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513 results for “molecular characters”
Figure 7 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 7. Paratya walkeri sp. nov.: a, maxilliped 3; b, pereiopod 1; c, pereiopod 2; d, pereiopod 3; e, dactylus. Scale lines 0.2 mm.
Figure 6 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 6. Paratya walkeri sp. nov.: a, head region and rostrum; b, antenna 1 peduncle and stylocerite; c, scaphocerite; d, left mandible; e, enlarged incisors; f, right mandible; g, enlarged incisors; h, maxilla 1; i, maxilla 2; j, maxilliped 1; k, maxilliped 2. Scale lines 0.2 mm.
Figure 2 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 2. Neighbour-joining analysis of Paratya using Tamura-3-parameter, gamma distribution shape parameter of 0.81, homogenous pattern among lineages and 2000 bootstrap pseudoreplicates. Bootstrap values>72% displayed. Sequence data from Cook et al. (2006); Baker et al. (2004), Cook (2006), Hurwood et al. (2003), McCluskey (2007) and this study.
Figure 8 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 8. Paratya walkeri sp. nov.: a, pereiopod 4; b, dactylus 4; c, pereiopod 5; d, dactylus 5; e, telson; f, telson terminal spines; g, pleopod 1 of female. Scale lines 0.2 mm.
Figure 1 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 1. Maps: a, distribution of Paratya in Australia. Sources include data from Cook et al. (2006); Baker et al. (2004), Cook (2006), Hurwood et al. (2003), McCluskey (2007) and data from this study; b, distribution of Paratya specimens analysed in this study. Maps created in Cartographica.
Figure 5 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 5. Paratya australiensis: a–e, P. australiensis Kemp; f–j, P. australiensis Shoalhaven morphotype; a, rostrum; b, left mandible incisors; c, right mandible incisors; d, first pereiopod; e, second pereiopod; f, rostrum; g, left mandible incisors; h, right mandible incisors; i, first pereiopod; j, second pereiopod. Scale lines 0.2 mm.
Figure 3 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 3. Sub-tree of Paratya arrostra Riek, 1953, showing supported subclades. Themajority of material collected across a wide geographical area in this study grouped within a single clade (E), which is equivalent to Lineage 4B in Cook et al. (2006). Previous haplotypes from Cook et al. (2006) form the other sub-clades, but no specific geographical information is known for these sequences. Sub-clades A and B contain some specimens from this study.
Figure 4 in New species of Paratya (Decapoda: Atyidae) from Australian inland waters - linking morphological characters with molecular lineages
Figure 4. Sub-tree of Paratya tasmaniensis Riek, 1953, showing supported sub-clades. Sub-clade A predominantly has material from Tasmania but with a single specimen collected at Hamilton, Victoria. Sub-clade B contains specimens from the Glenelg River catchment, south-west Victoria through to the Hastings River in New South Wales. Sub-clade E contains sequences from Cook (2006) from the Strathbogie area, and sub-clades C and D are from Cook et al. (2006) and McCluskey (2007).
Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales.
Fig. 2. The 50 in Verification Of Four Species Of The Mud Lobster Genus Thalassina (Crustacea: Decapoda: Gebiidea: Thalassinidae) Using Molecular And Morphological Characters
Fig. 2. The 50% majority-rule consensus tree resulting from maximum likelihood analysis of (a) partial PEPCK sequences (substitution rate parameters: TC = 0.5206, TA = 0.1254, TG = 0.0125, CA = 0.1254, CG = 0.0125, AG = 0.2036), - Ln likelihood 1935.877; (b) partial NaK sequences (TC = 0.5183, TA = 0.1061, TG = 0.0727, CA = 0.0972, CG = 0.0223, AG = 0.1834), - Ln likelihood 2117.352; (c) partial COI sequences (TC = 0.7231, TA = 0.1315, TG = 1.4301e–5, CA = 0.0153, CG = 0.0311, AG = 0.0991), - Ln likelihood 2729.365; (d) combined PEPCK, NaK and COI DNA sequences (TC = 0.5687, TA = 0.1190, TG = 0.0211, CA = 0.1190, CG = 0.0211, AG = 0.1511), - Ln likelihood 6914.207. The bootstrap values (ML/MP/BI) are shown at the branches. Bar indicates substitutions per site.
Fig. 3 in Verification Of Four Species Of The Mud Lobster Genus Thalassina (Crustacea: Decapoda: Gebiidea: Thalassinidae) Using Molecular And Morphological Characters
Fig. 3. Locations of examined specimens of T. squamifera (circles) and T. kelanang (triangles) by various authors. Museum catalogue numbers at each site are indicated. = Poore & Griffin, 1979; ● = Ngoc-Ho & de Saint Laurent, 2009; = Moh & Chong, 2009; O = Sakai & Turkay, 2012; ▲ = Moh & Chong, 2009, this study. Dotted line indicates Wallace's Line. Modified base map from http:// commons.wikimedia.org.
