排序方式： 共有45条查询结果，搜索用时 562 毫秒
1.
L.J. Hou M. Liu J.J. Lu S.Y. Xu D.N. Ou Y. Yang D.G. Zheng 《Environmental Geology》2006,49(7):937-945
The influences of exposure to the atmosphere on ammonium cycle in the intertidal surface sediments were in situ studied with
a geochemical approach at a typical station in the Yangtze Estuary during three tidal cycles in September 2003. During an
about 8-h emersion period of each diurnal tide, six high-resolution vertical profiles of adsorbed and dissolved ammonium were
measured. It was observed that both adsorbed and dissolved ammonium generally had an increasing trend in sediment cores during
the exposure. The rate of ammonium regeneration in sediments was estimated using the accumulation amount of ammonium including
adsorbed and soluble fractions during the daytime emersion. The calculation result showed that there was relatively high ammonification
rate (˜500 nmol N cm−3 day−1), which reflected that organic nitrogen in sediments was quickly decomposed with a residence time of ˜52.7 days. Due to the
dramatic temperature difference observed in sediment profiles, free convection was considered an important mechanism of regulating
the efflux of produced ammonium into overlying waters. The total estimated amount of regenerated ammonium was ˜1.35×105 t N year−1 in the intertidal flat of the Yangtze Estuary, which occupied 7.6% of the total inorganic nitrogen annually transported to
the estuarine ecosystem. 相似文献
2.
A.Yu. Likhacheva S. A. Veniaminov E. A. Paukshtis 《Physics and Chemistry of Minerals》2004,31(5):306-312
The thermal decomposition of ammonium-exchanged natural analcime is characterized by gas chromatography, IR spectroscopy and X-ray diffraction. The de-ammoniation and dehydroxylation proceed in parallel throughout the decomposition, which evidences the instability of the protonated analcime framework. The mechanism of degassing of NH4-analcime changes throughout its decomposition. At the initial step, the mechanism of de-ammoniation consists in thermal dissociation of NH4+ molecule onto NH3 and proton (framework OH group) and diffusion of NH3 out of the structure. Subsequent decomposition and removal of the OH groups lead to a progressive loss of crystallinity. At this step, an apparent activation energy for NH3 desorption is estimated to be 145(±13) kJ mol–1. This value is within the upper limit of the activation energy characteristic for the NH3 desorption from proton centres in large-pore zeolites. At the final step, the adsorption of NH3 and protons onto the defect centres in the amorphosed aluminosilicate framework results in a significant increase of an apparent activation energy for the de-ammoniation and dehydroxylation up to 270(±20) kJ mol–1. 相似文献
3.
Understanding the role of the oceans in the Earth's changing climate requires comprehension of the relevant metabolic pathways which produce climatically important trace gases. The global ocean represents one of the largest natural sources of nitrous oxide (N2O) that is produced by selected archaea and/or bacteria during nitrogen (N) metabolism. In this study, the role of nitrite (NO2−) in the production of N2O in the upper water column of the oligotrophic North Pacific Subtropical Gyre was investigated, focusing primarily on the lower euphotic zone where NO2− concentrations at the primary NO2− maximum reached 195 nmol L−1. Free-drifting sediment trap arrays were deployed to measure N cycle processes in sinking particulate material and the addition of selected N substrates to unpreserved sediment traps provided an experimental framework to test hypotheses regarding N2O production pathways and controls. Sinking particles collected using NO2−-amended, unpreserved sediment traps exhibited significant production of N2O at depths between 100 and 200 m. Subsequent stable isotope tracer measurements conducted on sediment trap material amended with 15NO2− yielded elevated δ15N values of N2O, supporting N2O production via a NO2− metabolism pathway. Experiments on seawater collected from 150 m showed N2O production via NO2− metabolism also occurs in the water-column and indicated that the concentration of NO2− relative to NH4+ availability may be an important control. These findings provide evidence for the production of N2O via nitrifer-denitrification in the lower euphotic zone of the open ocean, whereby NO2− is reduced to N2O by ammonia-oxidizing microorganisms. 相似文献
4.
