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877 results for “digestate”
DATASET: What is the best scale for implementing anaerobic digestion according to environmental and economic indicators?
<p>DATASET: What is the best scale for implementing anaerobic digestion according to environmental and economic indicators?</p> <p>Journal of Water Process Engineering, Volume 35, June 2020, 101235</p> <p>https://doi.org/10.1016/j.jwpe.2020.101235</p> <p> </p>
Organisation of the digestive, excretory and reproductive systems in cysts of Thulinius ruffoi
<p>The data show the organisation of the digestive, excretory and reproductive systems in cysts of T. ruffoi at specific and unspecified stages of encystment. Text files contain additional technical information.</p>
High-pressure flow digestion system
<p><span>Buildup of the presented high-pressure flow-through microwave-assisted digestion system. The gray shaded components including the digestion vessel indicate the pressurized part. The counter-current nitrogen stream enters the digestion system at the nitrog</span>en inlet port/ sample exit port and leaves the system at the pressure interface. (A, H) nitric acid 5% (v/v) rinsing solution, (B) sample (1% (w/w) wine), (C) waste (D) digested sample, (E) precision dispenser, (F) six-port high performance valve, (G) sample loop, (I) Knauer HPLC pump, (J) pressure interface including the nitrogen exit port, (K) cooling unit, (L) high pressure vessel, (M) magnetron, (N) nitrogen inlet port/ sample exit port, (O) pressure restriction loop</p>
Figure 6 in Zootechnical indices and digestibility in juveniles of tambaqui Colossoma macropomum fed a diet containing particulate maize
Figure 6. Regression Graph (linear model) for the variable coefficient: Apparent digestibility of crude protein for tambaqui fed diets with different particle size of corn (Ŷ = 72.2 – 1.21.X; (R2 = 52.0%; p= 0.0014)).
Figure 5 in Zootechnical indices and digestibility in juveniles of tambaqui Colossoma macropomum fed a diet containing particulate maize
Figure 5. Regression Graph (Quadratic Model) for the variable specific growth rate (TCE) after 68 days of experiment (Ŷ = 6.15 – 0.00279.X + 0.00000191.X2; (R2 = 53.7%; p= 0.0006)).
Figure 2 in Zootechnical indices and digestibility in juveniles of tambaqui Colossoma macropomum fed a diet containing particulate maize
Figure 2. Regression Graph (Model Quadratic) for variable weight gain in the 68 days of experiment (Ŷ = 61.3 – 0.0807.X + 0.0000574X2 (R2 = 58.5%; p= 0.0002)).
Figure 4 in Zootechnical indices and digestibility in juveniles of tambaqui Colossoma macropomum fed a diet containing particulate maize
Figure 4. Regression Graph (Quadratic Model) for variable Total feed consumption in the 68 days of experiment (Ŷ = 556.6 – 0.513.X + 0.000321.X2; (R2 = 65.6%; p<0.0001)).
Figure 3 in Zootechnical indices and digestibility in juveniles of tambaqui Colossoma macropomum fed a diet containing particulate maize
Figure 3. Regression Graph (Cubic Model) for apparent feed conversion variable after 68 days of experiment (Ŷ = 1.27 – 0.00284X + 0.00000783X2 – 0.00000000570X3; (R2 = 58.,1%; p= 0.0007)).
Figure 1 in Zootechnical indices and digestibility in juveniles of tambaqui Colossoma macropomum fed a diet containing particulate maize
Figure 1. Regression Graph (Model Quadratic) for variable weight final after 68 days of experiment (Ŷ = 72.3 – 0.809.X + 0.0000576X2; (R2 = 58.5%; p= 0.0002)).
Figure 2 in Obtainment and characterization of digestive aspartic proteases from the fish Caranx hippos (Linnaeus, 1766)
Figure 2. pH and temperature effect on EE acidic proteases. (A) Optimal temperature; (B) Thermal stability; (C) Optimal pH; (D) pH stability.
Data for 'Accounting for digestion enzyme bias in Casanovo' (Melendez et al., 2024)
<p>This upload contains two archives and an explanatory README.md that accompany <a href="https://doi.org/10.1101/2024.05.16.594602">Accounting for digestion enzyme bias in Casanovo (Melendez et al., 2024)</a>. The archive named 'mgf_data' contains all of the mgf files used in the paper. The archive named 'mztab_data' contains mztab formatted sequencing (and enzyme classification) predictions from all models trained in the paper. The README file describes the structure of each archive, the contents of each mgf and mztab file, and the sections of the paper that each mgf or mztab file relates to.</p>
Figure 1 in Experimental evidence that the invasive snail Potamopyrgus antipodarum (Gray, 1843) survives passage through the digestive tract of common riverine fish
Figure 1. The Number of ingested P. antipodarum individuals per fish (red bars) and the number of snails that survived passing through the digestive tract (green bars). Values are mean ± standard deviation.
