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22,710 results for “Plant”
Individual-based plant-pollinator networks are structured by phenotypic and microsite plant traits
<p>Dataset associated with the manuscript "Individual-based plant-pollinator networks are structured by phenotypic and microsite plant traits" (Arroyo-Correa et al. 2020), including plant-pollinator interactions, individual plant attributes and the plant polygon map created with drone flights. </p>
Figure 8 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 8. Phyllocnistis maxberryi sp. n., pupa. A Ventral view of head B ventral view of cocoon-cutter C frons D lateral view of head E lateral view of cocoon-cutter F dorsal of sixth abdominal tergum G spines on sixth abdominal tergum H lateral view of spines on seventh abdominal tergum I view of abdominal tip Į dorsal view of A9–10 K lateral seta on sixth abdominal tergum L ventral view of A9–10. Scale bars 100 µm.
Figure 6 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 6. Phyllocnistis tropaeolicola sp. n., genitalia. A Male, ventral view B right valva, mesal view C aedeagus D female, lateral view E ventral view of terminal segments. (Scale bar 0.5 mm except for figure B, 0.25 mm.)
Figure 2 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 2. Adults of three new Phyllocnistis species from Costa Rica. A Phyllocnistis drimiphaga sp. n., holotype female B P. maxberryi sp. n., holotype female (abdomen removed for dissection) C P. tropaeolicola sp. n., holotype male.
Figure 10 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 10. Life history of Phyllocnistis drimiphaga sp. n. A Leaf mines on abaxial side of leaf surface, white square enclosing early mine, arrow pointing to pupal cocoon fold B close-up view of early mine, arrow pointing to egg shell remains C same as figure B, but showing frass pattern (photo taken with sunlight projecting through the leaf from behind) D nearly mature old mine on adaxial side E nearly mature old mine on abaxial side (photo taken from adaxial side) F opened mine showing mature sapfeeding larva in situ G opened young pupal cocoon fold showing cocoon-spinning larva in situ H pupal cocoon fold on adaxial mine I opened pupal cocoon fold showing pupa in situ (dorsal view) Į protruded and attached pupal shell (arrow) on pupal cocoon fold of an abaxial leaf mine K opened pupal cocoon fold on adaxial mine showing Ageniaspis cocoons in situ.
Figure 1 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 1. Habitats and larval host plants of Phyllocnistis species. A Cerro de la Muerte, Villa Mills region, 3000 m and below, in Cordillera de Talamanca B Volcán Barva, ALAS transect, 2000 m, in Braulio Carillo National Park C habitat of P. drimiphaga in Cerro de la Muerte, km 70 Pan-American Hwy, road to El Paraíso del Quetzal, 2700 m, arrow pointing to host plant where mines were found D young stem shoots and leaves of Drimys granadensis of C, growing from base of the tree E flowers and leaves of D. granadensis F habitat of P. maxberryi in Cerro de la Muerte, km 95 Pan-American Hwy, trail front of La Georgina in Villa Mills, 3100 m, arrow pointing to host plant where mines were found G young growth of Gaiadendron punctatum in front, and mature trees with yellow fruits in behind, at ALAS transect in Vara Blanca, 2000 m H habitat of P. tropaeolicola in Cerro de la Muerte, on km 95 Pan-American Hwy, near La Gegina in Mills, 3100 m, arrow pointing to host plant where mines were found I Tropaeolum emarginatum, details of host plants that are shown in H.
Figure 12 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 12. Life history of Phyllocnistis tropaeolicola sp. n. A Leaf mines on a young leaf, arrows pointing at young to middle instar larvae B mature leaf mine with pupal cocoon fold (arrow), white square enclosing early stage mine region C mature sap-feeding larva in pre-cocoon chamber D detailed view of figure C E opened mine showing nearly mature sap-feeding larva in situ F opened young pupal cocoon fold showing cocoon-spinning instar in situ G pupal cocoon fold, arrow pointing to the slender exit H opened pupal cocoon fold showing pupa in situ, dorsolateral view.
Figure 11 in Systematics, host plants, and life histories of three new Phyllocnistis species from the central highlands of Costa Rica (Lepidoptera, Gracillariidae, Phyllocnistinae)
Figure 11. Life history of Phyllocnistis maxberryi sp. n. A Leaf mines on young growing Gaiadendron shoot B mature mine with pupal cocoon fold (arrow) C nearly mature mine and mature sap-feeding larva (left arrow), and oviposition location (right arrow) D close-up view of mature sap-feeding larva E opened mine showing mature sap-feeding larva in situ F opened young pupal cocoon fold showing cocoonspinning larva in situ G pupal cocoon fold, arrow pointing at thinner pupal exit H opened pupal cocoon fold showing pupa in situ, dorsal view I pupa in situ, lateral view.
Fig. 7. Begonia acetosella Craib. A. Plant habit. B – C. Leaf variation. D. Female bud. E. Female flower. F in A revision and one new species of Begonia L. (Begoniaceae, Cucurbitales) in Northeast India
Fig. 7. Begonia acetosella Craib. A. Plant habit. B – C. Leaf variation. D. Female bud. E. Female flower. F. Reverse of flower. G. Styles. Photographs by Rebecca Camfield of a plant in cultivation at the Royal Botanic Garden Edinburgh (accession 19980065).
