In Situ Measures of Dissolved Organic Carbon Flux in a Rural Stream

1984 ◽  
Vol 41 (6) ◽  
pp. 964-973 ◽  
Author(s):  
Frank T. Kuserk ◽  
Louis A. Kaplan ◽  
Thomas L. Bott

Dissolved organic carbon (DOC) dynamics were measured in a second-order stream located in a pasture in southeastern Pennsylvania. In situ measurements made at six stations in early summer showed a diel patern of net DOC release from the streambed communities with predawn minima and afternoon maxima. When an 18-m section of the stream was covered with black plastic for 1 mo to exclude algal growth and measures were repeated in late summer, a net removal of DOC occurred in the covered section, while in an adjacent uncovered section DOC was released. When a bovine manure extract was introduced into the covered section, the DOC removal rate increased by more than an order of magnitude. Jewel-weed (Impatiens capensis L.) extract also elicited an elevated rate of DOC removal. When these extracts were added individually to microcosms, removal rates in the dark were 57 and 65% of the in situ uptake estimates for the manure extract and leachate, respectively. Abiotic controls showed that nearly all of the DOC removal was biotic uptake. DOC flux measurements in a third-order section of White Clay Creek, located on an adjacent watershed, also revealed a net DOC release from the uncovered streambed. Introduction of a bovine manure extract elicited a DOC removal rate an order of magnitude less than in the pasture stream. A companion microcosm experiment yielded an uptake rate that was 178% of the in situ estimate.

2016 ◽  
Vol 13 (12) ◽  
pp. 3833-3846 ◽  
Author(s):  
Emily C. O'Donnell ◽  
Jemma L. Wadham ◽  
Grzegorz P. Lis ◽  
Martyn Tranter ◽  
Amy E. Pickard ◽  
...  

Abstract. Determining the concentration and composition of dissolved organic carbon (DOC) in glacial ecosystems is important for assessments of in situ microbial activity and contributions to wider biogeochemical cycles. Nonetheless, there is limited knowledge of the abundance and character of DOC in basal ice and the subglacial environment and a lack of quantitative data on low-molecular-weight (LMW) DOC components, which are believed to be highly bioavailable to microorganisms. We investigated the abundance and composition of DOC in basal ice via a molecular-level DOC analysis. Spectrofluorometry and a novel ion chromatographic method, which has been little utilized in glacial science for LMW-DOC determinations, were employed to identify and quantify the major LMW fractions (free amino acids, carbohydrates, and carboxylic acids) in basal ice from four glaciers, each with a different type of overridden material (i.e. the pre-entrainment sedimentary type such as lacustrine material or palaeosols). Basal ice from Joyce Glacier (Antarctica) was unique in that 98 % of the LMW-DOC was derived from the extremely diverse free amino acid (FAA) pool, comprising 14 FAAs. LMW-DOC concentrations in basal ice were dependent on the bioavailability of the overridden organic carbon (OC), which in turn was influenced by the type of overridden material. Mean LMW-DOC concentrations in basal ice from Russell Glacier (Greenland), Finsterwalderbreen (Svalbard), and Engabreen (Norway) were low (0–417 nM C), attributed to the relatively refractory nature of the OC in the overridden palaeosols and bedrock. In contrast, mean LMW-DOC concentrations were an order of magnitude higher (4430 nM C) in basal ice from Joyce Glacier, a reflection of the high bioavailability of the overridden lacustrine material (> 17 % of the sediment OC comprised extractable carbohydrates, a proxy for bioavailable OC). We find that the overridden material may act as a direct (via abiotic leaching) and indirect (via microbial cycling) source of DOC to the subglacial environment and provides a range of LMW-DOC compounds that may stimulate microbial activity in wet subglacial sediments.


Sensors ◽  
2020 ◽  
Vol 20 (3) ◽  
pp. 859
Author(s):  
Suzanne R. Jacobs ◽  
Björn Weeser ◽  
Mariana C. Rufino ◽  
Lutz Breuer

In situ spectrophotometers measuring in the UV-visible spectrum are increasingly used to collect high-resolution data on stream water quality. This provides the opportunity to investigate short-term solute dynamics, including diurnal cycling. This study reports unusual changes in diurnal patterns observed when such sensors were deployed in four tropical headwater streams in Kenya. The analysis of a 5-year dataset revealed sensor-specific diurnal patterns in nitrate and dissolved organic carbon concentrations and different patterns measured by different sensors when installed at the same site. To verify these patterns, a second mobile sensor was installed at three sites for more than 3 weeks. Agreement between the measurements performed by these sensors was higher for dissolved organic carbon (r > 0.98) than for nitrate (r = 0.43–0.81) at all sites. Higher concentrations and larger amplitudes generally led to higher agreement between patterns measured by the two sensors. However, changing the position or level of shading of the mobile sensor resulted in inconsistent changes in the patterns. The results of this study show that diurnal patterns measured with UV-Vis spectrophotometers should be interpreted with caution. Further work is required to understand how these measurements are influenced by environmental conditions and sensor-specific properties.


