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505 results for “apples”
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Dataset underpinning the paper "Terahertz plasmon resonances in two-dimensional electron systems: Modeling approaches" by S. Siaber et al 2019 Phys. Rev. Appl.
<p>Dataset underpinning the paper "Terahertz plasmon resonances in two-dimensional electron systems: Modeling approaches" by S. Siaber et al 2019 Phys. Rev. Appl.</p>
FIGURE 6 in New species and record of Zygophiala (Capnodiales, Mycosphaerellaceae) on apple from Montenegro
FIGURE 6. Conidiophores, conidiogenous cells and conidia of Zygophiala cylindrica ZMHS23. Scale bar = 10 μm.
FIGURE 4 in New species and record of Zygophiala (Capnodiales, Mycosphaerellaceae) on apple from Montenegro
FIGURE 4. Conidiophores, conidiogenous cells and conidia of Zygophiala montenegroensis ZMHS29. Scale bar = 10 μm.
FIGURE 3. Zygophiala montenegroensis ZMHS29. a. 1 in New species and record of Zygophiala (Capnodiales, Mycosphaerellaceae) on apple from Montenegro
FIGURE 3. Zygophiala montenegroensis ZMHS29. a. 1-month-old colony on PDA. b. Flyspeck signs on apple peel. c, e, g. Conidiophores, conidiogenous cells and conidia. f. Conidiophore. d, h–k. Conidia. Scale bars = 5 μm.
FIGURE 2 in New species and record of Zygophiala (Capnodiales, Mycosphaerellaceae) on apple from Montenegro
FIGURE 2. One of equally most parsimonious trees determined from ITS -ACT-TEF matrix sequences. The tree is rooted to Z. tardicrescens. Isolates taken from flyspeck signs on apple fruit. (Tree length = 352, CI = 0.8324, RI = 0.9149, RC = 0.7615, HI = 0.1676). Bootstrap values>50% shown above the tree branches.
FIGURE 5. Zygophiala cylindrica ZMHS23. a. 1 in New species and record of Zygophiala (Capnodiales, Mycosphaerellaceae) on apple from Montenegro
FIGURE 5. Zygophiala cylindrica ZMHS23. a. 1-month-old colony on PDA. b. Flyspeck signs on apple peel. c, f–k. Conidia. d, e. Conidiophores, conidiogenous cells and conidia. Scale bars = 5 μm.
FIGURE 1 in New species and record of Zygophiala (Capnodiales, Mycosphaerellaceae) on apple from Montenegro
FIGURE 1. One of 100 equally most parsimonious trees determined from ITS sequences. The tree is rooted to Teratosphaeria (JX556227). Isolates were taken from flyspeck signs on apple fruit. (Tree length = 114, CI = 0.8860, RI = 0.9078, RC = 0.8043, HI = 0.1140). Bootstrap
FIGURE 5 in First Report Of Anisandrus Maiche (Coleoptera: Curculionidae: Scolytinae) Infesting Apple Trees
FIGURE 5. Weekly capture in 2023 of Anisandrus maiche and Xylosandrus germanus in ethanol-baited traps along the woody edge of apple orchards.
FIGURE 1 in First Report Of Anisandrus Maiche (Coleoptera: Curculionidae: Scolytinae) Infesting Apple Trees
FIGURE 1. Adult beetle found in gallery, identified to Anisandrus maiche using morphological characteristics (Rabaglia et al., 2009). including A) median tuft of long setae at posterior margin of pronotum; B) impressed 2nd declivital interstriae and striae, and the raised 3rd declivital interstriae with numerous distinct granules; C) Procoxae contiguous; and D) Elytral declivity without a dorsal semi-circular carina.
FIGURE 2. A in First Report Of Anisandrus Maiche (Coleoptera: Curculionidae: Scolytinae) Infesting Apple Trees
FIGURE 2. A. Slides made from sections of gallery wall, with possible Ambrosiella ascospores (arrows) and clesitothecia debris (circles). B. Ambrosiella ascospores. Scale bars: 100µm.
FIGURE 1. A–B in Aptenia ×vascosilvae (A. cordifolia × A. haeckeliana) (Aizoaceae), the new nothospecies from which the horticulturally popular cultivar Aptenia 'Red Apple' was derived
FIGURE 1. A–B. Habit of Aptenia ×vascosilvae (B: a population of A. ×vascosilvae naturalised on Tabarca Island, Alicante province, Spain). C. A. cordifolia. D. A. haeckeliana. E. Flowers of A. cordifolia (purple flower) and A. haeckeliana (yellowish flower). F. Leaves of A. cordifolia (basally cordate) and A. haeckeliana (basally cuneate) (photos by E. Laguna).
