Measurements of dissolved organic carbo ,

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Seamounts and organic matter—Is there an effect? The case of Sedlo and Seine seamounts,Part 2. Composition of suspended particulate organic matter

The suspended particulate organic matter (sPOM) around two isolated NE Atlantic seamounts, Seine (33°46′N 14°21′W; summit at ∼170 m) and Sedlo (40°19′N 26°40′W; summit at ∼780 m), was studied over a period of 2 years during four 2–4-week oceanographic surveys. Elemental (C and N), chlorophyll a and lipid biomarker concentrations and N stable isotopic values were variable close to the surface (40–90 m), although some chlorophyll a enrichment above the summits was discerned sporadically. Results from near-surface waters showed a generally “fresh”, mainly phytoplankton signature in sPOM with some seasonality, which was more pronounced around Sedlo. sPOM concentrations and composition changed with depth, apparently controlled by seasonality and proximity to the seamounts. A few metres above the Seine summit, the suspended particulate organic carbon (sPOC) concentrations and labile polyunsaturated fatty acids (% of lipids) were higher than elsewhere at similar depths (∼200 m) in summer 2004. In the same season at Sedlo, polyunsaturated fatty acids were also relatively more abundant (up to 43% of total lipids) around the topographic feature throughout the water column, indicating supply of more labile sPOM, perhaps by advection, downwelling or passive sinking of locally produced phytoplankton and/or in situ production. The high-quality sPOM that seems to be present around the seamounts could provide an important food source to the biological community.     

Seamounts and organic matter—Is there an effect? The case of Sedlo and Seine Seamounts: Part 1. Distributions of dissolved and particulate organic matter

The temporal and spatial variability in the water-column distribution of dissolved organic carbon (DOC), and the particulate organic matter, collected both with bottles (POM-b) and in situ pumps (POM-p), was studied around Sedlo and Seine, two seamounts located in subtropical waters of the northeast Atlantic Ocean. Seine and Sedlo presented high POM-b concentrations, compared with reported background concentrations from the Azores-Madeira region, although our results show large regional, temporal and intra-seamount variability around the two seamounts. On the contrary, the POM-p pool, which contributed only 25–56% of the POC-b at surface, represented a fairly constant fraction of the suspended POM. Seine was characterized by higher POC-b concentrations than Sedlo, presumably as result of a combined mechanism of advection from the far field, and retention/accumulation of organic carbon, favoured by the secondary circulation around the seamount. Passive accumulation of POM-b was also evident at the southern flank of Sedlo during one the surveys, coinciding with a change in the local circulation around the seamount caused by the intrusion of a Mediterranean water eddy (Meddy). Average PON concentrations at the two seamounts were comparable in magnitude, and hence the C/N ratios were higher in Seine, adding support to the hypothesis of advection of allochtonous highly refractory organic matter into Seine. The contribution of DOC to the apparent oxygen utilization (AOU) in the upper 1000 m was significantly higher in Seine (25%) than in Sedlo (11%). This points to a proportionally more important role of dissolved material to the overall carbon remineralization rates in the water column of Seine.     

Distribution of dissolved organic carbon in and near the Prydz Bay, Antarctica

INTRODUCTIONDissolvedorganiccarbon (DOC)makesupthesecondlargestofthebioactivepoolsofcar bonintheocean ,secondtothelargestpoolofdissolvedinorganiccarbon .Theglobaldissolvedorganiccarbonpoolisestimatedtobe 6 85Gt,avaluecomparabletothemassofCO2 intheat mosphere (Hedges,1 992 ) .Thesizeofthereservoir,aswellasitsdynamics ,indicatesthatDOCplaysacentralroleintheoceancarboncycle .AsitrelatestogreenhousegasessuchasCO2 andassociatesclimatecycle ,oceanicDOCbiogeochemicalcycleshavebeenoneoftheh…     

River or mangrove? Tracing major organic matter sources in tropical Brazilian coastal waters

