scholarly journals Effects of nitrate and phosphate supply on chromophoric and fluorescent dissolved organic matter in the Eastern Tropical North Atlantic: a mesocosm study

2015 ◽  
Vol 12 (10) ◽  
pp. 7209-7255
Author(s):  
A. N. Loginova ◽  
C. Borchard ◽  
J. Meyer ◽  
H. Hauss ◽  
R. Kiko ◽  
...  

Abstract. The Eastern Tropical North Atlantic (ETNA) is an open ocean region with little input of terrestrial dissolved organic matter (DOM), suggesting that pelagic production has to be the main source of DOM. Inorganic nitrogen (DIN) and phosphorus (DIP) concentrations affect pelagic production, leading to DOM modifications. The quantitative and qualitative changes in DOM are often estimated by its optical properties. Colored DOM (CDOM) is often used to estimate dissolved organic carbon (DOC) concentrations by applied techniques, e.g. through remote sensing, whereas DOM properties, such as molecular weight, can be estimated from the slopes of the CDOM absorption spectra (S). Fluorescence properties of CDOM (FDOM) allow discriminating between different structural CDOM properties. The investigation of distribution and cycling of CDOM and FDOM was recognized to be important for understanding of physical and biogeochemical processes, influencing DOM. However, little information is available about effects of nutrient variability on CDOM and FDOM dynamics. Here we present results from two mesocosm experiments conducted with a natural plankton community of the ETNA, where effects of DIP ("Varied P") and DIN ("Varied N") supply on optical properties of DOM were studied. CDOM accumulated proportionally to phytoplankton biomass during the experiments. S decreased over time indicating accumulation of high molecular weight DOM. In Varied N, an additional CDOM portion, as a result of bacterial DOM reworking, was determined. It increased the CDOM fraction in DOC proportionally to the supplied DIN. The humic-like FDOM component (Comp.1) was derived by bacteria proportionally to DIN supply. The bound-to-protein amino acid-like FDOM component (Comp.2) was released irrespectively to phytoplankton biomass, but depending on DIP and DIN concentrations, as a part of an overflow mechanism. Under high DIN supply, Comp.2 was removed by bacterial reworking processes, leading to an accumulation of humic-like Comp.1. No influence of nutrient availability on amino acid-like FDOM component in peptide form (Comp.3) was observed. Comp.3 potentially acted as an intermediate product during formation or degradation Comp.2. Our findings suggest that changes in nutrient concentrations may lead to substantial responses in the quantity and "quality" of optically active DOM and, therefore, might bias results of the applied techniques for an estimation of DOC concentrations in open ocean regions.

2015 ◽  
Vol 12 (23) ◽  
pp. 6897-6914 ◽  
Author(s):  
A. N. Loginova ◽  
C. Borchard ◽  
J. Meyer ◽  
H. Hauss ◽  
R. Kiko ◽  
...  

Abstract. In open-ocean regions, as is the Eastern Tropical North Atlantic (ETNA), pelagic production is the main source of dissolved organic matter (DOM) and is affected by dissolved inorganic nitrogen (DIN) and phosphorus (DIP) concentrations. Changes in pelagic production under nutrient amendments were shown to also modify DOM quantity and quality. However, little information is available about the effects of nutrient variability on chromophoric (CDOM) and fluorescent (FDOM) DOM dynamics. Here we present results from two mesocosm experiments ("Varied P" and "Varied N") conducted with a natural plankton community from the ETNA, where the effects of DIP and DIN supply on DOM optical properties were studied. CDOM accumulated proportionally to phytoplankton biomass during the experiments. Spectral slope (S) decreased over time indicating accumulation of high molecular weight DOM. In Varied N, an additional CDOM portion, as a result of bacterial DOM reworking, was determined. It increased the CDOM fraction in DOC proportionally to the supplied DIN. The humic-like FDOM component (Comp.1) was produced by bacteria proportionally to DIN supply. The protein-like FDOM component (Comp.2) was released irrespectively to phytoplankton or bacterial biomass, but depended on DIP and DIN concentrations. Under high DIN supply, Comp.2 was removed by bacterial reworking, leading to an accumulation of humic-like Comp.1. No influence of nutrient availability on amino acid-like FDOM component in peptide form (Comp.3) was observed. Comp.3 potentially acted as an intermediate product during formation or degradation of Comp.2. Our findings suggest that changes in nutrient concentrations may lead to substantial responses in the quantity and quality of optically active DOM and, therefore, might bias results of the applied in situ optical techniques for an estimation of DOC concentrations in open-ocean regions.


