碳纳米管和纳米二氧化钛复合光催化剂处理海洋柴油污染的研究

利用溶胶凝胶法自制了碳纳米管和纳米二氧化钛的复合光催化剂,采用投射电子显微镜和X光衍射仪对粉体的粒径、物象、形貌和热稳定性等进行表征。通过研究光照条件、催化剂的投加量、油的初始浓度、催化剂制备的煅烧条件等因素,考察了自制碳纳米管和纳米二氧化钛的复合催化剂对降解模拟海洋柴油污染的海水去除率的影响。研究发现,在可见光照条件下,400℃煅烧2 h的复合催化剂,投加量为0.4 g/L、柴油的初始浓度为0.6 g/L、反应的光照时间为4 h时效果最好,去除率可达到67.65%。     

Evaluating the economic damage of climate change on global coral reefs

This paper evaluates the global economic damage arising from the effects of climate change and associated carbon dioxide concentrations on the loss of coral reefs. We do this by first estimating the effects of sea surface temperature and carbon dioxide concentrations on coral cover. We develop a statistical relationship between coral coverage and sea surface temperature that indicates that the effects are dependent on the temperature range. For example, we find that increasing sea surface temperature causes coral coverage to decrease when sea surface temperature is higher than 26.85 °C, with the estimated reduction being 2.3% when sea surface temperature increases by 1%. In addition, we find that a 1% carbon dioxide increase induces a 0.6% reduction in global coral coverage. We also estimate the resultant loss in economic value based on a meta-analysis of the recreational and commercial value of reef coverage and a crude proportional approach for other value factors. The meta-analysis shows that the coral reef value decreases by 3.8% when coral cover falls by 1%. By combining these two steps we find that the lost value in terms of the global coral reef value under climate change scenarios ranges from US$3.95 to US$23.78 billion annually.     

Effects of anthropogenic seawater acidification on acid-base balance in the sea urchin Psammechinus miliaris

The purple-tipped sea urchin, Psammechinus miliaris, was exposed to artificially acidified seawater treatments (pH(w) 6.16, 6.63 or 7.44) over a period of 8 days. Urchin mortality of 100% was observed at pH(w) 6.16 after 7 days and coincided with a pronounced hypercapnia in the coelomic fluid producing an irrecoverable acidosis. Coelomic fluid acid-base measures showed that an accumulation of CO(2) and a significant reduction in pH occurred in all treatments compared with controls. Bicarbonate buffering was employed in each case, reducing the resultant acidosis, but compensation was incomplete even under moderate environmental hypercapnia. Significant test dissolution was inferred from observable increases in the Mg(2+) concentration of the coelomic fluid under all pH treatments. We show that a chronic reduction of surface water pH to below 7.5 would be severely detrimental to the acid-base balance of this predominantly intertidal species; despite its ability to tolerate fluctuations in pCO(2) and pH in the rock pool environment. The absence of respiratory pigment (or any substantial protein in the coelomic fluid), a poor capacity for ionic regulation and dependency on a magnesium calcite test, make echinoids particularly vulnerable to anthropogenic acidification. Geological sequestration leaks may result in dramatic localised pH reductions, e.g. pH 5.8. P. miliaris is intolerant of pH 6.16 seawater and significant mortality is seen at pH 6.63.     

南海西部盐水层CO2埋存潜力评估

南海西部东方1-1、崖城13-1和乐东等气田具有CO2含量高的特点,每年从生产出的天然气中分离出大量的CO2。为了减少CO2在大气中的排放,考虑在莺歌海地区选择合适的盐水层埋存体,拟进行CO2地质埋存示范工程。根据CO2在盐水层中的各种埋存机理,并考虑盐水层构造特征对CO2运移分布的影响,提出了一种较为准确的CO2埋存潜力评估方法,并利用此方法对筛选出的5个备选盐水层进行了评估。评估结果表明,各盐水层埋存潜力巨大,都远远大于示范工程期限内预计的CO2埋存总量,并可将这些盐水层作为将来海南省及临近广东省人为CO2的埋存场所。南海西部东方1-1、崖城13-1和乐东等气田具有CO2含量高的特点,每年从生产出的天然气中分离出大量的CO2。为了减少CO2在大气中的排放,考虑在莺歌海地区选择合适的盐水层埋存体,拟进行CO2地质埋存示范工程。根据CO2在盐水层中的各种埋存机理,并考虑盐水层构造特征对CO2运移分布的影响,提出了一种较为准确的CO2埋存潜力评估方法,并利用此方法对筛选出的5个备选盐水层进行了评估。评估结果表明,各盐水层埋存潜力巨大,都远远大于示范工程期限内预计的CO2埋存总量,并可将这些盐水层作为将来海南省及临近广东省人为CO2的埋存场所。     

