南黄海大气颗粒物中营养元素的季节分布

根据2006-07—2007-10南黄海海域4个季节的综合调查,分析了颗粒物(TSP)、总碳、氮、磷、钠、钙和镁等化学要素的季节变化,初步探讨了影响各参数季节变化的原因及其来源。结果显示各要素分布具有明显的季节变化规律,且不同要素分布特征不同。TSP的平均浓度为春季最高、夏季最低;总碳、钠和钙的平均浓度为冬季最高、夏季最低;硝酸盐的平均浓度为春季冬季夏季秋季,磷酸盐则为夏季秋季春季冬季;镁的平均浓度表现为秋季春季夏季冬季。TSP、总碳、氮均呈现离岸近处浓度高的趋势,特别是山东半岛南部海区以及长江口北部海区。与北黄海相比,研究区域内TSP和总碳的季节变化规律相似,但浓度普遍低于前者;硝酸盐浓度略高于前者,而磷酸盐则差异不大。大气颗粒物中氮:磷大于16:1,这可能是造成南黄海潜在磷限制的重要因素。钙主要来自陆源,镁在夏季陆源与海源相当,其他季节主要来自海源。日益增强的人类活动及其影响下的陆-海物质交换是影响南黄海大气颗粒物含量及分布的重要因素。     

长江口及东海海域大气气溶胶中水溶性离子的分布特征

2006年夏季、冬季和2007年春季、秋季在长江口及东海海域进行了大面积走航采样,通过离子色谱法分析了气溶胶中主要水溶性离子的质量浓度,探讨了其季节变化和海域分布.分析结果表明,K+和Ca2+季节变化显著,海域分布呈现近岸高外海低的趋势,Na+和Mg2+海域分布差异显著;NH4+-N,NO3--N和SO42--S的春、...     

连云港近海海域水质的季节和年际变化

根据1992～2005年连云港近海海域水质监测资料,对该海域水质的季节变化和年际变化进行研究.结果表明,近海水质有明显的季节变化特征,其中盐度从春、夏季到秋季缓慢降低,冬季升高;溶解无机氮(DIN)与盐度恰恰相反,夏秋季最高且监测的超标率高.溶解氧季节性非常明显,依次为冬季>春季>秋季>夏季.总体上春冬季水质好于夏秋季.年际变化显示,1992～2005年pH和盐度均有降低趋势,尤其是2003年以后降幅更加明显;DO和COD年际变化相对平稳但季节变化幅度较大;2000年12月后油类浓度明显降低且年际变化平稳;近几年DIN有明显增加趋势,无机氮已成为该海域主要污染物.     

黄河口及莱州湾海域磷的时空分布及浮游生物对低磷胁迫的响应

本文利用2019—2021年在黄河口及莱州湾海域进行的4次陆海同步调查结果,分析了环莱州湾主要入海河口和排污口陆源输入磷的季节变化、黄河口及莱州湾海域内不同形态磷及不同碱性磷酸酶活性(APA)的时空分布特征,探讨了海域内磷受限状况及浮游植物和浮游细菌对低磷胁迫的响应。结果表明,磷的陆源输入中黄河贡献最大,小清河次之;总磷(TP)入海通量呈现出夏季>春季>秋季>冬季的季节变化,春、夏、秋季磷输入以颗粒态磷(PP)为主,冬季以溶解态磷(DP)为主;受农业施肥及河道内浮游生物活动的影响,春季陆源DP以溶解有机磷(DOP)为主,其他季节以活性磷酸盐(PO₄-P)为主。研究海域内TP浓度及构成不仅受陆源输入的影响,还受浮游生物消亡、海上养殖活动和沉积物释放等作用共同调控,TP浓度呈现出春季>夏季≈秋季>冬季的季节变化、近岸高远岸低的分布特征,高值区主要位于黄河和小清河河口区域;TP构成上,春季以DP为主,夏、秋季DP与PP相当,冬季以PP为主;春、秋季DP以DOP为主,而夏、冬季DP以PO₄-P为主。海域内浮游植物普遍受到...     

