獐子岛养殖海域颗粒有机碳、颗粒氮的时空分布特征

2011年8月、10月、12月和2012年4月对大连獐子岛养殖海域共14个站位进行了大面调查。对其中颗粒有机碳(POC)和颗粒氮(PN)的时空分布特征进行了研究。结果表明,獐子岛养殖海域水体中POC质量浓度的季节变化趋势是:夏季秋季春季冬季。夏季POC质量浓度最高,表、底层的质量浓度分别为0.159~1.672 mg/L和0.045~0.834 mg/L,平均值分别为(0.867±0.451)mg/L和(0.319±0.204)mg/L。冬季表、底层POC质量浓度最低,表、底层POC质量浓度分别为0.020~0.530 mg/L和0.061~0.458 mg/L。平均值分别为(0.240±0.125)mg/L和(0.221±0.129)mg/L。四个季节的POC质量浓度平面分布较为均匀。PN质量浓度的季节变化趋势是:夏季秋季冬季春季。夏季PN的质量浓度最高,表、底层PN的质量浓度分别为0.026~0.439 mg/L和0.020~0.393 mg/L,平均值分别为(0.193±0.067)mg/L和(0.172±0.060)mg/L。春季表、底层PN质量浓度最低,表、底层PN质量浓度分别为0.059~0.178 mg/L和0.024~0.212 mg/L,平均值分别为(0.120±0.047)mg/L和(0.100±0.050)mg/L。PN与POC的分布特征相似,空间分布均匀。叶绿素a(Chl-a)质量浓度的变化趋势为:夏季秋季春季冬季。POC、PN和Chl-a的垂直分布规律相似,春季底层质量浓度高于表层,夏秋两季表层质量浓度高于底层,冬季表、底层质量浓度基本一致。根据C/N以及POC/Chl-a的比值对POC的来源进行初步分析,表明该海域的POC主要来源于海洋生物,并且受陆源的影响较小。     

Distribution of particulate organic carbon and nitrogen in the Bering Sea and northern North Pacific Ocean

Particulate matter was collected in the Bering Sea and the northern North Pacific Ocean during the cruise of R. V. Hakuho-maru, Ocean Research Institute of Tokyo University in summer of 1975. The particulate matter was analyzed for organic carbon and nitrogen, chlorophylla and amino acids.The concentrations of particulate organic carbon and nitrogen were measured with the range of 16–422gC l^–1 and 1–85gN l^–1, 19–186gC l^–1 and 1–26gN l^–1, 46–1,038gC l^–1 and 6–79gN l^–1 and 19–246gC l^–1 and 2–25gN l^–1 in the Oyashio, the Deep Bering Sea, the continental shelf of Bering Sea and the northern North Pacific, respectively. Particulate organic carbon and nitrogen decreased with depth throughout the areas. The average concentrations of organic carbon and nitrogen in the entire water column tended to decrease in the following order; the continental shelf > Oyashio > northern North Pacific > Deep Bering Sea.C/N of particulate matter varied in the range of 3–15 (7 on average) in surface waters throughout the areas and these values tended to increase with depth to 5–20 (11 on average) in deep waters without significant regional variability.Linear regressions between chlorophylla and particulate organic carbon in the euphotic layers indicate that detrital organic carbon accounted for 34.2, 44.9, 49.1 and 25.2 % of particulate organic carbon in the Oyashio, the Deep Bering Sea, the continental shelf and the northern North Pacific, respectively.Particulate amino acid was determined in the range of 10.3–78.0g l^–1, 104–156g l^–1 and 10.4–96.4g l^–1 in the Deep Bering Sea, the continental shelf and the northern North Pacific, respectively. Aspartic acid, glutamic acid, serine, glycine and alanine were found as dominant species of amino acid of particulate matter.     

