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Figure 3 in Eriophyoid (Trombidiformes: Eriophyoidea) mite species associated with boxes worldwide with a new record of Eriophyes canestrinii (Nalepa, 1890) from Iran
Figure 3. Deformation on Buxus sempervirens hyrcana bud caused by Eriophyes canestrinii.
Figure 2 in Eriophyoid (Trombidiformes: Eriophyoidea) mite species associated with boxes worldwide with a new record of Eriophyes canestrinii (Nalepa, 1890) from Iran
Figure 2. High population of Eriophyes canestrinii collected on Buxus sempervirens hyrcana (×100).
Figure 1. Localities associated with two new Maratus species from southeastern Australia. M in Two new peacock spiders from southeastern Australia (Araneae: Salticidae: Euophryini: Maratus Karsch 1878)
Figure 1. Localities associated with two new Maratus species from southeastern Australia. M. nimbus was found near standing or intermittent water at three locations in the south (1-2, 5), but also at Sturt National Park in the arid interior (3-4). Only a single location is known for M. sapphirus. Background courtesy of NASA Visible Earth.
Effects of nest-site availability on male-male competition and the foraging costs associated with paternal care in a resource-defense species
<p><strong>Effects of nest-site availability on male-male competition and associated costs of nest site maintenance and paternal care in a resource-defense species</strong></p> <p>This repository contains the .csv files used for the statistical analyses of the study "Effects of nest-site availability on male-male competition and associated costs of nest site maintenance and paternal care in a resource-defense species". In case of questions, please email Laís A. Grossel: <a href="mailto:laisgrossel@gmail.com">laisgrossel@gmail.com</a></p> <p><strong>Data files and structure</strong></p> <p>We have files for the analysis with field and experimental data.</p> <p>With the file <strong>field.csv</strong> we tested the probability of males obtaining a nest and receiving eggs from females. In this file, we have the headers:</p> <ul> <li><strong>maleID:</strong> identity of males in the field</li> <li><strong>DSW:</strong> dorsal scute width, in mm</li> <li><strong>mass:</strong> to the nearest 0.001 g</li> <li><strong>nest_possession:</strong> with 2 levels: 0 if the male did not possess a nest and 1 if the male possessed a nest</li> <li><strong>nest_opening:</strong> in cm</li> <li><strong>parental_status:</strong> with 3 levels: 0 if the male did not have a nest, 1: if the male had a nest but no eggs, and 2: if the male had a nest and eggs</li> </ul> <p>With the file <strong>experiment_nests.csv</strong> we tested predictions related with the nest possession. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>nestID:</strong> identity of the nests</li> <li><strong>occupation:</strong> if the nest was once occupied during the experiment, with 2 levels: 0 if it was never occupied and 1 if it was occupied at least once</li> <li><strong>occupied_scans:</strong> number of scans with any male inside the nest</li> <li><strong>vacant_scans:</strong> number of scans without any male inside the nest</li> <li><strong>total_scans:</strong> total number of observation scans </li> <li><strong>owners:</strong> number of different owners of the nest (at least 6 consecutive scans)</li> <li><strong>turnover:</strong> if there was at least a substitution of the nest owner without figths, with 2 levels: 0 if there was not any substitution and 1 if there was a substitution</li> <li><strong>turnovers_number:</strong> number of substitutions of the nest owner without figths</li> <li><strong>takeover:</strong> if there was at least a takeover attempt of the nest after figths, with 2 levels: 0 if there was not any attempt and 1 if there was an attempt</li> <li><strong>takeovers_number:</strong> number of takeover attempts of the nest after figths</li> <li><strong>fight:</strong> if there was at least a figth inside or close to the nest, with 2 levels: 0 if there was not any figth and 1 if there was a figth</li> <li><strong>fights_number:</strong> number of figths inside or close to the nest</li> <li><strong>canibalism:</strong> if there was at least a cannibalism event inside the nest, 2 levels: 0 if there was not any cannibalism event and 1 if there was a cannibalism event</li> <li><strong>canibalism_number:</strong> number of cannibalism events inside the nest</li> </ul> <p>With the file <strong>experiment_males.csv</strong> we tested predictions related to the males owners. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>maleID:</strong> identitity of the males</li> <li><strong>DSW:</strong> dorsal scute width, in mm</li> <li><strong>nest_possession:</strong> with 2 levels: 0 if the male never possessed a nest during the experiment and 1 if the male possessed a nest at least once (6 consecutive scans)</li> <li><strong>nestID:</strong> identity of the nest possessed by the male</li> <li><strong>inside_scans:</strong> number of scans with the male inside his nest</li> <li><strong>outside_scans:</strong> number of scans with the male outside his nest</li> <li><strong>total_scans:</strong> total number of scans in which the male was the owner of the nest</li> <li><strong>takeover:</strong> if the male suffered a takeover attempt of his nest, with 2 levels: 0 if the male did not suffer any attempt and 1 if the male suffered an attempt</li> <li><strong>eggs:</strong> if the male received eggs from a female, with 2 levels: 0 if the male did not receive eggs and 1 if the male received eggs</li> <li><strong>eggs_number:</strong> number of eggs received </li> <li><strong>cannibalism:</strong> if the owner male cannibalized the eggs inside the nest, 2 levels: 0 if the male did not cannibalize eggs and 1 if the male cannibalized eggs</li> <li><strong>cannibalism_number:</strong> number of cannibalism events by the owner male </li> </ul> <p>With the file <strong>fights-takeovers.csv</strong> we tested predictions related with nest takeovers. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>nestID:</strong> identity of the nest possessed by the male</li> <li><strong>focalID:</strong> identitity of the focal males (the owner nest)</li> <li><strong>DSW:</strong> dorsal scute width, in mm</li> <li><strong>fight:</strong> if the male was involved in at least a figth, with 2 levels: 0 if the male was not involved in any figth and 1 if the male was involved in a figth</li> <li><strong>takeover:</strong> if the male suffered a takeover attempt of his nest, with 2 levels: 0 if the male did not suffer any attempt and 1 if the male suffered an attempt. Obs: the nest takeover always happens after a fight. If there was a takeover, then there was a fight too.</li> <li><strong>res_focal: </strong>result of the figth or takeover for the focal male, with 2 levels: 0 if the focal male did not lose the figth or the nest and 1 if the focal male lost the figth or the nest</li> <li><strong>intruderID:</strong> identity of the intruder male involved in the figth or the takeover with the owner male</li> <li><strong>intruder_DSL: </strong>dorsal scute width of the intruder male, in mm</li> <li><strong>dyad:</strong> identity of the two individuals involved in the figth or takeover (owner male and intruder male)</li> <li><strong>DSW_difference:</strong> difference between the dorsal scute width of the dyad (focal male minus intruder male)</li> </ul> <p>With the file <strong>foraging.csv</strong> we tested a prediction related with males foraging. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>nestID:</strong> identity of the nest possessed by the male</li> <li><strong>maleID:</strong> identitity of the males</li> <li><strong>parental_status:</strong> with 2 levels: 0 if the male did not have eggs in the nest and 1: if the male had eggs</li> <li><strong>inside_scans:</strong> number of scans with the male inside his nest</li> <li><strong>outside_scans:</strong> number of scans with the male outside his nest</li> <li><strong>total_scans:</strong> total number of scans in which the male was the owner of the nest</li> </ul>
Fig. 13 in Histopathological characterisation of retinal lesions associated to Diplostomum species (Platyhelminthes: Trematoda) infection in polymorphic Arctic charr Salvelinus alpinus
Fig. 13. Diplostomum sp. metacercaria in a choroidal vessel. Scale bar = 200 μm.
New Zealand native forest plant cover data for Popovic et al. MEE (2019), Untangling direct species associations from indirect mediator species effects with graphical models.