Fig. 2 in Low Level Genetic Diversity of Opalinid Morphotypes from the Digestive Tract of Hoplobatrachus rugulosus (Batrachia, Amphibia) in Thailand
Fig. 2. Scanning electron micrographs of opaline cells fixed in 2.5% glutaraldehyde. All opaline cells are covered with flagella throughout their body. (A) Opalinid cell with somatic ridges caused by the flagellar metachronal beating clearly defined in a spiral arrangement. (B) Fan-shaped opalinid cell with a broad anterior end and tapering posterior. (C) Uniformly elongated opalinid cell with a slightly tapering posterior end. (D) Fan-shaped opalinid cell of a similar morphotype to B but of a smaller size. Scale bar: A, C and D: 50 μm; B: 10 μm.
Fig. 1 in Low Level Genetic Diversity of Opalinid Morphotypes from the Digestive Tract of Hoplobatrachus rugulosus (Batrachia, Amphibia) in Thailand
Fig. 1. Light micrographs of opaline cells from life. (A) The opaline falx (arrow). (B) Multiple nuclei throughout the cell (arrowheads). A bend at the mid-body level is noticeable. (C) Flagella covering the body of the opaline cell (arrow). Several scores of nuclei are clearly visible (small circular clear whitish areas). (D) Prominent ridges signifying the metachronal beating of the flagella cover the opaline body in a random arrangement (arrow). (E) Flagella beating in a metachronal fashion (arrow). Opalinid cell nuclei (arrowheads). Scale bar: A and C: 100 μm; B, D and E: 50 μm.
FIGURE 4 in Partial characterization of digestive proteases in juveniles of Microphis brachyurus (short-tailed pipefish) (Syngnathiformes: Syngnathidae)
FIGURE 4 | SDS-PAGE zymogram of alkaline digestive proteases of short-tailed pipefish (Microphis brachyurus) juveniles: Molecular weight marker (MWM), rabbit phosphorylase B (97.4 kDa), bovine serum albumin (66.2 kDa), ovalbumin (42.7 kDa), carbon anhydrase (31.0 kDa) and lysozyme (14.4 kDa); control (without inhibitor); inhibitors were the same as in Fig. 3.
FIGURE 3 in Partial characterization of digestive proteases in juveniles of Microphis brachyurus (short-tailed pipefish) (Syngnathiformes: Syngnathidae)
FIGURE 3 | Residual activity (%) of digestive proteases using several inhibitors on multienzyme extracts of short-tailed pipefish (Microphis brachyurus) juveniles. Alkaline proteases with no inhibitor (Alk control), tosylphenylanylchloromethyl ketone (TPCK), phenanthroline (PHEN), ethyl-diamine tetra-acetic acid (EDTA), tosyllysyl- chloromethyl ketone (TLCK), ovalbumin (OVO), soybean trypsin inhibitor (SBT1), phenyl methyl sulphonyl fluoride (PMSF), acidic proteases with no inhibitor (Acid control), pepstatin A (mean ± SD, n = 3). Columns with different letters represent significant differences (p <0.05).
Figure 3 in Diversity of cellulolytic and xylanolytic fungi associated with the digestive tract of aquatic insect larvae in streams of the Amazon Forest and Cerrado in Brazil
Figure 3. Percentage of fungal isolates from the DT of Stenochironomus (Diptera: Chironomidae) from trunks in Amazon Forest (A), trunks in Cerrado (B) and leaves in Cerrado (C) producers and non-producers of xylanase (Xyl) and cellulase (CMCase).
Figure 2 in Diversity of cellulolytic and xylanolytic fungi associated with the digestive tract of aquatic insect larvae in streams of the Amazon Forest and Cerrado in Brazil
Figure 2. Principal component analysis (PCA) of the physicochemical parameters of the streams sampled in the Amazon Forest - Amazonas (A) and Cerrado - Tocantins (T) in the north of Brazil.
Figure 1 in Diversity of cellulolytic and xylanolytic fungi associated with the digestive tract of aquatic insect larvae in streams of the Amazon Forest and Cerrado in Brazil
Figure 1. Map of the sampling sites of Stenochironomus (Diptera:Chironomidae) in low-order streams in the Adolpho Ducke Forest Reserve in the state of Amazonas (Amazon Forest Biome) and at the Lajeado State Park (LSP) in the state of Tocantins, (Cerrado Biome) Brazil.
Figure 2 in Diversity and enzymatic capabilities of fungi associated with the digestive tract of larval stages of a shredder insect in Cerrado and Amazon Forest, Brazil
Figure 2. Percentage of fungal isolates from the DT of Triplectides (Trichoptera: Leptoceridae) in Cerrado (A) and Amazon Forest (B) biomes producers and non-producers of xylanase (Xyl) and cellulase (CMCase).
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.