The genus Oceanapia Norman, 1869 comprises 95 species worldwide, 20 from the Atlantic Ocean and seven from Brazil. Oceanapia includes sponges with hollow body and numerous fistulae; spicules are oxeas or strongyles and microscleres, if present, are sigmas or toxas. Specimens were collected by trawl at Rio Grande do Norte, Pernambuco and Pará States, Brazil. Two new species are described from the Northeast Region of Brazil: Oceanapia cordia sp. nov. and Oceanapia magna sp. nov. For two preoccupied combinations, new names are proposed, Oceanapia hechteli nom. nov. and Oceanapia topsenti nom. nov. Oceanapia stalagmitica (Wiedenmayer, 1977) is recorded and described for the first time from Brazil. A taxonomic study of seven specimens of Oceanapia from the North and Northeast region (Brazil) is given, including description, illustrations and geographical distribution. The two new species are compared with all other descriptions of Oceanapia from the Atlantic Ocean.
The objective of this study was to investigate some life history traits of the palaemonid shrimp Typton carneus collected from a reef in northeastern Brazil. Samples of the sponges Amphimedon compressa, A. viridis, Desmapsamma anchorata, Dysidea etheria, Haliclona implexiformis and Tedania ignis were analyzed and shrimps were removed from them. A total of 41 individuals were found in Te. ignis, three in H. implexiformis and one in D. etheria; the latter two sponges are new records of sponge hosts for Ty. carneus. Of the specimens associated with Te. ignis, 24 were males, 10 ovigerous females, six non-ovigerous females and one juvenile male. Fecundity varied between 19 to 56 eggs (37 ± 14) per female, and the mean egg volume was 0.033 ± 0.010 mm³. Eleven heterosexual pairs were obtained. Characteristics of the pairs suggest a monogamous mating system for the studied population, such as: the absence of sexual dimorphism in weaponry and body size and presence of paired non-brooding and brooding females carrying eggs in different development stages; and a sex ratio that does not differ from the expected 1:1. However, the lack of size-assortative pairing as well as the low proportion of pairs, compared to solitary individuals, have been observed in polygamous mating systems.
Eurypon Gray, 1867 comprises 49 valid species distributed worldwide, and in an extensive bathymetric range. Three Eurypon species are known for Brazil, all endemic from the Northeast region. Here, we describe three new species of Eurypon. Two of which are recorded from shallow waters (down to 100 m) off Pernambuco and Paraíba States, and one species is from deep waters (157 m) off Rio Grande do Norte State. Eurypon oxychaetum sp. nov. has large subtylostyles (1025-2125 µm, length), styles, two categories of acanthostyles and oxychaetes; Eurypon potiguaris sp. nov. has large tylostyles (1000-2315 µm, length), two categories of acanthostyles, and thin oxeas; Eurypon verticillatum sp. nov. is a blue sponge with exclusive verticillate acanthostyles. The new species were compared with all other Atlantic species of the genus. A replacement name for the secondary homonym Eurypon topsenti is proposed: Eurypon pulitzeri nom. nov. The presence of verticillate acanthostyles and oxychaetes spicules are reported for the first time in Table 1 genus.
Three species of Desmacella Schmidt, 1870 are described from the Brazilian coast: Desmacella microsigmata sp. nov., Desmacella tylovariabilis sp. nov. and Desmacella annexa Schmidt, 1870. The new species were compared with Desmacella species from the Atlantic Ocean, which differ by the size of their spicules and by the presence of microspined sigmas. Desmacella annexa was found to have microspined toxiform microxeas and sigmas. Desmacella now contains 31 species distributed worldwide.
The members of Lissodendoryx Topsent, 1892a are recognized by a spicule combination of ectosomal tylotes or strongyles, isodictyal reticulate architecture, arcuate isochelae and sigmas (Hofman & Van Soest 1995; Van Soest 2002). Five subgenera of Lissodendoryx, are recognized (Van Soest 2002): Lissodendoryx (Acanthodoryx) Lévi, 1961, L. (Anomodoryx) Burton, 1934, L. (Ectyodoryx) Lundbeck, 1909, L. (Lissodendoryx) Topsent, 1892a, and L. (Waldoschmittia) de Laubenfels, 1936. Lissodendoryx (Anomodoryx) is defined by the presence of a single megasclere type (Van Soest 2002). Currently has six recognized species (Van Soest et al. 2014) including two from Brazil (Muricy et al. 2011): L. (A.) recife (Boury-Esnault, 1973) and L. (A.) tylota (Boury-Esnault, 1973). In this paper, a new species of L. (Anomodoryx) is described from the mesophotic zone off Bacia Potiguar (Rio Grande do Norte State, Northeastern Brazil). The specimen was preserved in ethanol 80% and deposited in the Porifera Collection of the Universidade Federal de Pernambuco (UFPEPOR).
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