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Fig. 1 A in Comparative analysis of metacyclogenesis and infection curves in different discrete typing units of Trypanosoma cruzi
Fig. 1 A Microphotographs of 10-day incubation cultures of Trypanosoma cruzi epimastigotes in LIT medium with Field's staining and magnification (100 ×), metacyclic forms are indicated by red arrows. B Epimastigote production, evaluated for 12 days in a LIT medium. C Metacyclogenetic curve representing the dynamic process of metacyclic trypomastigote formation in T. cruzi. In x is the time (days) while the y-axis indicates the number of metacyclic trypomastigotes (MT) per milliliter. The data points provide information on the efficacy and kinetics of metacyclic trypomastigote production. D Dynamics of metacyclogenesis in T. cruzi, capturing both the starting point and the peak of the process. The data presented provide a better understanding of the timing and efficiency of metacyclic trypomastigote production. E This comparative approach uses brackets to indicate statistically significant differences (p <0.05) between DTUs in both the onset and peak phases of metacyclogenesis. In this graph, it can be seen whether there are DTUs with noticeable variations during the kinetics of metacyclogenesis
Fig. 2 in Comparative analysis of metacyclogenesis and infection curves in different discrete typing units of Trypanosoma cruzi
Fig. 2 Mosaic of microphotographs showing T. cruzi CDT infections in Vero cells for 120 h, using different DTUs. Samples were fixed with formaldehyde and stained with Field's stain. This representation captures the different stages and dynamics of infection in the different DTUs, and the cell morphological changes induced. White arrows indicate the presence of amastigotes at 24 h. By 72 h, amastigote nests become visible, and at 96–120 h, nests along with cell-derived trypomastigotes are observed
Data and code for "Air pollution impacts from warehousing in the United States uncovered with satellite data"
<div> <div> <p>This repository (ver 2024.06.11) contains data and code supporting the analyses and visualizations in the manuscript "Air pollution impacts from warehousing in the United States uncovered with satellite data" in the journal <em>Nature </em><em>Communications</em> (DOI forthcoming). A description of the data files and code can be found in the README. </p> </div> </div>
Fig. 5 Mollusc fossils from unit 3 a in A study on benthic molluscs and stable isotopes from Kutch, western India reveals early Eocene hyperthermals and pronounced transgression during ETM2 and H2 events
Fig. 5 Mollusc fossils from unit 3 a Broken shell of Pteria sp. b Partially preserved Anomia sp. c–e Nuculana sp. c within green shale, d external view of left valve, e internal view of left valve. f Articulated specimen of Caestocorbula sp. g Aphrodina sp. (white arrow) and Claibornicardia sp. (yellow arrow) in shell limestone h–j Claibornicardia sp. h internal view of left valve, i external view of left valve, j internal view of right valve. k, l Turritella sp. Scale bars 10 mm
Figure 2 in First report of Meloidogyne javanica on Ginger and Turmeric in the United States
Figure 2: Healthy ginger (left) and ginger infected with Meloidogyne javanica (right) showing stunted growth of the rhizomes, collected from nematode-infested soils on an organic farm in Wheeler County, Georgia.
Figure 1 in First report of Meloidogyne javanica on Ginger and Turmeric in the United States
Figure 1: Ginger (Zingiber officinale) (A) and turmeric (Curcuma longa) infected with Meloidogyne javanica from an organic farm in Wheeler County, Georgia showing severely galled roots. Numerous egg masses of the nematode are evident protruding from galled roots of both ginger (C) and turmeric (D).
Fig. 2. A in Carcharocles-bitten sperm whale tooth from the Neogene of the Coastal Eastern United States
Fig. 2. A possible origin of the Otodus tooth bite traces on the root of the Neogene sperm whale tooth CMM-V-8955. An Otodus sp. (foreground) is biting the rostrum of a sperm whale (background). That the bite traces occur on the tooth of the sperm whale hints at a live antagonistic interaction between these two macropredators.
Fig. 1 in Carcharocles-bitten sperm whale tooth from the Neogene of the Coastal Eastern United States
Fig. 1. Otodus-bitten sperm whale tooth (CMM-V-8955) from the Neogene of the Aurora Phosphate Mine, North Carolina, USA; in lingual (A1) and anteromedial (A2) views, showing all three bite traces, as indicated by the numbers 1–3; A3, enlarged view of the two primary bite traces, one of which shows the serration marks left as the shark tooth cut into the sperm whale tooth. The specimen was whitened with sublimed ammonium chloride to enhance contrast.
Figures 1–8 in Taxonomic notes on velvet ants of the genus Timulla Ashmead, 1899 (Hymenoptera: Mutillidae) in the United States of America and Canada
Figures 1–8. Lateral habitus of Timulla males. 1) Timulla barbata (Fox, 1899). 2) Timulla ornatipennis (Bradley, 1916). 3) Timulla dubitata dubitata (Smith, 1855). 4) Timulla dubitata fugitiva Mickel, 1937. 5) Timulla euterpe (Blake, 1879). 6) Timulla euterpe (Blake, 1879). 7) Timulla vagans rufinota Mickel, 1937. 8) Timulla vagans vagans (Fabricius, 1798). Scale line = 2.0 mm.