Concentration of particulate trace metals and particulate organic carbon in marine surface waters by a bubble flotation mechanism

The transport of particulate organic carbon (POC) and particulate trace metals (PTM) to the sea surface by rising bubbles in samples of surface water collected in Narragansett Bay was examined using an adsorptive bubble separation technique. Recoveries of POC ranged from 30 to 59% while those of the particulate form of the trace metals, Al, Mn, Fe, V, Cu, Zn, Ni, Pb, Cr and Cd were generally greater than 50%. The recovery data were used to arrive at a rough order of magnitude estimate of the bubble transport of POC and PTM under open-ocean conditions. While transport rates of the trace metals to the sea surface by both bubble transport and atmospheric deposition varied over approximately 3 orders of magnitude, the ratio of bubble transport to atmospheric deposition for most metals varied over approximately one order of magnitude, perhaps suggesting some degree of coupling between atmospheric PTM and bubble-transported PTM.     

Dissolved and particulate organic carbon and nitrogen in the Northwestern Mediterranean

The distribution of dissolved organic carbon (DOC) and nitrogen (DON) and particulate organic carbon (POC) and nitrogen (PON) was studied on a transect perpendicular to the Catalan coast in the NW Mediterranean in June 1995. The transect covered a hydrographically diverse zone, including coastal waters and two frontal structures (the Catalan and the Balear fronts). The cruise was conducted during the stratified period, characterized by inorganic nutrient depletion in the photic zone and a well established deep chlorophyll a maximum. DOC concentrations were measured using a high-temperature catalytic oxidation method, and DON was determined directly, with an update of the Kjeldahl method, after removal of inorganic nitrogen.The ranges of DOC and DON concentrations were 44–95 μM-C and 2.8–6.2 μM-N. The particulate organic matter ranged between 0.9 and 14.9 μM-C and from 0.1 to 1.7 μM-N. The DOC : DON molar ratio averaged 15.5±0.4, and the mean POC : PON ratio was 8.6±0.6. The distribution of dissolved organic matter (DOM) was inverse to that of the salinity. The highest concentrations of DOM were found in coastal waters and in the stations affected by the Catalan front, located at the continental shelf break.It was estimated that recalcitrant DOM constituted 67% of the DOM pool in the upper 50 m. The data suggest that accumulation of DOC due to the decoupling of production and consumption may occur in the NW Mediterranean during stratification and that the organic matter exported from the photic layer is dominated by C-rich material.     

Vertical distributions of dissolved organic carbon and nitrogen in the Southern Ocean

Detailed vertical profiles of dissolved organic carbon (DOC), nitrogen (DON) and DOC/DON ratios in the Australian sector of the Southern Ocean (56°–65°S around 140°W transect) were obtained by a high-temperature catalytic oxidation method with a modified Shimadzu TOC-5000 unit. The simultaneous analyses of DOC and total dissolved nitrogen (TDN) gave high precision results (±0.7 μMC and ±0.3 μMN). In surface layers, DOC concentrations were lower (45–55 μM) than those generally obtained from other oceanic environments (60–90 μM). The surface concentrations of DON varied from 4 to 9 μM, but within the range generally reported for other ocean regions. Surface excesses of DOC and DON were calculated against nearly constant subsurface concentrations. A consistent contribution of low C/N ratio (2.7–5.0) was found in the mid-surface layer (30–75 m), suggesting more extensive degradation of carbon-enriched materials and/or enhanced supply of nitrogen-enriched ones.     

南大洋浮游植物现存量对颗粒有机碳的贡献

根据中国第15、16次南极考察观测的颗粒有机碳、叶绿素a浓度的数据,探讨浮游植物现存量对南大洋颗粒有机碳的贡献。结果表明,普里兹湾内浮游植物碳对颗粒有机碳的贡献高于湾北部的大洋区,真光层上部浮游植物碳对颗粒有机碳的贡献高于深层水。同时分析两个航次测区叶绿素a浓度和航程途中叶绿素a浓度的分布,以期了解浮游植物在南大洋颗粒有机碳来源中的作用。     

The clay mineralogy of particulate material from some surface seawaters of the eastern Atlantic Ocean

