南极普里兹湾及其邻近海域溶解有机碳的分布

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.     

Air-sea carbon fluxes and their controlling factors in the Prydz Bay in the Antarctic

The Prydz Bay in the Antarctic is an important area in the Southern Ocean due to its unique geographic feature. It plays an important role in the carbon cycle in the Southern Ocean. To investigate the distributions of carbon dioxide in the atmosphere and surface seawater and its air-sea exchange rates in this region, the Chinese National Antarctic Research Expedition （CHINARE） had set up several sections in the Prydz Bay. Here we present the results from the CHINARE-XVI cruises were presented onboard R/V Xue/ong from November 1999 to April 2000 and the main driving forces were discussed controlling the distributions of partial pressure of carbon dioxide. According to the partial pressure of carbon dioxide distributions, the Prydz Bay can be divided into the inside and outside regions. The partial pressure of carbon dioxide was low in the inside region but higher in the outside region during the measurement period. This distribution had a good negative correlation with the concentrations of ehlorophyll-a in general, suggesting that the partial pressure of carbon dioxide was substantially affected by biological production. The results also indicate that the biological produetion is most likely the main driving force in the marginal ice zone in the Southern Ocean in summer. However, in the Antarctic divergence sector of the Prydz Bay （about 64°S）, the hydrological processes become the controlling factor as the sea surface partial pressure of carbon dioxide is much higher than the atmospheric one due to the upwelling of the high DIC CDW, and this made the outside of Prydz Bay a source of carbon dioxide. On the basis of the calculations, the CO2 flux in January （austral summer） was -3.23 mmol/（m^2 · d） in the inner part of Prydz Bay, i.e. , a sink of atmospheric CO2, and was 0.62 mmol/（m^2 · d） in the outside part of the bay, a weak source of atmospheric CO2. The average air-sea flux of CO2 in the Prydz Bay was 2.50 mmol/（m^2 · d）.     

Features of physical oceanography in the oceans near the Prydz Bay during the 1998/1999 austral summer

1Introduction The Prydz Bay has its open water in the northadjacent to the Indian Ocean sector of the SouthernOcean.It borders on the ice shelf to its south,andthe Antarctic Continent to its east and west.It is thelargest water stretching southward into t…     

长江口跨越锋面颗粒磷季节分布变化特征及影响因素

根据2006年夏、冬季以及2007年春、秋季“海监49号”科学考察船的调查数据,分析了长江口跨越锋面区域(31.00°～31.78°N、121.04°～123.99°E)颗粒总磷(PP),颗粒无机磷(PIP),颗粒有机磷(POP)的季节变化和空间分布特征.结果表明,PIP是水体颗粒磷的主要存在形式;受长江径流输沙量的影...     

Measurements of dissolved organic carbon (DOC) in sea water by high temperature combustion method

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.     

Size fractionated biomass and productivity of phytoplankton and new production in the Prydz Bay and the adjacent Indian sector of the Southern Ocean during the austral summer 1998/1999

INTRODUCTIONComparedwithotheroceansintheworld ,thereisrelativelyhigherlevelofnutrients (ni trate ,phosphate ,silicate)intheSouthernOcean .Butprimaryproductivitiesarelow ,andnewproductionisalsoonlyinthemiddlelevelthere .Itiscommonlyconsideredthatthelowerpro ductivitiesintheSouthernOceaniscausedbylowtemperature ,lowlight,lowstabilityofwa ter,scarcityoftraceelementsuchasironandgrazingbyzooplankton (Burkilletal.,1 995) ,etc.ThemostexistedstudiesconcentratedontheAtlanticSectoroftheSouthernO…     

