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Fig. 2 in Taxonomy and biostratigraphy of the elasmobranchs and bony fishes (Chondrichthyes and Osteichthyes) of the lower-to-middle Eocene (Ypresian to Bartonian) Claiborne Group in Alabama, USA, including an analysis of otoliths
Fig. 2. Tallahatta Formation surface exposures in Alabama, with sampled localities indicated by closed circles.
Fig. 22 in Taxonomy and biostratigraphy of the elasmobranchs and bony fishes (Chondrichthyes and Osteichthyes) of the lower-to-middle Eocene (Ypresian to Bartonian) Claiborne Group in Alabama, USA, including an analysis of otoliths
Fig. 22. Stenoscyllium cf. S. priemi Noubhani & Cappetta, 1997, teeth. A–C. MSC 35760.1, lower Tallahatta Formation. A. Labial view. B. Mesial view. C. Lingual view. D–F. MSC 35760.2, lower Tallahatta Formation. D. Labial view. E. Distal view. F. Lingual view. Scale bars = 2 mm.
Fig. 26 in Taxonomy and biostratigraphy of the elasmobranchs and bony fishes (Chondrichthyes and Osteichthyes) of the lower-to-middle Eocene (Ypresian to Bartonian) Claiborne Group in Alabama, USA, including an analysis of otoliths
Fig. 26. Carcharhinus mancinae sp. nov. referred specimens. A–C. MSC 38426.16, upper lateral tooth, basal Gosport Sand. A. Lingual view. B. Labial view. C. Mesial view. D–F. MSC 38424.1, upper lateral tooth, basal Gosport Sand. D. Lingual view. E. Labial view. F. Mesial view. G–I. MSC 38424.5, upper lateral tooth, basal Gosport Sand. G. Lingual view. H. Labial view. I. Mesial view. J–L. MSC 38424.3, upper lateral tooth, basal Gosport Sand. J. Lingual view. K. Labial view. L. Mesial view. M–O. MSC 38426.3, symphysial? tooth, basal Gosport Sand. M. Lingual view. N. Labial view. O. Mesial view. P–R. MSC 38426.2, lower anterior tooth, basal Gosport Sand. P. Lingual view. Q. Labial view. R. Mesial view. S–U. MSC 37522.3, upper lateral tooth, basal Gosport Sand. S. Lingual view. T. Labial view. U. Mesial view. V–X. MSC 38424.2, lower lateral tooth, basal Gosport Sand. V. Lingual view. W. Labial view. X. Mesial view. Y–AA. MSC 37522.1, lower posterolateral tooth, basal Gosport Sand. Y. Lingual view. Z. Labial view. AA. Mesial view. BB–DD. MSC 38426.4, upper lateral tooth, basal Gosport Sand. BB. Lingual view. CC. Labial view. DD. Mesial view. EE–GG. MSC 38416, lower anterior tooth, basal Gosport Sand. EE. Lingual view. FF. Labial view. GG. Mesial view. HH–JJ. MSC 188.40, lower anterolateral tooth, basal Gosport Sand. HH. Lingual view. II. Labial view. JJ. Mesial view. Scale bars = 1 cm.
Fig. 23 in Taxonomy and biostratigraphy of the elasmobranchs and bony fishes (Chondrichthyes and Osteichthyes) of the lower-to-middle Eocene (Ypresian to Bartonian) Claiborne Group in Alabama, USA, including an analysis of otoliths
Fig. 23. Galeorhinus de Blainville, 1816 and Pachygaleus Cappetta, 1992, teeth. A–F. Galeorhinus aff. G. duchaussoisi Adnet & Cappetta, 2008. A–C. MSC 35756.1, lower Tallahatta Formation. A. Labial view. B. Lingual view. C. Mesial view. D–F. MSC 37691, basal Lisbon Formation. D. Labial view. E. Lingual view. F. Mesial view. — G–J. G. louisi Adnet & Cappetta, 2008, MSC 37353.2, lower Tallahatta Formation. G. Labial view. H. Lingual view. I. Mesial view. J. Close–up of labial wrinkling. — K–M. G. aff. G. duchaussoisi, MSC 37353.4, Tallahatta Formation. K. Labial view. L. Lingual view. M. Mesial view. — N–P. Galeorhinus ypresiensis (Casier, 1946), MSC 37693.1, Gosport Sand. N. Labial view. O. Lingual view. P. Mesial view. — Q–V. Pachygaleus lefevrei (Diameries, 1891). Q–S. MSC 37688, basal Lisbon Formation. Q. Labial view. R. Lingual view. S. Mesial view. T–V. MSC 35763, lower Tallahatta Formation. T. Labial view. U. Lingual view. V. Mesial view. Scale bars = 2 mm.
