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Figs 157–170 in Review of Aphidiinae parasitoids (Hymenoptera: Braconidae) of the Middle East and North Africa: key to species and host associations
Figs 157–170. Forewing (♀): 157. Praon orpheusi. 158. Praon pubescens. 159. Praon rosaecola. 160. Praon unitum. 161. Praon uroleucon. 162. Praon volucre. 163. Praon yomenae. 164. Toxares deltiger. 165. Trioxys asiaticus. 166. Trioxys cirsii. 167. Trioxys complanatus. 168. Trioxys curvicaudus. 169. Trioxys metacarpalis. 170. Trioxys moshei.
Fig. 2 in Morphological Characteristics Of Dicrocoelium Dendriticum (Digenea, Dicrocoeliidae), Parasitizing Three Host Species In The Central Regions Of Ukraine
Fig. 2. Frequency distribution of body length of Dicrocoelium specimens from naturally infected cattle, sheep and goat (n = 30).
Figs. 2–5 in New record of Machaeriobia machaerii (Kieffer, 1913) (Diptera, Cecidomyiidae) in Brazil and association with host-plant species
Figs. 2–5. Diagnostic characters of Machaeriobia machaerii in the specimens from Ribeirão Preto, São Paulo State. 2. Simple tarsal claws, 3. One-segmented palpus, 4. Bulbous ovipositor of female pupa, 5. Larval thoracic spatula.
Fig. 2 in Sensitive, quantitative detection of Besnoitia darlingi and related parasites in intermediate hosts and to assess felids as definitive hosts for known and as-yet undescribed related parasite species
Fig. 2. Coccidia-specific PCR to confirm the presence of DNA of various parasite species used to test the analytic specificity of the BdanjoRT1 real-time PCR. (1) Besnoitia darlingi, (2) B. neotomofelis, (3) B. oryctofelisi, (4) B. besnoiti (Evora isolate), (5) B. bennetti (Texas), (6) B. tarandi (Bt-CA-Quebec1), (7) Toxoplasma gondii, (8) Hammondia hammondi, (9) Neospora caninum, (10) H. heydorni, (11) Cystoisospora felis, (12) C. rivolta, (13) C. burrowsi, (14) C. canis, (15) Sarcocystis cruzi and (16) Crytosporidium parvum. Presence of (17) Giardia duodenalis and (18) Tritrichomonas foetus DNA was shown by amplification using species or genus-specific primers, respectively. C, negative control; M, marker.
Fig. 3 in Sensitive, quantitative detection of Besnoitia darlingi and related parasites in intermediate hosts and to assess felids as definitive hosts for known and as-yet undescribed related parasite species
Fig. 3. Analytic sensitivity (A) and standard curve (B) obtained for the threshold cycle (Cq) values obtained in the BdanjoRT1 real-time PCR using varying amounts of genomic Besnoitia darlingi DNA (approximately equivalent to the DNA content of 10.000 [blue], 1000 [green], 100 [red], 10 [brown] and 1 [black] B. darlingi tachyzoites) diluted in 100 ng/μl mouse DNA. Cq values used for regression are displayed as circles. Results on samples resembling DNA of 0.1 tachyzoite were not included in regression, since only two of four samples had reacted with a Cq value of 37.8 or 38.3 (displayed grey in A and as crosses in B). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Sensitive, quantitative detection of Besnoitia darlingi and related parasites in intermediate hosts and to assess felids as definitive hosts for known and as-yet undescribed related parasite species
Fig. 1. Location of the primers and the probe of the Besnoitia darlingi/B.neotomofelis /B. oryctofelisi-specific real-time PCR assay BdanjoRT1 within the ITS-1 region of the rRNA gene. The sequences of the ITS-1 region of B. akodoni (AY545987, bold), B. jellisoni (AF076860, bold), B. neotomofelis (HQ909085, bold), B. darlingi (AF489696, bold) and B. oryctofelisi (AY182000, bold), were aligned relative to sequences of other Besnoitia spp. including B. besnoiti from Portugal, Spain and Germany, B. bennetti reported from the USA and Belgium, B. tarandi from Canada and Finland and those of Neospora caninum, Hammondia heydorni, Toxoplasma gondii and H. hammondi by using Clustal V (DNAStar, Madisin, Wisconsin, USA). Deletions and substitutions in the sequences relative to and within the clade of B. acodoni, B. jellisoni, B. neotomofelis, B. darlingi and B. oryctofelisi are indicated by black background. Sequences of the primer BdanjoRev and the Probe Bb11-12 are displayed in their complementary form. The probe Bb11-12 was established for a real-time PCR to detect B. besnoiti, but it is universal and can be used for the detection of all Besnoitia spp. mentioned here.
