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1,854 results for “Host plant”
Comparative transcriptomics reveal contrasting fungal strategies in a plant pathogen (Fusarium graminearum) versus an endophyte (Metarhizium anisopliae) during initial host colonization
GEO Series GSE277787. Fusarium graminearum. 24 samples. Type: Expression profiling by high throughput sequencing.
Multiple paths of plant host toxicity are associated with the fungal toxin cercosporin
GEO Series GSE142976. Arabidopsis thaliana. 15 samples. Type: Expression profiling by high throughput sequencing.
Genome-wide analysis of Botrytis cinerea genes targeting plant cell walls of different hosts [tomato]
GEO Series GSE57586. Botrytis cinerea B05.10. 3 samples. Type: Expression profiling by high throughput sequencing.
Fragmentation of tRNA in Phytophthora infestans asexual life cycle stages and during host plant infection [life cycle]
GEO Series GSE62674. Phytophthora infestans. 8 samples. Type: Non-coding RNA profiling by high throughput sequencing.
RNA-seq time-course analysis of the transcriptional dynamics of the two root-infecting fungi Colletotrichum tofieldiae (mutualistic) and Colletotrichum incanum (pathogenic) and their plant host Arabid
GEO Series GSE70094. Arabidopsis thaliana; Colletotrichum tofieldiae; Colletotrichum incanum. 63 samples. Type: Expression profiling by high throughput sequencing.
An artificial host system enables the obligate parasitic plant Cuscuta campestris to grow and complete its life cycle in vitro
GEO Series GSE178396. Cuscuta campestris. 8 samples. Type: Expression profiling by high throughput sequencing.
Intraspecific difference among herbivore lineages and their host-plant specialization drive the strength of trophic cascades
<p>Dataset from the publication Intraspecific difference among herbivore lineages and their host-plant specialization drive the strength of trophic cascades</p>
Figure 2 in Notes on mating behaviour and a possible new host plant for Megacyllene angulata (Fabricius, 1775) (Cerambycidae, Coleoptera)
Figure 2. Specimens of Megacyllene angulata performing mating behavior. (A) Male and female specimens clustered in a region of the vine. (B) Males frantically pursued females. (C) Copulations interrupted by aggressive behaviors of other males. (D) Couple in copulation, immobile on the region of the vine not directly exposed to sunlight.
Figure 3 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 3. Nomenclature of Phyllocnistis forewing fasciae and strigulae.
Data from: Pleistocene sea level fluctuation and host plant habitat requirement influenced the historical phylogeography of the invasive species Amphiareus obscuriceps (Hemiptera: Anthocoridae) in its native range
Background: On account of repeated exposure and submergence of the East China Sea (ECS) land bridge, sea level fluctuation played an important role in shaping the population structure of many temperate species across the ECS during the glacial period. The flower bug Amphiareus obscuriceps (Poppius, 1909) (Hemiptera: Anthocoridae) is an invasive species native to the Sino-Japanese Region (SJR) of East Asia. We tested the hypothesis of the ECS land bridge acting as a dispersal corridor or filter for A. obscuriceps during the glacial period. Specifically, we tested whether and the extent to which dispersal ability and host plant habitat requirement influenced the genetic structure of A. obscuriceps during the exposure of the ECS land bridge. Results: Phylogenetic and network analyses indicated that A. obscuriceps is composed of two major lineages, i.e., China and Japan. Divergence time on both sides of the ECS was estimated to be approximately 1.07 (0.79-1.32) Ma, which was about the same period that the sea level increased. No significant Isolation by Distance (IBD) relationship was found between Фst and Euclidean distances in the Mantel tests, which is consistent with the hypothesis that this species has a good dispersal ability. Our Last Glacial Maximum (LGM) niche modeling of plants that constitute preferred habitats for A. obscuriceps exhibited a similar habitat gap on the exposed ECS continental shelf between China and Japan, but showed a continuous distribution across the Taiwan Strait. Conclusion: Our results suggest that ecological properties (habitat requirement and dispersal ability), together with sea level fluctuation during the Pleistocene across the ECS, have shaped the genetic structure and demographic history of A. obscuriceps in its native area. The host plant habitat requirement could also be a key to the colonization of the A. obscuriceps species during the exposure of the ECS land bridge. Our findings will shed light on the potential role of habitat requirement in the process of biological invasion in future studies.
