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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) 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="12"><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><i>Leidybatus jugosus</i></th><td>2</td><td></td><td>1</td><td></td><td>68</td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>71</b></td></tr><tr><th><i>Burnhamia daviesi</i></th><td>6</td><td></td><td></td><td></td><td>1</td><td></td><td></td><td></td><td>1</td><td></td><td>4</td><td><b>12</b></td></tr><tr><th><i>Eoplinthicus yazooensis</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td></td><td><b>1</b></td></tr><tr><th>Batomorphii indet.</th><td></td><td></td><td></td><td></td><td>4</td><td></td><td></td><td></td><td>3</td><td></td><td></td><td><b>7</b></td></tr><tr><th>Myliobatidae indet.</th><td>750</td><td>4</td><td>4</td><td>1</td><td>845</td><td>1</td><td></td><td>22</td><td>762</td><td></td><td>197</td><td><b>2586</b></td></tr><tr><th><i>Cylindracanthus ornatus</i></th><td></td><td></td><td></td><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>Cylindracanthus rectus</i></th><td></td><td></td><td></td><td></td><td>40</td><td></td><td>4</td><td></td><td>2</td><td></td><td></td><td><b>46</b></td></tr><tr><th><i>Cylindracanthus</i> sp.</th><td>4</td><td>4</td><td>3</td><td></td><td>55</td><td></td><td></td><td></td><td>6</td><td></td><td></td><td><b>72</b></td></tr><tr><th><i>Pycnodus</i> sp.</th><td>8</td><td></td><td>1</td><td></td><td>11</td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>20</b></td></tr><tr><th>Lepisostidae indet.</th><td></td><td></td><td>1</td><td></td><td>2</td><td></td><td></td><td></td><td>10</td><td>23</td><td></td><td><b>36</b></td></tr><tr><th><i>Egertonia isodonta</i></th><td>35</td><td></td><td>2</td><td></td><td>17</td><td></td><td></td><td></td><td>37</td><td></td><td>37</td><td><b>128</b></td></tr><tr><th><i>Paralbula</i> aff. <i>P. marylandica</i></th><td>17</td><td></td><td></td><td></td><td>52</td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>69</b></td></tr><tr><th><i>Phyllodus toliapicus</i></th><td>8</td><td></td><td></td><td></td><td>15</td><td></td><td></td><td></td><td>3</td><td></td><td></td><td><b>26</b></td></tr><tr><th><i>Albula eppsi</i></th><td>23</td><td>2</td><td>1</td><td></td><td>6</td><td></td><td></td><td></td><td>1</td><td></td><td></td><td><b>33</b></td></tr><tr><th><i>Albula oweni</i></th><td>15</td><td></td><td></td><td></td><td>3</td><td></td><td>1</td><td></td><td>6</td><td></td><td></td><td><b>25</b></td></tr><tr><th><i>Albula</i> sp.</th><td></td><td></td><td></td><td></td><td>3</td><td></td><td></td><td></td><td>1</td><td></td><td></td><td><b>4</b></td></tr><tr><th>Osteoglossidae indet.</th><td>2</td><td></td><td></td><td></td><td>11</td><td>1</td><td></td><td></td><td>1</td><td></td><td>1</td><td><b>16</b></td></tr><tr><th>Ariidae indet.</th><td></td><td></td><td>2</td><td></td><td>17</td><td>1</td><td></td><td></td><td>34</td><td>12</td><td></td><td><b>66</b></td></tr><tr><th><i>Sphyraena</i> sp.