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1.
利用切向超滤技术分离和提取九龙江口水体中溶解相(粒径0.45μm)、胶体相(分子量 1 k Da,粒径0.45μm)和真溶解相(分子量1 k Da)的活性磷酸盐(SRP)和溶解态总磷(DTP),初步探讨了不同相中各形态磷的环境化学行为。研究表明,切向超滤过程的SRP和DTP系统空白分别为ND～0.001 mg/dm~3和ND～0.005 mg/dm~3,均未高于方法检出限;样品质量回收率为92.3%～100.0%,满足80.0%～120.0%质量技术要求。真溶解相中SRP、溶解态有机磷(DOP)和DTP占溶解相比例为65.3%～92.3%,存在形式以真溶解相为主;胶体相中SRP、DOP和DTP的含量分别为0.13～4.19、3.25～19.20μg/dm~3和3.39～23.40μg/dm~3,占溶解相比例为1.2%～17.0%;真溶解相和溶解相中的各形态磷含量主要受陆源输入控制。 相似文献
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南极普里兹湾及其邻近海域溶解有机碳的分布 总被引：5，自引：0，他引：5
中国南极科学考察第16航次期间(1999年11月～2000年4月),在南极普里兹湾及邻近海域的不同站位与水深采集海水样品用于溶解有机碳测定,通过高温催化氧化法完成样品的分析.结果表明,在调查期间,南极普里兹湾及其邻近海域各测站上层水体(0～100m)溶解有机碳浓度的变化范围为14.3～181.1μmol/dm3,平均为52.5μmol/dm3,该变化幅度比Ross海、太平洋等海域的相应值略大.溶解有机碳垂直分布的特征是0大于25大于50大于100m,即随深度的增加溶解有机碳浓度逐渐减小,与生物活动在垂直方向上的强弱变化相关.根据200m以深水柱溶解有机碳的垂直分布,可确定研究海域难降解溶解有机碳的浓度为40.4μmol/dm3,与其他研究所报道的数值(～42μmol/dm3)相近.上层水体(0～100m)过剩溶解有机碳的空间分布显示,64°S以北海域溶解有机碳过剩较多,而64°S以南海域则过剩溶解有机碳较少.溶解有机碳浓度与分布特征显示,普里兹湾及其邻近海域溶解有机碳浓度与南大洋其他海域相当,具有低溶解有机碳的一般特征.溶解有机碳浓度的空间分布呈现由西南向东北方向逐渐增加的趋势,这可能与南极陆架夏季上层水的北向扩展有关.生物活动及水体运动是研究海域溶解有机碳分布的主要影响因素. 相似文献
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海水中胶体有机碳的测定──高温燃烧法和紫外/过硫酸钾法的比较 总被引：5，自引：0，他引：5
利用切向超滤(cross-flow ultrafiltration)技术对海水中胶体有机碳(COC)和真溶解有机碳(UOC)进行了分离,并分别用高温燃烧法和紫外/过硫酸钾法对胶体有机碳和真溶解有机碳进行了测定。测定结果表明,切向超滤能定量分离海水中的胶体有机碳,高温燃烧法和紫外/过硫酸钾法对胶体有机碳和真溶解有机碳的测定结果没有明显的系统误差,表明这两种方法的氧化效率基本相同,胶体粒子的存在,对紫外/过硫酸钾法的氧化效率没有显着影响。 相似文献
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利用错流超滤技术提取天然胶体,研究了胶体的有机碳浓度、粒径和来源对海水小球藻(Chlorellaspp.)、亚心形扁藻(Platymonassubcordiformis)和球等鞭金藻(Isochrysisgalbana)生长的影响。结果表明,当粒径为10kDa—0.2μm、胶体有机碳浓度为4.8—238.4μmol/L时,胶体使小球藻、扁藻和金藻的生长率分别提高了4.0%—7.0%、19.1%—28.9%和2.9%—8.7%。