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Fig. 2 in Activity and expression of midgut proteases from Mexican and US Trichoplusia ni (Hübner) strains exposed to Bacillus thuringiensis
Fig. 2. Zymogram of midgut proteins from Trichoplusia ni with either 2% Xen- Tari (A) or 1% Cry1Ac-HD73 (B) as substrate. GT and G represent the GTO strain. Migration of molecular markers is indicated on the lef, and proposed T. ni protease numbering (P1 – P7) on right, based on migration in the gel.
Fig. 4 in Activity and expression of midgut proteases from Mexican and US Trichoplusia ni (Hübner) strains exposed to Bacillus thuringiensis
Fig. 4. Relative DNA detected by semi-quantitative RT-PCR using the imageJ sofware, comparing the tnapn1 versus the rs5 control transcript as amplification reference. Trichoplusia ni strains NLX, GTOX and USX represent NL, US and GTO afer 5 generations being exposed to XenTari.
Fig. 3 in Activity and expression of midgut proteases from Mexican and US Trichoplusia ni (Hübner) strains exposed to Bacillus thuringiensis
Fig. 3. Detection of protease activity in midgut extracts from different Trichoplusia ni strains using class-specific substrates. (A) N-a-benzolyl-L-arginine-pNA (BApNA) for detection of trypsin-like activity; (B) N-succinyl-ala-ala-pro-phepNA (SAAPFpNA) for detection of chymotrypsin-like activity; and (C) N-succinylala-ala-pro-leu-pNA (SAAPLpNA) for detection of elastase-like activity.
Fig. 1 in The effects of non-host plant extracts on the oviposition deterrent and ovicidal activity of Conopomorpha sinensis Bradley (Lepidoptera: Gracillariidae)
Fig. 1. The effect of 5 plant extracts on oviposition activity index (OAI) values of Conopomorpha sinensis in the choice test. Plant extracts with oviposition activity indexes of ≥ 0.3 are considered as attractants, whereas those of ≤ −0.3 are considered to be deterrents. Negative values indicate that more eggs were deposited in the control group than those in groups receiving treatment with plant extracts.
Fig. 3. Activity patterns for 14 in Camera-Trapping Survey Of Mammals In And Around Imbak Canyon Conservation Area In Sabah, Malaysian Borneo
Fig. 3. Activity patterns for 14 mammal species (with n ≥ 8) photocaptured in and around Imbak Canyon Conservation Area in central Sabah, Malaysian Borneo. Dotted bar indicates percent frequency of independent photographs taken during the day time (0600–1800 hours); Black bar indicates percent frequency of independent photographs taken during night time (1800–0600 hours). Species are listed in order of decreasing frequency of diurnal activity. Numbers in parentheses indicate sample size.
Extended data of the article "Lockbox enrichment facilitates manipulative and cognitive activities for mice": Supplementary Figure
<p><span>Figure and results of the distance traveled in the Free Exploratory Paradigm, Open Field Test, and Elevated Plus Maze Test during habituation are shown</span>.</p>
Fig. 8 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig. 8. Diagram of Principal Component Analysis during collection periods [Temp(W), water temperature; Sal(W), water salinity; OD(W), water dissolved oxygen; pH(W), pH of water; Fe(W), water iron; Mn(W), water manganese; Cu(S), copper from sediment; Cr(S), chromium from sediment; Ni(S), nickel from sediment; Zn(S), zinc from sediment].
Fig. 7 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig. 7. Dendrogram of Bray-Curtis similarity between the points sampled in the Port Complex of SÃo LuÍs, MaranhÃo, Brazil.
Fig. 3 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig. 3. Temporal and spatial variation of different granulometric size fractions contribution (%) to the sediment total weight at SÃo LuÍs Harbor, MaranhÃo, Brazil. The number below the x-axis indicate the sampling stations.
