Atmospheric CO2 concentrations over the last glacial termination

A record of atmospheric carbon dioxide (CO2) concentration during the transition from the Last Glacial Maximum to the Holocene, obtained from the Dome Concordia, Antarctica, ice core, reveals that an increase of 76 parts per million by volume occurred over a period of 6000 years in four clearly distinguishable intervals. The close correlation between CO2 concentration and Antarctic temperature indicates that the Southern Ocean played an important role in causing the CO2 increase. However, the similarity of changes in CO2 concentration and variations of atmospheric methane concentration suggests that processes in the tropics and in the Northern Hemisphere, where the main sources for methane are located, also had substantial effects on atmospheric CO2 concentrations.     

Atmospheric CO2 and climate on millennial time scales during the last glacial period

Reconstructions of ancient atmospheric carbon dioxide (CO2) variations help us better understand how the global carbon cycle and climate are linked. We compared CO2 variations on millennial time scales between 20,000 and 90,000 years ago with an Antarctic temperature proxy and records of abrupt climate change in the Northern Hemisphere. CO2 concentration and Antarctic temperature were positively correlated over millennial-scale climate cycles, implying a strong connection to Southern Ocean processes. Evidence from marine sediment proxies indicates that CO2 concentration rose most rapidly when North Atlantic Deep Water shoaled and stratification in the Southern Ocean was reduced. These increases in CO2 concentration occurred during stadial (cold) periods in the Northern Hemisphere, several thousand years before abrupt warming events in Greenland.     

Saturation of the southern ocean CO2 sink due to recent climate change

Based on observed atmospheric carbon dioxide (CO2) concentration and an inverse method, we estimate that the Southern Ocean sink of CO2 has weakened between 1981 and 2004 by 0.08 petagrams of carbon per year per decade relative to the trend expected from the large increase in atmospheric CO2. We attribute this weakening to the observed increase in Southern Ocean winds resulting from human activities, which is projected to continue in the future. Consequences include a reduction of the efficiency of the Southern Ocean sink of CO2 in the short term (about 25 years) and possibly a higher level of stabilization of atmospheric CO2 on a multicentury time scale.     

Atmospheric CO2: principal control knob governing Earth's temperature

Ample physical evidence shows that carbon dioxide (CO(2)) is the single most important climate-relevant greenhouse gas in Earth's atmosphere. This is because CO(2), like ozone, N(2)O, CH(4), and chlorofluorocarbons, does not condense and precipitate from the atmosphere at current climate temperatures, whereas water vapor can and does. Noncondensing greenhouse gases, which account for 25% of the total terrestrial greenhouse effect, thus serve to provide the stable temperature structure that sustains the current levels of atmospheric water vapor and clouds via feedback processes that account for the remaining 75% of the greenhouse effect. Without the radiative forcing supplied by CO(2) and the other noncondensing greenhouse gases, the terrestrial greenhouse would collapse, plunging the global climate into an icebound Earth state.     

The impact of agricultural soil erosion on the global carbon cycle

Agricultural soil erosion is thought to perturb the global carbon cycle, but estimates of its effect range from a source of 1 petagram per year(-1) to a sink of the same magnitude. By using caesium-137 and carbon inventory measurements from a large-scale survey, we found consistent evidence for an erosion-induced sink of atmospheric carbon equivalent to approximately 26% of the carbon transported by erosion. Based on this relationship, we estimated a global carbon sink of 0.12 (range 0.06 to 0.27) petagrams of carbon per year(-1) resulting from erosion in the world's agricultural landscapes. Our analysis directly challenges the view that agricultural erosion represents an important source or sink for atmospheric CO2.     

