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Figure 4 in Husbandry, captive breeding, larval development and stages of the Malayan horned frog Megophrys nasuta (Schlegel, 1858) (Amphibia: Anura: Megophryidae)
Figure 4. Megophrys nasuta larvae in stages 25 to 45. Drawings: M. Wildenhues.
Figure 3 in Husbandry, captive breeding, larval development and stages of the Malayan horned frog Megophrys nasuta (Schlegel, 1858) (Amphibia: Anura: Megophryidae)
Figure 3. Megophrys nasuta larvae in stages 18 to 22. Drawings: R. Bach.
Figure 7 in Husbandry, captive breeding, larval development and stages of the Malayan horned frog Megophrys nasuta (Schlegel, 1858) (Amphibia: Anura: Megophryidae)
Figure 7. Megophrys nasuta larvae in stages 30 to 34. Photos: M. Wildenhues.
Figure 6 in Husbandry, captive breeding, larval development and stages of the Malayan horned frog Megophrys nasuta (Schlegel, 1858) (Amphibia: Anura: Megophryidae)
Figure 6. Megophrys nasuta larvae in stages 25 to 29. Photos: M. Wildenhues.
Figure 9 in Husbandry, captive breeding, larval development and stages of the Malayan horned frog Megophrys nasuta (Schlegel, 1858) (Amphibia: Anura: Megophryidae)
Figure 9. Megophrys nasuta larvae in stages 41 to 46. Photos: M. Wildenhues.
HRDIC and EBSD data for the study of early stage plasticity of a Ni-base superalloy
<p>We used High-Resolution Digital Image Correlation (HRDIC) to study the strain localisation and slip activity of a Ni-base superalloy sample, which was subjected to an in-situ tensile test inside a scanning electron microscope (SEM). </p> <p>Displacement data for HRDIC were calculated using two methods: the integrated method, which correlates with the initial reference frame, and the differential method, which correlates with the previous step. Both datasets are available and saved in separate folders in the .zip file named 'HRDIC and EBSD data'.</p> <p>EBSD data for the region of interest (ROI) can be found in the same .zip file along with a Jupyter Notebook to read and visualise to both datasets. </p>
Table 1 in Agistemus collyerae (Acari: Trombidiformes: Stigmaeidae) in South Africa: first record, introduction pathways and a re-description including additional life stages
<p><b>Table 1</b> Measurements of <i>Agistemus collyerae</i> collected from South Africa, and comparison with New Zealand female specimens. All measurements are lengths unless otherwise noted. Leg length was measured from coxa to tip of empodium. Measurements are given in μm. SA = South Africa; NZ = New Zealand.