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FIGURE 1. Thismia bokorensis from the type locality. A–B. Flowers. C in Flora of Bokor National Park VII: Thismia bokorensis (Burmanniaceae), a new species representing a new generic record
FIGURE 1. Thismia bokorensis from the type locality. A–B. Flowers. C. Flowering plant.
THE SIGNIFICANCE OF ORGANIZING ACADEMIC FOREIGN REPRESENTATIVE OFFICES WITHIN THE DEPARTMENT OF INTERNATIONAL COOPERATION TO INVOLVE FOREIGN STUDENTS IN THE EDUCATIONAL PROCESS OF HIGHER EDUCATION INSTITUTIONS.
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BURI BAKHSHI THE SON OF SADIQ – REPRESENTATIVE OF THE VALLEY BAKHSHICHILIK
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LadiesDebating_HTO: A Knowledge Graph for representing the "Edinburgh Ladies' Debating Society Digital Collection" (1865 - 1880) following Heritage Textual Ontology
<p>This Knowlege Graph represents the information of the "Edinburgh Ladies’ Debating Society<strong>"</strong> (years: 1865 - 1880) collection in RDF (ttl format). This collection consists of the complete runs of two Edinburgh journals, <strong>‘The Attempt’ (10 volumes, 1865-74)</strong> and its successor ‘<strong>The Ladies’ Edinburgh Magazine’ (6 volumes, 1875-80)</strong>. These publications were produced by a leading Edinburgh women’s club, known during the period as the Edinburgh Essay Society or the Ladies’ Edinburgh Essay Society, but subsequently as the Ladies’ Edinburgh Debating Society. The Society existed from 1865 to 1935. The raw dataset is provided by the NLS in this <a href="https://data.nls.uk/data/digitised-collections/edinburgh-ladies-debating-society/">link</a>. As other NLS data collections, they are originally provided using two XMLs schemas: METS for descriptive, structural, technical and administrative metadata (Title, Author, Publisher, etc); and ALTO for encoding the OCR text of a page.</p> <p>In this work, we have extracted the information from METS and ALTO XMLS using <a href="https://github.com/francesNLP/defoe">defoe</a> tool. The KG uses the <a href="https://w3id.org/hto">HTO</a> to represent the information extracted. Furthermore, during the information extraction phase, we have employed several techniques to mitigate two common OCR errors: long-S and the line-break hyphenation.</p>
TABLE 3. Means and standard deviations for 16 morphometric characters measured from males representing 12 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 3</b>. Means and standard deviations for 16 morphometric characters measured from males representing 12 populations belonging to <i>Anadolua</i> genus.