顶空气相色谱法测定海水二甲基硫和浮游植物细胞二甲基硫丙酸的研究

建立了顶空ＧＣ／ＦＰＤ测定海水中二甲基硫（ＤＭＳ）和浮游植物细胞中二甲基硫丙酸（ＤＭＳＰ）的方法，并研究盐度、温度、气液相比ＤＭＳ诸因素对ＤＭＳ顶空灵敏度的影响。该法对ＤＭＳ测定的相对标准偏差均小于６％，平均回收率为１０６％，最低检出限为２０ｎｇ／Ｌ。细胞ＤＭＳＰ先经碱作用转化为ＤＭＳ，在５０℃下作用时间不少于６ｈ，峰高与浓度的双对数线性相关系数大于０．９９。对１９９４年冬、１９９５年夏采自胶州湾     

环境因对三种常见微藻细胞中二甲基硫丙酸含量影响的初步研究

３种常见的海洋浮游藻类－－扁藻、杜氏藻和牟氏角刺藻作为实验材料,采用正交方法设计实验条件,研究盐度、和光强的变化对藻类细胞内二甲基硫丙酸（ＤＭＳＰ）含量的影响。结果表明,３种藻类细胞ＤＭＳＰ含量相差很大。扁藻ＤＭＳＰ含量最高,其次为杜氏藻,牟氏角刺藻呈最低,种间差别的影响明显高于环境条件的变化对藻ＤＭＳＰ含量的影响。３种环境因陬对藻细胞ＤＭＳＰ含量的影响效果不同,盐度变化引起藻细胞ＤＭＳＰ含量的变     

青岛沿岸海区海藻体中DMSP含量测定

实验研究海藻体中二甲基硫基丙酸酯（Ｄｉｍｅｔｈｙｌｓｕｌｆｏｎｉｕｍｐｒｏｐｉｏｎａｔｅ,ＤＭＳＰ）的简单测定方法。改进顶空进样方法灵敏度低的缺点,采用碱解和萃取吸收同时进行气相色谱火焰光度检测法测定不同种类的底栖藻中所含的ＤＭＳＰ。并以此测定不同季节胶州湾部分地区近岸表层水体浮游藻所含的ＤＭＳＰ,同时还测定水体中的磷酸盐浓度。结果表明在底栖藻中ＤＭＳＰ含量随季节呈现一定的规律性变化,不同藻体内ＤＭＳＰ含量相差可达两个数量级,而单位水体微藻中的ＤＭ－ＳＰ亦随季节呈现一定的规律性变化     

二甲基硫光化学氧化反应的动力学研究

实验研究水溶液中二甲基硫（ＤＭＳ）的光化学氧化反应的动力学。结果表明，在入射光频率与强度一定条件下，ＤＭＳ进行光化学氧化反应的速率会受到介质、ｐＨ、重金属离子的影响。Ｈｇ２＋能显著加快人工海水介质中ＤＭＳ的光氧化速率。ＤＭＳ进行光氧化的一级速率常数为４．４６×１０－５～３０．４×１０－５ｓ－１，其在光照下的人工海水介质中的半寿期为３．６ｈ。这说明光化学过程对于影响和控制ＤＭＳ在海洋中的浓度和分布起着十分重要的作用     

影响海水中二甲基硫分布的生物因素

二甲基硫(ＤＭＳ)是海水中有机硫化物的重要组成部分,也是参与硫的生物地球化学循环的重要物质,其海空通量约为０．６×１０１２～１．６×１０１２ｍｏｌ／ａ,占海洋中硫释放量的５５%～８０%。对ＤＭＳ在海水中的浓度及分布进行分析,是评价其在全球硫循环中所起作用的重要基础。为此,国际上已有不少学者对ＤＭＳ的来源、分布、海空通量进行了较系统的研究工作。由于充分认识到ＤＭＳ在全球海洋痕量气体的排放中占有举足轻重的地位,并对全球气候变化和酸雨的形成产生重大影响,有关ＤＭＳ的浓度与分布、通量与循环的研究已成为当今国际…     

海水中二甲基硫(DMS)的测定方法及其来源的研究

本文综述了目前国内外有关海水中二甲基硫（ＤＭＳ）的测定方法及其来源的研究,指出ＤＭＳＰ是海洋生物降解产生ＤＭＳ的主要来源。     

近200ka来赤道大西洋的二甲硫产量变化

按照Ｇａｉａ理论,浮游植物可能是阻止地球气候达到极限的生物地球化学反馈圈中的主要成分。１９８７年,Ｃｈａｒｓｌｏｎ等提出从浮游植物释放到大洋表层水的二甲硫（ＤＭＳ）是海洋对流层中硫酸盐气溶胶和云凝聚中心的主要来源。因此,由于强日射和高温时期的ＤＭＳ产量提高,ＤＭＳ的释放提供了潜在的全球气候调节机制。硫酸盐气溶胶是仅次于温室气体对大气辐射产生影响的第二个最大的调节机制。尤其在北半球,人为的硫化合物强烈地影响了气溶胶水平,但是ＤＭＳ是开放大洋气溶胶颗粒的主要天然发生器。海洋气溶胶通过直接散布和吸收辐射以及…     