</p><table><tbody><tr><th></th><th>NZ female</th><th>SA female</th><th>SA male</th><th>SA deutonymphs</th></tr></tbody><tbody><tr><th></th><td>(n=6)</td><td>(n=8)</td><td>(n = 2)</td><td>(n=1)</td></tr><tr><th><b>BODY SIZE</b></th></tr><tr><th>Length (excl. gnathosoma)</th><td>224 – 298</td><td>234 – 262</td><td>193 – 201</td><td>188</td></tr><tr><th>Length (incl. gnathosoma)</th><td>323 – 416</td><td>335 – 379</td><td>308</td><td>277</td></tr><tr><th>Width (at level of c2)</th><td>171 – 242</td><td>172 – 207</td><td>156 – 160</td><td>137</td></tr><tr><th><b>GNATHOSOMA</b></th></tr><tr><th><i>m</i></th><td>21 – 25</td><td>18 – 23</td><td>20 – 23</td><td>18</td></tr><tr><th><i>n</i></th><td>23 – 27</td><td>18 – 27</td><td>18 – 19</td><td>19</td></tr><tr><th><i>or1</i></th><td>11 – 12</td><td>11 – 14</td><td>12 – 13</td><td>10</td></tr><tr><th><i>or2</i></th><td>11 – 12</td><td>10 – 14</td><td>10 – 14</td><td>9</td></tr><tr><th>Moveable cheliceral digit</th><td>31 – 36</td><td>36 – 39</td><td>35 – 40</td><td></td></tr><tr><th>Palp</th><td>72 – 80</td><td>71 – 85</td><td>86 – 89</td><td>63</td></tr><tr><th>Palp tibial claw</th><td>13 – 18</td><td>15 – 17</td><td>19 – 20</td><td>7</td></tr><tr><th><b>DORSUM</b></th></tr><tr><th>Eyes (diameter)</th><td></td><td>9 – 10</td><td></td><td>8</td></tr><tr><th>Post-ocular bodies (diameter)</th><td></td><td>6 – 8</td><td></td><td>7</td></tr><tr><th><i>ve</i></th><td>24 – 27</td><td>15 – 17</td><td>15 – 16</td><td>13</td></tr><tr><th><i>sci</i></th><td>30 – 39</td><td>21 – 28</td><td>23</td><td>19</td></tr><tr><th><i>sce</i></th><td>31 – 38</td><td>23 – 28</td><td>22 – 24</td><td>18</td></tr><tr><th><i>c1</i></th><td>24 – 31</td><td>20 – 26</td><td>15 – 17</td><td>15</td></tr><tr><th><i>c2</i></th><td>35 – 39</td><td>21 – 31</td><td>23 – 27</td><td>18</td></tr><tr><th><i>d1</i></th><td>30 – 37</td><td>20 – 25</td><td>17</td><td>17</td></tr><tr><th><i>d2</i></th><td>32 – 39</td><td>23 – 28</td><td>23 – 26</td><td>16</td></tr><tr><th><i>e1</i></th><td>42 – 46</td><td>29 – 34</td><td>12 – 13</td><td>22</td></tr><tr><th><i>e2</i></th><td>42 – 45</td><td>27 – 34</td><td>25 – 27</td><td>24</td></tr><tr><th><i>f</i></th><td>34 – 42</td><td>31 – 35</td><td>32 – 34</td><td>25</td></tr><tr><th><i>h1</i></th><td>38 – 43</td><td>34 – 39</td><td>13 – 14</td><td>26</td></tr><tr><th><i>h2</i></th><td>32 – 38</td><td>32 – 36</td><td>21 – 26</td><td>22</td></tr><tr><th><i>ve – ve</i></th><td>27 – 45</td><td>28 – 34</td><td>30 – 31</td><td>33</td></tr><tr><th><i>c1 – c1</i></th><td>36 – 43</td><td>26 – 36</td><td>34 – 40</td><td>26</td></tr><tr><th><i>d1 – d1</i></th><td>61 – 73</td><td>52 – 64</td><td>54 – 56</td><td>48</td></tr><tr><th><i>e1 – e1</i></th><td>33 – 34</td><td>24 – 34</td><td>27</td><td>22</td></tr><tr><th><i>f – f</i></th><td>65 – 80</td><td>58 – 65</td><td>38 – 42</td><td>44</td></tr><tr><th><i>h1 – h1</i></th><td>15 – 18</td><td>13 – 21</td><td>9</td><td>13</td></tr><tr><th><b>VENTER</b></th></tr><tr><th><i>g</i></th><td>35 – 39</td><td>27 – 37</td><td>-</td><td></td></tr><tr><th>Aedeagus</th><td>-</td><td>-</td><td>48 – 55</td><td>-</td></tr><tr><th><b>LEGS</b></th></tr><tr><th>Leg I</th><td>185 – 200</td><td>184 – 195</td><td>187 – 