Modelling trace metal concentration distributions in estuarine waters

The concentration of dissolved organic carbon (DOC) was measured every few months from September 2000 through October 2001 at a coastal location in the center of Suruga Bay, Japan (34°51′N, 138°38′E). Water samples were collected three times per day (midday, night and predawn). DOC concentrations ranged from 91.3 to 45.2 μM C on the surface to 100 m depth. Diel variation in DOC concentrations, among the three sampling times, was greater in the upper 20 m, with a maximum difference of 21.7 μM C in July 2001, and reflected in diel DOC inventory variations from the surface to 50 m. Diel variations were controlled by both physical and biological factors. DOC concentrations were significantly correlated with potential density in the deeper layers (100–1000 m), indicating that the distribution of DOC concentrations in the deeper layer was mainly due to mixing. Most DOC concentrations in the upper layer (0–50 m) did not display the same relationship as in the deeper layer. Using the relationship with potential density at 100–1000 m, the DOC concentration in the upper layer, due simply to mixing, was calculated. The difference between the calculated and observed DOC was used to estimate biological contribution. The biological contributions to the DOC inventory in the upper layer (0–50 m) were found greatly in November 2000 and April 2001. This indicates that excess DOC accumulated, by biological processes, in the upper layer during these periods. In November 2000, the excess DOC in the inventory was constant throughout the sampling days (0.36–0.37 mol C m⁻²), whereas diel variations of DOC in the vertical profile were large and contrary to the variation between 10 and 20 m. This suggests that the excess DOC was contributed biologically during daytime in the uppermost layer and reached to the 50 m depth by deeper mixing. As a result, the inventory appeared to be stable over a day because of the compensating effects of DOC production and consumption throughout 50 m. In contrast, in spring and summer, there was a distinct diel inventory decrease in the nighttime, with apparent rates ranging from −0.61 to −0.35 μM C h⁻¹. It is probable that the DOC, which accumulated during the daytime, was mostly labile, with a turnover time of a few hours. The results indicate that the dynamics of diel DOC variations varied seasonally, and suggest that these variations need to be considered when estimating seasonal DOC pools in the coastal ocean.     

Spatial distributions and seasonal variations of particulate phosphorus in the Jiaozhou Bay in North China

Based on the measurements of particulate phosphorus(PP) in the Jiaozhou Bay from May 2003 to April 2004,the spatial distribution,seasonal variation and biogeochemical characteristics of PP were investigated to understand the fates and roles of phosphorus in the Jiaozhou Bay ecosystem.The concentration of the total PP ranged from 0.07 to 2.09 μmol/dm3.The concentration of POP was from 0.01 to 1.83 μmol/dm3,with an average of 0.32 μmol/dm3,which accounted for 49.6% in total PP.The concentration of PIP was fro...     

The chemical distribution characteristics of variant form phosphorus in the seawater of the South China Sea

According to two cruises investigation information in summer and winter during 1998 and1999, the phosphorous concentration distribution and changes of summer and winter were discussed pri-marily in the South China Sea. The results show that the phosphate concentration of surface seawater insummer is distinctly lower than that in winter, averaging 0.04 μmol/dm3 in summer and 0.35 μmol/dm3 in winter. The organic phosphorous concentration of surface seawater in summer is higher than thatin winter, averaging 0.12μmol/dm3 in summer and 0.04 μmol/dm3 in winter respectively. The season-al changes of total phosphorus are similar to phosphate, averaging 0.22 μmol/dm3 in summer and 0.61μmol/dm3 in winter respectively. In vertical direction, phosphate, TDP and TP content are the lowestin upper 50 m water column, and increase in linearity rapidly with water depth, increasing slowly under500 m, reach to maximum about 1 000 m, then decrease slightly with water depth increasing. The ver-tical distribution is typical in summer, and there is small dispersed for phosphorus concentration for thesame depth of different stations. However, in winter there is a large disperse for phosphate, TDP andTP, specifically for phosphate at 200 m at which the concentration is maximum. This result indicatesthat there are large differences in hydrology and biology conditions that affect largely the chemical envi-ronment of the South China Sea. The organic phosphorus is the predominant in surface seawater of theSouth China Sea, but the inorganic phosphorus is the predominant in layers below depth of 150 m. Theorganic phosphorus concentration in deep water usually decreases with water depth increasing. The or-ganic phosphorus in summer is remarkably more than that in winter because of the strong biology activi-ties in summer.     

