Distribution coefficient of Mg2+ ions between calcite and solution at 10–50°C

The distribution coefficient (λ_Mg) of Mg²⁺ ions between calcite and solution was found to be 0.012 ± 0.001 (10°C), 0.014 ± 0.001 (15°C), 0.019 ± 0.001 (25°C), 0.024 ± 0.001 (30°C), 0.027 ± 0.001 (35°C) and 0.040 + 0.003 (50°C). This indicates a remarkable dependence on temperature. The effect of the Mg²⁺/Ca²⁺ molar ratio in a parent solution on λ_Mg for calcite is small, where the molar ratio lies in the range 0.04-2. However, the λ_Mg value for aragonite tends to decrease with increasing Mg²⁺/Ca²⁺ ratio in the parent solution. The largest Mg content of calcite in the Ca(HCO₃)₂-Mg²⁺ → calcite system is around 2 mol% in the temperature range 10–50°C. Neither homogeneous nor heterogeneous distribution laws hold for aragonite precipitation, and the temperature effect on the coprecipitation of Mg²⁺ ions with aragonite is very small.     

Distribution coefficient of Mg ions between calcite and solution at 10–50°C

The distribution coefficient (λ_Mg) of Mg²⁺ ions between calcite and solution was found to be 0.012 ± 0.001 (10°C), 0.014 ± 0.001 (15°C), 0.019 ± 0.001 (25°C), 0.024 ± 0.001 (30°C), 0.027 ± 0.001 (35°C) and 0.040 + 0.003 (50°C). This indicates a remarkable dependence on temperature. The effect of the Mg²⁺/Ca²⁺ molar ratio in a parent solution on λ_Mg for calcite is small, where the molar ratio lies in the range 0.04-2. However, the λ_Mg value for aragonite tends to decrease with increasing Mg²⁺/Ca²⁺ ratio in the parent solution. The largest Mg content of calcite in the Ca(HCO₃)₂-Mg²⁺ → calcite system is around 2 mol% in the temperature range 10–50°C. Neither homogeneous nor heterogeneous distribution laws hold for aragonite precipitation, and the temperature effect on the coprecipitation of Mg²⁺ ions with aragonite is very small.     

铀、钍在碳酸钙-海水界面的附着行为研究

运用实验模拟的手段,对铀(U)、钍(Th)在碳酸钙-海水界面的附着行为进行了初步研究,通过测定相关的分异系数(D)定量评估了文石和方解石两种碳酸钙矿物对U和Th的捕集作用。实验结果显示,不仅U和Th之间存在显著差异,而且两种碳酸钙矿物之间也存在明显不同。U介于碳酸钙和海水之间的分异系数(DU)分别在1.5~3.5(文石)和0.04~0.19(方解石)区间内变化,分异行为非常微弱但其分异系数随着碳酸钙沉淀速率的增加而逐渐上升。这表明U元素主要是以共沉淀的方式进入到文石或方解石沉淀中,但由于其在海水溶液中主要以2 22 3UO(CO)nn的形式存在,因而只能以占据晶格缺陷的方式进入碳酸钙。与之相反的是,文石和方解石都对Th表现出极强的捕集能力,所测定的分异系数(DTh)分别在240~6 330(文石)和430~6 160(方解石)范围内变化,但DTh与碳酸钙沉淀速率之间无明显关联。Th在碳酸钙表面的附着行为可界定为单纯的吸附作用,这一行为应与Th主要以Th(OH)4的形式赋存于溶液中有关。     

