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1.
对海洋沉积物中有机碳的主要测定方法优缺点进行了讨论和对比。 重铬酸钾—硫酸亚铁法主要难题是在计算时无法知道沉积物中有机碳的氧化数,因而所测值不够准确。 高温燃烧法对碳酸盐含量高的样品,测定误差较大。 经改进的过硫酸钾氧化法是个比较好的方法,可连续测定沉积物中的无机碳和有机碳。 相似文献
2.
为探讨南海的海水碳酸盐现况，本文利用“海研一号”三个航次（第266、287及316航次）的机会，搜集南海东北角的碳酸盐因子，如温度盐度、pH值、总碱度及总二氧化碳等。南海深层水具有西菲律宾海水深约2200m的水团特性，实测结果显示此两水团的碳酸盐因子并没有明显的差异。由滞留时间、无机碳及有机碳分解速率计算结果显示，南海深层水的滞留时间以40a较为合理。 相似文献
3.
根据2007年8月(夏季),11月(秋季),2008年1月(冬季)和2010年4月(春季)在胶州湾海域测得的p H、溶解无机碳(DIC)、总碱度(Alk),以及通过以上参数计算得到的二氧化碳分压(p CO2)的数据,结合现场的化学、水文、生物等参数,探讨和分析了该海域的二氧化碳各参数的分布特征、季节变化和影响因素。结果表明:胶州湾p H、DIC、Alk和p CO2的年变化范围分别为:7.77—8.30,1949.2—2201.8μmol/kg,2033.9—2382.5μmol/kg和89.9—745.3μatm,均呈现明显的时空变化。温度是影响胶州湾碳酸盐体系的主要影响因素之一,同时陆地径流和降水会降低海水碳酸盐体系中各参数的含量,但是人类活动和生物活动也会在一定程度上增加DIC、Alk和p CO2的含量。 相似文献
4.
南海北部4万年以来有机碳和碳酸盐含量变化及古海洋学意义 总被引：5，自引：0，他引：5
南海北部陆坡的17937柱状样上部4万年来有机碳和碳酸盐的含量分布特征显示：有机碳含量总体显示出冰期高、间冰期低的特征,碳酸盐则相反。C／N元素比分布范围和二组分分析说明该站位的有机碳以海洋自生有机碳为主,全新世达80％以上。根据海洋沉积物中总有机碳含量和两类不同来源有机碳所占比例计算得出的海洋自生生物产生的有机碳含量在MIS2时期最高,说明末次冰期海洋生产力提高。冰期冬季风强化,海水混合程度加强,营养物质利用更充分以及陆源输入增多导致营养物质增加。碳酸盐含量主要受陆源物质稀释的影响,为“大西洋型”旋回。碳酸盐旋回在全新世早中期存在低碳酸钙事件,可能与该时期的强降雨冲刷所致陆源稀释作用增强、海水溶解作用增强以及海洋表层生产力的降低等综合作用相关。 相似文献
5.
海洋碳循环是全球碳循环的重要组成部分,是影响全球变化的关键控制环节。海洋是地球最大的碳库,是地球吸纳CO2的重要缓冲器。海水中溶解无机碳是海洋CO2系统的重要参数,利用AS-C3型溶解性无机碳分析仪进行不同盐度海水溶解无机碳的测量,利用t检验法检验使用仪器的测量精度,探寻盐度与海水总溶解无机碳的关系。实验结果表明:AS-C3型溶解性无机碳分析仪的测量精度在±0.3μmol/L左右,测量过程中无系统差异;海水盐度与总溶解无机碳呈正相关关系,即盐度增大,海水总溶解无机碳增加。最后总结了海水总溶解无机碳测量时的影响因素,如N2纯度、气流状况、实验过程中的温度控制等。 相似文献
6.