<p>Forest cover measurements were collected at 1246 native forest sites that form part of a network of permanent 20 x 20 m plots spread throughout New Zealand. A total of 1831 plant species were present in these plots, with the most common being herbs, graminoids, ferns, shrubs and trees. Plant cover (in ordinal categories) was assessed for each species in several tiers at different heights. The cover data we analysed (<em>NZ_native_forest_cover.csv) </em>were the maximum cover recorded over all the tiers at the 964 sites identified as native forests, containing 1311 species with at least one presence. <em>NZ_native_forest_species.csv</em> contains species data including species name, exotic/native, and plant type (tree, shrub, etc.), corresponding to the plant species in the columns of <em>NZ_native_forest_cover.csv</em>.</p> <p>We acknowledge the use of data drawn from the Natural Forest plot data collected between January 2002 and March 2007 by the LUCAS programme for the Ministry for the Environment, New Zealand.</p> <p> </p>
Datasets associated with: Comparing temperature data sources for use in species distribution models: From in-situ logging to remote sensing. Global Ecology and Biogeography
<p>Data associated with the paper 'Comparing temperature data sources for use in species distribution models: From in-situ logging to remote sensing. Global Ecology and Biogeography' by Lembrechts JJ et al., published in Global Ecology and Biogeography.</p> <p>Contains a dataset containing all extracted and measured temperature variables for all 106 measurement plots (climatedata), as well as the climate and species data used in the Species Distribution Models (SDMs). </p> <p>For details on the content of the table, see the readme-file, for details on methodology, see the original paper. </p>
Figure 4 in Chewing lice (Phthiraptera: Amblycera, Ischnocera) species found on birds in Turkey, with new records and a new host association
Figure 4. Cuclotogaster heterographus, male, original.
Figure 3 in Chewing lice (Phthiraptera: Amblycera, Ischnocera) species found on birds in Turkey, with new records and a new host association
Figure 3. Cuclotogaster heterographus, female, original.
Figure 5 in Chewing lice (Phthiraptera: Amblycera, Ischnocera) species found on birds in Turkey, with new records and a new host association
Figure 5. Cuclotogaster heterographus, male genitalia, original.
Figure. Relative abundance of species in the Phyllonorycter parasitoid complex. in Hymenopterous parasitoids associated with Phyllonorycter coryli (Nic.) and Phyllonorycter nicellii (Stt.) on hazel in Poland
Figure. Relative abundance of species in the Phyllonorycter parasitoid complex.
Fig. 3 in Male and female association in Trichomyia Haliday in Curtis, 1839 using a molecular approach (Diptera, Psychodidae, Trichomyiinae), and description of new species from Brazil
Fig. 3. Dendrogram of genetic similarity among Trichomyia species analyzed, F, female.
Fig. 10 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus
Fig. 10. Crinotonia attenuatus (Bruce), new combination, male (PCL 3.2 mm). Scale bar = 5 mm.
Figure 1 in Unusual shallow-water boreal gastropod species associations at the Northern part of Arctic archipelago Novaya Zemlya
Figure 1. Map of studied areas off Novaya Zemlya.
Fig. 2 in From wildlife to humans: The global distribution of Trichinella species and genotypes in wildlife and wildlife-associated human trichinellosis
Fig. 2. Global distribution of Trichinella spiralis in wildlife reported in this review.
Fig. 1 in A new species of Torymus (Hymenoptera: Torymidae) associated with two genera of Bruchinae (Coleoptera: Chrysomelidae) in México
Fig. 1. Regional distribution of Torymus moazopi n. sp. in Mexico.
Fig. 3 in A new species of Torymus (Hymenoptera: Torymidae) associated with two genera of Bruchinae (Coleoptera: Chrysomelidae) in México
Fig. 3. Torymus moazopi sp. nov. (Allotype) (Male): (a) lateral habitus; (b) head, frontal view.