福建九龙江口秋茄红树林鹧鸪菜几种营养元素含量的季节变化

研究了福建九龙江口秋茄(Kandelia candel)红树林潮间带的红藻鹧鸪菜(Caloglossa leprieurii)的氮、磷、钾、钠、钙与镁6种营养元素含量的季节变化。氮、磷、钾与钠均以春季含量最高；钙与镁分别以秋季和冬季最高。氮与磷含量冬季最低，钾含量秋季最低；钠、钙、镁均以夏季含量最低，6种元素含量的季节变化模式不一致。营养元素含量的季节变化表明鹧鸪菜春季富集的营养物质较多，与春季有较高的生物量一致。营养元素含量的季节变化反映了鹧鸪菜的生长与环境因子的季节变化。鸥鸪菜的氮、磷含量高于土壤含量。并明显高于水体氮、磷含量，说明鹧鸪菜能强烈富集环境中的氮、磷，因此鸥鸪菜类的大型藻类的存在可能是红树林区赤潮极少发生的原因之一。     

中国东部海域大气气溶胶入海通量的研究

根据中国东部海域气溶胶浓度及分级采样资料,计算得出黄海、东海及日本以南海域沙尘气溶胶的代表元素铝(Al)每月干沉降通量分别为42.8、18.3、5.2mg/m2;其中各海域春季的干沉降通量均占全年干沉降通量的40%以上.相应每月总沉降通量分别为54.1、29.8、10.5mg/m2.渤海、黄海、东海及日本以南海域每年沙尘气溶胶总沉降通量分别为26.4、9.3、5.1、1.8g/m2.东海污染元素总沉降通量以春季最大,夏、秋季次之,冬季最小.日本以南海域锑(Sb)元素总沉降通量的季节分布为冬季最大,夏、秋季次之,秋季最小;硒(Se)元素总沉降通量的最大值出现在夏季,其他季节分布比较均匀.     

流沙湾海水中总有机碳的时空分布及其影响因素研究

于2008年2月(冬季)、5月(春季)、8月(夏季)和11月(秋季)对流沙湾进行了4次采样调查,研究分析了流沙湾海水中总有机碳的空间分布和季节变化特征,并探讨了TOC与温度、盐度、pH、叶绿素a和底泥TOC之间的相关关系.结果发现,在2008年度流沙湾海水TOC的浓度为0.992 ～ 5.437 mg/L,平均值为2.414 mg/L,呈现春季＞夏季＞秋季＞冬季的变化趋势,整个流沙湾海域海水TOC的平面分布相对比较均匀,表层稍大于底层.在内外湾分布上,冬、夏季节内湾TOC大于外湾,而春、秋季节外湾大于内湾;在垂直分布上,冬、夏和秋季表层大于底层,而春季底层大于表层;在地域分布上,冬、夏季节从流沙镇一侧海域到西联镇一侧海域逐渐减小,秋季变化趋势相反,春季时,两侧无明显变化.相关关系的分析结果表明,流沙湾海水TOC与温度、pH呈现出正相关关系,与温度的相关关系较为显著,与盐度则呈现不显著的负相关关系;与叶绿素a存在一定的相关关系,在叶绿素a浓度小于2.6μg/L,两者呈现正相关关系,而在叶绿素a浓度大于2.6 μg/L,两者呈现负相关关系;与底泥TOC呈现出了一定的正相关关系.     