The concentrations of the clay minerals montmorillonite and illite have been determined in 28 samples of particulate material from surface (0–～5 m) waters along the eastern margins of the Atlantic Ocean, and the concentrations of chlorite and kaolinite have been determined in nineteen of the samples.The average concentration of the four clays in the particulate material decreases in the following order: illite (～42%) > kaolinite (～25%) > chlorite (～19%) > montmorillonite (～14%). There are specific trends in the latitudinal distributions of illite and kaolinite in the particulate material; illite decreases and kaolinite increases towards low latitudes. These trends are also found in eolian dusts and deep-sea sediments from the same region, and these clays are considered to have a detrital origin.The concentrations of montmorillonite in the particulate material and deep-sea sediments are similar in the North Atlantic. However, in the South Atlantic the sediments contain about twice as much montmorillonite as does the particulate material. It is suggested that whereas the montmorillonite in North Atlantic deep-sea sediments is largely detrital, that in South Atlantic sediments is both detrital and authigenic.     

Distributions of particulate and dissolved organic and inorganic phosphorus in North Pacific surface waters

Several operationally defined fractions of phosphorus (P) were measured along a surface water transect in the North Pacific. The P content in all fractions was found to increase northward from the edge of the subtropical to the subarctic region. Particulate organic P (POP) concentrations increased from 9 to 110 nmol L^− 1, whereas the particulate inorganic P (PIP) concentrations increased from 1 to 13 nmol L^− 1. A significant correlation between POP, PIP and chlorophyll a suggested that these P pools are associated directly or indirectly with phytoplankton cells. PIP comprised 10–20% of the total particulate P pool across the transect, indicating it is an important component of the marine P cycle in this region. Dissolved non-reactive P (assumed to consist predominantly of non-reactive organic P compounds, thus referred to as DOP) concentration increased from 0.10 to 0.22 μmol L^− 1, whereas soluble reactive P (SRP) concentration increased from 0.01 to 1.42 μmol L^− 1 along the transect. The proportion of DOP and SRP varied widely, with a large proportion of DOP in areas with low total dissolved P concentrations in lower latitudes and a large proportion of SRP in areas with high total dissolved P concentrations in higher latitudes. High demand for DOP in the lower latitudinal region would diminish the concentration of this pool relative to higher latitudinal regions where SRP is more abundant and would be preferentially utilized. The availability of SRP could have a significant impact on the concentration and probably on the composition of DOP. We show that P fractionation provides an important insight for discussing the marine P cycle.     

空白校正对元素分析仪测定海水中颗粒有机碳结果准确性的影响分析

颗粒有机碳(POC)在海洋生态系统乃至全球碳循环中发挥着重要作用,其准确获取至关重要。目前,元素分析仪测定POC是最准确和常用的分析方法,但取样忽略了水体溶解有机碳(DOC)可能带来的影响。针对空白样品如何获取才能有效去除DOC影响的问题,本文设计比较了5种取样方法对POC测定结果的影响,以及滤膜对数据的影响。结果显示, 1) 5种样品取样方法所得的结果差异显著,不进行空白校正会对结果产生较大误差;2)文献和本文设计的空白样取样方法均出现了空白值大于样品值的异常情况; 3)样品继续抽人工海水100 mL即可有效洗去滤膜上吸附的DOC; 4)未过滤的滤膜450℃灼烧5h后可以有效去除滤膜上吸附的碳,但是存放时间越久滤膜从空气中吸附碳的概率越大。本研究确定的人工海水法可以有效去除DOC对测定结果的影响,样品测定结果重复性、精密度高,可准确用于海水POC样品的测定。     

Chemical forms and dynamics of amino acid-containing particulate organic matter in Pacific surface waters

Particulate combined amino acids (PCAA) are the most abundant identified constituents of particulate organic matter (POM) in Pacific Ocean surface waters, but their chemical forms are unclear. In the present study, chemical characterization of amino acid-containing materials in surface POM from subarctic to subtropical waters along 165 °E in the Pacific was carried out by one- and two-dimensional gel electrophoresis. At least four chemical forms of amino acid-containing POM were distinguished: proteins, acidic materials containing peptides, protein/peptide-specific dye-stainable low-molecular-mass materials (stainable materials) and non-stainable materials, all of which were considered to be major components of detrital POM. Seventeen distinct protein containing components were distinguished in samples across the transect. A majority of stainable materials was estimated to comprise 6–8 amino acid residues, while less than six amino acid residues made up the non-stainable materials. Among the four chemical forms, acidic materials and non-stainable materials were major components, accounting for 31–42% and 49–63% of PCAA, respectively, along the transect. Proteins were common, but they were quantitatively less than 2% of PCAA. Stainable materials were regionally variable and more abundant in subarctic waters than in subtropical waters. The mechanistic processes by which such amino acid-containing POM occurs as detrital POM are discussed.     