The influence of mangrove-fringed tropical estuaries on coastal carbon budgets has been widely recognised. However, a quantitative differentiation between riverine and mangrove-derived inputs to the dissolved (DOM) and microparticulate organic matter (POM) pool of these environments has been hitherto not possible. Based on lignin-derived phenols and stable carbon isotopes a chemical signature for mangrove, terrestrial and marine-derived organic matter was established for a mangrove estuary in North Brazil. A mixing model was applied to calculate the contribution of each of the three sources to the DOM and POM pool in the estuary throughout 18 tidal cycles in the course of one year. Best source assignment for POM was reached with the yield of lignin phenols and δ¹³C as paired indicators, while the origin of DOM was best identified by the yield of lignin phenols and the acid to aldehyde ratio of vanillyl phenols. Although only about 6% of the fluvial catchment area is covered by mangroves, their contribution to the estuarine DOM and POM pool generally exceeded several times the terrigenic input from the hinterland. This outwelling of mangrove-derived organic matter was enhanced during the rainy season. DOM and POM were exported from the mangrove to the estuary in similar proportions. Most mangrove-POM was rapidly removed from the water column, while mangrove-DOM behaved conservatively. In contrast, terrestrial DOM was almost entirely removed in the outer part of the estuary, which was accompanied by a concomitant increase in terrestrial POM. This seems to be the result of a geochemical barrier zone for this type of DOM in the estuary. Generally, a high proportion of mangrove-DOM was present in the outer part of the estuary, even at high tide. This indicates DOM outwelling from mangroves in adjacent bays or estuaries and points to similar driving forces controlling this process on a regional scale. Mangroves probably play a more important role than rivers for marine carbon budgets along the North Brazilian coast south of the Amazon estuary.     

Variation of reactivity of particulate and sedimentary organic matter along the Zhujiang River Estuary

To investigate organic matter source and reactivity in the Zhujiang River (Pearl River)Estuary and its adjacent areas, particulate organic carbon (POC), particulate hydrolysable amino acids (PHAA), and Chl a during two cruises in July 1999 and July 2000 were measured. The highest POC and PHAA concentration was observed in the waters with maximum Chl a. The spectra distribution,relative content (dry weight in milligram per gram), PHAA-C% POC and other indicators such as the ratios of amino acids vs. amino sugars (AA/AS) and glucosamine vs. galactosamine (Glum/Gal) suggested that particulate amino acids in the water column and sediments in the Zhujiang River Estuary were mainly derived from biogenic processes rather than transported from terrestrial erosion. In inner estuary where high turbidity was often observable, organic matter was mainly contributed by re-suspension of bottom sediments with revealed zooplankton, microbial reworked characteristics, which suggest that these organic matters were relatively “old“. In the estuarine brackish region, organic matter in water column is mainly contributed by relatively fresh, easily degradable phytoplankton derived organic matter.During physical - biological processes within the eastuary, organic matter derived from phytoplankton was subjected to alteration by zooplankton grazing and bacterial reworking.     

Nitrogen forms and decomposition of organic carbon in the southern Bohai Sea core sediments

Study on form characteristics of nitrogen in marine sediments is the primary method to research its biogeochemical cycling and nitrogen form characteristics in core sediments can reflect the process and results of early diagenesis in a certain degree. In this paper, Sequential extraction process in natural grain size was used for studying the existent forms of nitrogen in five core sediments of the southern Bohai Sea for the first time. Nitrogen was divided into two parts -transferable and fixed based on whether it could be extracted by the reagent. Distributions and early diagenesis of transferable nitrogen forms in the southern Bohai Sea were researched integratedly. Results indicate that IEF - N and OSF-N are predominant forms in transferable part in the studied core sediments. Contents of different nitrogen forms vary differently with depth, and have different diagenesis process. Decomposition constant of organic nitrogen (ON) and OC are about 15.51 × 10~(-3)a~(-1)and 4.79× 10~(-3)a~(-1) respective     

Microbial enzymatic response to catchment‐scale variations in supply of dissolved organic carbon