嵊泗海域大气总悬浮颗粒物的特征

以嵊泗海域为研究区域,研究了该区域大气总悬浮颗粒物(TSP)含量及TSP中重金属含量随季节变化的特征,通过对TSP中各重金属元素的相关系数、富集因子以及气象要素的分析来判断重金属的来源.结果表明:冬季该海域TSP含量最大,为夏季的4倍之多,季节变化很显著;冬季该海域TSP中重金属(Cu、Pb、Cd)含量最高,秋、春季次之,夏季最低.冬季Cu、Pb和Cd含量分别为夏季的17、27和27倍.TSP含量和TSP中的Cu、Pb、Cd含量的相关性不强,或基本不相关;但Cu、Pb、Cd含量之间的相关系数却很大,其中Pb与Cd含量的相关系数达到了0.95,说明它们的关系密切,可能来自同一个源.富集因子由大到小对应的3种重金属依次为Cd、Pb和Cu.从富集因子年平均值来看,Cu、Pb、Cd都被富集;冬季3种重金属都被严重富集,夏季3种重金属都没有被富集.冬季,嵊泗群岛盛行西北风且风速很大,非常有利于把上海及其周边城市的污染物输送到嵊泗海域,造成冬季该海域的TSP中重金属含量严重富集;春季,嵊泗群岛盛行的风向开始转变为东南风,风从海洋吹向大陆,所以春季该海域TSP中重金属含量急剧减少;夏季,嵊泗群岛的风向转变为东风,风还是从海洋吹向大陆,加之夏季是1年中降雨量最多的季节,加速了TSP中重金属的沉降速度,致使夏季该海域TSP中3种重金属含量都达到了最低值;秋季,嵊泗群岛的风向又转变为西北风,有利于陆源污染物的传输,虽然风速小于冬季,但依然造成重金属含量的严重富集.可以推断,嵊泗海域的TSP中重金属主要来源于上海及其周边城市的陆源污染物.     

钦州湾海水中石油烃时空变化特征及其影响因素

2009年1月至11月对广西钦州典型养殖海湾-钦州湾海域表层海水石油烃进行了4次采样调查,分析该海域石油烃污染状况,探讨石油烃的时空分布特征及其影响因素。结果表明,钦州湾表层海水石油烃的质量浓度在0.001~0.095 mg/L之间,平均值为0.022 mg/L;季节变化呈现夏季最高,秋、冬季次之,春季最低的特点,夏、冬季海水受到不同程度石油污染,春、秋季均达到国家《海水水质标准》二类标准。水平分布上总体呈现春、秋季节外湾大于内湾,夏、冬季节内湾大于外湾的特征。钦州湾水产养殖活动及陆地径流输入是影响石油烃时空变化的主要因素。春季石油烃的质量浓度与温度和溶解氧等环境因子有着较好的相关性,夏季石油烃和溶解无机磷存在显著正相关。总体上钦州湾海域目前受石油烃污染程度较轻,仍有一定接纳自净能力。     

闽浙沿岸流扩展范围的季节特征及其对典型海湾的影响

根据2006~2007年春、夏、秋、冬季4个航次的监测数据分析闽浙沿岸流扩展范围和温度、盐度、营养盐含量平面分布季节变化特征,结果显示:调查期间,闽浙沿岸流主要分布于浙闽沿岸海域,具有明显的季节变化特征,冬季闽浙沿岸流扩展范围最大,可影响至广东南澳岛海域,秋季次之,可影响至厦门湾、东山湾海域,春季可扩展至泉州湾附近海域,夏季影响范围最小,仅局限于浙江北部沿岸海域.选取福建罗源湾、厦门湾和东山湾,分析闽浙沿岸流对典型海湾的影响,结果显示:冬季闽浙沿岸流给福建典型海湾带来了大量的营养盐物质,罗源湾、厦门湾和东山湾均受其影响,海水营养盐含量明显提高,秋季次之,春季影响略小,夏季基本不受闽浙沿岸流影响.     

Dry and wet deposition of nutrients from the tropical Atlantic atmosphere: Links to primary productivity and nitrogen fixation

Atmospheric deposition fluxes of soluble nutrients (N, P, Si, Fe, Co, Zn) to the tropical North Atlantic were determined during cruise M55 of the German SOLAS programme. Nutrient fluxes were highest in the east of the section along 10°N, owing to the proximity of source regions in West Africa and Europe, and lowest in the west, for both dry and wet deposition modes. In common with other recent studies, atmospheric P and Si inputs during M55 were strongly depleted relative to the stoichiometry of phytoplankton Fe, N, P and Si requirements. Atmospheric N inputs were equivalent to 0.1–4.7% of observed primary productivity during the cruise. Atmospheric nutrient supply was also compared to observed nitrogen fixation rates during M55. While atmospheric Fe supply may have been sufficient to support N fixation (depending on the relationship between our simple Fe leaching experiment and aerosol Fe dissolution in seawater), atmospheric P supply was well below the required rate. The stable nitrogen isotope composition of nitrate–N in aerosol and rain was also determined. Results of a simple model indicate that atmospheric deposition and nitrogen fixation introduce similar amounts of isotopically light nitrogen into surface waters of the study region. This implies that nitrogen isotope-based methods would overestimate nitrogen fixation here by a factor of 2, if atmospheric inputs were not taken into account.     