</p><table><tbody><tr><th><b>Localities</b></th><th></th><th></th><th></th><th></th><th></th><th></th><th></th><th><b>Characters</b></th><th></th><th></th><th></th><th></th><th></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td></td><td></td><td></td><td></td><td></td><td></td><td>(m ± sd, except NSF)</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>TLB</td><td>TL</td><td>TLP</td><td>MIDLC</td><td>MADLC</td><td>LHF</td><td>MWHF</td><td>MWFS</td><td>MLS</td><td>MWS</td><td>MWBE</td><td>MLAT</td><td>MWAT</td><td>MLC</td><td>LCMIT</td><td>NSF</td></tr><tr><th><i>A. schwarzi</i> (Muğla-Sandras) N=4</th><td>26.40 ±0.59</td><td>5.26 ±0.11</td><td>7.09 ±0.09</td><td>1.72 ±0.13</td><td>4.79 ±0.09</td><td>18.90 ±0.67</td><td>4.05 ±0.13</td><td>1.06 ±0.01</td><td>0.99 ±0.04</td><td>0.84 ±0.00</td><td>2.41 ±0.05</td><td>1.44 ±0.11</td><td>1.06 ±0.02</td><td>1.80 ±0.02</td><td>0.64 ±0.03</td><td>66.75 ±3.09</td></tr><tr><th><i>A. schwarzi</i> (Denizli-Babadağ) N=10</th><td>23.47 ±1.46</td><td>5.50 ±0.13</td><td>6.30 ±0.10</td><td>1.60 ±0.12</td><td>4.93 ±0.19</td><td>18.57 ±0.40</td><td>3.87 ±0.16</td><td>1.04 ±0.05</td><td>1.04 ±0.01</td><td>0.91 ±0.06</td><td>2.28 ±0.05</td><td>1.42 ±0.09</td><td>0.88 ±0.04</td><td>1.69 ±0.08</td><td>0.52 ±0.02</td><td>65.00 ±2.71</td></tr><tr><th><i>A. schwarzi</i> (İzmir-Bozdağ) N=5</th><td>20.84 ±0.71</td><td>5.37 ±0.14</td><td>6.84 ±0.18</td><td>1.83 ±0.12</td><td>5.08 ±0.08</td><td>18.50 ±0.38</td><td>3.96 ±0.11</td><td>1.00 ±0.08</td><td>1.10 ±0.05</td><td>0.83 ±0.02</td><td>2.43 ±0.07</td><td>1.40 ±0.12</td><td>0.85 ±0.85</td><td>1.63 ±0.09</td><td>0.65 ±0.07</td><td>65.60 ±3.21</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_I) N=3</th><td>22.33 ±1.04</td><td>4.76 ±0.09</td><td>6.18 ±0.13</td><td>1.53 ±0.05</td><td>4.72 ±0.13</td><td>18.60 ±0.96</td><td>3.60 ±0.20</td><td>0.91 ±0.06</td><td>1.00 ±0.05</td><td>0.84 ±0.05</td><td>2.19 ±0.08</td><td>1.34 ±0.07</td><td>0.74 ±0.09</td><td>1.74 ±0.07</td><td>0.54 ±0.04</td><td>70.00 ±3.60</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_II) N=4</th><td>20.92 ±1.11</td><td>4.82 ±0.10</td><td>6.34 ±0.09</td><td>1.65 ±0.19</td><td>4.89 ±0.16</td><td>18.62 ±0.29</td><td>3.95 ±0.19</td><td>0.93 ±0.03</td><td>1.01 ±0.05</td><td>0.90 ±0.03</td><td>2.22 ±0.07</td><td>1.35 ±0.03</td><td>0.85 ±0.03</td><td>1.71 ±0.03</td><td>0.48 ±0.01</td><td>67.75 ±4.35</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Tahtalıdağ) N=1</th><td>24.40</td><td>5.14</td><td>6.84</td><td>1.84</td><td>4.84</td><td>18.30</td><td>3.90</td><td>1.06</td><td>0.96</td><td>0.84</td><td>2.37</td><td>1.57</td><td>1.00</td><td>1.92</td><td>0.56</td><td>74.00</td></tr><tr><th><i>A. schwarzi</i> (UŞak-Şaphane) N=6</th><td>19.87 ±1.48</td><td>4.81 ±0.14</td><td>6.26 ±0.24</td><td>1.79 ±0.07</td><td>4.79 ±0.19</td><td>18.83 ±0.40</td><td>3.63 ±0.10</td><td>0.97 ±0.02</td><td>1.14 ±0.06</td><td>0.84 ±0.04</td><td>2.10 ±0.06</td><td>1.41 ±0.12</td><td>0.98 ±0.08</td><td>1.77 ±0.10</td><td>0.59 ±0.04</td><td>64.00 ±3.16</td></tr><tr><th><i>A. schwarzi</i> (Kütahya-Civanağa) N=4</th><td>21.17 ±0.89</td><td>5.35 ±0.14</td><td>6.36 ±0.16</td><td>1.72 ±0.11</td><td>4.94 ±0.10</td><td>18.00 ±0.82</td><td>3.42 ±0.15</td><td>0.96 ±0.02</td><td>1.07 ±0.05</td><td>0.71 ±0.03</td><td>2.17 ±0.09</td><td>1.37 ±0.03</td><td>1.02 ±0.09</td><td>1.65 ±0.05</td><td>0.57 ±0.01</td><td>62.2 ±2.22</td></tr><tr><th><i>A. schwarzi</i> (Denizli