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Fig. 7 in Expression profile of two HSP70 chaperone proteins in response to extreme thermal acclimation in Xestia c-nigrum (Lepidoptera: Noctuidae)
Fig. 7. Expression levels of 2 HSP70s at different developmental stages relative to expression levels in 2nd instars at 25 °C. The data are denoted as the mean ± SEM (error bar), and the different lowercase or uppercase letters indicate a significant differenwce in the means as assessed using multi-comparison tests (P <0.05).
Fig. 4 in Expression profile of two HSP70 chaperone proteins in response to extreme thermal acclimation in Xestia c-nigrum (Lepidoptera: Noctuidae)
Fig. 4. Phylogenetic tree of Xc-HSC70 and Xc-HSP70 amino acid sequences from different species. A 3-letter code has been included to indicate the order name of the corresponding insect and vertebrate orders (COL = Coleoptera, LEP = Lepidoptera, DIP = Diptera, HYM = Hymenoptera, and VER =Vertebrata). The values indicated on the branches correspond to bootstrap percentages (BP).
Fig. 3 in Expression profile of two HSP70 chaperone proteins in response to extreme thermal acclimation in Xestia c-nigrum (Lepidoptera: Noctuidae)
Fig. 3. Schematic structure of the Xc-HSC70 gene. Exons are shown as boxes in which white boxes represent untranslated regions, whereas the black boxes are the protein-coding exons; introns are indicated as lines between the boxes. The numbers above and below the drawing represent the sizes (base pairs) of each exon and intron, respectively. The start codon (ATG) and stop codon (TAA) are also indicated. The genomic DNA sequence of Xc-HSC70 has been deposited in GenBank under accession no. KF731994.
Fig. 2 in Expression profile of two HSP70 chaperone proteins in response to extreme thermal acclimation in Xestia c-nigrum (Lepidoptera: Noctuidae)
Fig. 2. Nucleotide and deduced amino acid sequences of the Xc-HSP70 gene. The signature sequences of the HSP70 family are shown in boxes, the nuclear localization signal sequence is underlined, the consensus sequence EEVD at the C-terminus is indicated in italics, and the start and stop codons are in bold. The nucleotides and amino acids are numbered along the lef and right margins. The sequence encoding Xc-HSP70 has been deposited in GenBank under accession no. HQ698836.
Fig. 1 in Expression profile of two HSP70 chaperone proteins in response to extreme thermal acclimation in Xestia c-nigrum (Lepidoptera: Noctuidae)
Fig. 1. Nucleotide and deduced amino acid sequences of Xc-HSC70. The signature sequences of the HSP70 family are shown in boxes, the nuclear localization signal sequence is underlined, the consensus sequence EEVD at the C-terminus is indicated in italics, and the start and stop codons are in bold. The nucleotides and amino acids are numbered along the lef and right margins. The sequence encoding Xc-HSC70 has been deposited in GenBank under accession no. KC844151.
Fig. 3 in Effects of male age and mating status on response to the female sex pheromone of Copitarsia decolora (Lepidoptera: Noctuidae)
Fig. 3. Activation latencies (black bars) and landing latencies (gray bars) (Q1 <Median <Q2) of virgin and mated Copitarsia decolora males to female sex pheromone extract (3FE) in wind tunnel bioassays. Mated males were tested 24 h and 48 h afer mating (24 AM and 48 AM, respectively). Bars within a behavior headed by the same letter are not significantly different (Tukey's mean separation test, n = 10, P <0.05).
Fig. 1 in Effects of male age and mating status on response to the female sex pheromone of Copitarsia decolora (Lepidoptera: Noctuidae)
Fig. 1. Activation latencies (black bars) and landing latencies (gray bars) (Q1 <Median <Q2) by age group of virgin males in response to a glandular extract of female sex pheromone (3FE) in wind tunnel bioassays. Bars within a behavior headed by the same letter are not significantly different (Tukey's mean separation test, n = 10, P <0.05).
Fig. 4 in Effects of male age and mating status on response to the female sex pheromone of Copitarsia decolora (Lepidoptera: Noctuidae)
Fig. 4. Depolarization (mean ± SEM) of antennae in response to a glandular extract of female sex pheromone (3FE) of virgin and mated males. Mated males were tested 24 h and 48 h afer mating (24 AM and 48 AM, respectively). Bars headed by the same letter are not significantly different (Tukey's mean separation test, n = 6, P <0.05).
Fig. 3 in Response of two chemotypes of Melaleuca quinquenervia (Myrtales: Myrtaceae) saplings to colonization by specialist herbivores
Fig. 3. Total mean (± SE) leaf biomass shed via abscission by Melaleuca quinquenervia saplings subjected to unrestricted or restricted herbivory by Oxyops vitiosa and Boreioglycaspis melaleucae. **: P = 0.01.
Fig. 1 in Response of two chemotypes of Melaleuca quinquenervia (Myrtales: Myrtaceae) saplings to colonization by specialist herbivores
Fig. 1. Mean (± SE) dry weight biomass of leaves shed via abscission by saplings of 2 Melaleuca quinquenervia chemotypes subjected to 2 levels of herbivory by Oxyops vitiosa and Boreioglycaspis melaleucae.
Fig. 1 in Effects of the antennal sensilla distribution pattern on the behavioral responses of Tribolium castaneum (Coleoptera: Tenebrionidae)
Fig. 1. Tribolium castaneum antennal ultrastructure observations. Dorsal view of the whole antenna with 11 antennal segments with a black line indicating where antennae were cut. Sensilla basiconica were found only on the last 3 segments of the antennae and sensilla trichodea on all antennal segments.
