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1.
南大洋普里兹湾沉积物中生物硅含量与分布   总被引：1，自引：2，他引：1  
利用中国第18,21次南极考察获得的沉积物样品,对南大洋普里兹湾沉积物中生物硅(BSiO2)的含量以及分布特征进行了初步研究.结果表明:普里兹湾表层沉积物中生物硅含量丰富,生物硅含量在4.89%~85.41%之间变化,平均为30.90%.最高值出现在湾内的IV-10站.生物硅的垂向分布与间隙水中硅酸盐呈现相反的变化趋势.表层沉积物中生物硅和有机碳分布趋势与表层海水中叶绿素a、初级生产力的分布趋势密切相关,最大值均出现在普里兹湾环流中心区域,较好地反映了上层水体中初级生产力的变化状况.  相似文献   

2.
《海洋科学》2012,36(2)
根据2008年8月与11月在东山湾海域获得的调查资料对表层水中溶解态Fe（II）和Fe（III）含量、浮游植物叶绿素a、营养元素及其浓度等环境参数进行分析。结果表明,夏、秋季海水中Fe（II）浓度及其在总溶解铁中所占比例均与浮游植物叶绿素a呈正相关,其相关系数分别为0.7959、0.9219。现场围隔实验表明,海水中总溶解态Fe含量在24 h内有较大的变化,最大减少量达到17.4%。DS2站点海水中Fe（II）浓度及其在总溶解铁中所占比例随光照强度增加而增加。最高值与初始值相比较,叶绿素a较高的DS2站点海水中Fe（II）浓度增加较叶绿素a较低的DS5号站点高0.053μg/L。Fe（II）和Fe（III）加富实验研究了溶解态的Fe（II）和Fe（III）在海水中相互转化。高浓度的Fe（II）在海水中被氧化成Fe（III）,海水中浮游植物也会引发光还原作用使Fe（III）还原成Fe（II）。  相似文献   

3.
东山湾海水中Fe(II)和Fe(III)相互转化围隔实验研究   总被引：1，自引：0，他引：1  
根据2008 年8 月与11 月在东山湾海域获得的调查资料对表层水中溶解态Fe(II)和Fe(III)含量、浮游植物叶绿素a、营养元素及其浓度等环境参数进行分析。结果表明, 夏、秋季海水中Fe(II)浓度及其在总溶解铁中所占比例均与浮游植物叶绿素a 呈正相关, 其相关系数分别为0.7959、0.9219。现场围隔实验表明, 海水中总溶解态Fe 含量在24 h 内有较大的变化, 最大减少量达到17.4%。DS2 站点海水中Fe(II)浓度及其在总溶解铁中所占比例随光照强度增加而增加。最高值与初始值相比较, 叶绿素a 较高的DS2 站点海水中Fe(II)浓度增加较叶绿素a 较低的DS5 号站点高0.053μg/L。Fe(II)和Fe(III)加富实验研究了溶解态的Fe(II)和Fe(III)在海水中相互转化。高浓度的Fe(II)在海水中被氧化成Fe(III),海水中浮游植物也会引发光还原作用使Fe(III)还原成Fe(II)。  相似文献   

4.
讨论了1997年冬季在北太平洋西北海域7个站位的表层至200m水深水柱中溶解及颗粒态234Th,颗粒态有机碳(POC)、氮(PON)及叶绿素a浓度的垂直分布剖面.溶解态、颗粒态及总的234Th的放射性在真光层中显著低于母体238U的放射性,总的234Th放射性在水深大于100m时趋于平衡.利用234Th-238U在海洋表层海水中的放射性不平衡推导出了北太平洋西北海域冬季真光层海水中234Th的平均停留时间和输出通量以及颗粒态有机碳和有机氮的输出通量.在亚北极环流区溶解态234Th的停留时间为40~50d,而在黑潮-亲潮共同影响区为20d左右.颗粒态有机碳和有机氮从真光层的输出通量范围分别为3.8~8.2和0.50~0.98mmol/(m2·d),西部海区高于东部海区,南部海区高于北部海区.在黑潮-亲潮共同影响区较高的颗粒态有机碳输出通量表明光照量及陆源营养盐物质的提供是两个决定生产力的主要因素.叶绿素a的水深分布和POC/PON的值同Redfield的比值的一致性表明这个海区的冬季颗粒物主要由浮游植物构成.北太平洋西北海域在冬季的颗粒有机碳输出通量可高于世界大洋一些海区春、夏季的颗粒有机碳输出通量.  相似文献   

