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Fig. 3 in Integrated pest management of the German cockroach (Blattodea: Blattellidae) in manufactured homes in rural North Carolina
Fig. 3. Total population levels and decrease (%) of German cockroach populations from all participants during the Pre-IPM, IPM-education, and IPM-education plus bait intervention phases for 6 manufactured homes in rural North Carolina.
Fig. 1 in Integrated pest management of the German cockroach (Blattodea: Blattellidae) in manufactured homes in rural North Carolina
Fig. 1. Population fluctuations of German cockroaches from Oct 2011 to Mar 2014 in 6 manufactured homes in rural North Carolina during the Pre-IPM, IPMeducation, and IPM-education plus bait intervention phases.
Fig. 12 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 12. Enlarged labial palp (lef) showing sensillum chaeticum (C) and sensillum styloconicum (S); and enlarged apical maxillary palp (right) showing apical sensilla basiconica (A1, A2, A3), medial sensilla basiconica (M1, M2, M3), and lateral sensilla basiconica (L1, L2).
Fig. 1 in Conotelus sp. (Coleoptera: Nitidulidae), a new insect pest of passion fruit in the Amazon Biome
Fig. 1. Adults (a, b) of Conotelus sp. (Coleoptera: Nitidulidae) and damage (c, d) caused by this species in passion fruit flowers (Passiflora edulis f. flavicarpa).
Fig. 11 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 11. Apical maxillary palp showing apical sensilla basiconica (A1, A2, A3), medial sensilla basiconica (M1, M2, M3), and lateral sensilla basiconica (L1, L2) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
Fig. 8 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 8. Labrum (L) showing distribution and number of sensilla chaetica (C1–C15) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
Fig. 7 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 7. Ventral and lateral view of larval mouthparts showing labrum (L), mandible (M), maxillae (MX), labium (LI), antennae (A), stemma (ST), and long tactile setae (LTS) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
Fig. 4 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 4. SEM images of larval antennae of Plutella xylostella at different instars: A) 1st instar, B) 2nd instar, C) 3rd instar, and D) 4th instar.
Fig. 15 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 15. Multiple sequence alignment of the partialsequence of the Or83b gene in Spodoptera litura, Chilo partellus, Plutella xylostella, and Maruca vitrata with the reference sequence of Spodoptera litura Or83b (Accession No. JQ811935) using ClustalW sofware. Grey shades represent completely conserved bases. Primer sequences used for amplification of the partial Or83b gene are underlined.
Fig. 1 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 1. Dorsal surface of the larval head showing short tactile setae (STS) and long tactile setae (LTS) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
Fig. 6 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 6. Antenna is segmented (I–III), showing the presence of sensilla styloconica (S1, S2), sensilla basiconica (B1, B2, B3), and sensillum chaeticum (C) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
Fig. 3 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 3. SEM images of larval antennae of Chilo partellus at different instars: A) 1st instar, B) 2nd instar, C) 3rd instar, D) 4th instar, E) 5th instar, and F) 6th instar.
Fig. 5 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 5. SEM images of larval antennae of Maruca vitrata at different instars: A) 1st instar, B) 2nd instar, C) 3rd instar, D) 4th instar, and E) 5th instar.
Fig. 2 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 2. SEM images of larval antennae of Spodoptera litura at different instars: A) 1st instar, B) 2nd instar, C) 3rd instar, D) 4th instar, and E) 5th instar.
Fig. 2 in Conotelus sp. (Coleoptera: Nitidulidae), a new insect pest of passion fruit in the Amazon Biome
Fig. 2. Population fluctuations of Conotelus sp. (Coleoptera: Nitidulidae) adults in passion fruit (Passiflora edulis f. flavicarpa) plantations. Right Y-axis denotes temperature and relative humidity.
Fig. 10 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 10. Enlarged maxillae (MX) showing maxillary palp (MP), galea (G), stipes (ST), and cardo (CA), with galea showing the distribution of sensilla styloconica (S1–S4) and sensilla chaetica (C) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
Fig. 16 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 16. Multiple sequence alignment of the deduced amino acid sequence of the partial Or83b gene of Spodoptera litura, Chilo partellus, Plutella xylostella, and Maruca vitrata with the reference sequence of Spodoptera litura Or83b (Accession No. AFN22085) using ClustalW sofware. Grey shades represent completely conserved residues.
Fig. 14 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 14. Phylogenetic tree produced for the Or83b amino acid sequences of lepidopteran species collected from the NCBI database and Or83b amino acid sequences of Spodoptera litura, Chilo partellus, Plutella xylostella, and Maruca vitrata generated in this study, analyzed using MEGA6 sofware. The rectangular boxes indicate the template sequences generated in this study.
Fig. 9 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 9. Mandible (M) showing sensilla chaetica (C1, C2) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
Fig. 13 in Comparison of sensory structures present on larval antennae and mouthparts of lepidopteran crop pests
Fig. 13. Ventral labium (LI) surface of mouthparts showing hypopharynx (H), labial palp (LP), spinneret (SP), sensilla chaetica (C), and sensilla styloconica (S) in 4 species of Lepidoptera: A) Spodoptera litura, B) Chilo partellus, C) Plutella xylostella, and D) Maruca vitrata.
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.