Figures 3–6. Adult male genitalia. 3 in A new species of Paranthrene Hübner (Lepidoptera: Sesiidae) from the northern midwest United States
Figures 3–6. Adult male genitalia. 3) Paranthrene sogaardi. new species 4) Paranthrene tabaniformis. 5) Paranthrene sogaardi new species aedeagus. 6) Paranthrene tabaniformis aedeagus.
Figures 7–10. Paranthrene sogaardi new species. 7 in A new species of Paranthrene Hübner (Lepidoptera: Sesiidae) from the northern midwest United States
Figures 7–10. Paranthrene sogaardi new species. 7) Dorsal view. 8) Lateral view. 9) Frons. 10) Michigan collection site of Paranthrene tabaniformis.
Figure 2 in Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 2: Grass species
Figure 2. Cumulative percent shatter over four time periods (maturity, maturity + 2 wk, maturity + 3 wk, maturity + 4 wk) for each species. The darker the bar, the greater percent of sampled site-years that corresponded to the percent shatter value. This normalizes across species with different sampling efforts. Species sampled in just a single site-year are indicated by a single black square, which represents 100% of the sampling effort. Species are denoted by their EPPO codes
Figure 3 in Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 2: Grass species
Figure 3. Cumulative percent seed shatter for all species from planting date to soybean physiological maturity (black vertical line) across the participating states in 2016 and 2017.
Figure 1. Heat map indicating the cumulative percent seed shatter across the participating states for a in Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 2: Grass species
Figure 1. Heat map indicating the cumulative percent seed shatter across the participating states for a window starting from soybean physiological maturity to 4 wk past physiological maturity in 2016 and 2017. States were included in these maps only if they conducted sampling during the week indicated. (e.g., In 2017, Arkansas sampled on October 2, October 18, and November 3, none of which are within ±3 d of the October 10 maturity date or maturity +2 wk on October 24 in the state that year. Hence only data from maturity +3 wk are for Arkansas for 2017.)
Figure 8 in Seedbank Persistence of Palmer Amaranth (Amoronthus polmeri) and Waterhemp (Amoronthus tuberculotus) across Diverse Geographical Regions in the United States
Figure 8. Effects of experimental site by burial depth by year on percentage seed viability for Amoronthus polmeri and Amoronthus tuberculotus. Vertical bars represent ± standard error of the mean.
Figure 4 in Seedbank Persistence of Palmer Amaranth (Amoronthus polmeri) and Waterhemp (Amoronthus tuberculotus) across Diverse Geographical Regions in the United States
Figure 4. Monthly soil temperature (averaged over a 15-min concurrent recording period on a daily basis for the entire experimental period) at the top and at 15 cm below the soil surface (left y-axis) and monthly soil volumetric water content at 15 cm below soil surface (right y-axis) for each of the seven sites where the seed material of Amoronthus polmeri and Amoronthus tuberculotus was exposed to burial conditions during 2014–2016. Data presented for Missouri include only two experimental years (2015 and 2016).
Figure 1 in Seedbank Persistence of Palmer Amaranth (Amoronthus polmeri) and Waterhemp (Amoronthus tuberculotus) across Diverse Geographical Regions in the United States
Figure 1. Experimental sites across Midsouth United States, where Amoronthus polmeri and Amoronthus tuberculotus seed material was exposed to burial trials for a period of 1 to 3 yr before viability test evaluation. Numbers in parentheses represent the latitude and longitude of the experimental sites.
Figure 6 in Seedbank Persistence of Palmer Amaranth (Amoronthus polmeri) and Waterhemp (Amoronthus tuberculotus) across Diverse Geographical Regions in the United States
Figure 6. Interaction of experimental site by burial depth on percentage seed damage and loss averaged across 2014–2016 for Amoronthus polmeri and Amoronthus tuberculotus. Damaged seeds include broken, shrunk, or malformed seeds and those lost due to deterioration or futile germination, which were impossible to count. Vertical bars represent ± standard error of the mean. Supplemental information is also provided in Supplementary Tables S1 and S2, where the actual values averaged across three replications per treatment and five locations of seed material origins are shown.
Figure 3 in Seedbank Persistence of Palmer Amaranth (Amoronthus polmeri) and Waterhemp (Amoronthus tuberculotus) across Diverse Geographical Regions in the United States
Figure 3. Amoronthus polmeri seeds as they appeared under a dissection microscope (A) before the seed retrieval and cleaning processes and (B) after the cleaning process. The same criteria were used for A. tuberculotus seeds.
Figure 7 in Seedbank Persistence of Palmer Amaranth (Amoronthus polmeri) and Waterhemp (Amoronthus tuberculotus) across Diverse Geographical Regions in the United States
Figure 7. Percentage seed viability as affected by burial depth and retrieval time (in months) for Amoronthus polmeri and Amoronthus tuberculotus. Vertical bars represent ± standard error of the mean (i.e., 0.612 and 0.649 for A. polmeri and A. tuberculotus, respectively).
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.