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opencc-by-4.0Jun 2018View details →

Supplementary data for "Heterometallic perovskite-type metal-organic framework with an ammonium cation: structure, phonons, and optical response"

Optimised structures of [NH4][Na0.5M0.5(COOH)3] (M = Al, Cr) Phonon output for [NH4][Na0.5Cr0.5(COOH)3] Gif of the T’(NH4+) mode (no. 23). The c-axis is the vertical direction. For further information please see the associated publication.

opencc-by-nc-sa-4.0Jul 2019View details →

Thermal decomposition data of uranium containing microspheres produced via internal gelation and ammonium diuranate powder

A combination of simultaneous thermal analysis, evolved gas analysis and non-ambient XRD techniques was used to characterise and investigate the thermal decomposition behaviour in the NH3 − UO3 − H2O class of materials. One compound was prepared according to a typical ammonium diuranate precipitation reaction, and could be identified as 3UO3·NH3·5H2O. Microspheres prepared by the sol-gel method via internal gelation were associated to the composition 3UO3·2NH3·4H2O under the specified conditions. The products were analysed using the techniques listed below, the resulting data are part of this dataset. <ul> <li>TGA, combined with EGA-MS (Tmax = 1300 °C, heating rate = 2 °C/min)</li> <li>TG-DSC, combined with EGA-MS (Tmax = 1300 °C, heating rate = 10 °C/min)</li> <li>ambient XRD (dried products after synthesis)</li> <li>in-situ high temperature XRD (including initial and final scans, taken at 35 °C) <ul> <li>Tmax for 3UO3·NH3·5H2O = 1300 °C; Tmax for 3UO3·2NH3·4H2O = 650 °C</li> <li>Samples measured directly on a Pt/Rh heating strip (Pt/Rh phase visible in patterns, blank scan included)</li> </ul> </li> </ul>

opencc-by-4.0May 2024View details →

Data for: Klein et al., Viscosity of aqueous ammonium nitrate--organic particles: Equilibrium partitioning may be a reasonable assumption for most tropospheric conditions, egusphere-2024-1459

Experimental data This folder contains the experimental and modelled data to the figures shown in the main manuscript and Appendix. Figure 3B AIOMFAC-VISC (AIOMFAC-VISC modelling of sucrose) Figure 3B Experimental (Viscosity measurements of sucrose) Figure 4 (Viscosity measurements of ammonium nitrate - sucrose - water mixtures) Figure 5 A and C (Viscosity estimations of ammonium nitrate - sucrose - water mixtures using mixing rules) Figure 5 B and D (Viscosity estimations of ammonium nitrate - sucrose - water mixtures using AIOMFAC-VISC) Figure 6 (Viscosity estimations of inorganic - sucrose - water mixtures using mixing rules) Figure 7 (Mixing times for ammonium nitrate - sucrose - water and Toluene SOA - sucrose - water aerosol particles for varies cities)  Figure A2 (Viscosity estimations of ammonium nitrate - sucrose - water mixtures using a mass fraction based mixing rules)

opencc-by-4.0Oct 2024View details →

Dataset: Post-treatment of high-rate activated sludge effluent via zeolite adsorption and recovery of ammonium-nitrogen

Dataset used to write journal article (doi:10.1016/j.biortech.2024.130837) covering the post-treatment of high-rate activated sludge effluent via zeolite adsorption and recovery of ammonium-nitrogen to produce potential alternative fertilising products. The data included is data gathered from column experiments (for breakthrough modelling and to compare different N recovery methods). Metal and cation content results for the treated wastewater and adsorption outputs is also included

openCC (other)May 2024View details →

Nitrogen cycling and metabolic rates of aquacultured and wild Acropora coral from Guam in response to ammonium loading rates during 2020-2022

Rates from aquacultured corals and coral fragments collected in Guam in response to ammonium loading. These data are from two separate experiments, one using aquacultured corals and artificial seawater and light. The second was done with wild collected Acropora pistillata from two reef sites in Guam. The first site was West Hagåtña Bay (N13.479650, E144.741750; N13.479833, E144.741733) which had more nearby urban influences and was near the sewage outfall for the city (Redding et al. 2013). The second site was Luminao Reef (N13.4652417, E144.6477483; N13.465467, E144.648050) which was a more isolated reef on the seaward side of the breakwater for Guam’s major port. We measured respiration, gross primary production, 15N ammonium uptake to corals, related nitrogen cycling fluxes in the tanks (reminerization, net uptake, nitrification).

openCC (other)Apr 2020View details →

Effects of microarthropod exclusion and water amendments on fluffgrass rhizosphere ammonium (NH4) at the Jornada Basin LTER, 1986-1987

