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FIGURE 158 in Review of Gonatocerus (Hymenoptera: Mymaridae) in the Palaearctic region, with notes on extralimital distributions
FIGURE 158. Gonatocerus (Lymaenon) longior Ƥ (holotype): slide.
FIGURES 65, 66 in Review of Gonatocerus (Hymenoptera: Mymaridae) in the Palaearctic region, with notes on extralimital distributions
FIGURES 65, 66. Gonatocerus (Lymaenon) aureus Ƥ (neotype): 65, slide; 66, habitus.
FIGURES 58–60 in Review of Gonatocerus (Hymenoptera: Mymaridae) in the Palaearctic region, with notes on extralimital distributions
FIGURES 58–60. Gonatocerus (Lymaenon) africanus Ƥ (paratype): 58, antennae; 59, wings; 60, habitus.
FIGURE 108. Distribution map for Collaria meilleurii and C in Taxonomic revision of Collaria Provancher, 1872 (Hemiptera: Miridae) with the description of a new species from the Afrotropical region
FIGURE 108. Distribution map for Collaria meilleurii and C. oculata.
Distribution of economic damages due to climate-driven sea-level rise across European regions and sectors
<p>The datasets generated during and/or analysed during the study</p>
Fig. 2 in A Diminutive New Speciesof DicronocephalusHope (Coleoptera: Scarabaeidae: Cetoniinae) from Xizang Zizhiqu (Tibet Autonomous Region), China, with a Distributional Analysis of the Genus
Fig. 2. Parameres of Dicronocephalus dabryi (left) and Dicronocephalus diminuata (right).
Fig. 6 in Distribution, systematics and nomenclature of the three taxa of Common Stonechats (Aves, Passeriformes, Muscicapidae, Saxicola) that breed in the Caucasian region
Fig. 6. Males in worn summer plumage, ventral (A, B) and dorsal (C, D) view. A, C, Saxicola maurus variegatus, coll. No. 28005/106, Azerbaijan, Ismailli Distr., vicinity of Ismailly, 40°46.99′ N, 48°06.73′ E, 540 m a.s.l., 2 July 1973, ad., V.M. Loskot leg. (NMNH); B, D, Saxicola maurus armenicus, coll. No. 25070/86, Armenia, Syunik Prov., vicinity of Goris, 39°31.16′ N, 46°21.42′ E, 1,650 m a.s.l., 13 June 1960, sad., M.I. Golovushkin leg. (NMNH).
Data from: 'Species traits to guide moth conservation in anthropogenic regions: a multi-species approach using distribution trends in Flanders'
<p>These data are related to the investigation of species traits as a guidance for moth conservation in the highly anthropogenic European region of Flanders (northern part of Belgium) based on Multi-Species Change Indices (MSCIs).</p> <p><strong>Abstract</strong></p> <ol> <li>Insects appear to decline rapidly in recent decades. This so-called sixth mass extinction garnered significant media attention, raising public awareness.</li> <li>Macro-moths—a species-rich and ecologically diverse insect group—face severe declines, particularly in urbanised and intensively farmed areas.</li> <li>Flanders is a highly anthropogenic region, serving as a case study where the impact on macro-moths of stressors like intensive agriculture, industrialization and urbanization has been quantified through a recently compiled Red List. Here, for 717 macro-moth species, we calculated relative changes in distribution area between a reference period (1980-2012) and the subsequent period (2013-2022). By correlating these species-specific trends with ten key ecological and life-history traits, we calculated more general Multi-Species Change Indices (MSCIs).</li> <li>These MSCIs showed that species associated with wet biotopes and heathlands declined on average by 20-25%, while (sub)urban species increased by more than 60%. Species feeding on lichens or mosses increased by 31%, while grass-feeding species decreased by 20%. Both very small (+34%) and very large species (+15%) increased, whereas medium-sized species decreased by 5%. Monophagous (+17%), migrant (+88%), and colour-invariable species (+5%) increased, while colour-variable species decreased (-8%). Finally, Holarctic (-21%) and Palearctic species (-5%) decreased, while Mediterranean (+27%) and Western-Palearctic species (+9%) increased.</li> <li>Our trait-based approach identifies key threats and mitigation strategies for moths in anthropogenic regions, offering evidence-based insights for crafting efficient management recommendations and informed conservation policies to safeguard moth communities.</li> </ol>