191</td><td>148</td></tr><tr><th>ωI</th><td>13 – 16</td><td>9 – 12</td><td>9 – 10</td><td>7</td></tr><tr><th>ωI♂</th><td>-</td><td>-</td><td>10 – 13</td><td>-</td></tr><tr><th>ϕI</th><td>10 – 14</td><td>8 – 11</td><td>9</td><td>5</td></tr><tr><th>leg II</th><td>166 – 189</td><td>168 – 188</td><td>169 – 174</td><td>138</td></tr><tr><th>ωII</th><td>10 – 13</td><td>6 – 10</td><td>9 – 11</td><td>5</td></tr><tr><th>ωII♂</th><td>-</td><td>-</td><td>11 – 13</td><td>-</td></tr><tr><th>ϕII</th><td>9 – 10</td><td>4 – 6</td><td>5 – 6</td><td>3</td></tr><tr><th>leg III</th><td>169 – 187</td><td>173 – 194</td><td>166 – 175</td><td>141</td></tr><tr><th>ωIII</th><td>8 – 10</td><td>5 – 6</td><td>5</td><td>3</td></tr><tr><th>ϕIII</th><td>7 – 10</td><td>3 – 5</td><td>4</td><td>2</td></tr><tr><th>leg IV</th><td>185 – 210</td><td>188 – 198</td><td>184 – 186</td><td>144</td></tr><tr><th>ωIV♂</th><td>-</td><td>-</td><td>5 – 6</td><td>-</td></tr></tbody></table>
Table 2 in Agistemus collyerae (Acari: Trombidiformes: Stigmaeidae) in South Africa: first record, introduction pathways and a re-description including additional life stages
<p><b>Table 2</b> <i>Agistemus collyerae</i> specimens detected on agricultural imports from other countries by South Africa.</p><table><tbody><tr><th><b>country</b></th><th><b>crop</b></th><th><b>commodity</b></th><th><b>import date(s)</b></th><th><b>specimens</b></th></tr></tbody><tbody><tr><th>Yemen</th><td>citrus (unspecified <i>Citrus sp</i>.)</td><td>budwood</td><td>Aug 1991</td><td>1 female</td></tr><tr><th>Australia</th><td>mandarin orange (<i>Citrus reticulata</i>) nectarine (<i>Prunus persica var. nucipersica</i>) peach (<i>Prunus persica)</i> citrus (unspecified <i>Citrus sp.</i>)</td><td>budwood budwood budwood budwood</td><td>Jan 2013 Feb 2007, Jan 2010, Feb 2010 Jan 2010, Mar 2013 Jan 2010</td><td>2 deutonymphs 5 females, 6 males 2 females, 1 male 3 females</td></tr><tr><th>Italy</th><td>olive (<i>Olea europaea</i>)</td><td>rooted cuttings</td><td>Oct 2007</td><td>Unable to locate specimen</td></tr><tr><th>Spain</th><td>apricot (<i>Prunus armeniaca</i>) grapes (<i>Vitis vinifera)</i></td><td>fresh fruit fresh fruit</td><td>Jun 2009 Oct 2015</td><td>1 female 1 female</td></tr><tr><th>Chile</th><td>grapevine (<i>Vitis vinifera)</i></td><td>budwood</td><td>Mar 2014</td><td>1 female</td></tr><tr><th>USA</th><td>nectarine (Prunus persica var. nucipersica) peach (<i>Prunus persica)</i> citrus (unspecified C <i>itrus sp.</i>)</td><td>budwood budwood budwood</td><td>Nov 2010 Nov 2011, Jan 2012, Nov 2012 May 2016</td><td>2 females 2 females, 1 male 1 female</td></tr><tr><th>France</th><td>nectarine (<i>Prunus persica var. nucipersica</i>)</td><td>budwood</td><td>Jan 2017</td><td>1 female</td></tr></tbody></table>
Table 1 in Effect of the seed maturation stage and pre-germination treatments on emergence of Erythrina crista-galli L.
