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2,185 results for “integrated taxonomy”
Figure 12 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 12. Hypostomus cari, new species, Holotype, NºP 25422, 127.3 mm SL, Parnaíba River, Alto Parnaiba, Maranhão, Brazil.
Figure 13 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 13. Colour in life of Hypostomus cari, Parnaíba River basin. A, ºFRN 5668, 111.7 mm SL, Mulato Creek, Amarante, Piauí, Brazil. B, ºFRN 3043, 111.7 mm SL, Cachoeira do Pintado, tributary to the Água Quente River, Barreiras do Piauí, Piauí, Brazil.
Figure 11 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 11. Type locality of Hypostomus pusarum, Ceará*Mirim River, Ceará*Mirim, Rio Grande do Norte, Brazil.
Figure 15 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 15. Type locality of Hypostomus cari, new species, Parnaíba River, Alto Parnaíba, Maranhão, Brazil.
Figure 8 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 8. Intraspecific variation of Hypostomus pusarum. A, lighter, smaller, and closely spaced spots in ventral region, 123.2 mm SL. B, darker, larger, and more widely spaced spots, 117.4 mm SL. ºFRN 608, ºmbuzeiro River, Jaguaribe River basin, São Nicolau, Ceará, Brazil.
Figure 6 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 6. Hypostomus pusarum photographed in life immediately asser capture. A, ºFPB 7886, 183.4 mm SL, Ceará*Mirim River basin, Ceará* Mirim, Rio Grande do Norte, Brazil. B, ºFRN 0607, 120.1 mm SL, ºmbuzeiro River, tributary of the Jaguaribe River, Aiuaba, Ceará, Brazil.
Figure 9 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 9. Intraspecific variation between individuals of Hypostomus pusarum collected in the same locality. A, dark spots on dorsum, 78.5 mm SL. B, no dark spots on body, spots only on tips of dorsal and caudal fins, 70.1 mm SL. ºFRN 5643, Lagoa de Remígio Dam, Remígio, Paraíba, Brazil.
Figure 7 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 7. Ontogenetic development of interradial spots on the dorsal fin of Hypostomus pusarum (A) ºFRN 0255, 62.6 mm SL, Seridó River, upstream of Ilha de Santana, Caicó, Rio Grande do Norte, Brazil, (B) ºFRN 1127, 116.9 mm SL, Ceará*Mirim River, between Ceará*Mirim and Taipu, Rio Grande do Norte, Brazil, and (C) ºFPB 7701, 170.4 mm SL, Ceará*Mirim River, Jardim de Angicos, Rio Grande do Norte, Brazil.
Figure 5 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 5. On the less, holotype of Plecostomus pusarum: CAS*Sº 22225, 142.6 mm SL. Ceará*Mirim River, Ceará*Mirim, Rio Grande do Norte, Brazil. Photo: Department of Ichthyology, California Academy of Sciences. On the right, topotype of Hypostomus pusarum: ºFRN 1127, 130.1 mm SL. Ceará*Mirim River, Estrela do Norte farm, between Ceará*Mirim and Taipu, Rio Grande do Norte.
Figure 3 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 3. Genetic distances (Kimura 2 parameters) among species of the genus Hypostomus from the NCCD ecoregion, the Hypostomus aff. pusarum, and other species of the São Francisco and Parnaíba ecoregions. Basin abbreviations: APO (Apodi*Mossoro), PAR (Piranhas*Acu), PBN (Paraiba do Norte), and SAFR (Sao Francisco).
Figure 4 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 4. Maximum likelihood tree with phylogenetic relationships of the Hypostomus pusarum complex and Hypostomus aff. pusarum. Ŋe tree is associated with the occurrence of populations. On the right, a haplotype network for the COI molecular marker of the species of the H. pusarum complex and Hypostomus aff. pusarum. Each circle represents a haplotype and the size of the circles is proportional to the number of individuals that have the haplotype. Black dashes between circles indicate mutational steps. Abbreviations of the hydrographic basins: Ceará* Mirim (CEA), Jaguaribe (JAG), Granjeiro (GÞ), Choró (CHO), Trairí (TÞ), Salgado (SAL), São Francisco (SFR) and Parnaíba (PNB). Ecoregion abbreviations: north*east Caatinga and Coastal Drainage (NCCD), São Francisco (SAFR) and Parnaíba (PNBA).
Figure 10 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 10. Distribution of Hypostomus pusarum in the three ecoregions: Northeastern Caatinga and Coastal Drainages (NCCD), São Francisco (SAFR) and Parnaíba (PNBA).
Figure 2 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 2. Phylogenetic tree with Bayesian inference for the COI marker, including Hypostomus aff. pusarum, the H. pusarum complex clade, and other congeners. Ŋe numbers above the branches are posterior probability values. Basin abbreviations: APO (Apodi*Mossoró), PAR (Piranhas*Açu), PBN (Paraíba do Norte), and SAFR (São Francisco). mGMYC, generalized mixed Yule coalescent multiple; sGMYC, generalized mixed Yule coalescent single; ABGD, automatic barcode gap discovery; bPTP, Bayesian implementation of Poisson tree processes; e mPTP, maximum likelihood implementation of Poisson tree processes.