南海北部涠洲岛海域Merulinidae珊瑚文石骨骼和海水间微量元素分配系数：来自珊瑚种属和瑞利分馏的影响

微量元素在珊瑚文石骨骼和海水间的分配过程是控制海水中微量元素进入珊瑚骨骼的关键环节,表征该分配过程的分配系数（K_D）常用于时间序列上的海水微量元素含量重建。由于缺乏珊瑚和海水的原位研究,我们对珊瑚文石骨骼与海水之间微量元素的分配行为的了解非常有限,这严重阻碍了我们对于准确的海水化学定量数据的获取。本研究中,我们选取了南海北部涠洲岛海域的两种典型的造礁石珊瑚种（网状菊花珊瑚（Goniastrea retiformis）和八重山扁脑珊瑚（Platygyra yaeyamaensis））和周围原位表层海水中的5种微量元素（Cu、Zn、Pb、Cd和Cr）进行研究,估算了这些微量元素在珊瑚文石骨骼和海水之间的分配系数。研究结果表明：各个微量元素在网状菊花珊瑚和八重山扁脑珊瑚文石骨骼和海水间的分配系数分别为3.65和3.49（Cu）;0.57和0.97（Zn）;1.06和1.42（Pb）;0.88和1.01（Cd）;0.66和0.60（Cr）。结合前人报道的各个种属珊瑚的分配系数,我们发现不同珊瑚种属Cu、Zn、Pb和Cd的K_D值存在显著差异,而Cr的K_D值差异则相对较小。此外,微量元素K_D值还在一定程度上受到瑞利分馏的影响,该影响与K_D值的大小有关。本研究为珊瑚文石骨骼和海水间分配系数提供了较为准确的K_D值,为未来的珊瑚研究提供了重要的基础数据,并扩展了我们对海洋生物成因矿物晶格的化学特征的认识。     

Adsorption of uranyl complex ions on hydrous titanium oxide (HTO)——Ⅱ. Infrared spectrum investigation

-The i. r. spectra of Na4 [UO2 (CO3)3], Na [UO2 (OH)3] and the surface species of uranium on HTO underthe condition of flowing natural seawater and concentrated seawater (NaCl-NaHCO3-U) were recorded, with the bands of urany! of surface species obtained and the finding that iigands of surface species besides HTO are mainly water and OH, and there are some CO32- groups under the condition of natural seawater. Some relations between the complex properties and the j. r. spectroscopic characters for uranyl complexes were studied, and the transferred change quantity of surface complex was calculated.Structure models for surface species of adsorption are herein presented and the mechanism for uranium adsorption is deduced.     

The uranium content and the activity ratio234U/238U in marine organisms and sea water in the western North Pacific

The uranium content and activity ratio A²³⁴U/A²³⁸U were determined in open ocean water, marine plankton, marine algae and sea water in the environment in which plankton and algae live. The average uranium content of 3.34±0.28×10⁻⁶ g/l and the average activity ratio of 1.13±0.04 were obtained in open ocean water. The uranium contents in plankton and algae were respectively from 1.7 to 7.8×10⁻⁷ g/g and 0.4 to 23.5×10⁻⁷ g/g on dry basis with the respective concentration factors of 48 to 260 and 10 to 733. The activity ratio in plankton and algae ranged from 1.07 to 1.18 which coincided well with those in the environmental sea water.     

Seasonal variation of Mn adsorption on to calcareous surfaces in the English Channel, and its implication on the manganese distribution coefficient

Dissolved and particulate manganese in seawater samples derived from the English Channel has been analyzed using graphite furnace atomic absorption (GFAAS), and inductively coupled plasma atomic emission (ICP—AES) spectroscopies. Because of the high contents of carbonate minerals found in the suspended matter samples, the English Channel constitutes an ideal field area for the study of the Mn²⁺/Ca²⁺/CaCO₃ system. Owing to the chemical speciation of particulate manganese and the combined use of the X-ray diffraction and electron spin resonance spectroscopy we have shown the importance of the carbonate phase in the stabilization of manganese (II). This has been confirmed by p-pH measurements in the field. All these studies have also indicated that: (1) manganese is associated with calcite in the form of a solid solution, Mn_xCa_1−xCO₃; and (2) significant increases in the concentrations of particulate manganese, especially in offshore waters, occur in summer. This seasonal phenomenon has been attributed to the proliferation of coccolithophorids, which are known to be covered with calcified skeletons at high specific surface areas. To appraise the implication of the coccolithophorid-blooms phenomenon on the Mn²⁺/Ca²⁺/CaCO₃ system, we have used the manganese distribution coefficient, D_i, between the liquid phase and CaCO₃ particles. Overall we have shown that: (1) D_i in summer (i.e. when coccoliths considered as very fine-grained calcite are abundant) is much higher than that obtained in winter; and (2) in the vicinity of the French coast, D_i does not vary significantly even in summer. This is because of the high content of chalk-derived particles found in the near-shore waters.     