海水中二甲基硫（DMS）的测定方法及其来源的研究

本文综述了目前国内外有关海水中二甲基硫（ＤＭＳ）的测定方法及其来源的研究,指出了ＤＭＳＰ是海洋生物降解产生ＤＭＳ的主要来源。     

电子传递系统活力测定法及其在海洋生态系统中的应用

本文介绍了ＥＴＳ的概念，ＥＴＳ活力测定法的原理和方法，概述了ＥＴＳ活力在海洋中的时空变化及其影响因子和在海洋生态研究中的应用，最后对该法作简要的评价并提出展望。     

海洋活性肽的研究进展

随着人们对海洋资源认识的提高,以及现代生物技术在海洋药物研究中的应用,反相ＨＰＬＣ、２ＤＮＭＲ、ＦＡＢＭＳ、手性色谱(包括ＧＣ、ＨＰＬＣ)等技术的发展,使得对海洋活性肽的研究易于进行。近１０多年来,海洋活性肽类,特别是海洋环肽的研究也取得了很大进展,其中从海鞘(Ｔ     

Dimethyl sulfide in the atmospheric surface layer of the Equatorial Pacific Ocean

This paper reports a case study of atmospheric stability effect on dimethyl sulfide(DMS) concentration in the air. Investigation includes model simulation and field measurements over the Pacific Ocean. DMS concentration in surface sea water and in the air were measured during a research cruise from Hawaii to Tahiti. The diurnal variation of air temperature over the sea surface differed from the diurnal cycle of sea surface temperature because of the high heat capacity of sea water. The diurnal cycle of average DMS concentration in the air was studied in relation to the atmospheric stability parameter and surface heat flux. All these parameters had minima at noon and maxima in the early morning. The correlation coefficient of the air DMS concentration with wind speed (at 15 m high) was 0. 64. The observed concentrations of DMS in the equatorial marine surface layer and their diurnal variability agree well with model simulations. The simulated results indicate that the amplitude of the cycle and the mean     

The concentration and distribution of dimethyl sulfide in the marine atmospheric boundary layer near the equator

Ｔｈｅｃｏｎｃｅｎｔｒａｔｉｏｎａｎｄｄｉｓｔｒｉｂｕｔｉｏｎｏｆｄｉｍｅｔｈｙｌｓｕｌｆｉｄｅｉｎｔｈｅｍａｒｉｎｅａｔｍｏｓｐｈｅｒｉｃｂｏｕｎｄａｒｙｌａｙｅｒｎｅａｒｔｈｅｅｑｕａｔｏｒ￥ＬｉＸｉｎｇｓｈｅｎｇ；ＬｉＺｈｅ；Ｆ．Ｐａｒｕｎｇｏ...     

离子迁移谱现场观测渤海和北黄海二甲基硫的研究

渤海、黄海是高产二甲基硫(Dimethyl Sulfide,DMS)的大陆架海区.该海区DMS的现场调查研究有助于准确评估海洋DMS释放量及其对全球气候变化的负反馈作用.目前,无论是基于模型还是直接测量法的通量估算均以表层海水或低层大气DMS浓度为基础,因此,先进的检测技术对其通量估算的准确度具有决定性作用.气相色谱法...     

Sea to Air Flux of Dimethyl Sulfide and Its Effect on the Environment

Reviews on the cunent studies on the sea to air flux ofdimethyl sulfide (DMS) have been made at home and abroad, pointing out that the flux of DMS is influenced by many factors.There is great difference between the results coming fiom different models. Besides, this paper focuses on the oxidation mechanisms of DMS by OH and NO3 radicals after it enters the atmosphere, the oxidation products' contribution to acid rain and fog and the relationships among the DMS, CCN and climate system.     