Çameli) N=5</th><td>22.32 ±4.16</td><td>5.44 ±0.12</td><td>6.81 ±0.15</td><td>1.63 ±0.03</td><td>5.12 ±0.13</td><td>18.98 ±1.24</td><td>4.00 ±0.19</td><td>0.98 ±0.03</td><td>1.13 ±0.03</td><td>0.79 ±0.03</td><td>2.28 ±0.03</td><td>1.45 ±0.06</td><td>0.88 ±0.04</td><td>1.62 ±0.04</td><td>0.57 ±0.01</td><td>64.00 ±3.67</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Konya-Rezebeli) N=4</th><td>22.62 ±1.11</td><td>5.36 ±0.30</td><td>6.43 ±0.30</td><td>2.20 ±0.09</td><td>4.84 ±0.27</td><td>17.27 ±0.48</td><td>4.00 ±0.09</td><td>1.04 ±0.07</td><td>1.13 ±0.07</td><td>0.89 ±0.10</td><td>2.43 ±0.05</td><td>1.33 ±0.11</td><td>1.44 ±0.05</td><td>2.22 ±0.16</td><td>0.87 ±0.06</td><td>46.00 ±1.82</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Antalya-GündoğmuŞ) N=1</th><td>24.00</td><td>5.32</td><td>6.63</td><td>2.21</td><td>4.89</td><td>16.60</td><td>4.00</td><td>0.95</td><td>1.05</td><td>0.84</td><td>2.58</td><td>1.28</td><td>1.19</td><td>2.31</td><td>0.97</td><td>49.00</td></tr><tr><th><i>A. moli</i> <b>sp. nov.</b> (Konya-Sultandağ) N=5</th><td>21.90 ±1.51</td><td>4.72 ±0.08</td><td>6.28 ±0.09</td><td>1.81 ±0.04</td><td>4.59 ±0.10</td><td>17.80 ±0.45</td><td>3.74 ±0.17</td><td>0.93 ±0.05</td><td>1.12 ±0.06</td><td>0.87 ±0.05</td><td>2.24 ±.06</td><td>1.71 ±0.16</td><td>1.14 ±0.05</td><td>1.33 ±0.11</td><td>0.65 ±0.03</td><td>51.80 ±2.39</td></tr></tbody></table><p>m—Mean; sd—Standard deviation; N—individuals</p>
TABLE 5. Means and standard deviations for 15 morphometric characters measured from females representing 10 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 5</b>. Means and standard deviations for 15 morphometric characters measured from females representing 10 populations belonging to <i>Anadolua</i> species.</p><table><tbody><tr><th><b>Characters</b> (mm ± sd)</th></tr></tbody><tbody><tr><th><b>Localities</b></th><td>TLB</td><td>TLP</td><td>MIDLC</td><td>MADLC</td><td>MLHF</td><td>MWHF</td><td>MWFS</td><td>MLS</td><td>MWS</td><td>MWBE</td><td>MLAT</td><td>MWAT</td><td>MLC</td><td>MLO</td><td>MWO</td></tr><tr><th><i>A. schwarzi</i> (Muğla-Sandras) N=3</th><td>25.66 ±1.52</td><td>7.37 ±0.19</td><td>1.96 ±0.08</td><td>5.40 ±0.16</td><td>24.00 ±3.00</td><td>4.33 ±0.15</td><td>1.16 ±0.05</td><td>1.14 ±0.02</td><td>0.89 ±0.05</td><td>2.66 ±0.08</td><td>1.08 ±0.05</td><td>0.27 ±0.02</td><td>1.63 ±0.04</td><td>21.06 ±0.40</td><td>1.90 ±0.10</td></tr><tr><th><i>A. schwarzi</i> (Denizli-Babadağ) N=6</th><td>25.00 ±2.61</td><td>6.96 ±0.25</td><td>2.06 ±0.13</td><td>5.29 ±0.21</td><td>19.83 ±1.25</td><td>4.15 ±0.26</td><td>1.08 ±0.03</td><td>1.30 ±0.09</td><td>0.92 ±0.03</td><td>2.46 ±0.12</td><td>1.15 ±0.07</td><td>0.26 ±0.02</td><td>1.43 ±0.04</td><td>19.80 ±1.58</td><td>1.96 ±0.08</td></tr><tr><th><i>A. schwarzi</i> (İzmir-Bozdağ) N=8</th><td>24.90 ±1.15</td><td>7.89 ±0.31</td><td>2.08 ±0.10</td><td>5.54 ±0.15</td><td>22.00 ±1.00</td><td>4.76 ±0.39</td><td>1.16 ±0.06</td><td>1.13 ±0.09</td><td>0.88 ±0.03</td><td>2.72 ±0.14</td><td>1.06 ±0.07</td><td>0.29 ±0.06</td><td>1.50 ±0.06</td><td>21.81 ±0.55</td><td>2.20 ±0.29</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_I) N=2</th><td>23.75 ±0.64</td><td>6.45 ±0.41</td><td>2.00 ±0.07</td><td>5.37 ±0.30</td><td>18.50 ±0.71</td><td>3.90 ±0.00</td><td>1.08 ±0.04</td><td>1.29 ±0.04</td><td>0.84 ±0.07</td><td>2.31 ±0.08</td><td>0.92 ±0.00</td><td>0.32 ±0.01</td><td>1.44 ±0.00</td><td>20.20 ±0.00</td><td>2.00 ±0.00</td></tr><tr><th>A. schwarzi (Antalya-Gömbe_II) N=6</th><td>21.07 ±3.37</td><td>6.28 ±0.41</td><td>1.73 ±0.20</td><td>4.62 ±0.22</td><td>17.67 ±0.42</td><td>3.90 ±0.18</td><td>0.98 ±0.05</td><td>1.09 ±0.04</td><td>0.83 ±0.04</td><td>2.27 ±0.17</td><td>0.94 ±0.06</td><td>0.37 ±0.04</td><td>1.28 ±0.08</td><td>18.41 ±0.58</td><td>2.03 ±0.05</td></tr><tr><th><i>A. schwarzi</i> (UŞak-Şaphane) N=4</th><td>21.70 ±0.57</td><td>6.60 ±0.21</td><td>1.89 ±0.04</td><td>5.14 ±0.20</td><td>20.60 ±0.36</td><td>3.85 ±0.06</td><td>1.06 ±0.03</td><td>1.28 ±0.09</td><td>0.92 ±0.03</td><td>2.43 ±0.03</td><td>1.09 ±0.07</td><td>0.36 ±0.07</td><td>1.22 ±0.03</td><td>22.02 ±0.83</td><td>2.17 ±0.09</td></tr><tr><th><i>A. schwarzi</i> (Kütahya-Civanağa) N=3</th><td>22.33 ±1.15</td><td>6.82 ±0.29</td><td>2.16 ±0.19</td><td>5.04 ±0.28</td><td>18.17 ±0.80</td><td>3.63 ±0.35</td><td>1.05 ±0.00</td><td>1.26 ±0.05</td><td>0.91 ±0.03</td><td>2.45 ±0.03</td><td>0.93 ±0.04</td><td>0.48 ±0.03</td><td>1.28 ±0.05</td><td>19.47 ±0.47</td><td>2.13 ±0.06</td></tr><tr><th><i>A. schwarzi</i> (Denizli Çameli) N=5</th><td>23.04 ±1.51</td><td>7.50 ±0.30</td><td>2.16 ±0.20</td><td>5.61 ±0.11</td><td>21.54 ±0.93</td><td>4.54 ±0.29</td><td>1.09 ±0.03</td><td>1.33 ±0.04</td><td>0.95 ±0.05</td><td>2.62 ±0.09</td><td>1.19 ±0.06</td><td>0.19 ±0.04</td><td>1.40 ±0.02</td><td>22.04 ±1.65</td><td>2.06 ±0.11</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Konya-Rezebeli) N=3</th><td>22.73 ±0.64</td><td>5.80 ±0.16</td><td>1.60 ±0.06</td><td>4.19 ±0.08</td><td>15.97 ±0.15</td><td>3.97 ±0.06</td><td>0.89 ±0.00</td><td>1.09 ±0.03</td><td>0.79 ±0.00</td><td>2.24 ±0.03</td><td>0.80 ±0.04</td><td>0.28 ±0.03</td><td>1.22 ±0.05</td><td>13.97 ±0.15</td><td>1.80 ±0.10</td></tr><tr><th><i>A. moli</i> <b>sp. nov.</b> (Konya-Sultandağ) N=6</th><td>22.25 ±1.17</td><td>6.98 ±0.22</td><td>2.22 ±0.14</td><td>5.22 ±0.16</td><td>20.95 ±0.83</td><td>4.02 ±0.19</td><td>1.10 ±0.06</td><td>1.28 ±0.03</td><td>0.81 ±0.04</td><td>2.49 ±0.07</td><td>1.12 ±0.05</td><td>0.43 ±0.03</td><td>1.45 ±0.07</td><td>21.59 ±1.11</td><td>2.08 ±0.10</td></tr></tbody></table><p>m—Mean; sd—Standard deviation; N—individuals</p>
Data from: A robust and representative lower bound on object processing speed in humans
