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1,918 results for “molecular evidence”
FIGURE 6 in Morphological and molecular evidence for the occurrence of three Hippocampus species (Teleostei: Syngnathidae) in Brazil
FIGURE 6. Hippocampus erectus: A. Hippocampus villosus Günther 1880, from Bahia, Brazil; holotype BMNH 1879.5.14.464 kindly provided by James Maclaine; B. from Florida, USA/Redpath Museum-Mc Gill University, kindly provided by Sara Lourie. C. H. erectus, couple from Brazil (Pernambuco); D. H. patagonicus; E. H. reidi from Brazil, couples of Rio Grande do Sul and Pernambuco States, respectively.
FIGURE 5. A in Morphological and molecular evidence for the occurrence of three Hippocampus species (Teleostei: Syngnathidae) in Brazil
FIGURE 5. A. Hippocampus erectus, male; B. Hippocampus reidi, female; from Figueiredo & Menezes (1980). C. Hippocampus patagonicus from Brazil, male 112 mm (Note: the dark diagonal streaks on the back of head and parallel streaks on the trunk and tail, and also the elongated dark spot at the top of the first dorsal fin rays described by Figueiredo & Menezes,1980 to H. erectus); D. H. patagonicus from Argentina, Holotype MACN 8808, kindly provided by Diego Luzzatto.
FIGURE 4 in Morphological and molecular evidence for the occurrence of three Hippocampus species (Teleostei: Syngnathidae) in Brazil
FIGURE 4. Neighbor-Joining tree of the Hippocampus species analyzed, using K2P distances. Bootstrap values>70 shown.
FIGURE 3 in Morphological and molecular evidence for the occurrence of three Hippocampus species (Teleostei: Syngnathidae) in Brazil
FIGURE 3. Hippocampus erectus: A. MCZ 35290; B. USNM161345; C. TCWC 7312.04; D. RMMU 2337a; E. PH 122e. Hippocampus reidi: F. MCZ 158435; G. USNM 131966a; H. USNM 131966b; I. MCZ 59348; J, PH 28r. Hippocampus patagonicus: K. MZUSP 51138; L. FURG 830206; M. RMMU 2859a; N. MCP 2687; O. PH 48p.
FIGURE 8 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 8. Gene tree for mtCOI showing proportional differences between individual females of Centropages mohamedi sp. nov. and C. orsinii from neritic waters of the central Red Sea. Numbers at branch points are bootstrap values (i.e., percentage of trees with that branch point among 1000 subreplicates). The specimen numbers correspond to those in Table 1.
FIGURE 7 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 7. SEM micrograph of Centropages mohamedi sp. nov. male from the Red Sea. (A) Rostrum, ventral view; (B) Basis of right leg 4, posterior view; (C) Fused exopodal segments 2 and 3 of male left leg 5; (D) Third exopodal segment of male right leg 5 (serration of distal part indicated by arrow).
FIGURE 5 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 5. Centropages mohamedi sp. nov. Female (holotype). (A) Leg 1; (B) Leg 2; (C) Leg 3; (D) Leg 4; (E) Leg 5; (F) Endopod of left leg 5; (G) Left medial process of second exopodal segment of female leg 5; (H) Right medial process of second exopodal segment of female leg 5. Scale bars in mm.
FIGURE 4 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 4. Centropages mohamedi sp. nov. Female (holotype). (A) Antenna; (B) Mandibular gnathobase; (C) Mandibular palp; (D) Maxillule; (E) Maxilla, (F) Maxilliped. Scale bars in mm.
FIGURE 3 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 3. SEM micrographs of Centropages mohamedi sp. nov. female. (A) Rostrum, lateral view; (B) Urosome, lateral view; (C) Genital double somite, lateral view, (D) Maxillipod basis (middle seta with proximal, spirally located spinule indicated by arrow), lateral view; (E) Medial process of second exopodal segment of female leg 5 indicated by arrow; (F) Enlarged medial process of second expodal segment of female leg 5.
FIGURE 2 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 2. Centropages mohamedi sp. nov. Female (holotype). (A) Habitus, dorsal view; (B) Habitus, lateral view; (C) Rostrum, lateral view; (D) Urosome, dorsal view; (E) Urosome, ventral view; (F) Urosome, lateral view; (G–H) Antennule. Scale bars in mm.
FIGURE 6 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 6. Centropages mohamedi sp. nov. Male (allotype). (A) Habitus, dorsal view; (B) Rostrum, ventro-lateral view; (C) Urosome, dorsal view; (D) Right antennule; (E) Right leg 4; (F) Basis of right leg 4, posterior view; (G) Leg 5, posterior view. Scale bars in mm.
