Pricing carbon consumption: synthesizing an emerging trend     

Clayton Munnings  William Acworth  Oliver Sartor  Yong-Gun Kim  Karsten Neuhoff 《Climate Policy》2019,19(1):92-107

Nearly every carbon price regulates the production of carbon emissions, typically at midstream points of compliance such as power plants, consistent with typical advice from the literature. Since the early 2010s however, policymakers in Australia, California, China, Japan and Korea have implemented carbon prices that regulate the consumption of carbon emissions, where points of compliance are further downstream, such as distributors or final consumers. This article identifies the pivot towards placing the point of compliance for carbon prices further downstream as an emerging international trend, describes the designs of different prices on carbon consumption around the world, and explains the various motivations of the policymakers implementing them. Findings reveal that policymakers tend to layer prices on carbon consumption on top of prices on carbon production in an effort to improve economic outcomes by addressing incomplete pass-through of the carbon price from producer to consumer, thereby facilitating more cost-effective abatement. Policymakers also use prices on carbon consumption to reduce emissions leakage or because large producers of carbon are not within their jurisdiction. The prevalence of prices on carbon consumption will likely increase as evidenced by proposals in China and Europe.

Key policy insights

• The recent surge in the number of jurisdictions implementing prices on carbon consumption represents an emerging international trend.

• Policymakers use prices on carbon consumption in an effort to improve economic outcomes and capture environmental benefits.

• While this article offers insights that detail initial challenges and successes, whether these prices on carbon consumption actually achieve their intended goals is an academically rich topic that requires further research on individual policies.

  相似文献   

Modeling locally varying anisotropy of CO2 emissions in the United States     

Jeff B. Boisvert  Clayton V. Deutsch 《Stochastic Environmental Research and Risk Assessment (SERRA)》2011,25(8):1077-1084

In a spatial property modeling context, the variables of interest to be modeled often display complex nonlinear features. Techniques to incorporate these nonlinear features, such as multiple point statistics or cummulants, are often complex with input parameters that are difficult to infer. The methodology proposed in this paper uses a classical vector-based definition of locally varying anisotropy to characterize nonlinear features and incorporate locally varying anisotropy into numerical property models. The required input is an exhaustive field of anisotropy orientation and magnitude. The methodology consists of (1) using the shortest path distance between locations to define the covariance between points in space (2) multidimensional scaling of the domain to ensure positive definite kriging equations and (3) estimation or simulation with kriging or sequential Gaussian simulation. The only additional parameter required when kriging or simulating with locally varying anisotropy is the number of dimensions to retain in multidimensional scaling. The methodology is demonstrated on a CO₂ emissions data set for the United States in 2002 and shows an improvement in cross validation results as well as a visual reproduction of nonlinear features.  相似文献   

Erratum to: Segregating gas from melt: an experimental study of the Ostwald ripening of vapor bubbles in magmas     

Nicole C. Lautze  Thomas W. Sisson  Margaret T. Mangan  Timothy L. Grove 《Contributions to Mineralogy and Petrology》2011,161(2):349

  相似文献   

Origin of ~2.5 Ga potassic granite from the Nellore Schist Belt,SE India: textural,cathodoluminescence, and SHRIMP U–Pb data     

K. Vijaya Kumar  W. G. Ernst  C. Leelanandam  J. L. Wooden  M. J. Grove 《Contributions to Mineralogy and Petrology》2011,162(4):867-888