Figure 1 in Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil
Figure 1. Principal component analysis (PCA) with morphological data of the Hypostomus pusarum complex and Hypostomus aff. pusarum. Basin abbreviations: SAFR (Sao Francisco).
Figure 10 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 10. Shells of Mioawateria species. (A) Mioawateria personata (Powell, 1942) holotype Institute of Geological and Nuclear Sciences Limited (GNS) TM3761; (B) Mioawateria blakeana (Dall, 1881) comb. n., Smithsonian National Museum of Natural History (USNM) 87427; (C) Mioawateria brachis (Dall, 1919) comb. n., holotype USNM 96486; (D) Mioawateria isogonia (Dall, 1908) comb. n., holotype USNM 123112. Scale bar = 3 mm.
Figure 9 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 9. Shells of deep-sea raphitomid species previously assigned to Gymnobela. (A) Spergo africana (Sysoev, 1996) comb. n., holotype Natural History Museum of the United Kingdom (NHMUK) 1993114; (B) Spergo bululi (Stahlschmidt, Poppe and Tagaro, 2018) comb. n., holotype Muséum National d'Histoire Naturelle (MNHN) IM-2000-30,406; (C) Spergo oculifera (Kantor and Sysoev, 1986) comb. n., holotype Zoological Museum of Moscow University (ZMMU) Lc 22338; (D) Austrobela fulvotincta (Dautzenberg and Fischer, 1896) comb. n., syntype Musée océanographique de Monaco (MOM) INV-18461; (E) Theta chrysopelex (Barnard, 1963) comb. n., holotype Iziko South African Museum ISAM A9857; (F) Theta homeotata (Watson, 1886) comb. n., holotype NHMUK 1887.2.9.1115; (G) Austrobela gypsata (Watson, 1881) comb. n., syntype NHMUK 1887.2.9.979–80; (H) Theta latistriata (Kantor and Sysoev, 1986) comb. n., holotype ZMMU Lc 22341. Scale bar = 10 mm.
Figure 8 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 8. Shells of Gymnobela species vouchers. (A) G. bairdii (Verrill and Smith, 1884), syntype Smithsonian National Museum of Natural History (UNSM) 37824; (B) G. rotundata Sysoev, 1990, holotype Zoological Museum of Moscow University (ZMMU) Lc 5718; (C) G. abyssorum (Locard, 1897), lectotype Muséum National d'Histoire Naturelle (MNHN) IM-2000-2750; (D) G. chyta (Watson, 1881), holotype Natural History Museum of the United Kingdom (NHMUK) 1887.2.9.1108; (E) G. granulisculpturata Sysoev, 1990, holotype ZMMU Lc 5725; (F) G. verecunda (Barnard, 1963), lectotype ISAM A9697; (G) G. mitrodeta Sysoev, 1997, holotype MNHN IM-2000-3121; (H) G. laticaudata Sysoev, 1990, holotype ZMMU Lc 5735; (I) G. engonia figured in Bouchet and Warén 1980 (fig. 123). Scale bar: A, C, F–G, I = 10 mm; B, H = 3.3 mm; D–E = 5 mm.
Figure 4 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 4. Shells of Gymnobela primary species hypotheses (PSHs)/species studied herein. (A) G. frielei (Verril, 1885), holotype Smithsonian National Museum of Natural History (USNM) 44653; (B) G4/ G. frielei Australian Museum (AMS) C.571666; (C) G4/G. frielei AMS C.571702; (D) G4/G. frielei AMS C.482314; (E) G4/G. frielei AMS C.571812; (F) G4/G. frielei AMS C.571677; (G) G4/G. glaucocreas (Barnard, 1963), holotype Iziko South African Museum (ISAM) A9821; (H) G3/G. angulosa Sysoev, 1988, holotype Zoological Museum of Moscow University (ZMMU) Lc-22363 (I) G3/G. angulosa AMS C.571649; (J) G3/ G. angulosa AMS C.571648; (K) G3/G. angulosa, Bavarian State Collection of Zoology (ZSM) mol 20070770. Scale bar = 10 mm.
Figure 2 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 2. Maximum likelihood (ML, left) tree and Bayesian consensus phylogram (BI, right) based on analyses of the concatenated sequence dataset. Numbers above branches indicate nodal support by Bayesian posterior probabilities (BPP) and ML bootstrap (BS). BPP values of 1 and BS values of 100% are represented by asterisks. Sequences of samples collected outside Australian waters are underlined. Samples whose shells are figured (scale bar = 10 mm) are in bold. The shell image of P1 has been digitally edited (grey area) to simulate an intact spire. Vertical bars mark distinct primary species hypotheses (PSHs) as delimited by the Automatic Barcode Gap Discovery (ABGD) method.
Figure 7 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 7. Bathymetric ranges of taxa studied herein as inferred from museum records of sequenced specimens. Primary species hypotheses (PSHs)/species represented by a single record are indicated with a circle.
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