How early does the brain decode object categories? Addressing this question is critical to constrain the type of neuronal architecture supporting object categorization. In this context, much effort has been devoted to estimating face processing speed. With onsets estimated from 50 to 150 ms, the timing of the first face-sensitive responses in humans remains controversial. This controversy is due partially to the susceptibility of dynamic brain measurements to filtering distortions and analysis issues. Here, using distributions of single-trial event-related potentials (ERPs), causal filtering, statistical analyses at all electrodes and time points, and effective correction for multiple comparisons, we present evidence that the earliest categorical differences start around 90 ms following stimulus presentation. These results were obtained from a representative group of 120 participants, aged 18-81, who categorized images of faces and noise textures. The results were reliable across testing days, as determined by test-retest assessment in 74 of the participants. Furthermore, a control experiment showed similar ERP onsets for contrasts involving images of houses or white noise. Face onsets did not change with age, suggesting that face sensitivity occurs within 100 ms across the adult lifespan. Finally, the simplicity of the face-texture contrast, and the dominant midline distribution of the effects, suggest the face responses were evoked by relatively simple image properties and are not face specific. Our results provide a new lower benchmark for the earliest neuronal responses to complex objects in the human visual system.
Genomic evidence that governmentally produced Cannabis sativa poorly represents genetic variation available in state markets
<p>The National Institute on Drug Abuse (NIDA) is the sole producer of <i>Cannabis </i>for research purposes in the United States, including medical investigation. Previous research established that cannabinoid profiles in the NIDA varieties lacked diversity and potency relative to the <i>Cannabis </i>produced commercially. Additionally, microsatellite marker analyses have established that the NIDA varieties are genetically divergent form varieties produced in the private legal market. Here, we analyzed the genome of multiple <i>Cannabis </i>varieties from diverse lineages including two produced by NIDA, and we provide further support that NIDA's varieties differ from widely available medical, recreational, or industrial <i>Cannabis</i>. Furthermore, our results suggest that NIDA's varieties lack diversity in the single copy portion of the genome, the maternally inherited genomes, the cannabinoid genes, and in the repetitive content of the genome. Therefore, results based on NIDA's varieties are not generalizable regarding the effects of <i>Cannabis </i>after consumption. For medical research to be relevant, material that is more widely used would have to be studied. Clearly, having research to date dominated by a single, non-representative source of <i>Cannabis</i> has hindered scientific investigation.</p>
Figure 4 in The enigmatic milliped genus Pandirodesmus Silvestri 1932 and description of a new species from Tobago represented by males (Polydesmida: Leptodesmidea: Chelodesmidae: Chelodesminae: Pandirodesmini)
Figure 4. Distributions of Pandirodesmus and Pandirodesmini. Red dot, P. rutherfordi. Red star, P. disparipes.
