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752 results for “Nemacheilidae”
Fig. 3 in Kapuasia, a genus name for 'Nemacheilus' maculiceps (Teleostei: Nemacheilidae)
Fig. 3. Kapuasia maculiceps, Borneo: Kapuas drainage. ZRC 56404, 69.7 mm SL. Note that nostril condition (fused nares) is anomalous.
Fig. 4 in Kapuasia, a genus name for 'Nemacheilus' maculiceps (Teleostei: Nemacheilidae)
Fig. 4. Kapuasia maculiceps; a, ZRC 61464, 64.3 mm SL; mouth; b, ZRC 65285, 86.6 mm SL; close up of anterior part of lower lip. Arrow: mental groove.
Fig. 6. Kapuasia maculiceps, ZRC 61464, 56.2 in Kapuasia, a genus name for 'Nemacheilus' maculiceps (Teleostei: Nemacheilidae)
Fig. 6. Kapuasia maculiceps, ZRC 61464, 56.2. mm SL; pectoral fin, dorsal view; note tubercles near tip of first and second branched rays.
Figure 2 in Karstsinnectes cehengensis (Cypriniformes: Nemacheilidae), a new species of cave fish from Guizhou, China
Figure 2. Phylogenetic tree reconstructed based on mitogenome and seven nuclear genefragments. In this phylogenetic tree, Bayesian posterior probabilities (BPP) from BI analyses/ultrafast bootstrap supports (UBP) from ML analyseswere noted beside nodes. The scale bar represents 0.04 nucleotide substitutions per site. Numbers within parentheses correspond to the ID numbers in Table 2.
Figure 1 in Karstsinnectes cehengensis (Cypriniformes: Nemacheilidae), a new species of cave fish from Guizhou, China
Figure 1. Distribution of the species of Karstsinnectes in Southwest China, with its potential distribution regions.
Figure 4 in Karstsinnectes cehengensis (Cypriniformes: Nemacheilidae), a new species of cave fish from Guizhou, China
Figure 4. The three-dimensional reconstructed model of the skeleton of Karstsinnectes cehengensis Luo, Zhao & Zhou, sp. nov. (paratype GZNU20230223003, standard length 33.5 mm). A. Dorsal view; B. Ventral view; C. Latera view.
Figure 5 in Karstsinnectes cehengensis (Cypriniformes: Nemacheilidae), a new species of cave fish from Guizhou, China
Figure 5. Karstsinnectes cehengensis Luo, Zhao & Zhou, sp. nov. (A–B) and K. anophthalmus (C) in life. A from holotype GZNU2023 0106002. A, C were photographed by Tao Luo, B by Jiajun Zhou.
Figure 3 in Karstsinnectes cehengensis (Cypriniformes: Nemacheilidae), a new species of cave fish from Guizhou, China
Figure 3. Morphological characteristics of holotype GZNU20230106002 of Karstsinnectes cehengensis Luo, Zhao & Zhou, sp. nov. in preservative (10% formalin), photographed by Tao Luo. A. Latera view; B. Dorsal view; C. Ventral view. Scale bars = 5.0 mm.
Figure 3 in The complete mitochondrial genome of Barbatula quignardi (Băcescu-Meşter, 1967) (Teleostei, Nemacheilidae)
Figure 3. – Maximum Likelihood phylogenetic tree of Barbatula mitogenomes; bootstrap values beside the nodes.
Figure 1 in The complete mitochondrial genome of Barbatula quignardi (Băcescu-Meşter, 1967) (Teleostei, Nemacheilidae)
Figure 1. – Voucher of the sequenced mitogenome, MNHN- IC-2010-1064 (FFFtag4260), 41.7 mm SL, Lez River at Prades-leLez (Hérault Dept.), 24th Nov. 2010, Denys and ONEMA coll.
Figure 5 in Barbatula leoparda (Actinopterygii, Nemacheilidae), a new endemic species of stone loach of French Catalonia
Figure 5. – Distribution map of the three recognized Barbatula spp. in France and Spain adapted and modified from Kottelat and Freyhof (2007): Barbatula leoparda in yellow, Barbatula barbatula in blue and Barbatula quignardi in orange. Locations: Têt River at Nefiach (1), Tech River at Céret (2) and at Elne (3).
