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310 results for “host use”

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zenodo32/100

Fig. 5 in Composition and Host-Use Patterns of a Scarab Beetle (Coleoptera: Scarabaeidae) Community Inhabiting the Canopy of a Lowland Tropical Rainforest in Southern Venezuela

Fig. 5. Number of individuals sampled per scarab beetle species on host trees regressed on the number of utilized host trees, Venezuela, 1997–1999.

opennotspecifiedMar 2019View details →
zenodo32/100

Figs. 1–3 in Composition and Host-Use Patterns of a Scarab Beetle (Coleoptera: Scarabaeidae) Community Inhabiting the Canopy of a Lowland Tropical Rainforest in Southern Venezuela

Figs. 1–3. Study site in Venezuela. 1) Crane used for access to the canopy of the lowland rainforest; 2) Canopy of the lowland rainforest; 3) Window trap in the canopy of the crane plot.

opennotspecifiedMar 2019View details →
zenodo32/100

Fig. 6 in Composition and Host-Use Patterns of a Scarab Beetle (Coleoptera: Scarabaeidae) Community Inhabiting the Canopy of a Lowland Tropical Rainforest in Southern Venezuela

Fig. 6. Total number of individuals sampled per scarab beetle species regressed on the number of months of occurrence, Venezuela, 1997–1999.

opennotspecifiedMar 2019View details →
zenodo32/100

Figs. 1–4 in Lignyodes enucleator Panzer (Coleoptera: Curculionidae: Curculioninae: Tychiini) Associated with Fraxinus syriaca Boiss. (Oleaceae) — The First Records from Israel and of Host Plant Use

Figs. 1–4. The Syrian ash, Fraxinus syriaca, at the Hermon Field School, Hula Valley, Israel: 1) General view;

opennotspecifiedDec 2016View details →
zenodo32/100

FIGURE 3 in Using DNA barcoding to identify host-parasite interactions between cryptic species of goby (Coryphopterus: Gobiidae, Perciformes) and parasitic copepods (Pharodes tortugensis: Chondracanthidae, Cyclopoida)

FIGURE 3. Maximum likelihood tree derived from COI sequences of our copepod samples (labeled as P. tortugensis) plus voucher sequences from related copepods in the suborder Ergasilida (see Table 5 for a list). Sequences of copepods confamilial to P. tortugenis (Chondracanthidae) are labelled to species (and shaded blue in the online colour version), and members other taxa are labeled to family (and shaded pink in the colour online version). Support values for bipartitions are indicated, and divergence represented by dark blue scale bar = 3 %.

opennotspecifiedOct 2021View details →
zenodo32/100

FIGURE 1 in Using DNA barcoding to identify host-parasite interactions between cryptic species of goby (Coryphopterus: Gobiidae, Perciformes) and parasitic copepods (Pharodes tortugensis: Chondracanthidae, Cyclopoida)

FIGURE 1. Maximum likelihood tree derived from COI sequences of our goby samples plus voucher sequences from all Coryphopterus species except C. punctipectophorus. Voucher sequences are identified by GenBank sequence ID. Sequences from several other goby species are included as outgroups (not all are identified in the figure; see Table 4 for a list). Support values for bipartitions are indicated, and divergence represented by scale bar = 6%.

opennotspecifiedOct 2021View details →
zenodo32/100

FIGURE 2 in Using DNA barcoding to identify host-parasite interactions between cryptic species of goby (Coryphopterus: Gobiidae, Perciformes) and parasitic copepods (Pharodes tortugensis: Chondracanthidae, Cyclopoida)

FIGURE 2. Differences in body depth between goby species. A boxplot of body depth (as a % of body length in SL) for the three gobies, with sample sizes in parentheses. For the boxplot: box boundaries represent 25th and 75th percentiles respectively; line inside box indicates the median, lower and upper error lines indicate 10th and 90th percentiles respectively, and circles show data falling outside 10th and 90th percentiles.

opennotspecifiedOct 2021View details →
zenodo32/100

FIGURE 1 in The longhorn beetles (Coleoptera: Cerambycidae) of Kentucky with notes on larval hosts, adult nectar use, and semiochemical attraction

FIGURE 1. Distribution of specimen records and Level III ecoregions within Kentucky (A), and heatmap of specimen density and the counties of Kentucky (B).

opennotspecifiedJan 2023View details →
dryad32/100

Data from: Use of an exotic host plant shifts immunity, chemical defense, and viral burden in wild populations of a specialist insect herbivore