Light scattering and size distribution of particles in the surface waters of the North Pacific Ocean

The volume scattering function and size distribution of suspended particles in the surface water were determined in the North Pacific. The relationship between the scattering coefficient estimated from observed volume scattering function and cross-section concentration of the particles greater than 2.4m in diameter was found to be linear in both northern and southern regions of central North Pacific. Difference in the constant of proportionality between two regions, however, was very great. Moreover the constant in the southern region was too large compared with the values obtained by the Mie theory. This is considered to be due to the fact that particles smaller than 2.4m which were not measureable by the Coulter Counter, were neglected in the calculation of cross-section concentration. If small particles are taken into consideration, total cross-section concentration and scattering coefficient in the two regions tend to follow a linear relation. From the correlation between the scattering coefficient computed from size distribution and the volume scattering function, the refractive index of particles was estimated to be 1.03–1.05. By the same procedure, the refractive index of particles in Tateyama Harbour where the water was very turbid, was estimated to be also 1.03–1.05. This is in contrast to the result for the refractive index of particles originating from the river which flows into the harbour. This index was found to be 1.10–1.20.     

Total particulate and organic fluxes in anoxic Framvaren waters

Cylindrical sediment traps were deployed at various depths in the anoxic water of Framvaren for two periods of one year (1981–1982 and 1983–1984). The traps were emptied three times during 1981–1982 and five times during 1983–1984. The vertical fluxes of total suspended material, organic carbon and nitrogen were calculated on a daily and annual basis. The average annual sediment flux 20 m above the bottom was approximately 60 g m⁻² y⁻¹ and the flux of organic carbon was 20 g m⁻² y⁻¹. On the basis of an average C/N ratio of 8 and a constant carbon flux below a depth of 20 m, it is concluded that little mineralization of the organic matter takes place in the anoxic water column. Assuming a primary production of the order to 50–100 g m⁻² y⁻¹, 22–24% of that reaches the anoxic water masses. Further breakdown of organic matter takes place in the surface sediments.     

北太平洋西部和印度洋东部及其邻近海域表层水体中137Cs的分布

对北太平洋西部海域、苏禄海及印尼海、中国南海、印度洋东部海域、孟加拉湾及安达曼海等表层水体中放射性核素137Cs的活度进行了测定。结果表明,上述海域表层水体中137Cs活度显示了较大的变化范围,最低值出现在南极附近的南大洋(1.1Bqm-3),较高的活度值则出现在北太平洋西部海域及中国南海(3Bqm-3)。在所研究水域范围内,137Cs活度的纬度分布特征并没有完全有效地反映出137Cs的全球理论大气沉降趋势及其纬度效应。综合本研究及Miyake等人(1988)的测定结果,我们计算出137Cs自表层海水中的析出速率在苏禄海及印尼海约为0.016/a,在孟加拉湾及安达曼海约为0.033/a,在中国南海约为0.029/a,这一结果明显低于西北太平洋日本沿海表层水体中137Cs的析出速率。这可能是因为在这些海域,横向及纵向的水体混合过程相对都较慢,而且颗粒物对137Cs的吸附析出过程也比较弱所致。     

Biological organic carbon export estimated from the annual carbon budget observed in the surface waters of the western subarctic and subtropical North Pacific Ocean from 2004 to 2013