In a geochemical and geochronological investigation of Archean and Proterozoic magmatism in the Nellore Schist Belt, we conducted SHRIMP U–Pb analyses of zircons from two cospatial granitic bodies at Guramkonda and Vendodu. The former is a Ba- and Sr-rich hornblende-bearing tonalite, whereas the latter is a Rb-, Zr-, Pb-, Th-, U-, and REE-rich biotite-bearing leucogranite. The Guramkonda tonalite displays a restitic texture with remnants of trapped granitic melt, whereas the Vendodu leucogranite contains residual/partially melted plagioclase grains. Both rock types contain two generations of zircon: tonalite contains a group of euhedral zoned zircons enclosed within plagioclase and a group of subhedral patchy zircons associated with trapped melt (quartz + feldspar matrix), and leucogranite also contains a group of doubly terminated euhedral zircons included within orthoclase as well as a group of zircons with visible cores mantled by later rim growth. Cathodoluminescence images also clearly document two distinctly textured varieties of zircon: the tonalite contains a population characterized by narrowly spaced uninterrupted oscillatory zoning and a second population lacking zoning but exhibiting a random distribution of dark (U-rich) and light (U-poor) regions; the leucogranite contains U-rich zoned zircons and U-poor zircon cores mantled by U-rich rims. The REE chemistry of zircon cores from the Vendodu leucogranite is very similar to the REE of zoned zircons from the Guramkonda tonalite. Zircon ages from both plutons exhibit bimodal distributions in U–Pb concordia diagrams. The tonalite defines an age of 2,521 Ma ± 5 Ma for zoned magmatic zircons and 2,485 Ma ± 5 Ma for unzoned newly precipitated zircons, whereas the leucogranite has an age of 2,518 Ma ± 5 Ma for U-poor zircon cores (relics of the tonalite pluton) and 2,483 Ma ± 3 Ma for U-rich zoned magmatic zircons. The trace element geochemistry of the ~2,520 Ma zircons is distinctly different from the ~2,485 Ma zircons, irrespective of the host rock. Our textural, CL image, and SHRIMP U–Pb analyses document the origin of the leucogranite by partial melting of the tonalite. High alkalis (Na₂O + K₂O), Rb, Nb, HREE, FeO^t/MgO and low Ca, Al, Ba, Sr, and large negative Eu anomalies characterize the leucogranite as a thermal minimum melt, whereas the very low K and Rb of the tonalite attests to its residual nature. We suggest that the leucogranite formed by high-T (900–950°C), moderate-pressure (<10 kbar) dehydration partial melting of the tonalite under reducing conditions. The calculated source compositions of the leucogranite melt and the tonalite residue show strong similarities to melts that are considered to have been produced in a subduction-zone environment. The leucogranite probably formed in a post-collisional realm immediately after accretion of the tonalitic crust.  相似文献   

The structure of methane gas hydrate bearing sediments from the Krishna-Godavari Basin as seen from Micro-CT scanning     

Emily V.L. Rees  Jeffery A. Priest Chris R.I. Clayton 《Marine and Petroleum Geology》2011,28(7):1283-1293

The Indian National Gas Hydrate Program (NGHP) Expedition 1, of 2006, cored through several methane gas hydrate deposits on the continental shelf around the coast of India. The pressure coring techniques utilized during the expedition (HYACINTH and PCS) enabled recovery of gas hydrate bearing, fine-grained, sediment cores to the surface. After initial characterization core sections were rapidly depressurized and submerged in liquid nitrogen, preserving the structure and form of the hydrate within the host sediment. Once on shore, high resolution X-ray CT scanning was employed to obtain detailed three-dimensional images of the internal structure of the gas hydrate. Using a resolution of 80 μm the detailed structure of the hydrate veins present in each core could be observed, and allowed for an in depth analysis of orientation, width and persistence of each vein. Hydrate saturation estimates could also be made and saturations of 20-30% were found to be the average across the core section with some portions showing highs of almost 60% saturation. The majority of hydrate veins in each core section were found to be orientated between 50 and 80° to the horizontal. Analysis of the strikes of the veins suggested a slight preferential orientation in individual sample sections, although correlation between individual sections was not possible due to the initial orientation of the sections being lost during the sampling stage. The preferred vein orientation within sample sections coupled with several geometric features identified in individual veins, suggest that hydraulic fracturing by upward advecting pore fluids is the main formation mechanism for the veined hydrate deposits in the K-G Basin.  相似文献   

Evidence for Late Riphean granite formation in the Polar Urals     

A. A. Soboleva  A. F. Karchevskii  L. I. Efanova  N. B. Kuznetsov  M. Grove  I. D. Sobolev  M. V. Maurin 《Doklady Earth Sciences》2012,442(2):181-187

  相似文献   

Experiments on liquid immiscibility along tholeiitic liquid lines of descent   总被引：4，自引：2，他引：2  

Bernard Charlier  Timothy L. Grove 《Contributions to Mineralogy and Petrology》2012,164(1):27-44

Crystallization experiments have been conducted on compositions along tholeiitic liquid lines of descent to define the compositional space for the development of silicate liquid immiscibility. Starting materials have 46–56 wt% SiO₂, 11.7–17.7 wt% FeO_tot, and Mg-number between 0.29 and 0.36. These melts fall on the basaltic trends relevant for Mull, Iceland, Snake River Plain lavas and for the Sept Iles layered intrusion, where large-scale liquid immiscibility has been recognized. At one atmosphere under anhydrous conditions, immiscibility develops below 1,000–1,020°C in all of these compositionally diverse lavas. Extreme iron enrichment is not necessary; immiscibility also develops during iron depletion and silica enrichment. Variations in melt composition control the development of silicate liquid immiscibility along the tholeiitic trend. Elevation of Na₂O + K₂O + P₂O₅ + TiO₂ promotes the development of two immiscible liquids. Increasing melt CaO and Al₂O₃ stabilizes a single-liquid field. New data and published phase equilibria show that anhydrous, low-pressure fractional crystallization is the most favorable condition for unmixing during differentiation. Pressure inhibits immiscibility because it expands the stability field of high-Ca clinopyroxene, which reduces the proportion of plagioclase in the crystallizing assemblage, thus enhancing early iron depletion. Magma mixing between primitive basalt and Fe–Ti–P-rich ferrobasalts can serve to elevate phosphorous and alkali contents and thereby promote unmixing. Water might decrease the temperature and size of the two-liquid field, potentially shifting the binodal (solvus) below the liquidus, leading the system to evolve as a single-melt phase.  相似文献   