Calibration and evaluation of a carbonate microsensor for studies of the marine inorganic carbon system

Accurate and rapid determination of inorganic carbon constituents in ocean environments is important for understanding the carbon cycle, especially in the context of ocean-acidification research. A microsensor capable of directly measuring carbonate ion (CO₃ ^2–) concentrations would be desirable. In this study, a carbonate microsensor with a polymeric liquid membrane was fabricated, and two calibration methods were used to evaluate its performance. The first method was based on continuous titration. Small increments of HCl were added to seawater or Na₂CO₃ solution to adjust the total alkalinity and pH values and thus obtain a series of carbonate concentrations. The second method used a series of discrete standards. Varying amounts of HCl or NaOH were added to separate seawater aliquots, and the CO₃ ^2– concentration of each standard was calculated from the resulting total alkalinity and total dissolved inorganic carbon. Both methods were found to be adequate for achieving accurate calibration of the CO₃ ^2– sensor, and both are suitable for field work. The discrete standards method, however, is more convenient and may provide a better linear range at low CO₃ ^2– concentrations (detection range: 2–300 μmol/kg) than the continuous titration method in seawater (detection range: 10–250 μmol/kg). This CO₃ ^2– microsensor can be used for 5–7 d and detects changes in carbonate concentration as low as 2 μmol/kg in the inorganic carbon constituents of the environments where marine calcareous organisms grow. The CO₃ ^2– microelectrode was further assessed by applying it to the measurement of pore-water CO₃ ^2– concentration profiles in a marine sediment core.     

The kinetic interactions of metal ions with humic acids

Complexation of europium (III) and UO₂²⁺ by humic acid was found to be very fast (< 1 m). However, passage through ion exchange resin removed a fraction which decreased as the contact time increased over a 2–3 day period. The dissociation kinetics for UO₂²⁺-humate were described by an equation with five first order terms with rate constants ranging from 40.6 m⁻¹ to 5.64×10⁻³ m⁻¹. The percentage of UO₂²⁺ dissociating by the slower paths, comparable to that eluting with the humic acid through the ion exchange resin is assigned to internal site-bound cations (strong binding). The faster dissociating fraction corresponded roughly to the UO₂²⁺ removed by the cation exchange resin (weak binding). The time dependence of the weak to strong binding ratio was associated with change in the conformation of the macromolecular humic acid as the cations neutralized the charge repulsions of the anionic humate.     