</th><td>1</td><td>5</td><td>2</td><td></td><td>17</td><td></td><td></td><td></td><td>43</td><td>2</td><td>1</td><td><b>71</b></td></tr><tr><th><i>Eutrichiurides plicidens</i> comb. nov.</th><td></td><td></td><td>1</td><td></td><td>7</td><td></td><td></td><td></td><td>3</td><td></td><td></td><td><b>11</b></td></tr><tr><th><i>Trichiurides sagittidens</i></th><td></td><td>4</td><td>1</td><td></td><td>5</td><td></td><td></td><td></td><td>10</td><td>12</td><td>1</td><td><b>33</b></td></tr><tr><th><i>Trichiurus oshosunensis</i></th><td></td><td></td><td>2</td><td></td><td>31</td><td></td><td></td><td></td><td></td><td></td><td></td><td>33</td></tr></tbody></table>
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="2"><b>Meridian lower upper Tallahatta “lower” “upper” Lisbon/ lower Tallahatta Sand Tallahatta Tallahatta /Lisbon Lisbon Lisbon Gosport Gosport Fm. Member Fm. Fm. contact Fm. Fm. contact Sand</b></th><th><b>Gosport Sand</b></th><th><b>Total</b></th></tr></thead><tbody><tr><th><i>Myliobatis</i> sp. 1</th><td>5</td><td>307</td><td></td><td><b>312</b></td></tr><tr><th><i>Myliobatis</i> sp. 2</th><td></td><td>18 207 1 48</td><td colspan="2">13 <b>287</b></td></tr><tr><th><i>Pseudaetobatus belli</i></th><td>15</td><td>210</td><td></td><td><b>225</b></td></tr><tr><th><i>Rhinoptera</i> sp. <i>Meridiania</i> cf. <i>M. convexa</i></th><td>16</td><td>14 18 181 1 5 1525 1 1</td><td colspan="2">131 <b>1891</b> 2 <b>4</b></td></tr><tr><th><i>Leidybatus jugosus</i></th><td></td><td>2 28 41</td><td></td><td><b>71</b></td></tr><tr><th><i>Burnhamia daviesi</i></th><td></td><td>6 1 1</td><td>4</td><td><b>12</b></td></tr><tr><th><i>Eoplinthicus yazooensis</i></th><td></td><td></td><td colspan="2">1 <b>1</b></td></tr><tr><th>Batomorphii indet.</th><td></td><td>4</td><td>3</td><td><b>7</b></td></tr><tr><th>Myliobatidae indet.</th><td></td><td>750 4 74 776 1 7 762</td><td>212</td><td><b>2586</b></td></tr><tr><th><i>Cylindracanthus ornatus</i></th><td></td><td>2 1</td><td></td><td><b>3</b></td></tr><tr><th><i>Cylindracanthus rectus</i></th><td></td><td>24 16 4 2</td><td></td><td><b>46</b></td></tr><tr><th><i>Cylindracanthus</i> sp.</th><td></td><td>4 4 13 45 6</td><td></td><td><b>72</b></td></tr><tr><th><i>Pycnodus</i> sp.</th><td></td><td>8 2 10</td><td></td><td><b>20</b></td></tr><tr><th>Lepisostidae indet.</th><td></td><td>1 2 10</td><td>23</td><td><b>36</b></td></tr><tr><th><i>Egertonia isodonta</i></th><td></td><td>35 12 7 37</td><td colspan="2">37 <b>128</b></td></tr><tr><th><i>Paralbula</i> aff. <i>P. marylandica</i></th><td></td><td>17 52</td><td></td><td><b>69</b></td></tr><tr><th><i>Phyllodus toliapicus Albula eppsi Albula oweni</i></th><td></td><td>8 15 3 23 2 1 6 1 15 3 1 6</td><td colspan="2"><b>26 33 25</b></td></tr><tr><th><i>Albula</i> sp.</th><td></td><td>3 1</td><td></td><td>4</td></tr></tbody></table>
