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Figure 6 from: Jia A, Chen B, Lu H, Xing Y, Li B, Fan X (2024) Multigene phylogeny and morphology reveal three new species of Cytospora isolated from diseased plant branches in Fengtai District, Beijing, China. MycoKeys 101: 163-189. https://doi.org/10.3897/mycokeys.101.116272
Figure 6 Cytospora fengtaiensis from Acer palmatum 'Atropurpureum' (BJFC CF20230405) A, B habit of conidiomata on branch C transverse section through conidiomata D longitudinal section through conidiomata E conidiophores and conidiogenous cells F conidia. Scale bars: 1 mm (A); 200 µm (B–D); 10 µm (E, F).
Figure 7 from: Jia A, Chen B, Lu H, Xing Y, Li B, Fan X (2024) Multigene phylogeny and morphology reveal three new species of Cytospora isolated from diseased plant branches in Fengtai District, Beijing, China. MycoKeys 101: 163-189. https://doi.org/10.3897/mycokeys.101.116272
Figure 7 Cytospora haidianensis from Salix babylonica (BJFC CF20230411) A, B habit of conidiomata on branch C transverse section through conidiomata D longitudinal section through conidiomata E, F conidiophores and conidiogenous cells G conidia. Scale bars: 1 mm (A); 200 µm (B–D); 10 µm (E–G).
Figure 1 from: Jia A, Chen B, Lu H, Xing Y, Li B, Fan X (2024) Multigene phylogeny and morphology reveal three new species of Cytospora isolated from diseased plant branches in Fengtai District, Beijing, China. MycoKeys 101: 163-189. https://doi.org/10.3897/mycokeys.101.116272
Figure 1 Disease symptoms associated with Cytospora species collected from Fengtai District, Beijing, China AAcer palmatum 'Atropurpureum' BAcer pictum subsp. Mono. CEuonymus japonicusDMalus 'American' EMalus × micromalusFPinus bungeanaeGSalix babylonicaHSorbaria sorbifolia.
Rapid phagosome isolation enables unbiased multiomic analysis of human microglia phagosomes 2
<p><span>Proteomic data of iPSC-derived microglia phagosomes and controls</span></p>
Supplementary material 8 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
Table of coordinates used
Supplementary material 7 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
Haplotype network of the COI data analyzed of D. pampeana
Supplementary material 2 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
Scree plots obtained from the morphometric and meristic data analyzed
Supplementary material 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
Tukey box plot of most distinctive meristic data observed in analyzed specimens of Diapoma pampeana
Figure 4 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 4 Most discriminant axes obtained from the PCA analyses performed using morphometric and meristic data of studied specimens of Diapoma pampeana (in each plot, the loadings are scaled to 90% of the PC scores). Size-corrected measurements: A. PC1 vs. PC2 plot; B. PC3 vs. PC4 plot. Meristic data; C. PC1 vs. PC2 plot; D. PC3 vs. PC4 plot. Only these variables that most loaded the components are indicated as follows: E- depth at dorsal-fin origin; F- snout to dorsal-fin origin; G- snout to pelvic-fin origin; H- Snout to anal-fin origin; I- distance between dorsal- and adipose-fin origins; J- dorsal fin to caudal-fin base; K- anal-fin base length; L- caudal peduncle length; M- longitudinal scales; N- lateral-line scales; P- scales between lateral line-dorsal origin; Q- scales between lateral line-pelvic origin; R- circumpeduncular scales; S- predorsal scales; T- number of branched anal-fin rays; U- gill rakers on upper limb of branchial arch; V- gill rakers on lower limb of branchial arch; W- number of maxillary teeth; X- number of dentary teeth.
Figure 3 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 3 Geographic distribution of Diapoma pampeana. A. View within South America; B. View within Brazil and Uruguay. All studied specimens from the Pando (Circle), Santa Lucía (triangle), Yi (diamond), and Upper Negro (star; holotype represented by not-filled pattern) are depicted. Other records presented by Ito et al. (2022) are also included.
Figure 1 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 1 Coloration in life of D. pampeana (A, B) from the Pando stream, Canelones Uruguay. Photo by J. Pfleiderer.
Figure 6 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 6 Bayesian topology of phylogenetic relationships among the analyzed Diapoma species (comparing specimens of D. pampeana from the Pando stream and Upper Negro basin) based on COI sequence data. Numbers at nodes correspond to posterior probabilities.
Supplementary material 6 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
Uncorrected pairwise genetic distances using the COI data matrix
Supplementary material 3 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
Total variance accounted for the PCA performed for the morphometric and meristic data
Supplementary material 1 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
All COI sequences analyzed in the present work
Figure 2 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 2 Extern morphology of studied specimens of Diapoma pampeana. A. MLP 11443, male, 30.6 mm SL, Uruguay, Pando Stream; B. MLP 11445, female, 35.1 mm SL, Uruguay, Pando Stream; C. MHNM 1125, female, 31.3 mm SL, Uruguay, Canelón Grande Stream; D. MHNM 4018, male, 29.8 mm SL, Uruguay, marginal lagoon to Rio Yi; E. MHNM 4018, female, 29.3 mm SL, Uruguay, marginal lagoon to Rio Yi. Photographs of the specimens from the Upper Negro are available in Ito et al. (2022). Scale bar: 1 mm.
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.
Unraveling the Effect of Rh Isolation on Shallow d States of Gallium–Rhodium Alloys
<p>Dataset for "Unraveling the Effect of Rh Isolation on Shallow d States of Gallium–Rhodium Alloys"</p> <p>https://pubs.acs.org/doi/full/10.1021/acs.jpcc.3c04350</p>
Original pictures of isolation, culture and immunofluorescence staining of primary fibroblasts from cervical tissue in vitro
Open the record for dataset details and reuse information.
Fig. 1. Terpenoids 1–10 isolated from a in Botryane, noreudesmane and abietane terpenoids from the ascomycete Hypoxylon rickii
Fig. 1. Terpenoids 1–10 isolated from a single cultivation of the fungus Hypoxylon rickii.
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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.