A comparison of annual and seasonal carbon dioxide effluxes between sub-Arctic Sweden and High-Arctic Svalbard

Recent climate change predictions suggest altered patterns of winter precipitation across the Arctic. It has been suggested that the presence, timing and quantity of snow all affect microbial activity, thus influencing CO₂ production in soil. In this study annual and seasonal emissions of CO₂ were estimated in High-Arctic Adventdalen, Svalbard, and sub-Arctic Latnjajaure, Sweden, using a new trace gas-based method to track real-time diffusion rates through the snow. Summer measurements from snow-free soils were made using a chamber-based method. Measurements were obtained from different snow regimes in order to evaluate the effect of snow depth on winter CO₂ effluxes. Total annual emissions of CO₂ from the sub-Arctic site (0.662–1.487 kg CO₂ m^–2 yr^–1) were found to be more than double the emissions from the High-Arctic site (0.369–0.591 kg CO₂ m^–2 yr^–1). There were no significant differences in winter effluxes between snow regimes or vegetation types, indicating that spatial variability in winter soil CO₂ effluxes are not directly linked to snow cover thickness or soil temperatures. Total winter emissions (0.004–0.248 kg CO₂ m^–2) were found to be in the lower range of those previously described in the literature. Winter emissions varied in their contribution to total annual production between 1 and 18%. Artificial snow drifts shortened the snow-free period by 2 weeks and decreased the annual CO₂ emission by up to 20%. This study suggests that future shifts in vegetation zones may increase soil respiration from Arctic tundra regions.     

流体水化学观测方法在断层土壤气观测中的应用

利用现有水化学观测仪器设备对某些灵敏气体进行观测,比如使用水氡、水质、气体观测仪器设备进行断层土壤气氡、二氧化碳、气体观测的实验研究,并且给出了集气、采气装置的构成方式.氡气和气体观测采用真空负压采样法,使用水氡观测仪器和气相色谱仪.而土壤二氧化碳观测方法可采用碱溶液吸收法,采样时采用真空负压采样法或常压自然吸收法两种方式,还提出了氡气观测中设计采样装置时应注意的事项.     

On the scavenging of SO2 by cloud and raindrops: II. An experimental study of SO2 absorption and desorption for water drops in air

For the purpose of testing our previously described theory of SO₂ scavenging a laboratory investigation was carried out in the UCLA 33 m long rainshaft. Drops with radii between 250 and 2500 m were allowed to come to terminal velocity, after which they passed through a chamber of variable length filled with various SO₂ concentrations in air. After falling through a gas separating chamber consisting of a fluorocarbon gas the drops were collected and analyzed for their total S content in order to determine the rate of SO ₂ absorption.The SO₂ concentration in air studied ranged between 1 and 60% (v). Such relatively large concentrations were necessary due to the short times the drops were exposed to SO₂ in the present setup. The present experimental results were therefore not used to simulate atmospheric conditions but rather to test our previously derived theory which is applicable to any laboratory or atmospheric condition. Comparison of our studies with the results from our theory applied to our laboratory conditions led to predicted values for the S concentration in the drops which agreed well with those observed if the drops had radii smaller than 500 m. In order to obtain agreement between predicted and observed S concentrations in larger drops, an empirically derived eddy diffusivity for SO₂ in water had to be included in the theory to take into account the effect of turbulent mixing inside such large drops.In a subsequent set of experiments, drops initially saturated with S (IV) were allowed to fall through S-free air to determine the rate of SO ₂ desorption. The results of these studies also agreed well with the results of our theoretical model, thus justifying the reversibility assumption made in our theoretical models.In a final set of experiments, the effects of oxidation on SO₂ absorption was studied by means of drops containing various amounts of H₂O₂. For comparable exposure times to SO₂, the S concentration in drops with H₂O₂ was found to be up to 10 times higher than the concentration in drops in which no oxidation occurred.     

