Thermogenic organic matter dissolved in the abyssal ocean

Formation and decay of thermogenic organic matter are important processes in the geological carbon cycle, but little is known about the fate of combustion-derived and petrogenic compounds in the ocean. We explored the molecular structure of marine dissolved organic matter (DOM) for thermogenic signatures in different water masses of the Southern Ocean. Ultrahigh-resolution mass spectrometry via the Fourier transform-ion cyclotron resonance technique (FT-ICR-MS) revealed the presence of polyaromatic hydrocarbons (PAHs) dissolved in the abyssal ocean. More than 200 different PAHs were discerned, most of them consisting of seven condensed rings with varying numbers of carboxyl, hydroxyl, and aliphatic functional groups. These unambiguously thermogenic compounds were homogenously distributed in the deep sea, but depleted at the sea surface. Based on the structural information alone, petrogenic and pyrogenic compounds cannot be distinguished. Surface depletion of the PAHs and first estimates for their turnover rate (> 1.2 · 10¹² mol C per year) point toward a primarily petrogenic source, possibly deep-sea hydrothermal vents, which is thus far speculative because the fluxes of combustion-derived and petrogenic matter to the ocean are not well constrained. We estimate that > 2.4% of DOM are thermogenic compounds, and their global inventory in the oceans is > 1.4 · 10¹⁵ mol C, significantly impacting global biogeochemical cycles.     

Marine organisms and their contribution to organic matter in the ocean

The best estimates of marine biomass can be made for the algal component. Estimates of the biomass of small animals and bacteria both in the water column and the sediment remain beset with sampling and enumeration problems and, in the past, the contribution of the microfauna has often been ignored.Marine phytoplankton are the major source of organic matter in the oceans by means of photosynthesis but their contribution is not necessarily related to the size of the organism. In some instances the nanoplankton are the major contributors. Factors affecting distribution and production are discussed.The chemical composition of phytoplankton production and variation within it is less well understood. The amount, nature, variation, and mechanism of extracellular production, of algal spoliation during ingestion by herbivores, of algal autolysis and of herbivore excretory products is not well understood and neither is the relative contribution to the non-living “dissolved” and “particulate” organic carbon pools.     

Fractionation during remineralization of organic matter in the ocean

Remineralization ratios (–O₂:P, C_org.:P, N:P) in the ocean are estimated from ocean tracer data using a new approach, which takes into account the effects of local exchange across neutral surfaces. This approach is applied to temperature, salinity, phosphate, nitrate, dissolved oxygen, alkalinity, and dissolved inorganic carbon data from the low- and mid-latitude Pacific, Indian, and South Atlantic Oceans. The consideration of local exchange effects tends to reduce the –O₂:P and C_org.:P remineralization estimates above 1500 m compared to earlier estimates. Below 1500 m, exchange effects can be neglected (except in the South Atlantic) and earlier estimates appear robust. In the deep South Atlantic, the consideration of these effects leads to increased –O₂:P and C_org.:P remineralization ratio estimates, bringing them more in line with the robust deep ocean estimates. For reasonable, open ocean mixing coefficient values and several choices for phosphate remineralization rate profiles, –O₂:P (C_org.:P) remineralization ratios in the ocean increase from about 140 (100) at 750 m depth to about 170 (130) at 1500 m and remain so deeper down. Such an increase down through the upper ocean thermocline implies significant fractionation during remineralization of organic matter—nutrients are released higher in the water column than inorganic carbon. These results also argue for a –O₂:P (C_org.:P) uptake ratio in new production of about 140–150 (100–110). N:P remineralization ratios decrease from about 15 at 750 m to about 12 at 1500–2000 m. This may reflect a “true” N:P remineralization (and uptake) ratio of about 16, modified by denitrification.These results imply that applications of derived, quasi-conservative tracers, based on the assumption of constant remineralization ratios, may be subject to significant error for depths less than 1500 m. In addition, present Ocean General Circulation Models of the natural carbon cycle in the ocean–atmosphere system assume remineralization to occur without fractionation but have problems simulating observed, pre-industrial levels of atmospheric pCO₂, given observed ocean inventories of alkalinity and dissolved inorganic carbon. Implementation of uptake and (depth-dependent) remineralization ratios estimated here would likely reduce this problem considerably. Furthermore, calculations with a simple global carbon cycle model show that fractionation in the modern ocean, as estimated in the present work, has reduced atmospheric pCO₂ by more than 20 ppm below the level it would have had without fractionation.     