Figure 6 in Gall-inducing arthropods in a Neotropical savanna area in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil): effects of plant species richness and super-host abundance
Figure 6. Effect of plant species richness on the galling species per plant species in an area of Neotropical savanna in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil).
Data from: Adaptation to resistant hosts increases fitness on susceptible hosts in the plant parasitic nematode Globodera pallida
Trade-offs between virulence (defined as the ability to infect a resistant host) and life-history traits are of particular interest in plant pathogens for durable management of plant resistances. Adaptation to plant resistances (i.e., virulence acquisition) is indeed expected to be associated with a fitness cost on susceptible hosts. Here, we investigated whether life-history traits involved in the fitness of the potato cyst nematode Globodera pallida are affected in a virulent lineage compared to an avirulent one. Both lineages were obtained from the same natural population through experimental evolution on resistant and susceptible hosts, respectively. Unexpectedly, we found that virulent lineages were more fit than avirulent lineages on susceptible hosts: they produced bigger cysts, containing more larvae and hatching faster. We thus discuss possible reasons explaining why virulence did not spread into natural G. pallida populations.
Figure 9 from: Huemer P, Schmid J (2021) Relict populations of Lyonetia ledi Wocke, 1859 (Lepidoptera, Lyonetiidae) from the Alps indicate postglacial host-plant shift to the famous Alpenrose (Rhododendron ferrugineum L.). Alpine Entomology 5: 101-106. https://doi.org/10.3897/alpento.5.76930
Figure 9 Habitat of Lyonetia ledi in Engadine/Switzerland with Rhododendron ferrugineum.
Figures 103-104 from: Tang C-T, Mikó I, Nicholls JA, Schwéger S, Yang M-M, Stone GN, Sinclair F, Bozsó M, Melika G, Pénzes Z (2016) New Dryocosmus Giraud species associated with Cyclobalanopsis and non-Quercus host plants from the Eastern Palaearctic (Hymenoptera, Cynipidae, Cynipini). Journal of Hymenoptera Research 53: 77-162. https://doi.org/10.3897/jhr.53.9890
Figures 103-104 - Dryocosmus konradi sp. n., galls (photos by C.-T. Tang).
Figure 4 in Immature stages, phenology, distribution and host plants of the Andean Moon Moth Cercophana frauenfeldii Felder, 1862 (Lepidoptera: Saturniidae)
Figure 4 Fourth instar Chaetotaxy of C. frauenfeldii.
Figures 28-29 from: Zacharczenko B, Wagner D, Hatfield M (2014) A new cryptic Sympistis from eastern North America revealed by novel larval phenotype and host plant association (Lepidoptera, Noctuidae, Oncocnemidinae). ZooKeys 379: 93-107. https://doi.org/10.3897/zookeys.379.5765
Figures 28-29 - Sympistis forbesi pupa 28 ventral 29 lateral.
Figure 10 from: Tartally A, Koschuh A, Varga Z (2014) The re-discovered Maculinea rebeli (Hirschke, 1904): Host ant usage, parasitoid and initial food plant around the type locality with taxonomical aspects (Lepidoptera, Lycaenidae). ZooKeys 406: 25-40. https://doi.org/10.3897/zookeys.406.7124
Figure 10 - Anton Koschuh on his way to Zeiritz (23.06.2012) (photo: AT).
Figure 3 from: Pujade-Villar J, Wang Y, Guo R, Chen X (2015) Revision on Palaearctic species of Periclistus Förster with description of a new species and its host plant gall (Hymenoptera, Cynipidae). ZooKeys 596: 65-75. https://doi.org/10.3897/zookeys.596.5945
Figure 3 - Distribution map of Periclistus species in the Palaearctic regions.
Fig. 1 in Mylabrini diversity and host plants in a Saharan oasis ecosystem with an updated checklist of Meloidae from Algeria (Coleoptera)
Fig. 1 – Location of Ouled Djellal Wilaya; sampling sites: 1, Oued El Assel, 2, Oued Djdai 3, Saad.
Fig. 5 in The Australian issid planthopper genus Orinda Kirkaldy, 1907: New subgenera, new species, host plant and identification key (Hemiptera: Fulgoromorpha: Issidae)
Fig. 5. Habitat of Orinda (Montorinda) eungellana sp. nov., Eungella National Park, 17 Mar. 2020.
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.