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The diversity of Porifera from Ponta do Ouro (Mozambique) has been evaluated; this paper presents the first taxonomic effort devoted to sponges in the area, while studies of closeby areas are quite dated. Overall, 55 specimens were examined, leading to 26 described species; among these, four are new (Hyattella sulfurea Calcinai & Belfiore sp. nov., H. pedunculata Calcinai & Belfiore sp. nov., Amphimedon palmata Calcinai & Belfiore sp. nov. and Phoriospongia mozambiquensis Calcinai & Belfiore sp. nov.) and four (Chondrosia corticata Thiele, 1900, Callyspongia (Cladochalina) aerizusa Desqueyroux-Faundez, 1984, Clathria (Thalysias) hirsuta Hooper & Levi, 1993 and Ciocalypta heterostyla Hentschel, 1912) are new records for the Indian Ocean. For Callyspongia (Euplacella) abnormis Pulitzer-Finali, 1993, Callyspongia (Callyspongia) pulitzeri Van Soest & Hooper, 2020 and Amphimedon brevispiculifera (Dendy, 1905) this represents the first record after their initial discovery. The majority of the species have a wide distribution in the Indo-Pacific Ocean, but species from South and East Africa have also been recorded. These data highlight the characteristic of Ponta do Ouro as a transitional zone, located between a tropical and temperate biogeographic province, as well as the importance of increasing biodiversity knowledge of this biogeographic border to monitor possible shifts in the area as a consequence of climate crisis.
A new genus and species of Sternaspidae (Annelida: Polychaeta) from the deep eastern Atlantic
(2020)
Based on specimens recently collected in sediments from 2700 m depth off Mauritania (Northwest Africa; type locality) and from 2700–4400 m depth off Angola (Southwest Africa), a new genus and species, Mauretanaspis longichaeta gen. et spec. nov., is described. The new genus and species are characterized by a unique combination of characters: ventro-caudal shield covered by firmly adhering sediment, lateral margins strongly bent and merging into integument; introvert hooks tapering; eight pre-shield segments; absence of peg chaetae; exceptionally long posteriormost lateral chaetae equaling body length; posterior shield chaetae equaling shield length. A comparative table of characters for all currently recognised sternaspid genera and a key to all species with ventro-caudal shield covered by firmly adhering sediment are provided.
The endozoic ciliates of the family Clevelandellidae Kidder, 1938 typically inhabit the hindgut of wood-feeding panesthiine cockroaches. To assess the consistency of species delimitation in clevelandellids, we tested the utility of three sources of taxonomic data: morphometric measurements, cell geometrical information, and 18S rRNA gene sequences. The morphometric and geometrical data delimited the clevelandellid morphospecies consistently and unambiguously. However, only Paraclevelandia brevis Kidder, 1937 represented a homogenous taxon in both morphological and molecular analyses; the morphospecies Clevelandella constricta (Kidder, 1937) and C. hastula (Kidder, 1937) contained two or three distinct, more or less closely related genotypes each; and the genetic homogeneity of the morphospecies C. panesthiae (Kidder, 1937) and C. parapanesthiae (Kidder, 1937) was not corroborated by the 18S rRNA gene sequences at all. Moreover, the 18S rRNA gene phylogenies suggested the C. panesthiae-like morphotype to be the ancestral phenotype from which all other clevelandellid morphotypes arose. The only exception was the C. constricta-like morphotype, which very likely branched off before the diversification of the C. panesthiae-like progenitor. The present molecular analyses also suggested that a huge proportion of the clevelandellid diversity still waits to be discovered, since examination of only four panesthiine populations revealed 10 distinct clevelandellid genotypes/molecular species.
Two new species of Grandidierella Coutière, 1904 from Singapore waters are described based on specimens collected during the Comprehensive Marine Biodiversity Survey (CMBS) between 2010–2015. Grandidierella pawaiensis sp. nov. differs from the rest in the genus by a combination of characters; (1) gnathopod 1 carpus proximoventral corner with apically acute process, (2) inner face of carpus of gnathopod 1 proximoventral corner with curved process, (3) proximal margin of dactylus of gnathopod 1 male with excavation, and (4) gnathopod 2 basis anterior margin crenulate. Grandidierella sungeicina sp. nov. on the other hand, is distinguishable from other related species of Grandidierella found in the tropical region by its paired mid-dorsal projections on pereonites 2 to 5, 1 ventrodistal triangular projection on pereonite 4, and gnathopod 2 ischium with 1 large trapezoid projection.
An integrative redescription of Hypsibius pallidoides Pilato, Kiosya, Lisi, Inshina & Biserov, 2011 was undertaken following a reexamination of the type material and new material using highquality light microscopy, scanning electron microscopy and methods of molecular taxonomy. Detailed morphological investigations revealed a unique complex of characters that precluded the attribution of this species to the genus Hypsibius Ehrenberg, 1848. Furthermore, phylogenetic analyses indicated the affi nity of this species within the subfamily Pilatobiinae (Hypsibiidae). Notahypsibius gen. nov. is erected for H. pallidoides and two putatively related species: H. scaber Maucci, 1987 and Ramazzottius arcticus (Murray, 1907). An emended diagnosis for the genus Pilatobius is given, while the subfamily Pilatobiinae lacks a cohesive morphological diagnosis despite representing, at the same time, a wellsupported molecular clade. Obvious controversy between the results of the morphological and molecular analyses of the phylogeny of Hypsibioidea is discussed. The distribution of morphological characters such as the claw type, organization of the bucco-pharyngeal apparatus, and egg shell sculpture type within Eutardigrada is analyzed and their phylogenetic signifi cance discussed.
