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875 results for “Infestation”
Figs. 7–9 in Armored scales (Hemiptera: Diaspididae) infesting Hass avocado intercepted in Florida and a new parasitoid-host association for Davidsonaspis aguacatae
Figs. 7–9. Parasitized Davidsonaspis aguacatae adult female: 7. Encarsia lounsburyi adult female and adjacent D. aguacatae crawler; pl–pygidial lobe, t–tentorium. 8. Details of D. aguacatae crawler; ant–antenna, l–leg, ms–maxillary stylet, pl–pygidial lobe. 9. Details of E. lounsburyi adult female.
Fig. 1 in Field survey of Asian citrus psyllid (Hemiptera: Liviidae) infestations associated with six cultivars of Poncirus trifoliata (Rutaceae)
Fig. 1. Comparisons among cultivars of Citrus, citranges, and pure Poncirus trifoliata with respect to infestations of Asian citrus psyllid (ACP) in 5-yr-old trees at a grove in east-central Florida during 2016. a) Percentage of branches with flush suitable for oviposition by Asian citrus psyllid. b) Average infestation densities of immature Asian citrus psyllids (counts of eggs and nymphs combined) per flush shoot. Error bars are standard errors of the mean.
Fig. 2 in Warble infestations by Hypoderma tarandi (Diptera; Oestridae) recorded for the first time in West Greenland muskoxen
Fig. 2. Neighbour-Joining dendrogram showing the genetic relationship between Hypoderma spp. based on 579 bp of the Cox-1 gene using Kimura-2-parameter distance with Dermatobia hominis included as an out group. Warbles H84 and H194 are obtained from two muskoxen on Greenland whereas the other sequences were obtained from GenBank with accession number given after each species. Bootstrap values are indicated at the nodes (1000 replicates). Scale bar: number of base substitutions per site.
Fig. 2 in Apparent fatal winter tick (Dermacentor albipictus) infestation in captive reindeer (Rangifer tarandus)
Fig. 2. Dorsal (A) and ventral view (B) of an adult female Dermacentor albipictus collected from captive reindeer. Inset image shows large goblet cells on the spiracular plate.
Fig. 4 in Spatio-temporal variation in prevalence and intensity of trematodes responsible for waterfowl die-offs in faucet snail-infested waterbodies of Minnesota, USA
Fig. 4. Models of Cyathocotyle bushiensis (Cb) and Sphaeridiotrema spp. (Sg) metacercarial prevalence (prev) and intensity (int) in the waterbodies we studied in northern Minnesota during 2011‾2013; a) East Winnibigoshish index area, b) West Winnibigoshish index area, c) Lower Twin Lake, d) Crow Wing River, e) White Earth ponds, f) Shell River. Depth_cm is water depth at the sampling location. Dist.scaup is the minimum Euclidean distance between a given waypoint and the nearest point sampled under a raft of scaup in either the same season, or up to two seasons prior in that same year. Log.abund is the log transformed snail abundance at a sampling point. Size.mean is the mean snail size at a sampling point. Year2012 and Year2013 are comparisons between samples collected in 2011 vs 2012 and 2011 vs 2013, respectively.
Fig. 3 in Spatio-temporal variation in prevalence and intensity of trematodes responsible for waterfowl die-offs in faucet snail-infested waterbodies of Minnesota, USA
Fig. 3. Average intensity of (a) Cyathocotyle bushiensis (Cb) and (b) Sphaeridiotrema spp. (Sg) metacercariae in each of the waterbodies studied in northcentral Minnesota during nine seasons in 2011‾2013 with 95% confidence intervals. Note that waterbody specific y-axis scales are used to highlight differences within a waterbody.
Fig. 2 in Spatio-temporal variation in prevalence and intensity of trematodes responsible for waterfowl die-offs in faucet snail-infested waterbodies of Minnesota, USA
Fig. 2. Average prevalence of (a) Cyathocotyle bushiensis (Cb) and (b) Sphaeridiotrema spp. (Sg) metacercariae in each of the waterbodies studied in northcentral Minnesota during nine seasons in 2011‾2013 with 95% confidence intervals.
