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Figure 5 from: Vanegas-Ríos JA, Serra Alanís WS, Azpelicueta MM, Litz T, Malabarba LR (2024) Population variation of Diapoma pampeana (Characiformes, Characidae, Stevardiinae) from an isolated coastal drainage in Uruguay, with new records: comparing morphological and molecular data. Zoosystematics and Evolution 100(1): 69-85. https://doi.org/10.3897/zse.100.112778
Figure 5 Neighbor-Joining topology of analyzed Diapoma specimens based on Tamura-Nei model and COI sequence data. Bootstrap values (10000 replicates) are shown below the branches. SBL = 0.783.
Fig. 1. a in Color pattern variation in Cichla temensis (Perciformes: Cichlidae): Resolution based on morphological, molecular, and reproductive data
Fig. 1. a) Four defined color pattern grades in Cichla temensis used to group live specimens in the field. Specimens within each grade occur along a continuum of color and pattern variation. Grades 1 and 4 represent the extremes of variation. The more brightly colored Grade 4 (specimen TL = 548mm) variant is known as the three-barred peacock or tucunaré açu in Brazil. At the other extreme, Grade 1 (specimen TL = 541mm) is known as the speckled peacock or tucunaré paca and is dark and comparatively non-descript. Grade 2 (specimen TL = 613mm) and Grade 3 (specimen TL = 585mm) represent transitional degrees of variation between the extremes of paca and açu. All variant grades were collected in both Region 1 and Region 2 (Fig. 2); b) Cichla monoculus was collected in Region 1 (specimen TL = 382mm) and displays a pattern of bars 1, 2 and 3 similar to, but shorter than those of C. temensis without postorbital markings but with an abdominal bar; c) Cichla orinocensis was collected in Region 2 (specimen TL = 412mm) and is differentiated by three ocellar marks in place of vertical bars 1, 2 and 3. Postorbital markings are absent.
Figure 5 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 5 Phlomoides henryi Y.Zhao & C.L.Xiang A habitat B plant with linear-tuberous roots C inflorescence D verticillaster E flowers F dissected flower G appendages at base of posterior filaments H fruiting calyces I dissected calyces J bracts K floral leaves L stem leaves. Photographs by Yue Zhao, except C by Li Chen.
Figure 4 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 4 SEM of both sides of leaves of Phlomoides henryi and related species A, BP. henryiC, DP. bracteosaE, FP. brevifloraG, HP. macrophyllaI, JP. nyalamensisK, LP. tibeticaM, NP. milingensisO, PP. rotataA, C, E, G, I, K, M, OSEM of adaxial leaves B, D, F, H, J, L, N, PSEM of abaxial leaves.
Figure 2 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 2 Different types of trichomes of PhlomoidesA short simple non-glandular trichomes (P. macrophylla) B short simple non-glandular trichomes (P. breviflora) C long simple non-glandular trichomes (P. henryi) D symmetrically non-glandular stellate (P. breviflora) E non-glandular stellate with central long branch (P. bracteosa) F bi- or trifurcate non-glandular stellate (P. nyalamensis) G sub-sessile/ sessile glandular trichomes (P. macrophylla) H simple glandular trichomes of (P. bracteosa) I branched glandular trichomes (P. breviflora).
Figure 1 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 1 Phylogeny of Phlomoides inferred by Bayesian Inference (BI), based on the combined plastid dataset cpDNA. Support values displayed on the branches follow the order BI-PP/ML-BS (" * " indicates PP = 1.00 or BS = 100%, "-" indicates incongruent relationship between BI and ML tree.
Figure 3 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 3 Photos of bracts, SEM of bracts of Phlomoides henryi and related species A, BP. henryiC, DP. bracteosaE, FP. brevifloraG, HP. macrophyllaI, JP. nyalamensisK, LP. tibeticaM, NP. milingensisO, PP. rotata. A, C, E, G, I, K, M, O photos of bracts B, D, F, H, J, L, N, PSEM of bracts.
Supplementary material 2 from: Xiudan W, Luan L, Yang Z (2024) Discovery of a new species of Synergus (Hymenoptera, Cynipidae, Synergini) based on morphology and molecular data. ZooKeys 1193: 81-94. https://doi.org/10.3897/zookeys.1193.105756
appendix S2
Supplementary material 1 from: Xiudan W, Luan L, Yang Z (2024) Discovery of a new species of Synergus (Hymenoptera, Cynipidae, Synergini) based on morphology and molecular data. ZooKeys 1193: 81-94. https://doi.org/10.3897/zookeys.1193.105756
appendix S1
Figure 1 from: Xiudan W, Luan L, Yang Z (2024) Discovery of a new species of Synergus (Hymenoptera, Cynipidae, Synergini) based on morphology and molecular data. ZooKeys 1193: 81-94. https://doi.org/10.3897/zookeys.1193.105756
Figure 1 Maximum-likelihood tree derived from COI sequences of 45 species of Synergus from the EP, with 1000 bootstrap replicates. Numbers on nodes are SH-aLRT and bootstrap values.
