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7,883 results for “Tropic”
Accompanying data for "The Response of Tropical Rainfall to Idealized Small-Scale Thermal and Mechanical Forcing", by Martin Velez-Pardo and Timothy W. Cronin
<p>Data accompanying the manuscript "The Response of Tropical Rainfall to Idealized Small-Scale Thermal and Mechanical Forcing", by Martin Velez-Pardo and Timothy W. Cronin.</p>
FIGURE 17 in Systematics of the Octopleura Clade of Miconia (Melastomataceae: Miconieae) in Tropical America
FIGURE 17. Distributions of Miconia renatoi, M. sessilis, M. spiciformis, and M. variabilis.
FIGURE 10 in Systematics of the Octopleura Clade of Miconia (Melastomataceae: Miconieae) in Tropical America
FIGURE 10. Elevation ranges of the Octopleura clade species across their range.
Decadal survival of tropical pioneer seeds in the soil seedbank is accompanied by fungal infection and dormancy release
<p>Pioneer trees require high-light environments for successful seedling establishment. Consequently, seeds of these species often persist in the soil seed bank (SSB) for periods ranging from several weeks to decades. How they survive despite extensive pressure from seed predators and soilborne pathogens remains an intriguing question.</p> <p>This study aims to test the hypotheses that decades-old seeds collected from the SSB in a lowland tropical forest remain viable by i) escaping infection by fungi, which are major drivers of seed mortality in tropical soils, and/or ii) maintaining high levels of seed dormancy and seed coat integrity when compared to inviable seeds.</p> <p>We collected seeds of <em>Trema micrantha</em> and <em>Zanthoxylum ekmanii </em>at Barro Colorado Island, Panama, from sites where adult trees previously occurred in the past 30 years. We used carbon dating to measure seed age and characterized seed coat integrity, seed dormancy, and fungal communities.</p> <p>Viable seeds from the SSB ranged in age from 9 to 30 years for <em>T. micrantha</em>, and 5 to 33 years for <em>Z. ekmanii.</em> We found no evidence that decades-old seeds maintain high levels of seed dormancy or seed coat integrity. Fungi were rarely detected in fresh seeds (no soil contact), but phylogenetically diverse fungi were detected often in seeds from the SSB. Although fungal infections were more commonly detected in inviable seeds than in viable seeds, a lack of differences in fungal diversity and community composition between viable and inviable seeds suggested that viable seeds are not simply excluding fungal species to survive long periods in the SSB.</p> <p><em>Synthesis: </em>Our findings reveal the importance of a previously understudied aspect of seed survival, where the impact of seed-microbial interactions may be critical to understand long-term persistence in the SSB.</p>
Fig. 8 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 8. Head shields and colour pattern of the head
Fig. 21 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 21. Holotype of Demansia torquata (BMNH 1946.1.17.41).
Fig. 10 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 10. Distribution of Demansia olivacea
Fig. 11 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 11. Holotype of Demansia quaesitor (NTM R16836).
Fig. 6 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 6. Head shields and colour pattern of the head and
Fig. 16 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 16. Holotype of Demansia rufescens (WAM R52747).
Fig. 4 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 4. Holotype of Demansia calodera (WAM R54992).
Fig. 9 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 9. Holotype of Elapocephalus ornaticeps (AM R31918).
Fig. 18 in Revision of the Small Tropical Whipsnakes Previously Referred to Demansia olivacea (Gray, 1842) and Demansia torquata (Günther, 1862) (Squamata: Elapidae)
Fig. 18. Holotype of Demansia shinei (NTM R6489).
Fig. 2 in Natural-Licks Use By Orangutans And Conservation Of Their Habitats In Bornean Tropical Production Forest
Fig. 2. Two pairs of females with infants drink the seepage water at a natural-lick.
Fig. 6 in Natural-Licks Use By Orangutans And Conservation Of Their Habitats In Bornean Tropical Production Forest
Fig. 6. Visitation time of each orangutan class to the naturallicks.
Fig. 4 in Natural-Licks Use By Orangutans And Conservation Of Their Habitats In Bornean Tropical Production Forest
Fig. 4. Visiting proportion of each orangutan class: flanged male, female with infant, and others.
Fig. 3 in Natural-Licks Use By Orangutans And Conservation Of Their Habitats In Bornean Tropical Production Forest
Fig. 3. Proportion of visitation frequency of top 3 species among the natural-licks.