Forests and climate change: forcings, feedbacks, and the climate benefits of forests

The world's forests influence climate through physical, chemical, and biological processes that affect planetary energetics, the hydrologic cycle, and atmospheric composition. These complex and nonlinear forest-atmosphere interactions can dampen or amplify anthropogenic climate change. Tropical, temperate, and boreal reforestation and afforestation attenuate global warming through carbon sequestration. Biogeophysical feedbacks can enhance or diminish this negative climate forcing. Tropical forests mitigate warming through evaporative cooling, but the low albedo of boreal forests is a positive climate forcing. The evaporative effect of temperate forests is unclear. The net climate forcing from these and other processes is not known. Forests are under tremendous pressure from global change. Interdisciplinary science that integrates knowledge of the many interacting climate services of forests with the impacts of global change is necessary to identify and understand as yet unexplored feedbacks in the Earth system and the potential of forests to mitigate climate change.     

Global iron connections between desert dust, ocean biogeochemistry, and climate

The environmental conditions of Earth, including the climate, are determined by physical, chemical, biological, and human interactions that transform and transport materials and energy. This is the "Earth system": a highly complex entity characterized by multiple nonlinear responses and thresholds, with linkages between disparate components. One important part of this system is the iron cycle, in which iron-containing soil dust is transported from land through the atmosphere to the oceans, affecting ocean biogeochemistry and hence having feedback effects on climate and dust production. Here we review the key components of this cycle, identifying critical uncertainties and priorities for future research.     

土壤呼吸强度的影响因素及其研究进展

探讨了土壤呼吸的研究情况和各因素对土壤呼吸的影响,提出了土壤呼吸研究尚需解决的问题和研究方向,并进行了展望.     

CO_2体积分数升高对土壤-植物系统碳过程的影响

从土壤和植物2个方面,综述了大气二氧化碳体积分数升高对生态系统碳过程的影响。大气CO2体积分数升高,提高了植物的光合速率,促进了生物量的累积,改变了植物的碳结构。高CO2体积分数导致植物基质（C／N）的变化将直接影响枯落物的分解速率。大气CO2体积分数升高通过影响植物生长而间接地对土壤生态过程产生影响。由于高CO2体积分数下碳输入和输出的关系还存在很多不确定性,因此还不能推断高CO2体积分数下土壤碳库是增加还是减少。不同的生态系统类型,对高CO2体积分数的响应状况也不一致。今后应定量研究CO2体积分数升高条件下生态系统各分室碳库的动态,明确土壤、植物和大气碳库储量变化及其之间的碳通量,以便定量化生态系统碳收支对高CO2体积分数升高的响应。另外,还应加强CO2体积分数升高与其他全球变化因子的耦合作用研究,探讨其相互作用的机制,将有助于全面了解全球变化条件下生态系统的碳循环过程。     

Trends in Stomatal Density and 13C/12C Ratios of Pinus flexilis Needles During Last Glacial-Interglacial Cycle

Measurements of stomatal density and delta(13)C of limber pine (Pinus flexilis) needles (leaves) preserved in pack rat middens from the Great Basin reveal shifts in plant physiology and leaf morphology during the last 30,000 years. Sites were selected so as to offset glacial to Holocene climatic differences and thus to isolate the effects of changing atmospheric CO(2) levels. Stomatal density decreased approximately 17 percent and delta(13)C decreased approximately 1.5 per mil during deglaciation from 15,000 to 12,000 years ago, concomitant with a 30 percent increase in atmospheric CO(2). Water-use efficiency increased approximately 15 percent during deglaciation, if temperature and humidity were held constant and the proxy values for CO(2) and delta(13)C of past atmospheres are accurate. The delta(13)C variations may help constrain hypotheses about the redistribution of carbon between the atmosphere and biosphere during the last glacial-interglacial cycle.     