1986 ◽  
Vol 43 (6) ◽  
pp. 1259-1270 ◽  
Author(s):  
Bruce J. Peterson ◽  
John E. Hobbie ◽  
Teresa L. Corliss

The carbon cycle of the Kuparuk River, a meandering tundra stream, is dominated by inputs of eroding peat and leaching dissolved organic carbon from the tundra. Net production of epilithic algae is about 13 g C∙m−2∙yr−1, an order of magnitude less than inputs of allochthonous particulate organic carbon and two orders of magnitude less than inputs of dissolved organic carbon. The streamwater has a mean total organic carbon concentration of 6.8 mg∙L−1, and the annual export of organic carbon from the watershed is 2–3 t∙km−2∙yr−1; both are similar to the average for temperate streams. However, because of the low primary productivity of tundra vegetation, the export of organic carbon from the watershed via the river is a larger fraction (2–6%) of the total watershed net primary production than the 0.1–0.4% usually found for temperate rivers.


2008 ◽  
Vol 5 (4) ◽  
pp. 1165-1173 ◽  
Author(s):  
R. Sempéré ◽  
M. Tedetti ◽  
C. Panagiotopoulos ◽  
B. Charrière ◽  
F. Van Wambeke

Abstract. The distribution and bacterial availability of dissolved neutral sugars were studied in the South East Pacific from October to December 2004 during the BIOSOPE cruise. Four contrasting stations were investigated: Marquesas Islands (MAR), the hyper-oligotrophic South Pacific Gyre (GYR), the eastern part of the Gyre (EGY), and the coastal waters associated to the upwelling area off Chile (UPW). Total (free and combined) dissolved neutral sugar (TDNS) concentrations were in the same order of magnitude at MAR (387±293 nM), GYR (206±107 nM), EGY (269±175 nM), and UPW (231±73 nM), with the highest and lowest concentrations found at MAR (30 m, 890 nM) and EGY (250 m, 58 nM), respectively. Their contribution to dissolved organic carbon (TDNS-C×DOC−1%) was generally low for all sites varying from 0.4% to 6.7% indicating that South East Pacific surface waters were relatively poor in neutral sugars. Free dissolved neutral sugar (FDNS; e.g. sugars analyzed without hydrolysis) concentrations were very low within the detection limit of our method (5–10 nM) accounting for <5% of the TDNS. In general, the predominant sugars within the TDNS pool were glucose, xylose, arabinose, and galactose, while in the FDNS pool only glucose was present. TDNS stock to bacterial production ratios (integrated values from the surface to the deep chlorophyll maximum) were high at GYR with respect to the low primary production, whereas the opposite trend was observed in the highly productive area of UPW. Intermediate situations were observed for MAR and EGY. Bioavailability of dissolved organic matter (DOM) exposed to natural solar radiation was also experimentally studied and compared to dark treatments. Our results showed no or little detectable effect of sunlight on DOM bacterial assimilation in surface waters of UPW and GYR, while a significant stimulation was found in MAR and EGY. The overall results clearly suggest that DOM is less labile at GYR compared to UPW, which is consistent with the observed accumulation of dissolved organic carbon and the elevated C/N ratios reported by Raimbault et al. (2008).


2019 ◽  
Vol 124 (6) ◽  
pp. 3755-3778
Author(s):  
Sergio R. Signorini ◽  
Antonio Mannino ◽  
Marjorie A. M. Friedrichs ◽  
Pierre St‐Laurent ◽  
John Wilkin ◽  
...  

2013 ◽  
Vol 13 (10) ◽  
pp. 5117-5135 ◽  
Author(s):  
B. Ervens ◽  
Y. Wang ◽  
J. Eagar ◽  
W. R. Leaitch ◽  
A. M. Macdonald ◽  
...  

