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Figure. Interferon alpha-A based phylogenetic tree (neighbor joining method) constructed by MEGA 6.1 for Punjab urial in comparison with other mammalian species sequences available from GenBank (NCBI). in Characterization of interferon alpha of major histocompatibility complex class I in Punjab urial (Ovis vignei punjabiensis)
Figure. Interferon alpha-A based phylogenetic tree (neighbor joining method) constructed by MEGA 6.1 for Punjab urial in comparison with other mammalian species sequences available from GenBank (NCBI).
Figure 5 in Morphological and molecular characterization of Myxobolus puntiusii n. sp. (Cnidaria: Myxosporea) infecting Puntius sophore Hamilton, 1822 from Ranjit Sagar Wetland, Punjab (India)
Figure 5. Phylogenetic tree generated by maximum likelihood showing the phylogenetic position of Myxobolus puntiusii n. sp. (KU156662) with other myxosporeans. GenBank accession numbers are given and number above nodes indicates bootstrap confidence values. Scale bar: amount of inferred evolutionary change along the branch lengths.
Figure 2 in Morphological and molecular characterization of Myxobolus puntiusii n. sp. (Cnidaria: Myxosporea) infecting Puntius sophore Hamilton, 1822 from Ranjit Sagar Wetland, Punjab (India)
Figure 2. Line drawing of myxospores of Myxobolus puntiusii n. sp. a. Ziehl–Neelsen stain (frontal view). b. Fresh myxospore (sutural view). c. Myxospore showing sporoplasmic nuclei with extruded polar filament (iron–hematoxylin stain).
Figure 3 in Morphological and molecular characterization of Myxobolus puntiusii n. sp. (Cnidaria: Myxosporea) infecting Puntius sophore Hamilton, 1822 from Ranjit Sagar Wetland, Punjab (India)
Figure 3. Photomicrograph of myxospores of Myxobolus puntiusii n. sp. a. Fresh myxospores under dark field microscope. b. Fresh myxospores under phase contrast microscope.
Figure 1 in Morphological and molecular characterization of Myxobolus puntiusii n. sp. (Cnidaria: Myxosporea) infecting Puntius sophore Hamilton, 1822 from Ranjit Sagar Wetland, Punjab (India)
Figure 1. Photomicrograph of infected caudal fin of Puntius sophore showing plasmodia of Myxobolus puntiusii n. sp.
Figure 1 in Selection and molecular characterization of Bacillus thuringiensis strains efficient against soybean looper (Chrysodeixis includens) and Spodoptera species
Figure 1 Comparison of growth inhibitory symptoms of Spodoptera frugiperda larvae exposed to Bacillus thuringiensis β-exotoxins after eight days of inoculation. a: Positive control (strain HD-125); b: Negative control (water); c: Strain 773.
Figure 5 in Selection and molecular characterization of Bacillus thuringiensis strains efficient against soybean looper (Chrysodeixis includens) and Spodoptera species
Figure 5 Toxicity of Bacillus thuringiensis strains against three Spodoptera species. Means followed by the same letter do not differ statistically from one another by the Scott-Knott test at the 5% probability level.
Figure 4 in Selection and molecular characterization of Bacillus thuringiensis strains efficient against soybean looper (Chrysodeixis includens) and Spodoptera species
Figure 4 Profile of total and digested trypsin proteins produced by Bacillus thuringiensis strains eficiente against Chrysodeixis includens. (D) Proteins digested with trypsin; MM: SeeBlue® Plus2 Pre-Stained Standard Marker (Invitrogen, USA).
Figure 3 in Selection and molecular characterization of Bacillus thuringiensis strains efficient against soybean looper (Chrysodeixis includens) and Spodoptera species
Figure 3 Plasmid profiles of Bacillus thuringiensis efficient strains against Chrysodeixis includens. a: DNA extraction according to Fagundes et al. (2011); b: DNA extraction using QIAGEN kit (Invitrogen, USA).MM:1 Kb DNA ladder plus (Invitrogen, USA.The red rows indicate megaplasmids.
