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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>
Fig. 3. Karyotypes after FISH with 5S in Contributions to the systematic of Pimelodidae (Osteichthyes, Siluriformes): basic and molecular cytogenetics on seven species of Pimelodus from three Brazilian hydrographic systems
Fig. 3. Karyotypes after FISH with 5S rDNA probes (red) and 18S rDNA probe (green). a. Pimelodus absconditus; b. Pimelodus britskii; c. Pimelodus maculatus; d. Pimelodus microstoma; e. Pimelodus mysteriosus; f. Pimelodus ortmanni; g. Pimelodus paranaensis. Scales bar = 10 μm.
Fig. 2. Karyotypes arranged from C-banded 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. 2. Karyotypes arranged from C-banded chromosomes. a. Pimelodus absconditus; b. Pimelodus britskii; c. Pimelodus maculatus; d. Pimelodus microstoma; e. Pimelodus mysteriosus; f. Pimelodus ortmanni; g. Pimelodus paranaensis. B chromosomes in the boxes. Scales bar = 10 μm.
Fig. 5 in Contributions to the systematic of Pimelodidae (Osteichthyes, Siluriformes): basic and molecular cytogenetics on seven species of Pimelodus from three Brazilian hydrographic systems
Fig. 5. Cytogenetics data and phylogenetic relationships between Pimelodidae (modified from Lundberg et al., 2011). N= Neopimelodines; S= Sorubimines; CP= Calophysus-Pimelodus Clade; C = Calophysines; PI = Pimelodus Group; 2n = number diploid; p = short arm; q = long arm; S = simple; M = multiple.
Figs 1, 2. Auxis spp. from Syrian marine waters. 1, A in First record of frigate tuna Auxis thazard (Osteichthyes: Scombriformes: Scombridae) in the Syrian marine waters, the Eastern Mediterranean
Figs 1, 2. Auxis spp. from Syrian marine waters. 1, A. thazard (Lacepède, 1800); 2, A. rochei (Risso, 1810). A, corselet; B, vertical line indicating where the tip of the pectoral fin reaches; C, dark wavy lines in the dorsal scaleless area.
Fig. 5 in First Japanese Record and a Revised Diagnosis for Dictyosoma tongyeongensis (Osteichthyes: Perciformes: Stichaeidae)
Fig. 5. Head of three species of Dictyosoma. A, Dictyosoma tongyeongensis—FAKU 135567, 216.5 mm SL; B, one of PKU 3568, 241.5 mm SL (paratype); C, D. burgeri [form "a" sensu Yatsu et al. (1978)]—BSKU 39371, 180.1 mm SL; D. D. burgeri [form "b" sensu Yatsu et al. (1978)]—FAKU 135521, 212.0 mm SL; E. D. rubrimaculatum—NSMT-P 18401, 117.5 mm SL (holotype).
Fig. 3 in First Japanese Record and a Revised Diagnosis for Dictyosoma tongyeongensis (Osteichthyes: Perciformes: Stichaeidae)
Fig. 3. Radiographs of (A) Dictyosoma tongyeongensis and (B) D. burgeri. Arrow indicates anteriormost dorsal-fin pterygiophore.
Fig. 2. Dictyosoma tongyeongensis. A in First Japanese Record and a Revised Diagnosis for Dictyosoma tongyeongensis (Osteichthyes: Perciformes: Stichaeidae)
Fig. 2. Dictyosoma tongyeongensis. A: FAKU 135518, 227.8 mm SL, Notojima, Ishikawa, Japan; B: dark individual, FAKU 135664, 216.7 mm SL, Notojima, Ishikawa, Japan; C: holotype, NIBR-P 17843, 275.2 mm SL, Tongyeong, southern coast of Korean Peninsula.
Fig. 1 in First Japanese Record and a Revised Diagnosis for Dictyosoma tongyeongensis (Osteichthyes: Perciformes: Stichaeidae)
Fig. 1. Collection sites of Dictyosoma tongyeongensis examined in the present study. Solid star: type specimens; solid circle: other specimens.
