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Fig. 42 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Fig. 42. Phylogenetic placement of Tetracneminae specimens inferred from ML analysis of concatenated sequences of 28S and COI. The analysis was conducted in RAxML and branch support, expressed as a percentage, was assessed with 1,000 rapid bootstrap replicates. Clade 1 = Leptomastidea hypogeococci; clade 2 = Anagyrus cachamai; clade 3 = Anagyrus quilmes. Encyrtus spp. (the outgroup) belong to the subfamily Encyrtinae.
Figs. 27–33 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 27–33. Cheiloneurus sp. near banksi (Rockley, Christ Church Parish, Barbados): 27, female antenna; 28, female head (frontal view); 29, female mesosoma and metasoma; 30, female fore wing; 31, male antenna; 32, male fore wing; 33, male genitalia.
Figs. 34–36 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 34–36. Prochiloneurus spp. males (34–35, P. argentinensis, Loreto, Misiones, Argentina [photographs courtesy of D. A. Aquino]; 36, P. narendrani, Mona Island, Puerto Rico): 34, habitus; 35, antennae; 36, habitus.
Fig. 1. A in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Fig. 1. A gall-like formation caused by the feeding of Harrisia cactus mealybug, Hypogeococcus sp., on Stenocereus fimbriatus columnar cactus in Caja de Muertos Island, Puerto Rico.
Figs. 12–13 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 12–13. Leptomastidea hypogeococci sp. n. female (holotype): 12, mesosoma and metasoma; 13, fore and hind wings.
Figs. 14–17 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 14–17. Leptomastidea hypogeococci sp. n. male (paratype, Cabo Rojo, Puerto Rico, USA): 14, antenna; 15, body; 16, fore and hind wings; 17, genitalia.
Figs. 9–11 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 9–11. Leptomastidea hypogeococci sp. n. female (holotype): 9, slide; 10, head (frontal view); 11, antenna.
Figs. 37–41 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 37–41. Anagyrus tanystis female (holotype): 37, slide; 38, head (frontal view); 39, antennae; 40, mesosoma and metasoma; 41, fore wing.
Figs. 2–3 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 2–3. Leptomastidea abnormis female (San Miguel de Tucumán, Tucumán, Argentina): 2, antenna; 3, fore wing.
Fig. 8 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Fig. 8. Leptomastidea hypogeococci sp. n. female, photographed live (from colony, San Juan, Puerto Rico, USA): habitus.
Figs. 25–26 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 25–26. Cheiloneurus sp. near banksi (Rockley, Christ Church Parish, Barbados): 25, habitus of female; 26, habitus of male.
Figs. 18–21 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 18–21. Leptomastidea hypogeococci sp. n. (paratypes, Seacrest Scrub Natural Area, Palm Beach County, Florida, USA): 18, female antenna; 19, female fore wing; 20, male antenna; 21, male fore wing.
Figs. 22–24 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Figs. 22–24. Stemmatosteres sp. male (Cuesta del Toquero, Jujuy, Argentina): 22, habitus; 23, head and antennae; 24, gaster.
Fig. 43 in Complex of primary and secondary parasitoids (Hymenoptera: Encyrtidae and Signiphoridae) of Hypogeococcus spp. mealybugs (Hemiptera: Pseudococcidae) in the New World
Fig. 43. Genetic variation in mitochondrial COI among specimens of 3 Tetracneminae (Encyrtidae) species inferred using the UPGMA method in MEGA6. The tree is drawn to scale, and branch lengths represent uncorrected p-distance. Branch support was assessed with 1,000 bootstrap replicates.
Figure 2 in Peptidoglycan from Immunobiotic Lactobacillus rhamnosus Improves Resistance of Infant Mice to Respiratory Syncytial Viral Infection and Secondary Pneumococcal Pneumonia
Figure 2. – Photography of a juvenile lemon shark identified as Negaprion acutidens with an estimated total length of 70 cm (Photo MI).
Figure 1 in Peptidoglycan from Immunobiotic Lactobacillus rhamnosus Improves Resistance of Infant Mice to Respiratory Syncytial Viral Infection and Secondary Pneumococcal Pneumonia
Figure 1. – The Chesterfield islands (A) lie in the Coral Sea with New Caledonia (NC) to the east and Australia (AUS) to the west. The atoll structure of the Chesterfield (B) includes a V shaped barrier reef in the South (C) where the juvenile lemon sharks were observed (arrow).
Fig. 2 in Anticoccidial activity of the secondary metabolites in alpine plants frequently ingested by wild Japanese rock ptarmigans
Fig. 2. The efficacy of the natural components against E. tenella sporozoites. The viability of sporozoites was determined at various concentrations of the compounds that showed effectiveness at 100 μM. The half maximal inhibitory concentration (IC50) value was determined from the approximate curves obtained from these results. SPZ: sporozoite.
Fig. 1 in Anticoccidial activity of the secondary metabolites in alpine plants frequently ingested by wild Japanese rock ptarmigans
Fig. 1. Direct effects of the natural components derived from alpine plants on E. tenella sporozoites. The viability of sporozoites treated with each natural component derived from alpine plants or lasalocid (positive control) with the viability of the DMSO-treated group set as 100%. The final concentration was 100 μM for the natural components, and 1 μM for lasalocid. SPZ: sporozoite; Las: lasalocid. Outliers were tested using Thompson's test (p <0.05), and the student's t-test was utilized to compare the data with the DMSO-treated group as a control (**p <0.01, ***p <0.001, ****p <0.0001).
Fig. 3 in Anticoccidial activity of the secondary metabolites in alpine plants frequently ingested by wild Japanese rock ptarmigans
Fig. 3. Confirmation of the active compounds using commercially available compounds and their efficacy. (A) The viability of sporozoites treated with each commercially available compound or lasalocid (positive control) was compared to the viability of the DMSO-treated group, which was set as 100%. The final concentration was 100 μM for the synthetic compounds, and 1 μM for lasalocid. SPZ: sporozoite, Las: lasalocid. The student's t-test was used for the comparisons (****p <0.0001) without outliers, as tested using Thompson's test (p <0.05). (B) The viability of sporozoites was determined at each concentration of the synthetic compounds that showed effectiveness at 100 μM. The half maximal inhibitory concentration (IC50) value was determined by approximating the curves obtained from the results.
Fig. 4 in Anticoccidial activity of the secondary metabolites in alpine plants frequently ingested by wild Japanese rock ptarmigans
Fig. 4. The inhibitory effects of the natural components derived from alpine plants on sporozoite cell invasion. The invasion rate of sporozoites treated with each natural component derived from alpine plants or lasalocid (positive control) with the viability of the DMSO-treated group set as 100%. Each compound was used at its maximum non-toxic concentration. Las: lasalocid. The student's t-test was utilized to compare the data with the DMSO-treated group as a control (**p <0.01, ***p <0.001, ****p <0.0001). Outliers were identified and removed using Thompson's test (p <0.05).
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.