The northeastern Atlantic and Mediterranean small mussel drills of the Ocinebrina aciculata complex are here revised and consist of at least 3 species. The type species, Ocinebrina aciculata (Lamarck, 1822), characterized by a slender shell with rounded whorls and primary and secondary spiral cords of approximately similar size, lives throughout the northeastern Atlantic and Mediterranean Sea at depths usually ranging between 0 and 105 m. Its synonymy is here stabilized by a neotype selection for Murex corallinus Scacchi, 1836. Ocinebrina corallinoides Pallary, 1912 (=Ocinebrina buzzurroi Cecalupo and Mariani, 2008, new synonymy), characterized by a strongly elongate and weakly convex shell and primary and secondary spiral cords of approximately similar size, is endemic to the Gulf of Gabès and is here considered a distinct species, pending genetic studies. Ocinebrina reinai n. sp. is here described from the central Mediterranean Sea (where it is sympatric with O. aciculata) on the basis of morphological diagnostic features of shell (rarest presence of labral tooth, commoner presence of infrasutural apertural denticle, dark spots on the ribs and spiral sculpture with differently sized primary and secondary cords and smaller threads) and radula, confirmed by genetic data. Divergence in COI sequences with sympatric samples of O. aciculata (>7%), confirm their status as a distinct species. A comparative table reporting diagnostic features of the congeneric species of the complex and those with which the new species was previously misidentified is offered.
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Five new species of Homoscleromorpha (Porifera) of four genera, Oscarella, Plakortis, Plakina and Corticium, are described from vertical walls of reef caves at depths ranging from 23 to 28 m in the Caribbean Sea. Oscarella nathaliae sp. nov. has a leaf-like thinly encrusting, flat body, loosely attached to the substrate and a perforated, not lobate surface. Oscarella nathaliae sp. nov. contains two bacterial morphotypes and is characterized by two mesohylar cell types with inclusions. Plakortis myrae sp. nov. has diods of two categories: abundant large ones (83–119 mm long) and rare small ones (67–71 mm long) with sinuous, S-bent centres; triods Y- or T-shaped (18–5 mm long), and abundant microrhabds (5–12 mm long). Plakortis edwardsi sp. nov. has diods of one category with thick, sinuous, S-bent centres (110 to 128 mm long); triods T-shaped (actines 28–59 mm long). It is the only species of this genus showing small diods (22–31 mm long). Plakortis dariae sp. nov. has diods of two categories: large ones (67–112 mm long) and small, rare, irregular ones, slightly curved, often deformed with one end blunt (30–59 mm long); triods rare and regular (actines 20–44 mm long long). Corticium diamantense sp. nov. has oscula situated near its border, regular non-lophose calthrops of one size class, very rare tetralophose calthrops and candelabra with the fourth actine ramified basally in 4–5 microspined rays. In addition, a re-description of Plakina jamaicensis Lehnert & van Soest 1998 is based on newly collected material and the type specimen. P. jamaicensis has a convoluted brainlike surface; well developed sub-ectosomal cavities; irregular sinuous diods, triods, calthrops, rare monolophose calthrops, rare dilophose calthrops, rare trilophose calthrops and common tetralophose calthrops. Molecular ‘barcoding’ sequences for mitochondrial cob are given for Plakortis edwardsi sp. nov., P. dariae sp. nov., Plakina jamaicensis and Corticium diamantense sp. nov. An identification key for all western Atlantic Homoscleromorpha is provided.
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