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Fig. 3 in Morphological and molecular description of Ixodes woyliei n. sp. (Ixodidae) with consideration for co-extinction with its critically endangered marsupial host
Fig. 3 Scanncng electron mccrographs of Ixodes woyliei n. sp. Female. a Gnathosoma, dorsal vcew. b Gnathosoma, ventral vcew. c Hspostome. Scale-bars: a-b, 100 μm; c, 20 μm
Figs. 9–14 in Taxonomic studies on the genus Caryopemon (Coleoptera: Chrysomelidae: Bruchinae) of China and Myanmar with some new host plants
Figs. 9–14. Caryopemon luteonotatus; 9, dorsal view; 10, ventral view; 11, hind femur; 12, median lobe, ventral view; 13, median lobe, lateral view; 14, lateral lobes, ventral view. Scale bars = 1 mm.
Figure 7 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 7: Hemp plant dry weights (g) two hemp cultivars (Eletta Campana = fiber, Cherry Blossom x T1 = CBD) exposed to two RKN species, M. enterolobii and M. hapla. Factor levels not connected by the same letter are significantly different according to Tukey's HSD where P ≤ 0.05. PCBxT1 = Cherry Blossom x T1, PEC = Eletta (Trial 5).
Figure 3 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 3: Hemp plant dry weights (g) with a mixed population of root-knot species and 11 hemp cultivars; all plants were inoculated with 10,000 RKN eggs. Factor levels not connected by the same letter are significantly different according to Tukey's HSD with P ≤ 0.05 (Trial 2).
Figure 2 in A Seinhorst Model Determined the Host-Parasite Relationships of Meloidogyne javanica Infecting Fenugreek cv. UM202
Figure 2: Effect of increasing nematode population densities (from 0.125 on the left to 128 J2s g-1 soil on the right) of M. javanica on the growth of fenugreek cv. UM-202, showing a reduction in plant growth. Symptoms of nematode attack (a marked reduction of plant growth) were evident at the P level of 8 J2s g-1 soil. However, the tolerance limits (T) of fenugreek plant shoot length i were 1.3 J2s g-1 soil.
Figure 3 in A Seinhorst Model Determined the Host-Parasite Relationships of Meloidogyne javanica Infecting Fenugreek cv. UM202
Figure 3: Relationship between initial population densities (Pi) of M. javanica and relative shoot length (A) and relative shoot dry weights (B) of fenugreek cv. UM-202, grown in pots under glasshouse conditions for 90 days. Each point represents the average of four replicated plants. Lines represent the predicted function calculated by fitting the Seinhorst model to data using the SeinFit program. Statistics for fitted models of shoot length and shoot dry weight were R2 = 0.90, sum of squares (SS) = 0.12; and R2 = 0.92, SS = 0.072, respectively.
Figure 1 in A Seinhorst Model Determined the Host-Parasite Relationships of Meloidogyne javanica Infecting Fenugreek cv. UM202
Figure 1: Scanning electron microscopy (SEM) images of the perineal pattern of M. javanica, which show a rounded to flattened dorsal arch and conspicuous lateral lines that separate the dorsal and ventral regions of the patterns. (A) A close view of the distinct lateral line in a perineal pattern distinguishes this species from other Meloidogyne spp. (B) An inner area was marked by coarsely broken striae and contained the vulva and anus.
Figure 2 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 2: Hemp plant dry weights (g) for inoculated (+) and uninoculated (-) plants with a mixed population of root-knot species and six European hemp cultivars. Factor levels not connected by the same letter are significantly different according to Tukey's HSD with P ≤ 0.05 (Trial 1).
Figure 1 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 1: Root galls caused by RKN (M. javanica and M. incognita mixed population) on hemp roots (cv. Carmagnola Selezionata, left) compared to cucumber roots (cv. Dasher II, middle) (Trial 1) and cv. Cherry Blossom x T1 (right; Trial 2) (Photos J. Coburn).
Figure 5 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 5: Hemp plant dry weights (g) for two cannabigerol (CBG) hemp cultivars and a nematicide in naturally RKN-infested soil. P values (P ≤ 0.05) represent significant differences between cultivars by treatment (PG = Gold, PP= Panacea; NA = naturally infested soil, V = Velum, ST = steamed soil.). Velum was applied at 0.48 kg a.i./Ha. Factor levels not connected by the same letter are significantly different according to Tukey's HSD with P ≤ 0.05 (Trial 4).