Fig. 2 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 2. Parasites recovered from analyzed guignas in Chile: A-anterior extremity of female Molineus sp. (40x); B- caudal extremity of female Molineus sp. with caudal spine (40x); C- oral extremity of female Angiostrongylus sp. (40x); D-lateral view of caudal extremity of female Angiostrongylus sp. (40x); E-caudal extremity of male Angiostrongylus sp., caudal bursa and spicules can be observed (40x); F- lateral view of the rounded caudal extremity of female Oslerus sp. (40x); G-lateral view of the caudal extremity of male Oslerus sp., with characteristic short and stout spicules (40x); H- oral extremity of female Troglostrongylus sp. (100x); I- lateral view of the caudal extremity of male Troglostrongylus sp., long spicules and caudal bursa can be observed (40x).
Fig. 3 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 3. Parasite richness (number of species/genera) in the analyzed guignas from Chile (a) overall, (b) by geographic zone and (c) by sex. Error bars represent standard error of 5%.
Fig. 1 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 1. Geographical locations and parasitism status of analyzed guigna samples in Chile. Dotted line boxes delimit the two geographic zones (Center, South) studied in Chile.
Fig. 6 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 6. Distribution of parasite infection intensity (total number of helminths per guigna) in the analyzed guignas from Chile.
Fig. 4 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 4. Richness of gastrointestinal parasites in guignas from Chile, compared (a) by geographic zone and (b) by sex. p values show the statistical significance in the Mann-Whitney U test between (a) center-south and (b) females-males.
Fig. 1 in Oviposition preference of rugose spiraling whitefly (Hemiptera: Aleyrodidae) on five host plant species
Fig. 1. Photo showing the cage arrangement. Six cages (1.83 × 1.83 × 1.83 m with 20 × 20 Mesh Lumite) were constructed in a shadehouse in a north-south row. Each cage had 5 potential host plants and a source plant containing adult whiteflies.
Fig. 2 in Oviposition preference of rugose spiraling whitefly (Hemiptera: Aleyrodidae) on five host plant species
Fig. 2. The cumulative number of eggs deposited on different plants during the experiment. The average cumulative number of eggs was always greatest on gumbo limbo.
Figure. 3 in Niche separation between the cosmopolitan species Drosophila melanogaster and the tropical Asian species Drosophila ananassae based on larval host-plant species
Figure. 3. Statistical interaction between Drosophila species and larval host plant in determining the number of male flies eclosing in the present experiment. Blue circles represent replicates for Drosophila ananassae and Drosophila melanogaster when raised on cucumberfruit (Averrhoa bilimbi). Red circles indicate replicates where D. ananassae or D. melanogaster were raised on banana (Musa sp.). The number of male flies eclosing from each replicate are presented as squareroot transformed data (variable: TFlies), since the transformed data were used in the ANOVA to determine the statistical significance of this statistical interaction. Da. = Drosophila ananassae, Dm.= Drosophila melanogaster.
Figure 2 in Niche separation between the cosmopolitan species Drosophila melanogaster and the tropical Asian species Drosophila ananassae based on larval host-plant species
Figure 2. Number of Drosophila ananassae and Drosophila melanogaster eclosing in the present experiment, pooling across fruit types. Da. = Drosophila ananassae, Dm.= Drosophila melanogaster.
Figure 1 in Niche separation between the cosmopolitan species Drosophila melanogaster and the tropical Asian species Drosophila ananassae based on larval host-plant species
Figure 1. Number of male flies eclosing from cucumberfruit (Averrhoa bilimbi) vs. banana (Musa species), pooled across Drosophila Species.
Fig. 2 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species
Fig. 2. Schematic representation of the experimental system used to test the host selection behavior of the isopods in the single-host treatments. A: Tachaea chinensis at 20-min acclimation. B: T. chinensis after release.
Fig. 3 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species
Fig. 3. Schematic representation of the experimental system used to test the host selection behavior of the isopods in the common vs un-common host treatments. A: Tachaea chinensis at 20-min acclimation. B: T. chinensis after release.
Fig. 7 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species
Fig. 7. Average predation proportion of Tachaea chinensis in each freshwater decapod's species treatment. Fishers exact test, *P <0.05, **P <0.01.
Fig. 9 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species
Fig. 9. Attachments of Tachaea chinensis on various freshwater decapods during this study. The arrows indicate the position of the isopod on the host. (a) T. chinensis on the left-side of the carapace of Palaemon paucidens; (b) T. chinensis on the right-side of the carapace of Procambarus clarkii; (c) T. chinensis attached on the right-side of the carapace of Neocaridina spp.; and (d) T. chinensis initially clinging on the abdomen of Macrobrachium nipponense.
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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.