针对复杂硝酸铵水盐体系溶解度的测定,传统分析方法操作步骤繁琐,且试剂较贵,引入一种简单准确的分析方法,即热分解法,对LiNO3-KNO3-NH4NO3-H2O体系和NaNO3-KNO3-NH4NO3-H2O体系中硝酸铵和水的含量进行精确分析。结果表明,热分解温度控制在230～240℃,若控制样品质量为1.5 g,分解时间不低于36 h,能将LiNO3-KNO3-NH4NO3-H2O体系中的硝酸铵和水彻底分解,且随着样品中硝酸铵含量增加,热分解时间也将延长,分析相对误差能控制在0.2%以内。针对复杂NaNO3-KNO3-NH4NO3-H2O体系,热分解温度控制在230～255℃,若控制样品质量为1.5 g,分解时间不少于44 h,且随着样品中硝酸铵含量的增加,相应延长热分解时间,能将复杂NaNO3-KNO3-NH4NO3-H2O体系中的硝酸铵和水彻底分解,分析相对误差能控制在0.2%以内。 相似文献
5.
Fuminori Hashihama Toru Hirawake Sakae Kudoh Jota Kanda Ken Furuya Yukuya Yamaguchi Takashi Ishimaru 《Polar Science》2008,2(2):109-120
We investigated the size fraction and pigment-derived class compositions of phytoplankton within the euphotic zone of the Antarctic marginal ice zone between 63.3°S and 66.5°S along the 140°E meridian on two consecutive cruises in the late austral summer and early austral autumn of 2003. We observed significant temporal and spatial variations in phytoplankton size and taxonomic composition, although chlorophyll a concentrations were generally below 1 μg l−1 during both periods. Microphytoplankton (>20 μm), mainly diatoms, were prominent in the euphotic zone in the southernmost area around 66.5°S during late summer. In the rest of the study area during both cruises, the phytoplankton community was dominated by pico- and nano-sized populations (<20 μm) throughout the euphotic zone. The small-size populations mostly consisted of diatoms and haptophytes, although chlorophytes were dominant in extremely cold water (−1.5°C) below the overlying warm water around 65.5°S during late summer. From late summer to early autumn, chlorophytes declined in abundance, probably due to increasing temperature within the euphotic zone (−1 to 0°C). These pico- and nano-phytoplankton-dominated populations were often accompanied by relatively high concentrations of ammonium, suggesting the active regeneration of nutrients within the small-size plankton community. 相似文献
6.
Hai Wang Zheng‐Xin Chen Xiao‐Yu Zhang Si‐Xi Zhu Ying Ge Scott‐X. Chang Chong‐Bang Zhang Cheng‐Cai Huang Jie Chang 《洁净——土壤、空气、水》2013,41(7):657-664
The effects of plant species richness on both above‐ and belowground plant biomass, plant nitrogen (N) pool size, and substrate N concentrations were studied in a full‐scale subsurface vertical‐flow constructed wetland (CW). Results showed that (i) plant species richness increased belowground plant biomass and its N pool size but had no effect on aboveground plant biomass and its N pool size; (ii) plant species richness increased substrate N removal, especially ammonium N removal; and (iii) plant species richness had no effect on plant N use efficiency, suggesting that the N pool size increased with increasing plant species richness. More N accumulation could be removed through harvesting plant biomass. We concluded that the N removal performance of the CW improved by plant species richness through increasing belowground biomass and relevant N pool size. 相似文献
7.