海水小球藻生长率的相对增长百分数(Y)值与胶体有机碳浓度(CCOC)呈线性正相关;亚心形扁藻和球等鞭金藻的Y与CCOC呈多项式相关;胶体对扁藻生长的刺激作用大于球等鞭金藻和海水小球藻。粒径为10kDa—0.2μm的胶体对3种藻的促进作用大于1—10kDa的胶体。河口、河流和生源胶体使小球藻的生长率提高1.5%—14.1%,不同来源的3种胶体对海水小球藻的促进作用依序是河流胶体>生源胶体>河口胶体。以上结果表明,天然胶体含有微藻生长所必需的营养元素,对微藻的生长有显著的刺激作用。 相似文献
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依据2013 年夏季和秋季对黄海海域两个航次的调查结果,对该海域溶解无机氮的季节变化,垂直变化,平面分布状况及其影响因素进行了初步分析和探讨。结果表明,该海域溶解无机氮的分布及组成存在明显的季节性：秋季NO3-N的平均浓度为（7.09±4.15）μmol/dm3,远高于夏季（3.21±3.31） μmol/dm3;夏季NH4-N 含量（0.99±0.95）μmol/dm3 较秋季（0.79±0.82）μmol/dm3 高;夏、秋两个季节溶解无机氮的主要组成部分均为NO3-N,其比例约为70 %和90 %。受浮游植物生长、海水层化以及黄海冷水团存留的影响,调查海域夏季表层溶解无机氮的浓度较低,底层浓度较高;此外,研究海域表层溶解无机氮的分布明显受陆源输入控制,表层溶解无机氮的整体呈现出近岸高外海低的现象,NH4-N的高值区主要出现在靠近城市的近岸海区。该论文可以为该海域氮盐的海洋化学循环研究及赤潮等有害藻华的预防提供科学的理论依据。 相似文献
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纳米粒子在大亚湾痕量金属迁移和转换过程中的重要作用 总被引：1，自引：0，他引：1
利用切向超滤技术对大亚湾纳米粒子 (0 .4 5μm～ 10 3 Daltons)进行了有效分离 ,并计算其回收率。测定了大亚湾胶体态和溶解态 (<10 3 Daltons)痕量金属 (Cu、Pb和 Cd)的含量。平均来说 ,14% Cu、2 0 % Pb和 2 4 % Cd实际上与胶体物质密切相关 ,说明胶体物质在这些金属的迁移和转换过程中具有重要作用 相似文献
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南日岛海域溶解态Cu、Pb、Cd含量及其与营养盐的关系 总被引：3，自引：0，他引：3
本文首次报道了福建南日岛海域溶解态Cu、PB、Cd的含量，探讨了它们与营养盐的关系。1990年5月溶解态Cu、Pb、Cd的平均含量分别为0．84、0．230、0．023μg／dm3；1990年10月分别为0. 78、0．290、0. 033μg／dm3。其5月溶解态Cu与无机氮N（NO3-＋NO2-＋NH4 ）线性回归的相关式为Cu（μg／dm3）＝-0. 789＋0．328N（μmol／dm3），相关系数r＝0．853，原子比△Cu：△N＝5．17×10－3：1。 相似文献
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海水中磷氮不同形态的同时测定 总被引：1，自引：0，他引：1
采用过硫酸钾-硼酸-氢氧化钠混合试剂作为氧化剂,同时测定海水中总磷、氮和总溶解态磷、氮,从而建立了海水中磷、氮不同形态的分析流程及步骤。总磷、总溶解态磷浓度为0.35～1.09μmol/dm3时,相对标准偏差小于6.6%;总氮、总溶解态氮浓度为11.8～54.8μmol/dm3时,相对标准偏差小于5.6%。总磷、总溶解态磷和总氮、总溶解态氮的回收率分别为95.0%～106.0%和94.0%～106.0%。本文的分析方法可用于对近岸海水及河口水中磷、氮不同形态的同时测定。 相似文献
11.
