Biogeochemical data from diel cycles in a turbid-water pond and a clear-water pond in Brussels
<p><span>The dataset comprises one file containing geo-referenced information with corresponding timestamps. The names of the two ponds are written in French according to the official name defined by Brussels Environment (BE) (i.e. Leybeek and Silex).</span></p> <p><strong><span>Field sampling</span></strong></p> <p><span>Sampling was done every hour from a pontoon by collecting directly surface waters with 60ml polypropylene syringes for gases (CO<sub>2</sub>, CH<sub>4</sub>, N<sub>2</sub>O). Contents of the syringes were transferred with a silicone tube in 60 ml borosilicate serum bottles (Weathon) for CH<sub>4</sub> and N<sub>2</sub>O, poisoned with 200 µl of a saturated solution of HgCl<sub>2</sub>, and sealed with a butyl stopper and crimped with aluminium cap, without a headspace for further analysis at home laboratory. CO<sub>2</sub> measurements were carried out directly on the field with a Li-Cor Li-840 CO<sub>2</sub>/H<sub>2</sub>O gas analyser using the headspace technique by equilibrating four syringes with 30 mL of sample water and 30 mL of atmospheric air by vigorous shaking during 5 min (Borges et al., 2019). The Li-Cor Li-840 was calibrated before and after each cruise with ultrapure N<sub>2</sub> and a suite of gas standards (Air Liquide Belgium) with CO<sub>2</sub> mixing ratios of 388, 813, 3788 and 8300 ppm. The overall precision of pCO<sub>2</sub> measurements was ±2.0%. Water temperature, specific conductivity, and %O<sub>2</sub> were also measured every hour in-situ with VWR MU 6100H probe. 2L polyethylene containers were filled with water three to four times a day and processed at home laboratory for nutrients (soluble reactive phosphorus (SRP), ammonium (NH<sub>4</sub><sup>+</sup>), nitrate (NO<sub>3</sub><sup>-</sup>), and nitrite (NO<sub>2</sub><sup>-</sup>)), chlorophyll-<em>a</em> (Chl-<em>a</em>) and total suspended matter (TSM). </span></p> <p><strong><span>Meteorological data</span></strong></p> <p><span>Meteorological data including hourly air temperature, rainfall, wind speed and atmospheric pressure were retrieved online from </span><span><a href="https://wow.meteo.be/en"><span>https://wow.meteo.be/en</span></a></span><span> from the closest meteorological station of the two ponds (Institute of St-Lambert in Brussels, at 50.8408 °N, 4.4234 °E) located from 2.5km of Pêcheries pond and 5km from Silex pond.</span></p> <p><strong><span>CH<sub>4</sub> and N<sub>2</sub>O measurements by gas chromatography and </span></strong><strong><span>δ</span></strong><strong><sup><span>13</span></sup></strong><strong><span>C-CH<sub>4</sub> by <span>cavity ring-down spectrometry</span></span></strong></p> <p><span>Measurements of N<sub>2</sub>O and CH<sub>4</sub> concentrations dissolved in water and in the gas were made with the headspace technique (20ml of ultra-pure N<sub>2</sub>, Air Liquid Belgium, Weiss, 1981) and a gas chromatograph (GC) (SRI 8610C) with a flame ionisation detector for CH<sub>4</sub> and an electron capture detector for N<sub>2</sub>O calibrated with CO<sub>2</sub>:CH<sub>4</sub>:N<sub>2</sub>O:N<sub>2</sub> gas mixtures (Air Liquide Belgium) with mixing ratios of 1, 10 and 30 ppm for CH<sub>4</sub>, 404, 1018, 3961 ppm for CO<sub>2</sub>, and 0.2, 2.0 and 6.0 ppm for N<sub>2</sub>O. The precision of measurement based on duplicate samples was ±3.9% for CH<sub>4</sub> and ±3.2% for N<sub>2</sub>O.</span></p> <p><span>The </span><span>δ</span><sup><span>13</span></sup><span>C-CH<sub>4</sub> was measured in the headspace gas (20 ml of synthetic air, Air Liquid Belgium) equilibrated with the water sample (total volume 60 ml). The gas samples were diluted to achieve a final CH4 partial pressure below 10 ppm, aligning with the instrument's recommended operational concentration range. This prepared gas was then injected into a cavity ring-down spectrometer (G2201-I, Isotopic Analyzer, Picarro) equipped with a Small Sample Introduction Module 2 (SSIM, Picarro). The data were corrected using calibration curves of </span><span>δ</span><sup><span>13</span></sup><span>C-CH<sub>4</sub> as a function of concentration, based on two gas standards from Airgas Specialty Gases with certified </span><span>δ</span><sup><span>13</span></sup><span>C-CH<sub>4</sub> values of -23.9±0.3 ‰ and -69.0±0.3 ‰.