南大洋大气有机胺分布及来源特征研究

依托中国第36次南极科学考察,利用船载走航气溶胶及气体组分在线分析仪对南大洋大气中气态和颗粒态有机胺进行了在线观测。获得了南大洋开阔海域及普里兹湾大气中高分辨气态和颗粒态有机胺的组成及分布,并对其来源特征进行了分析。结果表明：南大洋大气有机胺以气态三甲胺（TMA）和二甲胺（DMA）为主要存在形态,其均值分别为(104.0±285.2)、(3.5±6.0) ng/m3。普里兹湾大气中有机胺的平均浓度显著高于南大洋开阔海域,气态TMA和DMA均值分别达到(289.0±396.6)、(5.6±16.1) ng/m3。南大洋大气中气态TMA、DMA和氨气（NH3）在不同区域内均具有良好的线性关系,表明三者具有同源性。从来源分析,南大洋大气有机胺主要受到海洋生物活动的影响,但在海冰边缘区及南极近岸海域,企鹅等动物的生物活动会导致大气中有机胺的浓度显著升高。     

海口湾海水重金属的行为特征

本文对海口湾溶解态铜、铅、锌、镉进行了测定.铜的变化范围为:0.47～1.16μg/dm3,平均值为0.78μg/dm3;铅的变化范围为:0.94～2.36μg/dm3,平均值为1.36μg/dm3;锌的变化范围为:1.28～4.83μg/dm3,平均值为3.14μg/dm3;镉的变化范围为:0.005～0.072μg/dm3,平均值为0.030μg/dm3,Cu、Zn的溶解态含量在龙昆路生活污水排污沟口、秀英工业排污沟口及海甸溪口的测站相对较高,Pb、Cd溶解态含量较低,湾内各站平面分布较为均匀.它们的溶解态含量垂直变化趋势为:Cu、Pb、Zn底层大于表层,而Cd表层大于底层.对Cu、Pb、Zn、Cd的颗粒态含量也进行了测定,指出海口湾海水中的颗粒物对重金属的净化起一定作用.对铜的溶解态中的强络合态和不稳态铜也进行了研究,强络合态占总溶解态的比例均在85%以上,对生物起毒性作用有关的不稳态铜含量很低,均小于5nmol/dm3,表明目前海口湾海水中的重金属铜不会对生物生长产生影响.     

南极普里兹湾浮游植物现存量与初级生产力粒级结构和新生产力研究

报道1998～1999年夏季在南极普里兹湾及其毗邻海域对细胞丰度、优势种类组成、生物量和初级生产力的粒级结构、新生产力及其环境制约机制的研究.结果表明,调查海区具有显著的空间区域化特征.普里兹湾及其毗邻陆架区浮游植物现存生物量和生产力均较高,大陆坡和深海区明显降低;营养盐浓度由于浮游植物的消耗则有相反的分布趋势.浮游植物生物量和生产力受水体的垂直稳定度、浮游动物摄食、水温和光照等环境条件的控制.粒度分级测定结果表明,对调查海区叶绿素a的贡献,小型浮游生物为52.2%,微型为29.4%,微微型为18.4%;对初级生产力的贡献,小型为52.4%,微型为28.7%,微微型为18.9%.研究海区的平均新生产力和f比分别为230.6mg/(m2·d)和0.43.     

