Haliclona (Halichoclona) vansoesti

Muricy, Guilherme, Esteves, Eduardo L., Monteiro, Leandro C., Rodrigues, Beatriz Roma & Albano, Rodolpho M., 2015, A new species of Haliclona (Demospongiae: Haplosclerida: Chalinidae) from southeastern Brazil and the first record of Haliclona vansoesti from the Brazilian coast, Zootaxa 3925 (4), pp. 536-550 : 543-547

publication ID

https://doi.org/ 10.11646/zootaxa.3925.4.3

publication LSID

lsid:zoobank.org:pub:F02FAC72-AD74-496D-9811-B8B4313A783E

DOI

https://doi.org/10.5281/zenodo.5618325

persistent identifier

https://treatment.plazi.org/id/CD0A878E-3D29-8E68-FF29-7CB1FCD2FD58

treatment provided by

Plazi

scientific name

Haliclona (Halichoclona) vansoesti
status

 

Haliclona (Halichoclona) vansoesti View in CoL de Weerdt, de Kluijver & Gomez, 1999

( Figures 3‒4 View FIGURE 3 View FIGURE 4 ; Table 2 View TABLE 2 )

Synonyms:

Haliclona (Halichoclona) vansoesti View in CoL de Weerdt, de Kluijver & Gomez, 1999: 49; de Weerdt, 2000: 49; Valderrama & Zea, 2013: 372; Rützler et al., 2014: 80.

Haliclona (Halichoclona) View in CoL sp., Monteiro & Muricy, 2004: 683.

Diagnosis. Haliclona (Halichoclona) with a very loose connection between ectosome and choanosome, a whitish or cream translucent ectosome combined with a purplish or violet to pink, lavender, or light salmon choanosome, a cavernous structure and a friable or crisp consistency. Microscleres absent.

Material examined. MNRJ 3809, Palmas Island, S shore, Rio de Janeiro, between 6–12 m depth, coll. E. Vilanova, G. Muricy, L. Monteiro, January 11, 2001. MNRJ 3863, Cagarra Islet, NE shore, Rio de Janeiro, between 6–12 m depth, coll. E. Vilanova, G. Muricy, L. Monteiro, January 11, 2001. MNRJ 3915, Cagarra Island, S shore, Rio de Janeiro, coll. L. Monteiro, February 1, 2001. MNRJ 8981, Rasa Island, W shore ("Portinho"), Rio de Janeiro, 10 m depth, coll. L. Monteiro, February 23, 2005. UERJPOR 6, 9, 10, 12, 15, 30 and 34, Maricás Archipelago, 10‒12 m depth, colls. E. L. Esteves & B. Condor, February 14, 2013.

Description ( Figs. 3 View FIGURE 3 A‒I, 4A‒C): Shape thickly encrusting, very irregular, up to 25 cm wide by 1‒3 cm thick, with abundant, short tube-shaped projections 2‒30 mm high topped by circular oscules 2‒10 mm in diameter ( Fig. 3 View FIGURE 3 A‒H). Oscular tubes are cylindrical or vulcaniform, with relatively thin walls (0.5‒2.0 mm thick), slightly translucent ( Fig. 3 View FIGURE 3 I). Some specimens also present blind fistular projections, which are more irregular, lower and thinner than the oscular tubes ( Fig. 3 View FIGURE 3 C‒E). Choanosome color variable from light purple or violet to pink, lavender, light salmon or cream. The surface is translucent, usually whitish or lighter than the choanosome. Below 10 m depth and without artificial illumination the sponge looks light blue ( Fig. 3 View FIGURE 3 H). After fixation it becomes white to cream ( Fig. 4 View FIGURE 4 A‒C). Surface irregular, uneven, reticulate, very loosely connected to the choanosome, easily detachable ( Fig. 4 View FIGURE 4 C). Consistency friable and fragile, slightly compressible, rather inelastic.

Skeleton: Ectosomal skeleton easily detachable, formed by a slightly disorganized isotropic, predominantly paucispicular tangential reticulation of oxeas, slightly denser than that of the choanosome ( Fig. 4 View FIGURE 4 D). Subectosomal and choanosomal lacunae are common ( Fig. 4 View FIGURE 4 E–F). Choanosomal skeleton cavernous, formed by a relatively disorganized isotropic reticulation of oxeas similar to that of the ectosome but mostly unispicular ( Fig. 4 View FIGURE 4 F). Amount of spongin very low in both the choanosome and ectosome.

Spicules: oxeas smooth, fusiform, slightly curved, with acerate or hastate tips: 139.1‒175.5 (± 11.1)–217.5 µm long by 2.4–7.3 (± 1.4)–12.5 µm wide ( Table 2 View TABLE 2 , Fig. 4 View FIGURE 4 G).

Ecology. Haliclona (Halich.) vansoesti is one of the most common sponge species on the islands off Rio de Janeiro State on horizontal and especially on vertical rocky surfaces, mainly between 10‒20 m depth.

Distribution. Curaçao (type locality), Jamaica, St. Vincent, Martinique (de Weerdt et al., 1999), Colombian Caribbean ( Valderrama & Zea, 2013), Belize (Rützler et al., 2014), and Brazil, where it is reported so far only from Rio de Janeiro State ( Monteiro & Muricy, 2004; present study; Fig. 1 View FIGURE 1 ).

