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Titel Application of a UV-Vis submersible probe for capturing changes in DOC concentrations across a mire complex during the snowmelt and summer periods
VerfasserIn Armine Avagyan, Benjamin Runkle, Lars Kutzbach
Konferenz EGU General Assembly 2013
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 15 (2013)
Datensatznummer 250078642
 
Zusammenfassung
An accurate quantification of dissolved organic carbon (DOC) is crucial for understanding changes in water resources under the influence of climate, land use and urbanization. However, the conventionally used methods do not allow high frequency in situ analyses in remote or hostile environments (e.g., industrial wastewater or during environmental high-flow events, such as snowmelt or floods). In particular, missing measurements during the snowmelt period in landscapes of the boreal region can lead to significant miscalculations in regional carbon budgets. Therefore, the aim of the study was to test the performance of a portable, submersible UV-Vis spectrophotometer (spectro::lyser, s::can Messtechnik GmbH, Austria) during the snowmelt period in a boreal mire-forest catchment, and to provide a conceptual understanding of the spatial and temporal dynamics of DOC concentrations during and after snowmelt. During 2011, water samples were collected from the near-pristine Ust-Pojeg mire complex in northwestern Russia (61˚ 56’N, 50˚ 13’E). Sampling started during the spring snowmelt period and continued until late fall. The mire presented a mosaic of different landscape units. The mire consisted of minerogeous (fen), ombrogenous (bog), and transitional forest-mire (lagg) zones. Water samples were taken from the surface across the mire (22 points at 50-m intervals). DOC concentrations were analyzed directly at the study site using a portable, submersible UV-Vis spectrophotometer, which uses high-resolution absorbance measurements over the wavelength range 200–742.5 nm at 2.5-nm intervals as a proxy for DOC content. Because the DOC composition of fluids varies by site, a local calibration replaced the default settings of the spectro::lyser (Global Calibration) to enhance the accuracy of the measurements. To evaluate the local calibration and correct for drift, the same samples (n = 157) were additionally analyzed using the wet persulfate oxidation method (O-I-Analytica, Aurora Model 1030, USA). Based on ordinary least squares regression, the local calibration showed good agreement between the results obtained from the high-resolution absorption measurements and the wet persulfate oxidation method (r2= 0.99, root-mean-square error = 1.7 mg L-1). The measurement campaign revealed spatial and temporal variability of DOC concentrations, and demonstrated that at the beginning of the snowmelt period, surface carbon was flushed away by meltwater, whereas deeper layers remained frozen. During this time, the surface DOC concentrations fluctuated within the range of 8–15 mg L-1 (April 07) across the entire mire complex. After April 18, the concentrations diverged between the sites; the DOC concentration reached 30 mg L-1in the surface water at the lagg zone but was 15 mg L-1 at the bog site (April 25). The DOC surface water concentration continued to increase during summer and fall, ranging from 19 to 74 mg L-1 across the mire, with an average of 45 ± 14 mg L-1. The study indicates that high-resolution spectroscopic measurements provide a simple, fast, robust and non-destructive method for measuring DOC contents, with a short duration (17-20 seconds) and portability of the sample analysis rendering this method particularly advantageous for in-situ measurements at remote field locations.