At each localized sphere for dynamics of organic matter in the sea, the total amount of nutrient substances is constant, and
the total and inorganic substances must keep a steady state within a certain time.
Based on the simplified assumptions, the mechanism of this steady state in the sea was analyzed using the data of primary
productivity, especialy nutrient absorption of diatom. When a certain amount of phosphate was supplied to different volume
of a basic medium, the absorded-phosphate per pigment unit (chlorophyll-a μg per liter) of diatom was constant. The absorbed-phosphate per pigment unit and initial concentration of phosphate in the
medium had linear relationship within about 200 μg phosphate per liter of the medium. The curves of experimental phosphate
absorption and growth of diatom were found to be consistent with the theoretical one. 相似文献
12.
This study examines the mechanism of oxidation of dissolved organic matter (DOM) in a high-temperature combustion (HTC) carbon analyzer. The HTC analyzer, which is commonly used to measure the concentration of dissolved organic carbon (DOC) in seawater, is still largely empirical in its operation, and little information is yet available on the chemical and physical mechanisms responsible for oxidation of DOM. To examine the role of water, which has been hypothesized to be a source of reactive oxidants in HTC analyzers, several experiments were conducted using gaseous hexane samples and several wet/dry carrier gases. Because the quantity of O2(g) needed to oxidize an injected sample of DOM is quite small, a substantial effort has been made to exclude O2(g) from the combustion furnace of the HTC instrument. In this modified, “air-tight” instrument, the efficiency of conversion of hexane into CO2 was greatest in dry O2 and slightly lower in moist O2. Hexane was only slightly oxidized in dry N2, but it was largely converted into CO2 when moist N2 was used as the carrier gas. These experiments confirm that water provides reactive oxidizing species (perhaps hydroxyl radical) that rapidly convert hexane into CO2 in the combustion tube of a carbon analyzer. Additional experiments with aqueous solutions of potassium hydrogen phthalate and a variety of carrier gases support this basic hypothesis. 相似文献
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Stable carbon isotope distribution of particulate organic matter in the ocean: a model study 总被引：4，自引：0，他引：4
Matthias Hofmann Dieter A. Wolf-Gladrow Taro Takahashi Steward C. Sutherland Katharina D. Six Ernst Maier-Reimer 《Marine Chemistry》2000,72(2-4)
The stable carbon isotopic composition of particulate organic matter in the ocean, δ13CPOC, shows characteristic spatial variations with high values in low latitudes and low values in high latitudes. The lowest δ13CPOC values (−32‰ to −35‰) have been reported in the Southern Ocean, whereas in arctic and subarctic regions δ13CPOC values do not drop below −27‰. This interhemispheric asymmetry is still unexplained. Global gradients in δ13CPOC are much greater than in δ13CDIC, suggesting that variations in isotopic fractionation during organic matter production are primarily responsible for the observed range in δ13CPOC. Understanding the factors that control isotope variability is a prerequisite when applying δ13CPOC to the study of marine carbon biogeochemistry. The present model study attempts to reproduce the δ13CPOC 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, μi, of the phytoplankton. In the Atlantic Ocean, where most field data are available, both parametrizations reproduce the latitudinal variability of the mean δ13CPOC distribution. The interhemispheric asymmetry of δ13CPOC can mostly be attributed to the interhemispheric asymmetry of CO2 concentration in the water. However, the strong seasonal variations of δ13CPOC as reported by several authors, can only be explained by a growth rate-dependent fractionation, which reflects variations in the cellular carbon demand. 相似文献