Actinide speciation in aquatic systems

Nuclear test explosions and reactor wastes have deposited an estimated 16 × 10¹⁵ Bq of plutonium into the world's aquatic systems. However, plutonium concentration in open ocean waters is on the order 10^− 5 Bq/kg, indicating that most of the plutonium is quite insoluble in marine waters and has been incorporated into sediments. Actinide ions often are not in a state of thermodynamic equilibrium and their solubility and migration behavior is related to the form in which the nuclides were introduced into the aquatic system.Actinide solubility depends on such factors as the pH (hydrolysis), Eh (oxidation state), reaction with complexants (e.g., carbonate, phosphate, humic acid, etc.), sorption to surfaces of minerals and/or colloids etc., in the water. The most significant of these variables is the oxidation state of the metal ion. The simultaneous presence of more than one oxidation state for some actinides (e.g., plutonium) in a solution complicates actinide environmental behavior. Both Np(V)O₂⁺ and Pu(V)O₂⁺, the most significant states in natural, oxic waters are relatively noncomplexing and resistant to hydrolysis and subsequent precipitation. The solubility of NpO₂⁺ can be as high as 10^− 4 M while that of PuO₂⁺ is limited by reduction to the insoluble tetravalent species, Pu(OH₄), (pK_sp = 56). The net solubility of hexavalent UO₂²⁺ in sea water is also limited by hydrolysis; however, it has a relatively high concentration due to formation carbonate complexes. The insoluble trivalent americium hydroxocarbonate, Am(CO)₃(OH), is limiting species for the solubility of Am(III) in sea water. Thorium is found exclusively as the tetravalent species and its solubility is limited by the formation of quite insoluble Th(OH)₄.The chemistry of actinide ions in the environment is reviewed to show the spectrum of reactions that can occur in natural waters which must be considered in assessing the environmental behavior of actinides. While much is understood about sorption of actinides on surfaces, the mode of migration of actinides in such waters and the potential effects of these radioactive species on marine bioto, much more is needed for a satisfactory understanding of the behavior of the actinides in the environment.     

C波段紧缩极化SAR海冰探测能力评估

The C-band synthetic aperture radar(SAR) data from the Bohai Sea of China, the Labrador Sea in the Arctic and the Weddell Sea in the Antarctic are used to analyze and discuss the sea ice full polarimetric information reconstruction ability under compact polarimetric modes. The type of compact polarimetric mode which has the highest reconstructed accuracy is analyzed, along with the performance impact of the reconstructed pseudo quad-pol SAR data on the sea ice detection and sea ice classification. According to the assessment and analysis, it is recommended to adopt the CTLR mode for reconstructing the polarimetric parameters σ_(HH)~0,σ_(VV)~0, H and α,while for reconstructing the polarimetric parameters σ_(HV)~0, ρ_(H-V), λ_1 and λ_2, it is recommended to use the π/4 mode.Moreover, it is recommended to use the π/4 mode in studying the action effects between the electromagnetic waves and sea ice, but it is recommended to use the CTLR mode for studying the sea ice classification.     

239,240Pu and137Cs in the East China and the Yellow Seas

The distribution and inventory of artificial radionuclides,^239,240Pu and¹³⁷Cs were determined in the East China and the Yellow Seas in 1987. Almost all of^239,240Pu and 50 to 80% of¹³⁷Cs in the continental shelf area are retained in the sediment column.^239,240Pu sediment inventory in the sea area is larger than the fallout input and tends to increase southwardly. This excess^239,240Pu and the lateral distribution are attributable to the supply of^239,240Pu by the Yangtze River discharge. On the contrary,¹³⁷Cs sediment inventory shows a decrease to the south, and the fact can be accounted for by the southward dispersion of fine silt particles discharged from the Yellow River. Total¹³⁷Cs inventory is smaller than the estimated fallout input, and the fact seems to indicate dispersion of¹³⁷Cs out of the shelf region. Vertical profiles of^239,240Pu and¹³⁷Cs contents in sediments differ from that of natural²¹⁰Pb, implying the effect of varied accumulation rates of the artificial radionuclides over the sediment particle mixing by benthic organisms. Apparent maximum sediment particle mixing coefficient (D _B ) calculated from the excess²¹⁰Pb profiles in stations located between the inner and outer shelves ranged from 1.4 to 8.3 cm²y^–1. ThisD _B value is higher than that in the Okinawa Trough (1.0 cm²y^–1), but lower than previously estimatedD _B value (26 cm²y^–1) in the outer shelf mud.     

