Model-Simulated Atmospheric Carbon Dioxide: Comparisons with Satellite Retrievals and Ground-Based Observations

Atmospheric CO2 concentrations from January 2010 to December 2010 were simulated using the GEOS-Chem（Goddard Earth Observing System-Chemistry） model and the results were compared to satellite Gases Observing Satellite（GOSAT） and ground-based the Total Carbon Column Observing Network（TCCON） data. It was found that CO2 concentrations based on GOSAT satellite retrievals were generally higher than those simulated by GEOS-Chem. The differences over the land area in January and April ranged from 1 to 2 ppm, and there were major differences in June and August. At high latitudes in the Northern Hemisphere in June, as well as south of the Sahara, the difference was greater than 5 ppm. In the high latitudes of the Northern Hemisphere the model results were higher than the GOSAT retrievals, while in South America the satellite data were higher. The trend of the difference in the high latitudes of the Northern Hemisphere and the Saharan region in August was opposite to June. Maximum correlation coefficients were found in April, reaching 0.72, but were smaller in June and August. In January, the correlation coefficient was only 0.36. The comparisons between GEOS-Chem data and TCCON observations showed better results than the comparison between GEOS and GOSAT. The correlation coefficients ranged between 0.42（Darwin） and 0.92（Izana）. Analysis of the results indicated that the inconsistency between satellite observations and model simulations depended on inversion errors caused by data inaccuracies of the model simulation＇s inputs, as well as the mismatch of satellite retrieval model input parameters.     

洋底高原：了解地球内部的窗口

洋底高原是洋壳的重要组成部分,它是分布在洋底的一种面积广大、且具有异常洋壳厚度的区域。洋底高原通常规模巨大,绝大多数喷发于大洋环境,岩石组成主要为镁铁质到超镁铁质,岩石类型主要为拉斑玄武岩。大多数洋底高原的岩石组成较为相似,而且均形成于一期或两期时间较短却大规模集中喷发的岩浆活动,目前认为是大规模的热地幔物质从地幔深部上升到岩石圈底部,由于巨大地幔柱头部（地幔羽）引起的熔融作用形成的。正是由于洋底高原与地幔柱之间具有这种十分密切的关系,因此对洋底高原的研究将成为我们了解地球内部的窗口。以ODP对翁通-爪哇和凯尔盖朗（Kerguelen）海台的研究为例,简单介绍了洋底高原的基本特征、地幔柱在其形成过程中的作用以及目前在这一领域还未解决的一些问题。     

Origin of CO2-rich fluid inclusions in leucosomes from the Skagit migmatites, North Cascades, Washington, USA

CO₂–CH₄ fluid inclusions are present in anatectic layer-parallel leucosomes from graphite-bearing metasedimentary rocks in the Skagit migmatite complex, North Cascades, Washington. Petrological evidence and additional fluid inclusion observations indicate, however, that the Skagit Gneiss was infiltrated by a water-rich fluid during high-temperature metamorphism and migmatization. CO₂-rich fluid inclusions have not been observed in Skagit metasedimentary mesosomes or melanosomes, meta-igneous migmatites, or unmigmatized rocks, and are absent from subsolidus leucosomes in metasedimentary migmatites. The observation that CO₂-rich inclusions are present only in leucosomes interpreted to be anatectic based on independent mineralogical and chemical criteria suggests that their formation is related to migmatization by partial melting. Although some post-entrapment modification of fluid inclusion composition may have occurred during decompression and deformation, the generation of the CO₂-rich fluid is attributed to water-saturated partial melting of graphitic metasedimentary rocks by a reaction such as biotite + plagioclase + quartz + graphite ± Al₂SiO₅+ water-rich fluid = garnet + melt + CO₂–CH₄. The presence of CO₂-rich fluid inclusions in leucosomes may therefore be an indication that these leucosomes formed by anatexis. Based on the inferences that (1) an influx of fluid triggered partial melting, and (2) some episodes of fluid inclusion trapping are related to migmatization by anatexis, it is concluded that a free fluid was present at some time during high-temperature metamorphism. The infiltrating fluid was a water-rich fluid that may have been derived from nearby crystallizing plutons. Because partial melting took place at pressures of at least 5 kbar, abundant free fluid may have been present in the crust during orogenesis at depths of at least 15 km.     