Taxonomic remarks. The specimens from Rio de Janeiro studied here are very similar to Haliclona (Halich.) vansoesti from the Caribbean identified by de Weerdt. et al. (1999), de Weerdt (2000) and Valderrama & Zea (2013). They share the four traits considered most characteristic of the species by de Weerdt et al. (1999) and de Weerdt (2000), and whose combination distinguishes it from all other species of the subgenus: a very loose connection between ectosome and choanosome, a whitish translucent ectosome combined with a purplish choanosome, a cavernous structure and a brittle or crisp consistency. They also share the thick encrusting shape, raised oscules, the general skeletal organization and the shape and size of oxeas. The main differences between them are the greater variation in shape and color, a more irregular surface, and especially the higher oscular tubes in Brazilian specimens when compared to those from the Caribbean (2‒30 mm high in Brazil vs. "slightly raised elevations" in the Caribbean; de Weerdt et al., 1999). We consider these differences as simple intraspecific variations, because the range of variation of these characters in Brazilian specimens is wider and includes the typical morphology of Caribbean specimens. On the other hand, H. (Halich.) vansoesti sensu Rützler et al. (2014) from Bahamas differs from our specimens and from all other records by its black color after fixation in ethanol instead of a whitish cream color and by its slightly longer oxeas: 160–280 µm long in Rützler et al. (2014) specimens vs. 140–218 om in Brazilian specimens (present study), 120–221 µm in the original description (de Weerdt et al., 1999; de Weerdt, 2000), and 166–214 µm in Colombian specimens ( Valderrama & Zea, 2013). The Bahamian specimens studied by Rützler et al. (2014) are thus atypical and may either belong to a sibling species or represent a case of high intraspecific variation. The conspecificity of the southeastern Brazilian and the typical Caribbean specimens of H. (Halich.) vansoesti was confirmed through phylogenetic analysis of molecular data (see below).

Phylogenetic analysis. The maximum likelihood phylogenetic tree based on the small subunit 18S rRNA gene included three samples of putative H. (Halich.) vansoesti from SE Brazil and representative sequences of each of the five clades described in a recent molecular phylogenetic analysis of Demospongiae that included marine Haplosclerida (= Haploscleromorpha; Redmond et al., 2013). It indicates that sequences of the putative H. (Halich.) vansoesti from SE Brazil form a monophyletic cluster with the same gene sequence from Caribbean ( Panama) specimens of H. (Halich.) vansoesti , with high bootstrap support, falling within phylogenetic clade B of Redmond et al. (2013) ( Fig. 5 View FIGURE 5 ). BLAST searches also showed that Brazilian samples share 99% nucleotide identity with this Caribbean species. They were phylogenetically closer to H. (Halich.) vansoesti than to any other species of Haliclona , further supporting the hypothesis that they belong to the same species. In our analysis we recovered the same five clades (A–E) found by Redmond et al. (2013), and as in their study H. (Halich.) vansoesti fell within clade B.

The maximum likelihood phylogenetic tree based on COI sequences included three samples of putative H. (Halich.) vansoesti from Rio de Janeiro and representative sequences from Redmond et al. (2011) ( Fig. 6 View FIGURE 6 ). In their analysis, Redmond et al. (2011) described two monophyletic clades for this marker: clade A, composed mainly of Haliclona and Callyspongia species and clade B, formed by two Haliclona and Callyspongia species and Amphimedon queenslandica Hooper & van Soest, 2006. In our analysis, the COI sequences for the putative H. (Halich.) vansoesti from SE Brazil form a monophyletic cluster with high bootstrap support outside these two clades that does not include any other Haliclona species.

TABLE 2. Spicule measurements (oxeas length and width in µm) of 11 specimens of Haliclona (Halichoclona) vansoesti from Rio de Janeiro State, SE Brazil. Measurements are expressed as minimum – average (± standard deviation) – maximum. N = 30.

Specimen Length Width
MNRJ 3809 146.4 ‒ 162.8 (± 8.8) ‒ 180.0 4.8 ‒ 7.2 (± 1.5) ‒ 9.6
MNRJ 3863 148.8–168.5 (± 11.3) ‒ 192.0 3.6 ‒ 6.7 (± 1.2) ‒ 9.6
MNRJ 3915 170.4–187.3 (± 6.8)–201.6 7.2–9.4 (± 0.6) ‒ 9.6
MNRJ 8981 144.0–161.4 (± 8.4)–180.0 3.6–6.5 (± 1.3)–9.6
UERJPOR 0 6 177.2 ‒ 199.0 (± 11.2)–216.6 5.2–8.8 (± 1.9)–12.0
UERJPOR 0 9 147.0–170.4 (± 12.6) ‒ 195.5 3.5–5.5 (± 1.1)–7.4
UERJPOR 10 156.2–178.8 (± 13.0)–210.3 2.8–6.0 (± 1.8)–10.7
UERJPOR 12 140.4–185.1 (± 20.7)–217.5 3.7–7.6 (± 2.4)–11.2
UERJPOR 15 144.7–172.7 (± 13.8)–195.3 3.7–8.1 (±2.0)–12.5
UERJPOR 30 139.1–158.3 (± 10.8)–176.6 2.6–4.8 (± 1.0)–6.5
UERJPOR 34 181.7 ‒ 189.2 (± 5.1) ‒ 197.2 8.0 ‒ 9.2 (± 0.6)–10.6
MNRJ

Museu Nacional/Universidade Federal de Rio de Janeiro

Kingdom

Animalia

Phylum

Porifera

Class

Demospongiae

Order

Haplosclerida

Family

Chalinidae

Genus

Haliclona

Loc

Haliclona (Halichoclona) vansoesti

Muricy, Guilherme, Esteves, Eduardo L., Monteiro, Leandro C., Rodrigues, Beatriz Roma & Albano, Rodolpho M. 2015
2015
Loc

Haliclona (Halichoclona)

Monteiro 2004: 683
2004
Loc

Haliclona (Halichoclona) vansoesti

Valderrama 2013: 372
Weerdt 2000: 49
Kluijver 1999: 49
1999
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