Figure 6 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 6: Cannabis sativa (cv. Panacea) 60 days after planting in RKN-infested field soil. (Left) naturally infested soil, (middle) nematicide-treated (fluopyram) soil, (right) steamed soil (Photo J. Coburn).
Figure 4 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 4: Hemp plant dry weights (g) for RKN inoculated (+) and uninoculated (-) plants with two CBD and two Chinese fiber hemp cultivars. Factor levels not connected by the same letter are significantly different according to Tukey's HSD with P ≤ 0.05 (Trial 3).
Figure 2 in New Hosts and Records in Portugal for the Root-Knot Nematode Meloidogyne luci
Figure 2: Phylogenetic relationship of MelOidOgyne spp. sequences based on the alignment of sequences of cytochrome oxidase subunit I (A) and cytochrome oxidase subunit II (B) of mitochondrial DNA with available sequences of other MelOidOgyne species. The phylogenetic tree was generated in MEGA7 using the Neighbour-Joining method. The percentage of replicate trees in which the associated MelOidOgyne spp. clustered together in the bootstrap test (500 replicates) is shown next to the branches. The evolutionary distances were computed using the Jukes-Cantor method. All positions with less than 95% site coverage were eliminated. That is, fewer than 5% alignment gaps, missing data, and ambiguous bases were allowed at any position. *Recently, reclassified as M. lUCi, according to Stare et al. (2017).
Figure 1 in New Hosts and Records in Portugal for the Root-Knot Nematode Meloidogyne luci
Figure 1: Esterase phenotypes of protein homogenates from five egglaying females of MelOidOgyne species isolates. C – M. lUCi (positive control); 1 – M. ethiOpiCa isolate from Brazil; J3 – M. jaVaniCa (reference isolate); 2 – M. lUCi (COrdyline aUStraliS); 3 – M. lUCi (SOlanUM lyCOperSiCUM) and 4 – M. lUCi (OXaliS COrniCUlata).
Figure 5 in Seasonal Abundance of Economically Important Fruit Flies (Diptera: Tephritidae: Dacinae) in Bangladesh, in Relation to Abiotic Factors and Host Plants
Figure 5. Distribution and mean monthly trap captures of Dacus longicornis, in relation with abiotic factors and host fruit availability.
Figure 4 in Seasonal Abundance of Economically Important Fruit Flies (Diptera: Tephritidae: Dacinae) in Bangladesh, in Relation to Abiotic Factors and Host Plants
Figure 4. Distribution and mean monthly trap captures of Zeugodacus cucurbitae (A) and Z. tau (B), in relation with abiotic factors and host fruit availability.
Figure 3 in Seasonal Abundance of Economically Important Fruit Flies (Diptera: Tephritidae: Dacinae) in Bangladesh, in Relation to Abiotic Factors and Host Plants
Figure 3. Distribution and mean monthly trap captures of Bactrocera rubigina (A) and B. correcta (B), in relation with abiotic factors.
Figures 6–9 in Adventive Thysanoptera Species in the Hawaiian Islands: New Records and Putative Host Associations
Figures 6–9. Thrips new to Hawaii. 6. Head and pronotum of Adraneothrips alajuela. 7. Abdominal tergites 1 and 2 of A. alajuela. 8. Head and pronotum of Azaleothrips siamensis. 9. Head and antenna of Sophiothrips annulatus.
Figure 2 in Seasonal Abundance of Economically Important Fruit Flies (Diptera: Tephritidae: Dacinae) in Bangladesh, in Relation to Abiotic Factors and Host Plants
Figure 2. Distribution and mean monthly trap captures of Bactrocera dorsalis (A) and B. zonata (B), in relation with abiotic factors and host fruit availability.
Figures 1–5 in Adventive Thysanoptera Species in the Hawaiian Islands: New Records and Putative Host Associations
Figures 1–5. Thrips new to Hawaii. 1. Leaf-damage on Colocasia esculenta by Biltothrips minutus (photo: S. Chun). 2. Head of Indusiothrips seshadrii. 3. Head and pronotum of Monilothrips kempi. 4. Head and thorax of Trichromothrips priesneri. 5. Forewing of Coremothrips pallidus.
ScienceDex guides
Understand access before you commit
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.