5.
本文报道了1990年10月日本以南海水重金属垂直分布的一些结果,讨论了溶解态铜、镉和镍的浓度同生物地球化学环境的关系.表层水中溶解态铜的浓度比500m以浅层的浓度高;在4000m以深,溶解态铜达最大值8.2nmol/dm3.溶解态镍的浓度由表层的3.4nmol/dm3变化到深层的8.5nmol/dm3.最高值出现于较冷的水体中.溶解态镉的垂直剖面属良好的营养盐型分布,溶解态镉与磷酸盐呈线性相关,原子比是△Cd:△N:△P=3.5×10-4:14:1.  相似文献   

6.
南黄海西部冬季表层水中的溶解态重金属分布特征分析   总被引：1，自引：0，他引：1  
分析了2007年1月的南黄海西部调查得到的表层海水中的溶解态重金属数据资料,研究了海水中溶解态重金属的分布特征及影响机制.结果表明各溶解态重金属的空间分布大致呈现近岸海区向远岸逐渐减少的趋势;但调查海域远岸水体南部(34°N以南)溶解态重金属质量浓度整体上比中部和北部海域的略高;而近岸分布无明显规律.重金属Cu,Pb,Zn和Cd之间具有良好的正相关性,苏北站位Cu和As与盐度以及与悬浮物含量间呈相反的显著相关性.说明重金属分布除受到来自近岸污染的影响,还可能受到海水水动力学及黄海暖温高盐水舌的影响;苏北海域As的分布可能受到该海域特定的氧化还原水环境影响.  相似文献   

7.
利用2006年夏、冬季两个航次采集的长江口、杭州湾及邻近海域表层海水水样,分别采用石墨炉无火焰原子吸收分光光度法和火焰原子吸收分光光度法,测定了海水中溶解态Cu、Pb、Cd、总Cr的含量以及溶解态Zn的含量,研究了该海域表层海水中溶解态Cu、Pb、Zn、Cd和总Cr的平面分布状况,结果表明:(1)夏季表层海水中溶解态Cu、Pb、Zn、Cd和总Cr的平均质量浓度分别为0.90、0.54、5.80、0.080和0.46 μg/dm3;冬季则分别为1.01、0.81、9.32、0.070和0.31 μg/dm3,上述重金属元素含量基本达到国家一类海水水质标准,仅夏、冬季Pb的部分站位以及冬季Zn的部分站位达到国家二类海水水质标准.(2)表层海水溶解态Cu、Pb、Zn的质量浓度总体平面分布规律为:冬季高于夏季;Cd和总Cr的质量浓度总体平面分布规律为:夏季高于冬季.(3)影响近岸海域表层海水溶解态重金属分布的因素比较复杂,入海径流和排污口等输入海域的重金属对海水表层的重金属分布具有决定性的作用,同时,盐度、pH值、悬浮颗粒物质、营养盐等也是重要的影响因子.  相似文献   

8.
利用2008年秋季胶州湾两个航次的调查结果,对该海域营养盐等生源要素的分布特征进行了分析,并通过相关性分析及陆海同步调查数据对其来源做了初步探讨.结果表明,胶州湾秋季两个航次的叶绿素、营养盐、化学需氧量、温度、光照、盐度、溶解氧等各调查要素相应的平面分布趋势基本相同,除盐度和温度外均表现出由河口向离岸逐渐降低的趋势.秋季可能成为胶州湾浮游植物生长限制因子的要素与叶绿素 a 相关性强弱顺序如下(“**”和“*”分别代表置信水平 P=0.01和 P=0.05):活性磷酸盐:0.889(**)、溶解无机氮:0.724(**)、溶解有机氮:0.549(**)、溶解有机磷:0.523(**)、颗粒态氮:0.474(**)、温度:–0.696(**)、活性硅酸盐:0.410(*)、颗粒态磷:–0.191、浊度:–0.096.由相关性分析结果及陆海同步调查结果可初步得出与叶绿素 a 相关性较强的各要素来源如下:化学需氧量、盐度、溶解无机氮、活性磷酸盐、溶解有机氮、溶解有机磷具有明显的陆源输入特征,颗粒态氮以浮游植物新陈代谢产生为主.  相似文献   

9.
作者以阳极溶出伏安法和氢氧化铁共沉淀—DDC—Ag法测定了黄河口表层海水中溶解态总砷、溶解态有机砷、溶解无机砷、砷(Ⅲ)和砷(Ⅴ)的含量。实验结果表明:1、黄河口区表层海水中丰水期溶解态无机砷的平均浓度(2.26μgL~(-1))高于枯水期的平均浓度(1.43μgL~(-1));2、枯水期内,表层海水中溶解态无机砷浓度与海水盐度之间存在良好的相关性,而在丰水期内无此相关关系;3、两航次中溶解态无机砷的平面分布呈明显的梯度分布,即由河口向渤海湾中部方向溶解态无机砷浓度递减。  相似文献   