台湾海峡大气微量金属的化学特征及其入海通量

2006～2007年，利用大容量气溶胶采样器在台湾海峡采集79个大气气溶胶样品．采用ICP—MS分析法测定了样品中Pb、Cu、Cd、V、Zn、Fe和Al等金属元素的含量．分析结果显示，台湾海峡大气微量金属含量呈现出明显的季节变化，对大部分元素而言，含量最低值出现在夏季，而最高值出现在冬季，气溶胶中微量金属的含量变化与海峡的气象条件等因素有关．通过富集因子、相关性分析和因子分析，对微量金属的来源进行了判别．台湾海峡大气微量金属的来源特征为：Cu、Pb、Cd、V主要来自污染源，而Al、Fe、Zn则主要来自地壳源．比较和分析了台湾海峡海域微量金属的大气与河流输入，Cu和Zn的大气输入低于九龙江和闽江的输入，而Pb、Cd的大气输入则超过了这2条河流的输入．     

中国近海大气气溶胶的时间和地理分布特征

通过对中国近海10个航次气溶胶观测资料的统计分析得出:(1)从黄海、东海至日本以南海域气溶胶中地壳元素年平均浓度明显减小,在春季尘暴多发期间地壳元素浓度离到岸距离接指数规律递减.污染元素气溶胶浓度分布与陆源排放量和离岸距离有一定关系.(2)海上陆源气溶胶浓度的季节分布为:春季最大,秋冬次之,夏季最小.受日本排放源的影响,日本以南海域污染元素浓度最大值出现在冬季.(3)Se元素浓度与海洋源密切相关.海盐元素从黄海、东海至日本以南海域浓度逐渐增加,主要受周围海况影响,与风速呈现一定程度的正相关.影响近海气溶胶浓度的主要因素有陆源气溶胶排放量、降水分布和大尺度天气形势.     

Atmospheric nitrogen deposition to the Mullica River-Great Bay Estuary

Measurements of nitrate and ammonium in precipitation and associated with aerosols were conducted at Rutgers University Marine Field Station in Tuckerton, New Jersey from March 2004 to March 2005 to characterize atmospheric nitrogen deposition to the Mullica River-Great Bay Estuary. The arithmetic means of nitrate and ammonium concentrations for precipitation samples were 2.3mgL(-1) and 0.42mgL(-1), respectively. Nitrate and ammonium concentrations in aerosol samples averaged 3.7microgm(-3) and 1.6microgm(-3), respectively. Wet deposition rates appeared to vary with season; the highest rate of inorganic nitrogen deposition (nitrate+ammonium) occurred in the spring with an average value of 1.33kg-Nha(-2)month(-1). On an annual basis, the total (wet and dry) direct atmospheric deposition fluxes into the Mullica River-Great Bay Estuary were 7.08kg-Nha(-2)year(-1) for nitrate and 4.44kg-Nha(-2)year(-1) for ammonium. The total atmospheric inorganic nitrogen directly deposited to the Mullica River-Great Bay Estuary was estimated to be 4.79x10(4)kg-Nyear(-1), and the total atmospheric inorganic nitrogen deposited to the Mullica River watershed was estimated to be 1.69x10(6)kg-Nyear(-1). Only a fraction of the nitrogen deposited on the watershed will actually reach the estuary; most of the nitrogen will be retained in the watershed due to utilization and denitrification during transport. The amount of N reaching the Mullica River-Great Bay Estuary indirectly is estimated to be 5.07x10(4)kg-Nyear(-1), approximately 97% is retained within the watershed. This atmospheric nitrogen deposition may stimulate phytoplankton productivity in the Mullica River-Great Bay ecosystem.     