Chemical studies on organic matter and carbon cycle in the ocean

Chemistry of organic materials of the suspended and sinking particles, and the evaluation of the particulate materials for the carbon cycle of the ocean are described in this paper. Organic carbon (POC) and nitrogen (PON) of the suspended particles collected from various areas of the North through South Pacific were determined with considerably high variabilities in their concentration. Higher values of the POC and PON were obtained in the surface water of the higher latitudinal areas of both northern and southern hemispheres and the equatorial Pacific, while the lower values of these organic elements were measured in the middle latitudinal areas of the Pacific. These facts clearly indicate that inorganic nutrients supply to the surface water layers from the underlying water is primarily determinative factor to govern the concentration of the POC and PON in the surface water layer. POC and PON concentrations in the intermediate through deep waters, however, are much less variable in time and space. Carbohydrates, free and combined amino acids and lipid materials were major organic constituents of the suspended particles. The organic composition of the particles was extensively variable in region, time and depth. Such change in the organic composition was mainly caused by the production and decay of the free and combined amino acids, lipid materials and water extractable carbohydrate. Sinking particle which has high sinking rate over 100 m day⁻¹ and can be collected only by sediment trap, also consists of carbohydrates, free and combined amino acids and lipid materials. A detailed analysis of the particle indicate that the sinking particle was much different from the suspended particle from the intermediate through deep waters in terms of the abundance of the biologically susceptible organic materials such as unsaturated hydrocarbon, fatty acid and water extractable carbohydrate often found in phytoplankton. These facts clearly indicate that the sinking particle plays an important role on the vertical transport of the biologically susceptible organic materials from the surface water to the deep water. Vertical flux of organic materials in various water depths was extensively measured in the North Pacific and Antarctic Ocean using the depth-series sediment trap system to collect the sinking particles from various depths of the waters. Regional and seasonal variabilities of the organic carbon flux at the various depths were obviously observed, however the attenuation rate of the organic carbon flux in the intermediate through deep water was not changed so much irrespective of the sampling time and region. The time-series sediment trap system was also using to determine the seasonal variation of the organic carbon flux. An average organic carbon flux at 1 km depth from this trap system was almost comparable to the amount of organic carbon degraded in the water deeper than 1 km depth, which was calculated from oxygen consumption rate of the deep water. Thus, it is clear that the sinking particle must play an important role in the carbon cycle of the deep water.     

The partitioning of organic carbon fluxes and sedimentary organic matter decomposition rates in the ocean

The partitioning of annual organic carbon fluxes from five stations located in the vicinity of the Pacific-Antarctic Ridge and the Peru continental margin suggests that 35–85% of the total near-bottom organic carbon flux is utilized at or near the sediment-water interface. These estimates have large uncertainties, but illustrate that assessments of organic carbon utilization can be made by several stepwise approaches which are generally applicable to a wide spectrum of marine environments.In one approach, the mineralization of organic carbon from the sediments was predicted from both sedimentary organic carbon and pore water nutrient profiles with comparable results. Neglecting sediment mixing, the rate constants of the anoxic sediments off Peru range from 0.1 × 10^?3 to 4 × 10^?3 y^?1, and rate constants derived for oxic SW Pacific sediments range from 3 × 10^?4 to 7 × 10^?4 y^?1. As with other values reported for sulfate reducing sediments by Toth and Lerman (1977) and for oxic central Pacific sediments by Müller and Mangini (1980), log-log plots of rate constants vs. sedimentation rate define two parallel linear relationships for oxic and anoxic sediments, respectively. The apparently enhanced rates for oxic environments may result from large benthic organisms which redistribute a portion of the available detritus and in doing so convert it into more easily accessible and metabolizable organic matter. In low-oxygen environments, bottom feeders and infauna are less abundant and more likely to irrigate rapidly accumulating sediments.     