Abstract. Cloud and fog droplets efficiently scavenge and process water-soluble compounds and, thus, modify the chemical composition of the gas and particle phases. The concentrations of dissolved organic carbon (DOC) in the aqueous phase reach concentrations on the order of ~ 10 mgC L−1 which is typically on the same order of magnitude as the sum of inorganic anions. Aldehydes and carboxylic acids typically comprise a large fraction of DOC because of their high solubility. The dissolution of species in the aqueous phase can lead to (i) the removal of species from the gas phase preventing their processing by gas phase reactions (e.g., photolysis of aldehydes) and (ii) the formation of unique products that do not have any efficient gas phase sources (e.g., dicarboxylic acids). We present measurements of DOC and select aldehydes in fog water at high elevation and intercepted clouds at a biogenically-impacted location (Whistler, Canada) and in fog water in a more polluted area (Davis, CA). Concentrations of formaldehyde, glyoxal and methylglyoxal were in the micromolar range and comprised ≤ 2% each individually of the DOC. Comparison of the DOC and aldehyde concentrations to those at other locations shows good agreement and reveals highest levels for both in anthropogenically impacted regions. Based on this overview, we conclude that the fraction of organic carbon (dissolved and insoluble inclusions) in the aqueous phase of clouds or fogs, respectively, comprises 2–~ 40% of total organic carbon. Higher values are observed to be associated with aged air masses where organics are expected to be more highly oxidised and, thus, more soluble. Accordingly, the aqueous/gas partitioning ratio expressed here as an effective Henry's law constant for DOC (KH*DOC) increases by an order of magnitude from 7 × 103 M atm−1 to 7 × 104 M atm−1 during the ageing of air masses. The measurements are accompanied by photochemical box model simulations. These simulations are used to contrast two scenarios, i.e., an anthropogenically vs. a more biogenically impacted one as being representative for Davis and Whistler, respectively. Since the simplicity of the box model prevents a fully quantitative prediction of the observed aldehyde concentrations, we rather use the model results to compare trends in aldehyde partitioning and ratios. They suggest that the scavenging of aldehydes by the aqueous phase can reduce HO2 gas phase levels significantly by two orders of magnitude due to a weaker net source of HO2 production from aldehyde photolysis in the gas phase. Despite the high solubility of dicarbonyl compounds (glyoxal, methylglyoxal), their impact on the HO2 budget by scavenging is < 10% of that of formaldehyde. The overview of DOC and aldehyde measurements presented here reveals that clouds and fogs can be efficient sinks for organics, with increasing importance in aged air masses. Even though aldehydes, specifically formaldehyde, only comprise ~ 1% of DOC, their scavenging and processing in the aqueous phase might translate into significant effects in the oxidation capacity of the atmosphere.


1985 ◽  
Vol 63 (12) ◽  
pp. 2332-2339 ◽  
Author(s):  
L. G. Goldsborough ◽  
G. G. C. Robinson

Annual sequences of biomass, species diversity, and community composition of epiphytic diatoms on a dense mat of Lemna minor L. growing in a freshwater marsh are described. In 2 successive years, maximum biomass occurred in early spring prior to occlusion of the water surface by the mat, while diversity reached relative maxima in the early summer (during a period of declining total biomass) and late fall. Ambient air temperature (possibly through a relationship with in situ metabolic activity and nutrient availability) was significantly correlated with community ordination scores on a temporal basis. Depth profile maxima of diatom abundance on vertically positioned artificial substrata occurred below the mat, suggesting that light limitation of algal growth within dense mats may be of lesser importance. Dominant diatom species in the spring and fall were generally ubiquitous in the surrounding marsh, while the major taxa in midsummer, Achnanthes hungarica, Amphora veneta, and Navicula twymaniana, may be specific to the Lemna microhabitat. The development of algal community specificity within a defined seasonal range is discussed in terms of the relative importance of host exudates versus exogenous nutrients as the basis for algal-substratum associations.


2009 ◽  
Vol 66 (9) ◽  
pp. 1522-1531 ◽  
Author(s):  
M. Demarty ◽  
Y. T. Prairie

We studied the in situ release of dissolved organic carbon (DOC) by growing a submerged freshwater macrophyte–epiphyte complex. Incubations with benthic chambers in five southeastern Quebec lakes show a net DOC production for different communities of Myriophyllum spicatum and Potamogeton spp. Daytime DOC release rates range from undetectable to 9.7 mg C·m–2·h–1. Although DOC release was restricted to daylight hours and thus suggestive of a photosynthesis-related process, we found no strong link between DOC release rates and concurrent illumination or temperature. We found no difference in DOC release rates between the three main colonizing species of the studied region. The overall mean DOC release rate was 4.57 mg C·m–2·h–1 (standard deviation (SD), ±0.65) or 56 µg C·g dry weight–1·h–1 (SD, ±8), which we suggest can be used for extrapolations at the lake scale.


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