This data package contains data on nitrogen availability (as ammonium, NH4+), measured with ion exchange resin bags, in fluffgrass (Dasyochloa pulchella) rhizosphere soil from 1986-1987. This study was conducted at the Chihuahuan Desert Rangeland Research Center to test how watering, and changing densities of soil microarthropods and nematodes, impacts fluffgrass growth and nutrient cycling. An ion exchange resin bag technique (Binkley 1984, Lajtha 1988) was used to determine ammonium availability. Twenty 6 x 6 m plots were established with a 3 m buffer between plots. Five plots were randomly assigned to one of four treatments:1) Chlordane (to exclude microarthropods), 2) Chlordane and water, 3) Water, and 4) Control. Two cation exchange bags were placed in the rhizosphere of a fluffgrass plant in each plot. Bags were left in the field 3 months, collected, brought to the lab and analyzed for available ammonium (NH4+) using a salicylate procedure. The data table contains bag collection date, treatment, and NH4+ (mg/kg) concentration. This study is complete.

openCC (other)Nov 2020View details →

Nitrate, ammonium, and water content of mesquite root tube soil from three habitats at the Jornada Basin LTER site, 1987

This data package contains data on measured root tube soil nutrients from soil cores collected under mesquite (Prosopis glandulosa)at three habitat types of the Jornada Experimental Range and New Mexico State University College Ranch. These habitat types include: 1)playa, 2)dunes, and (4)grassland. Soil core samples were collected in 1987 by hand-augering a reference core and a root tube core. Subsamples were analyzed for nitrate, ammonium, and soil moisture contents. This data set consists of the date of collection, collection site, nitrate concentration, ammonium concentration, and percent soil moisture. Collected variables also include treatments (irradiation and nematicide) that are not well-documented at this time. Data collection was completed in 1987.

openCC (other)Mar 2020View details →

SBC LTER: OCEAN: Sediment porewater ammonium and urea concentrations

This data set present the results of efforts to characterize the concentrations of ammonium and (selectively) urea in pore waters of permeable, sandy sediments on the inner continental shelf of the Santa Barbara Channel, including those adjacent to major kelp beds. Samples sites included Arroyo Burro, Mission Creek, Refugio and Mohawk. A second data file include depth profiles of ammonium and urea concentrations in the water column above each sediment sampling site, which were used to discern the strength of the vertical gradients of ammonium and urea concentrations between the surficial sediments and the water column.

opencc-by-4.0Feb 2024View details →

Data archive for: Resting cells of Skeletonema marinoi assimilate organic compounds and respire by dissimilatory nitrate reduction to ammonium in dark, anoxic conditions

Data archive for: “Resting cells of Skeletonema marinoi assimilate organic compounds and respire by dissimilatory nitrate reduction to ammonium in dark, anoxic conditions” <a href="https://doi.org/10.1111/1462-2920.16625">https://doi.org/10.1111/1462-2920.16625</a>   Dataset of single cell assimilation of organic/inorganic C/N by resting cells of the marine diatom Skeletonema marinoi captured using secondary ion mass spectrometry (SIMS) and stable isotopic tracers. The dataset also contains POC/PON changes over time during dormancy, DNRA (15N-NH4+ production), denitrification (15N-N2 production) and a germination assay to determine survival rate, most probable number analysis (MPN).   Two strains (GF04 and R05) were incubated in dark and anoxic conditions in two different incubation experiments. Incubation 1: Diatoms treated with antibiotics before entering dormancy compared to a control not treated with antibiotics then given 15N-NO3- in dark anoxic conditions. Incubation 2: Diatoms treated with antibiotics given, 15N & 13C urea, 15N & 13C urea + 14N-NO3-, 13C-acetate, 13C-acetate + 15N-NO3-, or 15N-NO3-. See the main manuscript for a extensive experimental setup.   Each file is uploaded as both a .CSV and .XLSX, so that you can choose which you prefer. DNRA_and_denitrification.csv/xlsx: DRNA and denitrification depending on volume (Incubation 1) DNRA_per_cell.csv/xlsx: DNRA per cell (Incubation 1 & 2) MPN_data.csv/xlsx: Most probable number analysis (Incubation 1 & 2) POC_PON.csv/xlsx: POC and PON per cell and volume (Incubation 1 & 2) SIMS_data.csv/xlsx: SIMS data (Incubation 1 & 2)

opencc-by-4.0Dec 2016View details →

Table 3 b in Description of Epistylis camprubii n. sp., a Species Highly Tolerant to Ammonium and Nitrite