Open-ocean deployment of a buoy-mounted aerosol sampler on the Bermuda Testbed Mooring: Aerosol iron and sea salt over the Sargasso Sea

We report results from the first deployment of a buoy-mounted aerosol sampler on the Bermuda Testbed Mooring (BTM) in the Sargasso Sea, in which a time-series of 21 aerosol samples were collected over the period May 5–September 29, 2004. These aerosol samples were analyzed for iron and soluble sodium (as a proxy for sea salt). Also analyzed was a time-series of 22 aerosol samples collected over the same period at the Tudor Hill atmospheric sampling tower on Bermuda. The buoy sampler worked as intended and successfully collected a time-series of aerosol samples, thus demonstrating that moored buoys can be used as oceanic observatories to provide information on the temporal (weekly, monthly and seasonal) variability in the concentration of aerosol iron (and other trace elements) over the surface ocean. The magnitude and time variation of aerosol Fe concentrations calculated from the BTM buoy samples are in close agreement with the corresponding aerosol Fe record from the Tudor Hill tower, which is located approximately 80 km northwest of the mooring site. Both the BTM and Tudor Hill samples record periods of high aerosol iron loadings in late June and late July 2004, reflecting the transport of soil dust from North Africa, with the highest concentration of aerosol iron at the BTM site (0.83 μg m⁻³) measured in late June. Concentrations of sea-salt aerosol calculated from the BTM samples are comparable to values measured over the Sargasso Sea and for samples collected at the Tudor Hill tower. Sea-salt aerosols do not appear to impede the collection of mineral aerosols by the buoy-mounted sampler.     

大气气溶胶中若干有机物的含量和季节变化

研究、探讨青岛近岸大气气溶胶中多芳烃类化合物的浓度水平、变化特征及影响因素。用高效液相色谱荧光检测法分析了青岛近岸大气气溶胶中的多环芳烃(PAHs)的含量水平,共检出13种多环芳烃化合物。结果表明该类化合物总量(∑PAHs)具有明显的季节特征,呈现春季<秋季<冬季的特征,人类活动可能是其主要来源。     

Study of continental material transported through the atmosphere to the oeean

I am deeply honored to have been selected as a recipient of the 1987 Okada Prize by the Oceanographical Society of Japan. The present paper reviews my work and recent studies of other investigators concerning mineral aerosol (dust) particles in the marine atmosphere over the Pacific Ocean. I would like to emphasize the importance of atmospheric deposition of continental substances to the ocean environment. From consecutive measurements of atmospheric dust concentrations and total deposition fluxes at 13 island stations in the Pacific Ocean, a strong seasonal transfort pattern of dust particles was found at most of the stations. High atmospheric dust concentrations occurred during the spring in both hemispheres. There was a latitudinal gradient in both the atmospheric dust concentration and flux, with the highest values observed at midlatitudes. When combined with observations of dust storms in Asia and isentropic trajectory analysis, it was clear that the dust over the central North Pacific was transported by the upper westerly winds from the arid desert regions in central and eastern Asia. Transport times were 1–2 weeks, and in some cases, atmospheric transport paths of over 10,000 km were observed. Infrequent short-term dust events contributed most of annual atmospheric dust flux to the open ocean. These sporadic inputs are major sources for both suspended mineral matter in the water column and the non-biogenic component of deep-sea sediments in the Pacific Ocean. The impact of atmospheric dust fluxes on chemical and biological processes in the water column remains to be determined.     

Preliminary study on concentrations and size distribution of marine aerosols over the East China Sea

In summer and winter, 1987,and in spring and autumn, 1988, the concentrations and size distribution of marine aerosols were measured over the East China Sea and the South Japan Sea. This paper deals with the study on the seasonal variation of the marine aerosols with the meteorological parameters, the differences and the relations between the marine and continental aerosols. The results show that the marine aerosol concentrations and size distribution over the East China Sea have distinct seasonal change characteristics, which may be attributed to the East Asian atmospheric circulation. The size distribution is discussed by using a three-parameter size distribution model.