Water ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1967 ◽  
Author(s):  
Min Xiao ◽  
Fengchang Wu ◽  
Yuanbi Yi ◽  
Zenglei Han ◽  
Zhongliang Wang

Characterization of dissolved organic matter (DOM) is useful in understanding environment quality and carbon cycling in the lake system. In this study, the fluorescence of DOM, major ions, and nutrients in water were investigated to understand the sources and the transformation of DOM in Dianchi Lake, the sixth largest freshwater lake in China. The dissolved organic carbon content in water above the deposition layer was higher than 5 mg C∙L−1 but lower than that in pore water. Two primary components of humic (C1) and protein-like components (C2) were identified using parallel factor (PARAFAC) modeling on sample fluorescence spectra. Organic components were related to mineral structures, and encapsulation of bacterial or algal cells into particulates could be disintegrated to release DOM. The aromaticity and the hydrophobicity of optical properties were regulated by percentages of chromophores (CDOM) of DOM in surface water, whereas by percentages of fluorophores (FDOM) in DOM in pore water, the underlying water layer was defined as a belt of transition. The molecular weight enhanced with percentages of C1 in CDOM increased in water above the sediment layer and the pore water at the northern lake site, but molecular weight attenuated with percentages decreased in pore water at the southern lake site. DOM not only originated from particulate decomposition but also derived from internal transformation among different, dissolved organic molecules. Small molecules were aggregated into larger ones, and, conversely, large molecules decomposed into small sizes. Another speculation is that dissolved molecules adsorbed or were encapsulated into particulates or were degraded and released into dissolved phases. The precise factors regulated composition, structure, and spectral properties of dissolved organic matter in the Dianchi Lake. This study highlights that sources of DOM and transformation mechanisms in the lake water could be correlated with nutrients and primary geochemical factors for mobility and distribution in different water compartments.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
J. Fouché ◽  
C. T. Christiansen ◽  
M. J. Lafrenière ◽  
P. Grogan ◽  
S. F. Lamoureux

Abstract Permafrost degradation may lead to mobilization of carbon and nutrients and enhance microbial processing rates of previously frozen organic matter. Although the pool size and chemical composition of dissolved organic matter (DOM) are fundamental determinants of the carbon cycle in Arctic watersheds, its source within the seasonally thawing active layer and the underlying permafrost remains largely uncharacterized. Here, we used 25 soil cores that extended down into the permafrost from nine sites across Arctic Canada to quantify dissolved organic carbon (DOC) and nitrogen stocks, and to characterize DOM optical properties. Organic permafrost stores 5–7 times more DOC and ammonium than the active layer and mineral permafrost. Furthermore, the permafrost layers contain substantial low molecular weight DOM with low aromaticity suggesting high biodegradability. We conclude that soil organic matter stoichiometry and cryogenic processes determine permafrost DOM chemistry, and that thawing will mobilize large amounts of labile DOC and ammonium into Arctic watersheds.


Author(s):  
K. Avarachen Mathew ◽  
Murat Van Ardelan ◽  
Susana Villa Gonzalez ◽  
Olav Vadstein ◽  
S. Vezhapparambu Veena ◽  
...  

2008 ◽  
Vol 5 (2) ◽  
pp. 281-298 ◽  
Author(s):  
P. Raimbault ◽  
N. Garcia ◽  
F. Cerutti