<p><b>Table 1.</b> Mean ± standard deviation for the ESI and MET variables. Equivalent letters mean that treatments do not differ statistically (one factor ANOVA, with Tukey test for multiple comparisons of means, <i>p</i> ≤ 0.05). TC – control; T1– sanded and soaked in water for 48 h; T2 – sanded and soaked in water for 24 h; T3 – soaked in water outside of heating at the initial temperature of 60 °C until reaching ambient temperature; T4 – only sanded; and T5 – immature seeds.</p><table><tbody><tr><th><b>Treatment</b></th><th><b>ESI</b></th><th><b>MET</b></th></tr></tbody><tbody><tr><th>TC</th><td>16.08 ± 8.52a</td><td>10.69 ± 4.66a</td></tr><tr><th>T1</th><td>10.45 ± 1.66ab</td><td>4.73 ± 1.06 b</td></tr><tr><th>T2</th><td>3.64 ± 1.42b</td><td>5.92 ± 1.50b</td></tr><tr><th>T3</th><td>13.18 ± 1.32a</td><td>10.96 ± 0.94a</td></tr><tr><th>T4</th><td>16.02 ± 3.96a</td><td>6.89 ± 1.21ab</td></tr><tr><th>T5</th><td>16.25 ± 2.15a</td><td>6.98 ± 0.26ab</td></tr></tbody></table><p>ESI = Emergence Speed Index; MET = Mean Emergence Time.</p>
Data for Paper: A rigorous optimization method for long-term multi-stage investment planning: Integration of hydrogen into a decentralized multi-energy system
<p>Data containing the results and figures presented in the paper "A rigorous optimization method for long-term multi-stage investment planning: Integration of hydrogen into a decentralized multi-energy system" by Luka Bornemann and Jelto Lange and Martin Kaltschmitt, submitted to the Journal Energy Reports.</p>
Planktonic foraminifera faunal data and derived sea-surface temperatures for the Marine Isotope Stage (MIS) 18 to MIS 28 interval of IODP Site U1387, Gulf of Cadiz
<p>Planktonic foraminifera faunal data and sea-surface temperature reconstructions for the early-middle Pleistocene interval between 750 and 1006 kilo years from IODP Site U1387 in the Gulf of Cadiz (southern Portuguese margin). This data was used to reconstruct the paleoecological and paleoclimatical changes at the southern Portuguese margin in Mega et al. (2025), The Early–Middle Pleistocene Transition in the Gulf of Cadiz (NE Atlantic) – an interplay between subtropical gyre and extremely cold surface waters. Clim. Past 21, 919-939, doi: 10.5194/cp-21-919-2025.</p> <p>The data is also available from the world data center Pangaea as a bundled data set:</p> <p>Voelker, Antje H L; Mega, Aline; Rodrigues, Teresa (2025): Planktonic foraminifera faunal data and sea-surface temperatures for the Marine Isotope Stage (MIS) 18 to MIS 28 interval of IODP Site 339-U1387, Gulf of Cadiz [dataset bundled publication]. PANGAEA, <a href="https://doi.org/10.1594/PANGAEA.974451" target="_blank" rel="nofollow noopener">https://doi.org/10.1594/PANGAEA.974451</a></p>
Repeated autologous fat grafting significantly increases mas-tectomy flap thickness in prepectoral multi-stage composite expander-to-implant breast reconstruction: exploring the con-cept of a reverse expansion
<p>Supplementary material 1 (Video): MRI sequences of a 37-year-old (A), 44-year-old (B) and 46-year-old (C) patient after bilateral mastectomy, sparing both the skin and nipple-areolar com-plexes, with prepectoral insertion of a breast tissue expander. These sequences were captured be-fore repeated sessions of autologous fat grafting to the mastectomy flap and reverse expansion of the expander. In D, E, and F, the corresponding MRI sequences were performed 3 months after 3 sessions of autologous fat grafting each and the exchange of the expander with a definitive im-plant.</p> <p>Supplementary material 2 (Video): Repeated contraction of bilateral pectoralis major muscles in a 37-year-old (A), 44-year-old (B) and 46-year-old (C) patient after bilateral mastectomy sparing both the skin and nipple-areolar complexes, with prepectoral expander-to-implant breast reconstruction and repeated autologous fat grafting sessions while gradually deflating the ex-pander. Note the almost complete absence of breast animation, even in the 44-year-old patient having the implant stabilized with a synthetic, non-absorbable mesh to prevent caudal “bottom-ing out” and lateral migration.</p>
Dataset: Aflatoxin B1 Metabolism of Reared Alphitobius diaperinus in Different Life-Stages
Open the record for dataset details and reuse information.