Fig. 1 in Spatio-temporal variation in prevalence and intensity of trematodes responsible for waterfowl die-offs in faucet snail-infested waterbodies of Minnesota, USA
Fig. 1. Map of study area in northcentral Minnesota depicting the study lakes with county boundaries, within the state and USA.
Fig. 5 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host
Fig. 5. Transverse section of S. herzbergii skin parasitized by copepods. (Hematoxylineosin staining). a. Detail of the outer and middle layer of the epidermis (hyperplasia and hypertrophy) (100X). b. Sacciforme cell (400X).
Fig. 4 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host
Fig. 4. Cross section of healthy skin of S. herzbergii. Detail of the epidermis and dermis (staining with hematoxylin-eosin) (400X).
Fig. 2 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host
Fig. 2. Hemorrhagic cutaneous lesions caused by the infestation of copepods on S. herzbergii. a. Ventral view. b. Pectoral fins and mouth.
Fig. 3 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host
Fig. 3. Cross section of healthy skin of S. herzbergii, showing the different layers that make it up (Hematoxylin-eosin staining) (100X).
Fig. 1 in Infestation of introduced raccoons (Procyon lotor) with indigenous ixodid ticks on the Miura Peninsula, Kanagawa Prefecture, Japan
Fig. 1. Map of the Miura Peninsula, Kanagawa Prefecture, Japan. The prefecture is located southeast of Kanto Plain. The square indicates our study area, which includes Yokosuka City and Hayama Town.
Fig. 2 in Infestation of introduced raccoons (Procyon lotor) with indigenous ixodid ticks on the Miura Peninsula, Kanagawa Prefecture, Japan
Fig. 2. Temporal change of raccoon infesting Haemaphysalis flava in the Miura Peninsula, Japan from April 2015 to June 2016.
Figure 2 in New record of Microtechnites bractatus (Say) (Hemiptera: Miridae) infesting Crotalaria spp. and injuries of Miridae in cultivated plants in the State of Paraná, Brazil
Figure 2 Damage of (A) Microtechnites bractatus and (B) Collaria scenica in black oats (Avena strigosa), ryegrass (Lolium multiflorum), beans (Phaseolus vulgaris), white clover (Trifolium repens), tifton 85 (Cynodon spp.), fescue (Festuca sp.), corn (Zea mays) and (viii) crotalaria (Crotalaria juncea).
Figure 4 in Host Plant Records for Fruit Flies (Diptera: Tephritidae: Dacini) in the Pacific Islands: 2. Infestation Statistics on Economic Hosts
Figure 4. Mean number of flies emerged per kg fruit and percent samples infested for the most infested hosts for Bactrocera facialis.
Figure 3 A–C in Host Plant Records for Fruit Flies (Diptera: Tephritidae: Dacini) in the Pacific Islands: 2. Infestation Statistics on Economic Hosts
Figure 3 A–C. Mean number of flies emerged per kg fruit and percent samples infested for the most infested hosts for Pacific fruit fly (Bactrocera xanthodes) (A), B. curvipennis (B), B. psidii (B), and B. trilineola (C).
Fig. 3 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?
Fig. 3. Parasite infestation in faeces and ambient temperature. Correlation between parasite infestation in Alpine mountain hare faeces (n = 52) and average, minimal, and maximal temperature found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. See text for details on statistics.
Fig. 2 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?
Fig. 2. Number of parasite types per faeces and severity of parasitic infestation. Correlation between number of parasite types per Alpine mountain hare faeces and severity of parasitic infestation (n = 28) found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. The severity of infestation is indicated by scattered ((+)), low (+), intermediate (++), and high (+++) infestation. See text for details on statistics.
Fig. 2. A in Multiple infestations of gastrointestinal parasites - Probable cause for high mortality of Spot-billed Pelican (Pelecanus philippensis) at Kokrebellur Community Reserve, India
Fig. 2. A. Larvae of Contracaecum sp. in fish, B. Adult Contracaecum sp. worms in the pelican, C. Eggs of Echinostoma sp. in pelican fecal and water samples, D. Eggs of Contracaecum sp. in pelican fecal and water samples and E. Eggs of Opisthorchis viverrini in pelican fecal samples.
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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
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.