A revision was done on the species of Enteromius Cope, 1867 (Cypriniformes: Cyprinidae) from the Lake Edward system with a smooth, flexible third unbranched dorsal fin ray without serrations. Specimens with these characteristics had previously been attributed to E. perince and E. stigmatopygus. A combination of a genetic (COI, mtDNA) and a morphometric approach was used. Based on the COI gene, we found two groups with a distance of 8.5%, though neither of the two corresponded to E. perince or E. stigmatopygus. One group revealed to be conspecific with E. alberti, previously a synonym of E. stigmatopygus, described from the Rutshuru River, May-Ya-Moto (DRC, Lake Edward system), and revalidated here. In addition, E. cercops, described from the Nzoia River (Kenya, Lake Victoria basin), is put in synonymy with E. alberti. The second group was most similar to E. mimus, but differed morphologically somewhat from the types of E. mimus. Therefore, specimens of this group were identified as E. cf. mimus. Morphologically, E. alberti can be separated from E. cf. mimus based on a higher number of lateral line scales and smaller values for interorbital width, pre-pelvic distance, body depth, maximum and minimum caudal peduncle depth, head width and head depth.
The chewing louse species Lipeurus megalops Piaget, 1880, is redescribed and illustrated. This species has previously been placed in the genus Oxylipeurus Mjöberg, 1910, but marked differences in preantennal structure, male and female genitalia, abdominal chaetotaxy, and structure of abdominal plates indicate that this species is not closely related to other species in this genus. We therefore erect a new genus, Calidolipeurus gen. nov. for this species. Calidolipeurus is presently monotypic, containing only Calidolipeurus megalops gen. et comb. nov. We also provide a preliminary key to the Oxylipeurus-complex.
The geographical range of the typically host-specific species of chewing lice (Phthiraptera) is often assumed to be similar to that of their hosts. We tested this assumption by reviewing the published records of twelve species of chewing lice parasitizing wild and domestic chicken, one of few bird species that occurs globally. We found that of the twelve species reviewed, eight appear to occur throughout the range of the host. This includes all the species considered to be native to wild chicken, except Oxylipeurus dentatus (Sugimoto, 1934). This species has only been reported from the native range of wild chicken in Southeast Asia and from parts of Central America and the Caribbean, where the host is introduced. Potentially, this discontinuous distribution is due to a low tolerance for dry environments, possibly exacerbated by competitive exclusion by Cuclotogaster heterographus (Nitzsch, 1866). Our examinations of O. dentatus also revealed that this species differs significantly from other species of Oxylipeurus in the male and female genitalia, head structure and chaetotaxy, and other morphological characters. We therefore here erect the monotypic genus Gallancyra gen. nov. for O. dentatus, and redescribe the type species.
The first Oriental species of the genus Trichopsomyia Williston, 1888, Trichopsomyia pilosa sp. nov. (Java), has been discovered and is now described. This Oriental species of Trichopsomyia has several characters strongly differing from the other species within this genus. It is hypothesized that it forms a separate group within Trichopsomyia. One species, Trichopsomyia formiciphila Downes, Skevington & Thompson, 2017, from Australia, is similar to the Oriental species described here, and the group is named after this first described species, hence the formiciphila group. The characters for a future phylogenetic analysis are discussed. The character states of the pilosity of the katepisternum and the shape of the metasternum hitherto used in a phylogenetic analysis of Syrphidae Latreille, 1802 are discussed too.
We describe three new parastenocaridid: Cottarellicaris sanctiangeli Bruno & Cottarelli sp. nov., Stammericaris vincentimariae Bruno & Cottarelli sp. nov. and Proserpinicars specincola Bruno & Cottarelli sp. nov., collected in the pools of five different caves located in Calabria (Southern Italy). We conducted a phylogenetic analysis based on the mitochondrial COI and ribosomal 18S sequences of C. sanctiangeli sp. nov. and S. vincentimariae sp. nov., and of four more species of Stammericaris and one Proserpinicaris available from literature. Based on the molecular study, the specimens of C. sanctiangeli sp. nov. are clearly separated from the species belonging to the closely-related genus Stammericaris. The morphological and molecular data indicate that the genera belonging to the two subfamilies Parastenocaridinae and Fontinalicaridinae form two monophyletic and distinct clades, thus supporting their status. We also provide insights on the genus Proserpinicaris based on morphological data only; in particular, the most important synapomorphic character of the genus, i.e., the taxonomic value of the hyaline structure inserted on the anterior surface of the male leg 4 basis, is discussed based on the development of the P4 endopod, as observed in the last copepodid stage of some species of this genus. Finally, we widen the biogeographic and ecological knowledge of the three genera.