A suite of exoenzyme activities was assayed in three New Zealand streams draining pasture, native forest, and a pine catchment. There were differences among catchments in activity of three of the five enzymes assayed (cello‐biohydrolase, N‐acetylglucosaminidase, and dihydroxylphenylalanine oxidation). A principal components analysis (PCA) demonstrates that patterns of enzyme activity can be used to separate the three stream types. An experimental addition of algal‐leachate, leaf‐litter leachate, and high dissolved organic carbon (DOC) water from a small seep also resulted in marked shifts in epilithic enzyme activities 1 day after DOC additions. Oxidative enzymes showed a particularly strong response to additions of humic DOC. As for the field samples, a PCA showed large differences among treatments indicating that exoenzyme patterns can be used to examine which DOC sources predominate in different streams. Application of this approach to describing differences among streams will require detailed seasonal sampling together with longer‐term experiments.     

Sources and transport of particulate organic carbon in the Amazon River and its estuary

Stable carbon isotope ratios have been used to study the sources of particulate organic carbon(POC) in the Amazon River and its tributaries, and to examine the transport of the riverine POC intothe oceanic environment. POC in the upper reaches of the Amazon River has more positive δ ~(13)C values(--24.5‰ to -- 28.0‰) than that in the middle and lower reaches (--27.9‰ to -- 30.1‰). Theδ ~(13)C of POC from the tributaries is generally more negative than that observed in the Amazon mainchannel. This δ ~(13)C datum shows that the POC in the Amazon main channel is predominantly of terres-trial origin rather than a result of in situ production. A large range of δ ~(13)C values (--17.5‰ to -28.4‰) is observed in the Amazon Estuary and plume. and is considered as the result of the mixing     

Lignin phenols used to infer organic matter sources to Sepetiba Bay – RJ,Brasil

Lignin phenols were measured in the sediments of Sepitiba Bay, Rio de Janeiro, Brazil and in bedload sediments and suspended sediments of the four major fluvial inputs to the bay; São Francisco and Guandu Channels and the Guarda and Cação Rivers. Fluvial suspended lignin yields (Σ8 3.5–14.6 mgC 10 g dw⁻¹) vary little between the wet and dry seasons and are poorly correlated with fluvial chlorophyll concentrations (0.8–50.2 μgC L⁻¹). Despite current land use practices that favor grassland agriculture or industrial uses, fluvial lignin compositions are dominated by a degraded leaf-sourced material. The exception is the Guarda River, which has a slight influence from grasses. The Lignin Phenol Vegetation Index, coupled with acid/aldehyde and 3.5 Db/V ratios, indicate that degraded leaf-derived phenols are also the primary preserved lignin component in the bay. The presence of fringe Typha sp. and Spartina sp. grass beds surrounding portions of the Bay are not reflected in the lignin signature. Instead, lignin entering the bay appears to reflect the erosion of soils containing a degraded signature from the former Atlantic rain forest that once dominated the watershed, instead of containing a significant signature derived from current agricultural uses. A three-component mixing model using the LPVI, atomic N:C ratios, and stable carbon isotopes (which range between –26.8 and –21.8‰) supports the hypothesis that fluvial inputs to the bay are dominated by planktonic matter (78% of the input), with lignin dominated by leaf (14% of the input) over grass (6%). Sediments are composed of a roughly 50–50 mixture of autochthonous material and terrigenous material, with lignin being primarily sourced from leaf.     

Analytical procedures to classify organic pollutants in natural waters, sediments, and benthic organisms

Procedures are described to extract, fractionate and analyze organic pollutants in environmental samples. The methods are based on organic solvent extraction to isolate the pollutants, liquid-solid adsorption chromatography to separate the various pollutants into four fractions, and analyses of the fractions using glass capillary gas-chromatography. Based on a number of considerations, the procedures were found suitable for the analyses of trace level organic pollutants in a variety of sample types. The data from these studies has provided important information on the biogeochemistry of organic pollutants in the aquatic environment.     

Does planktonic community structure determine downward particulate organic carbon flux in different oceanic provinces?