象山港氮、磷营养盐环流和分布规律的研究 总被引：8，自引：1，他引：7
采用定点监测分析方法,研究了象山港狭湾内设置的六个固定站位1992-2007年时间段内的硝酸氮(NO3-N)、亚硝酸氮(NO2-N)、铵氮(NH4-N)和磷酸盐(PO4-P)浓度的监测数据,探讨了象山港狭湾内(122°00'E以西)氮、磷营养盐的环流和分布规律.结果表明,(1)除个别年份外,16年内硝酸氮、亚硝酸氮、铵氮和磷酸盐浓度的空间分布,从港顶1号站向港口6号站呈降低趋势,其中以PO4-P、NO2-N的降低趋势最为明显,而NH4-N的降低趋势相对较弱.(2)NO3-N的空间变化规律较为复杂,并且3号站的浓度往往达到最大值.(3)无论是平水期(4月)还是丰水期(7月),表层盐度均低于底层,而表层温度高于底层;盐度从港顶1号站向港口6号站递增,而温度递减.这种分布规律基本上可用余环流模式进行解释,但余环流输运并不是促使营养盐入海的唯一原因,潮振荡的垂向剪切造成的纵向弥散和潮混合亦对营养盐输运有重大贡献.(4)与1992年相比,2007年各站的NO3-N浓度几乎都增加了一倍,PO4-P浓度增幅更大,说明象山港的氮、磷污染与日俱增. 相似文献
8.
Wet deposition of ammonium in Europe 总被引：2，自引：0，他引：2
Ammonium concentration data in precipitation have been compiled to derive a concentration and deposition field for ammonium in Europe. Measurements referring to a total number of 218 measuring sites have been considered. Because of changes in the ammonium concentrations due to the use of improper sampling procedures, a correction procedure is proposed. This makes allowance for the type of sampler used, the length of the sampling period, and whether or not light-protected sample bottles are used. Dependent on the specific sampling procedure used correction factors range from 0.75 to 1.20. According to our calculations, the total wet deposition flux of ammonium in Europe in the early 1980s amounts to 2.4 Mt NH4
+y-1. However, for some parts of Europe the flux cannot be estimated very reliably because of the low number or even the absence of measuring sites. Compared to earlier estimates for around 1960, the ammonium wet deposition flux has increased by approximately 25% during the period 1960–1980. 相似文献
9.
Jeffrey L. Collett Jr. Aaron Bator D. Eli Sherman Katharine F. Moore Katherine J. Hoag Belay B. Demoz Xin Rao Jill E. Reilly 《Atmospheric Research》2002,64(1-4)
Over the past decade, the chemical compositions of fogs and intercepted clouds have been investigated at more than a dozen locations across the United States. Sampling sites have been located in the northeast, southeast, Rocky Mountain, and west coast regions of the US. They include both pristine and heavily polluted locations. Frontal/orographic clouds (warm and supercooled), intercepted coastal stratiform clouds, and radiation fogs have all been examined. Sample pH values range from below 3 to above 7. Major ions also exhibit a wide concentration range, with clouds at some locations exhibiting high sea salt concentrations, while composition at other locations is dominated by ammonium and sulfate or nitrate. 相似文献
10.
The solubilities of ammonium chloride in aqueous ammonia decreased first and then increased with increasing ammonia concentrations, but the mechanism of this phenomenon has not been clarified. In the present work, the ATR-FTIR and Raman spectroscopy were employed to investigate the corresponding mechanism. The spectra analysis was focused on the region between 2500 and 4000 cm-1. It was firstly discovered that the N-H???N hydrogen bonds between ammonium ions and ammonia molecule was mainly formed in the NH4Cl-NH3-H2O system with concentrations higher than 10% ammonia, but N-H???O hydrogen bonds between ammonium ions and water molecule took advantage in the system with lower ammonia concentrations. Correspondingly, the phenomena of hydrogen bonding redshift and blueshift was observed respectively compared in NH3?H2O solution. Moreover, the hydrogen bonding structure of the saturated solution was obtained by means of MD simulation. The present work provides some theoretical basis for the separation of ammonium potassium chloride. 相似文献