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1.
海洋生物固氮作用研究进展 总被引:1,自引:0,他引:1
近年来,海洋生物固氮作用研究已成为海洋氮循环研究热点之一,因为它补充了海洋中的结合态氮,影响着海洋氮储库的收支平衡,进而调控海洋的初级生产力,并因此与海洋颗粒有机碳的迁出以及海洋对大气CO2的吸收密切相关.海洋生物固氮作用的研究主要是在近30a开展起来的,现有观点认为全球海洋生物固氮速率为100~200 Tg/a.15↑N2示踪法和乙炔还原法是最重要的生物固氮速率实测方法,而硝酸盐异常指数法、15↑N同位素收支平衡法、卫星遥测法等则是重要的间接估测方法.束毛藻曾被认为是全球海洋最重要的固氮生物,但近年来也发现了固氮生物在微微(pi-co)级和微(nano)级的分布,表明以往基于束毛藻的固氮速率可能是被低估的.海洋生物固氮作用营养盐限制的研究主要集中在铁和磷这2个元素的作用,但目前尚无定论.在中国边缘海生物固氮作用的研究还很匮乏,少数研究表明除黑潮区外,由束毛藻所支持的固氮速率并不高.就海洋固氮作用研究的未来发展,指出今后必须在更大时空尺度上开展海洋生物固氮作用研究,以弥补现有实测数据的不足,并获取固氮微生物种类组成的准确信息,在确定海洋生物固氮作用控制因素的同时,追踪新固定氮的流向,进而为海洋氮循环提供准确信息. 相似文献
2.
海洋生物固氮是指固氮生物利用固氮酶将氮气转化为生物可利用铵盐的海洋氮元素输入过程,和反硝化及厌氧氨氧化等氮流失途径一起制约着大洋氮收支平衡。而固氮速率的测定是研究海洋生物固氮的最直接方式。自发现海洋生物固氮作用以来,固氮速率的测定方法在不断更新改进,但总体来说仍存在较大不确定性。最近用15N2同位素示踪法及其他相关数据综合得到全球海洋固氮量为196.1 Tg N∙a−1,最高固氮速率发生在南太平洋热带地区。但分布受到多种因素的影响。其中,物理因素中的光照和温度是全球范围固氮速率分布的最佳预测因子,光照为固氮过程提供能量,温度通过影响固氮酶活性而发挥作用。在化学因素中,铁元素的缺乏成为固氮的重要限制因子。除此之外,还有生物因素,如浮游植物和异养固氮生物等,对固氮量的贡献影响较大。最近有研究对以往固氮作用区域和反硝化作用空间相互耦合的观点表示质疑,提出二者分布空间分离的新格局。研究多控制因素对固氮生物的耦合效应、明确不同物种对固氮总量的相对贡献以及进一步建立固氮速率的原位测定方法是未来海洋固氮作用研究的主要工作。 相似文献
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海洋中的氮循环是海洋生物地球化学研究的热点领域之一,而硝化过程是氮循环的关键一环,准确获取硝化速率对于丰富海洋氮循环的认识至关重要。15N标记同位素技术是目前国际上最为广泛使用的硝化速率测定方法,该方法的核心在于准确测定15N加富样品产生的15NO2-和15NO3-的含量,但目前的方法普遍存在测试时间较长、测试成本较高、所需样品体积较大或者检测限较高等问题。研究以低成本的膜进样质谱作为15N加富样品测试设备,建立了基于镉柱与氨基磺酸双还原体系测定15N加富样品中15NO3-含量的方法。经条件优化实验确定的具体方法:采用1 mol/L HCl配制15 mmol/L的氨基磺酸(SA)作为反应试剂除去样品原有的NO2-,然后利用镉柱将15NO 相似文献
5.
海水入侵调查方法研究进展 总被引:1,自引:0,他引:1
综述了国内外海水入侵调查方法,总结了水化学方法、水位观测、地球物理勘测方法、同位素示踪法在海水入侵监测和调查中的研究进展,指出各类方法在应用中应注意的问题,提出未来仍需积极探索不同的海水入侵调查方法,发展延时性地球物理勘测方法、应用新的同位素示踪剂等,同时联用多种调查方法,以获得可靠的结果。 相似文献
6.