Fig. 3 in Characterization of sounds in maize produced by internally feeding insects: investigations to develop inexpensive devices for detection of Prostephanus truncatus (Coleoptera: Bostrichidae) and Sitophilus zeamais (Coleoptera: Curculionidae) in small-scale storage facilities in sub-Saharan Africa
Fig. 3. Effects of distance on detectability of larval sound impulses. Horizontal axis indicates the mean distance between the larval pouch and the sensor; vertical axis indicates the log10-transformed mean rate of impulses detected at that distance. Bars indicate the standard error of mean transformed rate.
Fig. 1 in Characterization of sounds in maize produced by internally feeding insects: investigations to develop inexpensive devices for detection of Prostephanus truncatus (Coleoptera: Bostrichidae) and Sitophilus zeamais (Coleoptera: Curculionidae) in small-scale storage facilities in sub-Saharan Africa
Fig. 1. Spectral profiles of 4 distinctive types of larval sound impulses detected in cracked corn: HaNb, solid line; Ma, dashed line, Ha, dash-dot-dotted line, and La, dotted line. Horizontal axis indicates frequency in kHz and vertical axis indicates relative spectrum amplitude in dB.
Fig. 2 in Characterization of sounds in maize produced by internally feeding insects: investigations to develop inexpensive devices for detection of Prostephanus truncatus (Coleoptera: Bostrichidae) and Sitophilus zeamais (Coleoptera: Curculionidae) in small-scale storage facilities in sub-Saharan Africa
Fig. 2. Oscillogram of sound impulses recorded 10 cm from pouch containing Sitophilus oryzae larvae. Examples of 3 types of larval sound impulse occur during the 1 s period, and one example each of type (Ha, La, and HaNb) is marked above the impulse. Horizontal axis indicates time in seconds and vertical axis indicates relative signal amplitude.
Figures 13–16 in Re-characterization of two Lithosiini species recently described from the island of Taiwan, with establishing of a new combination and the corrected checklist of the genus Aberrasine Volynkin & Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
Figures 13–16. Aberrasine spp.: female genitalia. Depositories of the specimens: 13 and 15 in MWM/ZSM; 14 and 16 in NHMUK (©).
Figures 9–12 in Re-characterization of two Lithosiini species recently described from the island of Taiwan, with establishing of a new combination and the corrected checklist of the genus Aberrasine Volynkin & Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
Figures 9–12. Aberrasine spp.: male genitalia. Depositories of the specimens: 9 and 11 in MWM/ZSM; 10 and 12 in NHMUK (©).
Figures 1–8 in Re-characterization of two Lithosiini species recently described from the island of Taiwan, with establishing of a new combination and the corrected checklist of the genus Aberrasine Volynkin & Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
Figures 1–8. Aberrasine spp.: adults. Depositories of the specimens: 1, 2, 5 and 6 in MWM/ZSM; 3, 4, 7 and 8 in NHMUK (©).
Figures 13–16 in Anarta insolita umay, a new subspecies from Russian Altai and Mongolia, with re-characterization of Anarta insolita uigurica (Hacker, 1998) (Lepidoptera, Noctuidae, Noctuinae)
Figures 13–16. Anarta insolita sspp.: female genitalia (13, 14) and female distal abdominal segments (15, 16). Specimens are deposited in CAV.
Figures 9–12 in Anarta insolita umay, a new subspecies from Russian Altai and Mongolia, with re-characterization of Anarta insolita uigurica (Hacker, 1998) (Lepidoptera, Noctuidae, Noctuinae)
Figures 9–12. Anarta insolita sspp.: male genitalia. Depositories of specimens: 9 in ZSM; 10–12 in CAV.
Figures 1–8 in Anarta insolita umay, a new subspecies from Russian Altai and Mongolia, with re-characterization of Anarta insolita uigurica (Hacker, 1998) (Lepidoptera, Noctuidae, Noctuinae)
Figures 1–8. Anarta insolita sspp.: adults. Depositories of specimens: 1 in ZSM; 2–6 in CAV; 7 in PGM (photo by P. Gyulai); 8 in ZMB.
Figure 12 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 12. (A) Hemolytic activity (%) of the freshwater mussel shell powder. (B) BCI (%) of the freshwater mussel shell powder. *Significant differences for all pairwise analyses at p <0.05.
Figure 9 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 9. SEM-EDS of the different surfaces of the L. wheatleyi shells: (A) periostracum layer and (B) nacreous layer.
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.