TABLE 3 in A new genus and species of barnacle (Cirripedia, Verrucomorpha) associated with vents of the Lau Back-Arc Basin: its gross morphology, inferred first juvenile stage and affinities
<p>TABLE 3. — Comparison of two juvenile and four adult characters in two neoverrucid and one verrucid genus.</p><table><tbody><tr><th></th><th>Neoverruca</th><th>Imbricaverruca</th><th><i>Verruca</i></th></tr></tbody><tbody><tr><th>1) Juvenile pedunculate stages</th><td>Several stages pedunculate</td><td>Likely several stages</td><td>Peduncle vestigial</td></tr><tr><th>2) Juvenile carina</th><td>Higher than wide</td><td>Wider than high</td><td>Higher than wide</td></tr><tr><th>3) Adult median latus</th><td>Vestigial</td><td>Well-developed</td><td>Lost</td></tr><tr><th>4) Imbricating plates</th><td>Reduced in number, deciduous</td><td>Complete, well-developed</td><td>Lost</td></tr><tr><th>5) Fixed scutum & tergum</th><td>Normal, higher than wide</td><td>Reduced wider than high</td><td>As wide as high</td></tr><tr><th>6) Rostrum & carina</th><td>Normal, higher than wide*</td><td>Reduced, wider high</td><td>As wide as high</td></tr></tbody></table><p>*R-C gap less on movable side, as in all three genera.</p>
TABLE 2 in A new genus and species of barnacle (Cirripedia, Verrucomorpha) associated with vents of the Lau Back-Arc Basin: its gross morphology, inferred first juvenile stage and affinities
<p>TABLE 2. — Comparison between the primordial plates of the earliest juvenile stages of the principal suborders of thoracic Cirripedia (See Fig. 6 for corresponding figures and text for a full explanation).</p><table><tbody><tr><th><b>Taxon/Character</b></th><th><b>Carinal proportions</b></th><th><b>Carinal of position</b></th><th><b>Terga and scuta of each side</b></th></tr></tbody><tbody><tr><th>Lepadomorpha (Fig. 6A)</th><td>Higher than wide and longer than terga</td><td>Extending up between terga</td><td>Symmetrical</td></tr><tr><th>Scalpellomorpha (Fig. 6B)</th><td>Higher than wide and nearly as long as terga</td><td>Extending up between terga</td><td>Symmetrical</td></tr><tr><th>Verrucomorpha</th></tr><tr><th>Neoverrucidae (Fig. 6C)</th><td>Higher than wide and shorter than terga</td><td>Extending up between terga</td><td>Initially symmetrical</td></tr><tr><th>X-juvenile (Fig. 6D)</th><td>Wider than high, shorter than terga and perhaps displaced to one side</td><td>Not extending up between terga</td><td>Scuta if not terga initially symmetrical</td></tr><tr><th>Verrucidae (Fig. 6E)</th><td>About as wide as high, shorter than terga and displaced to one side</td><td>Not extending up between terga</td><td>Distinctly asymmetrical</td></tr><tr><th>Balanomorpha (Fig. 6F)</th><td>Higher than wide</td><td>Not extending up between terga</td><td>Symmetrical</td></tr></tbody></table>
Mr Burns: a post-electric play written by Anne Washburn / A tertiary performance staged by Te Kura o Toi Whakaari: NZ Drama School