Dissolved organic matter in the subterranean estuary of a volcanic island,Jeju: Importance of dissolved organic nitrogen fluxes to the ocean

We observed the origin, behavior, and flux of dissolved organic carbon (DOC), dissolved organic nitrogen (DON), colored dissolved organic matter (CDOM), and dissolved inorganic nitrogen (DIN) in the subterranean estuary of a volcanic island, Jeju, Korea. The sampling of surface seawater and coastal groundwater was conducted in Hwasun Bay, Jeju, in three sampling campaigns (October 2010, January 2011, and June 2011). We observed conservative mixing of these components in this subterranean environment for a salinity range from 0 to 32. The fresh groundwater was characterized by relatively high DON, DIN, and CDOM, while the marine groundwater showed relatively high DOC. The DON and DIN fluxes through submarine groundwater discharge (SGD) in the groundwater of Hwasun Bay were estimated to be 1.3 × 10⁵ and 2.9 × 10⁵ mol d^− 1, respectively. In the seawater of Hwasun Bay, the groundwater-origin DON was almost conservative while about 91% of the groundwater-origin DIN was removed perhaps due to biological production. The DON flux from the entire Jeju was estimated to be 7.9 × 10⁸ mol yr^− 1, which is comparable to some of the world's large rivers. Thus, our study highlights that DON flux through SGD is potentially important for delivery of organic nitrogen to further offshore while DIN is readily utilized by marine plankton in near-shore waters under N-limited conditions.     

Stable carbon isotope distribution of particulate organic matter in the ocean: a model study

The stable carbon isotopic composition of particulate organic matter in the ocean, δ¹³C_POC, shows characteristic spatial variations with high values in low latitudes and low values in high latitudes. The lowest δ¹³C_POC values (−32‰ to −35‰) have been reported in the Southern Ocean, whereas in arctic and subarctic regions δ¹³C_POC values do not drop below −27‰. This interhemispheric asymmetry is still unexplained. Global gradients in δ¹³C_POC are much greater than in δ¹³C_DIC, suggesting that variations in isotopic fractionation during organic matter production are primarily responsible for the observed range in δ¹³C_POC. Understanding the factors that control isotope variability is a prerequisite when applying δ¹³C_POC to the study of marine carbon biogeochemistry. The present model study attempts to reproduce the δ¹³C_POC distribution pattern in the ocean. The three-dimensional (3D) Hamburg Model of the Oceanic Carbon Cycle version 3.1 (HAMOCC3.1) was combined with two different parametrizations of the biological fractionation of stable carbon isotopes. In the first parametrization, it is assumed that the isotopic fractionation between CO₂ in seawater and the organic material produced by algae, _P, is a function of the ambient CO₂ concentration. The two parameters of this function are derived from observations and are not based on an assumption of any specific mechanism. Thus, this parametrization is purely empirical. The second parametrization is based on fractionation models for microalgae. It is supported by several laboratory experiments. Here the fractionation, _P, depends on the CO₂ concentration in seawater and on the (instantaneous) growth rates, μ_i, of the phytoplankton. In the Atlantic Ocean, where most field data are available, both parametrizations reproduce the latitudinal variability of the mean δ¹³C_POC distribution. The interhemispheric asymmetry of δ¹³C_POC can mostly be attributed to the interhemispheric asymmetry of CO₂ concentration in the water. However, the strong seasonal variations of δ¹³C_POC as reported by several authors, can only be explained by a growth rate-dependent fractionation, which reflects variations in the cellular carbon demand.     