Appendix 1 in Taxonomy and biostratigraphy of the elasmobranchs and bony fishes (Chondrichthyes and Osteichthyes) of the lower-to-middle Eocene (Ypresian to Bartonian) Claiborne Group in Alabama, USA, including an analysis of otoliths
<p><b>Appendix 1</b> (continued) Number of non-otolith taxa identified to lowest taxonomic ranking within each Claiborne Group unit. Shaded areas represent the stratigraphic range of taxa within Claiborne Group units in Alabama, USA.</p><table><thead><tr><th><b>Taxon</b></th><th colspan="5"><b>Meridian lower upper Tallahatta “lower” Tallahatta Sand Tallahatta Tallahatta /Lisbon Lisbon Fm. Member Fm. Fm. contact Fm.</b></th><th><b>“upper” Lisbon Fm.</b></th><th><b>Lisbon/ Gosport contact</b></th><th><b>lower Gosport Gosport Sand Sand</b></th><th><b>Total</b></th></tr></thead><tbody><tr><th>Lamnidae indet.</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>2</td><td><b>2</b></td></tr><tr><th><i>Macrorhizodus praecursor</i> Carcharhiniformes indet.</th><td>1</td><td>1</td><td></td><td></td><td>1 3</td><td>2</td><td>1</td><td>2 13 2</td><td><b>20 6</b></td></tr><tr><th><i>Premontreia</i> (<i>Oxyscyllium</i>) <i>subulidens</i></th><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td><b>1</b></td></tr><tr><th><i>Stenoscyllium</i> cf. <i>S. priemi</i></th><td></td><td>3</td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>3</b></td></tr><tr><th><i>Galeorhinus</i> aff. <i>G. duchaussoisi</i></th><td></td><td>2</td><td>1</td><td></td><td>4</td><td></td><td></td><td>3</td><td><b>10</b></td></tr><tr><th><i>Galeorhinus louisi</i></th><td></td><td></td><td>2</td><td></td><td></td><td></td><td></td><td></td><td><b>2</b></td></tr><tr><th><i>Galeorhinus ypresiensis</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td colspan="2">3 <b>3</b></td></tr><tr><th><i>Pachygaleus lefeveri</i></th><td></td><td>3</td><td></td><td></td><td>1 5</td><td></td><td></td><td></td><td><b>9</b></td></tr><tr><th><i>Hemipristis curvatus</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>6</td><td><b>6</b></td></tr><tr><th>Carcharhinidae indet.</th><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td><b>1</b></td></tr><tr><th><i>Carcharhinus mancinae</i> sp. nov.</th><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td>101 1</td><td><b>103</b></td></tr><tr><th><i>Negaprion gilmorei</i></th><td></td><td></td><td></td><td></td><td>6 18</td><td>1</td><td>2</td><td>1389 104</td><td><b>1519</b></td></tr><tr><th><i>Rhizoprionodon ganntourensis Scoliodon conecuhensis Abdounia beaugei</i></th><td></td><td>9 23 13</td><td>1</td><td></td><td>3 63 4 66 1 11</td><td></td><td>1</td><td>74 5 30 6 3 22</td><td><b>156 130 50</b></td></tr><tr><th><i>Abdounia enniskilleni</i></th><td></td><td></td><td></td><td></td><td>2 7</td><td>5</td><td></td><td>257 31</td><td><b>302</b></td></tr><tr><th><i>Abdounia minutissima Abdounia</i> sp.</th><td></td><td>7</td><td>1 1</td><td></td><td>3 40 10 2</td><td></td><td>1</td><td colspan="2">2 17 <b>71</b> 8 5 <b>26</b></td></tr><tr><th><i>Pseudabdounia claibornensis</i> gen. et comb. nov.</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>88 1</td><td><b>89</b></td></tr><tr><th><i>Pseudabdounia recticona</i> gen. et comb. nov.</th><td></td><td>6</td><td>1</td><td></td><td>26 133</td><td></td><td>2</td><td></td><td>168</td></tr></tbody></table>
Appendix 2 in Taxonomy and biostratigraphy of the elasmobranchs and bony fishes (Chondrichthyes and Osteichthyes) of the lower-to-middle Eocene (Ypresian to Bartonian) Claiborne Group in Alabama, USA, including an analysis of otoliths