Behavior features of heavy metals in the Haikou Bay waters

INThonUCrIONBecause of the discharge of industrial waste water, waste residue, waste gas and acid rain theheavy metals concentration in river and lake and eventually in seawater have been increasing.Therefore many studies on heavy metals innuencing marine ecological environment have beencarried out (Sun et al., 1990; Sunda and Guillard, 1976; Zhu et al., 1992). After entering intothe sea, heavy metals change, transfer and transform, and these processes have gained attentionfrom marine envi…     

2001/2002年夏季南极普里兹湾及其邻近海域的浮游植物

报道了 2 0 0 1 /2 0 0 2年夏季南极普里兹湾邻近海域 3 7个大面测站浮游植物的调查结果。经初步鉴定共有浮游植物 3门 3 7属 86种 ,其中硅藻在种类和细胞丰度上占绝对优势 ,其次为甲藻。主要优势种为克格伦拟脆杆藻 (Fragilariopsiskerguelensis)、细条伪菱形藻 (Pseu do nitzschialineola)、短拟脆杆藻 (Fragilariopsiscurta)和赖氏束盒藻 (Trichotoxonreinboldii)等南极特有种类和常见种类。调查区浮游植物分为两个群集 ,分布在 6 7°S以南的普里兹湾内的群集主要以克格伦拟脆杆藻、短拟脆杆藻、胡克星脐藻 (Asteromphalushookeri)和南极弯角藻 (Eu campiaantarctica)等南极特有种类和常见种类为主 ;分布在 6 7°S以北的大洋海域的群集主要以细条伪菱形藻、赖氏束盒藻、拟膨胀伪菱形藻 (Pseudo nitzschiaturgiduloides)和羽状环毛藻(Corethronpennatum)等南极常见种为主。调查区浮游植物的平均细胞丰度为 (8796± 2 92 85 )ind/L ,细胞多分布于海水的表层 ,密集区分布在 6 7°S以南的普里兹湾内 ,浮游植物的细胞丰度同硝酸盐的浓度密切相关。调查区浮游植物的多样性程度是低的。     

南极半岛近岸海域生物化学要素分布特征及影响因素

基于中国第30次南极科学考察在南极半岛(60°~63°S)近岸海域获取的调查资料,分析了该海域生物化学要素中溶解有机碳(DOC)、总氮(TN)和总磷(TP)分布特征并讨论地形和水团对其的影响。结果表明:2014年夏季南极半岛近岸海域水体DOC浓度变化范围为40.5~78.1μmol/L,平均浓度为66.3μmol/L;TN浓度变化范围为4.2~29.5μmol/L,平均浓度为14.9μmol/L;TP浓度变化范围为0.8~2.9μmol/L,平均浓度为2.0μmol/L。表层DOC呈现研究海域西北部D1断面和东南部D5断面浓度较高,中部DOC浓度较低;表层TN与TP浓度高值区出现在研究海域西部D1断面北部以及南部,中部和东部浓度较低;DOC,TN和TP浓度的垂直分布与海底地形和水团交汇密切相关,水团运动受阻于地形致使生物化学要素在垂直方向再分布。DOC,TN和TP空间分布反映了南极半岛近岸海域生物化学要素复杂的流通,将为合理开发和利用南极资源及环境影响评价提供科学依据。     

南海海域海水中各形态磷的化学分布特征

根据1998年7月和1999年1月两个航次的调查资料,对南海水体中磷的含量分布以及夏、冬季变化规律进行了探讨.结果表明,南海表层水体中磷酸盐夏季含量明显低于冬季,夏季平均含量为0.004μmol/dm3,而冬季为0.35 μmol/dm3;有机磷含量夏季高于冬季,含量分别为0.12,0.04 μmol/dm3;总磷含量的季节变化与无机磷酸盐类似,夏、冬季含量分别为0.22,0.61 μmol/dm3.在垂向分布上表层50 m水柱中PO₄3--P,总溶解态磷和总磷含量最小,随水深增加基本上呈线性快速增加,至500 m增加减缓,1 000 m左右为最大含量,然后随着水深略有下降.在夏季垂直分布比较典型,不同站位在一水深的含量离散性小,而冬季PO₄3--P,总溶解态磷和总磷的垂直分布则显得离散性大,尤其是PO₄3--P分布在200 m左右出现最大值,说明当年冬季南海各区域存在着较大水文、生物差异,很大的影响了化学环境的变化.在南海表层水中通常以有机磷占优势,在150 m深处以下的水中则以无机磷为主.深水中溶解的有机磷含量一般随水深减少.夏季的有机磷明显高于冬季,表明夏季的生物作用强烈.     