Reconstructing long‐term records of dissolved CO2

The dissolved CO₂ concentration of stream waters is an important component of the terrestrial carbon cycle. This study reconstructs long‐term records of dissolved CO₂ concentration for the outlets of two large catchments (818 and 586 km²) in northern England. The study shows that:

• 1. The flux of dissolved CO₂ from the catchments (as carbon per catchment area), when adjusted for that which would be carried by the river water at equilibrium with the atmosphere, is between 0 and 0·39 t km⁻² year⁻¹ for the River Tees and between 0 and 0·65 t km⁻² year⁻¹ for the River Coquet.
• 2. The flux of dissolved CO₂ is closely correlated with dissolved organic carbon (DOC) export and is unrelated to dissolved CO₂ export from the headwaters of the study catchments.
• 3. The evasion rate of CO₂ from the rivers (as carbon per stream area) is between 0·0 and 1·49 kg m⁻² year⁻¹, and calculated in‐stream productions of CO₂ are estimated as between 0·5 and 2·5% of the stream evasion rate.
• 4. By mass balance, it is estimated that 8% of the annual flux of DOC is lost within the streams of the catchment.

The study shows that the loss of CO₂ from the streams of the Tees catchment is between 3·1 and 7·5 kt year⁻¹ (as carbon) for the River Tees, which is the same order as annual CH₄ flux from peats within the catchment and approximately 50% of the net CO₂ exchange to the peats of the catchment. Copyright © 2005 John Wiley & Sons, Ltd.     

CO modelling of CW leo

Preliminary results are presented of fitting the spectral energy distribution and newly obtained¹²CO and¹³CO J =1-0, 2-1 and 3-2 line profiles of CW Leo. This is done with a model which includes a self-consistent calculation of the gas temperature.     

Syndeformational fluid trapping in quartz: determining the pressure-temperature conditions of deformation from fluid inclusions and the formation of pure CO2 fluid inclusions during grain-boundary migration

Abstract Observations and microthermometric data on fluid inclusions from a terrane that underwent deformation following peak metamorphic conditions show that grain-boundary migration recrystallization favours the entrapment of carbonic inclusions whereas microfracturing during brittle deformation favours the infiltration and eventual entrapment of aqueous fluids. Our results imply that pure CO₂ fluid inclusions in metamorphic rocks are likely to be the residue of deformation-recrystallization process rather than representing a primary metamorphic fluid.
Where the temperature of deformation can be deduced by other means, the densities of fluid inclusions trapped during recrystallization, which we call recrystallization-primary fluid inclusions, can be used to constrain the ambient pressure during deformation. Using these constraints, the data imply that the post-metamorphic Hercynian exhumation in Sardinia brought rocks at 300° C to within 3km of the surface. This conclusion is similar to that described for the rapidly uplifted Southern Alps in New Zealand.     

Charnockitic alteration: evidence for CO2 infiltration in granulite facies metamorphism

Charnockitic alteration (arrested orthopyroxene formation in biotite- and amphibole-bearing rocks) occurs in high-grade terranes of all ages. Three criteria are used to show that this alteration was produced in many locations by a migrating fluid phase: (i) diffuseness of the alteration—the alteration zones are often quite unlike discrete migmatitic veins; (ii) relation to deformation—most occurrences show alteration closely associated with warping of foliation or dilation cracks; (iii) open-system alteration—whilst some occurrences represent nearly isochemical alteration, slight changes in bulk composition, often loss of mafic constituents and gain of Na and Si, are evident in detailed mass-balance analysis. Y and sometimes Rb are characteristically depleted. Partial melting sometimes accompanied volatile infiltration, as evidenced by more discrete veins and euhedral orthopyroxene. It is quite unlikely, however, that open-system alteration was produced by escape of viscous quartzo-feldspathic melts. Pervasive migration of low-T lamprophyric (mafic–alkaline, CO₂-charged) interstitial liquids is a possibility by virtue of their extreme fluidity, but CO₂ infiltration was needed to generate these liquids. Vapour-deficient dehydration melting is another feasible mechanism of orthopyroxene formation which may have operated in conjunction with CO₂ infiltration. Characteristic development of charnockitic alteration in some prograde amphibolite to granulite facies transitions, as in the Dharwar Craton of South India, suggests that the alteration is a fundamental feature of the granulite facies metamorphism, implying active and causal participation of migrating fluids. In other high-grade terranes like the Adirondack Mountains of New York, this kind of alteration is rare, and fluid action does not seem to have been important in the metamorphism. A vapour phase participating in charnockitic metamorphism was necessarily one of relatively low H₂O, therefore presumably rich in CO₂. Consideration of possible large CO₂ sources leads to the conclusion that emanations from volatile-rich basalts emplaced in the lower crust are the most probable source of charnockitizing fluids. The ultimate source would therefore be enriched subcontinental lithosphere or asthenosphere. The Rb-depleted pyroxene gneiss (charnockitic) terranes may be characteristic of zones of large-scale transcurrent or oblique-motion faults which tap such great depths.     