<p><b>Appendix 2</b> (continued on next four pages) Number of non-otolith taxa identified to lowest taxonomic ranking from each Claiborne Group locality in Alabama, USA.</p><table><thead><tr><th><b>Taxon</b></th><th colspan="16"><b>ADl-1 Amo-8 ACh-7 Ach-14 Acon-6 Acov-1 ACov-11 Ach-8 ACl-3 AWa-2 AMo-4 ACl-4 Ach-21 Acl-14 Acl-15 Total</b></th></tr></thead><tbody><tr><th>Chondrichthyes indet.</th><td>1821</td><td>28</td><td>1</td><td></td><td></td><td></td><td>512</td><td></td><td></td><td></td><td>22</td><td>135</td><td>2</td><td></td><td>83</td><td><b>2604</b></td></tr><tr><th><i>Heterodontus</i> sp.</th><td>2</td><td></td><td></td><td></td><td></td><td></td><td>3</td><td></td><td></td><td></td><td></td><td>1</td><td>1</td><td></td><td></td><td><b>7</b></td></tr><tr><th><i>Orectolobus ziegenhinei</i></th><td></td><td></td><td></td><td>1</td><td></td><td></td><td>179</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>180</b></td></tr><tr><th><i>Ginglymostoma maroccanum</i></th><td>8</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>8</b></td></tr><tr><th><i>Ginglymostoma</i> sp.</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>21</td><td></td><td></td><td></td><td><b>21</b></td></tr><tr><th><i>Nebrius thielensi</i></th><td>30</td><td>1</td><td></td><td>1</td><td></td><td></td><td>115</td><td></td><td></td><td></td><td></td><td>22</td><td>1</td><td></td><td></td><td><b>170</b></td></tr><tr><th><i>Orectolobidae</i> indet.</th><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>1</b></td></tr><tr><th>Lamniformes indet.</th><td>149</td><td></td><td></td><td></td><td></td><td></td><td>96</td><td></td><td></td><td></td><td></td><td>6</td><td></td><td></td><td>3</td><td><b>254</b></td></tr><tr><th><i>Otodus</i> (<i>Otodus</i>) sp.</th><td>8</td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>9</b></td></tr><tr><th><i>Otodus</i> (<i>Carcharocles</i>) sp.</th><td></td><td></td><td>1</td><td>1</td><td>3</td><td></td><td>15</td><td></td><td></td><td></td><td></td><td></td><td>4</td><td></td><td></td><td><b>24</b></td></tr><tr><th><i>Anomotodon</i> sp.</th><td>2</td><td></td><td></td><td></td><td></td><td></td><td>2</td><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td>1</td><td><b>6</b></td></tr><tr><th><i>Striatolamia macrota</i></th><td>959</td><td></td><td></td><td>2</td><td>3</td><td>4</td><td>412</td><td>2</td><td>52</td><td>1</td><td>32</td><td>455</td><td>161</td><td></td><td>40</td><td><b>2123</b></td></tr><tr><th>Odontaspididae indet.</th><td>1</td><td></td><td></td><td></td><td></td><td></td><td>5</td><td></td><td>1</td><td></td><td>1</td><td>8</td><td>65</td><td></td><td>2</td><td><b>83</b></td></tr><tr><th><i>Brachycarcharias atlasi</i></th><td>61</td><td></td><td></td><td></td><td></td><td></td><td>48</td><td></td><td></td><td></td><td></td><td>4</td><td></td><td></td><td></td><td><b>113</b></td></tr><tr><th><i>Brachycarcharias lerichei</i></th><td>747</td><td></td><td></td><td></td><td>2</td><td></td><td>551</td><td></td><td>3</td><td></td><td></td><td>49</td><td>8</td><td>3</td><td>7</td><td><b>1370</b></td></tr><tr><th><i>Brachycarcharias twiggsensis</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>6</td><td>15</td><td></td><td></td><td><b>21</b></td></tr><tr><th><i>Hypotodus verticalis</i></th><td>46</td><td></td><td></td><td>2</td><td></td><td></td><td>70</td><td></td><td>1</td><td></td><td></td><td>1</td><td>1</td><td></td><td></td><td><b>121</b></td></tr><tr><th><i>Jaekelotodus robustus</i></th><td>21</td><td></td><td></td><td></td><td></td><td></td><td>115</td><td></td><td>11</td><td></td><td>3</td><td>2</td><td>5</td><td></td><td></td><td><b>157</b></td></tr><tr><th><i>Mennerotodus</i> sp.</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>5</td><td></td><td></td><td><b>5</b></td></tr><tr><th><i>Odontaspis winkleri</i></th><td>3</td><td></td><td></td><td></td><td></td><td></td><td>2</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>5</b></td></tr><tr><th><i>Tethylamna dunni</i></th><td>1</td><td></td><td></td><td></td><td>1</td><td></td><td>81</td><td></td><td>5</td><td></td><td></td><td>3</td><td>5</td><td></td><td></td><td><b>96</b></td></tr><tr><th>Lamnidae indet.