新的痕量同位素示踪剂在全球变化研究中的应用 总被引:3,自引:0,他引:3
最近,用高精度多通道电感耦合等离子体质谱仪测定某些过渡金属,如Mo,Fe,Cu,Zn等同位素的组成,表明它们可作为全球变化研究中生物地球化学过程的示踪剂,现有的研究文献表明,Mo的同位素可用于古氧化还原环境研究,初步结果显示,海水中δ^97/95Mo的变化与海洋有氧与缺氧沉积物有直接的关系,可记录缺氧沉积物的来源,以此为基础,可用δ^97/95Mo的收支来估算从陆地进入海洋中Mo的通量和全球Mo同位素的收支;Fe同位素在一定程度上控制着海洋生物生产力的水平,其丰度也对气候变化有影响,但生物与非生物过程都可引起铁同位素的分馏,其δ^56/54Fe的变化都可达1‰,所以Fe同位素不能单独用来界定地质记录的Fe参与的过程是生物还是非生物控制,Cu,Zn的同位素也被用来研究生物地球化学过程的示踪剂,但目前报道不多,综述了这一领域的主要进展,集中阐述了同位素示踪样品的制备、纯化与测定方法,同位素在海洋环境变化研究中的应用,最后提出了这一领域可能的发展方向。 相似文献
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反硝化与厌氧氨氧化作用是海洋结合态氮迁出的主要途径,15N示踪法是定量反硝化和厌氧氨氧化作用的新方法,它具有灵敏度高、可同步测量反硝化与厌氧氨氧化速率的优点.本研究开展了一系列方法学实验,以确定高纯氦气驱赶水样所含气体的时间、超声赶气时间、同位素比值质谱仪测量N2含量的精度、N2含量及其同位素组成测定的工作曲线以及示踪剂的最佳添加量等,从而确立起15N示踪同步测定海水反硝化和厌氧氨氧化速率的方法.所建立方法测量N2含量的相对标准偏差小于8%,可满足海洋反硝化与厌氧氨氧化速率测定的需要.应用该方法实测了厦门筼筜湖富氧与缺氧水体的反硝化与厌氧氨氧化速率,结果表明,缺氧底层水的反硝化速率[4.10~5.47μmol/(dm3·d)]比富氧表层水[0.43~0.46μmol/(dm3·d)]明显来得高,但缺氧底层水的厌氧氨氧化速率[0.00~0.12μmol/(dm3·d)]则比富氧表层水的速率[0.52~0.67μmol/(dm3·d)]低得多. 相似文献
8.
《热带海洋学报》2017,(2)
大气沉降向海洋表层输入大量的铝,然而关于铝对海洋浮游植物的影响却少有研究报道。目前,铝对在海洋碳和氮循环中起着重要作用的固氮生物影响的研究还较少。文章以Aquil培养基(无氮硅营养盐)半连续培养单细胞海洋固氮蓝藻Crocosphaera watsonii,利用流式细胞技术和~(15)N同位素示踪法,研究铝(0、0.2、2和20μmol×L~(–1))对Crocosphaera watsonii生长和固氮作用的影响。数据表明,3个铝处理组Crocosphaera watsonii细胞大小、光合色素含量和光系统Ⅱ(PSⅡ)原初光能转化效率(F_v/F_m)都显著降低,生长速率和固氮速率明显受到抑制。结果表明,在营养充足条件下,铝对Crocosphaera watsonii生长和固氮具有抑制性作用。 相似文献
9.
大气CO2浓度升高引起的海洋酸化可能对浮游植物造成不同程度的影响。而近海浮游植物不仅面临着海水酸化问题,还会受到海水溶解性CO2降低及pH升高(海水碱化)的影响。本实验以斑点海链藻(Thalassiosira punctigera)为研究对象,测定7个不同pCO2水平(25 μatm、50 μatm、100 μatm、200 μatm、400 μatm、800 μatm、1 600 μatm)下的生长、光合作用和呼吸作用速率、细胞粒径、叶绿素a和生物硅含量以及叶绿素荧光等参数。结果表明,与400 μatm相比,在海水酸化(pCO2 > 400 μatm)和海水碱化(pCO2 < 400 μatm) 条件下,斑点海链藻的生长速率和叶绿素a含量都显著降低,但是碱化条件下降低的程度更大。此外,碱化处理的藻细胞光合作用速率、最大量子产量(Fv/Fm)和最大相对电子传递速率(rETRmax)都显著低于400 μatm培养下的细胞,而呼吸作用速率显著升高,但是生物硅含量和细胞大小无明显变化。研究表明海水碱化和海水酸化均会抑制其生理活动,而且海水碱化对其影响更显著。这表明正常pCO2生长下的藻细胞具有最适的生理状态。本研究可为探究海水碳酸盐系统变化对海洋初级生产力的影响提供一定的数据支持。 相似文献
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利用15 N示踪法实测南海水体反硝化速率的研究发现,培养水样在长时间密闭放置过程中也会受到外界空气的污染,且其29N2/28N2比值恒定为0.007 35。根据空气背景中29N2/28N2比值恒定的特征,提出基于质量平衡关系校正空气N2污染的方法,通过将样品实测29N2浓度扣除由外界空气贡献的29N2浓度,可获得由生物反硝化作用所产生的29N2准确浓度,进而可计算出准确的反硝化速率。经空气29N2背景校正后,29N2浓度的偏差明显小于未经校正的结果,且29N2浓度与培养时间之间的线性相关性显著加强,凸显出空气29N2背景校正是获取准确反硝化速率的关键。鉴于15 N示踪法已被广泛应用于海洋水体与沉积物反硝化速率的测定中,所提出的空气29N2背景校正方法具有重要的意义。 相似文献
12.