Abstract. During the BIOSOPE cruise the RV Atalante was dedicated to study the biogeochemical properties in the South Pacific between the Marquesas Islands (141° W–8° S) and the Chilean upwelling (73° W–34° S). Over the 8000 km covered by the cruise, several different trophic situations were encountered, in particular strong oligotrophic conditions in the South Pacific Gyre (SPG, between 123° W and 101° W). In this isolated region, nitrate was undetectable between the surface and 160–180 m and only trace quantities (<20 nmoles l−1) of regenerated nitrogen (nitrite and ammonium) were detected, even in the subsurface maximum. Integrated nitrate over the photic layer, which reached 165 m, was close to zero. Despite this severe nitrogen-depletion, phosphate was always present in significant concentrations (≈0.1 μmoles l−1), while silicic acid was maintained at low but classical oceanic levels (≈1 μmoles l−1). In contrast, the Marquesas region (MAR) to the west and Chilean upwelling (UPW) to the east were characterized by high nutrient concentrations, one hundred to one thousand fold higher than in the SPG. The distribution of surface chlorophyll reflected the nitrate gradient, the lowest concentrations (0.023 nmoles l−1) being measured at the centre of the SPG, where integrated value throughout the photic layer was very low (≈ 10 mg m−2). However, due to the relatively high concentrations of chlorophyll-a encountered in the DCM (0.2 μg l−1), chlorophyll-a concentrations throughout the photic layer were less variable than nitrate concentrations (by a factor 2 to 5). In contrast to chlorophyll-a, integrated particulate organic matter (POM) remained more or less constant along the study area (500 mmoles m−2, 60 mmoles m−2 and 3.5 mmoles m−2 for particulate organic carbon, particulate organic nitrogen and particulate organic phosphorus, respectively), with the exception of the upwelling, where values were two fold higher. The residence time of particulate carbon in the surface water was only 4–5 days in the upwelling, but up to 30 days in the SPG, where light isotopic δ15N signal noted in the suspended POM suggests that N2-fixation provides a dominant supply of nitrogen to phytoplankton. The most striking feature was the large accumulation of dissolved organic matter (DOM) in the SPG compared to the surrounding waters, in particular dissolved organic carbon (DOC) where concentrations were at levels rarely measured in oceanic waters (>100 μmoles l−1). Due to this large pool of DOM in the SPG photic layer, integrated values followed a converse geographical pattern to that of inorganic nutrients with a large accumulation in the centre of the SPG. Whereas suspended particulate matter in the mixed layer had a C/N ratio largely conforming to the Redfield stochiometry (C/N≈6.6), marked deviations were observed in this excess DOM (C/N≈16 to 23). The marked geographical trend suggests that a net in situ source exists, mainly due to biological processes. Thus, in spite of strong nitrate-depletion leading to low chlorophyll biomass, the closed ecosystem of the SPG can accumulate large amounts of C-rich dissolved organic matter. The implications of this finding are examined, the conclusion being that, due to weak lateral advection, the biologically produced dissolved organic carbon can be accumulated and stored in the photic layer for very long periods. In spite of the lack of seasonal vertical mixing, a significant part of new production (up to 34%), which was mainly supported by dinitrogen fixation, can be exported to deep waters by turbulent diffusion in terms of DOC. The diffusive rate estimated in the SPG (134 μmolesC m−2 d−1), was quite equivalent to the particles flux measured by sediments traps.


2017 ◽  
Vol 14 (7) ◽  
pp. 1825-1838 ◽  
Author(s):  
Anja Engel ◽  
Hannes Wagner ◽  
Frédéric A. C. Le Moigne ◽  
Samuel T. Wilson

Abstract. In the ocean, sinking of particulate organic matter (POM) drives carbon export from the euphotic zone and supplies nutrition to mesopelagic communities, the feeding and degradation activities of which in turn lead to export flux attenuation. Oxygen (O2) minimum zones (OMZs) with suboxic water layers (< 5 µmol O2 kg−1) show a lower carbon flux attenuation compared to well-oxygenated waters (> 100 µmol O2 kg−1), supposedly due to reduced heterotrophic activity. This study focuses on sinking particle fluxes through hypoxic mesopelagic waters (< 60 µmol O2 kg−1); these represent  ∼  100 times more ocean volume globally compared to suboxic waters, but they have less been studied. Particle export fluxes and attenuation coefficients were determined in the eastern tropical North Atlantic (ETNA) using two surface-tethered drifting sediment trap arrays with seven trapping depths located between 100 and 600 m. Data on particulate matter fluxes were fitted to the normalized power function Fz =  F100 (z∕100)−b, with F100 being the flux at a depth (z) of 100 m and b being the attenuation coefficient. Higher b values suggest stronger flux attenuation and are influenced by factors such as faster degradation at higher temperatures. In this study, b values of organic carbon fluxes varied between 0.74 and 0.80 and were in the intermediate range of previous reports, but lower than expected from seawater temperatures within the upper 500 m. During this study, highest b values were determined for fluxes of particulate hydrolyzable amino acids (PHAA), followed by particulate organic phosphorus (POP), nitrogen (PN), carbon (POC), chlorophyll a (Chl a) and transparent exopolymer particles (TEP), pointing to a sequential degradation of organic matter components during sinking. Our study suggests that in addition to O2 concentration, organic matter composition co-determines transfer efficiency through the mesopelagic. The magnitude of future carbon export fluxes may therefore also depend on how organic matter quality in the surface ocean changes under influence of warming, acidification and enhanced stratification.


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