Confronting the nitrogen challenge: Options for governance and target setting

The release of excessive anthropogenic nitrogen contributes to global climate change, biodiversity loss, and the degradation of ecosystem services. Despite being an urgent global problem, the excess nitrogen is not governed globally. This paper considers possible governance options for dealing with excessive nitrogen through target setting, which is an approach commonly adopted to address global environmental problems. The articulation of the nitrogen problem and the numerous international institutions dealing with it, provide evidence of a nitrogen regime characterised by limited coordination and targets covering sources and impacts only partially. This calls for improving the nitrogen governance in the direction of more integrated approaches at the global scale. In this vein, the paper investigates two opposite governance options – here labelled as ‘holistic’ and ‘origin-based’ – and evaluates them for their capability to define solutions and targets for human-induced nitrogen. From the analysis, it emerges that origin-based solutions can be preferable to holistic solutions as they can be more specific and potentially have greater immediate results. Independent from which governance arrangement is chosen, what matters most is the speed at which an arrangement can deploy solutions to combat (fast-growing) nitrogen pollution.     

Assessment of the Uncertainties in the NO2 and O3 Measurements by Visible Spectrometers

The column amounts of nitrogen dioxide (NO2) and ozone (O3) were measured using a visible spectrometer based on the twilight zenith-sky technique at two observatories located at similar latitudes in the northern part of Japan separated by a distance of 150 km. The measurements began in April 1991 at the Moshiri Observatory (44.4°N, 142.3°E) and in April 1994 at the Rikubetsu Observatory (43.5°N, 143.8°E). Since weather conditions and the possible influence from tropospheric pollution were not always identical at these two observatories, the overall accuracy of the measurements was studied comparing these data sets. The first year data obtained at a solar zenith angle of 90 degrees indicated that the NO2 slant column values at sunrise and sunset agreed within 0.36 and 0.54 × 1016 cm-2, respectively, corresponding to 5 % (June) and to 12 % (December) of the columns. The O3 values agreed within 0.76 × 1019 cm-2, corresponding to 4 % (March) 6 % (August) of the columns, although a part of the difference was systematic. The O3 column amounts were also compared to those obtained by the Dobson spectrometer at Sapporo (43.5°N, 143.8°E), whose latitude is similar to these observatories. When an air mass factor of 17.5 was used, the two-year Moshiri vertical column values agreed with the Dobson direct sun values to within 15 Dobson Units, or 3 6 % of the column. The difference between the two values was found to be due partly to the change in the air mass factor caused by seasonal and day-to-day changes in the shape of the O3 vertical profiles. These results confirm the reliability of the NO2 and O3 measurements by visible spectrometers at these sites for the Network for the Detection of Stratospheric Change (NDSC).     

扩散法——EA-IRMS测定天然水体铵态氮同位素实验条件研究

稳定氮同位素是研究氮循环和氮污染源示踪的一个有效手段。然而目前国内对水体中铵态氮同位素测定方法研究较少,限制了水体氮循环和污染机理的深入探讨。本文采用改进的扩散法(EA-IRMS)测定水中铵态氮同位素,探讨了样品制备过程中扩散溶液的体积、浓度和扩散时间对回收率及氮同位素测定值的影响。实验得出最佳扩散条件为:1.50 mg/L氯化铵溶液400 mL扩散14天,回收率大于95%,且不会产生氮同位素分馏。本研究为高精度测定天然水体中铵态氮同位素提供了更可靠的实验条件。     

Transformation of ammonium nitrogen and response characteristics of nitrifying functional genes in tannery sludge contaminated soil

High concentrations of ammonium nitrogen released from tannery sludge during storage in open air may cause nitrogen pollution to soil and groundwater. To study the transformation mechanism of NH₄⁺-N by nitrifying functional bacteria in tannery sludge contaminated soils, a series of contaminated soil culture experiments were conducted in this study. The contents of ammonium nitrogen (as NH₄⁺-N), nitrite nitrogen (as NO₂^?-N) and nitrate nitrogen (as NO₃^?-N) were analyzed during the culture period under different conditions of pollution load, soil particle and redox environment. Sigmodial equation was used to interpret the change of NO₃^?-N with time in contaminated soils. The abundance variations of nitrifying functional genes (amoA and nxrA) were also detected using the real-time quantitative fluorescence PCR method. The results show that the nitrification of NH₄⁺-N was aggravated in the contaminated silt soil and fine sand under the condition of lower pollution load, finer particle size and more oxidizing environment. The sigmodial equation well fitted the dynamic accumulation curve of the NO₃^?-N content in the tannery sludge contaminated soils. The Cr(III) content increased with increasing pollution load, which inhibited the reproduction and activity of nitrifying bacteria in the soils, especially in coarse-grained soil. The accumulation of NO₂^?-N contents became more obvious with the increase of pollution load in the fine sand, and only 41.5% of the NH₄⁺-N was transformed to NO₃^?-N. The redox environment was the main factor affecting nitrification process in the soil. Compared to the aerobic soil environment, the transformation of NH₄⁺-N was significantly inhibited under anaerobic incubation condition, and the NO₃^?-N contents decreased by 37.2%, 61.9% and 91.9% under low, medium and high pollution loads, respectively. Nitrification was stronger in the silt soil since its copy number of amoA and nxrA genes was two times larger than that of fine sand. Moreover, the copy numbers of amoA and nxrA genes in the silt soil under the aerobic environment were 2.7 times and 2.2 times larger than those in the anaerobic environment. The abundance changes of the amoA and nxrA functional genes have a positive correlation with the nitrification intensity in the tannery sludge-contaminated soil.     