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” “upper” Tallahatta Sand Tallahatta Tallahatta /Lisbon Lisbon Lisbon Fm. Member Fm. Fm. contact Fm. Fm.</b></th><th><b>Lisbon/ Gosport contact</b></th><th><b>lower Gosport Sand</b></th><th><b>Gosport Sand</b></th><th><b>Total</b></th></tr></thead><tbody><tr><th><i>Physogaleus alabamensis</i> comb. nov. <i>Physogaleus secundus</i></th><td></td><td>31 131</td><td>1 1</td><td></td><td>185 232 1 53 555 1</td><td></td><td>15 38</td><td colspan="2">17 <b>507</b> 27 <b>786</b></td></tr><tr><th><i>Physogaleus</i> sp.</th><td></td><td></td><td></td><td></td><td>1 1</td><td></td><td></td><td></td><td><b>2</b></td></tr><tr><th><i>Galeocerdo eaglesomei</i></th><td></td><td></td><td></td><td></td><td>4 13</td><td>1</td><td>2</td><td>18</td><td><b>38</b></td></tr><tr><th><i>Galeocerdo clarkensis</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>83</td><td colspan="2">3 <b>86</b></td></tr><tr><th><i>Galeocerdo</i> sp.</th><td></td><td></td><td></td><td></td><td></td><td></td><td>16</td><td></td><td><b>16</b></td></tr><tr><th>Galeomorphii 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>Pristidae indet.</th><td></td><td></td><td></td><td></td><td>4</td><td></td><td>2</td><td colspan="2">7 <b>13</b></td></tr><tr><th><i>Anoxypristis</i> sp. <i>Pristis</i> sp.</th><td></td><td>1 27</td><td></td><td></td><td>11 4 91 27</td><td></td><td>2 36</td><td>66</td><td><b>18 247</b></td></tr><tr><th><i>Propristis schweinfurthi</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>2</td><td colspan="2">8 <b>10</b></td></tr><tr><th>Myliobatiformes indet.</th><td></td><td></td><td></td><td></td><td>1 288 3</td><td></td><td></td><td>60</td><td><b>352</b></td></tr><tr><th>“ <i>Dasyatis</i> ” aff. <i>D. charlisae</i></th><td></td><td></td><td></td><td></td><td>4 4</td><td></td><td></td><td></td><td><b>8</b></td></tr><tr><th>“ <i>Dasyatis</i> ” <i>jaekeli</i></th><td></td><td>3</td><td></td><td></td><td>13</td><td></td><td></td><td></td><td><b>16</b></td></tr><tr><th>“ <i>Dasyatis</i> ” sp.</th><td></td><td></td><td></td><td></td><td>6</td><td></td><td>2</td><td></td><td><b>8</b></td></tr><tr><th><i>Aturobatis</i> aff. <i>A. aquensis</i></th><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>Coupatezia</i> sp.</th><td></td><td>1</td><td></td><td></td><td>17</td><td></td><td></td><td></td><td><b>18</b></td></tr><tr><th><i>Hypolophodon sylvestris</i></th><td></td><td>7</td><td></td><td></td><td></td><td></td><td></td><td></td><td><b>7</b></td></tr><tr><th><i>Jacquhermania duponti</i></th><td></td><td></td><td></td><td></td><td>11</td><td></td><td>16</td><td colspan="2">1 <b>28</b></td></tr><tr><th><i>Aetobatis</i> sp.</th><td></td><td></td><td></td><td></td><td>12 103</td><td>1</td><td></td><td>11</td><td><b>127</b></td></tr><tr><th><i>Aetomylaeus</i> sp.</th><td>11</td><td>80</td><td></td><td></td><td>12 123 4</td><td></td><td>153</td><td>9</td><td>392</td></tr></tbody></table>
FIGURE 3 Halosaurus ovenii from the northeastern Atlantic Ocean, MHNUSC 25010 - 2, 578 in Halosaur fishes (Notacanthiformes: Halosauridae) from Atlantic Spanish waters according to integrative taxonomy
FIGURE 3 Halosaurus ovenii from the northeastern Atlantic Ocean, MHNUSC 25010 - 2, 578 mm total length.