Table 3b. Comparison between Epistylis camprubii and the other Epistylis species mentioned in the manuscript: characteristics of stalk, macronucleus and contractile vacuole.<table><tbody><tr><th>Species</th><th>Stalk width in vivo (µm)</th><th>Stalk striation / segmentation</th><th>Macronucleus</th><th>Contractile vacuole</th><th>Data source</th></tr></tbody><tbody><tr><th>Epistylis camprubii</th><td>3.1–8.4</td><td>Longitudinally striated, occasionally transeverse segmentation</td><td>C-shaped, transversely oriented; adoral half of the body</td><td>1, adoral third of the body, on dorsal wall of vestibulum</td><td>Present manuscript</td></tr><tr><th>E. balatonica</th><td>–</td><td>Longitudinally finely striated</td><td>Horinzotal horsehoe-shaped in the middle of the body</td><td>1, in the heigh of the peristomial lip</td><td>Stiller 1971</td></tr><tr><th>E. chrysemydis</th><td>13–25</td><td>Longitudinally striated, occasionally transeverse segmentation</td><td>C-shaped, transversely oriented; adoral half of the body</td><td>1, close or in the heigh of the peristomial lips, on ventral wall of vestibulum</td><td>Foissner et al. 1992</td></tr><tr><th>E. coronata</th><td>11–18</td><td>–</td><td>Semicircular, adoral half of the body</td><td>1, in the height of the peristomial lips, on dorsal wall of vestibulum</td><td>Foissner et al. 1992</td></tr><tr><th>E. entzii</th><td>18</td><td>–</td><td>3/4 circular, adoral half of the body</td><td>1, in the heigh of the peristomial lip, on dorsal wall of vestibulum</td><td>Foissner et al. 1992</td></tr><tr><th>E. epistyliformis</th><td>–</td><td>Transverse segmentation</td><td>Intenselly flattened, horsehoe-shaped</td><td>1, adoral third of the body</td><td>Stiller 1971</td></tr><tr><th>E. hentscheli</th><td>12–20, sometimes 25</td><td>Occasionally finely annulated</td><td>Semicircular, adoral half of the body</td><td>1, in the heigh of the peristomial lip, on ventral wall of vestibulum</td><td>Foissner et al. 1992</td></tr><tr><th>E. plicatilis</th><td>7–18</td><td>Longitudinally finely striated</td><td>Semicircular, adoral half of the body</td><td>1, in the heigh of the peristomial lip, on dorsal wall of vestibulum</td><td>Foissner et al. 1992</td></tr><tr><th>E. rotans / E. procumbens</th><td>–</td><td>Fine longitudinally striated, transverse segmentation</td><td>Reniform to semicircular, in transverse axis and adoral half of zooid</td><td>1, at level of peristomial lip, on dorsal wall Foissner et al. 1999 of vestibulum</td></tr><tr><th>E. rotans</th><td>–</td><td>Longitudinally striated, transeverse segmentation</td><td>C-shaped, transversely oriented, adoral third of the body</td><td>1, located in the adoral third of the body</td><td>Curds 1969</td></tr><tr><th>E. thienemanni</th><td>–</td><td>–</td><td>Flattened ribbon-like and horsehoe-shaped, adoral third of the body</td><td>1, located in the peristomial disc, on dorsal wall of vestibulum</td><td>Stiller 1971</td></tr><tr><th>E. variabilis</th><td>Variable</td><td>–</td><td>–</td><td>1, at the level of the peristomial lip</td><td>Stiller 1971</td></tr></tbody></table>

opencc-by-4.0Dec 2016View details →

Table 3 a in Description of Epistylis camprubii n. sp., a Species Highly Tolerant to Ammonium and Nitrite