<p>Defense against natural enemies constitutes an important driver of herbivore host range evolution in the wild. Populations of the Baltimore checkerspot butterfly, <em>Euphydryas phaeton </em>(Nymphalidae), have recently incorporated an exotic plant, <em>Plantago lanceolata </em>(Plantaginaceae), into their dietary range. To understand the tritrophic consequences of utilizing this exotic host plant, we examined immune performance, chemical defense, and interactions with a natural entomopathogen (Junonia coenia densovirus, <em>Parvoviridae</em>) across wild populations of this specialist herbivore. We measured three immune parameters, sequestration of defensive iridoid glycosides (IGs), and viral infection load in field-collected caterpillars using either <em>P. lanceolata</em> or a native plant, <em>Chelone glabra </em>(Plantaginaceae). We found that larvae using the exotic plant exhibited reduced immunocompetence, compositional differences in IG sequestration, and higher <em>in situ </em>viral burdens compared to those using the native plant. On both host plants, high IG sequestration was associated with reduced hemocyte concentration in the larval hemolymph, providing the first evidence of incompatibility between sequestered chemical defenses and the immune response (i.e., the "vulnerable host" hypothesis) from a field-based study. However, despite this negative relationship between IG sequestration and cellular immunity, caterpillars with greater sequestration harbored lower viral loads. While survival of virus-infected individuals decreased with increasing viral burden, it ultimately did not differ between the exotic and native plants. These results provide evidence that (1) phytochemical sequestration may contribute to defense against pathogens even when immunity is compromised, and (2) herbivore persistence on exotic plant species may be facilitated by sequestration and its role in defense against natural enemies.</p>

opencc-zeroFeb 2023View details →
zenodo32/100

Aggressive interactions among white-tailed deer and their impact on the use of 4-poster devices for host-targeted tick control

<p>Spreadsheet of data transcribed from images of deer and non-target wildlife with coded behaviors used in the manuscript &quot;Aggressive interactions among white-tailed deer and their impact on the use of 4-poster devices for host-targeted tick control&quot;. Data involves cameras placed at three sites in Maryland 2016-2017.</p>

opencc-by-4.0Jun 2023View details →
dryad32/100

How do host-plant use and seasonal life cycle relate to insect body size: A case study on European geometrid moths (Lepidoptera: Geometridae)

<p><span>We used European geometrid moths (&gt; 630 species) as a model group to investigate how life history traits linked to larval host plant use (i.e., diet breadth and host-plant growth form) and seasonal life cycle (i.e., voltinism, overwintering stage, and caterpillar phenology) are related to adult body size in holometabolous insect herbivores. To do so, we applied phylogenetic comparative methods to account for shared evolutionary history among herbivore species. We further categorised larval diet breadth based on the phylogenetic structure of utilised host plant genera. Our results indicate that species associated with woody plants are, on average, larger than herb feeders and increase in size with increasing diet breadth. Obligatorily univoltine species are larger than multivoltine species, and attain larger sizes when their larvae are restricted to the early season. Furthermore, adult body size is significantly smaller in species that overwinter in the pupal stage compared to those that overwinter as egg or caterpillar. In summary, our results indicate that the ecological niche of an holometabolous insect herbivore is strongly interrelated with its size at maturity.</span></p>

opencc-zeroSep 2023View details →
ClinicalTrials.gov32/100

Comparing the Therapeutic Effects of Using Ruxolitinib and Steroids Concurrently to Steroids Alone as Initial Treatment In Patients Diagnosed With Chronic Graft-versus-host Disease at a Grade of Moder

ClinicalTrials.gov study NCT06756061. IPD Sharing: NO. Countries: 1. Publications: 28.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Using Gut Microbial Gbu Gene Testing to Estimate Host TMAO Production Capacity

ClinicalTrials.gov study NCT05980884. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Prevention of Severe Acute Graft-versus-host Disease in Adult Patients Using a daGOAT Model

ClinicalTrials.gov study NCT05600855. IPD Sharing: YES. Countries: 1. Publications: 1.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov32/100

Using GM-CSF as a Host Directed Therapeutic Against COVID-19

ClinicalTrials.gov study NCT04400929. IPD Sharing: Not stated. Countries: 1. Publications: 30.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

The Use of Etanercept (Enbrel®) in the Treatment of Acute Graft-Versus-Host Disease

ClinicalTrials.gov study NCT00141713. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Disease's hidden death toll: Using parasite aggregation patterns to quantify landscape-level host mortality in a wildlife system

Open the record for dataset details and reuse information.

publicAug 2020View details →
dryad32/100

Data from: Using a comprehensive DNA barcode library to detect novel egg and larval host plant associations in a Cephaloleia Rolled-leaf Beetle (Coleoptera: Chrysomelidae)

Open the record for dataset details and reuse information.

publicApr 2013View details →
dryad32/100

Data from: Ecological and genetic factors influencing the transition between host-use strategies in sympatric Heliconius butterflies

Open the record for dataset details and reuse information.

publicJul 2013View details →
dryad32/100

Data from: Using host species traits to understand the consequences of resource provisioning for host–parasite interactions

Open the record for dataset details and reuse information.

publicSep 2018View details →

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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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