<p>DIRECTOR</p> <p>Stella Reid</p> <p>MUSICAL DIRECTOR</p> <p>Hayden Taylor</p> <p>PRODUCER</p> <p>Natasha James</p> <p>CHOREOGRAPHER</p> <p>Stella Reid</p> <p>FIGHT CHOREOGRAPHY</p> <p>Shane Rangi</p> <p>LIGHTING DESIGNER</p> <p>Grace Newton</p> <p>SOUND DESIGNER</p> <p>Oliver Devlin</p> <p>DIALECT COACH</p> <p>Jacque Drew</p> <p>SET DESIGNER</p> <p>Eden Winters</p> <p>COSTUME DESIGNER</p> <p>Tessa Saunders</p> <p>ASSISTANT SOUND DESIGNER</p> <p>Jade Alborn</p> <div> <p>PRODUCTION TEAM</p> <p>PRODUCTION MANAGER</p> <p>Olivia Cowley</p> <p>STAGE MANAGER</p> <p>Michael Lyell-O'Reilly</p> <p>HEAD MECHANIST</p> <p>Caleb Grainger</p> <p>PUTY STAGE MANAGER/SHOW CALLER</p> <p>Sarah Davitt</p> <p>DEPUTY STAGE MANAGER</p> <p>Joseph McAllum</p> <p>PRODUCTION ASSISTANT</p> <p>Isla McLarin</p> <p>MECHANIST</p> <p>Eilidh Hamilton</p> <p>MECHANIST</p> <p>Jack Tankersley</p> <p>SOUND OPERATOR/ENGINEER</p> <p>Paige Johns</p> <p>LIGHTING OPERATOR</p> <p>Luci McDougall</p> <p>COSTUME SUPERVISORS</p> <p>Sally Huges-Allen, Maysie Pyatt, Evan Stone, Kaitlyn Jacobs</p> <p> </p> <p>PRODUCTION TEAM</p> <p>COSTUME CONSTRUCTION</p> <p>Maxence Benoist, Lillian Denness,</p> <p>Renske Gordon, Evie Howard, Maria McCarthy, Dottie Olsen, Mikkel Rivett,</p> <p>Hannah van den Eikhof, Jordyn Williams</p> <p>SET CONSTRUCTION & SCENIC PAINTING</p> <p>Emile Commarieu, Molly Friis, Azalea Lewis-Milne, Lora Nankivell, Grace O'Brien, Weston Symes</p> <p> </p> <p> </p> <p>CAST</p> <p>ZACHARY BELL - МАТТ/ACT II, HOMER/ACT III CHORUS</p> <p>BRAYDEN CRESWELL- GIBSON/SIDESHOW BOB, FIRST FBI AGENT / TROY MCCLURE</p> <p>FIPE FOAI - ACT III BART</p> <p>EMILIO FUENTES MANCILLA - ACT III LISA/APU</p> <p>KIMIORA HONEYCOMBE - JENNY ACT II, MARGE/ACT III CHORUS</p> <p>JUSTICE KALOLO - SAM ACT II, BART/ACT III, CHORUS /ACT III SCRATCHY</p> <p>SARAH LAWRENCE - COLLEEN, ACT III CHORUS</p> <p>MAIZY METEKINGI - ACT III MARGE/FLANDERS</p> <p>IZZIE NEWTON-CROSS - ITCHY/NELSON</p> <p>SUGAR REA-BRUCE MARIA/ACT II, LISA/2ND FBI AGENT/EDNA KRABAPPEL</p> <p>TAMAHOU TEHEI - ACT III HOMER / WILLY</p> <p>PARIS TUIMASEVE-FOX - QUINCY/ACT II, MAGGIE/ACT III CHORUS</p> <p>CASSIDY KEMP-WOFFENDEN - MR BURNS</p> <p>IAN BLACKBURN - MR BURNS SWING</p> </div>
Comprehensive Transcriptomic Analysis of Spodoptera Frugi-perda Reveals Stage-Specific Gene Expression and P450-Mediated Adaptation Mechanisms
<p><em><span>Spodoptera frugiperda</span></em><span> is a highly adaptable agricultural pest with a complex life cycle, posing significant challenges to pest control. This study conducted a transcriptomic analysis across nine developmental stages, identifying 6,834 differentially expressed genes (DEGs) and 3,072 stage-specific genes (SSGs) critical for their development and adaptability. Significant gene expression shifts were observed during the transition from late larval stages to adulthood. Notably, a high number of SSGs in 6th instar larvae and adult males were enriched in pathways related to oxidative phosphorylation and neural signaling, indicating high metabolic and reproductive demands. Widely shared DEGs associated with ecdysone signaling and detoxification processes underscore robust adaptation mechanisms.</span></p>
Data from: A combination of sexual and ecological divergence contributes to rearrangement spread during initial stages of speciation