The mechanisms regulating N2O production in an estuarine sediment (Tama Estuary, Japan) were studied by comparing the change in N2O production with those in nitrification and denitrification using an experimental continuous-flow sediment–water system with15N tracer (15N-NO−3 addition). From Feburary to May, both nitrification and denitrification in the sediment increased (246 to 716 μmol N m−2 h−1and 214 to 1260 μmol N m−2 h−1, respectively), while benthic N2O evolution decreased slightly (1560 to 1250 nmol N m−2 h−1). Apparent diffusion coefficients of inorganic nitrogen compounds and O2at the sediment–water interface, calculated from the respective concentration gradients and benthic fluxes, were close to the molecular diffusion coefficients (0·68–2·0 times) in February. However, they increased to 8·8–52 times in May except for that of NO−2, suggesting that the enhanced NO−3 and O2supply from the overlying water by benthic irrigation likely stimulated nitrification and denitrification. Since the progress of anoxic condition by the rise of temperature from February to May (9 to 16 °C) presumably accelerated N2O production through nitrification, the observed decrease in sedimentary N2O production seems to be attributed to the decrease in N2O production/occurrence of its consumption by denitrification. In addition to the activities of both nitrification and denitrification, the change in N2O metabolism during denitrification by the balance between total demand of the electron acceptor and supply of NO−3+NO−2 can be an important factor regulating N2O production in nearshore sediments. 相似文献
13.
Keiji Horikawa Masao Minagawa Yoshihisa Kato Masafumi Murayama Seiya Nagao 《Journal of Oceanography》2006,62(4):427-439
N2 fixation is an important biological process that adds new nitrogen to oceans and plays a key role in modulating the oceanic
nitrate inventory. However, it is not known how, when, and where N2 fixation rates have varied in response to past climate changes. This study presents a new record of nitrogen isotopic composition
(δ15N) over the last 83 kyr from a sediment core (KH02-4 SUP8) taken in the Sulu Sea in the western equatorial Pacific region;
data allow the N2 fixation variability in the sea to be reconstructed. Sediments, sinking, and suspended particulate organic matter (POM) all
have lighter isotopic values compared to the δ15N values of substrate nitrate (av. 5.8‰) in North Pacific Intermediate Water. These lighter δ15N values are regarded as reflecting N2 fixation in the Sulu Sea surface water. A δ15N mass balance model shows that N2 fixation rates were significantly enhanced during 54–34 kyr in MIS-3 and MIS-2. It has been speculated that higher interglacial
denitrification rates in the Arabian Sea and the eastern tropical Pacific would have markedly decreased the global oceanic
N inventory and contributed to the increase in N2 fixation in oligotrophic regions, but such a model was not revealed by our study. It is possible that changes in N2 fixation rates in the Sulu Sea were regional response, and accumulation of phosphate in the surface waters due to enhanced
monsoon-driven mixing is thought to have stimulated enhancements of N2 fixation during MIS-3 and MIS-2. 相似文献
14.
The generalised gradient approximation based on density functional theory is used to study the structural and electronic properties of the endohedral fullerene dimer (N2@C60)2. Four N atoms sit at the cage centres in the form of two N_2 molecules. The density of states and Mulliken charge analysis explore that the energy levels from -6 to -10 eV are mainly influenced by the N2 molecules. 相似文献
15.