A previous study based on data from a NE Atlantic site provided evidence, using an existing foodweb/vertical-flux modelling approach, that the size-structure of the phytoplankton community — rather than primary production — can be the dominant control on downward particulate organic carbon (POC) flux. In order to assess whether taking community structure into account can also provide more reliable estimates of downward POC flux in other oceanic provinces, epipelagic observations (mainly size-fractionated primary production, biomass, community structure data and heterotrophic bacterial production) and POC flux data from deep-moored sediment traps were collated from the six different ocean regions for which suitable data are available. At each site the epipelagic data were used in conjunction with two standard versions of the foodweb/vertical-flux model (one permits direct sinking of large ungrazed algae out of surface waters, the other does not) and published empirical depth/POCflux algorithms to predict the POC flux to the deep ocean. Predictions were also made using published primary-production/POC-flux algorithms, and the two sets of predictions were compared to the deep-ocean POC flux measurements. While the version of the foodweb/ vertical-flux model permitting the direct sinking of ungrazed algae provided the most reliable predictor of POC flux for five of the six sites, no conventional algorithm provided comparable predictions for more than two sites. The reliability of these predictions is discussed in the context of recent modelling studies that explore the extent to which flow fields in the water column overlying deep-moored sediment traps confound attempts to relate particle flux measurements to observations of surface-water processes. The present study suggests that the sinking of ungrazed large cells, probably diatoms, may be the key determinant of the magnitude of the downward POC flux in a variety of ocean regions. Planned ocean-observing programmes may provide sufficient epipelagic data to allow this approach to be used to improve the accuracy of basin-scale estimates of downward POC flux and hence reduce the uncertainty of the magnitude of this flux within the oceanic carbon budget.     

Measurements of dissolved organic carbon (DOC) in sea water by high temperature combustion method

Dissolved organic carbon (DOC) is the largest organic carbon reservoir in sea water and plays an imporrant role in the marine carbon cycle and other biogeochemical processes in the ocean. Accurate and precise determinalion of the bOC concentration in sea water is thus a prerequisite for any interpretation of DOC biogeochemistry. A key factor in analytical quality control is an accurate determination of the blank. The assessment and distinction of DOC blanks are essential for the precise measurements of oceanic DOC. The total DOC blank includes instrument and water blanks in the high temperature catalytic oxidation (HTCO) method. DOC can be measured accurately using the HTCO method only when the instrument blank is correctly distinguished from the total DOC blank and corrected in the sample measurements. Low DOC blanks can be achieved by extensive conditioning of new catalysts and the whole instrument system, whereas instrument blanks can be quantified by subtracting the water blank from the total DOC blank. We have been able to produce low carbon nanopure water [≤2μmol/dm³(C)] and have a low instrumental blank [< 5-6 μmol/dm³(C)] when using the HTCO method. Results of concentrations and distributions of DOC in the Gulf of Mexico and the North Atlantic are oceanographically consistent. Results from DOC measurements on samples from the international DOC methods comparison program further confirmed our low values of both nenopure water and the instrument blank.     

Structural and functional shifts in zoobenthos induced by organic enrichment — Implications for community recovery potential

Habitat change induced by organic enrichment is a growing concern for the sustainability of benthic communities in coastal aquatic environments. This case study describes the spatial and temporal response patterns and the recovery potential of low-diversity benthic communities to organic enrichment at two fish farm locations, during the rearing periods (15 and 20 years, respectively) and the following recovery periods (2 years). The spatial extent of disturbance differed depending on the hydromorphological characteristics of the rearing sites, but degraded macrobenthic communities close to both fish farms were recorded soon after the activity started. Continued organic enrichment resulted in high species turnover-rates and in an altered benthic community composition at both locations. After fish farm abatement, a partial recovery was detected in species richness, but abundance and biomass values were reduced and changes in structural composition remained. Alterations in benthic biological traits were observed at both fish farm locations, implying that organic enrichment might cause changes in benthic community function within low-diversity benthic communities.     