Chromosomal rearrangements between sympatric species often contain multiple loci contributing to assortative mating, local adaptation, and hybrid sterility. When and how these associations arise during the process of speciation remains a subject of debate. Here, we address the relative roles of local adaptation and assortative mating on the dynamics of rearrangement evolution by studying how a rearrangement co-varies with sexual and ecological trait divergence within a species. Previously, a chromosomal rearrangement that suppresses recombination on the Z (sex) chromosome was identified in European corn borer moths (Ostrinia nubilalis). We further characterize this recombination suppressor and explore its association with variation in sex pheromone communication and seasonal ecological adaptation in pairs of populations that are divergent in one or both of these characteristics. Direct estimates of recombination suppression in pedigree mapping families indicated that more than 39% of the Z chromosome (encompassing up to ~10 megabases and ~ 300 genes) resides within a non-recombining unit, including pheromone olfactory receptor (OR) genes and a major quantitative trait locus (QTL) that contributes to ecotype differences (Pdd). Combining direct and indirect estimates of recombination suppression, we found that the rearrangement was occasionally present between sexually isolated strains (E versus Z) and between divergent ecotypes (univoltine versus bivoltine). However, it was only consistently present when populations differed in both sexual and ecological traits. Our results suggest that independent of the forces that drove the initial establishment of the rearrangement, a combination of sexual and ecological divergence is required for rearrangement spread during speciation.
Screening of tomato lines under combined stress in generative stage
<ol> <li>Identification of lines with superior performance under combined stress</li> <li>same as (i)</li> <li>Three individual trials, 2018 - 2019</li> <li><em>S. lycopersicum; S. pennellii; S. lycopersicum x S. pennellii</em></li> <li>Greenhouse @ University of Bonn (50.62 N 6.99 E)</li> <li>Growing plants in rockwool slabs with drip irrigation (as commercial practise); stressed plants received modified nutrient solution and only 50 % water</li> <li>General drop in fruit yield and quality under stress conditions; Performance of tested lines (eg water use efficiency) differ significantly.</li> <li>(viii) in progress</li> </ol> <p>(ix) to be discussed</p>
Screening of tomato lines under combined stress in generative stage
<ol> <li>Identification of lines with superior performance under combined stress</li> <li> same as (1)</li> <li>Three individual trials, 2018 - 2019</li> <li><em>S. lycopersicum; S. pennellii; S. lycopersicum x S. pennellii</em></li> <li>Greenhouse @ University of Bonn (50.62 N 6.99 E)</li> <li> Growing plants in rockwool slabs with drip irrigation (as commercial practise); stressed plants received modified nutrient solution and only 50 % water</li> <li> General drop in fruit yield and quality under stress conditions; Performance of tested lines (eg water use efficiency) differ significantly.</li> <li> in progress</li> <li>to be discussed</li> </ol>
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.