杭州湾作为典型的高浑浊度海湾,对其水体碳酸盐体系分布特征的研究相对较少。本文基于两个夏季航次(2018年和2019年)获取的调查资料,阐述夏季杭州湾水体中碳酸盐体系参数的空间分布特征,并进一步分析影响溶解无机碳偏离保守混合作用的主要过程及相对贡献。数据结果表明,杭州湾内表层溶解无机碳浓度与总碱度的变化范围分别为1 553～1 964 μmol/kg和1 577～2 101 μmol/kg,略低于长江口(1 407～2 110 μmol/kg和1 752～2 274 μmol/kg),溶解无机碳浓度和总碱度的空间分布受控于淡水与外海水混合的影响,在潮汐作用下,总体呈现出湾内低,向湾外逐渐升高的趋势。影响表层溶解无机碳非保守混合分布的主要过程中,海?气交换降低溶解无机碳浓度,呼吸作用增加溶解无机碳浓度,两个过程对溶解无机碳浓度变化量的贡献分别为(?42.3±11.7)%与(34.2±14.3)%,净效应呈现为相对平衡的状态。通过计算获得表层海水pCO2的平均值为799 μatm (675～932 μatm),海湾总体表现为大气CO2的源。此外,湾内海水碳酸盐缓冲因子的范围为12.8～23.8,对CO2的缓冲能力弱于邻近东海海水(缓冲因子平均值约为11.9),指示其与外部水体的交换可能会降低附近海域的酸化缓冲能力。相对其他河口/海湾而言,杭州湾内高浊度与强潮汐的特点使其湾内水体的碳酸盐体系分布特征具有区域特殊性。 相似文献
7.
8.
青岛近海冬末春初海水碳酸盐体系的特征 总被引：1，自引：0，他引：1
通过在青岛近岸海域采集海水样品,测定了海水pH、总碱度(TA)、溶解无机碳(DIC)以及溶解钙离子,并根据这些参数计算了海水中的碳酸氢根、碳酸根等分量以及海水二氧化碳分压(pCO_2)、碳酸钙饱和度等参数。各站点海水pH范围为8.09~8.18,平均8.13;TA范围为2309~2345(mol/kg,平均2325(mol/kg;DIC范围为2158~2200(mol/kg,平均2180(mol/kg;海水中溶解钙离子的浓度为0.3700~0.3732g/kg,平均0.3716g/kg。求得海水pCO_2范围为371~476(atm,平均415(atm;方解石和文石的饱和度范围分别为2.31~2.84和1.45~1.78,平均值分别为2.57和1.61。通过与温度、盐度进行比较,发现冬末春初青岛近岸海域海水总碱度、溶解无机碳和溶解钙离子具有较为均匀的特征,是冬季混合导致的结果。海水pH有一定的变化性,与营养盐和叶绿素a的关系显示,观测区西部已开始增强的生物生产使海水pH升高,pH是该季节影响海水pCO_2、碳酸钙饱和度等参数的主要因素。该季节青岛近海总体上表现为大气CO_2的弱源,但西部海区是大气CO_2的弱汇。 相似文献
9.
分析表观耗氧量、滴定碱度及总二氧化碳量等资料来研判红海及亚丁湾间之海水交换。结果显示,红海深层水的方解石及霰石饱和度均比亚丁湾和阿拉伯海深层水的饱和度高。红海全水柱之方解石和霰石都处於过饱和状态,亚丁湾和阿拉伯海中各深度之方解石亦呈过饱和状态,但霰石的饱和探度则大约在500m左右。分析深层水之生物体无机碳与有机碳的分解比值,可以发现此地区深层水中,大约有25％的总二氧化碳增加量是由无机碳酸钙溶解而来。 相似文献
10.
红海及亚丁湾间之海水交换 总被引：2，自引：0，他引：2
分析表观耗氧量、滴定碱度及总二氧化碳量等资料来研判红海及亚丁湾间之海水交换。结果显示，红海深层水的方解石及霰石饱和度均比亚丁湾和阿拉伯海深层水的饱和度高。红海全水柱之方解石和霰石都处於过饱和状态，亚丁湾和阿拉伯海中各深度之方解石亦呈过饱和状态，但霰石的饱和深度则大约在５００ｍ左右。分析深层水之生物体无机碳与有机碳的分解比值，可以发现此地区深层水中，大约在２５％的总二氧化碳增加量是由无机碳酸钙溶解而 相似文献
11.