Fig. 6 in Trichoplusia ni (Lepidoptera: Noctuidae) survival, immune response, and gut bacteria changes afer exposure to Azadirachta indica (Sapindales: Meliaceae) volatiles
Fig. 6. Transcription of the 23S gene of Enterobacteria (428 bp) and ribosomal protein S5 gene (782 bp) from rRNA samples of Trichoplusia ni NL strain larval midguts, afer exposure to 10 g of neem leaves, determined by reverse transcriptase polymerase chain reaction (RT-PCR). PCR product of RNA not subject- ed to RT-PCR was taken as a negative control. Lane 1, DNA ladder 100 bp; lane 2, PCR product of plasmid DNA with the Enterobacteria insert as positive control; lane 3, PCR products of the 23S gene of Enterobacteria and the ribosomal protein S5 gene of T. ni from unexposed larvae; lanes 4, 6, and 8, PCR of control RNA; lane 5, RT-PCR products in gut from VOC-exposed T. ni larva, showing both 23S and ribosomal protein S5 gene amplification (1st replication); lane 7, RT-PCR products in gut from VOC-exposed T. ni larva, showing both 23S and ribosomal protein S5 gene amplification (2nd replication).
Fig. 3 in Trichoplusia ni (Lepidoptera: Noctuidae) survival, immune response, and gut bacteria changes afer exposure to Azadirachta indica (Sapindales: Meliaceae) volatiles
Fig. 3. Mortality for NL and Gto strains of Trichoplusia ni exposed as neonate larvae for 7 d in sealed containers to VOCs from 1 or 10 g of dried neem stems compared with the unexposed controls. Data represent the mean ± standard deviation of 3 replicate experiments per treatment (90 larvae per replicate were tested).
Fig. 3 in Effects of the antennal sensilla distribution pattern on the behavioral responses of Tribolium castaneum (Coleoptera: Tenebrionidae)
Fig. 3. SEM photomicrographs of 6 types (A1, B1, C1, D1, E1, F1) of sensilla basiconica (SB) showing lateral view of the antennae of Tribolium castaneum. TEM photomicrographs 6 types (A2, B2, C2, D2, E2, F2) of sensilla basiconica (SB) showing the thin wall and continuous pores and dendrites. CW = cuticle wall, P = pores, D = dendrites, SBI = sensilla basiconica type 1, SBII = sensilla basiconica type II, SBIII = sensilla basiconica type III, SB IV = sensilla basiconica type IV, SBV = sensilla basiconica type V, SBVI = sensilla basiconica type VI.
Fig. 1 in Trichoplusia ni (Lepidoptera: Noctuidae) survival, immune response, and gut bacteria changes afer exposure to Azadirachta indica (Sapindales: Meliaceae) volatiles
Fig. 1. Setup of the bioassay container for neem VOC exposure of Trichoplusia ni neonates. A) View of tray with 30 cups placed inside the 11 L plastic container with airtight lid for VOC exposure; B) view of tray with 30 cups with artificial diet infested with 3 neonates each and cardboard lid to allow VOC exchange; C) view of 1 L container with artificial diet (bottom) and 1 oz (29.6 mL) cups (top) with 1 g milled dried neem stems or leaves.
Fig. 3 in Response of male Centruroides vittatus (Scorpiones: Buthidae) to aerial and substrate-borne chemical signals
Fig. 3: The movement of a male scorpion during a 3-minute trial. Scorpion position was marked by a dot every 5 seconds of the trial. In general, the movement path has more space between dots in the "no-stimulus" side (top) versus the "stimulus" side (bottom). The average distance (+/- standard deviation) traveled between 5 second plots: no-stimulus side = 15.3 +/- 7.8 mm (median = 12.5 mm), stimulus side = 10.8 +/- 5.9 mm (median = 8.0 mm). "BL" indicates occurrence of a backward lunge.
Fig. 1 in Response of male Centruroides vittatus (Scorpiones: Buthidae) to aerial and substrate-borne chemical signals
Fig. 1: Y-shaped arena for Experiments 1, 2, and 3 to test airborne chemical communication in C. vittatus.
Response of convectively coupled Kelvin waves to surface temperature forcing in aquaplanet simulations: data and code
<p>This is the data and code used for a journal paper entitled "Response of convectively coupled Kelvin waves to surface temperature forcing in aquaplanet simulations", written by Mu-Ting Chien and Daehyun Kim in 2024. This paper is in minor revision in the Journal of Advances in Modeling Earth System. The submitted paper is here: (https://essopenarchive.org/doi/full/10.22541/essoar.171322728.86206700/v1).</p>
The data on the optical properties of kombucha and kombucha proteinoids, as well as chaos calculations are provided for the paper titled "Kombucha Mats as Responsive Materials."
<p>The data on the optical properties of kombucha and kombucha proteinoids, as well as chaos calculations are provided for the paper titled "Kombucha Mats as Responsive Materials."</p>
Fig. 1 in The response of Phyllophaga brevidens and Phyllophaga lenis (Coleoptera: Scarabaeidae) to methyl 2-(methylthio) benzoate and light
Fig. 1. Numbers of Phyllophaga brevidens and Phyllophaga lenis adults trapped per species, sex, and treatment during 2 sampling periods in Tlaltizapan, Morelos, Mexico. A = attractant, L= light, C = control, M = males, F = females, nd = not determined.
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.