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583 results for “plant distributions”
Fig. 22 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 22. Male genitalia of Melitaea shahvarica sp. nov. (a = valva; b = aedeagus). Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, alt. 2200–2400 m.
Fig. 23 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 23. Eggs of Melitaea shahvarica sp. nov., Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, alt. 2200–2400 m. A–C. Lateral view. D–F. View from above. G–I. Micropile area.
Fig. 9 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 9. Adults of Melitaea timandra timandra Coutsis & van Oorschot, 2014. A–H. UPS. I–P. UNS. A–D. ♂, Turkmenistan, Sary-Yazy, alt. 300 m. E–H. ♀, Turkmenistan, Sary-Yazy, alt. 300 m. I–L. ♂, Turkmenistan, Sary-Yazy, alt. 300 m. M–P. ♀, Turkmenistan, Sary-Yazy, alt. 300 m.
Fig. 27 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 27. Biotope, host plant, and adult of Melitaea shahvarica sp. nov. in nature. A. Shahvar Mt., E Elburs Ridge. B. Biotope with Phlomoides molucelloides (Bunge) Salmaki. C. Host plant Ph. molucelloides. D. Female on Ph. molucelloides.
Fig. 21 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 21. Adults of Melitaea shahvarica sp. nov. A–H. UPS. I–P. UNS. A, I. Holotype, ♂ (SDM). B–H, J–P. Paratypes (EDMSU). A–C. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., alt. 2200–2400 m. D. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., Tohar v. vicinity, alt. 2200 m. E–H. ♀. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., alt. 2200– 2400 m. I–K. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., 2200–2400 m. L. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, Tohar v. vicinity, alt. 2200 m. M–P. ♀. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., alt. 2200–2400 m.
Fig. 25. I–IV in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 25. I–IV instar caterpillars of Melitaea shahvarica sp. nov. (a = view from above; b = lateral view). A. First instar caterpillar after hatching. B. First instar caterpillar before molting. C. Second instar caterpillar. D. Third instar caterpillar. E. Fourth instar caterpillar.
Fig. 26. V–VI in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 26. V–VI instar caterpillars of Melitaea shahvarica sp. nov. (a = view from above; b = lateral view). A. Fifth instar caterpillar. B. Sixth instar caterpillar. C. Sixth instar caterpillar, head capsule, front view. D. Sixth instar caterpillar, head capsule, lateral view.
Fig. 20 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 20. Eggs of Melitaea timandra binaludica subsp. nov., Iran, Kuh-e-Binalud Mts. A–C. Lateral view. D–F. View from above. G–I. Micropile area.
Fig. 19. Male genitalia and harpe. A–C in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 19. Male genitalia and harpe. A–C. Melitaea timandra timandra Coutsis & van Oorschot, 2014. D–I. M. timandra binaludica subsp. nov. A–C. Turkmenistan, Sary-Yazy, alt. 300 m. D–F. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m. G. Afghanistan, Bamian Prov., Band-e-Amir, alt. 3200 m. H. Afghanistan, Bamian Prov., Band-e-Amir, Dzhudoi-Kvak Gorge, alt. 3200 m. I. Afghanistan, Band-e-Amir, Hazarajat.
Data for: "Dynamic species distribution modeling reveals the pivotal role of human-mediated long-distance dispersal in plant invasion"
<p>All the data needed to reproduce the results and Figures of our article:</p> <p>Botella, C., Bonnet, P., Hui, C., Joly, A., & Richardson, D. M. (2022). Dynamic Species Distribution Modeling Reveals the Pivotal Role of Human-Mediated Long-Distance Dispersal in Plant Invasion. <em>Biology</em>, <em>11</em>(9), 1293. <a href="https://doi.org/10.3390/biology11091293">https://doi.org/10.3390/biology11091293</a></p> <p>Please, find the R scripts and guidelines to reproduce our results on the article's Github repository :</p> <p><a href="https://github.com/ChrisBotella/plectranthus_barbatus/tree/main">https://github.com/ChrisBotella/plectranthus_barbatus/tree/main</a></p>
Map of China Pumped Storage Hydropower Plant Geospatal Distribution
<p>A map of PSH geospatial distribution in China, updated as of April 2024.</p> <p>All information are collected by using open-source on Internet. If you want to cite this map, please retain the copyright of Jingcai Cai.</p> <p>This map will also be upload in ArcGIS online soon, also the dataset will be released soon.</p> <p>If you want to contact author, could sent e-mal to me to get the dataset and have deeper communication with him.</p>
Рис. 7. 3D–диаграммы пространственного распределениЯ обилиЯ моллюска B. cylindrica (А), фитомассы (В), проективного покрытиЯ (С), твердости грунта на глубине 5–10 см (D) на участке № 1 в 2010 г. (единицы иЗмерениЯ осей Х и Y даны в метрах). Fig. 7. 3D–diagrams of the abundance spatial distribution of the snail B. cylindrica (A), phytomass (B), plants projective cover (C), 0–10 cm layer soil penetration resistance (D) at the site 1 in 2010. (axes X and Y presented in meters). in Analysis of the spatial distribution patterns of the land snail populations: a geostatistic method approach
Рис. 7. 3D–диаграммы пространственного распределениЯ обилиЯ моллюска B. cylindrica (А), фитомассы (В), проективного покрытиЯ (С), твердости грунта на глубине 5–10 см (D) на участке № 1 в 2010 г. (единицы иЗмерениЯ осей Х и Y даны в метрах). Fig. 7. 3D–diagrams of the abundance spatial distribution of the snail B. cylindrica (A), phytomass (B), plants projective cover (C), 0–10 cm layer soil penetration resistance (D) at the site 1 in 2010. (axes X and Y presented in meters).