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Nahla S. El-Shenawy Richard Greenwood Ismail M. Abdel-Nabi Zohour I. Nabil 《Ocean Science Journal》2009,44(2):69-77
Passive sampling could provide the solution to problems associated with costly and time consuming sampling programmes and biomonitoring. Mussels (Mytilus edulis) and Chemcatcher passive sampler were simultaneously analyzed for sequestered pesticides and polychlorinated biphenyls (PCBs) by gas chromatography with mass spectrometry (GC/MSD). The Chemcatcher passive sampler based on a solid phase extraction disc with two types of diffusion-limiting membranes (polyethelene and polysulphone), were also compared. Diuron, atrazine, irgarol and lindane were accumulated in the polysulphone passive sampler in greater concentration than in the mussels or in the other passive samplers with polyethelene limiting-membrane. Mussels can accumulate in their tissue high concentration of non polar compounds such as PCB 52, dieldren and PCB 153; more than the passive sampler with polysulphone membrane. The device with polyethelene limiting membrane has high affinity capacity to concentrate high amount of phenenthrene, dieldrin, PCB 153 and PCB 52, so it acts as a sampler for non-polar compounds. The highest uptake rate of hydrophobic compounds by Chemcatcher was observed for analytes with log octanol-water partition coefficient (KOW) between 4.5 and 7.5. Laboratory-based studies using passive samplers to assess the potential for bioaccumulation could provide robust and reliable information at relatively low cost compared to biomonitoring data. Laboratory data obtained using passive samplers could be related to accumulation under field conditions where field assessments are required. 相似文献
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本文以2021年5月长江口南北支采集的表层水为研究对象,通过测定氢、氧同位素,溶解有机碳(DOC)浓度,有色溶解有机质(CDOM)的吸收光谱和荧光光谱参数,探讨了夏季长江口北支、南支(北港、北槽、南槽)水体溶解有机质的组成、分布及其影响因素。沿长江下游到河口近海,南、北支DOC浓度分别为1.68±0.16 mg/L和1.46±0.31mg/L,CDOM的吸光系数a350分别为2.37±0.61 m-1和1.59±0.24 m-1。南支整体具有“高类腐殖质、低类蛋白”的特征,北支则具有“低类腐殖质、低类蛋白”的特征,这可能与南北支的径流量差异有关。在南北支不同分汊河道(北支、南支北港、南支北槽和南支南槽)中,南槽和北支有类似的海水入侵特征,但南槽具有较强的类蛋白组分输入,而南支北港和北槽样品间无显著差异,均表现为河流有机质为主的特征。对比2011年长江南北支DOC和CDOM数据显示,作为长江主河道的南支在2021年无明显变化,而北支有显著的变化。这些结果综合表明长江口DOM的变化格局可能受水动力条件(径流量)、人类活动因素共同作用的影响。比较全... 相似文献
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厦门湾有色溶解有机物的光吸收特性研究 总被引：3，自引：0，他引：3
研究了厦门湾九龙江河口区、西海域、同安湾及东侧水道海水中有色溶解有机物(CDOM)的光吸收特性,分析了CDOM的河口行为,并讨论了CDOM光吸收特性与其荧光性质之间的关系。结果表明,厦门湾表层海水CDOM光吸收系数a(355)的水平分布表现为河口区最高、东侧水道最低、西海域和同安湾介于两者之间,底层水a(355)的分布与表层基本相似,表明陆源河流输入是厦门湾CDOM的主要来源;a(355)的垂直分布为表层高于底层,主要受水文和生物因素控制。厦门湾表层水CDOM光谱斜率S的平均值介于0.014—0.018nm-1,但河口低盐度区S值较小,反映陆源腐殖质的影响。a(355)在河口混合中呈保守行为,表明CDOM具有良好的保守性质。CDOM的吸收系数a(355)与其荧光强度之间表现为较好的相关关系,指示可以用灵敏度更高的荧光方法来研究CDOM的分布和行为。 相似文献
