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首页> 外文期刊>Deep-Sea Research >Measurement of dark, particle-generated superoxide and hydrogen peroxide production and decay in the subtropical and temperate North Pacific Ocean
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Measurement of dark, particle-generated superoxide and hydrogen peroxide production and decay in the subtropical and temperate North Pacific Ocean

机译:在亚热带和温带北太平洋中测量暗的,颗粒产生的超氧化物和过氧化氢的产生和衰减

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摘要

Reactive oxygen species (ROS), which include the superoxide radical (O-2(-)) and hydrogen peroxide (H2O2), are thought to be generated mostly through photochemical reactions and biological activity in seawater and can influence trace metal speciation in the ocean. This study reports the results of an inter comparison of two methods to measure particle-generated [O-2(-)] in seawater samples, as well as measurements of particle-generated O-2(-) and H2O2 concentrations, decay kinetics, and dark production rates in seawater samples at Station ALOHA and (O-2(-) only) in the southern California Current Ecosystem. O-2(-) was measured using two different methods relying on chemiluminescence detection. The first method measured the difference between steady-state [O-2(-)] in filtered and unfiltered seawater, while the second method (standard method) measured O-2(-) decay to baseline in freshly filtered seawater. Because both methods detected [O-2(-)] relative to the background signal from filtered seawater, both should have measured [O-2(-)] generated by particles (presumably biota). However, the O-2(-) concentrations determined by the first method were always much smaller than those obtained from the second (standard) method. Follow-up laboratory and field experiments showed that the increased signal in the standard method was due to a filtration artifact that could neither be eliminated nor consistently accounted for under the tested conditions. We therefore recommend the first method for measuring particle-generated [O-2(-)]. Measured by this method, Station ALOHA had particle-generated O-2(-) concentrations that ranged from undetectable to 0.02 nM, with production rates less than 0.6 nM hr(-1) and decay rate coefficients from 0.003 to 0.014 s(-1). The southern California Current Ecosystem had particle-generated O-2(-) concentrations that ranged from undetectable to 0.05 nM, with production rates up to 4.7 nM hr(-1) and decay rate coefficients from 0.006 to 0.017 s(-1). H2O2 concentrations were measured by chemiluminescence detection, using dark incubations of unfiltered water samples to simultaneously determine production and decay rates. H2O2 concentrations at Station ALOHA ranged from 7 to 88 nM. Dark production rates and decay rate coefficients were low (mostly < 1.5 nM hr(-1) and < 0.03 h(-1), respectively); higher values were detected when biota were pre-concentrated with net tows. These rates of ROS production are lower than those reported by previous studies in other regions of the Pacific Ocean, but could still be significant compared to photochemical production. (C) 2015 Elsevier Ltd. All rights reserved.
机译:活性氧(ROS),包括超氧自由基(O-2(-))和过氧化氢(H2O2),被认为主要是通过海水中的光化学反应和生物活性产生的,并且可以影响海洋中的痕量金属形态。这项研究报告了两种方法的相互比较结果,这两种方法用于测量海水样品中的颗粒产生的[O-2(-)],以及测量颗粒产生的O-2(-)和H2O2的浓度,衰减动力学,加利福尼亚州南部当前生态系统的ALOHA站和(仅O-2(-))海水样品的暗化速率。使用化学发光检测的两种不同方法测量O-2(-)。第一种方法测量过滤后和未过滤海水中稳态[O-2(-)]之间的差异,第二种方法(标准方法)测量新鲜过滤后的海水中O-2(-)衰减至基线。因为这两种方法都相对于滤过海水的背景信号检测到[O-2(-)],所以两种方法都应该测量由颗粒(大概是生物群)产生的[O-2(-)]。但是,通过第一种方法确定的O-2(-)浓度始终比通过第二种(标准)方法获得的O-2(-)浓度小得多。后续的实验室和现场实验表明,标准方法中信号的增加是由于过滤伪影所致,该伪影在测试条件下既无法消除也无法统一解决。因此,我们建议使用第一种方法来测量颗粒生成的[O-2(-)]。用这种方法测量,ALOHA站产生的颗粒物产生的O-2(-)浓度范围从不可检测到0.02 nM,生产率小于0.6 nM hr(-1),衰减率系数从0.003至0.014 s(-1) )。加利福尼亚南部的当前生态系统的颗粒物产生的O-2(-)浓度范围从不可检测到0.05 nM,生产率高达4.7 nM hr(-1),衰减率系数从0.006到0.017 s(-1)。通过化学发光检测测量H2O2浓度,使用未过滤的水样品的暗温培养同时测定产水量和腐烂率。 ALOHA站的H2O2浓度范围为7至88 nM。暗生产率和衰减率系数很低(分别<1.5 nM hr(-1)和<0.03 h(-1));当将生物群预先用净丝束浓缩时,检测到更高的值。这些ROS生成速率低于太平洋其他地区以前的研究报告,但与光化学生成相比仍可能是重要的。 (C)2015 Elsevier Ltd.保留所有权利。

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