 µm, tyle width 7–12–15 µm ( Fig. 6a–b View FIGURE 6 ). Tylostyles II are small and cortical: 210–283–340 / 2–6–8 µm, tyle width 7–8–10 ( Fig. 6c–d View FIGURE 6 ).
Microscleres ( Figs. 6e–i View FIGURE 6 , Tab. 4 View TABLE 4 ). Mature selenasters are ellipsoid to rounded, with fused spines, forming rounded or polygonal plates: total size 37–44–57 / 30–42–48 µm, hilum 4–6–9 µm in diameter ( Fig. 6e View FIGURE 6 ). Three types of immature selenasters: immature selenasters I straight, slender, spiny, with spines concentrated on the ends of the shafts: 17–20–23 / 2–4–6 µm; immature selenasters II elongated, stout, with large and numerous spines: 25–28–30 / 10–13–18 µm ( Fig. 6f View FIGURE 6 ); immature selenasters III ellipsoid, stout, with spines very closely set, but still recognizable in their individuality: 32–39–43 / 17–24–28 µm. Spherasters are large, smooth, with short and conical rays: 10–15–25 µm in diameter ( Fig. 6g View FIGURE 6 ). Micro-spheroxyasters have smooth rays, with an irregular center: 1–2–3 µm in diameter ( Fig. 6h–i View FIGURE 6 ).
Habitat. This species occurs in the intertidal zone, in a shaded microhabitat ( Bettcher et al. 2023), to 25 m depth ( Boury-Esnault 1973).
Geographical distribution ( Fig. 4 View FIGURE 4 ; Tab. 2 View TABLE 2 ). Caribbean Sea: Curaçao (Ardnt 1927 as P. melobesioides ), Barbados ( Hechtel 1969 as P. melobesioides ), Colombia ( David-Colón et al. 2023). Northeast Brazil: Pernambuco State ( Boury-Esnault 1973) and Bahia State ( Bispo et al. 2006; Bettcher et al. 2023).
Taxonomic remarks. Placospongia cristata is herein characterized by the combination of two categories of tylostyles, ellipsoid to rounded mature selenasters, spherasters of the typical golf-ball shape and micro-spheroxyasters. In the original description, Boury-Esnault (1973) reported only the presence of tylostyles, selenasters and spherasters as spicular components. Our re-examination of the holotype and its spicules in SEM allowed us to confirm the presence of micro-spheroxyasters, as supposed by van Soest (2009).
Besides the type locality in Pernambuco State, P. cristata was also described from Bahia State ( Bettcher et al. 2023) and the Colombian Caribbean ( David-Colón et al. 2023), with the first in situ photographs of this species. The specimens from Bahia State are thinly encrusting and orange-brown in color ( Bettcher et al. 2023), while the Caribbean specimens are thicker, with creeping and erect lobes or branches, and dark brown to chocolate-brown in color ( David-Colón et al. 2023). The spicules of these populations conformed with the holotype re-examined here, except for the larger and thicker size of tylostyles and selenasters in the Caribbean populations and the presence of a few spirasters in one specimen from Bahia State ( Tab. 4 View TABLE 4 ). Despite these small differences, we consider the Brazilian and Colombian populations to belong to a single species, widely distributed in the Tropical Atlantic realm.
Rützler (2002) and Mothes et al. (2006) suggested that P. cristata could be a junior synonym of P. melobesioides based on the shared presence of spherasters and absence of spirasters, despite the large geographical distance between Northeast Brazil and Borneo, type locality of P. melobesioides . The two species also share the rounded shape of the selenasters and the presence of micro-spheroxyasters (cf. Becking 2013 as spherules). However, as noted by van Soest (2009), the choanosomal tylostyles of P. cristata are much smaller (430–600 µm) than those of P. melobesioides (670–1010 µm; Tab. 3 View TABLE 3 ). Furthermore, in P. cristata the spherasters are more abundant and the selenasters are slightly smaller than in P. melobesioides (37–57 vs. 45–68 µm; Tab. 3 View TABLE 3 ). Therefore, we agree with van Soest (2009) that P. cristata and P. melobesioides are different species, although closely related.
The similarity between P. cristata and P. melobesioides led van Soest (2009) to propose that the records of P. melobesioides from the Central Western Atlantic ( Schmidt 1870; Arndt 1927; de Laubenfels 1936; Gonzáles-Farías 1989) could in fact belong to P. cristata . David-Colón et al. (2023) also considered the records of P. melobesioides from Barbados ( Hechtel 1969) and Gulf of Mexico (de Laubenfels 1953) and the record of P. intermedia from Panama ( Collin et al. 2005) as belonging to P. cristata . However, the record of P. melobesioides by de Laubenfels (1936) included only selenasters and was considered unrecognizable by Hechtel (1969). Schmidt (1870), de Laubenfels (1953) and Collin et al. (2005, as P. intermedia ) did not describe the spicules of their specimens, and Sollas (1888) did not find spherasters in Schmidt’s type slides. On the other hand, van Soest (2009) reexamined the specimens of Arndt (1927) and found spherasters similar to those of P. cristata , and all the spicules described by Hechtel (1969) conform to the holotype of P. cristata . Therefore, we agree that the records of P. melobesioides from Curaçao and Barbados (Ardnt 1927; Hechtel 1969) are likely synonyms of P. cristata , but all records of P. melobesioides from the Caribbean need to be reevaluated. The records of P. melobesioides from the Gulf of Mexico (González-Farías 1989) and from North Brazil ( Mothes et al. 2006) belong to the new species Placospongia beatrizae sp. nov. ( Tab. 7 View TABLE 7 ) and are discussed below in its taxonomic remarks.
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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Placospongia cristata Boury-Esnault, 1973
Sandes, Joana, Moraes, Fernando & Muricy, Guilherme 2024 |
Placospongia ruetzleri sensu
Bettcher, L. & Fernandez, J. C. & Gastaldi, M. & Bispo, A. & Leal, C. V. & Leite, D. & Avelino-Alves, D. & Clerier, P. H. & Rezende, D. & Gulart, C. M. & Pinheiro, U. & Hajdu, E. 2023: 450 |
Placospongia cristata
David-Colon, J. & Zea, S. & Marin-Casas, D. 2023: 507 |
Bettcher, L. & Fernandez, J. C. & Gastaldi, M. & Bispo, A. & Leal, C. V. & Leite, D. & Avelino-Alves, D. & Clerier, P. H. & Rezende, D. & Gulart, C. M. & Pinheiro, U. & Hajdu, E. 2023: 465 |
Bispo, R. & Johnsson, R. & Neves, E. 2006: 24 |
Hechtel, G. J. 1976: 253 |
Boury-Esnault, N. 1973: 276 |
Placospongia melobesioides sensu
Hechtel, G. J. 1969: 32 |
Arndt 1927: 142 |
Placospongia melobesioides sensu Schmidt 1870: 72
Collin, R. & Diaz, M. C. & Norenburg, J. & Rocha, R. M. & Sanchez, J. A. & Schulze, A. & Schwartz, M. & Valdez, A. 2005: 658 |
Laubenfels, M. W. de 1953: 540 |
Laubenfels, M. W. de 1936: 153 |
Schmidt, O. 1870: 72 |