Seasonal variations and distributions of dissolved free and total carbohydrates at the İzmir Bay, Aegean Sea

Seasonal variations and distributions of dissolved carbohydrate concentrations at the İzmir Bay were investigated with salinity, chlorophyll a (Chl a), and dissolved organic carbon (DOC) levels to understand their relationships. Samples were collected from surface, subsurface and bottom depths at seven stations. DOC concentrations ranged from 32.2 to 244.2 μmol/L, and in general, DOC levels increased from winter to summer, then slightly decreased in autumn. Monosaccharide (MCHO), polysaccharide (PCHO) and total dissolved carbohydrate (TDCHO) levels were found between 0.7-8.3, 0.7-19.5, and 2.6-24.6 μmol/L. DOC, MCHO, PCHO and TDCHO levels were found higher in middle-inner bays, under the influence of anthropogenic inputs, compared to outer bay. Seasonal changes of MCHO/DOC, PCHO/DOC and TDCHO/DOC ratios were statistically significant (p<0.05) and the ratios showed decrease trends from winter to summer-autumn seasons. Distributions of TDCHO/DOC ratios at wide ranges (2.5%-42.3%) indicated the presence of newly forming and degrading fractions of DOM. According to results of factor analysis, Chl a, MCHO and TDCHO were explained in the same factor groups. In conclusion, the results showed that dissolved carbohydrate levels in the İzmir Bay might be influenced by biological processes and terrestrial/anthropogenic inputs.     

南极冬季威德尔海海冰物理结构与叶绿素a垂直分布特征

2006年8-10月极星号ANT/XXⅢ-7航次,对南极威德尔海西北海域浮冰区进行海冰综合考察,采用海冰物理学、海冰化学和海冰生态学等多学科现场同步观测取样与分析研究新方法。结果显示,测区21个冰站不同冰龄和不同结构类型的海冰冰芯,叶绿素a含量总平均值为16.56μg/dm3,范围为2.10~84.40μg/dm3,叶绿素a相对总量的R值均值为0.79~0.83。冰体叶绿素a含量与分布取决于海冰冰晶物理结构及其所处冰层部位,并和海冰生成环境、冰体发育和成冰过程密切相关。研究结果证实南极冬季海冰叶绿素a含量普遍处于较高水平,海冰冰藻具有较强活性,由此表明从整体上南极冬季海冰具有较高初级生产能力。这对正确分析估算冬季南极海洋生物生产,重新评估南大洋碳通量及其在全球气候变化中的贡献,具有重要科学意义。     

南极普里兹湾海域湍流扩散系数估计

基于Thorpe尺度方法,利用CTD数据,计算了南极普里兹湾海域的Thorpe尺度和湍流扩散系数,分析了观测区域(64°～69°S,66°～80°E)湍流翻转现象的强弱及分布。结果表明,在海底和地形粗糙区存在较大的Thorpe尺度(较强湍流翻转)和湍流扩散系数,湍流扩散系数最大值能达到10^-2m²/s量级,比平坦开阔海洋高2～3个数量级,部分观测站位的湍流扩散系数和湍动能耗散率表现出大-小-大的垂向分布结构,总水深较深的区域尤为明显;深水区域的浮力频率在海表面到500 m层比较大,浅水区域该现象不明显;湍动能耗散率在(67.25°S,73°E)周围和经度为78°E的各站位都表现相对较大,能达到10^-6 w/kg量级,个别站位甚至能达到10^-5 w/kg量级。     

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。