Figure 6 in Depth distribution of plant-parasitic nematodes on bentgrass golf greens in Missouri and Indiana
Figure 6: PCR results using Meloidogyne-specific and M. naasi and M. marylandi-specific primers. DL: DNA Ladder; 1: Meloidogyne spp. (DNA ID:9); 2: M. naasi (DNA ID:9); 3: Meloidogyne spp. (DNA ID:4); 4: M. marylandi (DNA ID:4); and 5: Meloidogyne spp.(DNA ID:4).
Figure 3 in Depth distribution of plant-parasitic nematodes on bentgrass golf greens in Missouri and Indiana
Figure 3: PCR results using Hoplolaimus-specific and H. stephanus, H. columbus and H. galeatus-specific primers. DL: DNA Ladder; 1: Hoplolaimus spp. (DNA ID:10); 2: H. stephanus (DNA ID:10); 3: H. columbus (DNA ID:10); 4 H. galeatus (DNA ID:10); 5: Hoplolaimus spp. (DNA ID:3); 6: H. stephanus (DNA ID:3); 7: H. columbus (DNA ID:3); 8 H. galeatus (DNA ID:3); 9: Hoplolaimus spp. (DNA ID:4); 10: H. stephanus (DNA ID:4); 11: H. columbus (DNA ID:4); and 12 H. galeatus (DNA ID:4).
Figure 2 in Depth distribution of plant-parasitic nematodes on bentgrass golf greens in Missouri and Indiana
Figure 2: Phylogeny of the rDNA ITS region of Hoplolaimus spp. isolated from golf putting greens. Phylogenetic trees were constructed with the neighbor-joining algorithm using the Kimura two-parameter model with Litylenchus spp. (LC383724) as the outgroup. Bootstrap values are based on 1000 resamplings of the data set. DNAID codes correlate to Table 2.
Figure 1 in Depth distribution of plant-parasitic nematodes on bentgrass golf greens in Missouri and Indiana
Figure 1: Distribution of plant-parasitic nematode species sampled from creeping bentgrass putting greens in Missouri and eastern Kansas in 2021 and Indiana in 2022 in two independent pie charts. Samples were collected during the months of April, June, August and October of 2021 and 2022, respectively. "n" indicates total PPNs represented within each chart.
Figure 4 in Depth distribution of plant-parasitic nematodes on bentgrass golf greens in Missouri and Indiana
Figure 4: Scanning-electron micrographs of a lance nematode specimen collected form Site 5. A) four lip annules; B) the presence of an epiptygma; C) 25 longitudinal striae on the basal lip annule; and D) four lateral incisures.
Figure 5 in Depth distribution of plant-parasitic nematodes on bentgrass golf greens in Missouri and Indiana
Figure 5: Phylogeny of molecularly characterized Meloidogyne spp. isolated from golf coursed based on D2/D3 28S genes. phylogenetic trees were constructed with the neighborjoining algorithm using the Kimura two-parameter model with Litylenchus spp. (LC383724) as the outgroup. Bootstrap values are based on 1000 resamplings of the data set and displayed near branch nodes. DNAID codes correlate to Table 2.
Figure 4 in Within-plant distribution and rapid assessment of sugarcane rust mite population on sugarcane canopy
Figure 4 Relationship between sugarcane rust mite density and counting speed of the imprinting technique.
Figure 3 in Within-plant distribution and rapid assessment of sugarcane rust mite population on sugarcane canopy
Figure 3 Within-plant distribution of sugarcane rust mite population based on the imprinting tech- nique (mean ± SEM). The numbers within brackets are the proportions of mite populations within plants. Means across leaves with the same capital letters are not significantly different and means with the same lower letters on a given leaf position are not significantly different (Tukey,P <0.05).
ScienceDex guides
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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.