Fig. 1 in Verification Of Four Species Of The Mud Lobster Genus Thalassina (Crustacea: Decapoda: Gebiidea: Thalassinidae) Using Molecular And Morphological Characters
Fig. 1. SFDA ordination diagram of morphological and meristic characters for four species of Thalassina.
Linked collectors and determiners for: Revision of the genus Dinotoperla Tillyard, 1921 (Plecoptera: Gripopterygidae) using morphological characters and molecular data: Establishes two new genera, three new species and updates the larval taxonomy.
Natural history specimen data linked to collectors and determiners held within, "Revision of the genus Dinotoperla Tillyard, 1921 (Plecoptera: Gripopterygidae) using morphological characters and molecular data: Establishes two new genera, three new species and updates the larval taxonomy". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/e57764ce-8c26-4ab9-a6d2-0b8a324f828c">https://bionomia.net/dataset/e57764ce-8c26-4ab9-a6d2-0b8a324f828c</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/e57764ce-8c26-4ab9-a6d2-0b8a324f828c">https://gbif.org/dataset/e57764ce-8c26-4ab9-a6d2-0b8a324f828c</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: A taxonomic review of the coastal genus Iotarphia Cameron (Coleoptera: Staphylinidae: Aleocharinae) with a description of new species based on morphological and molecular characters.
Natural history specimen data linked to collectors and determiners held within, "A taxonomic review of the coastal genus Iotarphia Cameron (Coleoptera: Staphylinidae: Aleocharinae) with a description of new species based on morphological and molecular characters". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/aea7d978-e7e9-460a-b618-c7ece0e0534c">https://bionomia.net/dataset/aea7d978-e7e9-460a-b618-c7ece0e0534c</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/aea7d978-e7e9-460a-b618-c7ece0e0534c">https://gbif.org/dataset/aea7d978-e7e9-460a-b618-c7ece0e0534c</a>. Formatted as a Frictionless Data package.
Figure 2 in A new species of freshwater crab (Decapoda: Brachyura: Potamidae) from Dongyin Island, Matsu, Taiwan, defined by morphological and molecular characters, with notes on its biogeography
Figure 2. Nanhaipotamon dongyinense sp. nov.: (A–F) holotype male (31.3×25.8 mm) (NMNS 4557-001); (G, H) allotype female (26.5×22.2 mm) (NMNS 4557-002). (A) Third maxilliped; (B) male abdomen; (C) left G1, in situ; (D) left G1; (E) left G1, distal segment; (F) left G2; (G) female abdomen; (H) female gonopore.
Figure 3 in A new species of freshwater crab (Decapoda: Brachyura: Potamidae) from Dongyin Island, Matsu, Taiwan, defined by morphological and molecular characters, with notes on its biogeography
Figure 3. (A–C) Dorsal, frontal and ventral views of the fresh-preserved male paratype (CW 36.28 mm) (NMNS 4557-003) of Nanhaipotamon dongyinense sp. nov., Dongyin Island, Matsu, Taiwan; (D) live coloration of the female paratype (CW 29.66 mm) (NMNS 4557-008); (E) habitat; (F) a chimney around the entrance of burrow.
Figure 1 in A new species of freshwater crab (Decapoda: Brachyura: Potamidae) from Dongyin Island, Matsu, Taiwan, defined by morphological and molecular characters, with notes on its biogeography
Figure 1. Collection sites for Nanhaipotamon species used in this study. For locality names see Table I.
Figure 24 in Revision of the genus Bosmina Baird, 1845 (Cladocera: Bosminidae), based on evidence from male morphological characters and molecular phylogenies
Figure 24. Bosmina (Eubosmina) tanakai sp. nov.: adult male from Ichiyanagi Numa Pond, Aomori Prefecture, Japan. A, antenna II; B, distal anterior seta; C–E, limb I; F, tip of copulatory hook; G, subdistal lobe in distal view. Scale bars: 100 Mm.
Figure 22 in Revision of the genus Bosmina Baird, 1845 (Cladocera: Bosminidae), based on evidence from male morphological characters and molecular phylogenies
Figure 22. Bosmina (Eubosmina) tanakai sp. nov.: female from Ichiyanagi Numa Pond, Aomori Prefecture, Japan (A, D–G), and from Konuma (B) and Kussharo (C), Hokkaido Prefecture, Japan. A–C, body outline of large adult; D, E, postabdonem of large adult; F, midgut with loops of an atypical specimen; G, juvenile female. Scale bars: 100 Mm.
Figure 21 in Revision of the genus Bosmina Baird, 1845 (Cladocera: Bosminidae), based on evidence from male morphological characters and molecular phylogenies
Figure 21. Bosmina (Eubosmina) tanakai sp. nov.: ephippial female from Ichiyanagi Numa Pond, Aomori Prefecture, Japan. A, lateral view; B, head, lateral view; C, D, head, anterior view; E, F, region of lateral head pore; G, setae at anteroventral portion of valve; H, I, mucro, inner view. Scale bars: 100 Mm.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.