The annual flux of biologically produced organic carbon from surface waters is equivalent to annual net community production (NCP) at a steady state and equals the export of particulate and dissolved organic carbon (POC and DOC, respectively) to the ocean interior. NCP was estimated from carbon budgets of salinity-normalized dissolved inorganic carbon (nDIC) inventories at two time-series stations in the western subarctic (K2) and subtropical (S1) North Pacific Ocean. By using quasi-monthly biogeochemical observations from 2004 to 2013, monthly mean nDIC inventories were integrated from the surface to the annual maximum mixed layer depth and corrected for changes due to net air–sea CO₂ exchange, net CaCO₃ production, vertical diffusion from the upper thermocline, and horizontal advection. The annual organic carbon flux at K2 (1.49 ± 0.42 mol m^?2 year^?1) was lower than S1 (2.81 ± 0.53 mol m^?2 year^?1) (p < 0.001 based on t test). These fluxes consist of three components: vertically exported POC fluxes (K2: 1.43 mol m^?2 year^?1; S1: 2.49 mol m^?2 year^?1), vertical diffusive DOC fluxes (K2: 0.03 mol m^?2 year^?1; S1: 0.25 mol m^?2 year^?1), and suspended POC fluxes (K2: 0.03 mol m^?2 year^?1; S1: 0.07 mol m^?2 year^?1). The estimated POC export flux at K2 was comparable to the sum of the POC flux observed with drifting sediment traps and active carbon flux exported by migrating zooplankton. The export fluxes at both stations were higher than those reported at other time-series sites (ALOHA, the Bermuda Atlantic Time-series Study, and Ocean Station Papa).     

Stability and composition of terrestrially derived dissolved organic nitrogen in continental shelf surface waters

A linear decrease in dissolved organic carbon and nitrogen with increasing salinity offshore from the Georgia coast suggests that organic nitrogen compounds contributed to coastal waters by rivers are stable during the period (2–3 months) of their transfer over the continental shelf. While the C/N ratio decreased with distance from shore, total dissolved organic nitrogen (DON), total amino nitrogen, and primary amino nitrogen showed similar relative decreases, suggesting that nitrogen is associated with refractory organic compounds. Measured amino nitrogen accounted for about 20% of the total DON, leaving about 80% of the organic nitrogen undefined.     

Basin-scale distributions of stable nitrogen isotopes in the subtropical North Atlantic Ocean: Contribution of diazotroph nitrogen to particulate organic matter and mesozooplankton

New N inputs via biological N₂-fixation play a critical role in supporting oceanic primary production and influencing global biogeochemical cycles. Numerous studies have documented significant N₂-fixation rates in the North Atlantic, but relatively little is known of the pathways and fluxes of new N through planktonic food webs. Here, we report the natural abundance of ¹⁵N in, and contribution of diazotroph N (N_D) inputs to, suspended particles and mesozooplankton collected along two transects in the subtropical North Atlantic Ocean (STNA). Samples were collected in April-May 2000 along the two main transects to evaluate spatial trends of ¹⁵N within the Western Atlantic and across the basin. We found that N₂-fixation is a key component in supporting both primary and secondary productions throughout the STNA. N_D contribution was generally higher for suspended particles than for mesozooplankton, and we observed a high N_D contribution to suspended particles over large spatial scales in the western and central STNA. Mesozooplankton N_D incorporation suggests that diazotroph production supports oceanic food webs over longer timescales (e.g., weeks to months) than that of particle turnover (e.g., days). Larger mesozooplankton (1000-4000 ??m) generally incorporated more N_D than smaller mesozooplankton (250-1000 ??m), and thus may exert a stronger influence on an N_D movement within the water column. Spatial and vertical patterns of variation in mesozooplankton ??¹⁵N also suggest either broad geographical differences in an N_D contribution to secondary production, or temporal variations in N_D incorporation via mesozooplankton communities.     

Petroleum hydrocarbons and particulate organic matter in the Sea of Azov waters

The paper discusses the results of investigations on contamination of the Sea of Azov by petroleum hydrocarbons and particulate organic matter. After cessation of open sea observations in 1992, the contamination of the sea by petroleum hydrocarbons is predicted for the period from 1993 to 1997. Translated by Vladimir A. Puchkin.     

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.