Table 1 in A new species-group with new species of the genus Lasioseius (Acari: Mesostigmata: Blattisociidae) associated with Neotropical hispine beetles in furled leaves ofHeliconia
<p><b>Table 1</b> Co-occurrence of species of <i>Lasioseius</i> with beetles in host plant leaves, La Selva, Costa Rica. Abbreviations: coex, coexistent; <i>H.</i>, <i>Heliconia</i>; n/c, no data; ALAS, Arthopods of La Selva parataxonomist collectors; DJ, Derek Johnson, collector; EEL, Evert E. Lindquist, collector; MP, Maylin Paniagua, collector.</p><table><tbody><tr><th></th><th><b>Collection Records</b></th><th></th><th></th><th><i>Lasioseius new species</i></th><th></th></tr></tbody><tbody><tr><th><b>Coll. date</b></th><td><b>host beetle</b></td><td><b>host plant</b></td><td><b>collector</b></td><td><i>cassid.</i></td><td><i>serripes</i></td><td><i>fuscina</i></td><td><i>duobtu.</i></td></tr><tr><th>Feb '94</th><td><i>Chelobasis sp.</i></td><td><i>H. pogonantha</i></td><td>EEL/ALAS</td><td><b>+</b></td><td></td><td></td><td><b>+</b></td></tr><tr><th>Feb '94</th><td><i>Cephaloleia vicina</i> (= <i>bella</i>)</td><td><i>H. pogonantha</i></td><td>EEL/ALAS</td><td>+</td><td></td><td></td><td></td></tr><tr><th>18 Feb '94</th><td>Chrysomelidae</td><td>n/c</td><td>ALAS</td><td><b>+</b></td><td></td><td><b>+</b></td><td></td></tr><tr><th>15 Apr '94</th><td>Chrysomelidae</td><td>n/c</td><td>MP</td><td><b>+</b></td><td></td><td><b>+</b></td><td><b>+</b></td></tr><tr><th>June '97</th><td><i>Cephaloleia vicina</i> (= <i>bella</i>)</td><td><i>H. pogonantha</i></td><td>n/c</td><td>+</td><td></td><td></td><td></td></tr><tr><th>June '97</th><td><i>Cephaloleia bella</i></td><td>n/c</td><td>DJ</td><td>+</td><td></td><td></td><td></td></tr><tr><th>June '97</th><td><i>Cephaloleia belti</i></td><td>n/c</td><td>DJ</td><td>+</td><td></td><td></td><td></td></tr><tr><th>June '97</th><td><i>Cephaloleia ornatrix</i></td><td>n/c</td><td>DJ</td><td></td><td>+</td><td></td><td></td></tr><tr><th>2 June '97</th><td>hispines</td><td>Heliconiaceae leaves</td><td>EEL</td><td>+</td><td></td><td></td><td></td></tr><tr><th>12 June '97</th><td>n/c</td><td><i>Heliconia</i> leaves</td><td>ALAS</td><td></td><td><b>+</b></td><td><b>+</b></td><td></td></tr><tr><th>12 June '97</th><td>coex <i>Ceph. belti / ornatrix</i></td><td><i>Heliconia</i> leaves</td><td>ALAS</td><td><b>+</b></td><td><b>+</b></td><td><b>+</b></td><td></td></tr><tr><th>12 June '97</th><td><i>Ceph. aequilata</i> (= <i>dilaticollis</i>)</td><td><i>Calathea</i></td><td>ALAS</td><td></td><td></td><td></td><td>+</td></tr><tr><th>12 June '97</th><td><i>Cephaloleia erichsonii</i></td><td><i>Calathea</i></td><td>ALAS</td><td></td><td></td><td></td><td>+</td></tr><tr><th>8 July '97</th><td><i>Chelobasis perplexa</i></td><td>n/c</td><td>MP (739027,8)</td><td></td><td><b>+</b></td><td></td><td><b>+</b></td></tr><tr><th>8 July '97</th><td><i>Cephaloleia bella</i></td><td><i>H. pogonantha</i></td><td>MP</td><td>+</td><td></td><td></td><td></td></tr><tr><th>97?</th><td><i>Cephaloleia belti</i></td><td><i>Calathea</i></td><td>ALAS</td><td></td><td></td><td>+</td><td></td></tr><tr><th>May ’97</th><td><i>Chelobasis bicolor</i></td><td>n/c</td><td>DJ -Corcovado NP</td><td>+</td><td></td><td></td><td></td></tr></tbody></table>