TABLE 1 in Australia's deep-water octocoral fauna: historical account and checklist, distributions and regional affinities of recent collections
<p><b>TABLE 1.</b> Summary of the number of sampling stations and depth ranges of octocoral collections during 6 biodiversity surveys in four regions in offshore Australian waters; number of sampling stations are broken down by sampling gear type (see text for references of gear types and survey codes). The numbers and depth range of sampling stations where octocoral were collected are shown separately.</p><table><tbody><tr><th>Survey region</th><th>North Tasman</th><th>South-eastern Australia</th><th></th><th></th><th></th><th>South-western Australia</th><th>North-western Australia</th><th>Overall</th><th></th></tr></tbody><tbody><tr><th>Survey year</th><td>2003</td><td></td><td>1997</td><td></td><td>2007</td><td></td><td>2008</td><td></td><td>2005</td><td></td><td>2007</td><td></td><td>1997–2008</td></tr><tr><th>Survey Code</th><td>Tan0308</td><td></td><td>SS01/97</td><td></td><td>SS02/07</td><td></td><td>TT01/08</td><td></td><td>SS10/05</td><td></td><td>SS05/07</td><td></td><td>Grand Total</td></tr><tr><th>Depth range (m)</th><td>77–1927</td><td></td><td>670–1694</td><td>105–1255</td><td>729–3950</td><td>86–1092</td><td></td><td>78–1022</td><td></td><td>77–3950</td></tr><tr><th>Number of sampling stations</th><td>Total</td><td>SP-Sample1)</td><td>Total</td><td>SP-Sample1)</td><td>TOTAL</td><td>SP-Sample1)</td><td>TOTAL</td><td>SP-Sample1)</td><td>TOTAL</td><td>SP-Sample1)</td><td>TOTAL</td><td>SP-Sample1)</td><td>TOTAL</td><td>SP-Sample1)</td></tr><tr><th></th><td>57</td><td>47</td><td>28</td><td>27</td><td>46</td><td>45</td><td>77</td><td>57</td><td>74</td><td>64</td><td>54</td><td>51</td><td>336</td><td>291</td></tr><tr><th>Beam trawl</th><td>13</td><td>10</td><td></td><td></td><td></td><td></td><td></td><td></td><td>37</td><td>30</td><td>33</td><td>30</td><td>83</td><td>72</td></tr><tr><th>CSIRO Sherman sled</th><td>16</td><td>13</td><td>27</td><td>26</td><td>46</td><td>45</td><td></td><td></td><td>37</td><td>32</td><td>12</td><td>12</td><td>138</td><td>128</td></tr><tr><th>NIWA sled</th><td>2</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>2</td><td>1</td></tr><tr><th>Rock dredge</th><td>1</td><td>1</td><td></td><td></td><td></td><td></td><td>1</td><td>1</td><td></td><td></td><td></td><td></td><td>2</td><td>2</td></tr><tr><th>Commercial fish trawl</th><td>15</td><td>13</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>9</td><td>9</td><td>24</td><td>23</td></tr><tr><th>Ratcatcher trawl</th><td>10</td><td>9</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>10</td><td>9</td></tr><tr><th>Dropline</th><td></td><td></td><td>1</td><td>1</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>1</td><td>1</td></tr><tr><th>ROV <i>Jason</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td>76</td><td>56</td><td></td><td></td><td></td><td></td><td>76</td><td>56</td></tr></tbody></table><p>1) SP-Sample identifies the number of sampling stations from which octocorals were identified to species-level</p>
TABLE 3 in Australia's deep-water octocoral fauna: historical account and checklist, distributions and regional affinities of recent collections
<p><b>TABLE 3.</b> Octocoral genera sampled in>5% of the 320 sampling stations, showing the number of sampling stations at which they were collected in total and by survey region and the depth range of the collections.</p><table><tbody><tr><th>Genus</th><th>Number of sampling stations</th><th>min. depth (m)</th><th>max. depth (m)</th><th>N Tasman</th><th>SE Australia</th><th>SW Australia</th><th>NW