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首页> 外文期刊>Oceanographic Literature Review >Concerted measurements of lipids in seawater and on submicrometer aerosol particles at the Cabo Verde islands: Biogenic sources, selective transfer and high enrichments
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Concerted measurements of lipids in seawater and on submicrometer aerosol particles at the Cabo Verde islands: Biogenic sources, selective transfer and high enrichments

机译:海水中的脂质的齐齐欲测量和Cabo Verde群岛的丘疹气溶胶颗粒:生物源,选择性转移和高浓缩

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摘要

In the marine environment, measurements of lipids as representative species within different lipid classes have been performed to characterize their oceanic sources and their transfer from the ocean into the atmosphere to marine aerosol particles. The set of lipid classes includes hydrocarbons (HC); fatty acid methyl esters (ME); free fatty acids (FFA); alcohols (ALC); 1,3-diacylglycerols (1,3 DG); 1,2-diacylglycerols (1,2 DG); mono-acylglycerols (MG); wax esters (WE); triacylglycerols (TG); and phospholipids (PP) including phosphatidylglycerols (PG), phos-phatidylethanolamine (PE), phosphatidylcholines (PC), as well as glycolipids (GL) which cover sulfoquinovosyldiacylglycerols (SQDG), monogalactosyl-diacylglycerols (MGDG), digalactos-yldiacylglycerols (DGDG) and sterols (ST). These introduced lipid classes have been analyzed in the dissolved and paniculate fraction of seawater, differentiating between underlying water (ULW) and the sea surface microlayer (SML) on the one hand. On the other hand, they have been examined on ambient submicrometer aerosol particle samples (PM1) which were collected at the Cape Verde Atmospheric Observatory (CVAO) by applying concerted measurements. These different lipids are found in all marine compartments but in different compositions. Along the campaign, certain variabilities are observed for the concentration of dissolved ( P DLULW: 39.8 128.5 νgL-1, P DLSML: 55.7 121.5 vgL-1 and paniculate ( P PLULW: 36.4 93.5 νgL-1, P PLSML: 61.0 118.1 νgL-1) lipids in the seawater of the tropical North Atlantic Ocean. Only slight SML enrichments are observed for the lipids with an enrichment factor EFSML of 1.1 1.4 (DL) and 1.0 1.7 (PL). On PM 1 aerosol particles, a total lipid concentration between 75.2 219.5 ngm-3 (averaged; 119.9 ngm-3) is measured. As also bacteria besides phytoplankton sources influence the lipid concentrations in seawater and on the aerosol particles, the lipid abundance cannot be exclusively explained by the phytoplankton tracer (chlorophyll a). The concentration and enrichment of lipids in the SML are not related to physicochemi-cal properties which describe the surface activity. On the aerosol particles, an EFaer (the enrichment factor on the submicrometer aerosol particles compared to the SML) between 9-104 7-105 is observed. Regarding the individual lipid groups on the aerosol particles, a statistically significant correlation (R2 D 0:45, p D 0:028) was found between EFaer and lipophilicity (expressed by the KOW value), which was not present for the SML. But simple physicochemical descriptors are overall not sufficient to fully explain the transfer of lipids. As our findings show that additional processes such as formation and degradation influence the ocean atmosphere transfer of both OM in general and of lipids in particular, they have to be considered in OM transfer models. Moreover, our data suggest that the extent of the enrichment of the lipid class constituents on the aerosol particles might be related to the distribution of the lipid within the bubble air water interface. The lipids TG and ALC which are preferably arranged within the bubble interface are transferred to the aerosol particles to the highest extent. Finally, the connection between ice nucleation particles (INPs) in seawater, which are already active at higher temperatures (-10 to -15 -C), and the lipid classes PE and FFA suggests that lipids formed in the ocean have the potential to contribute to (biogenic) INP activity when transferred into the atmosphere.
机译:在海洋环境中,已经进行了脂质作为不同脂质类别中的代表性物种的测量,以表征其海洋来源及其从海洋转移到大气中的海洋气溶胶颗粒。该组脂质类包括烃(HC);脂肪酸甲酯(ME);游离脂肪酸(FFA);醇(ALC); 1,3-二酰基甘油(1,3 dg); 1,2-二酰基甘油(1,2 DG);单酰基甘油(Mg);蜡酯(我们);三酰基甘油(Tg);和磷脂(PP)包括磷脂基甘油(PG),Phos-phatiyyl乙醇胺(PE),磷脂酰胆碱(PC),以及覆盖磺基喹啉基甘氨酸(SQDG),单甘露乳糖基 - 二酰基甘油(MGDG),Digalactos-Yldiacylglycrols(DGDG)的糖脂(GL)和甾醇(st)。已经在海水的溶解和容量分数中分析了这些引入的脂质类别,在一方面脱离底层水(ULW)和海面微层(SML)。另一方面,通过应用协调测量,他们已经在环境亚微米的气溶液颗粒样品(PM1)上进行了检查。这些不同的脂质在所有海洋隔室中发现,但在不同的组合物中。沿着竞选,观察到溶解的浓度(p dlulw:39.8 128.5νgl-1,p dlsml:55.7 121.5 Vgl-1和Paniculate(p芭蕾舞:36.4 93.5νgl-1,plsml:61.0 118.1νgl- 1)热带北大西洋海水中的脂质。只有1.1.4(DL)和1.0 1.7(PL)的富集因子EFSML的脂质只观察到脂质的轻微SML富集。在PM 1气溶胶颗粒上,总脂质浓度测量75.2 219.5 ngm-3(平均; 119.9 ngm-3)。作为浮游植物来源的细菌,除了浮游动物和气溶胶颗粒中的脂质浓度,脂质丰度不能被浮游植物示踪剂(叶绿素A)解释。SML中的脂质的浓度和富集与描述表面活性的物理化学性质无关。在气溶胶颗粒上,efaer(亚尺寸尺气溶胶颗粒上的富集因子与SML)之间观察到9-104 7-105。关于气溶胶颗粒上的个体脂质基团,在Efaer和亲脂性(由Kow值表达)之间发现统计学上显着的相关性(R2 D 0:45,P D 0:028),其不存在SML。但简单的物理化学描述符整体不足以充分解释脂质的转移。正如我们的研究结果表明,诸如形成和降解的其他过程,特别是诸如血液的海洋气氛转移,特别是在OM转移模型中考虑它们。此外,我们的数据表明,气溶胶颗粒上的脂肪类成分的富集的程度可能与泡沫空气界面内脂质的分布有关。优选在气泡界面内布置在气泡界面的脂质Tg和Alc被转移到气溶胶颗粒到最大程度。最后,海水中的冰成核颗粒(Inps)之间的连接,其在较高温度(-10至-15 -11-10)和脂肪类PE和FFA中表明海洋中形成的脂质有可能贡献在转移到大气中时(生物生物)INP活动。

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    《Oceanographic Literature Review》 |2021年第5期|987-987|共1页
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