Characterizing air–sea CO2 exchange dynamics during winter in the coastal water off the Hugli-Matla estuarine system in the northern Bay of Bengal, India

The distribution of the fugacity of CO₂ ( $ f_{{{\text{CO}}_{ 2} }} $ ) and air–sea CO₂ exchange were comprehensively investigated in the outer estuary to offshore shallow water region (lying adjacent to the Sundarban mangrove forest) covering an area of ~2,000 km² in the northern Bay of Bengal during the winter. A total of ten sampling surveys were conducted between 1 December, 2011 and 21 February, 2012. Physico-chemical variables like sea surface temperature (SST), salinity, pH, total alkalinity (TAlk), dissolved inorganic carbon (DIC) and in vivo chlorophyll-a along with atmospheric variables were measured in order to study their role in controlling the CO₂ flux. Surface water $ f_{{{\text{CO}}_{ 2} }} $ ranged between 111 and 459 μatm which correlated significantly with the SST (r = 0.71, p < 0.001, n = 62). Neither DIC nor TAlk showed any linear relationship with varying salinity in the estuarine mixing zone, demonstrating the significant presence of non-carbonate alkalinity. An overall net biological control on the surface $ f_{{{\text{CO}}_{ 2} }} $ distribution was established during the study, although no significant correlation was found between chlorophyll-a and $ f_{{{\text{CO}}_{ 2} }} $ (water). The shallow water region studied was mostly under-saturated with CO₂ and acted as a sink for atmospheric CO₂. The difference between surface water and atmospheric $ f_{{{\text{CO}}_{ 2} }} $ ( $ \Updelta f_{{{\text{CO}}_{ 2} }} $ ) ranged from ?274 to 69 μatm, with an average seaward flux of ?10.5 ± 12.6 μmol m^?2 h^?1. The $ \Updelta f_{{{\text{CO}}_{ 2} }} $ and hence the air–sea CO₂ exchange was primarily regulated by the variation in sea surface $ f_{{{\text{CO}}_{ 2} }} $ , since atmospheric $ f_{{{\text{CO}}_{ 2} }} $ varied over a comparatively narrow range of 361.23–399.05 μatm.     

Mechanisms of enrichment of the rarer elements in marine manganese nodules

The rare-earth distribution has been determined in five manganese nodules from a range of marine environments. Manganese nodules from Loch Fyne, Scotland, and the Gulf of Aden are characterized by a low absolute abundance of the rare-earth elements and a low Ce/La ratio compared with deep-sea nodules. This difference is interpreted in terms of the diagenetic remobilization of manganese in the high sedimentation regimes leading to the effective fractionation of manganese from the rare-earth elements and the resultant depletion of the rare earths in nodules from these environments. The mechanism of incorporation of the rare-earth elements into manganese nodules is thought to be either the direct adsorption of these elements from seawater or the scavenging of the elements by colloidal iron oxide prior to their incorporation into the authigenic phase of nodules. There appears to be no evidence for the surface transfer of these elements from inorganic detritus into the authigenic phase of nodules as suggested by previous authors. The distribution of U and Th in the nodules is controlled by factors similar to those controlling the rare-earth abundance in nodules. The higher U/Th ratios in nodules from Loch Fyne and the Gulf of Aden is considered to be due to the preferential reduction of UO₂(CO₃)₃^4? to some lower-valency uranium species such as U₃O₈ in nodules from less oxidizing environments.     

Tropical seagrass-associated macroalgae distributions and trends relative to water quality