In order to clarify the chemical forms of minor metallic elements occurring in the ocean, a new method of separation of organic compounds of metals in sea water by using XAD-2 resin was contrived. By applying the new method of determination, it is found that, (1) More than 80 % of V, Fe, Cd and Cu dissolved in sea water are present in organic forms regardless of the depth; (2) A most part of Co and Pb are present in organic forms near the surface, but they change into inorganic forms in the deep layer up to 50 to 60%; (3) Of the total amounts of dissolved Al, Ni, Zn, Ag, Mo, and U, less than 30 % are present in organic forms in sea water anywhere in the ocean; (4) Up to 45% of Se is in organic forms. 相似文献
12.
Dissolved organic carbon (DOC) is the largest organic carbon reservoir in sea water and plays an imporrant role in the marine carbon cycle and other biogeochemical processes in the ocean. Accurate and precise determinalion of the bOC concentration in sea water is thus a prerequisite for any interpretation of DOC biogeochemistry. A key factor in analytical quality control is an accurate determination of the blank. The assessment and distinction of DOC blanks are essential for the precise measurements of oceanic DOC. The total DOC blank includes instrument and water blanks in the high temperature catalytic oxidation (HTCO) method. DOC can be measured accurately using the HTCO method only when the instrument blank is correctly distinguished from the total DOC blank and corrected in the sample measurements. Low DOC blanks can be achieved by extensive conditioning of new catalysts and the whole instrument system, whereas instrument blanks can be quantified by subtracting the water blank from the total DOC blank. We have been able to produce low carbon nanopure water [≤2μmol/dm3(C)] and have a low instrumental blank [< 5-6 μmol/dm3(C)] when using the HTCO method. Results of concentrations and distributions of DOC in the Gulf of Mexico and the North Atlantic are oceanographically consistent. Results from DOC measurements on samples from the international DOC methods comparison program further confirmed our low values of both nenopure water and the instrument blank. 相似文献
13.
Automatic determination of dissolved organic carbon in seawater in the sub-ppm range 总被引：1，自引：0，他引：1
G. Cauwet 《Marine Chemistry》1984,14(4):297-306
The improvement of a dissolved organic carbon (DOC) analysis technique is described. This continuous flow system, based on both persulfate and UV oxidations, allows the automatic determination of DOC in sea and estuarine waters. The use of FID detection gives a very high sensitivity, permitting the detection of small variations in carbon content. The efficiency of the method and its sensitivity are tested, together with the influence of initial pH and duration of nitrogen bubbling. The system can also be used to determine total or inorganic carbon. 相似文献
14.
A new method of determination of selenium and separation of Se(IV) and Se(VI) in sea water is described. The selenium is determined by fluorometric method using Se-DAN complex in cyclohexane media. Prior to the fluorometric determination, Se(IV) is separated from sea water by means of Se(IV)-DDTC complex which is adsorbed on the macroreticular resin. As to the separation of the total selenium from sea water sample, the reduction and coprecipitation method is used. Se(VI) is determined with the same method as used for the total selenium after the separation of Se(IV). The average recoveries are 92.5±1.3% for Se(IV) and 97.4±0.9% for Se. The standard deviation of analytical results is below 10%. 相似文献
15.
本文讨论了介绍了用气相色谱法测定海水中无机离子Ｓｅ（－Ⅱ，Ｏ，Ⅳ，Ⅵ）；Ｂｅ（Ⅱ）；Ｃｒ（Ⅲ，Ⅳ）；ＣＨ３Ｈｇ＾＋，ＮＯ３，ＮＯ２，Ｂｒ，Ｉ，ＣＮ的测定方法和色谱条件。 相似文献
16.