The sensitivity of polar ozone depletion to proposed geoengineering schemes

The large burden of sulfate aerosols injected into the stratosphere by the eruption of Mount Pinatubo in 1991 cooled Earth and enhanced the destruction of polar ozone in the subsequent few years. The continuous injection of sulfur into the stratosphere has been suggested as a "geoengineering" scheme to counteract global warming. We use an empirical relationship between ozone depletion and chlorine activation to estimate how this approach might influence polar ozone. An injection of sulfur large enough to compensate for surface warming caused by the doubling of atmospheric CO2 would strongly increase the extent of Arctic ozone depletion during the present century for cold winters and would cause a considerable delay, between 30 and 70 years, in the expected recovery of the Antarctic ozone hole.     

城市系统碳循环:特征、机理与理论框架

城市是地表受人类活动影响最深刻的区域,城市系统碳循环在全球和区域碳过程中具有重要的地位和作用.提出了城市“自然-社会”二元碳循环的概念,探讨了城市系统碳循环的一般特征;分析了城市系统碳循环的内部机理,主要包括:城市系统碳储量和碳输入/输出通量的主要过程和途径、城市系统碳储量、碳通量和碳流通的生命周期分析、城市系统碳输入和碳输出的类型划分等;提出了基于系统层次划分和碳流通过程的城市系统碳循环的研究框架,分析了城市自然系统和城市经济系统的主要碳流通过程和环节,构建了城市系统碳循环研究的思路和理论框架;最后提出了城市系统碳循环领域未来的研究重点.     

Biogeochemical Controls and Feedbacks on Ocean Primary Production

Changes in oceanic primary production, linked to changes in the network of global biogeochemical cycles, have profoundly influenced the geochemistry of Earth for over 3 billion years. In the contemporary ocean, photosynthetic carbon fixation by marine phytoplankton leads to formation of approximately 45 gigatons of organic carbon per annum, of which 16 gigatons are exported to the ocean interior. Changes in the magnitude of total and export production can strongly influence atmospheric CO2 levels (and hence climate) on geological time scales, as well as set upper bounds for sustainable fisheries harvest. The two fluxes are critically dependent on geophysical processes that determine mixed-layer depth, nutrient fluxes to and within the ocean, and food-web structure. Because the average turnover time of phytoplankton carbon in the ocean is on the order of a week or less, total and export production are extremely sensitive to external forcing and consequently are seldom in steady state. Elucidating the biogeochemical controls and feedbacks on primary production is essential to understanding how oceanic biota responded to and affected natural climatic variability in the geological past, and will respond to anthropogenically influenced changes in coming decades. One of the most crucial feedbacks results from changes in radiative forcing on the hydrological cycle, which influences the aeolian iron flux and, in turn, affects nitrogen fixation and primary production in the oceans.     

Isotopic composition of the martian atmosphere

Results from the neutral mass spectrometer carried on the aeroshell of Viking 1 show evidence for NO in the upper atmosphere of Mars and indicate that the isotopic composition of carbon and oxygen is similar to that of Earth. Mars is enriched in (15)N relative to Earth by about 75 percent, a consequence of escape that implies an initial abundance of nitrogen equivalent to a partial pressure of at least 2 millibars. The initial abundance of oxygen present either as CO(2) or H(2)O must be equivalent to an exchangeable atmospheric pressure of at least 2 bars in order to inhibit escape-related enrichment of (18)O.     

典型气候/环境因子变化对九段沙湿地碳固定潜力的影响

利用人工气候室模拟长江口区域几种典型气候/环境因子的变化特征（全球变暖、CO2增加和海水无机氮污染加剧等）,并从植物生长量和土壤呼吸角度综合分析了这些气候/环境因素的变化对九段沙湿地土壤有机碳汇聚能力的影响。初步结果表明,在实验范围内,与对照相比,单方面的温度升高、无机氮污染加剧和CO2浓度升高会提高九段沙土壤的有机碳汇聚能力。无机氮污染加剧协同升温对土壤呼吸有一定的消减作用,从而提高了土壤有机碳汇聚能力;无机氮污染加剧协同CO2浓度升高会促使土壤有机碳的排放,使其碳汇聚能力下降;CO2浓度升高和全球升温的共同作用不会显著降低有机碳汇聚能力;无机氮污染加剧和CO2浓度升高的基础上加入升温的三因素交互作用会促进土壤有机碳的排放,使其碳汇聚能力下降。因此,要尽力避免海水中无机氮污染加剧和CO2浓度升高两个因素,以及在此基础上升温情况的同时发生。     

