环球海洋大气气溶胶化学研究 Ⅰ.Na、Mg、K、Cl、Ca、Br、F的特征

利用我国“极地号”科学考察船的南极和环球科学考察,采集了太平洋、南极海域、南大西洋、印度洋及航线近岸海域大气的58个气溶胶样品,对Na、Mg、K、Cl、Ca、Br、F进行多元相关分析表明,气溶胶中的Na、Mg、K主要来自海洋,它们之间的比值接近其在大洋海水的平均比值;Cl和Ca在大洋上空也主要来自海水,但近岸海域大气,却明显受到陆源物质输送影响,呈现出不同的Cl/Na和Ca/Na比值;Ca、Br、F在大气中的富集,在大洋上空可能归因于海洋生物活动或海洋微表层富集作用,而在近岸大气,归因于陆源输送影响。     

南极中山站大气气溶胶的化学组成及其来源的判别

从1998年3月7日至1999年11月23日历时21个月，在南极中山站连续采集89个海洋气溶胶样品，本文提供全部样品的13种化学元素Cu、Pb、Zn、Cd、Fe、Al、Mn、Cr、V、K、Na、Ca、Mg含量的实测值．研究表明中山站气溶胶化学成份的含量具有季节性变化的特征．通过相关分析、因子分析、富集因子等方法判别不同时间段中山站气溶胶化学成份的来源。     

西北太平洋及中国东部近海秋季海洋气溶胶分布特征

2015年9月,分两个航次同时对西北太平洋及中国东部近海上空海洋气溶胶进行采集.对样品中的Na~+、K~+、Ca~(2+)、Mg~(2+)、Cl~-、NH~+_4、NO~-_3、SO~(2-)_4、甲基磺酸(MSA)等9种组分进行了分析,结合数理统计方法探究两个海域上空海洋气溶胶的来源.结果表明西北太平洋及中国东部近海海域气溶胶来源具有显著差异,西北太平洋海域气溶胶以海盐来源为主,中国东部近海海域则受陆源气溶胶影响较大,K~+、Ca~(2+)及二次气溶胶含量明显高于西北太平洋;此外,中国东部近海海域气溶胶中MSA含量平均值高于西北太平洋.本研究还估算了NH~+_4、NO~-_3、SO~(2-)_4在两个海域的干沉降通量,中国东部近海营养盐气溶胶干沉降通量远大于西北太平洋,营养盐的输入有利于海洋初级生产力的提高,也会促进生物来源气溶胶的产生.     

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．     

1998年南极中山站海洋气溶胶的化学组成及其来源判别

从1998年3月7日至1999年3月2日历时12个月,在南极中山站连续采集52个海洋气溶胶样品,提供全部样品的13种化学元素铜、铅、锌、镉、铁、铝、锰、铬、钒、钾、钠、钙、镁含量的实测值.研究表明中山站气溶胶化学成分的含量具有季节性变化的特征.通过富集因子、相关分析、因子分析等方法判别中山站气溶胶化学成分的来源.     

环球海洋大气气溶胶化学研究

1986年11月—1987年5月,在中国第三次南极考察和环球科学考察期间,收集了58个海洋气溶胶样品,采用中子活化法分析了Al,V,Mn,I,Br,Mg,Na,Cl等元素。应用因子分析、回归分析和富集因子分析对气溶胶中元素进行分类、定量评估和来源判别,讨论不同来源元素的特征,计算各主要来源的贡献分量。结果表明,海洋气溶胶中Al的99.99％是来自陆源地壳风化物,Na的99.2％。和Cl的99.99％是来自海水,V的91.4％。来自陆源污染物。因此,Al可作为海洋气溶胶中陆源地壳风化物的示踪元素,Na和Cl可作为海水源示踪元素,非地壳源的V则可选择为陆源污染物的示踪元素。     

珠江口海域底层大气中TSP与Cu、Pb、Cd质量现状与趋势

于2002-2005年在珠江口海域大万山岛海洋环境监测站设立一个大气监测站,采集了120多个大气气溶胶样品,测定TSP(总悬浮颗粒物)的含量与元素Cu、Pb、Cd的浓度.结果表明,Cu的浓度有增加并趋于稳定的趋势,Pb与Cd变化缓慢,浓度趋于稳定.     

珠江口海域气溶胶中重金属含量的时间变化特征及入海通量初步估算

采用2009～2011年珠江口海域获取的代表春、夏、秋、冬4个季节的240个气溶胶样品,分析重金属（Cu、Pb、Zn、ca）质量浓度和大气干沉降通量的年、季变化特征．结果表明：气溶胶中zn的质量浓度最高,其次是Pb和Cu,Cd的质量浓度最低,年平均质量浓度依次为69,2、31．2、12．6和0．58ng／m3．Cu、Pb和Zn的年平均质量浓度和入海通量表现为2009年〉2011年〉2010年．Cd的年平均质量浓度和入海通量呈现逐年递减的变化趋势．各金属质量浓度及大气干沉降通量均为秋季最高,冬春季次之,夏季最低,这种季节性差异主要与季风和雨水冲刷作用有关．气溶胶中Cu、Ph、Cd和Zn平均质量浓度的较低值出现在2010年夏季．Pb在4个季节的平均质量浓度低值均出现在2010年,平均质量浓度依次为18．9、3．8、56．7、20．2ng／m3,表明加强人为污染物排放的控制,可有效地降低气溶胶中重金属的含量,提高环境空气质量．通过评估金属元素分别从大气和河流进入珠江口海域的输入量,该海域金属物质输送入海仍以河流输入为主,但大气中Pb对该海域的输入具有重要作用．     

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.     