Resuspension-induced partitioning of organic carbon between solid and solution phases from a river–ocean transition

Laboratory experiments were conducted to evaluate the net exchange of organic carbon (OC) between sediments and overlying water during episodes of resuspension. Surface sediment samples collected from six locations within the Hudson River Estuary and the Inner New York Bight were resuspended in their respective bottom waters for periods ranging from 30 s to 2 h. After resuspension, dissolved organic carbon (DOC) concentration generally reached levels greater than that predicted by conservative mixing of pore water and bottom water, indicating net release of OC from the sediment particles. The amount of OC released during the 1-h extractions comprised ≤0.1% of the total sediment pool, but correlated positively (R²=0.65, P<0.052) with the amount of particulate organic carbon (POC) found in the high-density fraction of the sediment matrix. This suggests that the mineral-bound fraction of sedimentary OC was the major source for the excess DOC released into solution, and that across various sedimentary environments, only a small (but fairly constant) fraction of the total sedimentary POC may be poised for rapid transfer to the water column.     

Optical backscattering in the Arabian Sea—continuous underway measurements of particulate inorganic and organic carbon

Continuous surface measurements of temperature, salinity, fluorescence and optical backscattering were made during R/V Thompson cruise no. TN053 in the northern Arabian Sea (“Bio-Optical cruise”; October–November, 1995). The cruise covered the early NE monsoon period. Optical measurements involved alternate estimates of total backscattering and acidified backscattering approximately every 1.5–2 min (measured after addition of a weak acid to dissolve calcium carbonate). The difference between total and acidified backscattering equals “acid-labile backscattering”. Total and acid-labile backscattering were converted to the concentration of particulate organic carbon (POC) and particulate inorganic carbon (PIC; calcium carbonate), respectively, and discrete samples taken along the cruise track were used for calibration. Backscattering data were frequently coherent with temperature, salinity, and density variability. Acid-labile backscattering values revealed that calcium carbonate accounted for 10–40% of the total optical backscattering in the region, and the semi-continuous records demonstrated distinct patches of coccolith-rich water. The northern Arabian Sea had the highest acid-labile backscattering. Results suggest that PIC : POC ratios can vary over about four orders of magnitude. Highest surface values of PIC : POC approached one in several places. We also report qualitative observations of phytoplankton community structure made aboard ship, on fresh samples.     

Does sedimentary organic delta 13C record variations in quaternary ocean [CO2(aq)]?

Ocean surface water [CO2(aq)] variations based on glacial/interglacial changes in sediment delta 13Corg are shown to compare favorably with reconstructions based on ice core [CO2]. In particular, an approximate 80 microatmospheres increase in atmospheric pCO2 during the last glacial-interglacial transition is calculated to correspond to a 3-4 micromolar increase in ocean surface water [CO2(aq)] at atmospheric equilibrium. A widespread marine delta 13Corg decrease of 1-2% accompanied this event and was not preceded by an equivalent isotopic change in surface water total dissolved inorganic carbon. These observations support the hypothesis that [CO2(aq)] influences photosynthetic isotope fractionation between marine inorganic and organic carbon pools, and therefore that plankton/sediment delta 13Corg may serve as a proxy for surface water [CO2(aq)].     

Sources and implications of particulate organic matter from a small tropical river—Zuari River,India

Transitional ecosystems,estuaries and the coastal seas,are distinctively affected by natural and anthropogenic factors.Organic matter(OM)originating from terrestrial sources is exported by rivers and forms a key component of the global biogeochemical cycles.Most previous studies focused on the bulk biochemical and anthropogenic aspects affecting these ecosystems.In the present study,we examined the sources and fate of OM entrained within suspended particulate matter(SPM)of the Zuari River and its estuary,west coast of India.Besides using amino acid(AA)enantiomers(L-and D-forms)as biomarkers,other bulk biochemical parameters viz.particulate organic carbon(POC),δ13C,particulate nitrogen(PN),δ15N and chlorophyll a were analyzed.Surprisingly no significant temporal variations were observed in the parameters analyzed;nonetheless,salinity,POC,δ13C,PN,δ15N,glutamic acid,serine,alanine,tyrosine,leucine and D-aspartic acid exhibited significant spatial variability suggesting source differentiation.The POC content displayed weak temporal variability with low values observed during the post-monsoon season attributed to inputs from mixed sources.Estuarine samples were less depleted than the riverine samples suggesting contributions from marine plankton in addition to contributions from river plankton and terrestrial C3 plants detritus.Labile OM was observed during the monsoon and post-monsoon seasons in the estuarine region.More degraded OM was noticed during the pre-monsoon season.Principal component analysis was used to ascertain the sources and factors influencing OM.Principally five factors were extracted explaining 84.52%of the total variance.The first component accounted for 27.10%of the variance suggesting the dominance of tidal influence whereas,the second component accounted for heterotrophic bacteria and their remnants associated with the particulate matter,contributing primarily to the AA pool.Based on this study we ascertained the role of the estuarine turbidity maximum(ETM)controlling the sources of POM and its implications to small tropical rivers.Thus,changes in temporal and regional settings are more likely to affect the natural biogeochemical cycles of small tropical rivers.     