A new dry combustion method for the simultaneous determination of total organic carbon and nitrogen in seawater is presented. Concentrations of total organic carbon obtained using this method average about 2.0 mg/l in surface water and 1.5 mg/l in deep water in the Northwest Atlantic. These concentrations are significantly greater than those reported using wet oxidation and wet combustion methods, but are comparable to concentrations reported by Russian workers using a similar dry combustion method. Organic nitrogen concentrations average 0.44 mg/l in surface water and 0.12 mg/l in deep water, yielding CN ratios for total organic matter of 5 and 12 respectively. 相似文献
17.
Satoru Kanamori 《Journal of Oceanography》1982,38(3):131-136
A new method for shipboard calibration of an infrared absorption carbon dioxide analyser was devised, utilizing the oxidative decomposition reaction of oxalic acid by permanganate in acid solution. With the present method, shipboard analysis of total carbon dioxide in 2 ml of sea water can be carried out with an error of less than 0.5 %. Some improvements in the analyser system are also presented. 相似文献
18.
Daiki Nomura Toru Takatsuka Masao Ishikawa Toshiyuki Kawamura Kunio Shirasawa Hisayuki Yoshikawa-Inoue 《Estuarine, Coastal and Shelf Science》2009
Physico-chemical properties in the brine and under-ice water were measured in Saroma-ko Lagoon on the northeastern coast of Hokkaido, Japan, which is connected to the Sea of Okhotsk, during the period from mid-February through mid-March 2006. The brine within brine channels of the sea ice was collected with a new sampling method examined in this study. Salinity, dissolved inorganic carbon (DIC), total alkalinity (TA), dissolved oxygen (DO), nutrients and oxygen isotopic ratio (δ18O) contained in the brine within brine channels of the sea ice and in the under-ice water varied largely in both time and space during the ice melt period, when discharge from Saromabetsu River located on the southeast of the lagoon increased markedly due to the onset of snow melting. The under-ice plume expands as far as 4.5 km from the river mouth at mid-March 2006, transporting chemical components supplied from the river into the lagoon. The under-ice river water was likely transported into the sea ice through well-developed brine channels in the sea ice due to upward flushing of water through brine channels occurred by loading of snowfalls deposited over the sea ice. These results suggest that the river water plume plays an important role in supplying chemical components into the sea ice, which may be a key process influencing the biogeochemical cycle in the seasonally ice-covered Saroma-ko Lagoon. 相似文献
19.
M.D. MacKinnon 《Marine Chemistry》1979,8(2):143-162
A method based on a dynamic head-space extraction and high-temperature oxidation of the trapped organic matter is described for the determination of the volatile organic carbon (VOC) concentration in seawater. The VOC concentrations in various geographic regions have been measured and calculated as a fraction of the total organic carbon (VOC/TOC). The VOC concentrations ranged from 15–60 μg C/liter in most oceanic areas. This volatile component was found to be a small fraction (1.5–6%) of the TOC. The VOC concentrations are highest in coastal regions and in the surface zone while the VOC/TOC ratio is relatively constant with depth and location. The volatile organic components may be important to the cycling of organic matter in sea water and the dynamics of this role have been postulated. 相似文献
20.
酸洗法测定海洋沉积物有机碳和无机碳含量的致命缺陷 总被引：2，自引：0，他引：2
Organic and inorganic carbon contents of marine sediments are important to reconstruct marine productivity,global carbon cycle, and climate change. A proper method to separate and determine organic and inorganic carbons is thus of great necessity. Although the best method is still disputable, the acid leaching method is widely used in many laboratories because of its ease-of-use and high accuracy. The results of the elemental analysis of sediment trap samples reveal that organic and inorganic carbon contents cannot be obtained using the acid leaching method, causing an infinitely amplified error when the carbon content of the decarbonated sample is 12%±1% according to a mathematical derivation. Acid fumigation and gasometric methods are used for comparison, which indicates that other methods can avoid this problem in organic carbon analysis. For the first time, this study uncovers the pitfalls of the acid leaching method, which limits the implication in practical laboratory measurement, and recommends alternative solutions of organic/inorganic carbon determination in marine sediments. 相似文献