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zenodo28/100

Figure 6 from: Tanaka S (2024) Temperature-dependent phototaxis in overwintering adults of the grasshopper Patanga japonica (Orthoptera, Acrididae). Journal of Orthoptera Research 33(1): 71-86. https://doi.org/10.3897/jor.33.102749

Figure 6 A–C. The effect of blocking the sunlight in the D-area (A) on the number of P. japonica adults in the L-area and temperatures of the two areas (B, C). Cardboard screen was placed in front of the D-area at 13:00. Grey areas show the period during which adults were moving from L- to D-areas. D–K. The effect of heating of the L-area on the behavior of P. japonica adults. In D–G, yellow and black bars indicate the number of adults in the L- and D-areas. In H–K, yellow and black lines indicate the temperatures in the L- and D-areas. Asterisks indicate a significant difference with a t-test at the 5% level.

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 4 from: Tanaka S (2024) Temperature-dependent phototaxis in overwintering adults of the grasshopper Patanga japonica (Orthoptera, Acrididae). Journal of Orthoptera Research 33(1): 71-86. https://doi.org/10.3897/jor.33.102749

Figure 4 The numbers of P. japonica adults in the L-area of tubes (A, B), temperatures in the L- and D-area (C, D) and light intensities (< 20,000 lux, E, F) under outdoor conditions on Dec. 31 (A, C, E) and Jan. 1 (B, D, F). Ten adults were placed in the D- or L-area of each tube at 08:00.

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 3 from: Tanaka S (2024) Temperature-dependent phototaxis in overwintering adults of the grasshopper Patanga japonica (Orthoptera, Acrididae). Journal of Orthoptera Research 33(1): 71-86. https://doi.org/10.3897/jor.33.102749

Figure 3 The numbers of P. japonica adults on the walls of cages kept under outdoor and indoor conditions on Dec. 28 (A) and 29 (B). All adults were placed on the floor at 08:00 on the first day in the indoor cage. Temperature on the floor was monitored hourly (C, D). Pale orange areas indicate the time of sunlight on cages.

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 2 from: Tanaka S (2024) Temperature-dependent phototaxis in overwintering adults of the grasshopper Patanga japonica (Orthoptera, Acrididae). Journal of Orthoptera Research 33(1): 71-86. https://doi.org/10.3897/jor.33.102749

Figure 2 The proportion of P. japonica adults that stood within 10 min after being placed with their sides down at 08:00 (N = 8–12) on the cork floor under outdoor conditions from Jan. 20–29 (A), the time of day when those adults that remained motionless for >10 min after being placed with their sides down at 08:00 stood spontaneously (B), and the floor and their body temperatures when standing (C).

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 10 from: Tanaka S (2024) Temperature-dependent phototaxis in overwintering adults of the grasshopper Patanga japonica (Orthoptera, Acrididae). Journal of Orthoptera Research 33(1): 71-86. https://doi.org/10.3897/jor.33.102749

Figure 10 A. The relationship between body temperatures of P. japonica adults and temperatures on litter in the outdoor enclosure from Jan. 17 to Feb. 7. Sitting, adults sitting on litter; emerging, those that just emerged from litter; hiding, those that started moving to hide under litter. Dotted lines indicate that the two temperatures are similar. B, C. The proportions of days when the temperature on litter increased, remained unchanged, and decreased during 1 h before the first P. japonica emerged (B) and before the first adult hid under litter (C) in the outdoor enclosure from Jan. 12 to Feb. 25.

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 9 from: Tanaka S (2024) Temperature-dependent phototaxis in overwintering adults of the grasshopper Patanga japonica (Orthoptera, Acrididae). Journal of Orthoptera Research 33(1): 71-86. https://doi.org/10.3897/jor.33.102749

Figure 9 A–E. Daily changes in the percentage of P. japonica adults above litter in the outdoor enclosure containing 20 individuals. Each histogram represents the mean percentage of insects at that hour averaged over all the days of that specific period. Bars indicate one SD. F. The relationship between the daily maximum number of P. japonica adults above the litter surface and various daily maximum temperatures in the outdoor enclosure from Feb. 6 to 25. T-1 = temperature at the bottom of litter; T-2 = temperature on litter; AT = air temperature, shade. G. The relationship between the numbers of P. japonica adults above litter and temperatures at 18:00 in the outdoor enclosure from Feb. 27 to Apr. 12. T-1, temperature at the bottom of litter; T-2, temperature on litter; AT, air temperature, shade.

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 11 from: Tanaka S (2024) Temperature-dependent phototaxis in overwintering adults of the grasshopper Patanga japonica (Orthoptera, Acrididae). Journal of Orthoptera Research 33(1): 71-86. https://doi.org/10.3897/jor.33.102749

Figure 11 The number of P. japonica adults that appeared in the L-areas of tubes at 20°C under artificial illumination on Jan. 3 (A) and Jan. 8 (B). Treatment tubes were transferred to warm indoors from the cool outside at 20:00, causing them to rapidly heat. Control tubes experienced only a mild temperature increase because they had already been indoors for several hours. All adults were placed in D-areas at 20:00. Temperatures in the L-areas are shown. Note that no Control insects moved into the L-areas on both days.