Modulation of the particulate organic carbon flux to the ocean by a macrotidal estuary: Evidence from measurements of carbon isotopes in organic matter from the Gironde system

The isotopic composition of the organic carbon of the suspended particulate matter in the Gironde estuary and the Biscay shelf has been measured on a seasonal basis from 1977 to 1982. The δ¹³C values show a progressive change along the estuary and permit an estimate of the proportion of terrestrial carbon in each sample. It is estimated from these data that up to 80% of the continental POC is mineralized in the estuary and 3–16% of the riverborne flux is exported to the shelf.     

Inputs of organic carbon from Ria de Aveiro coastal lagoon to the Atlantic Ocean

Land/ocean boundaries constitute complex systems with active physical and biogeochemical processes that affect the global carbon cycle. An example of such a system is the mesotidal lagoon named Ria de Aveiro (Portugal, 40°38′N, 08°45′W), which is connected to the Atlantic Ocean by a single channel, 350 m wide. The objective of this study was to estimate the seasonal and inter-tidal variability of organic carbon fluxes between the coastal lagoon and the Ocean, and to assess the contribution of the organic carbon fractions (i.e. dissolved organic carbon (DOC) and particulate organic carbon (POC)) to the export of organic carbon to the Ria de Aveiro plume zone. The organic carbon fractions fluxes were estimated as the product of the appropriate fractional organic carbon concentrations and the water fluxes calculated by a two-dimensional vertically integrated hydrodynamic model (2DH). Results showed that the higher exchanges of DOC and POC fractions at the system cross-section occurred during spring tides but only resulted in a net export of organic carbon in winter, totalling 85 t per tidal cycle. Derived from the winter and summer campaigns, the annual carbon mass balance estimated corresponded to a net export of organic carbon (7957 = 6585 t yr⁻¹ POC + 1372 t yr⁻¹ DOC). On the basis of the spring tidal drainage area, it corresponds to an annual flux of 79 g m⁻² of POC and 17 g m⁻² of DOC out of the estuary.     

An optical model for the remote sensing of coloured dissolved organic matter in coastal/ocean waters

An optical model is developed for the remote sensing of coloured dissolved organic matter (CDOM) in a wide range of waters within coastal and open ocean environments. The absorption of CDOM (denoted as a_g) is generally considered as an exponential form model, which has two important parameters – the slope S and absorption of CDOM at a reference wavelength a_g(λ₀). The empirical relationships for deriving these two parameters are established using in-situ bio-optical datasets. These relationships use the spectral remote sensing reflectance (R_rs) ratio at two wavelengths R_rs(670)/R_rs(490), which avoids the known atmospheric correction problems and is sensitive to CDOM absorption and chlorophyll in coastal/ocean waters. This ratio has tight relationships with a_g(412) and a_g(443) yielding correlation coefficients between 0.77 and 0.78. The new model, with the above parameterization applied to independent datasets (NOMAD SeaWiFS match-ups and Carder datasets), shows good retrievals of the a_g(λ) with regression slopes close to unity, little bias and low mean relative and root mean square errors. These statistical estimates improve significantly over other inversion models (e.g., Linear Matrix-LM and Garver-Siegel-Maritorena-GSM semi-analytical models) when applied to the same datasets. These results demonstrate a good performance of the proposed model in both coastal and open ocean waters, which has the potential to improve our knowledge of the biogeochemical cycles and processes in these domains.     