Figure 7 from: Strong EE, Sirenko BI, McLean JH (2021) The only species of Mohnia Friele, 1879 (Caenogastropoda, Buccinoidea, Buccinidae) in the North Pacific represents an unrecognized new genus of Newtoniellidae (Triphoroidea). ZooKeys 1055: 69-87. https://doi.org/10.3897/zookeys.1055.68911
Figure 7 Radula morphology of Pseudomohnia sp., LACM 1997-168.10 A radular ribbon B detail of rachidian and lateral teeth C detail of rachidian D, E detail of lateral and marginal teeth F detail of inner and outer marginal teeth. Scale bars: 20 µm (C, F); 100 µm (A, B, D, E).
Figure 6 from: Strong EE, Sirenko BI, McLean JH (2021) The only species of Mohnia Friele, 1879 (Caenogastropoda, Buccinoidea, Buccinidae) in the North Pacific represents an unrecognized new genus of Newtoniellidae (Triphoroidea). ZooKeys 1055: 69-87. https://doi.org/10.3897/zookeys.1055.68911
Figure 6 Radula and jaw morphology of Pseudomohnia rogerclarki sp. nov., holotype, LACM 3776 A radular ribbon B detail of rachidian and lateral teeth C detail of rachidian D detail of lateral and marginal teeth E detail of inner and outer marginal teeth F jaw, inner surface. Scale bars: 10 µm (C); 20 µm (B, D, E); 100 µm (A, F).
Figure 4 from: Strong EE, Sirenko BI, McLean JH (2021) The only species of Mohnia Friele, 1879 (Caenogastropoda, Buccinoidea, Buccinidae) in the North Pacific represents an unrecognized new genus of Newtoniellidae (Triphoroidea). ZooKeys 1055: 69-87. https://doi.org/10.3897/zookeys.1055.68911
Figure 4 Radula morphology and gut contents of Pseudomohnia kurilana (Dall, 1913) comb. nov., lectotype, USNM 205224 A radular ribbon B detail of rachidian and lateral teeth C detail of rachidian D detail of marginal teeth E detail of inner and outer marginal teeth F sponge spicules from gut. Scale bars: 20 µm (C, D, E); 100 µm (A, B, F).
Figure 5 from: Strong EE, Sirenko BI, McLean JH (2021) The only species of Mohnia Friele, 1879 (Caenogastropoda, Buccinoidea, Buccinidae) in the North Pacific represents an unrecognized new genus of Newtoniellidae (Triphoroidea). ZooKeys 1055: 69-87. https://doi.org/10.3897/zookeys.1055.68911
Figure 5 Anatomy of Pseudomohnia gen. nov. APseudomohnia kurilana (Dall, 1913) comb. nov., lectotype, USNM 205224 B–EPseudomohnia sp., LACM 1997-168.10 A, B external anatomy, dorsal view, mantle cavity opened via mid-dorsal incision C foregut, dorsal view D foregut, left-lateral view E pallial gonoduct, left-lateral view. Scale bars 1 mm. Abbreviations: ae, anterior esophagus; bg, buccal ganglion; cs, longitudinal cleft in foot sole; ct, ctendium; dg, digestive gland; go, gonad; hg, hypobranchial gland; meg, mid-esophageal gland; od, odontophore; op, opercular lobe; os, osphradium; pg, pallial gonoduct; ppg, propodeal pedal gland; r, rectum; rm, retractor muscles; rs, radular sac; sg, salivary gland; si, siphon; sp, supra-esophageal ganglion; sto, stomach; t, cephalic tentacle.
Figure 3 from: Strong EE, Sirenko BI, McLean JH (2021) The only species of Mohnia Friele, 1879 (Caenogastropoda, Buccinoidea, Buccinidae) in the North Pacific represents an unrecognized new genus of Newtoniellidae (Triphoroidea). ZooKeys 1055: 69-87. https://doi.org/10.3897/zookeys.1055.68911
Figure 3 Protoconch and operculum morphology of Pseudomohnia gen. nov. A, B, EPseudomohnia kurilana (Dall, 1913) comb. nov. Lectotype, USNM 205224 C, D, FPseudomohnia rogerclarki sp. nov. Holotype, LACM 3776 A, C protoconch, apical view B, D protoconch, lateral view E, F Operculum. Black arrows indicate approximate position of inferred transition between protoconch and teleoconch. Scale bar: 1 mm.