Unveiling the Natural Dynamics of Parthenocarpy and Self-Compatibility in Apple Trees
<p><strong><span>Supplementary Materials:</span></strong></p> <p><span>Table S1. Three years parthenocarpy and self-compatible accession survey result.</span></p> <p><span>Table S2. Accessions used in GWAS for parthenocarpic and self-compatible traits. </span></p> <p><span>Table S3. Fruit set rate of parthenocarpy and self-compatible accessions. Light blue colour in the column of Number of fruits per cluster flower indicated fruit setting rates were comparable between bagged flowers and open-pollinated (OP) flowers. </span></p> <p><span>Table S4. Functional annotations of the associated SNPs located within the candidate genes for parthenocarpy trait. The significant SNPs (-Log10 (P) ≥3) associated <em>Malus</em> genes were identified within 20kb either side of the SNP on GDT2T genome database.</span></p> <p><span>Table S5. Functional annotations of the associated SNPs located within the candidate genes for self-compatible trait. The significant SNPs (-Log10 (P) ≥3) associated <em>Malus</em> genes were identified within 20kb either side of the SNP on GDT2T genome database.</span></p>
FIGURE 2. PCA diagrams for the first two factors, F1 and F2 in Common but new: Bartramia rosamrosiae, a "new" widespread species of apple mosses (Bartramiales, Bryophytina) from the Mediterranean and western North America
FIGURE 2. PCA diagrams for the first two factors, F1 and F2, with the variance explained by each. Italicized numbers correspond to the characters in Table 1. A: Bartramia (Anacolia) laevisphaera; M: Bartramia rosamrosiae sp. nov.; S: Bartramia stricta.
FIGURE 5 in Common but new: Bartramia rosamrosiae, a "new" widespread species of apple mosses (Bartramiales, Bryophytina) from the Mediterranean and western North America
FIGURE 5. Comparison of: A. Bartramia laevisphaera, B. B. stricta, C. B. rosamrosiae sp. nov.. First row: Cortex cells (scale bar 20 µm). Second row: Central strand illustrating the proportional differences (scale bar 100 µm). Third row: Leaf shape (scale bar A3 = 2 mm; B3–C3 = 1 mm) & distal margin (scale bar 50 µm). Last row): Cross section at leaf base (scale bar A4/B4 = 100 µm; C4 = 50 µm).
FIGURE 1 in Common but new: Bartramia rosamrosiae, a "new" widespread species of apple mosses (Bartramiales, Bryophytina) from the Mediterranean and western North America
FIGURE 1. Maximum likelihood tree based on the combined trnS-F and ITS matrix. Likelihood bootstrap percentages are depicted above (bold) the branch followed by posterior probabilities. Support values from the analyses including indel coding are depicted below the branches: with MPBSsic formatted in italics and PPsic underlined.
FIGURE 6 in Common but new: Bartramia rosamrosiae, a "new" widespread species of apple mosses (Bartramiales, Bryophytina) from the Mediterranean and western North America
FIGURE 6. Distribution of the species of Bartramia sect. Strictidium: Cross = B. breutelii; Triangles = B. rosamrosiae sp. nov.; Stars = B. (Anacolia) laevisphaera; Squares = B. stricta.
FIGURE 4 in Common but new: Bartramia rosamrosiae, a "new" widespread species of apple mosses (Bartramiales, Bryophytina) from the Mediterranean and western North America
FIGURE 4. Comparison of: A. Bartramia laevisphaera. B. B. stricta. C. B. rosamrosiae sp. nov. First row: Sporophyte dry (scale bar 2 mm). Second row: Plant dry (scale bar 2 mm). Third row: Plant wet (scale bar 2 mm).
FIGURE 3 in Common but new: Bartramia rosamrosiae, a "new" widespread species of apple mosses (Bartramiales, Bryophytina) from the Mediterranean and western North America
FIGURE 3. Canonical analysis based on the two discriminant functions F1 and F2 of the discriminant analysis. Gray dots are the centroids of each group.
Proximity to natural habitat and flower plantings increases insect populations and pollination services in South African apple orchards
<p><span><span><span><span><span><span><span><span><span><span><span>Introducing areas of wildflower vegetation within crop fields has been shown to enhance pollinator activity and pollination services to crops, and findings in Europe showed an interaction effect between floral treatments and landscape context. Natural fynbos patches in the South African Cape Floristic Region (CFR) are potential reservoirs for beneficial insects that could enhance pollinator populations and crop pollination in commercial apple orchards. However, the effect of proximity to natural habitat and floral enhancement treatments on crop pollinators and yield are yet to be fully tested in southern temperate regions.</span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span>To elucidate the impact of enhanced floral resources to apple flower visitors and crop yield, we established small experimental patches of flowers in non-productive areas of commercial apple (<i>Malus domestica</i>) orchards in the CFR. Experimental orchards were embedded in landscapes with varying proportions of natural habitat within 1 km. We used pollinator exclusion experiments to determine the benefits of insect pollination on apple yield, quality and economic value. </span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span>We found that the primary pollinators of apple flowers in the region is the endemic Cape honey bee<i>, Apis mellifera capensis</i>. Floral plantings enhanced overall pollinator abundance and honey bee flower visitation within the orchards, and positively affected apple size and economic value. Increased landscape complexity had a significantly positive effect on wild bees but not on honey bees. </span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span><i>Synthesis and applications</i>. We demonstrate that presence of floral plantings within orchards enhances pollinator activity within apple orchards and apple quality. This sustainable management practice may represent a profitable choice for growers, which could increase pollination services while reducing reliance on renting hives. These practices can indirectly contribute to increased landscape-scale resilience and connectivity, while also benefiting pollinators within the remaining natural habitat.</span></span></span></span></span></span></span></span></span></span></span></p>
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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.