Fig. 4 in First Record of the Rockfish Sebastes melanops from the Western North Pacific, with Comments on its Synonymy (Osteichthyes: Scorpaenoidei: Sebastidae)
Fig. 4. Unrooted neighbor-joining tree based on sequence variations of the mitochondrial control region. Sequences used here are referred to by catalog numbers of the specimens (determined here) or DDBJ registration numbers (indicated by asterisks, determined in previous studies). Numbers at branches indicate bootstrap probabilities in 1,000 bootstrap replications. The scale bar equals 0.01 of Kimura's (1980) distance.
Fig. 2 in First Japanese records of Anguilla luzonensis (Osteichthyes: Anguilliformes: Anguillidae) glass eels from Okinawa-jima Island, Ryukyu Archipelago, Japan
Fig. 2. Caudal fin and caudal pigmentation pattern of Anguilla luzonensis glass eel (fresh specimens), KYUM-PI-05434.
Fig. 3 in First Japanese records of Anguilla luzonensis (Osteichthyes: Anguilliformes: Anguillidae) glass eels from Okinawa-jima Island, Ryukyu Archipelago, Japan
Fig. 3. Neighbor-joining phylogenetic tree of species of Anguilla in the Indo-Pacific waters based on partial 16S rRNA sequences. The numbers beside internal branches indicate bootstrap probabilities for 1,000 replicates.
Fig. 3 in Heterogeneity Studies Of Wild Clarias Gariepinus (Osteichthyes, Clariidae) Using Sds-Polyacrylamide Gel Electrophoresis
Fig. 3. Dendrogram obtained from Classical Cluster analysis using Paired group Bray-Curtis similarity index on C. gariepinus from two natural populations in Ado-Ekiti and Ilesa.
Fig. 2 in Heterogeneity Studies Of Wild Clarias Gariepinus (Osteichthyes, Clariidae) Using Sds-Polyacrylamide Gel Electrophoresis
Fig. 2. Dendrogram from Classical Cluster analysis using Paired group Bray-Curtis similarity index on Clarias gariepinus obtained in Ilesa, Osun State.
Fig. 1 in Heterogeneity Studies Of Wild Clarias Gariepinus (Osteichthyes, Clariidae) Using Sds-Polyacrylamide Gel Electrophoresis
Fig. 1. Dendrogram obtained from Classical Cluster analysis using Paired group Bray-Curtis similarity index on Clarias gariepinus in Ado-Ekiti.
Fig. 5 in MORPHOLOGICAL CHARACTERISTICS OF HYBRID PIKEPERCH (SANDER LUCIOPERCA f × SANDER VOLGENSIS m) (OSTEICHTHYES, PERCIDAE)
Fig. 5. Canonical analysis based on the eight most important morphological characters (Table 2) selected by the forward stepwise discriminant function analysis for S. lucioperca (square), S. volgensis (triangle) and their F1 hybrid (circle). 95% confidence ellipses are drawn around group centroids, and
Fig. 3 in MORPHOLOGICAL CHARACTERISTICS OF HYBRID PIKEPERCH (SANDER LUCIOPERCA f × SANDER VOLGENSIS m) (OSTEICHTHYES, PERCIDAE)
Fig. 3. Plots of scores of the first and second principal components (PC) for meristic (a) and morphometric characters (b) of S. lucioperca (square), S. volgensis (triangle) and their F1 hybrid (circle).
Fig. 4 in MORPHOLOGICAL CHARACTERISTICS OF HYBRID PIKEPERCH (SANDER LUCIOPERCA f × SANDER VOLGENSIS m) (OSTEICHTHYES, PERCIDAE)
Fig. 4. Variable loadings of principal component (PC) analyses of meristic and morphometric characters of S. lucioperca (square), S. volgensis (triangle) and their F1 hybrid (circle). a – meristic PC1; b – meristic PC2; c – morphometric PC1; morphometric PC2. Full names of analysed characters are
Fig. 2. a – S in MORPHOLOGICAL CHARACTERISTICS OF HYBRID PIKEPERCH (SANDER LUCIOPERCA f × SANDER VOLGENSIS m) (OSTEICHTHYES, PERCIDAE)
Fig. 2. a – S. lucioperca; b-d – S. lucioperca × S. volgensis F1 hybrids; e – S. volgensis; f – hybrid with deformed mandible
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Allen Brain Atlas
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