Tropical coastal marine ecosystems including mangroves, seagrass beds and coral reef communities are undergoing intense degradation in response to natural and human disturbances, therefore, understanding the causes and mechanisms present challenges for scientist and managers. In order to protect our marine resources, determining the effects of nutrient loads on these coastal systems has become a key management goal. Data from monitoring programs were used to detect trends of macroalgae abundances and develop correlations with nutrient availability, as well as forecast potential responses of the communities monitored. Using eight years of data (1996–2003) from complementary but independent monitoring programs in seagrass beds and water quality of the Florida Keys National Marine Sanctuary (FKNMS), we: (1) described the distribution and abundance of macroalgae groups; (2) analyzed the status and spatiotemporal trends of macroalgae groups; and (3) explored the connection between water quality and the macroalgae distribution in the FKNMS. In the seagrass beds of the FKNMS calcareous green algae were the dominant macroalgae group followed by the red group; brown and calcareous red algae were present but in lower abundance. Spatiotemporal patterns of the macroalgae groups were analyzed with a non-linear regression model of the abundance data. For the period of record, all macroalgae groups increased in abundance (Ab_i) at most sites, with calcareous green algae increasing the most. Calcareous green algae and red algae exhibited seasonal pattern with peak abundances (Φ_i) mainly in summer for calcareous green and mainly in winter for red. Macroalgae Ab_i and long-term trend (m_i) were correlated in a distinctive way with water quality parameters. Both the Ab_i and m_i of calcareous green algae had positive correlations with NO₃⁻, NO₂⁻, total nitrogen (TN) and total organic carbon (TOC). Red algae Ab_i had a positive correlation with NO₂⁻, TN, total phosphorus and TOC, and the m_i in red algae was positively correlated with N:P. In contrast brown and calcareous red algae Ab_i had negative correlations with N:P. These results suggest that calcareous green algae and red algae are responding mainly to increases in N availability, a process that is happening in inshore sites. A combination of spatially variable factors such as local current patterns, nutrient sources, and habitat characteristics result in a complex array of the macroalgae community in the seagrass beds of the FKNMS.     

Vitamin B12 transudation from marine bottom muds

Transudation of vitamin B₁₂ from the surface layer of bottom muds in Maizuru Bay and in the Sea of Hiuchi was investigated in this report. The total counts of heterotrophs and bacteria producing vitamin B₁₂ in the bottom muds in these coastal regions were also examined. Results obtained were as follows:

1. In the marine bottom in these coastal regions, vitamin B₁₂ is continuously transuded from the surface layer of bottom muds to sea water. Accordingly, it is reasonably supposed that the surface layer of bottom muds, in which vitamin B₁₂ is produced and accumulated, is a source of provision of the vitamin in the coastal regions.
2. On an average, the quantity of transudation of vitamin B₁₂ from the surface layer of bottom muds to sea water is 2.6 μμg/cm²/hr and 5.2μμg/cm²/hr in Maizuru Bay and in the Sea of Hiuchi respectively.
3. In the surface layer of bottom muds in these coastal regions, the quantity of transudation of vitamin B₁₂ is correlated with the content of the vitamin and the counts of bacteria producing the vitamin.

     

Effect of the nonlinear interaction of tidal harmonics on their spatial structure as applied to the system of the white and Barents Seas

Using the three-dimensional nonlinear finite-element thermohydrodynamic model QUODDY-4, we obtain two solutions giving an idea of the role of the nonlinear interaction of tidal harmonics in the formation of their spatial structure. The first solution is induced by the total tide (M ₂ + S ₂ + K ₁ + O ₁) at the open boundary and by the total static tide inside the area under consideration; then, the solution obtained is subject to harmonic analysis. The second solution is obtained by specifying such tidal sea level elevations at the open boundary that meet individual tidal harmonics. These two solutions are compared. It is shown that the differences between the solutions for the S ₂, K ₁, and O ₁ waves can be significant, especially near the open boundary between the White and Barents seas. This conclusion remains valid also for the maximum velocities (major semiaxes of the ellipses) of the barotropic (depth-average) tidal current as well as for the average (over the tidal cycle) densities of the total tidal energy and components of the tidal-energy budget. The emergence of this feature indicates that there are resonance modes with frequencies that differ from those of the S ₂, K ₁, and O ₁ harmonics to a lesser extent than the M ₂ harmonic frequency. The same conclusion can be made by comparing the values of the amplification factor, which is defined as the ratio between the actual and static tides, for the system of the Barents and White seas as a whole and for Mezen Bay in the White Sea and Czech Bay in the Barents Sea, taken separately.     