10.
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   

11.
Abstract. The temporal variations of nutrients, chlorophyll a (chl a ), suspended particulate matter (SPM) and particulate organic carbon (POC) were measured over 12 months in three shallow coastal brackish water lagoons of the Amvrakikos Gulf, Ionian Sea. Two of the lagoons, Tsoukalio and Rodia, are interconnected but separated from Logarou by a narrow strip of land. Logarou has a better water exchange with the sea as indicated by the higher salinity and dissolved oxygen concentrations and the smaller variation of the above-mentioned parameters. Nitrate concentrations were largely the same in the three lagoons and higher than in the Amvrakikos Gulf. Phosphate concentrations in Logarou exceeded by far those of Tsoukalio/Rodia; the increased phosphate levels recorded in January caused an extended phytoplankton bloom with chl a concentrations higher than in the other two lagoons. Chl a in Tsoukalio was positively correlated with nitrate whereas in the most shallow lagoon, Logarou, it showed a positive correlation with light winds (force 4 and lower), probably caused by resuspension from the sediment. Increased phytoplankton biomass in Logarou coupled with the better water exchange may be related to the higher fish production in this lagoon.  相似文献   

12.
The spatial and temporal distribution of cadmium (Cd) and phosphate in the Southern Ocean are related to biology and hydrography. During a period of 18 days between transects 5/6 and 11, a phytoplankton spring bloom developed in the Polar Frontal region. Upper water Cd concentrations were not depleted and ranged from 0.2 to 0.8 nM at about 10 m depth. These relatively high Cd concentrations are attributed to upwelling of Upper Circumpolar Deep Water (0.5–1.2 nM in the core) in combination with low biological productivity (0.2 to 0.3 mg m−3 chlorophyll-a, 0.3 g C m−2 d−1). Total particulate Cd concentrations at 40 m depth were between 0.02 and 0.14 nM with the maximum in concentration in the Polar Frontal region. Most of the particulate Cd at this depth (85–94%) was detected in the first phase of a sequential chemical leaching treatment which includes adsorbed Cd as well as Cd incorporated in algae. The Polar Frontal region was characterized by minima in Cd concentration and Cd/phosphate ratio of seawater at both transects; values were the lowest at transect 11 after development of the spring bloom which was dominated by diatoms. This decreasing Cd/phosphate ratio in seawater during spring bloom development was attributed to preferential Cd gross uptake which more than compensated the process of preferential Cd recycling. Within the Upper Circumpolar Deep Water, Cd showed a maximum in concentration similar to that of the major nutrients. Both the Cd concentration and the Cd/phosphate ratio of the deeper water increased in southern direction, from 0.4 to 0.7 nM and from 0.2 to 0.3 nM/μM, respectively. Antarctic Intermediate Water has a Cd concentration of 0.21 nM with a Cd/phosphate ratio of 0.10 nM/μM. In Antarctic Bottom Water, Cd concentrations ranged from 0.60 to 0.82 nM.  相似文献   

13.
《Marine Chemistry》2001,76(3):189-209
  相似文献   

14.
A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn2+ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl?1, indicating that the oxidation of Fe2+ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters.  相似文献   

15.
The distributions of the trace metals iron (Fe), copper (Cu) and cadmium (Cd) along with hydrological parameters (salinity, temperature and reactive phosphate) across the New Zealand continental shelf near Otago Peninsula have been studied. This is a region in which the Subtropical Convergence (STC), a major oceanic front separating subtropical and subantarctic waters, is uniquely located close to land, permitting an examination of the influence of terrestrial sources of Fe and Cu on oceanic waters containing excess micronutrients. Acid-soluble (110 nmol kg−1) and dissolved (6.3 nmol kg−1) Fe concentrations were highest over the central shelf, and decreased rapidly across the mixing zone of the STC to about 5 nmol kg−1 for both forms. The distribution of acid-soluble and dissolved Cu were similar to their counterparts for Fe. Depth-concentration profiles for acid-soluble Fe and Cu suggest resuspension of shelf sediments is the main source. The ratio of oxine-labile to acid-soluble Fe varied from 0.03 to 0.26, with the highest values found in the near surface waters. Oxine-labile Fe and Cu also decreased in concentration in a seawards direction, and with depth, indicating the influence of near surface processes on the reactivity of these elements. Cd concentrations across the continental shelf were very low (<200 pmol kg−1) and exhibited no clear spatial trend and no correlation with phosphate. Comparison of the Cd/P ratio across the shelf indicated that the waters in this region were strongly depleted in Cd relative to P. Phosphate concentrations were lowest in neritic water and increased in the seawards direction because of mixing with nutrient-rich Subantarctic Surface Water.  相似文献   