Figure 2 in Barbatula leoparda (Actinopterygii, Nemacheilidae), a new endemic species of stone loach of French Catalonia
Figure 2. – Specimens of Barbatula spp. in ventral view. A: Holotype of Barbatula leoparda MNHN 2018- 0228, 62.6 mm SL ♀, Têt River at Nefiach, 7 Sep. 2016, Denys and ONEMA coll.; B: Barbatula barbatula MNHN 2013-0826, 72.9 mm SL ♂, stream Clauge (Rhône drainage) at La Loye, 1 Jul. 2013, Denys and ONEMA coll.; C: Holotype of Barbatula quignardi MGAB77, 52 mm SL ♂, Lez River, Jul. 1962, Băcescu coll.
Fig. 5 in Phylogeography of (Nemacheilidae): Responded to the Mid-Pleistocene Climate Transition in the Qinghai-Tibetan Plateau.
Fig. 5. Bayesian Skyline Plot (BSP) of the Tibetan stone loaches, T. stenura based on mtDNA (COI, Cyt b). The maximum time is set to the upper 95% HPD of the root height. The median estimate (solid line) and 95% HPD limits (Color area) are indicated. (a) Yangtze River populations (clade 4); (b) Subansiri River population (clade 3); (c) Nu River populations (clade 2); (d) the southwestern and central QTP populations (clade 1).
Fig. 3 in Phylogeography of (Nemacheilidae): Responded to the Mid-Pleistocene Climate Transition in the Qinghai-Tibetan Plateau.
Fig. 3. Bayesian estimates of divergence time for the lineages of T. stenura based on the mitochondrial genes (COI, Cyt b) data set. Dusty purple bars represent 95% highest posterior density for divergence estimates. The numbers on the nodes are million years ago (Mya).
Fig. 2 in Phylogeography of (Nemacheilidae): Responded to the Mid-Pleistocene Climate Transition in the Qinghai-Tibetan Plateau.
Fig. 2. ML tree for T. stenura on QTP and in its adjacent drainages based on a combination of genes including two mitochondrial genes (COI, Cyt b) and recombination activating protein 1 gene (Rag1-701 bp). Clade credibility values of major lineages are given for nodes with bootstrap support for ML (above branch) and posterior probability for Bayesian inferences (below branch). Major clades referred to in the text are listed to the right. Different colors were assigned for each clade: Clade 1, green; Clade 2, red; Clade 3, black; Clade 4, blue; Outgroups, black.
Fig. 4 in Phylogeography of (Nemacheilidae): Responded to the Mid-Pleistocene Climate Transition in the Qinghai-Tibetan Plateau.
Fig. 4. TCS network generated by Popart based on cytochrome b haplotypes for the T. stenura in QTP. Numbers in the networks represent haplotype designations and the areas of the circles are proportional to haplotype frequency; Black dots represent missing intermediate haplotypes.
Fig. 1 in Phylogeography of (Nemacheilidae): Responded to the Mid-Pleistocene Climate Transition in the Qinghai-Tibetan Plateau.
Fig. 1. Map of the study area and geographical distribution of sampling sites in this study. The sites are numbered according to table 1.
Figure 1 in Condition factor and length-weight relationships evaluation of 15 Oxynoemacheilus species (Cypriniformes: Nemacheilidae) from Iran
Figure 1. Box plot of (a) allometric coefficient b values, (b) Fulton's condition factor (K F) for 15 Oxynoemacheilus species from Iran.
Linked collectors and determiners for: Schistura madhavai, a new species of hill-stream loach from Sri Lanka, with redescription of S. notostigma (Teleostei: Nemacheilidae).
Natural history specimen data linked to collectors and determiners held within, "Schistura madhavai, a new species of hill-stream loach from Sri Lanka, with redescription of S. notostigma (Teleostei: Nemacheilidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/6e8828fd-d525-4cb4-be04-1febefc3b77e">https://bionomia.net/dataset/6e8828fd-d525-4cb4-be04-1febefc3b77e</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/6e8828fd-d525-4cb4-be04-1febefc3b77e">https://gbif.org/dataset/6e8828fd-d525-4cb4-be04-1febefc3b77e</a>. Formatted as a Frictionless Data package.
Fig. 3. Nemacheilus tebo, MZB 13367 in Nemacheilus Tebo, A New Loach From Sangkulirang Karst, East Kalimantan, Indonesia (Teleostei: Nemacheilidae)
Fig. 3. Nemacheilus tebo, MZB 13367, holotype, 56.1 mm SL; Indonesia: Kalimantan Timur: Lake Tebo area, site 2.
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