全球氦气勘探开发进展与利用现状

【研究目的】 由于氦气具有独特的物理特性,在科学研究、医学和高科技行业的用途越来越广泛。寻找更多的氦气资源,满足市场需求,是地质行业的责任。【研究方法】 按照统计分析原则,对全球氦气勘探成果与供需形势进行梳理、总结。【研究结果】 全球氦气资源分布极不均匀,主要氦气供应国为美国、卡塔尔、俄罗斯等。近期,许多公司开始在北美地区、俄罗斯、卡塔尔、坦桑尼亚等地开展氦气的勘探开发,其中北美部分地区的氦气资源位于富含氮气的储层中,具有广阔的开发前景,全球氦气勘探活动掀起新一轮热潮。【结论】 2021年全球氦市场出现供应缺口,当今全球氦气需求的增长开始转向亚洲和中东。建议高度重视氦气不可再生性和不可替代性,开展氦气资源潜力评价工程,勘查国内非烃类氦气矿床前景,加强国际合作,开展国内氦气储备地下空间评价与选址工作,增强中国的氦气储备能力。     

南阳凹陷原油含氮化合物组成及其控制因素

原油的含氮化合物总量及其组成特征不仅受原油运移距离影响,而且还受成油母质类型和成熟度影响.对南阳凹陷27个原油含氮化合物的研究表明,其油气运移指向的规律性不强,原因主要是由于原油运移距离较短,地质色层效应不明显.魏岗南部和北部原油的成熟度差异较大,但含氮化合物组成特征总体上非常相似,表明南阳凹陷原油的含氮化合物总量及其组成主要受控于成油母质类型.     

细菌反硝化法同时分析天然水中硝酸盐氮、氧同位素组成研究

细菌反硝化法是目前同时分析天然水中硝酸盐氮、氧同位素组成的最新方法。该方法包括反硝化菌的选取与培养,利用反硝化菌将硝酸根完全转化成N2O气体以及N2O气体的提取、纯化和同位素测定。该方法采用硝酸盐标准,对测试结果需进行试剂本底、同位素分馏、同位素交换校正。与传统方法相比,细菌反硝化法可同时分析低浓度微量水中硝酸盐的氮、氧同位素组成,且速度更快捷,结果更可靠。     

页岩孔隙度测量实验方法分析与评价

页岩气是目前国内外非常规油气领域研究的热点,有效的页岩孔隙度值是评价页岩储层物性的重要参数。由于页岩本身具有易碎的特点,导致钻取柱体样品难度大,很多学者采用碎样法计算孔隙度,但碎样法与柱体法的差别及测定结果的有效性并未见相关研究成果。本文对相同样品通过三种不同方法:氦气膨胀法测孔隙度(柱体),真、视密度法及低温氮气吸附实验法(样品粉碎至40~60目)分别计算孔隙度。结果发现三种方法测定的三组孔隙度数值不同,每种方法在样品制备上及实验方法的差别是影响实验结果的主要因素,为检验三组孔隙度值的有效性,采用数理统计中的单因素方差分析法进行分析,结果表明页岩柱体与粉碎至40~60目范围内的页岩样品测量的孔隙度值虽有差别,但在有效范围内,具有一致性。但是将页岩粉碎后,页岩中的有效孔隙变化程度较大,故用柱体测定的有效孔隙度法优于其他两种碎样方法。     

Retrieval of stratospheric O3 and NO2 vertical profiles using zenith scattered light observations

Daily zenith scattered light intensity observations were carried out in the morning twilight hours using home-made UV-visible spectrometer over the tropical station Pune (18‡31′, 73‡51′) for the years 2000–2003. These observations are obtained in the spectral range 462–498 nm for the solar zenith angles (SZAs) varying from 87‡ to 91.5‡. An algorithm has been developed to retrieve vertical profiles of ozone (O₃) and nitrogen dioxide (NO₂) from ground-based measurements using the Chahine iteration method. This retrieval method has been checked using measured and recalculated slant column densities (SCDs) and they are found to be well matching. O₃ and NO₂ vertical profiles have been retrieved using a set of their air mass factors (AMFs) and SCDs measured over a range of 87–91.5‡ SZA during the morning. The vertical profiles obtained by this method are compared with Umkehr profiles and ozonesondes and they are found to be in good agreement. The bulk of the column density is found near layer 20–25 km. Daily total column densities (TCDs) of O₃ and NO₂ along with their stratospheric and tropospheric counterparts are derived using their vertical profiles for the period 2000–2003. The total column, stratospheric column and tropospheric column amounts of both trace gases are found to be maximum in summer and minimum in the winter season. Increasing trend is found in column density of NO₂ in stratospheric, tropospheric and surface layers, but no trend is observed in O₃ columns for above layers during the period 2000–2003     

无机盐改性对沸石覆盖技术控制底泥氮磷释放的影响研究

通过试验,考察了无机盐改性对沸石覆盖控制底泥氮磷释放效果的影响,并对沸石覆盖技术控制底泥氮磷释放的机理进行初步探讨,结果表明:①NaCl及CaCl2改性对沸石吸附氨氮的性能影响不大;CaCl2改性可以提高沸石Ca2 的交换量而降低Na 的交换量,NaCl改性则可以明显降低Ca2 的交换量和增加Na 的交换量.②NaCl及CaCl2改性对沸石覆盖技术控制底泥氨氮的释放影响不大,而对控制底泥磷的释放则影响较大,沸石覆盖控制底泥磷释放效率从大到小依次为CaCl2改性沸石＞天然沸石＞NaCl改性沸石.③沸石覆盖技术控制底泥氨氮释放的机理为沸石的物理吸附和阳离子交换作用,控制底泥磷释放的机理包括沸石的机械阻挡作用和沸石与铵所交换出来的Ca2 对磷酸盐的固定作用.