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The Vallecitos syncline is a westerly structural extension of the San Joaquin Basin. The Vallecitos oil field, comprised of eight separate areas that produce from Cretaceous and Paleogene reservoirs, accounted for 5.4 MMB of oil and 5.6 BCF associated of gas through 2010. However, exploration for oil and gas in the Vallecitos area is challenging due to structural complexity and limited data. The purpose of this study is to evaluate whether source rocks are actively generating petroleum in the Vallecitos syncline and to improve our understanding of burial history and timing of hydrocarbon generation. We conducted biomarker analysis on twenty-two oil samples from the Vallecitos syncline. Source-related biomarkers show two genetic groups of oil, which originated from two different source rocks. These results differ from earlier published interpretations in which the Kreyenhagen Formation is the only source rock in the Vallecitos syncline, and suggest that the Cretaceous Moreno Formation in the syncline also is an active source rock.Stratigraphic evidence and modeling suggest that late Cenozoic episodes of erosion due to folding and uplift removed significant overburden on the flanks of the syncline. To better understand the petroleum systems and clarify the total active source rocks in the area, 2D burial histories were generated through the Vallecitos syncline. A published cross-section through the deepest part of the syncline was selected to conduct thermal history, basin evolution, and migration analyses. The 2D model results indicate that the lower Kreyenhagen Formation has various maturities within the formation at different locations in the present-day syncline. The basal part of the Kreyenhagen Formation is in the dry gas window and maturity decreases away from the central part to the flanks. It remains immature along shallow portions of the present-day flanks. In contrast, the basal part of the Moreno Formation achieved extremely high maturity (past the gas generation zone) but is in the oil generation zone on the flanks of the syncline at shallow depth. All of our geochemical and 2D model results suggest that there are two active source rocks in the Vallecitos syncline. Accordingly, we propose that there are two active petroleum systems in the Vallecitos syncline. 相似文献
18.
The first objective of this introductory paper is to summarize our present understanding of the quantities of total organic carbon produced in the ocean by photosynthesis and non-biotic photochemical reactions, and the amount entering the ocean from rivers, the atmosphere, and the sediments. In this overview it will become apparent that our knowledge of the primary mechanisms and processes involved with the input of organic matter to the ocean via rivers, the atmosphere, sediments, and in situ photochemical reactions is fragmentary and often completely lacking. This becomes critical when we attempt to estimate the input of certain naturally occurring organic compounds and some synthetic organic compounds, since their primary input to the sea is generally via the atmosphere, rivers, and dumping. Thus the second objective of this paper is to emphasize our need to understand the mechanisms involved in these other input processes and the necessity of developing field programs and mathematical models to evaluate the input of specific organic compounds via these pathways. Polychlorinated biphenyls are used as examples of how necessary it is to understand these other input routes in order to evaluate the cycling of pollutant substances in the ocean. 相似文献
19.
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. 相似文献
20.
错流超滤技术在海水胶体态铀、钍、镭同位素和有机碳研究中的应用 总被引：17，自引：3，他引：14
建立了由预过滤装置、蠕动泵、中空纤维超滤膜(AmiconH10P10-20,标称截留分子量10KDa)和连接管组成的错流超滤系统,利用荧光标记的40KDa葡聚糖和已知放射性活度的234Th示踪剂评估了超滤膜的截留和吸附性质,探讨了234Th在超滤过程中的渗透行为,考查了该系统用于实际海水样品时铀、钍、镭同位素和有机碳的质量平衡状况.结果表明,10Kda中空纤维超滤膜对40Kda葡聚糖具有良好的截留效率(85%),而吸附损失率为18%.铀、钍、镭同位素和有机碳在超滤过程中均达到极佳的质量平衡,回收率R=95%～98%,优于大多数文献报道的值.234Th在超滤过程中的渗透行为可以很好地用渗透模型加以描述.研究组分胶体态含量占“溶解”态含量的份额大小顺序如下:钍同位素、有机碳、镭同位素约等于铀同位素,这与钍为强颗粒活性元素、铀和镭为水溶性元素的地球化学性质相吻合. 相似文献