Table 2 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany
<p><b>Table 2</b> Maximum temperature of water (°C) in the mosquito-positive ovitraps during the field studies at the different study sites</p><table><tbody><tr><th>Study</th><th>Site</th><th><i>Ae. japonicus japonicus</i></th><th><i>Cx.pipiens</i> s.l.</th><th><i>An. plumbeus</i></th><th><i>Ae. geniculatus</i></th></tr></tbody><tbody><tr><th>2017</th><td>Alfter</td><td>26.8</td><td>34.7</td><td>31.3</td><td>20.3</td></tr><tr><th></th><td>Dormagen</td><td>22.1</td><td>27.2</td><td>17.3</td><td>21.7</td></tr><tr><th>2018</th><td>Alfter</td><td>22.6</td><td>19.8</td><td>20.6</td><td>n.n.</td></tr><tr><th></th><td>Bonn SÜd</td><td>24.7</td><td>24</td><td>17.3</td><td>n.n.</td></tr><tr><th></th><td>Heimerzheim</td><td>24.3</td><td>24.6</td><td>23.2</td><td>22.7</td></tr><tr><th></th><td>Lohmar</td><td>28.6</td><td>25.8</td><td>28.6</td><td>16.6</td></tr><tr><th></th><td>Siegburg</td><td>25.8</td><td>30</td><td>27</td><td>23.1</td></tr><tr><th></th><td>Troisdorf</td><td>26.8</td><td>27.7</td><td>25.2</td><td>n.n.</td></tr></tbody></table><p><i>n.n.</i> Species not present</p>
Table 1 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany
<p><b>Table 1</b> Total number and percentages of positive samples and occurrence of mosquito species per trap</p><table><tbody><tr><th>Study</th><th></th><th><i>Aedes japonicus japonicus</i></th><th><i>Culex pipiens</i> s.l.</th><th><i>Anopheles plumbeus</i></th><th><i>Aedes geniculatus</i></th><th>Total</th></tr></tbody><tbody><tr><th>2017</th><td>Total positive traps (<i>n</i>)</td><td>97</td><td>199</td><td>47</td><td>38</td><td>381</td></tr><tr><th></th><td>Positive traps/analysable traps (%)</td><td>15.4</td><td>31.7</td><td>7.5</td><td>6.1</td><td>60.7</td></tr><tr><th></th><td>Traps multiple species (<i>n</i>)</td><td>56</td><td>58</td><td>39</td><td>25</td><td>80</td></tr><tr><th></th><td>Multiple species/positive traps (%)</td><td>57.7</td><td>29.1</td><td>83</td><td>65.8</td><td>21</td></tr><tr><th>2018</th><td>Total positive traps (<i>n</i>)</td><td>441</td><td>285</td><td>137</td><td>19</td><td>882</td></tr><tr><th></th><td>Positive traps/analysable traps (%)</td><td>20.3</td><td>13.1</td><td>6.3</td><td>0.9</td><td>40.7</td></tr><tr><th></th><td>Traps multiple species (<i>n</i>)</td><td>180</td><td>139</td><td>113</td><td>11</td><td>206</td></tr><tr><th></th><td>Multiple species/positive traps (%)</td><td>40.8</td><td>48.8</td><td>82.5</td><td>57.9</td><td>23.4</td></tr></tbody></table><p>Calculations based on a total of 628 samples in 2017 and 2168 samples in 2018.The number of positive ovitraps with more than one species divided by the total number of positive ovitraps represents the portion of positive ovitraps with multiple species.See Additional file 1: Table S1 for all combinations of species and Additional file 2: dataset S1 for all samplings</p>
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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.
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.