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Fig. 2 in Organization of fish assemblages in blackwater Atlantic Forest streams

Fig. 2. Rarefaction curves calculated for each mesohabitat category (sand, leaf-litter and trunks), considering a total of 31 mesohabitats sampled in 13 blackwater streams of the alluvial plain of the Serra do Mar in the State of São Paulo. EstimateS 9.1 was used to plot species rarefaction curve (100 runs).

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Fig. 3 in Genetic diversity and population structure of Brycon nattereri (Characiformes: Bryconidae): a Neotropical fish under threat of extinction

Fig. 3. Haplotype network based on partial sequencing of the D-loop region (mtDNA) of 92 individuals of Brycon nattereri from the Laranjinha River. Circle sizes are pro- portional to haplotype frequency.

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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>

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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 &ldquo;lower&rdquo; &ldquo;upper&rdquo; 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>

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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="5"><b>Meridian lower upper Tallahatta &ldquo;lower&rdquo; &ldquo;upper&rdquo; 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>&ldquo; <i>Dasyatis</i> &rdquo; 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>&ldquo; <i>Dasyatis</i> &rdquo; <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>&ldquo; <i>Dasyatis</i> &rdquo; 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>

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Fig. 3 in Water temperature affects aggressive interactions in a Neotropical cichlid fish

Fig. 3. Mean ± SE of initial (third day) and final (eighth day) frequencies of a. restrained aggression and b. overt aggression of group-housed fish. Different letters show differences among treatments. Mixed Model ANOVA completed by Fisher-LSD post hoc test.

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Fig. 5 in Fish movement in an Atlantic Forest stream

Fig. 5. Relationship between distance (m) moved by fishes and seasons (dry and rainy) of all moving species from Ubatiba stream, Southeast, Brazil.

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Fig. 2 in Fish movement in an Atlantic Forest stream

Fig. 2. Schematic representation of the study area. Numbers were designated according to the distance of each stretch to the first stretch (0 m). Arrows indicate the water flow.

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Fig. 1. Ubatiba stream system showing all the four sampling sites. P1 in Fish movement in an Atlantic Forest stream

Fig. 1. Ubatiba stream system showing all the four sampling sites. P1 is the most upstream site and P4 is the most downstream site.

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Fig. 8 in Optimal fishing samplers to reveal the morphological structure of a fish assemblage in a subtropical tidal flat

Fig. 8. Redundancy analysis (RDA): individual species-gear relationships explained by morphological shape variability, using incidence data. In blue, fishing gear acronyms: beach seine (BS), cast net (CN), fish trap (FT), hook and line (HL), inner encircling gillnet (EG1), large gillnet (LG), marginal encircling gillnet (EG2), otter trawl (OT), small gillnet (SG).

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Fig. 4 in Optimal fishing samplers to reveal the morphological structure of a fish assemblage in a subtropical tidal flat

Fig. 4. Morphospace represented by shape variation of all species in the nine fishing gears grouped, using the relative warps: a. 1 and 2; b. 1 and 3. Acronyms: Anc tri, Anchoa tricolor; Bat sop, Bathygobius soporator; Bot oce, Bothus ocellatus; Cen par, Centropomus parallelus; Chi spi, Chilomycterus spinosus; Dia rho, Diapterus rhombeus; Elo sau, Elops saurus; Epi mar, Epinephelus marginatus; Hip rei, Hippocampus reidi; Lut ana, Lutjanus analis; Lut cya, Lutjanus cyanopterus; Mal del, Malacoctenus delalandii; Myr pun, Myrophis punctatus; Oph gom, Ophichthus gomesii; Pol vir, Polydactylus virginicus; Sca cri, Scartella cristata; Sco bra, Scomberomorus brasiliensis; Sel set, Selene setapinnis; Sel vom, Selene vomer; Sph tes, Sphoeroides testudineus; Str mar, Strongylura marina; Sym tes, Symphurus tesselatus; Tra myo, Trachinocephalus myops. Threatened species (Hip rei, Lut ana, Lut cya, Epi mar) are highlighted in red.

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FIG. 6 in The ways of fish beyond the sea: fish circulation and consumption in the Atacama desert, northern Chile, during the Formative period (500 cal B.C. - 700 cal A.D.)

FIG. 6. — Headless dried fish offered to a 4-6 years old infant in the route of Calate-Loa River mouth.

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FIG. 7 in The ways of fish beyond the sea: fish circulation and consumption in the Atacama desert, northern Chile, during the Formative period (500 cal B.C. - 700 cal A.D.)

FIG. 7. — Composite food made of two kind of fishes tied together by a braided rope: a complete anchoveta and a boneless fillet of a bigger fish. Topater 01 cemetery (Gallardo 2017: fig. 2). Scale bar: 5 cm.

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FIG. 15 in Food worthy of kings and saints: fish consumption in the medieval monastery Studenica (Serbia)

FIG. 15. — Sturgeon fishing at the exit of the Danube Gorges, cover of the fourth volume (De Piscibus in Aquis Danubii Viventibus) of L. F. Marsigli's Danubius Pannonico-Mysicus (Marsigli 1726).

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FIG. 9 in The ways of fish beyond the sea: fish circulation and consumption in the Atacama desert, northern Chile, during the Formative period (500 cal B.C. - 700 cal A.D.)

FIG. 9. — Graphic that indicates the relation between cranial and postcranial skeletal units in routes, Quillagua and interior oasis sites from the Atacama Desert during the Formative period. Both inferior bars show the same relation in reference skeletons from Trachurus murphyi Nichols, 1920 (60 cranial and 41 postcranial elements) and Cilus gilberti (Abbott, 1899) (60 cranial and 42 postcranial elements). Abbreviation: NISP, number of identified specimens.

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FIG. 2 in The ways of fish beyond the sea: fish circulation and consumption in the Atacama desert, northern Chile, during the Formative period (500 cal B.C. - 700 cal A.D.)

FIG. 2. — Altitudinal profile of the region with the position from the different localities mentioned in the article. Sites in italics: main geographical landmarks. Ab- breviation: m a.s.l., meters above sea level.

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FIG. 4 in The ways of fish beyond the sea: fish circulation and consumption in the Atacama desert, northern Chile, during the Formative period (500 cal B.C. - 700 cal A.D.)

FIG. 4. — Radiocarbon datations from the Formative sites of the Atacama Desert considered in this study. Marine and human material samples were excluded. Calibration made by SHCAL13 curve (Hogg et al. 2013) using Calib 704 (Stuiver et al. 2005).

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FIG. 6 in Food worthy of kings and saints: fish consumption in the medieval monastery Studenica (Serbia)

FIG. 6. — The distribution of mammal, bird and fish remains from medieval contexts at Studenica Monastery (after Marković 2015: 396, fig. 1).

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FIG. 4. — Fishing with net from a in Food worthy of kings and saints: fish consumption in the medieval monastery Studenica (Serbia)

FIG. 4. — Fishing with net from a boat, detail of the 13th century fresco from Mileševa Monastery (courtesy of the BLAGO Fund).

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FIG. 3 in Food worthy of kings and saints: fish consumption in the medieval monastery Studenica (Serbia)

FIG. 3. — Representation of various fish species, detail of the 14th century fresco from Gračanica Monastery (courtesy of the BLAGO Fund).

opencc-zeroNov 2019View details →

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Last verified 2026-04-30Open record

International Brain Laboratory public data

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Last verified 2026-04-29Open record

OpenNeuro

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openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record