Tilt corrections over complex terrain and their implication for CO<Subscript>2</Subscript> transport

Observational data from sonic anemometers are commonly rotated from sonic to streamline coordinates, a procedure that is called tilt correction. Tilt corrections are often used to post-process air velocity data collected from sonic anemometers to allow objective interpretation of air flow data relative to the Earth. Since streamline coordinates depend on dynamical characteristics of the flow, the tilt correction depends not only on temporal and spatial variations of the flow, but also on local circulations. We found that ensemble- averaged slope flows are approximately parallel to the terrain slope close to the ground within the canopy layer, but not above, due to the influence of the diurnal variation of local vertical circulations. As a result, the diurnal variation of the observed vertical velocity in streamline coordinates at 21.5 m above the ground over 11-m tall forest canopies can be opposite to that calculated from the continuity equation. To estimate CO₂ transport over sloping terrain, a workable reference coordinate system is needed such that multiple sonic anemometers have a common reference relative to the Earth. Streamline coordinate systems can be the choice of the common reference coordinate system only if flow, at least ensemble-averaged flow, is parallel to terrain slopes. The choice of the reference coordinate system and its implication in investigation of CO₂ transport are discussed. The National Center for Atmospheric Research is sponsored by the National Science Foundation.     

The Atmospheric Oxidation of the HS Radical: Reaction with NO2

The atmospheric reaction between HS and NO₂ was theoretically investigated at 298 K and 1 atm of pressure. Our results show that the first reaction step will lead to the formation of HSNO₂ or HSONO, spontaneously and exothermically. HSONO easily decomposes into HSO + NO. On the other hand, HSNO₂ can hardly dissociate in the reactants, and its isomerization to other adducts is much hindered. Production of HNO + SO and SNO + OH was found to be unfavorable. Thus, the main products would be HSO + NO and HSNO₂, and new investigations focusing on the atmospheric fate of HSNO₂ are suggested. A general discussion of the fate of HS under atmospheric conditions is presented. Recent investigations indicate that NO₂, O₂ and N₂O should be the most important oxidants of HS, while the O₃ influence will not be significant.     

岩溶发育对温室气体CO2的调节能力研究

温室效应是当今世界上许多国家及其政府关注的重要问题之一。从地质角度研究全球最大碳库－－碳酸盐岩在其岩溶发育过程中对温室气体ＣＯ２的调节能力,从而为更全面,定量地考察温室气体ＣＯ２循环提供新思路及依据。     

Measurements of Reaction Coefficients of NO2 and HONO on Aerosol Particles

The reaction coefficients of nitrogen dioxide and nitrous acid with monodisperse sodium chloride and ammonium sulphate aerosols have been measured in a flow reactor at atmospheric pressure. These experiments were performed at relative humidities above and below the deliquescence points of both aerosols (r.h. 50 and 85%) at 279 K. The results for NO₂ afford a reaction coefficient in the range (2.8–10) × 10^-4 and for HONO, (2.8–4.6) × 10^-3. For both species, there appears to be an enhancement of the reaction coefficient on sodium chloride aerosol at 50% r.h. The results are compared with reaction coefficients determined by other experimental methods. A good agreement is found for both gases between this method and the coated denuder method previously developed in our research laboratories (Msibi et al., 1993) and with the majority of other published data for NO₂. In the case of HONO, our estimate of reaction coefficient is smaller than, or at the lower limits of the ranges reported by other published studies.     

The ocean as source or sink of reactive trace-gases

Summary After a brief review on recent experimental work on the uptake resp release of SO₂ and NH₃ by the ocean, new results on the distribution of these reactive trace-gases in the marine atmosphere are presented. In the case of SO₂ there is no doubt that the ocean acts as a sink. In the case of NH₃ new observations and calculations show that under certain conditions the ocean may be a NH₃ source.     

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。     

Neoproterozoic chemostratigraphy

Chemostratigraphy has diverse applications to investigating the rock record, such as reconstructing paleoenvironments, determining the tectonic setting of sedimentary basins, indirect dating, and establishing regional or global correlations. Chemostratigraphy is thus an integral component of many investigations of the ancient sedimentary record. In this contribution, we review the principle inorganic geochemical methods that have been applied to the Neoproterozoic sedimentary record. Analysis of the traditional stable and radiogenic isotope systems, such as δ¹³C, δ¹⁸O, δ³⁴S, and ⁸⁷Sr/⁸⁶Sr, is routine, particularly in successions rich in carbonate. These mainstay applications have yielded invaluable data and information bearing on the chronology and evolution of this eventful era in Earth history. Alongside the growing database of traditional data, a series of novel geochemical techniques have given rise to important new models and constraints on Neoproterozoic biogeochemical change. In particular, a range of proxies for water column redox, mainly obtained from black shales, have shed light on the pace and tempo of Neoproterozoic oxygenation and its link to the appearance of early animal evolution. Increased integration of diverse geochemical, sedimentological, and paleontological datasets, and the gradual radiometric calibration of the stratigraphic record promise to bring the details of the evolution of the Neoproterozoic Earth system into ever greater focus.