</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>2</td><td></td><td></td><td></td><td><b>2</b></td></tr><tr><th><i>Macrorhizodus praecursor</i></th><td>1</td><td></td><td></td><td>1</td><td></td><td></td><td>1</td><td></td><td>2</td><td></td><td>2</td><td></td><td>12</td><td></td><td>1</td><td>20</td></tr><tr><th>Scombridae indet.</th><td></td><td></td><td></td><td></td><td></td><td></td><td>2</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>2</b></td></tr><tr><th><i>Palaeocybium proosti</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td></td><td>4</td><td>1</td><td></td><td></td><td><b>6</b></td></tr><tr><th><i>Scomberomorus bleekeri</i></th><td>5</td><td>3</td><td>1</td><td>3</td><td></td><td></td><td>134</td><td></td><td></td><td></td><td></td><td>4</td><td></td><td></td><td></td><td><b>150</b></td></tr><tr><th><i>Scomberomorus stormsi</i></th><td>3</td><td></td><td></td><td></td><td></td><td></td><td>7</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>2</td><td><b>12</b></td></tr><tr><th><i>Scomberomorus</i> sp.</th><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>1</b></td></tr><tr><th><i>Gymnosarda</i> sp.</th><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>1</b></td></tr><tr><th><i>Fisherichthys</i> aff. <i>F. folmeri</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>5</td><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td><b>6</b></td></tr><tr><th>Ostraciidae indet.</th><td>3</td><td></td><td></td><td>1</td><td></td><td></td><td>5</td><td></td><td></td><td></td><td></td><td>1</td><td>1</td><td>1</td><td></td><td><b>12</b></td></tr><tr><th>Balistidae indet.</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td></td><td></td><td><b>1</b></td></tr><tr><th><i>Progymnodon hilgendorphi</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>2</td><td>118</td><td>1</td><td></td><td></td><td><b>121</b></td></tr><tr><th>Teleostei indet.</th><td>17</td><td>793</td><td></td><td>1</td><td>1</td><td></td><td>171</td><td>19</td><td></td><td></td><td>8</td><td>87</td><td>33</td><td></td><td>3</td><td>1133</td></tr><tr><th>Totals</th><td>5689</td><td>853</td><td>3</td><td>52</td><td>25</td><td>5</td><td>6394</td><td>33</td><td>107</td><td>1</td><td>120</td><td>5747</td><td>836</td><td>4</td><td>497</td><td>20366</td></tr></tbody></table><p><b>Appendix 2</b> (continued)</p><p>Number of non-otolith taxa identified to lowest taxonomic ranking from each Claiborne Group locality in Alabama, USA.</p>
Fig. 6 in Contributions to the systematic of Pimelodidae (Osteichthyes, Siluriformes): basic and molecular cytogenetics on seven species of Pimelodus from three Brazilian hydrographic systems
Fig. 6. Idiogram for the seven studied Pimelodus species with data obtained with different methodologies. Heterochromatin (black), 5S rDNA (red) and 18S rDNA (green).
Fig. 1. Karyotypes arranged from Giemsa-stained chromosomes. a in Contributions to the systematic of Pimelodidae (Osteichthyes, Siluriformes): basic and molecular cytogenetics on seven species of Pimelodus from three Brazilian hydrographic systems
Fig. 1. Karyotypes arranged from Giemsa-stained chromosomes. a. Pimelodus absconditus; b. Pimelodus britskii; c. Pimelodus maculatus; d. Pimelodus microstoma; e. Pimelodus mysteriosus; f. Pimelodus ortmanni; g. Pimelodus paranaensis. Pairs of the AgNORs and B chromosomes are in the boxes. Scales bar = 10 μm.
Fig. 4. C in Contributions to the systematic of Pimelodidae (Osteichthyes, Siluriformes): basic and molecular cytogenetics on seven species of Pimelodus from three Brazilian hydrographic systems
Fig. 4. C-banded metaphase of Pimelodus ortmanni. Arrows indicate the heterochromatic B chromosomes. Scales bar = 10 μm.
