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Lipids of marine Archaea: Patterns and provenance in the water-column and sediments

机译:海洋古生细菌的脂质:水柱和沉积物中的模式和物源

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We measured archaeal lipid distributions from globally distributed samples of freshwater, marine, and hypersaline suspended particulate matter. Cluster analysis of relative lipid distributions identified four distinct groups, including: (1) marine epipelagic (<100 m) waters, (2) marine mesopelagic (200-1500 m) and upwelling waters, (3) freshwater/estuarine waters, and (4) hypersaline waters. A pronounced difference in lipid composition patterns is the near absence of ring-containing glycerol dialkyl glycerol tetraethers (GDGTs) at high salinity. Different archaeal communities populate marine (mesophilic Crenarchaeota and Euryarchaeota), and hypersaline environments (halophilic Euryarchaeota) and community shifts can regulate differences in lipid patterns between marine and hypersaline waters. We propose that community changes within meosphilic marine Archaea also regulate the lipid patterns distinguishing epipelagic and mesopelagic/upwelling zones. Changes in the relative amounts of crenarchaeol and caldarchaeol and low relative abundances of ringed structures in surface waters differentiate lipids from the epipelagic and mesopelagic/upwelling waters. Patterns of lipids in mesopelagic (and upwelling) waters are similar to those expected of the ammonia-oxidizing Group I Crenarchaeota, with predominance of crenarchaeol and abundant cyclic GDGTs; non-metric multidimensional analysis (NMDS) shows this pattern is associated with high nitrate concentrations. In contrast, limited culture evidence indicates marine Group II Euryarchaeota may be capable of producing mainly caldarchaeol and some, but not all, of the ringed GDGTs and we suggest that these organisms, along with the Crenarchaeota, contribute to lipids in epipelagic marine waters. Calculated TEX86 temperatures in mesopelagic samples (reported here and in published data sets) are always much warmer than measured in situ temperatures. We propose lipids used in the temperature proxy derive from both Euryarchaeaota and Crenarchaeota, and observed values of TEX86 are subject to changes in their ecology as influenced by nutrient fluctuations or other perturbations. Applications of published core-top TEX86-SST correlations require that (1) the surface waters are always composed of similar communities with the same temperature response and (2) that deeper water GDGT production is not transported to the sediments. Our lipid distribution patterns demonstrate both surface-water archacal community differences (which accompany greater nutrient influxes, shoaling of mesopelagic Crenarchaeota during upwelling periods, and possibly due to an influx of terrestrial Archaea), and changes in organic matter transport through the water column can affect the distribution of lipids recorded in sediments. We therefore suggest that reported temperature shifts in ancient applications indicate TEX86 lipids recorded not only temperature changes, but also changes in archaeal ecology, nutrient concentrations, and possibly oceanographic conditions. (c) 2007 Elsevier Ltd. All rights reserved.
机译:我们从淡水,海洋和高盐悬浮颗粒物的全球分布样本中测量了古细菌脂质的分布。相对脂质分布的聚类分析确定了四个不同的组,包括:(1)海洋表层水(<100 m),(2)海洋中弹性水(200-1500 m)和上升流水,(3)淡水/河口水,和( 4)高盐水。脂质组成模式的显着差异是在高盐度下几乎不存在含环的甘油二烷基甘油四醚(GDGT)。不同的古细菌群落分布在海洋(中温Crenarchaeota和Euryarchaeota)和高盐环境(嗜盐Euryarchaeota)中,群落的变化可以调节海洋和高盐海水之间的脂质模式差异。我们建议中生海洋古生菌内的群落变化也调节区分上表层和中生界/上升流区的脂质模式。地表水中Crenarchaeol和Caldarchaeol相对含量的变化以及环状结构相对较低的相对丰度,使脂质与上表层水和中弹性/上涌水区分开来。中生(和上升流)水中的脂质模式类似于氨氧化性I类Crenarchaeota所预期的模式,其中以Crenarchaeol和丰富的环状GDGT为主。非度量多维分析(NMDS)显示此模式与高硝酸盐浓度有关。相比之下,有限的文化证据表明,海洋第二类Euryarchaeota可能能够主要生产卡他古醇和一些但不是全部的环状GDGT,我们建议这些生物与Crenarchaeota一起有助于上表层海水中的脂质。中生骨样品中计算出的TEX86温度(此处和在已发表的数据集中报告)总是比实地测得的温度高得多。我们建议用于温度代理的脂质均来自Euryarchaeaota和Crenarchaeota,并且TEX86的观测值受营养成分波动或其他干扰的影响,其生态学也会发生变化。公开发表的核心-顶部TEX86-SST相关性的应用要求(1)地表水总是由具有相同温度响应的相似群落组成,以及(2)更深层水GDGT的产生不会传输到沉积物中。我们的脂质分布模式既表明了地表水古细菌群落的差异(伴随着大量营养物的涌入,中流古时的Crenarchaeota浅滩的上升,也可能是由于陆生古生菌的涌入),并且有机物通过水柱的运输变化会影响沉积物中记录的脂质分布。因此,我们建议在古代应用中报告的温度变化表明TEX86脂质不仅记录了温度变化,而且还记录了古细菌生态学,养分浓度以及可能的海洋学条件的变化。 (c)2007 Elsevier Ltd.保留所有权利。

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