</span></p> <p><strong><span>Chlorophyll-<em>a</em>, total suspended matter, and dissolved inorganic nutrients</span></strong></p> <p><span>Water was filtered through Whatman GF/F glass microfiber filters (porosity 0.7 µm) with a diameter of 47 mm for TSM and Chl-<em>a</em> determination. Chl-<em>a</em> was extracted from filters that were kept frozen before analysis (-20°C) with 90% acetone and concentrations was determined by fluorimetry (Kontron model SFM 25) (Yentsch and Menzel, 1963). Filters used for determination of TSM were pre-weighed before filtration and weighed after filtration of a known volume of water (after oven drying at 50°C). Filtered water was used for the determination of dissolved nutrients. NH<sub>4</sub><sup>+</sup> was measured by the nitroprusside-hypochlorite-phenol staining method (Grasshoff and Johannsen, 1972), NO<sub>2</sub><sup>-</sup> and NO<sub>3</sub><sup>-</sup> were measured before and after reduction of NO<sub>3</sub><sup>-</sup> to NO<sub>2</sub><sup>-</sup> by a cadmium-copper column, using the Griess acid reagent staining method (Grasshoff and Kremling, 2009), SRP was measured by the ammonium molybdate, ascorbic acid and potassium antimony tartrate staining method (Koroleff, 1983).</span></p> <p><strong><span>References</span></strong></p> <p><span>Borges AV, F Darchambeau, T Lambert, C Morana, G H Allen, E Tambwe, A Toengaho Sembaito, T Mambo, J Nlandu Wabakhangazi, J-P Descy, CR Teodoru, S Bouillon (2019) Variations in dissolved greenhouse gases (CO2, CH4, N2O) in the Congo River network overwhelmingly driven by fluvial-wetland connectivity, Biogeosciences, 16, 3801-3834. </span><span><a href="https://doi.org/10.5194/bg-16-3801-2019"><span>https://doi.org/10.5194/bg-16-3801-2019</span></a></span><span> </span></p> <p><span>Grasshoff, K., and Johannsen, H (1972). A new sensitive and direct method for the automatic determination of ammonia in sea water. ICES J. Mar. Sci. 34 (3), 516–521. </span><span><a href="https://doi.org/10.1093/icesjms/34.3.516"><span>https://doi.org/10.1093/icesjms/34.3.516</span></a></span><span>.</span></p> <p><span>Grasshoff, K., Kremling, K., and Ehrhardt, M. (2009). Methods of Seawater Analysis: Determination of Nitrite. </span><span>John Wiley & Sons.</span></p> <p><span>Koroleff, J. (1983). Determination of total phosphorus by alkaline persulphate oxidation. </span><span>Methods of Seawater Analysis. Verlag Chemie, Wienheim, pp. 136–138.</span></p> <p><span>Weiss, R. F. (1981). Determinations of carbon dioxide and methane by dual catalyst flame ionization chromatography and nitrous oxide by electron capture chromatography. <em>Journal of Chromatographic Science</em>, <em>19</em>(12), 611-616. </span><span><a href="https://doi.org/10.1093/chromsci/19.12.611"><span>doi.org/10.1093/chromsci/19.12.611</span></a></span><span> </span></p> <p><span>Yentsch, C. S., & Menzel, D. W. (1963). </span><span>A method for the determination of phytoplankton chlorophyll and phaeophytin by fluorescence. In <em>Deep Sea Research and Oceanographic Abstracts</em> (Vol. 10, No. 3, pp. 221-231). </span><span>Elsevier. </span><span><a title="Persistent link using digital object identifier" href="https://doi.org/10.1016/0011-7471(63)90358-9" target="_blank" rel="noopener"><span><span>https://doi.org/10.1016/0011-7471(63)90358-9</span></span></a><span> </span></span></p>
ShareScore
32/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 4
- Access
- 16
- Reuse readiness
- 8
- Engagement
- 0