Australia</th></tr></tbody><tbody><tr><th><i>Acanthogorgia</i></th><td>35</td><td>81</td><td>1150</td><td>7</td><td>13</td><td>6</td><td>9</td></tr><tr><th><i>Anthomastus</i></th><td>41</td><td>230</td><td>1694</td><td>2</td><td>33</td><td>4</td><td>2</td></tr><tr><th><i>Anthothela</i></th><td>26</td><td>181</td><td>1525</td><td></td><td>19</td><td>6</td><td>1</td></tr><tr><th><i>Chironephthya</i></th><td>24</td><td>78</td><td>751</td><td>4</td><td></td><td>4</td><td>16</td></tr><tr><th><i>Chrysogorgia</i></th><td>66</td><td>124</td><td>2395</td><td>6</td><td>47</td><td>5</td><td>8</td></tr><tr><th><i>Corallium</i></th><td>19</td><td>311</td><td>2173</td><td>1</td><td>16</td><td>2</td><td></td></tr><tr><th><i>Dendronephthya</i></th><td>43</td><td>77</td><td>1081</td><td>3</td><td></td><td>11</td><td>29</td></tr><tr><th><i>Keratoisis</i></th><td>32</td><td>257</td><td>2898</td><td>8</td><td>24</td><td></td><td></td></tr><tr><th><i>Lepidisis</i></th><td>38</td><td>330</td><td>3950</td><td>15</td><td>21</td><td>1</td><td>1</td></tr><tr><th><i>Narella</i></th><td>37</td><td>440</td><td>2559</td><td>3</td><td>30</td><td>2</td><td>2</td></tr><tr><th><i>Pennatula</i></th><td>20</td><td>95</td><td>1273</td><td>12</td><td>1</td><td></td><td>7</td></tr><tr><th><i>Pleurogorgia</i></th><td>20</td><td>915</td><td>1525</td><td></td><td>20</td><td></td><td></td></tr><tr><th><i>Primnoisis</i></th><td>29</td><td>670</td><td>1511</td><td>1</td><td>28</td><td></td><td></td></tr><tr><th><i>Thouarella</i></th><td>37</td><td>342</td><td>1375</td><td>5</td><td>32</td><td></td><td></td></tr><tr><th><i>Tokoprymno</i></th><td>23</td><td>729</td><td>1694</td><td></td><td>23</td><td></td><td></td></tr></tbody></table>
Supplementary material 1 from: Palchetti MV, Cantero JJ, Morales-Fierro V, Barboza GE, Moreira-Muñoz A (2021) Living in extreme environments: distribution of Lycium humile (Solanaceae), an endemic halophyte from the Altiplano-Puna region, South America. PhytoKeys 185: 1-15. https://doi.org/10.3897/phytokeys.185.71377
Occurences of Lycium humile in South America
Figure 4 from: Palchetti MV, Cantero JJ, Morales-Fierro V, Barboza GE, Moreira-Muñoz A (2021) Living in extreme environments: distribution of Lycium humile (Solanaceae), an endemic halophyte from the Altiplano-Puna region, South America. PhytoKeys 185: 1-15. https://doi.org/10.3897/phytokeys.185.71377
Figure 4 Saline environments of the Altiplano-Puna region (South America) in which Lycium humile grows A Salar del Hombre Muerto (Catamarca, Argentina) B Los Colorados (Salta, Argentina) C Salar de Uyuni (Potosí, Bolivia).
Figure 2 from: Palchetti MV, Cantero JJ, Morales-Fierro V, Barboza GE, Moreira-Muñoz A (2021) Living in extreme environments: distribution of Lycium humile (Solanaceae), an endemic halophyte from the Altiplano-Puna region, South America. PhytoKeys 185: 1-15. https://doi.org/10.3897/phytokeys.185.71377
Figure 2 Lectotype of Lycium humile Phil. (SGO 055683). Digital image by courtesy of the Museo Nacional de Historia Natural.
Distribution. Pacific coast of the Canal Zone region in Panama. in Molossidae
Distribution. Pacific coast of the Canal Zone region in Panama.
Fig. 2 in Current Distribution Of The European Grayling, Thymallus Thymallus, And Huchen, Hucho Hucho, In The Transcarpatian Region Of Ukraine
Fig. 2. Distribution of the huchen, Hucho hucho, in the Transcarpatian Region of Ukraine: potential distribution — information obtained from interviewing inspectors of the Transcarpathian Fish Protection Inspection, forestry inspectors, and local people; places of catches — sites, where huchen were actually caught and/or recorded during scientific surveys, in recreational or poacher's fishing gears, places of introduction — sites were huchen were released intentionally or escaped accidentally.
Distribution. Restricted to upper Changena River region, Bocas del Toro Province, W Panama. in Phyllostomidae
Distribution. Restricted to upper Changena River region, Bocas del Toro Province, W Panama.
Distribution. Andean regions of W Venezuela, Colombia, Ecuador, and Peru. in Phyllostomidae
Distribution. Andean regions of W Venezuela, Colombia, Ecuador, and Peru.
Distribution. Andean altiplano, in S Peru (Puno Region) and W Bolivia (La Paz Department). in Ctenomyidae
Distribution. Andean altiplano, in S Peru (Puno Region) and W Bolivia (La Paz Department).
Distribution. High-elevation regions of Ethiopia. in Nesomyidae
Distribution. High-elevation regions of Ethiopia.
Distribution. Endemic to E edge of the Central Highlands of Madagascar (Anjozorobe region). in Nesomyidae
Distribution. Endemic to E edge of the Central Highlands of Madagascar (Anjozorobe region).
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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.
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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.