FIGURE 1 in A new species of Centropages (Copepoda: Calanoida: Centropagidae) from the central Red Sea based on morphological and molecular evidence
FIGURE 1. Sampling sites of Centropages mohamedi sp. nov. and C. orsinii off Jeddah and entrance of Obhur Creek, central Red Sea.
FIGURES 1–4. H in Two closely related Homidia species (Entomobryidae, Collembola) revealed by morphological and molecular evidence
FIGURES 1–4. H. pseudofascia sp. nov., colour pattern: 1–3, adults; 1, lateral view; 2, dorsal view; 3, ventral view; 4, dorsal view of juvenile.
FIGURES 18–20. H in Two closely related Homidia species (Entomobryidae, Collembola) revealed by morphological and molecular evidence
FIGURES 18–20. H. pseudofascia sp. nov.: 18, chaetotaxy of Abd. IV–V; 19, manubrial plaque; 20, apical denes and mucro.
FIGURES 21–24. H in Two closely related Homidia species (Entomobryidae, Collembola) revealed by morphological and molecular evidence
FIGURES 21–24. H. fascia, colour pattern: 21–23, adults; 21, lateral view; 22–23, dorsal view; 24, dorsal view of juvenile.
FIGURES 5–12. H in Two closely related Homidia species (Entomobryidae, Collembola) revealed by morphological and molecular evidence
FIGURES 5–12. H. pseudofascia sp. nov.: 5, cephalic chaetotaxy; 6, basal Ant. II; 7, distal Ant. III; 8, apical bulb of Ant. IV; 9, prelabral and labral chaetae; 10, maxillary outer lobe; 11. labial chaetotaxy; 12, papilla E of labial palp.
FIGURES 25–29. H in Two closely related Homidia species (Entomobryidae, Collembola) revealed by morphological and molecular evidence
FIGURES 25–29. H. fascia: 25, prelabral and labral chaetae; 26, labial chaetae; 27, labial palp; 28, chaetotaxy of Abd. V; 29, manubrial plaque.
FIGURES 13–17. H in Two closely related Homidia species (Entomobryidae, Collembola) revealed by morphological and molecular evidence
FIGURES 13–17. H. pseudofascia sp. nov.: 13, chaetotaxy of Th. II–III; 14, trochanteral organ; 15, chaetotaxy of Abd. I–III; 16, anterior face of VT; 17, posterior face and lateral flap of VT.
FIGURE 8 in Uca (Xeruca), a new subgenus for the Taiwanese fiddler crab Uca formosensis Rathbun, 1921 (Crustacea: Decapoda: Ocypodidae), based on morphological and molecular evidence
FIGURE 8. Urocardiac ossicles of Uca tangeri (A, NCHUZOOL 13655, CW 26.9 mm, ♂), U. stylifera (B, NCHUZOOL 13578, CW 21.9 mm, ♂), U. acuta (C, NCHUZOOL 13665, CW 19.0 mm, ♂), U. lactea (D, NCHUZOOL 13213, CW 15.4 mm, ♂), U. tetragonon (E, NCHUZOOL 13666, CW 17.0 mm, ♀), and U. vocans (F, NCHUZOOL 13667, CW 20.2 mm, ♂). A, B, E, F, scale = 10 mm; C, D, scale = 5 mm.
FIGURE 4 in Uca (Xeruca), a new subgenus for the Taiwanese fiddler crab Uca formosensis Rathbun, 1921 (Crustacea: Decapoda: Ocypodidae), based on morphological and molecular evidence
FIGURE 4. Carapaces of Uca formosensis and other species with similar morphology. A, U. formosensis (NCHUZOOL 13672, CW 29.6 mm, left-handed; modified from Shih et al. 1999); B, U. bellator (NCHUZOOL 13653, CW 18.7 mm, lefthanded); C, U. seismella (USNM 137666, holotype, CW 13.0 mm, right-handed; modified from Crane 1975); D. U. polita (USNM 137667, holotype, CW 22.5 mm, right-handed; modified from Crane 1975); E, U. arcuata (NCHUZOOL 13660, CW 38.2 mm, left-handed); F, U. urvillei (NCHUZOOL 13661, CW 30.1 mm, left-handed); G, U. tetragonon (NCHUZOOL 13664, CW 18.3 mm, right-handed); H, U. jocelynae (NMNS 6177-001, holotype, CW 21.7 mm, right-handed).
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.