Fig. 6 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig. 6. Number of species, density and diversity of Shannon of the benthic macrofauna found in the Port Complex of SÃo LuÍs, MaranhÃo, Brazil: (A) Number of species, (B) Density, (C) Shannon diversity and (D) Lumbrineris sp.
Fig 5 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig 5. Temporal and spatial variation of metals and semimetals concentrations (mg kg-1) in the sediment at SÃo LuÍs Harbor, MaranhÃo, Brazil: (A) Lead, (B) Copper, (C) Chrome, (D) Nickel, (E) Zinc and (F) Arsenic.
Fig. 2 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig. 2. Temporal and spatial variation of sub superficial salinity (A), temperature (B), dissolved oxygen (C) and pH (D) at SÃo LuÍs Harbor, MaranhÃo, Brazil.
Fig. 1 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig. 1. Map of the location of Port Complex of SÃo LuÍs, MaranhÃo, Brazil, indicating the eight sampling points.
Fig. 4 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil
Fig. 4. Temporal and spatial variation of total iron (A), dissolved iron (B), manganese (C) and zinc (D) concentrations (mg kg-1) in the sub superficial water at SÃo LuÍs Harbor, MaranhÃo, Brazil. The thick black bar indicates the maximum allowed by resolution 357/05.
Fig. 1 in The lizard that never sleeps: activity of the pampa marked gecko Homonota uruguayensis
Fig. 1. Daily activity of Homonota uruguayensis (Vaz-Ferreira & Sierra de Soriano, 1961) (histogram) and hourly means of environmental temperatures (air temperature: solid line, substrate temperature: dotted lines) in autumn (a), winter (b), spring (c) and summer (d) in the study area at Rosário do Sul, Rio Grande do Sul State, Brazil, between May 2010 and January 2011.
Fig. 2 in The lizard that never sleeps: activity of the pampa marked gecko Homonota uruguayensis
Fig. 2. Relative frequency of active Homonota uruguayensis (Vaz-Ferreira & Sierra de Soriano, 1961) at different air (Ta) and substrate (Tsb) temperatures (2 °C intervals) in the study area at Rosário do Sul, Rio Grande do Sul State, Brazil, between May 2010 and January 2011.
Fig. 4 in Feeding behavior and activity period of three Neotropical bat species (Chiroptera: Phyllostomidae) on Musa paradisiaca inflorescences (Zingiberales: Musaceae)
Fig. 4. Activity period of (A) two glossophagine species (Anoura caudifer + Glossophaga soricina) and Phyllostomus discolor on Musa paradisiaca inflorescence, and of (B) two approaching strategies (upside landing and hovering) performed by two glossophagine species in an orchard located in the state of São Paulo, Brazil.
Fig. 3 in Feeding behavior and activity period of three Neotropical bat species (Chiroptera: Phyllostomidae) on Musa paradisiaca inflorescences (Zingiberales: Musaceae)
Fig. 3. Phyllostomus discolor (Wagner, 1843) with its wings completely open and its head directed toward the flowers performing the downside landing strategy on the banana inflorescence in an orchard located in the state of SÃo Paulo, Brazil. Photo: Wilson Uieda.
Fig. 2 in Feeding behavior and activity period of three Neotropical bat species (Chiroptera: Phyllostomidae) on Musa paradisiaca inflorescences (Zingiberales: Musaceae)
Fig. 2. Glossophaga soricina (Pallas, 1766) with its wings folded alongside the body performing the upside landing strategy on the banana inflorescence in an orchard located in the state of SÃo Paulo, Brazil. Photo: Wilson Uieda.
Figs 2, 3 in Native bee fauna of tomato crops: a comparison of active sampling and pan trapping methods
Figs 2, 3. Richness (Fig. 2) and abundance (Fig. 3) of flower visiting bees sampled bY different pan trap colors in nine tomato crops in GoiÁs state, BraZil. Boxplots represent means while vertical lines represent the 95% confidence interval. Each point represents value for each sampling unit.
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.