A sulfur dioxide climate feedback on early Mars

Ancient Mars had liquid water on its surface and a CO2-rich atmosphere. Despite the implication that massive carbonate deposits should have formed, these have not been detected. On the basis of fundamental chemical and physical principles, we propose that climatic conditions enabling the existence of liquid water were maintained by appreciable atmospheric concentrations of volcanically degassed SO2 and H2S. The geochemistry resulting from equilibration of this atmosphere with the hydrological cycle is shown to inhibit the formation of carbonates. We propose an early martian climate feedback involving SO2, much like that maintained by CO2 on Earth.     

杉树再生技术营林在节能减排中的价值探析

大量CO2的排放,给人类带来了严重的生态灾害,因此节能减排成为了国际社会广泛关注的问题,发展低碳经济、植树造林增加碳汇等成为世界各国减排的主要手段,但很少关注民族本土性生态功能和作用在节能减排中的价值。通过田野调查表明,侗族林农运用杉树再生技术形成的人工林对CO2的固化效果,体现出长效性和高效性,在节能减排中有着其独特的价值。     

Mass-independent oxygen isotope fractionation in atmospheric CO as a result of the reaction CO + OH

Atmospheric carbon monoxide (CO) exhibits mass-independent fractionation in the oxygen isotopes. An 17O excess up to 7.5 per mil was observed in summer at high northern latitudes. The major source of this puzzling fractionation in this important trace gas is its dominant atmospheric removal reaction, CO + OH --> CO2 + H, in which the surviving CO gains excess 17O. The occurrence of mass-independent fractionation in the reaction of CO with OH raises fundamental questions about kinetic processes. At the same time the effect is a useful marker for the degree to which CO in the atmosphere has been reacting with OH.     

Carbon isotope constraints on the deglacial CO₂ rise from ice cores

The stable carbon isotope ratio of atmospheric CO(2) (δ(13)C(atm)) is a key parameter in deciphering past carbon cycle changes. Here we present δ(13)C(atm) data for the past 24,000 years derived from three independent records from two Antarctic ice cores. We conclude that a pronounced 0.3 per mil decrease in δ(13)C(atm) during the early deglaciation can be best explained by upwelling of old, carbon-enriched waters in the Southern Ocean. Later in the deglaciation, regrowth of the terrestrial biosphere, changes in sea surface temperature, and ocean circulation governed the δ(13)C(atm) evolution. During the Last Glacial Maximum, δ(13)C(atm) and atmospheric CO(2) concentration were essentially constant, which suggests that the carbon cycle was in dynamic equilibrium and that the net transfer of carbon to the deep ocean had occurred before then.     

Oceanic Uptake of Fossil Fuel CO2: Carbon-13 Evidence

The delta(13)C value of the dissolved inorganic carbon in the surface waters of the Pacific Ocean has decreased by about 0.4 per mil between 1970 and 1990. This decrease has resulted from the uptake of atmospheric CO(2) derived from fossil fuel combustion and deforestation. The net amounts of CO(2) taken up by the oceans and released from the biosphere between 1970 and 1990 have been determined from the changes in three measured values: the concentration of atmospheric CO(2), the delta(13)C of atmospheric CO(2) and the delta(13)C value of dissolved inorganic carbon in the ocean. The calculated average net oceanic CO(2) uptake is 2.1 gigatons of carbon per year. This amount implies that the ocean is the dominant net sink for anthropogenically produced CO(2) and that there has been no significant net CO(2) released from the biosphere during the last 20 years.