Amphibole stability in primitive arc magmas: effects of temperature,H<Subscript>2</Subscript>O content,and oxygen fugacity     

Michael J. Krawczynski  Timothy L. Grove  Harald Behrens 《Contributions to Mineralogy and Petrology》2012,164(2):317-339

  相似文献   

Early petrologic processes on the ureilite parent body     

S. J. Singletary  T. L. Grove 《Meteoritics & planetary science》2003,38(1):95-108

Abstract— We present a petrographic and petrologic analysis of 21 olivine‐pigeonite ureilites, along with new experimental results on melt compositions predicted to be in equilibrium with ureilite compositions. We conclude that these ureilites are the residues of a partial melting/smelting event. Textural evidence preserved in olivine and pigeonite record the extent of primary smelting. In pigeonite cores, we observe fine trains of iron metal inclusions that formed by the reduction of olivine to pigeonite and metal during primary smelting. Olivine cores lack metal inclusions but the outer grain boundaries are variably reduced by a late‐stage reduction event. The modal proportion of pigeonite and percentage of olivine affected by late stage reduction are inversely related and provide an estimation of the degree of primary smelting during ureilite petrogenesis. In our sample suite, this correlation holds for 16 of the 21 samples examined. Olivine‐pigeonite‐liquid phase equilibrium constraints are used to obtain temperature estimates for the ureilite samples examined. Inferred smelting temperatures range from ～1150°C to just over 1300°C and span the range of estimates published for ureilites containing two or more pyroxenes. Temperature is also positively correlated with modal percent pigeonite. Smelting temperature is inversely correlated with smelting depth—the hottest olivine‐pigeonite ureilites coming from the shallowest depth in the ureilite parent body. The highest temperature samples also have oxygen isotopic signatures that fall toward the refractory inclusion‐rich end of the carbonaceous chondrite‐anhydrous mineral (CCAM) slope 1 mixing line. These temperature‐depth variations in the ureilite parent body could have been created by a heterogeneous distribution of heat producing elements, which would indicate that isotopic heterogeneities existed in the material from which the ureilite parent body was assembled.  相似文献   

Effect of iron and carbonation on the diffusion of iodine and rhenium in waste encasement concrete and soil fill material under hydraulically unsaturated conditions     

Dawn M. Wellman  Kent E. Parker  Laura Powers  Greg A. Whyatt  Libby N. Clayton  Shas V. Mattigod  Marcus I. Wood 《Applied Geochemistry》2008,23(8):2256-2271

Assessing long-term performance of Category 3 cement wasteforms and accurate prediction for radionuclide encasement requires knowledge of the radionuclide–cement interactions and mechanisms of retention (i.e. sorption or precipitation). A set of sediment-concrete half-cell diffusion experiments was conducted under unsaturated conditions (4% and 7% by weight moisture content) using carbonated and non-carbonated concrete–soil half cells. Results indicate the behavior of Re and I release was comparable within a given half-cell test. Diffusivity in soil is a function of moisture content; a 3% increase in moisture content affords a one to two order of magnitude increase in diffusivity. Release of I and Re was 1–3 orders of magnitude less from non-carbonated, relative to carbonated, concrete monoliths. Inclusion of Fe in non-carbonate monoliths resulted in the lowest concrete diffusivity values for both I and Re. This suggests that in the presence of Fe, I and Re are converted to reduced species, which are less soluble and better retained within the concrete monolith. The release of I and Re was greatest from Fe-bearing, carbonated concrete monoliths, suggesting carbonation negates the effect of Fe on the retention of I and Re within concrete monoliths. This is likely due to enhanced formation of microcracks in the presence of Fe, which provide preferential paths for contaminant migration. Although the release of I and Re were greatest from carbonated concrete monoliths containing Fe, the migration of I and Re within a given half cell is dependent on the moisture content, soil diffusivity, and diffusing species.  相似文献