Authigenic carbonate mineral formation in the Pagassitikos palaeolake during the latest Pleistocene, central Greece

The Pagassitikos Gulf in Greece is a semi-enclosed bay with a maximum depth of 102 m. According to the present-day bathymetric configuration and the sea level during the latest Pleistocene, the gulf would have been isolated from the open sea, forming a palaeolake since ~32 cal. ka b.p. Sediment core B-4 was recovered from the deepest sector of the gulf and revealed evidence of a totally different depositional environment in the lowest part of the core: this contained light grey-coloured sediments, contrasting strongly with overlying olive grey muds. Multi-proxy analyses showed the predominance of carbonate minerals (aragonite, dolomite and calcite) and gypsum in the lowest part of the core. Carbonate mineral deposition can be attributed to autochthonous precipitation that took place in a saline palaeolake with high evaporation rates during the last glacial–early deglacial period; the lowest core sample to be AMS ¹⁴C dated provided an age of 19.53 cal. ka b.p. The palaeolake was presumably reconnected to the open sea at ~13.2 cal. ka b.p. during the last sea-level rise, marking the commencement of marine sedimentation characterised by the predominance of terrigenous aluminosilicates and fairly constant depositional conditions lasting up to the present day.     

Scale dependence of accumulation-dispersal coefficient of marine organisms

An attempt is made to find a relation betweenK, the absolute value of accumulation-dispersal coefficient of marine organisms referred to a region or a group (Kawai, 1986a), andL, the square root of the area of the region or the group over which the distribution density of organisms is averaged.K is estimated as shown below. For appropriate sampling time-intervals,K becomes greater than other coefficients such as population growth coefficient. Using this result, an order of magnitude ofK dependent onL is estimated from various data of temporal change in density. With the aid of a dependenceQL ^–2/3 (Kawai, 1985b), a relationKL ^–2/3 is predicted for 30 cmL 30 km, whereQ andK are the root-mean-square values of area-averaged horizontal divergence of near-surface flows and of the accumulation-dispersal coefficient, respectively. The reason whyK tends to have the order of magnitude of weak or mediumQ is discussed. The doubling-halving time of the distribution density due to accumulation-dispersal,T, is related toK byT=(log_e2)/¦K¦L ^2/3. Finally, sampling time-intervals to estimate accumulation-dispersal coefficients are referred to.     

酸化过程对不同碳酸钙含量的海洋沉积物中总氮及其同位素分析的影响

为节约成本和样品,一些学者同时分析海洋沉积物中的碳、氮及其同位素（TOC、TN、δ¹³C和δ¹⁵N）。分析沉积物中的δ¹³C,需要对样品进行酸化去除无机碳,但是这一酸化过程会使TN和δ¹⁵N的分析结果产生偏差,且偏差范围与沉积物中无机碳含量（CaCO₃）有关。本研究选取了低CaCO₃含量（1-16%）和高CaCO₃含量（20-40%）的海洋沉积物样品,比较了酸化过程对TN和δ¹⁵N的影响。研究结果表明,酸化过程对海洋沉积物中TN和δ¹⁵N的分析结果产生了显著影响。对于低CaCO₃含量的样品,酸化导致样品中TN流失了约0-40%,δ¹⁵N偏移了约0-2‰;而对于高CaCO₃含量的样品,酸化导致样品中TN流失了约10-60%,δ¹⁵N偏移了约1-14‰。表明酸化对TN和δ¹⁵N的影响已经超过了仪器的误差范围0.002%（TN）和0.08‰（δ¹⁵N）,将影响TN和δ¹⁵N的环境指示意义。因此,即使海洋沉积物样品中CaCO₃含量很低,也必须用原样分析TN和δ¹⁵N以避免酸化过程的影响。