Particulate organic carbon in the global ocean derived from SeaWiFS ocean color

Satellite remote sensing offers new means of quantifying particulate organic carbon, POC, concentration over large oceanic areas. From SeaWiFS ocean color, we derived 10-year data of POC concentration in the surface waters of the global ocean. The 10-year time series of the global and basin scale average surface POC concentration do not display any significant long-term trends. The annual mean surface POC concentration and its seasonal amplitude are highest in the North Atlantic and lowest in the South Pacific, when compared to other ocean basins. POC anomalies in the North Atlantic, North Pacific, and global concentrations seem to be inversely correlated with El Niño index, but longer time series are needed to confirm this relationship. Quantitative estimates of POC reservoir in the oceanic surface layer depend on the choice of what should represent this layer. Global average POC biomass is 1.34 g m^?2 if integrated over one optical depth, 3.62 g m^?2 if integrated over mixed layer depth, and up to 6.41 g m^?2 if integrated over 200-m layer depth (when assumed POC concentration below MLD is 20 mg m^?3). The global estimate of total POC reservoir in the surface 200-m layer of the ocean is 228.61×10¹³ g. We expect that future estimates of POC reservoir may be even larger, when more precise calculations account for deep-water organic-matter maxima in oligotrophic regions, and POC biomass located just below the seasonal mixed layer in spring and summer in the temperate regions.     

Tracing terrigenous dissolved organic matter and its photochemical decay in the ocean by using liquid chromatography/mass spectrometry

Reversed-phase liquid chromatography/mass spectrometry (LC/MS) is introduced as a new molecular fingerprinting technique for tracing terrigenous dissolved organic matter (DOM) and its photochemical decay in the ocean. DOM along a transect from the mangrove-fringed coast in Northern Brazil to the shelf edge was compared with mangrove-derived porewater DOM exposed to natural sunlight for 2–10 days in a photodegradation experiment. DOM was isolated from all samples via solid-phase extraction (C18) for LC/MS analysis. DOM in the estuary and ocean showed a bimodal mass distribution with two distinct maxima in the lower m/z range from 400 to 1000 Da (intensity-weighted average of 895 Da). Terrigenous porewater DOM from the mangroves was characterized by a broad molecular mass distribution over the detected range from 150 to 2000 Da (intensity-weighted average of 1130 Da). Polar compounds, i.e., those that eluted early in the reversed-phase chromatography, absorbed more UV light and had on average smaller molecular masses than the more apolar compounds.     

Binding of monomeric organic compounds to marcomolecular dissolved organic matter in seawater

Several monomeric organic compounds, including amino acids, sugars, and fatty acids, were found to bind abiologically to dissolved macromolecular materials in particle-free seawater at natural substrate concentrations. The binding primarily occurred in ocean surface waters, at rates slower than in situ biological utilization rates of most of the compounds. Seasonal patterns of binding in Gulf of Maine waters may have been related to seasonal variations in macroalgal exudation of polyphenolic materials. Enhanced reactivity of relatively hydrophobic monomers implicated hydrophobic effects as potentially important in marine organic condensations. The resultant condensates showed high particle reactivity, consistent with low concentrations of dissolved condensed materials in seawater.     

Mechanisms of pore water organic matter adsorption to montmorillonite

The extent and mechanisms of adsorption of marine pore water organic matter to montmorillonite were studied in a series of batch and sequential adsorption experiments. Pore water natural organic matter (pNOM) and easily extracted natural organic matter (eNOM) were collected from Liberty Bay (Puget Sound, WA, USA) sediments. The pNOM and eNOM were each divided into two size fractions using a 1000 D ultrafilter. Batch adsorption isotherms were approximately linear, and the >1000 D fractions of both pNOM and eNOM had larger partition coefficients (K_d) than the <1000 D fractions. A two-component fit of the sequential adsorption data indicated that pNOM and eNOM contained a similar amount of NOM (30%) that was not surface reactive toward montmorillonite. After correcting the batch adsorption K_ds for the non-reactive components, the K_ds estimated by batch and sequential adsorption were identical (2.7 l/kg for >1000 D pNOM and eNOM, and 1.6 l/kg for <1000 D pNOM and eNOM). Mechanisms of adsorption were investigated by systematically changing conditions (pH, temperature and ionic composition) of >1000 D fractions during batch isotherm experiments. Adsorption of NOM was found to decrease with increased temperature, suggesting that hydrophobic effects were not the dominant adsorption mechanisms in this system. Ion exchange was also not an important adsorption mechanism because adsorption increased with ionic strength. The observed enhancement in adsorption with ionic strength indicated that van der Waals interactions were important in the adsorption of NOM. Ligand exchange was found to be a significant mechanism since the presence of SO₄²⁻ in solution reduced the amount of NOM adsorbed. Ca²⁺ enhanced adsorption slightly more than Na⁺, suggesting that cation bridging was involved. The relative contributions of van der Waals interactions, ligand exchange and cation bridging were estimated to be approximately 60%, 35% and 5%, respectively, for adsorption of NOM in a CaCl₂ solution.     