Distribution and cycling of dimethylsulfide in surface microlayer and subsurface seawater

Laboratory experiments, along with in situ investigation in Funka Bay, Japan, were conducted to determine the enrichment factor (EF) of dimethylsulfide (DMS) in the sea surface microlayer, as well as its the production and consumption rates. The EF of DMS in the microlayer was largely affected by various factors including sampling methods, sampling thickness, temperature, salinity, and DMS concentration in bulk water. In all cases but the sealed system, a part of DMS in the microlayer was always unavoidably lost during sampling. High temperature, great wind speed, and slow sampling would increase the extent of loss of DMS due to volatilization. In the field, the screen-collected samples usually exhibited greater microlayer enrichment for DMS than the plate-collected samples, showing that the screen sampler might be more effective for collecting the in situ microlayer DMS. The production and consumption rates of DMS in the surface microlayer were higher than those in the bulk water and these two rates were significantly correlated with the microlayer DMS concentrations. Moreover, the EF of DMS appeared to be related to the microlayer production rate of DMS, providing evidence supporting the observed DMS enrichment in the microlayer. The DMS production and consumption rates were not directly related to its concentrations in the bulk water, suggesting that the processes of production and consumption of DMS were very complex. In the surface microlayer, the biological turnover time of DMS varied from 0.4 to 1.9 days, with an average of 0.9 days, which was about 540-fold greater than the mean DMS sea–air turnover time (2.4 min). Thus, the biological process occurring within the microlayer can be neglected when we consider the sea–air exchange of DMS. Considering the microlayer production rate of DMS (an average of 9.7 nM day⁻¹) to be too small to counteract the sea-to-air removal of DMS, the main source of DMS in the microlayer appears to be through vertical transport by turbulent diffusion from the underlying water.     

Spatial variations of dimethylsulfide and dimethylsulfoniopropionate in the surface microlayer and in the subsurface waters of the South China Sea during springtime

Spatial variations in dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) were surveyed in the surface microlayer and in the subsurface waters of the low productivity South China Sea in May 2005. Overall, average subsurface water concentrations of DMS and DMSP of dissolved (DMSPd) and particulate (DMSPp) fractions were 1.74 (1.00-2.50), 3.92 (2.21-6.54) and 6.06 (3.40-8.68) nM, respectively. No enrichment in DMS and DMSPp was observed in the microlayer. In contrast, the microlayer showed a DMSPd enrichment, with an average enrichment factor (EF, defined as the ratio of the microlayer concentration to subsurface water concentration) of 1.40. In the study area, none of the sulfur components were correlated with chlorophyll a. An important finding in this study was that DMS, DMSP and chlorophyll a concentrations in the surface microlayer were respectively correlated with those in the subsurface water, suggesting a close linkage between these two water bodies. The ratios of DMS:Chl-a and DMSPp:Chl-a showed a gradually increasing trend from North to South. This might be due to changes in the proportion of DMSP producers in the phytoplankton community with the increased surface seawater temperature. A clear diurnal variation in the DMS and DMSP concentrations was observed at an anchor station with the highest concentrations appearing during the day and the lowest concentrations during the night. The higher DMS and DMSP concentrations during daytime might be attributed to the light-induced increase in both algal synthesis and exudation of DMSP and biological production of DMS. The mean flux of DMS from the investigated area to the atmosphere was estimated to be 2.06 micromo lm(-2)d(-1). This low DMS emission flux, together with the low DMS surface concentrations was attributed to the low productivity in this sea.     

格陵兰海气溶胶光学深度、海冰、浮游植物与二甲基硫的关系及其对未来气候的影响

dimethylsulphide (DMS)的海空通量是海洋生物气溶胶的主要来源之一,对气候（特别是北冰洋的气候）具有重要的辐射影响。利用卫星数据得到的气溶胶光学深度(AOD)作为气溶胶负荷的代表,在夏季和秋季表现的尤其明显。春季海冰的融化是北极气溶胶前体的重要来源。然而,早春的高浓度气溶胶可能与南方大陆污染的平流有关(北极霾)。更高的AOD通常在研究区域的南部出现。海冰浓度(SIC)和AOD呈正相关,而云盖(CLD)和AOD则呈负相关。SIC和CLD的季节性峰值均在AOD峰值的前一个月。AOD与SIC之间存在强烈的正相关关系。融冰与叶绿素（CHL)几乎在3月至9月呈正相关,但与春季和初夏的AOD呈负相关。春季和初夏较高的AOD有可能是由融冰和春季强风在该地区的结合影响。由于春季风的升高和冰的融化,在春季出现了DMS通量的峰值。从3月到五月,DMS浓度和AOD及融冰都呈正相关。早秋季升高的AOD可能与浮游植物合成的生物气溶胶的排放有关。到2100年,格陵兰海的DMS通量将增加3倍以上。生物气溶胶的显著增加可以部分抵消格陵兰海的增温现象。     

Responses of DMS in the seawater and atmosphere to iron enrichment in the subarctic western North Pacific (SEEDS-II)