F I G U R E 7 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 7 Gouania hofrichteri sp. nov., PMR VP4595, holotype, male, 30.35+3.67 mm, Souda Beach, Plakias, Crete, Greece. Lateral view of specimen preserved in 4% formaldehyde (top). Lateral, dorsal and ventral view, alive (below). Photographs by M. Wagner and M. Kovacˇic
F I G U R E 9 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 9 Gouania willdenowi (Risso 1810), PMR VP4574, neotype, male, 46.11+6.56 mm, Cagnes-sur-mer, Nice, France. Lateral view of specimen preserved in 4% formaldehyde (top). Lateral, dorsal and ventral view, alive (below). Photographs by M. Wagner and M. Kovacˇic
F I G U R E 1 0 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 1 0 Results of DNA-barcoding analyses. (a) Net between-group mean distances (mean and S.E.). The phylogeny shown in this figure is based on Wagner et al. (2019). (b) DNA-barcoding gap represented by boxplots showing maximum intraspecific and minimum interspecific divergences in %
F I G U R E 6 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 6 Gouania orientalis sp. nov., PMR VP4585, holotype, male, 32.8+4.93 mm, Plakias, Crete, Greece. Lateral view of specimen preserved in 4% formaldehyde (top). Lateral, dorsal and ventral view, alive (below). Photographs by M. Wagner and M. Kovacˇic
F I G U R E 8 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 8 Gouania pigra (Nardo, 1827), PMR VP3529, neotype, female, 43.12+5.03 mm, Glavotok, Krk, Croatia. Lateral view of specimen preserved in 4% formaldehyde (top). Lateral, dorsal and ventral view, alive (below). Photographs by M. Wagner and M. Kovacˇic
F I G U R E 5 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 5 Head osteology of Gouania species. (a) G. adriatica sp. nov. (PMR VP4618 – Holotype), (b) G. orientalis sp. nov. (PMR VP4585 – Holotype), (c) G. hofrichteri sp. nov. (ZSM-PIS- 047656 – Paratype), (d) G. pigra (Nardo 1827) (PMR VP3531 – Other material) and (e) G. willdenowi (Risso 1810) (ZSM-PIS-0476654 – Other material). Red, ceratobranchial 5; orange, premaxillary bone; blue, maxillary bone; green, nasal bone
F I G U R E 3 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 3 Gouania adriatica sp. nov., PMR VP4618, holotype, male, 41.41+6.77 mm, Stoja, Pula. Lateral view of specimen preserved in 4% formaldehyde (top). Lateral, dorsal and ventral view, alive (below). Photographs by M. Wagner and M. Kovacˇic
F I G U R E 4 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 4 Sucking discs and disc-papillae of Gouania species. (a) G. adriatica sp. nov. (PMR VP4618 – Holotype), (b) G. orientalis sp. nov. (PMR VP4585 – Holotype), (c) G. hofrichteri sp. nov. (PMR VP4595 – Holotype), (d) G. pigra (Nardo 1827) (ZSM-PIS-047649 – Other material) and (e) G. willdenowi (Risso 1810) (PMR VP4574 – Neotype). (f) Males of Gouania can have seemingly perfused prominent finger-like extensions on sucking disc edge in region A.A, B and C correspond to disc regions. Photographs by M. Wagner
F I G U R E 1 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 1 Geographical distribution ranges and ecology. (a) Distribution ranges of single Gouania species. The data shown are based on genetic, morphological and field observations as well as on historical findings mentioned by Hofrichter (1995) (all his records combined the species in G. willdenowi described here). Type and location of water currents are based on data provided by El-Geziry and Bryden (2010). Numbers 1–23 indicate sampling sites (compare with Supporting Information Table S1). (b) Female Gouania pigra (Nardo, 1827) in the interstitial of pebbles (photo taken in aquarium); see Supporting Information Video S1 for behaviour. (c) Trstenik (Pelješac, Croatia) – a site where G. pigra, G. adriatica sp. nov. and G. hofrichteri sp. nov. were found in sympatry. Photographs by M. Wagner
F I G U R E 2 in Unravelling the taxonomy of an interstitial fish radiation: Three new species of Gouania (Teleostei: Gobiesocidae) from the Mediterranean Sea and redescriptions of G. willdenowi and G. pigra
F I G U R E 2 Comparative morphological overview and lateral line system. (a) Main morphological characteristics of head region of (a) G. adriatica sp. nov. (PMR VP4618 – Holotype), (b) G. orientalis sp. nov. (PMR VP4585 – Holotype), (c) G. hofrichteri sp. nov. (PMR VP4595 – Holotype) and (d) G. pigra (Nardo 1827) (PMR VP3529 – Neotype). (e) Position of pores (bold) and neuromasts (italic) shown on the example of G. willdenowi (Risso 1810) (PMR VP4574 – Neotype) and the main morphological characteristics in the head region of this species. (f) Longitudinal infralateral and suborbital transversal rows of superficial neuromasts can be placed on the well-defined bottom of a deep (+) or shallow (–) groove. U, upper opercular tip; Abbreviations: L, lower opercular tip; SR, supralabial row; NR, nasal row; LIR, longitudinal infralateral; STR, suborbital transversal row; POR, postorbital transversal row; PTR, preopercular transversal row; SLR, subopercular longitudinal row; MR, mandibular row; AVR, anterior ventral row; PVR, posterior ventral row; ADR, anterior dorsal row; PDR, posterior dorsal row; HR, hyomandibular row; SR1, supraopercular row; SR2, suprapectoral row; DLR, dorsolateral longitudinal row; VLR, ventrolateral longitudinal row. Photographs by M. Wagner and M. Kovacˇic
Fig 10 in Correction: Integrated Taxonomy Reveals Hidden Diversity in Northern Australian Fishes: A New Species of Seamoth (Genus Pegasus)
Fig 10. Molecular species identification of Pegasus species using Genetic treeML trees. (A) sequences from the 16S gene; (B) sequences from the COI gene. Trees are based on the K2 evolutionary distance model and are shown here with mined Pegasus and Eurypegasus sequences from GenBank. The trees are shown here with an E. draconis outgroup. Bootstrap support values (following 1000 replicates) are shown above the nodes. https://doi.org/10.1371/journal.pone.0251680.g001
Figure 4 in Diadromous fishes from Saint-Pierre and Miquelon archipelago: diagnoses, taxonomy, nomenclature and distribution
Figure 4. – Pungitius pungitius (Linnaeus, 1758): syntypes LSL 34 and 35; scale bar = 1cm; with the permission of the Linnean Society of London (A); MNHN-IC-2022-0020, 32.7 mm SL, Saint-Pierre and Miquelon, Saint-Pierre Island, Milieu Pond (B).