Table 3a. Comparison between Epistylis camprubii and the other Epistylis species mentioned in the manuscript: characteristics of zooid and persitome.<table><tbody><tr><th>Species</th><th>Body lenght in vivo (µm)</th><th>Body width in vivo (µm)</th><th>Zooid shape</th><th>Peristomial disc diameter in vivo (µm)</th><th>Peristomial disc shape</th><th>Peristomial lip height in vivo (µm)</th><th>Peristomial lip width in vivo (µm)</th><th>Number of peristomial lips</th><th>Data source</th></tr></tbody><tbody><tr><th>Epistylis camprubii</th><td>35.3–98.1</td><td>18.0–65.2</td><td>Vase-shaped</td><td>11.2–21.3</td><td>Rounded, pointed, rarely umbilicated</td><td>5.0–10.6</td><td>16.2–31.7</td><td>1</td><td>Present manuscript</td></tr><tr><th>E. balatonica</th><td>90–100</td><td>45–55</td><td>Vase-shaped</td><td>–</td><td>–</td><td>–</td><td>–</td><td>2</td><td>Stiller 1971</td></tr><tr><th>E. chrysemydis</th><td>120–220</td><td>60–110</td><td>Vase-shaped</td><td>–</td><td>Umbilicated</td><td>–</td><td>50–80</td><td>2</td><td>Foissner et al. 1992</td></tr><tr><th>E. coronata</th><td>70–120</td><td>–</td><td>Vase-shaped</td><td>–</td><td>Slightly umbilicated and oblique</td><td>–</td><td>32–65</td><td>1</td><td>Foissner et al. 1992</td></tr><tr><th>E. entzii</th><td>125–190</td><td>80</td><td>Cylindrical</td><td>–</td><td>Convex, slightly oblique</td><td>–</td><td>–</td><td>1</td><td>Foissner et al. 1992</td></tr><tr><th>E. epistyliformis</th><td>43–62</td><td>20–27</td><td>Vase-shaped</td><td>–</td><td>Convex, sometimes – conical</td><td>–</td><td>1</td><td>Stiller 1971</td></tr><tr><th>E. hentscheli</th><td>110–170</td><td>38–60</td><td>Asymmetric and bell-shaped, narrowed down to the stem</td><td>–</td><td>Convex, slightly oblique</td><td>–</td><td>–</td><td>1</td><td>Foissner et al. 1992</td></tr><tr><th>E. plicatilis</th><td>90–160</td><td>25–50</td><td>Funnel-shaped</td><td>–</td><td>Not umbilicated</td><td>–</td><td>36–60</td><td>1</td><td>Foissner et al. 1992</td></tr><tr><th>E. rotans / E. procumbens</th><td>60–140</td><td>2–2½ times as long as wide</td><td>Irregular (sigmoidal – shape, bent at right</td><td>Flat or slightly convex, slightly</td><td>–</td><td>–</td><td>1</td><td>Foissner et al. 1999</td></tr><tr><th></th><td></td><td></td><td>angles, slightly tilted backwards)</td><td>oblique</td><td></td><td></td><td></td><td></td></tr><tr><th>E. rotans</th><td>70–100</td><td>–</td><td>Vase-shaped</td><td>–</td><td>Arched</td><td>–</td><td>–</td><td>1</td><td>Curds 1969</td></tr><tr><th>E. thienemanni</th><td>67–120</td><td>–</td><td>Vase-shaped</td><td>–</td><td>Conical</td><td>–</td><td>–</td><td>1</td><td>Stiller 1971</td></tr><tr><th>E. variabilis</th><td>50–100</td><td>–</td><td>Funnel-shaped</td><td>–</td><td>Slightly convex and obliquely protuberant</td><td>–</td><td>–</td><td>1</td><td>Stiller 1971</td></tr></tbody></table>

opencc-by-4.0Nov 2024View details →

Supplementary Datasets for "Oceanic enrichment of ammonium and its impacts on phytoplankton community composition under a high-emissions scenario"

These are the four supplementary datasets used in the analysis and work presented in the publication  Oceanic enrichment of ammonium and its impacts on phytoplankton community composition under a high-emissions scenario

opencc-by-4.0Oct 2024View details →

Derived daily timeseries of weather, soil moisture and temperature, flow and nitrogen species (nitrate and nitrite, ammonium) concentrations data for the North Wyke Farm Platform National Biosciences Research Infrastructure, England

For a selection of catchments from the North Wyke Farm Platform in southwest England, where land use conversions have been introduced, daily time series data covering weather conditions (minimum temperature, maximum temperature, total rainfall, wind speed and solar radiation), near-surface soil status (moisture content and temperature), flow and concentrations of key nitrogen species (nitrate and nitrite, ammonium) have been filtered based on attached data quality tags . The datasets run between 2013 and March 2024. For the main climate variables, data gaps were infilled with preceding- and following-on daily data, observations from a nearby weather station or existing national datasets to generate a continuous data series for modelling. For the other data series, annual and seasonal summary statistics on data coverage are provided. Information on significant field events, such as ploughing, drilling and harvest, fertiliser applications and manure spreading were also tabulated.

opencc-by-4.0Oct 2021View details →

Porewater concentrations of nitrate, nitrite, ammonium, manganese, and iron in sediments from the Atacama and Kermadec Trench regions

The file presents data collected during cruises on RV Tangaroa (TAN1711, 2017) to the Kermadec Trench and RV Sonne (SO261, 2018) to the Atacama Trench. Sample collection and analyses are described, and results are discussed in Thamdrup, B. et al. Anammox bacteria drive fixed nitrogen loss in hadal trench sediments. Proc. Natl. Acad. Sci. USA, in press, doi: 10.1073/pnas.2104529118.