Figure 2 from: Strong EE, Sirenko BI, McLean JH (2021) The only species of Mohnia Friele, 1879 (Caenogastropoda, Buccinoidea, Buccinidae) in the North Pacific represents an unrecognized new genus of Newtoniellidae (Triphoroidea). ZooKeys 1055: 69-87. https://doi.org/10.3897/zookeys.1055.68911
Figure 2 Distribution of Pseudomohnia gen. nov. in the North Pacific. Squares, Pseudomohnia kurilana (Dall, 1913) comb. nov.; circles, Pseudomohnia rogerclarki sp. nov.; stars, Pseudomohnia sp. Symbols with black fill are type localities. Scale in kilometers.
Figure 1 from: Strong EE, Sirenko BI, McLean JH (2021) The only species of Mohnia Friele, 1879 (Caenogastropoda, Buccinoidea, Buccinidae) in the North Pacific represents an unrecognized new genus of Newtoniellidae (Triphoroidea). ZooKeys 1055: 69-87. https://doi.org/10.3897/zookeys.1055.68911
Figure 1 Shell morphology of Pseudomohnia gen. nov. A, BPseudomohnia kurilana (Dall, 1913) comb. nov A lectotype, USNM 205224. Kuril Islands BZIN 57494/1. Kuril Islands C, DPseudomohnia sp. LACM 1997-156.7 Aleutian Islands E–IPseudomohnia rogerclarki sp. nov. Aleutian Islands E holotype, LACM 3776 FLACM 1997-174 GLACM 1997-174 HLACM 1997-163.21 ILACM 1997-165.20. Scale bar: 1 cm.
Figure 3 in A primitive representative of the Parabathynellidae (Bathynellacea, Syncarida) from the Yilgarn Craton of Western Australia
Figure 3. Billibathynella humphreysi sp. nov. (holotype). (A) Right thoracopod I " (frontal); (B) pleotelson and furcal rami " (dorsal); (C) pleotelson, furcal rami, and uropod " (lateral); (D) left uropod " (dorsal). Scale bars: 0.5 mm.
FIGURE 3 in Description of Electrogena sartorii sp. nov., a new representative of the genus Electrogena Zurwerra & Tomka, 1985 (Ephemeroptera: Heptageniidae), from Iran using molecular and morphological data
FIGURE 3. Whole larva in dorsal view with body coloration of Electrogena sartorii sp. nov.
Fig. 38 in Erichsonius (Sectophilonthus) jelineki sp. nov., the first representative of the genus from the Seychelles (Coleoptera: Staphylinidae: Staphylininae)
Fig. 38. Mount Trois Frères, the type locality of Erichsonius jelineki sp. nov. Arrows indicate the places at which the specimens were collected.
Figure 1 from: Rasnitsyn AP (2021) First Jurassic representative of the extinct family Peleserphidae (Hymenoptera, Proctotrupoidea). In: Proshchalykin MYu, Gokhman VE (Eds) Hymenoptera studies through space and time: A collection of papers dedicated to the 75th anniversary of Arkady S. Lelej. Journal of Hymenoptera Research 84: 295-300. https://doi.org/10.3897/jhr.84.65493
Figure 1 Arkadiserphus leleji sp. nov., holotype A general appearance, side view B interpretation (cly, clypeus; cx1, cx2, cx3, pro-, meso- and metacoxa; f1, f2, pro- and mesofemur; md, mandible; N1, N2, N3, pro-, meso- and metanotum; ppd, propodeum; scl2, mesoscutellum; ti3, hind tibia; tl3, hind trochantellus; I–VII, metasomal terga; 1–6, metasomal sterna) C fore wing (vein names standard). Scale bar: 1 mm.
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.