Seeking a handle on climate change: Examining the comparative effectiveness of energy efficiency improvement and renewable energy production in the United States

This study examines the comparative effectiveness of two important proposed solutions to climate change—energy efficiency improvement and the development and use of renewable energy sources. We focus specifically on their impacts on carbon dioxide emissions by conducting fixed effects regression analysis of panel data pertaining to U.S. states. The analysis reveals a negative relationship between both remedies and carbon dioxide emissions. Although the effects of these potential solutions are statistically equivalent, renewable energy production has a slight edge. Reflecting upon these findings and the larger environmental problem, we caution against exclusive reliance on efficiency improvement and renewable energy to the neglect of other important actions, such as lifestyle modifications. A broad range of social changes, which incorporate the remedies investigated in this paper, are needed to limit long-term global temperature increases to the desired level.     

Negative-emissions technology portfolios to meet the 1.5 °C target

Our carbon-intensive economy has led to an average temperature rise of 1 °C since pre-industrial times. As a consequence, the world has seen increasing droughts, significant shrinking of the polar ice caps, and steady sea-level rise. To stall these issues’ worsening further, we must limit global warming to 1.5 °C. In addition to the economy’s decarbonization, this endeavour requires the use of negative-emissions technologies (NETs) that remove the main greenhouse gas, carbon dioxide, from the atmosphere. While techno-economic feasibility alone has driven the definition of negative-emissions solutions, NETs’ diverse, far-reaching implications demand a more holistic assessment. Here, we present a comprehensive framework, integrating NETs’ critical performance aspects of feasibility, effectiveness, and side impacts, to define the optimal technology mix within realistic outlooks. The resulting technology portfolios provide a useful new benchmark to compare carbon avoidance and removal measures and deliberately choose the best path to solve the climate emergency.     

国外CO2地质储存现状与展望

温室气体CO2的大量排放给全球气候和环境带来的巨大影响,受到了世界各国的关注。实现CO2的深度减排是人类可持续发展的必由之路。CO2地质储存是缓解碳排放行之有效的方法之一。本文通过以下几方面论述了国外CO2地质储存的现状以及对未来的展望：1）CO2捕集机理,2）CO2地质储存,3）CO2地质储存项目现状与未来预测,4）CO2地质储存场地储量评估,5）CO2地质储存监测技术,6）CO2地质储存模拟工具,7）CO2地质存储经费等。     

国外 CO2地质储存现状与展望

温室气体CO2的大量排放给全球气候和环境带来的巨大影响,受到了世界各国的关注.实现CO2的深度减排是人类可持续发展的必由之路.CO2地质储存是缓解碳排放行之有效的方法之一.本文通过以下几方面论述了国外CO2地质储存的现状以及对未来的展望:1)CO2捕集机理,2)CO2地质储存,3)CO2地质储存项目现状与未来预测,4) CO2地质储存场地储量评估,5)CO2地质储存监测技术,6)CO2地质储存模拟工具,7)CO2地质存储经费等.     

Solar Photocatalytic Decolorization and Detoxification of Industrial Batik Dye Wastewater Using P(3HB)‐TiO2 Nanocomposite Films

Solar photocatalytic decolorization and detoxification of batik dye wastewater using titanium dioxide (TiO₂) immobilized on poly‐3‐hydroxybutyrate (P(3HB)) film was studied. The effects of initial dye concentration, catalyst concentration, P(3HB) film thickness, and fabrication methods of the nanocomposite films were evaluated against methylene blue, a standard organic dye. It was observed that 0.4 g of P(3HB)‐40 wt% TiO₂ removed 96% of the color under solar irradiation. P(3HB) and TiO₂, mixed concurrently in chloroform followed by stirring for 24 h showed a more even distribution of the photocatalyst on the polymer surface and yielded almost 100% color removal. The photocatalytic films were able to completely decolorize real industrial batik dye wastewater in 3 h and induced a chemical oxygen demand (COD) reduction of 80%. Reusability of the 0.4 g P(3HB)‐40 wt% TiO₂ film in decolorizing the batik dye wastewater was also possible as it gave a high consistent value of decolorization percentage (>80%) even after the sixth repeated usage. Recovery step of the photocatalysts was also not required in this simple treatment system. The decolorized batik dye wastewater had less/no toxic effects on mosquito larvae, Aedes aegypti, and microalgae, Scenedesmus quadricauda indicating simultaneous detoxification process along with the decolorization process.