Fungal responses to plant invasion are greater under soil warming than simulated nitrogen deposition data
<p>This file includes the data associated with analyzing scripts for the following github entry: <a href="https://gitlab.ethz.ch/manthony/swan-x-invasion">https://gitlab.ethz.ch/manthony/swan-x-invasion</a>. </p> <p>This project studied the combined effects of nitrogen deposition, soil warming, and Alliaria petiolata (garlic mustard) invasion on soil fungal communities, functional genes, and soil physical and chemical properties.</p>
Response of psychrophilic plant endosymbionts to experimental temperature increase
<p>Countless uncertainties remain regarding the effects of global warming on biodiversity, including the ability of organisms to adapt and how that will affect obligate symbiotic relationships. The present study aimed to determine the consequences of temperature increase on the adaptation of plant endosymbionts (endophytes) that grow better at low temperatures (psychrophilic). We isolated fungal endophytes from a high-elevation (paramo) endemic plant. Initial growth curves were constructed at different temperatures (4–25°C). Then, experiments were carried in which only the psychrophilic isolates were subjected to repeated increments in temperature. After the experiments, the final growth curves showed significantly slower growth than the initial curves, and some isolates even ceased to grow. While most studies suggest that the distribution of microorganisms will expand as temperatures increase because most of these organisms grow better at 25°C, the results from our experiments demonstrate that psychrophilic fungi were negatively affected by temperature increases. These outcomes raise questions concerning the potential adaptation of beneficial endosymbiotic fungi in the already threatened plant ecosystems. Assessing the consequences of global warming at all trophic levels is urgent because many species on Earth depend on their microbial symbionts for survival. Associations are mutually beneficial, results from our study have implications on the potential survival of these plants and high-elevation ecosystems.</p>
Dataset for "Intraspecies diversity reveals a subset of highly variable plant immune receptors and predicts their binding sites"
<p>Datasets for preprint (https://doi.org/10.1101/2020.07.10.190785) entitled:</p> <p>"Intraspecies diversity reveals a subset of highly variable plant immune receptors and predicts their binding sites"</p> <p>Contains:</p> <p>- All data files for scripts quoted in the preprint and deposited at https://github.com/krasileva-group/hvNLR</p> <p>- Clade Membership Tables</p> <p>- Clade Alignment Files</p> <p>- Clade Trees</p> <p>- Excel files for Figure S1, Figure S2, and Table 1</p>
Figs. 17-20 in Stink Bugs (Heteroptera, Pentatomidae) And An Unique Host Plant In The Brazilian Subtropics
Figs. 17-20. Loxa deducta: 17, adults on fruits of privet; 18, fifth instar on a privet leaf; 19, egg mass on a privet leaf. 20, fifth instar of Acrosternum impicticorne on privet fruits. (Scales: 2mm, fig. 17; 1mm, figs. 18-19; 0,5mm, fig. 20).
Figs. 1-7 in Stink Bugs (Heteroptera, Pentatomidae) And An Unique Host Plant In The Brazilian Subtropics
Figs. 1-7. Seasonal abundance of nymphs and adults of the most common pentatomids found on privet Ligustrum lucidum during a one-year period in northern Paraná state, Brazil.
Figure 5 in Geographic distribution, host plants, and morphological variation of the currently radiating phytophagous ladybird beetle Henosepilachna diekei
Figure 5. Elytra height of seven populations of Henosepilachna diekei. (A) Females; (B) males. The host plants were denoted in the parentheses as M, Mikania; L, Leucas; D, Dicliptera; P, Plectranthus. The different letter on the right shoulder of each box indicates significant difference (P <0.05) after adjustment of P-value for multiple comparisons (NS, P ≥ 0.05).
Figure 6 in Biodiversity of the scentless plant bugs (Hemiptera: Rhopalidae) in southern South America
Figure 6. Distribution of Jadera Stål species in Argentina. Pale colour: known distributions. The number of known species for each province is provided, with an asterisk indicating the number of newly recorded species.
Figure 1 in Biodiversity of the scentless plant bugs (Hemiptera: Rhopalidae) in southern South America
Figure 1. Distribution of Liorhyssus Stål species in Argentina. Pale colour: known distributions; dark colour: new distributions. The number of known species for each province is provided, with an asterisk indicating the number of newly recorded species.
Figure 7 in Biodiversity of the scentless plant bugs (Hemiptera: Rhopalidae) in southern South America
Figure 7. Known records for the species of Rhopalidae from Argentina over the years (cumulative relative frequencies 0–100%).
Figure 5 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic
Figure 5. Coxigenital region of Aceria rhodiolae females from (A) Russia, and (B,C,E) Nunavik, Canada. (A,B) Differential interference contrast light microscopy, (C,E) scanning electron micrograph, (D) line drawing. Scale on (B) also applies to (A). Notations on (D) indicate palp, leg and idiosomal setae, and coxal apodemes (ap1, ap2, ap; pra, prosternal apodeme). Other arrows elsewhere indicate characteristic ridges on coxal plates (a,b,c); genital flange (fl), and underlying postgenital plate (pp), which bears setae 3a and extends anterolaterally into lateral flaps (f) that flank the genital coverflap; and ventral ridges on femur, genu, and coxal fields (E).
Figure 8 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic
Figure 8. (A) Healthy infructescence of a Rhodiola rosea plant from Nunavik (Canada) versus (B) a mite-infested inflorescence (mostly pale green or yellowish) that partly (centrally) developed into fruits (yellow to red). (C) Dried inflorescences from Labrador (Canada) with a few (upper right) to most (lower left) flowers galled, and a galled leaf (isolated, in the middle). (D) Dried inflorescences from western Russia that were preserved in an herbarium for over 100 years. (E,F) Enlargement of a galled flower and galled leaf from Labrador (same scale). Arrows point at some of the galled flowers (B‒D) or leaves (C). The scale on (C) also applies to (D), and is approximate for (A,B).
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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.
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.