T. Yoshinari M. A. Altabet S. W. A. Naqvi L. Codispoti A. Jayakumar M. Kuhland A. Devol 《Marine Chemistry》1997,56(3-4)
Nitrous oxide (N2O) is a trace gas that is increasing in the atmosphere. It contributes to the greenhouse effect and influences the global ozone distribution. Recent reports suggest that regions such as the Arabian Sea may be significant sources of atmospheric N2O.In the ocean, N2O is formed as a by-product of nitrification and as an intermediary of denitrification. In the latter process, N2O can be further reduced to N2. These processes, which operate on different source pools and have different magnitudes of isotopic fractionation, make separate contributions to the 15N and18O isotopic composition of N2O. In the case of nitrification in oxic waters, the isotopic composition of N2O appears to depend mainly on the 15N/14N ratio of NH+4 and the 18O/16O ratio of O2 and H2O. In suboxic waters, denitrification causes progressive 15N and 18O enrichment of N2O as a function of degree of depletion of nitrate and dissolved oxygen. Thus the isotopic signature of N2O should be a useful tool for studying the sources and sinks for N2O in the ocean and its impact on the atmosphere.We have made observations of N2O concentrations and of the dual stable isotopic composition of N2O in the eastern tropical North Pacific (ETNP) and the Arabian Sea. The stable isotopic composition of N2O was determined by a new method that required only 80–100 nmol of N2O per sample analysis. Our observations include determinations across the oxic/suboxic boundaries that occur in the water columns of the ETNP and Arabian Sea. In these suboxic waters, the values of δ15N and δ18O increased linearly with one another and with decreasing N2O concentrations, presumably reflecting the effects of denitrification. Our results suggest that the ocean could be an important source of isotopically enriched N2O to the atmosphere. 相似文献
16.
In the present study, we report N_2 fixation rate(~(15)N isotope tracer assay) and the diazotroph community structure(using the molecular method) in the western tropical North Pacific Ocean(WTNP)(13°–20°N, 120°–160°E). Our independent evidence on the basis of both in situ N_2 fixation activity and diazotroph community structure showed the dominance of unicellular N_2 fixation over majority of the WTNP surface waters during the sampling periods.Moreover, a shift in the diazotrophic composition from unicellular cyanobacteria group B-dominated to Trichodesmium spp.-dominated toward the western boundary current(Kuroshio) was also observed in 2013. We hypothesize that nutrient availability may have played a major role in regulating the biogeography of N_2 fixation.In surface waters, volumetric N_2 fixation rate(calculated by nitrogen) ranged between 0.6 and 2.6 nmol/(L·d) and averaged(1.2±0.5) nmol/(L·d), with 10 μm size fraction contributed predominantly(88%±6%) to the total rate between 135°E and 160°E. Depth-integrated N_2 fixation rate over the upper 200 m ranged between 150 μmol/(m~2·d)and 480 μmol/(m~2·d)(average(225±105) μmol/(m~2·d). N_2 fixation can account for 6.2%±3.7% of the depthintegrated primary production, suggesting that N_2 fixation is a significant N source sustaining new and export production in the WTNP. The role of N_2 fixation in biogeochemical cycling in this climate change-vulnerable region calls for further investigations. 相似文献
17.
微藻固碳是一种新型节能减排技术,具有长期可持续发展的潜力。本文对两株富油微藻(球等鞭金藻和微拟球藻)进行了富碳培养下生长特性及中性脂积累特性的研究。两株富油微藻的最佳培养条件为10%CO2浓度和f培养基。本研究对两株富油微藻的最大生物量产率、总脂含量、最大油脂产率、微藻的C含量和CO2固定率进行了测定。球等鞭金藻的各参数指标分别为:142.42±4.58g/(m2·d),39.95%±0.77%,84.47±1.56g/(m2·d),45.98%±1.75%和33.74±1.65g/(m2·d)。微拟球藻的各参数指标分别为:149.92±1.80g/(m2·d),37.91%±0.58%,89.90±1.98g/(m2·d),46.88%±2.01%和34.08±1.32g/(m2·d)。实验结果显示,两株海洋微藻均属于高固碳优良藻株,适合应用于微藻烟气减排技术开发,具备用于海洋生物质能耦合CO2减排开发的潜力。 相似文献
18.
采用化学沉淀法成功制备了Cu2+/SnO2复合纳米光催化剂,采用XRD、SEM等测试手段对复合纳米光催化剂的粒径、形态等进行表征。在紫外光条件下,分别改变催化剂掺杂比、催化剂煅烧温度、催化剂投加量、柴油初始含量和光照时间等单因素,探究不同条件对Cu2+/SnO2复合纳米光催化剂降解海洋柴油污染物的影响。结果表明,自制复合纳米光催化剂可以有效降解海水中的柴油污染物,在紫外光作用下,于400℃下煅烧Cu/Sn掺杂比为0. 03的Cu2+/SnO2复合纳米光催化剂、投加量为0. 2 g/dm3、柴油初始含量为0. 15 g/dm3、H2O2溶液含量为0. 2 g/dm3、溶液的p H为7、光照时间3 h时效果最好,海水中柴油的去除率最高,达到86. 98%。Cu2+/SnO2复合纳米光催化剂用聚丙烯纳米球负载后可以实际应用于海洋中,便于回收。 相似文献