Radon-222 in medicinal groundwaters of Szczawno Zdrój (Sudety Mountains, SW Poland)

 Radon is a significant component of the groundwaters that discharge in the springs of Szczawno Zdrój and are recognized as medicinal. However, among the five exploited springs adjoining each other, it is only in Marta Spring that radon occurs in large concentrations (up to 325.6 Bq/dm³). Therefore, the authors have made an attempt to describe and clarify this fact. They found out from their own research and archival data that ²²²Rn dissolves in the waters of Marta Spring after acidulous waters of deep circulation have mixed with poorly mineralized shallow waters in their outflow zone. The genesis of the gas is determined by the content of its parent nuclide, ²²⁶Ra, in the sandstones in the vicinity of the intake. The volume of the rocks providing radon to the waters of this intake has been estimated at several hundred cubic metres. No seasonal fluctuations in radon concentration have been observed and ²²²Rn concentration changes do not seem to be influenced by changes in the concentration of other chemical components of the waters or by the discharge of the intake. The process of dissolving ²²²Rn in the medicinal groundwaters of Marta Spring is the last, the shortest, and the most local of the processes that form the chemical composition and the physical properties of these waters. Received: 7 January 2000 · Accepted: 12 August 2000     

地球圈层相互作用中的深海过程和深海记录（II）：气候变化的热带驱动与碳循环

地球轨道变化驱动冰期旋回的理论是气候演变研究在20世纪的最大突破。然而以65°N太阳辐射量为准的传统轨道理论，忽视了低纬区和碳循环的作用。本项目以“西太平洋暖池”为重点，通过地质资料和气候数值模拟的结合，揭示了“西太平洋暖池”和东亚季风发育的阶段性，发现了暖池海区冰消期表层水升温超前于北半球冰盖的融化。在南沙海区发现了碳同位素有40~50万年长周期，经过全球对比和对意大利上新世地层的实测与分析，证明这是世界大洋碳储库对于地球运行轨道偏心率长周期的响应，并推测是通过浮游植物群改变有机碳在海洋碳沉积中的比例所致。研究表明热带驱动和碳循环在气候演变中重要性，其正确认识是预测气候长期演变趋势的前提。是“深海973”项目总结报道之后的续篇，对上述成果作专题讨论。     

Can biomass burning produce a globally significant carbon-isotope excursion in the sedimentary record?

Negative carbon-isotope excursions have been comprehensively studied in the stratigraphic record but the discussion of causal mechanisms has largely overlooked the potential role of biomass burning. The carbon-isotopic ratios (δ¹³C) of vegetation, soil organic matter and peat are significantly lower than atmospheric carbon dioxide (CO₂), and thereby provide a source of low ¹³C CO₂ when combusted. In this study, the potential role of biomass burning to generate negative carbon isotope excursions associated with greenhouse climates is modeled. Results indicate that major peat combustion sustained for 1000 yr increases atmospheric CO₂ from 2.5× present atmospheric levels (PAL) to 4.6× PAL, and yields a pronounced negative δ¹³C excursion in the atmosphere ( 2.4‰), vegetation ( 2.4‰) and the surface ocean ( 1.2‰), but not for the deep ocean ( 0.9‰). Release of CO₂ initiates a short-term warming of the atmosphere (up to 14.4 °C, with a duration of 1628 yr), which is consistent with the magnitude and length of an observed Toarcian excursion event. These results indicate that peat combustion is a plausible mechanism for driving negative δ¹³C excursions in the rock record, even during times of elevated pCO₂.