Data from: Molecular phylogenetics and biogeography of galaxiid fishes (Osteichthyes: Galaxiidae): dispersal, vicariance, and the position of Lepidogalaxias salamandroides
The galaxiid fishes exhibit a gondwanan distribution. We use mitochondrial DNA sequences to test conflicting vicariant and dispersal biogeographic hypotheses regarding the southern hemisphere range of this freshwater group. Although phylogenetic resolution of cytochrome b and 16S rRNA sequences is largely limited to more recent divergences, our data indicate that the radiation can be interpreted as a number of relatively recent dispersal events superimposed on an ancient gondwanan radiation. Genetic relationships contradict the findings of recent morphological analyses of galaxioid fishes. In particular, a number of hypotheses regarding phylogenetic placement of the enigmatic Lepidogalaxias are examined. While most workers consider Lepidogalaxias to be an unusual scaled member of the southern hemisphere galaxioids, it has also been suggested that this species is related to the northern hemisphere esocoids. Our data strongly suggest that this species is not a galaxiid; the alternative hypothesised esocoid relationship cannot be rejected. The species-rich genus Galaxias is shown to be polyphyletic and the generic taxonomy of the Galaxiinae is reassessed in the light of phylogenetic relationships. Juvenile saltwater-tolerance is phylogenetically distributed throughout the Galaxiinae and the loss of this migratory phase may be a major cause of speciation.
FIGURE 2. Clupisoma prateri Hora, 1937, CAS 88908 in A new species of the Asian schilbid catfish genus Clupisoma from Myanmar, with a redescription of Clupisoma prateri Hora (Osteichthyes: Siluriformes: Schilbidae)
FIGURE 2. Clupisoma prateri Hora, 1937, CAS 88908 (122 mm SL).
FIGURE 1 in A new species of the Asian schilbid catfish genus Clupisoma from Myanmar, with a redescription of Clupisoma prateri Hora (Osteichthyes: Siluriformes: Schilbidae)
FIGURE 1. Clupisoma roosae, new species, holotype, NRM 40030 (160 mm SL).
FIGURE 3 in Leporinus amazonicus, a new anostomid species from the Amazon lowlands, Brazil (Osteichthyes: Characiformes)
FIGURE 3. Inner view of the teeth of Leporinus amazonicus n. sp. (INPA 22860, 218 mm SL, paratype).
FIGURE 1. Leporinus amazonicus n in Leporinus amazonicus, a new anostomid species from the Amazon lowlands, Brazil (Osteichthyes: Characiformes)
FIGURE 1. Leporinus amazonicus n. sp., lateral view of the holotype (INPA 22861, 218 mm SL).
FIGURE 4. Glyptothorax striatus, PUCMF 1058, 100.8 in Glyptothorax radiolus, a new species of sisorid catfish (Osteichthyes: Siluriformes) from northeastern India, with a redescription of G. s t r i a t u s McClelland 1842
FIGURE 4. Glyptothorax striatus, PUCMF 1058, 100.8 mm SL; dorsal, lateral and ventral views.
FIGURE 9 in Phylogeny and taxonomy of Petroschmidtia teraoi (Katayama, 1943) (Osteichthyes: Perciformes: Zoarcidae)
FIGURE 9. Left nasal (na) and infraorbitals (io) of Petroschmidtia teraoi, lateral view.
FIGURE 7 in Phylogeny and taxonomy of Petroschmidtia teraoi (Katayama, 1943) (Osteichthyes: Perciformes: Zoarcidae)
FIGURE 7. Pelvic girdle of Petroschmidtia teraoi, dorsal view. Right side rays omitted.
Supplementary material 1 from: Simanovsky SA, Medvedev DA, Tefera F, Golubtsov AS (2023) Divergent karyotypes in five genera of the African endemic fish family Distichodontidae (Cithariniformes, Osteichthyes). Comparative Cytogenetics 17: 251-262. https://doi.org/10.3897/compcytogen.17.107744
Supporting information
Supplementary material 3 from: Luo T, Mao M-L, Lan C-T, Song L-X, Zhao X-R, Yu J, Wang X-L, Xiao N, Zhou J-J, Zhou J (2023) Four new hypogean species of the genus Triplophysa (Osteichthyes, Cypriniformes, Nemacheilidae) from Guizhou Province, Southwest China, based on molecular and morphological data. ZooKeys 1185: 43-81. https://doi.org/10.3897/zookeys.1185.105499
Morphological characters and measurement data
Supplementary material 2 from: Luo T, Mao M-L, Lan C-T, Song L-X, Zhao X-R, Yu J, Wang X-L, Xiao N, Zhou J-J, Zhou J (2023) Four new hypogean species of the genus Triplophysa (Osteichthyes, Cypriniformes, Nemacheilidae) from Guizhou Province, Southwest China, based on molecular and morphological data. ZooKeys 1185: 43-81. https://doi.org/10.3897/zookeys.1185.105499
GPS information on the geographical distribution of 39 hypogean species of the genus Triplophysa
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.