opencc-by-4.0Feb 2024View details →
zenodo28/100

RESULTS OF SURGICAL TREATMENT OF RECURRENT PULMONARY ECHINOCOCCOSIS DEPENDING ON MORPHOLOGICAL MODIFICATIONS

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opencc-by-4.0Mar 2024View details →
zenodo28/100

Fig. 9 in Arachidonic acid-dependent carbon-eight volatile synthesis from wounded liverwort (Marchantia polymorpha)

Fig. 9. Proposed biosynthetic pathway to form C8 volatiles in M. polymorpha thalli.

opennotspecifiedNov 2014View details →
zenodo28/100

Fig. 1. Structures for compounds 1–5 in Arachidonic acid-dependent carbon-eight volatile synthesis from wounded liverwort (Marchantia polymorpha)

Fig. 1. Structures for compounds 1–5.

opennotspecifiedNov 2014View details →
zenodo28/100

Data for LRRK2 kinase inhibition reverses G2019S mutation-dependent effects on tau pathology spread

<p>Data that was analyzed and used to create figures in the paper.</p>

opencc-by-4.0Feb 2024View details →
zenodo28/100

Deep learning reveals the metabolic dependency of hypoxic tumor cells and the critical function of FLAD1 mediated mitochondrial metabolic reprogramming

Open the record for dataset details and reuse information.

opencc-by-4.0Apr 2024View details →
zenodo28/100

Pressure-dependent magnetism of the Kitaev candidate Li2RhO3

<p>Collection of the figures data for the pressure study of Li2RhO3</p>

opencc-by-4.0Sep 2024View details →
zenodo28/100

DEPENDENCE OF ITS PHYSICAL AND CHEMICAL PROPERTIES ON THE STRUCTURE OF BRIQUETTES

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opencc-by-4.0Nov 2024View details →
zenodo28/100

Multivocal Study on Microservice Dependencies

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opencc-by-4.0May 2024View details →
zenodo28/100

Data and scripts for "Servicesheds connect people to the landscapes upon which they depend"

Open the record for dataset details and reuse information.

opencc-by-4.0Oct 2024View details →
zenodo28/100

Open Source Software Dependency Dataset

<p>Open Source Software Dependency Dataset</p>

opencc-by-4.0Nov 2024View details →
dryad28/100

Context dependent benefits of aphids for bacteria in the phyllosphere.

<p>Insect herbivores, like aphids, are common on plants yet how they interact with plant microbiomes remains largely unknown. For instance, for the widespread bacterial epiphyte and potential aphid pathogen <i>Pseudomonas syringae</i>, aphids could impact bacterial populations by serving as secondary hosts or by altering the epiphytic habitat through feeding and/or waste secretion. Here we examined if the pea aphid, <i>Acyrthosiphon pisum</i>, could influence epiphytic populations of <i>P. syringae</i>. First, we quantified epiphytic growth ability without aphids and virulence to aphids across 21 diverse <i>P. syringae</i> strains. For eight strains that varied in these traits we then assessed the influence of aphid presence on epiphytic bacterial growth. In some cases, <i>P. syringae</i> benefited significantly from the presence of aphids, with up to 3.8 times more cell doublings. This benefit was not correlated with strain traits, but rather with initial population densities; smaller bacterial populations received relatively more benefit from aphids, and larger populations received less benefit. Honeydew, the sugary waste product of aphids, in the absence of aphids was sufficient to increase <i>P. syringae</i> density on leaves. We conclude that aphid honeydew can sometimes increase <i>P. syringae</i> epiphytic growth, but that the bacteria may not benefit from using aphids as hosts.</p>

opencc-zeroOct 2021View details →
zenodo28/100

Survey Material and Data - Illusion of visual stability through active perceptual serial dependence

<p>Survey Material and Data.</p>

opencc-by-4.0Sep 2021View details →
dryad28/100

Data from: Orientation of mouse H19 ICR affects imprinted H19 gene expression through promoter methylation–dependent and –independent mechanisms

<p>The mouse <em>Igf2/H19</em> locus is regulated by genomic imprinting, in which the paternally methylated <em>H19</em> imprinting control region (ICR) plays a critical role in mono-allelic expression of the genes in the locus. Although the maternal allele–specific insulator activity of the <em>H19</em> ICR in regulating imprinted <em>Igf2</em> expression has been well established, the detailed mechanism by which the <em>H19</em> ICR controls mono-allelic <em>H19</em> gene expression has not been fully elucidated. In this study, we evaluated the effect of <em>H19</em> ICR orientation on imprinting regulation in mutant mice in which the <em>H19</em> ICR sequence was inverted at the endogenous locus. When the inverted-ICR allele was paternally inherited, the methylation level of the <em>H19</em> promoter was decreased and the <em>H19</em> gene was derepressed, suggesting that methylation of the <em>H19</em> promoter is essential for complete repression of <em>H19</em> gene expression. Unexpectedly, when the inverted allele was maternally inherited, the expression level of the <em>H19</em> gene was lower than that of the WT allele, even though the <em>H19</em> promoter remained fully hypomethylated. These observations suggested that the polarity of the <em>H19</em> ICR is involved in controlling imprinted <em>H19</em> gene expression on each parental allele, dependent or independent on DNA methylation of the <em>H19</em> promoter.</p>

opencc-zeroNov 2021View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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