Organic carbon to Th ratios of marine organic matter

Uncertainties in the determinations of particulate organic carbon flux from measurements of the disequilibrium between ²³⁴Th and its mother isotope uranium depend largely on the determination of the organic carbon to ²³⁴thorium (OC : ²³⁴Th) ratio. The variability of the OC : ²³⁴Th ratio in different size fractions of suspended matter, ranging from the truly dissolved (< 3 or 10 kDa) fraction to several millimeter sized marine snow, as well as from sediment trap material was assessed during an eight-day cruise off the coast of California in Spring 1997. The affinity of polysaccharide particles called TEP (transparent exopolymer particles) and inorganic clays to ²³⁴Th was investigated through correlations. The observed decrease in the OC : ²³⁴Th ratio with size, within the truly dissolved to small particle size range, is consistent with concepts of irreversible colloidal aggregation of non-porous nano-aggregates. No consistent trend in the OC : ²³⁴Th ratio was observed for particles between 1 or 10 to 6000 μm. Origin and fate of marine particles belonging to this size range are diverse and interactions with ²³⁴Th too complex to expect a consistent relationship between OC : ²³⁴Th ratio and size, if all categories of particles are included. The relationship between OC and ²³⁴Th was significant when data from the truly dissolved fraction were excluded. However, variability was very large, implying that OC flux calculations using different collection methods (e.g. sediment trap, Niskin bottles or pumps) would differ significantly. Therefore a large uncertainty in OC flux calculations based on the ²³⁴Th method exist due to individual decisions as to which types or size classes of particles best represent sinking material in a specific area. Preferential binding of ²³⁴Th to specific substance classes could explain the high variability in the relationship between OC and ²³⁴Th. At 15 m, in the absence of lithogenic material, the OC : ²³⁴Th ratio was a function of the fraction of TEP or TEP-precursors in OC, confirming that acidic polysaccharides have a high affinity for ²³⁴Th and that TEP carry a ligand for ²³⁴Th. Preferential binding to TEP might change distribution patterns of ²³⁴Th considerably, as TEP may sink when included in large aggregates, or remain suspended or even ascend when existing as individual particles or microaggregates. In the presence of lithogenic matter, at depths below 30 m, the ratio between ²³⁴Th and OC was linearly related to the ratio between alumino silicates and C. The affinity of inorganic substances to ²³⁴Th is known to be relatively low, suggesting that a coating of acidic polysaccharides was responsible for the apparently high affinity between ²³⁴Th and lithogenic material. Overall, OC : ²³⁴Th ratios of all material collected during this investigation can best be explained by differential binding of ²³⁴Th to both TEP and TEP-precursors, as well as to lithogenic minerals, which were very abundant in an intermediate nepheloid layer between 50 and 90 m.     