SeaWiFS遥感资料分析中国海域气溶胶光学厚度的季节变化和分布特征

通过与地基气溶胶观测数据的对比,确认了SeaWiFS气溶胶光学厚度产品用于研究中国海域气溶胶分布和变化特征的有效性。在此基础上,分析了中国海域气溶胶光学厚度的季节变化和地理分布特征。研究结果表明,中国东部海域平均气溶胶光学厚度存在以中纬度为中心的纬向分布;受沙尘、季风气候的影响,中国海域气溶胶光学厚度存在季节变化,不同海区有不同的季节变化和分布特征。渤海、黄海及东海有类似的变化特征,春季都受到沙尘气溶胶的影响,使中国东部海域气溶胶光学厚度普遍高于0.160,且对东海的影响最大;夏、秋季逐渐减小,冬季有所回升。南海气溶胶光学厚度均值为0.150,随时间变化不明显,但地理分布变化显著;受季风气候的影响,从春季到冬季,气溶胶光学厚度高值中心从高纬海域向低纬海域转移,范围也逐渐扩大。冬季南海大部分海域气溶胶光学厚度都达到0.160以上,是整个中国海域冬季气溶胶光学厚度最大的海区。气溶胶光学厚度的季节变化和地理分布特征为研究中国海区域气候变化和海洋生态提供了依据。     

Atmospheric input of trace elements to the western Pacific Ocean and the Kuroshio ocean area

ＡｔｍｏｓｐｈｅｒｉｃｉｎｐｕｔｏｆｔｒａｃｅｅｌｅｍｅｎｔｓｔｏｔｈｅｗｅｓｔｅｒｎＰａｃｉｆｉｃＯｃｅａｎａｎｄｔｈｅＫｕｒｏｓｈｉｏｏｃｅａｎａｒｅａ￥ＱｉａｎＦｅｎｌａｎ；ＹｕＨｏｎｇｊｉａｎ；ＬａｎＹｏｕｃｈａｎｇ；ＣｈｅｎＺｈｉ；Ｚｈｏｕ...     

Characteristics of sulfate in atmosphere over Xiamen waters and its fluxes to waters

One hundred and seven marine aerosol samples were collected during December 1988 to March 1990, and 3 dry deposition samples, 16 rain samples and 2 Cascade Impacter samples were collected from March to May 1990 at the southeast coast of the Xiamen Island. All the samples were analyzed for SO42-, NO3-, Cl-, Na+ , NH4+, using ion chromatography.The results indicate that the concentration of sulfate in marine aerosols over the Xiamen waters appears to be of seasonal variation, in an order of winter > spring > autumn > summer. The mean sulfate concentration lor the total marine aerosol samples over the Xiamen waters is 9. 37 μg/m3, respectively 0. 89 and 8. 48 μg/m3 for the seasalt and non-sea-salt sulfate. The distribution of sulfate shows a bimodal form with a peak in the coarse particle range which is derived from the sea-salt sulfate, and a peak in the fine particle range which is derived from the non-sea-salt sulfate. The total deposition of sulfate to the Xiamen waters is estimated to be 4. 68g/m2      

Non-sea-salt sulfate in the marine boundary layer and its possible impact on chloride depletion

1Introduction Sulfurisoneofthemostimportantelements whosebiogeochemicalcyclesarepivotaltotheatmo- sphericenvironmentandtotheclimaticchanges.The predominant,stablechemicalspeciesofsulfurinthe atmosphereissulfuricacidorsulfatewhichunderor- dinaryconditionsexistsmainlyinsmallaerosolparti- cles(Chinetal.,1996;Kerminenetal.,2000;Restadet al.,1998).Sulfuricacidorsulfate-dominatedaerosols areubiquitousintheloweratmosphere.Inthemarine boundarylayer(MBL),non-sea-saltsulfuricacidorsulfate(nss-SO42-)…     

Trends in the solubility of iron,aluminium, manganese and phosphorus in aerosol collected over the Atlantic Ocean

The solubility of iron, aluminium, manganese and phosphorus has been determined in aerosol samples collected between 49°N and 52°S during three cruises conducted in the Atlantic Ocean as part of the European Union funded IRONAGES programme. Solubilities (defined at pH 4.7) determined for Fe and Al in samples of Saharan dust were significantly lower (medians 1.7% and 3.0%, respectively) than the solubilities of these metals in aerosols from other source regions (whole dataset medians 5.2% and 9.0%, respectively). Mn solubility also varied with aerosol source, but the median solubility of Mn in Saharan dust was very similar to the median for the dataset as a whole (55% and 56%, respectively). The observed solubility of aerosol P was ∼ 32%, with P solubility in Saharan aerosol perhaps as low as 10%. Laboratory studies have indicated that aerosol Fe solubility is enhanced by acid processing. No relationship could be found between Fe solubility and the concentrations of acid species (non-seasalt SO₄²⁻, NO₃⁻) nor the net acidity of the aerosol, so we are unable to confirm that this process is significant in the atmosphere. In terms of the supply of soluble Fe to oceanic ecosystems on a global scale, the observed higher solubility for Fe in non-Saharan aerosols is probably not significant because the Sahara is easily the dominant source of Fe to the Atlantic. On a smaller scale however, higher solubility for aerosol Fe may alter our understanding of Fe cycling in regions such as the remote Southern Ocean.     

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.     

Ocean manganese nodule and sediment reference materials

In this article, sampling locations, sample types, sample processing methods, and certified values of ocean manganese nodule and sediment reference materials available throughout the world are briefly described. Recommended or information values of major, minor, and trace constituents in those samples have also been collected, and a review of the main characteristics of their property values is presented.     

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。