塔里木盆地寒武系层状硅质岩与硅化岩的元素、δ30Si、δ18O地球化学研究

塔里木盆地寒武系发育层状硅质岩和硅化岩,层状硅质岩主要发育于塔东下寒武统深水沉积相区;硅化岩发育于塔东上寒武统斜坡沉积区与西部台地区寒武系白云岩中。根据显微结构特征,可将硅化岩分为放射状硅化岩与交代残余结构硅化岩两种。分析结果表明,层状硅质岩在Al—Fe-Mn三元图中位于正常海水沉积硅质岩区内,在微量元素平均地壳标准化图解上显示平缓右倾的特征;层状硅质岩Si同位素组成护。δ30Si为0．99‰～1．4‰,O同位素组成δ18O为21．4‰～24．4‰,与沉积型硅质岩相吻合,指示了正常海水沉积成因。硅化岩区别于层状硅质岩的典型特征是具有高U异常的特征;罗西斜坡放射状硅化岩具有较高的微量元素和稀土元素含量（∑REE为18．8～96．9μg／g）与较低的Si、O同位素值（δ18O和δ30Si值分别为15．8‰和1．7‰）;西部台地区交代残余结构硅化岩具有较低微量元素和稀土元素含量（∑REE为0．58～2．61μg／g）与较高的δ30Si（1．0‰～3．8‰）、δ18O（21．6‰～27．0‰）值特征。盆地东西部硅化岩的地球化学差异可能与硅化流体的温度差异有关,罗西斜坡放射状硅化岩硅化温度相对更高;另一方面,硅化过程对h430SiO4选择性较高,因而形成的交代石英具有较高的铲勘值。根据古城4井硅化岩包裹体均一温度与交代石英的O同位素值计算得到交代流体的δ18O值为9．1‰,该值与酸性岩浆水的δ18O值相似,指示了硅化流体可能来自于岩浆或变质水;以δ18O值（9．1‰）作为西部台地区硅化流体的O同位素值,计算得到西部台地区硅化岩硅化流体温度为101．3～158．5℃。根据石英O同位素温度计计算的硅化流体温度呈东高西低的趋势,指示了硅化流体可能来自台地东部。     

The economic impact of extreme sea-level rise: Ice sheet vulnerability and the social cost of carbon dioxide

The possibility of extreme sea-level rise is one of the commonly cited reasons for concern about climate change. Major increases in sea level would likely be driven by the melting or collapse of major ice sheets. This possibility has implications for the social cost of carbon dioxide, which is a key policy value as well as a useful summary measure of damage caused by greenhouse gas emissions.This paper extends earlier work on the importance of low-probability, high-impact events for the social cost of carbon dioxide to incorporate the possibility of extreme sea-level rise.To estimate its impact, an integrated assessment model is used, which allows a probabilistic assessment of climate change damages based on the linkages between the economic and climate systems. In the model, the generic discontinuity damage is replaced with the possibility of large-scale damage from factors that are taken to be correlated with temperature rise and, crucially for this paper, explicit consideration of extreme sea-level rise.Estimates of the amount of increase in the social cost of carbon dioxide that can be expected from incorporating extreme sea-level rise show that the increase is significant, though not especially large in percentage terms.The paper contributes to the literature of how to represent uncertain climate impacts in integrated assessment models and the associated estimation of the social cost of carbon dioxide.     

Inference of surface concentrations of nitrogen dioxide (NO2) in Colombia from tropospheric columns of the ozone measurement instrument (OMI)

For the first time, maps of surface concentration of nitrogen dioxide (NO₂) are presented for the Colombian territory. NO₂ surface concentrations for the year 2007 are inferred based on two sources of tropospheric NO₂ column data: (1) a simulation using a three-dimensional global model (GEOS-Chem) and (2) measurements made by the ozone monitoring instrument (OMI) onboard the NASA Aura satellite. Results show monthly averages between 0.1 and 6 ppbv. We compare these inferred values to corrected ground measurements of NO₂. We find correlation coefficients of up to 0.91 between the inferred data and the corrected observational data. A significant source of NO₂ is biomass burning, which can be diagnosed by data of fire radiative power (FRP) from the Monitoring of Atmospheric Composition and Climate (MACC) reanalysis. We find a close relationship between high values of inferred NO₂ surface concentrations and biomass burning for a large area which encompasses the departments of Caquetá, Meta, Guaviare, Vichada, and Putumayo.     

Compositional zoning of fluid inclusions in the Archaean Junction gold deposit,Western Australia: A process of fluid ‐ wall‐rock interaction?