Simultaneous measurements of dimethylsulfide (DMS) in the seawater and atmosphere were conducted during SEEDS-II to investigate the responses of DMS to iron (Fe) fertilization in the subarctic North Pacific. No significant increases in the seawater DMS (DMSw) concentration were observed inside the fertilized patch compared to those outside the patch, while particulate dimethylsulfoniopropionate (DMSPp) concentration inside the patch increased 2-fold compared to those outside the patch in the phytoplankton bloom of major DMSP producers such as prasinophytes, cryptophytes, diatoms and prymnesiophytes. In the decline phase of the bloom, maximum DMSw was observed both inside the patch (ca. 6.2 nM) and outside the patch (ca. 9.3 nM). In this period, increases in mesozooplankton and decreases in the DMSP producers (prymnesiophytes and diatoms) were observed both sides of the patch, but larger inside the patch than outside the patch. Large decreases in the DMSPp inside the patch, which was probably related to the large increases in mesozooplankton inside the patch, did not result in increases in the DMSw concentration. Considering biological and nonbiological parameters, we discussed these results, although they could not be completely explained. Unfortunately, the impact of Fe fertilization on the atmospheric DMS (DMSa) concentration was not detected due to no significant changes in DMSw. However, it is noted that DMSa concentrations were dependent on the sea–air DMS flux in the air from higher latitudes and/or the Eurasian continent, though the DMS flux was a minor role to the budget of DMSw. Therefore if DMSw were significantly changed by Fe fertilization, DMSa might be affected through changes in the sea-air flux in this condition.     

BCC_CSM对北极海冰的模拟:CMIP5和CMIP6历史试验比较

本文利用北京气候中心气候系统模式(BCC_CSM)在最近两个耦合模式比较计划(CMIP5和CMIP6)的历史试验模拟结果,对北极海冰范围和冰厚的模拟性能进行了比较,结果表明:(1) CMIP6改善了CMIP5模拟海冰范围季节变化过大的问题,总体上更接近观测结果;(2)两个CMIP试验阶段中BCC_CSM模拟的海冰厚度都偏小,但CMIP6试验对夏季海冰厚度过薄问题有所改进。通过对影响海冰生消过程的冰面和冰底热收支的分析,我们探讨了上述模拟偏差以及CMIP6模拟结果改善的成因。分析表明,8?9月海洋热通量、向下短波辐射和反照率对模拟结果的误差影响较大,CMIP6试验在这些方面有较大改善;而12月至翌年2月,CMIP5模拟的北极海冰范围偏大主要是海洋热通量偏低所导致,CMIP6模拟的海洋热通量较CMIP5大,但北大西洋表层海流的改善才是巴芬湾附近海冰外缘线位置改善的主要原因。CMIP试验模拟的夏季海冰厚度偏薄主要是因为6?8月海洋热通量和冰面热收支都偏大,而CMIP6试验模拟的夏季海冰厚度有所改善主要是由于海洋热通量和净短波辐射的改善。海冰模拟结果的改善与CMIP6海冰模块和大气模块参数化的改进有直接和间接的关系,通过改变短波辐射、冰面反照率和海洋热通量,使BCC_CSM模式对北极海冰的模拟性能也得到有效提高。     

Natural air–sea flux of CO2 in simulations of the NASA-GISS climate model: Sensitivity to the physical ocean model formulation

Results from twin control simulations of the preindustrial CO₂ gas exchange (natural flux of CO₂) between the ocean and the atmosphere are presented here using the NASA-GISS climate model, in which the same atmospheric component (modelE2) is coupled to two different ocean models, the Russell ocean model and HYCOM. Both incarnations of the GISS climate model are also coupled to the same ocean biogeochemistry module (NOBM) which estimates prognostic distributions for biotic and abiotic fields that influence the air–sea flux of CO₂. Model intercomparison is carried out at equilibrium conditions and model differences are contrasted with biases from present day climatologies. Although the models agree on the spatial patterns of the air–sea flux of CO₂, they disagree on the strength of the North Atlantic and Southern Ocean sinks mainly because of kinematic (winds) and chemistry (pCO₂) differences rather than thermodynamic (SST) ones. Biology/chemistry dissimilarities in the models stem from the different parameterizations of advective and diffusive processes, such as overturning, mixing and horizontal tracer advection and to a lesser degree from parameterizations of biogeochemical processes such as gravitational settling and sinking. The global meridional overturning circulation illustrates much of the different behavior of the biological pump in the two models, together with differences in mixed layer depth which are responsible for different SST, DIC and nutrient distributions in the two models and consequently different atmospheric feedbacks (in the wind, net heat and freshwater fluxes into the ocean).