Fig. 5 in Natural-Licks Use By Orangutans And Conservation Of Their Habitats In Bornean Tropical Production Forest
Fig. 5. Duration of the visit of each orangutan class to the naturallicks.
Data and code for Spaulding-Astudillo and Mitchell (2023c), "Clear-sky convergence and the origin of tropical congestus clouds"
<p>Data and code for Spaulding-Astudillo and Mitchell (2023c), "Clear-sky convergence and the origin of tropical congestus clouds".</p><p>The Python code used to create Figures 1, 3-6 and supplementary Figure 1 are included in separate directories. Within each directory, we include experimental data generated by the Reference Forward Model (RFM; Dudhia 2017) that is needed to reproduce the figures. To create the figures, run the provided code in a Jupyter notebook or from the command line. Helper functions for data processing within the figure scripts have the nomenclature ..._data.py. Note that the provided code only allows you to visualize RFM data, not produce it yourself. To do so, you must download and run RFM yourself (https://eodg.atm.ox.ac.uk/RFM/). In addition, Figure 1 requires spatio-temporally averaged data from MERRA-2, ERA5, and CloudSat/CALIPSO (Betrand et al. 2023), which we provide in pickle files. See the main text for data citations, which will allow you to access the original, non-averaged climate data. </p><p>RFM data directories have the nomenclature /ctrl-..... For example, ctrl-RHmid-75-zmid-7-uniform-1 where:<br>RHmid=75% is the relative humidity at a mid-tropospheric height zmid=7.5 km. Uniform=True indicates that the tropospheric relative humidity is constant with height. When uniform=False, the relative humidity follows a C-shaped distribution between the surface and the tropopause. The helper functions in ..._data.py allow you to read the RFM output from .asc files. The nomenclature of the RFM output files is standardized: https://eodg.atm.ox.ac.uk/RFM/. </p><p> </p><p> </p><p> </p><p> </p><p> </p><p> </p><p> </p>
CO and CO2 mixing ratios and flux measurements from the Amazon tropical rainforest
<p>CO and CO2 mixing ratio and flux measurements from the Amazon tropical rainforest</p><p>This dataset belongs to the manuscript 'The emission of CO from tropical rain forest soils', submitted to the journal Biogeosciences in December 2023.</p><p>More details on this dataset can be found in this manuscript:</p><p>https://egusphere.copernicus.org/preprints/2023/egusphere-2023-2746/egusphere-2023-2746.pdf</p><p> For questions, please reach out to Hella van Asperen: hasperen@bgc.mpg-jena.de</p><p>########################################</p><p>Plateau tower CO and CO2 mixing ratio measurements</p><p>Plateau tower CO and CO2 mixing ratio measurements took place in a dry season campaign (28 Sep- 7 Oct 2020) and a wet season campaign (11-18 May 2021) at the K34 tower at field site ZF2 in the Amazon rain forest (-2.60898, -60.209106). Due to a problem in the beginning of the dry season campaign, the measurements at the tower were continued until outside the campaign period, until 18 October 2020. Measurements were performed by a Spectronus FTIR analyzer. Concentrations were measured at 3 heights (5,15 and 36m) every half hour. Canopy height is ~28m.</p><p>########################################</p><p>Valley CO and CO2 mixing ratio measurements</p><p>Valley CO and CO2 mixing ratio measurements took place in a dry season campaign (28 Sep- 7 Oct 2020) and a wet season campaign (11-18 May 2021) at a valley close to the K34 tower at field site ZF2 (-2.600026, -60.217079). Since no electricity was available, automatic battery-driven bag sampling was performed during the night at 3h time intervals, with 4 measurements per night from a 1m height inlet (~18:00, ~21:00, ~0:00, ~3:00). Bag samples were measured the following morning by a Spectronus FTIR-analyzer. </p><p>########################################</p><p>Plateau and valley chamber CO and CO2 fluxes</p><p>Flux chamber measurements were performed over soil and litter together on the plateau and in the valley at field site ZF2, in a dry season campaign (28 Sep- 7 Oct 2020) and a wet season campaign (11-18 May 2021). Five soil collars were installed in the valley, and five on the plateau. Each collar was measured 3 times during each campaign week (on different days). Measurements from the same collar are indicated as (for example) V1A, V1B, V1C. After each flux chamber measurement, soil moisture and soil temperature was measured.</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.