Dissolved organic nitrogen dynamics in the North Sea: A time series analysis (1995–2005)

Dissolved organic nitrogen (DON) dynamics in the North Sea was explored by means of long-term time series of nitrogen parameters from the Dutch national monitoring program. Generally, the data quality was good with little missing data points. Different imputation methods were used to verify the robustness of the patterns against these missing data. No long-term trends in DON concentrations were found over the sampling period (1995–2005). Inter-annual variability in the different time series showed both common and station-specific behavior. The stations could be divided into two regions, based on absolute concentrations and the dominant times scales of variability. Average DON concentrations were 11 μmol l⁻¹ in the coastal region and 5 μmol l⁻¹ in the open sea. Organic fractions of total dissolved nitrogen (TDN) averaged 38 and 71% in the coastal zone and open sea, respectively, but increased over time due to decreasing dissolved inorganic nitrogen (DIN) concentrations. In both regions intra-annual variability dominated over inter-annual variability, but DON variation in the open sea was markedly shifted towards shorter time scales relative to coastal stations. In the coastal zone a consistent seasonal DON cycle existed with high values in spring–summer and low values in autumn–winter. In the open sea seasonality was weak. A marked shift in the seasonality was found at the Dogger Bank, with DON accumulation towards summer and low values in winter prior to 1999, and accumulation in spring and decline throughout summer after 1999. This study clearly shows that DON is a dynamic actor in the North Sea and should be monitored systematically to enable us to understand fully the functioning of this ecosystem.     

Does suspended matter drained from the Isahaya freshwater reservoir cause organic enrichment in the northern Ariake Bay?

The inner part of Isahaya Bay was converted to a freshwater reservoir following the closure of the land claim dike in 1997. Turbid water drains into Isahaya Bay when water levels increase. We investigated whether particulate organic matter (POM) from the reservoir in Isahaya Bay has caused bottom organic enrichment in the northern part of Ariake Bay. Using potential end-members from before to after the rainy seasons, during which a frequent discharge from the reservoir was expected, stable isotope analyses were performed on sediments collected from Isahaya Bay and northern Ariake Bay. Each end-member was isotopically differentiated by δ¹³C and δ¹⁵N (riverine POM: ?28.5 to ?27.2‰ and 3.3–4.6‰; reservoir POM: ?25.7 to ?25.3‰ and 7.4–8.4‰; marine POM: ?21.8 to ?19.7‰ and 6.7–7.6‰; microphytobenthos estimated from consumers: ?16.1 to ?15.9‰ and 5.2–6.1‰, respectively). Sediment isotopic signatures fell within the mixing space defined by the signatures of the end-members. Marine POM contributed greatly to bottom sediments in both seasons in Isahaya Bay and Ariake Bay, ranging from ca. 60–70 and 40–60%, respectively. Reservoir POM contributed around 10% to bottom sediments. This percentage slightly increased in the sediment of Isahaya Bay after the rainy season, but decreased in the sediment of Ariake Bay. Thus, most of the POM discharged from the reservoir would not reach the northern part of Ariake Bay and would not be a major contributor to organic enrichment. This study is the first to quantitatively describe the contribution of drained reservoir POM outside Isahaya Bay.