The Junction gold deposit, in Western Australia, is an orogenic gold deposit hosted by a differentiated, iron‐rich, tholeiitic dolerite sill. Petrographic, microthermometric and laser Raman microprobe analyses of fluid inclusions from the Junction deposit indicate that three different vein systems formed at three distinct periods of geological time, and host four fluid‐inclusion populations with a wide range of compositions in the H₂O–CO₂–CH₄–NaCl ± CaCl₂ system. Pre‐shearing, pre‐gold, molybdenite‐bearing quartz veins host fluid inclusions that are characterised by relatively consistent phase ratios comprising H₂O–CO₂–CH₄ ± halite. Microthermometry suggests that these veins precipitated when a highly saline, >340°C fluid mixed with a less saline ≥150°C fluid. The syn‐gold mineralisation event is hosted within the Junction shear zone and is associated with extensive quartz‐calcite ± albite ± chlorite ± pyrrhotite veining. Fluid‐inclusion analyses indicate that gold deposition occurred during the unmixing of a 400°C, moderately saline, H₂O–CO₂ ± CH₄ fluid at pressures between 70 MPa and 440 MPa. Post‐gold quartz‐calcite‐biotite‐pyrrhotite veins occupy normal fault sets that slightly offset the Junction shear zone. Fluid inclusions in these veins are predominantly vapour rich, with CO₂?CH₄. Homogenisation temperatures indicate that the post‐gold quartz veins precipitated from a 310 ± 30°C fluid. Finally, late secondary fluid inclusions show that a <200°C, highly saline, H₂O–CaCl₂–NaCl–bearing fluid percolated along microfractures late in the deposit's history, but did not form any notable vein type. Raman spectroscopy supports the microthermometric data and reveals that CH₄–bearing fluid inclusions occur in syn‐gold quartz grains found almost exclusively at the vein margin, whereas CO₂–bearing fluid inclusions occur in quartz grains that are found toward the centre of the veins. The zonation of CO₂:CH₄ ratios, with respect to the location of fluid inclusions within the syn‐gold quartz veins, suggest that the CH₄ did not travel as part of the auriferous fluid. Fluid unmixing and post‐entrapment alteration of the syn‐gold fluid inclusions are known to have occurred, but cannot adequately account for the relatively ordered zonation of CO₂:CH₄ ratios. Instead, the late introduction of a CH₄–rich fluid into the Junction shear zone appears more likely. Alternatively, the process of CO₂ reduction to CH₄ is a viable and plausible explanation that fits the available data. The CH₄–bearing fluid inclusions occur almost exclusively at the margin of the syn‐gold quartz veins within the zone of high‐grade gold mineralisation because this is where all the criteria needed to reduce CO₂ to CH₄ were satisfied in the Junction deposit.     

Rhomboidal versus triangular spherical harmonic truncation: Some verification statistics

Abstract

In the construction of global primitive equation models, based on the spherical harmonic method, two forms of truncation are in general use. Theoretical considerations suggest the triangular truncation method is superior, but the easily coded rhomboidal truncation is more commonly used. A verification experiment employing the Canadian Operational Spectral Model has been performed to determine if the theoretical superiority of the triangular truncation can be realized in practice. It was found that at least in the restricted case of extra‐tropical forecasts of less than 48 h, that the two truncation methods produced forecasts of equivalent accuracy.     

融冰期北极楚科奇海陆架中心区硅限制与来源补充

相对氮亏损(N:P约为7,小于16)的太平洋入流水携带的营养盐是支撑北冰洋上层生态系统的重要物质基础。海冰消退,光限制消失,楚科奇海陆架存在强烈的营养盐消耗与利用,广泛认为其表现为氮限制,因此该区域重点关注氮元素循环,对于硅元素的相关研究较少。本文基于2016年中国第七次北极科学考察和中国-俄罗斯首次联合北极科学考察两个同步进行的航次调查结果,全面展示了融冰期整个楚科奇海陆架区的营养盐分布格局。结果显示,硝酸盐和亚硝酸盐表层基本耗尽;硅酸盐表现为中心低,周围高,陆架中心区是强烈的硅限制区域,受到硅和氮的共同限制。沿着太平洋入流方向,S01、R01、LV77-01站位30 m以深硅酸盐浓度高于太平洋入流水端员,说明沉积物孔隙水向底层水释放硅酸盐,因此在浅水陆架区孔隙水可作为上层海洋硅酸盐的潜在来源。本研究结合文献数据计算得到楚科奇海陆架沉积物-水界面硅酸盐年通量为630.78 mmol·m^-2·a^-1,总量为3.75×10¹¹ mol·a^-1,是太平洋入流水所携带硅酸盐年通量的一半(6.59×10¹¹ mol·a^-1),表明沉积物孔隙水也是楚科奇海陆架硅酸盐的重要来源。