The contribution of organic matter to the alkaline reserve of natural waters

The contribution of organic matter (humic compounds) to the alkaline reserve of seawater in the Sea of Japan, in the Razdol’naya River estuarine waters, and in the interstitial waters of the sediments of the Sea of Okhotsk was characterized using two procedures for alkalinity measurements: the method by Bruevich and that of the sample equilibrium with air. It was found that the surface waters of the Sea of Japan contained about 20 μmol/kg of alkalinity of organic origin, and this value twofold decreased with depth. For most of the actual cases of the calculations of the seawater carbonate system, this value may be neglected. Meanwhile, the contribution of organic alkalinity to the Razdol’naya River waters amounts to nearly 120 μmol/kg. It was shown that, if this value in the calculation of the carbonate system of the Razdol’naya River estuary-Amur Bay is neglected, this may cause gross errors in the values of the partial pressure of carbon dioxide (the error might be over 1500 μatm) and in the dissolved inorganic carbon (an error over 150 μmol/kg). The maximum absolute contribution of the humic matter (over 300 μmol/kg) was found for the interstitial waters in selected sediments of the Sea of Okhotsk. In the interstitial waters of these sediments, humic matter concentrations as high as 300 mg/l were detected. The data obtained show that the determination of the amount of humic matter must be an indispensable condition for an adequate analysis of estuarine carbonate systems and of the interstitial water in reduced marine sediments.     

Analysis of lignin-derived phenols in standard reference materials and ocean dissolved organic matter by gas chromatography/tandem mass spectrometry

A series of reference materials are proposed for intercomparison and quality control purposes during the quantification of lignin oxidation products (LOP) from diverse environmental matrices. These materials are all easily accessible and certified for diverse organic constituents (NIST and IHSS). They represent a suite of natural environmental matrices (from solids to aqueous) and are characterized by a wide range of organic carbon and lignin concentrations with abundant proportions of all major LOP. The variability of LOP concentrations and signatures for all these materials averages 3–5% and does not exceed 10%. Using these standards, a new quantification method was developed and validated for the determination of low-level CuO oxidation products using capillary gas chromatography–tandem mass spectrometry (GC/MS–MS). Tandem mass spectrometry provides both the high sensitivity and selectivity required for the identification and quantification of trace levels of dissolved lignin. The method is particularly useful for removing interference from co-eluting isotopes generated from the DOM matrix and during glucose amendment procedures of low-carbon samples. Such glucose amendment is not necessary, however, when the CuO to organic carbon weight-to-weight ratio can be kept at a value < 200–300.     

Terrigenous pyroclastic matter as a source of dissolved calcium in the ocean

It has been found experimentally that the intensity of the leaching under the interaction of volcanic ash and seawater decreases as Ca > Mg > Si, and the mobilization of calcium and magnesium is more intense compared to silicon by factors of 30?C70 and 20?C50, respectively. Calcium and magnesium supplied to seawater owing to the halmyrolysis of the terrigenous pyroclastic matter may then interact with the products of organic matter oxidation to fix the free carbon dioxide in the form of autochthonous carbonates. It was shown that the halmyrolysis of terrigenous pyroclastic matter could not provide the complete immobilization of the autochthonous CO₂ produced in the ocean by the oxidation of organic matter. Thus, some other sources exist for the reactive silicates of calcium and magnesium, and these might probably be the silicates of the continental runoff of solid substances.     

筼筜湖绿潮期间颗粒有机物及沉积有机物的来源研究

以原子碳氮比C_at/N_at、TOC/Chl a、δ13C和δ15N等为指标,分析了筼筜湖绿潮爆发期间悬浮颗粒有机物(POM)和沉积有机物(SOM)的来源。结果显示,筼筜湖的POM主要以外源输入为主。在靠近海水入口的引水渠,POM主要来自厦门西海域的陆源有机碎屑;位于筼筜湖上游的干渠,生活污水及餐饮业废水的有机质是其POM的主要贡献者;内、外湖POM的C_at/N_at(6.94~7.08)与浮游植物接近,但它们并不以浮游植物为主,而主要来自引水渠和干渠有机质的输入。以内湖为例,它们对内湖POM的联合贡献高达54%~97%。筼筜湖SOM的潜在来源多样,但不同湖区差异显著:在大型海藻覆盖区,主要以大型海藻和POM为主,而在无海藻覆盖的区域,则主要来自POM的自然沉降或与底栖微藻的联合贡献。结果表明,在来源复杂的潟湖系统,有机物的化学组成并不能很好的指示有机物的来源和成因,它在有机质的示踪方面并不如稳定同位素来得有效可靠。不过,基于多种指标的分析结果可能更准确。