Figures 2-9 from: Xiudan W, Luan L, Yang Z (2024) Discovery of a new species of Synergus (Hymenoptera, Cynipidae, Synergini) based on morphology and molecular data. ZooKeys 1193: 81-94. https://doi.org/10.3897/zookeys.1193.105756
Figures 2-9 Synergus dilatatus sp. nov. 2 general habitus (♀) 3 general habitus (♂) 4 antenna (♀) 5 antenna (♂) 6 head in anterior view (♀) 7 head in anterior view (♂) 8 head in dorsal view (♀) 9 head in lateral view (♀).
Figures 10-17 from: Xiudan W, Luan L, Yang Z (2024) Discovery of a new species of Synergus (Hymenoptera, Cynipidae, Synergini) based on morphology and molecular data. ZooKeys 1193: 81-94. https://doi.org/10.3897/zookeys.1193.105756
Figures 10-17 Synergus dilatatus sp. nov. 10 head in posterior view (♀) 11 mesosoma in lateral view (♀) 12 mesosoma in dorsal view (♀) 13 propodeum in dorsal view (♀) 14 metasoma in lateral view (♀) 15 metasoma in lateral view (♂) 16 fore wing (♀) 17 fore wing (♂).
Figure 5 from: Zhu A-H, Liu Z-B, Li Y, Liu H-G, Yuan Y, He S-H (2024) Molecular and morphological data reveal two new species of Tropicoporus (Hymenochaetaceae, Basidiomycota) from Australia and tropical Asia. MycoKeys 103: 57-70. https://doi.org/10.3897/mycokeys.103.119027
Figure 5 Microscopic structures of Tropicoporus zuzaneae (drawn from the holotype Dai 22171) a basidiospores b basidia and basidioles c cystidioles d hyphae from subiculum e hyphae from trama. Scale bars: 5 µm (a); 10 µm (b–e).
Figure 1 from: Zhu A-H, Liu Z-B, Li Y, Liu H-G, Yuan Y, He S-H (2024) Molecular and morphological data reveal two new species of Tropicoporus (Hymenochaetaceae, Basidiomycota) from Australia and tropical Asia. MycoKeys 103: 57-70. https://doi.org/10.3897/mycokeys.103.119027
Figure 1 Phylogeny of Tropicoporus generated by ML analyses based on combined ITS+nLSU sequences. Branches are labelled with maximum likelihood bootstrap higher than 75% and Bayesian posterior probabilities higher than 0.90. New species are indicated in bold.
Figure 3 from: Zhu A-H, Liu Z-B, Li Y, Liu H-G, Yuan Y, He S-H (2024) Molecular and morphological data reveal two new species of Tropicoporus (Hymenochaetaceae, Basidiomycota) from Australia and tropical Asia. MycoKeys 103: 57-70. https://doi.org/10.3897/mycokeys.103.119027
Figure 3 Microscopic structures of Tropicoporus oceanianus (drawn from the holotype Dai 18859) a basidiospores b basidia and basidioles c cystidioles d hymenial setae e hyphae from context f hyphae from trama. Scale bars: 5 µm (a); 10 µm (b–f).
Figures 16-21 from: Lin L, Yang Z, Zhang J (2024) Revalidation of the jumping spider genus Cheliceroides Żabka, 1985 based on molecular and morphological data (Araneae, Salticidae). ZooKeys 1196: 243-253. https://doi.org/10.3897/zookeys.1196.117921
Figures 16-21 Comparison of genital structures of Cheliceroides longipalpis Żabka, 1985 (16–18) and the type species of Colopsus, Colopsus cancellatus Simon, 1902 (19–21, modified from Kanesharatnam and Benjamin 2021) 16, 19 left palp, ventral view 17, 20 epigynum, ventral view 18, 21 epigynum, dorsal view.
Figures 1- 2 from: Lin L, Yang Z, Zhang J (2024) Revalidation of the jumping spider genus Cheliceroides Żabka, 1985 based on molecular and morphological data (Araneae, Salticidae). ZooKeys 1196: 243-253. https://doi.org/10.3897/zookeys.1196.117921
Figures 1- 2 Phylogenetic results 1 maximum-likelihood tree from the UCE dataset 2 maximum-likelihood tree from the 13-mitochondrial-PCG dataset; numbers along the branches indicate bootstrap support.
Figures 3-15 from: Lin L, Yang Z, Zhang J (2024) Revalidation of the jumping spider genus Cheliceroides Żabka, 1985 based on molecular and morphological data (Araneae, Salticidae). ZooKeys 1196: 243-253. https://doi.org/10.3897/zookeys.1196.117921
Figures 3-15 Cheliceroides longipalpis Żabka, 1985 3–6 living photos of male (3–4) and female (5–6) 7–8 male habitus, dorsal (7) and ventral (8) view 9–11 left male palp, prolateral (9), ventral (10) and retrolateral (11) view 12–13 female habitus, dorsal (12) and ventral (13) view 14–15 epigynum, ventral (14) and dorsal (15) view.
FIGURE 3 in A systematic assessment of Leporinus tigrinus (Characiformes: Anostomidae) using morphological and molecular data
FIGURE 3. Leporinus tigrinus, syntypes, MCZ 20446, 138.3–143.9 mm SL: "Goyaz", Brazil.
FIGURE 8 in A systematic assessment of Leporinus tigrinus (Characiformes: Anostomidae) using morphological and molecular data
FIGURE 8. (A) Dorsal fin and (B) anal fin of Leporinus tigrinus (MZUEL 20673, 112.0 mm SL)
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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)
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DANDI Archive for NWB datasets
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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.