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Supplementary material 1 from: Salini S, Gracy RG, Akoijam R, Rabbani MK, David KJ, Roca-Cusachs M (2023) Revision of Acesines Stål and Dunnius Distant, resurrection of Mycterizon Breddin (Hemiptera, Heteroptera, Pentatomidae, Pentatominae), and description of a new species from India. ZooKeys 1148: 79-117. https://doi.org/10.3897/zookeys.1148.95629
Part 1
Supplementary material 2 from: Salini S, Gracy RG, Akoijam R, Rabbani MK, David KJ, Roca-Cusachs M (2023) Revision of Acesines Stål and Dunnius Distant, resurrection of Mycterizon Breddin (Hemiptera, Heteroptera, Pentatomidae, Pentatominae), and description of a new species from India. ZooKeys 1148: 79-117. https://doi.org/10.3897/zookeys.1148.95629
Part 2
Figure 17 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 17. Morphology of MahaƲelo madagasus sp. nov. A, habitus dorsal. B, habitus frontal. C, habitus lateral. Scale bars: 1 mm. D, head with mouthparts removed, ventral. E, maxilla, ventral. F, mandible, ventral. G, meso- and metathorax, ventral. H, aedeagus, ventral. I, male genital segment, ventral. J, female genitalia, ventral. K, details of spermatheca.
Figure 2 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 2. Results of the phylogenetic analyses of the combined, morphological and molecular dataset under Bayesian inference. Statistical support for branches show posterior probabilities. Branch lengths are kept and shown in the same proportion all along the tree. Apomorphies tracked in WINCLADA are shown upon each branch. DNA helix graphic after taxon name indicates taxa for which molecular data were available; asterisk '*' indicates interspecific chimeras (combined data from two different species of the same genus).
Figure 4 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 4. Plots of proportional measurements (% SL) against standard lengths for non-type specimens of Pseudophycis palmata, P. barbata and holotype of P. palmata. A, caudal peduncle length; B, interorbital width; C, barbel length; D, pelvic fin length.
Figure 3 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 3. Collection localities for specimens of Pseudophycis spp. in museums. A, P. bachus, green and P. palmata, orange; B, P. barbata, blue; C, P. breviuscula, red.
Figure 7. Pseudophycis barbata. A, NMNZ P.037124, 450 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 7. Pseudophycis barbata. A, NMNZ P.037124, 450 mm SL, Bay of Plenty, east of north-east point, North Island, New Zealand (photograph C. Struthers, NMNZ); B, BMNH 1863.1.15.38, holotype of Pseudophycis barbata, 394 mm SL, Victoria, South Australia (photograph © The Trustees of the Natural History Museum, London).
Fig. 4 in Resurrection and Re-description of (Cuvier), Silver Pomfret from the Northern Indian Ocean.
Fig. 4. Image of Pampus candidus.
Fig. 5 in Resurrection and Re-description of (Cuvier), Silver Pomfret from the Northern Indian Ocean.
Fig. 5. First Gill raker of Pampus candidus.
Fig. 6 in Resurrection and Re-description of (Cuvier), Silver Pomfret from the Northern Indian Ocean.
Fig. 6. Radiograph of Pampus candidus.
Fig. 3 in Resurrection and Re-description of (Cuvier), Silver Pomfret from the Northern Indian Ocean.
Fig. 3. Image of Stomateus candidus MNHN-IC-A-5712.
FIGURE 4. The estimated delta K and mean lnL values for each K in Taxonomic reassessment of salamanders (genus Hynobius) from Tsushima Islands Japan, with a resurrection of Hynobius tagoi Dunn, 1923 (Amphibia: Caudata)
FIGURE 4. The estimated delta K and mean lnL values for each K.
Data from: A resurrection experiment finds evidence of both reduced genetic diversity and potential adaptive evolution in the agricultural weed Ipomoea purpurea
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Data from: The resurrection of the genus Bergia (Anthozoa, Zoantharia, Parazoanthidae)
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Ancestral genetic variation in phenotypic plasticity underlies rapid evolutionary changes in resurrected populations of waterfleas
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Data from: Bayesian morphological clock methods resurrect placoderm monophyly and reveal rapid early evolution in jawed vertebrates
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Global transcriptome analysis reveals major roles for protein quality control, autophagy, and reactive oxygen species scavenging during the acquisition of desiccation tolerance in the resurrection pla
GEO Series GSE53058. Dorcoceras hygrometricum. 24 samples. Type: Expression profiling by array.
Data from: Evolutionary changes in plant tolerance against herbivory through a resurrection experiment
Both theoretical and empirical works have highlighted the difference in the evolutionary implications of host resistance and tolerance against their enemies. However, it has been difficult to show evolutionary changes in host defences in natural populations; thus, evaluating theoretical predictions of simultaneous evolution of defences remains a challenge. We studied the evolutionary changes in traits related to resistance and tolerance against herbivory in a natural plant population using seeds from two collections made in a period of 20 years. In a common garden experiment, we compared defensive traits of ancestral (1987) and descendant (2007) subpopulations of the annual plant Datura stramonium that shows genetic variation for tolerance and to which the specialist herbivore Lema daturaphila is locally adapted. We also examined the effects of different plant genotypes on the herbivore for testing the plant genetic variation in resistance. Based on the response to the contemporary herbivore populations, results revealed a nonsignificant response in plant resistance traits (herbivore consumption, foliar trichomes and tropane alkaloids), but a significant one in tolerance. The survival of herbivores in laboratory experiments depended on the plant genotype, which suggests genetic variation in plant resistance. Although we cannot identify the selective agent for the change nor exclude genetic drift, the results are consistent with the expectation that when resistance fails to control herbivory, tolerance should play a more important role in the evolution of the interaction.
Figure 5 from: Liu Y, Dai J-H, Zhuang Q-Y, Zou C-Y, Ma K-N (2024) Resurrection of Perilimnastes (Sonerileae, Melastomataceae) with description of a new species P. nana. PhytoKeys 238: 11-31. https://doi.org/10.3897/phytokeys.238.116168
Figure 5 Distribution of Perilimnastes.
Figure 2 from: Hiller A, Werding B (2024) Description of a new species of the Petrolisthes galathinus complex from the Caribbean Sea, and resurrection of Petrolisthes occidentalis from the East Pacific (Crustacea, Anomura, Porcellanidae). ZooKeys 1191: 391-407. https://doi.org/10.3897/zookeys.1191.111570
Figure 2 Petrolisthes galathinus (Bosc), original drawing by Bosc (1802: pl. 6, fig. 2).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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