Figure 3 in Diadromous fishes from Saint-Pierre and Miquelon archipelago: diagnoses, taxonomy, nomenclature and distribution
Figure 3. – Gasterosteus aculeatus Linnaeus, 1758: syntypes LSL 29-31; scale bar = 1cm; with the permission of the Linnean Society of London (A); MNHN-IC-2022-0022, 33.7 mm SL, Saint-Pierre and Miquelon (B).
Figure 2 in Diadromous fishes from Saint-Pierre and Miquelon archipelago: diagnoses, taxonomy, nomenclature and distribution
Figure 2. – Apeltes quadracus (Mitchill, 1815): drawning of an individual from New York, USA given by Mitchill (1815: 430, Pl. 1) with its species description (A); MNHN-IC-2022-0021, 26.9 mm SL, Saint-Pierre and Miquelon, Saint-Pierre Island, Airport Pond (B).
Text-fig. 6. Fish remains from Volchaya Balka locality (Late Miocene, North Caucasus). a – Scardinius sp., SSC-RAS G-2/1, pharyngeal tooth of the first row, side view, occlusal view; b – Abramis cf. bjoerkna, SSC-RAS G-2/2, pharyngeal tooth of the first row: top – side view, bottom – occlusal view; c – Carassius sp., SSC-RAS G-2/3, pharyngeal tooth of the first row: top – side view, bottom – occlusal view; d – Alburnus sp., SSC-RAS G-2/4, fragment of pharyngeal bone (os pharyngicus inferius), medial view; e – Acipenser sp., SSC-RAS G-2/5, left hyomandibular: left – medial view, right – proximal view; f – Gobiidae gen. indet., SSC-RAS G-2/6, tail vertebra: left – lateral view, right – dorsal view; g – Gobiidae gen. indet., SSC-RAS G-2/7, dentary: top – medial view, bottom – dorsal view. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology
Text-fig. 6. Fish remains from Volchaya Balka locality (Late Miocene, North Caucasus). a – Scardinius sp., SSC-RAS G-2/1, pharyngeal tooth of the first row, side view, occlusal view; b – Abramis cf. bjoerkna, SSC-RAS G-2/2, pharyngeal tooth of the first row: top – side view, bottom – occlusal view; c – Carassius sp., SSC-RAS G-2/3, pharyngeal tooth of the first row: top – side view, bottom – occlusal view; d – Alburnus sp., SSC-RAS G-2/4, fragment of pharyngeal bone (os pharyngicus inferius), medial view; e – Acipenser sp., SSC-RAS G-2/5, left hyomandibular: left – medial view, right – proximal view; f – Gobiidae gen. indet., SSC-RAS G-2/6, tail vertebra: left – lateral view, right – dorsal view; g – Gobiidae gen. indet., SSC-RAS G-2/7, dentary: top – medial view, bottom – dorsal view.
Figure:1 Fish classification and taxonomy in Artificial Intelligence Applications in Fish Classification and Taxonomy: Advancing Our Understanding of Aquatic Biodiversity
Figure:1 Fish classification and taxonomy
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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.