16.
We investigated the water structure and nutrient distribution in the Suruga Bay from April 2000 to July 2002, especially the Offshore Water, which occupies a large part of the bay. The maximum salinity in the upper 200 m varied between 34.49 and 34.71, indicating a temporal change in the influence of Kuroshio Water on the Offshore Water. Seasonal variation in nutrient concentrations was largest from surface to 50 m. On the other hand, the variance in nutrient concentrations within each season was largest in the subsurface layer of 100–300 m in spring, summer and fall. In the Offshore Water, the change of nutrients was negatively correlated with that of salinity in each season. This suggests that an increasing intrusion of saline water brings about a lower nutrient concentration in the Offshore Water. Likewise, negative correlations were observed between the change of the maximum salinity and chlorophyll a (Δ [chl.a-int])/nutrients integrated in the upper 200 m. Δ[chl.a-int] was significantly correlated with the changes of nitrate and phosphorus, but there were no significant correlations between Δ[chl.a-int] and the change of silicate. These results suggest that the concentrations of chlorophyll a and nutrients in the Offshore Water were decreased due to the increasing intrusion of Kuroshio Water. The Offshore Water is likely to be related to the regulation of primary production by nitrate.  相似文献   

17.
Chlorophyll a of total and particles retained on 30 μm mesh plankton net were both determined in surface waters along two cruise tracks ranging from the Subtropical water to the marginal ice zone in the Pacific sector of the Southern Ocean in austral summer. Total surface chlorophyll a in the study area was mostly less than 1 μg chl a 1−1, and showed distributions with no obvious trend associated with different waters masses of the Antarctic and the Subantarctic, although total chlorophyll a concentrations changed greatly within each water mass. Particularly low concentrations of chlorophyll a were detected in the marginal ice zone. Chlorophyll a contained in 30 μm netplankton made up 5∼60% of total chlorophyll a: large near the marginal ice zone and becoming small with travel towards the north. High percentage shares of netplankton chlorophyll a were confirmed even in low total chlorophyll a concentrations in summer in the Southern Ocean. A positive relation was observed between the percentage of 30 μm netplankton and the “average total chlorophyll a”, although there was great scatter. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

18.
A detailed study of particulate and dissolved cadmium distributions on 83 seawater samples from six profiles in the open North Atlantic Ocean showed a relatively homogenous distribution. The mean concentration of cadmium was 60 ± 27 ng/kg and the median concentration of particulate cadmium was 0.2 ng/kg. Although there are regional differences in dissolved cadmium concentrations among stations, it is suggested that cadmium behaves essentially as an inert element in sea water.Particulate cadmium is enriched by about a factor of four in samples from less than 400 m compared to samples from deeper than 1000 m. The high concentrations in surface waters are suggested to be due to aeolian transport of anthropogenically derived cadmium.Additional analyses of cadmium in the Gulf of Maine show a mean value of 230 ng/kg. The higher values in the Gulf of Maine are ascribed to the influence of continental runoff. Twelve sediment samples from the open North Atlantic show a relatively homogenous distribution, ranging from 0.13 to 0.21 ppm on a dry-weight basis.  相似文献   

19.
Results of trace-metal analyses of water samples obtained during a cruise with the Soviet R.V. “Akademik Kurchatov” in the Indian Ocean are presented. The determinations were performed on board with atomic absorption spectrophotometry after a two-stage dithiocarbamate—Freon extraction procedure. Trace-metal concentrations found are in the same range as those found recently for similar open-ocean areas by other workers. The values for lead and zinc are probably high due to contamination. Vertical profiles indicate biogenic processes as controlling factors for the increase of cadmium, copper and nickel concentrations with depth. Iron shows an irregular depth distribution as a result of large random variations in concentration.  相似文献   

20.
The behavior of dissolved cadmium (Cd) in the Danube estuary was investigated through field sampling and mixing experiments using Danube River water and Black Sea water. The experiments were performed by mixing these two end-member waters in various proportions, with the addition of stable or radioactive Cd to the freshwater Danube end-member prior to the mixing. The release of Cd that resulted in maximum concentrations under field conditions was well simulated by mixing experiments. The experimental results were modeled assuming that the release of Cd was the sum of the contribution of physical effects resulting from dilution effects and the contribution of chemical effects resulting from dissolved Cd-complex formation (and isotopic exchange when concerned). In the absence of dissolved Cd-complexing ligands, the release of Cd due to the dilution of the particulate phase during mixing could explain part of the maximum concentrations observed in field conditions. Kinetic effects were established by comparing the theoretical and measured contribution of chemical effects resulting from dissolved Cd-complex formation. The non-equilibrium state observed during the mixing experiment suggested the presence of particulate labile Cd that was not easily mobilized. All these features supported the hypothesis that Cd released in estuaries is controlled both by the dilution of the particulate phase and by kinetic competitive complexation between particulate ligands (covering a large spectrum of nature and strength) and dissolved ligands.  相似文献   

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