This paper analyzes the role of the National Natural Science Foundation of China (NSFC) in advancing human geography in China by focusing on five key research areas: land use, urban systems and urban agglomeration, economic globalization, climate change and social and cultural geographies. All NSFC-funded human geography programs related to these five topics from 1986 to 2017 comprise the sample for analysis, and the research topics, content, teams, and peer-reviewed journal publications supported by these programs are investigated. Specifically, this paper analyzes the NSFC’s promotion of the expansion of research topics in response to national developmental needs and the shifting frontiers of human geography research internationally, its enhancement of interdisciplinary research, and its contributions to the assembly of specialized research teams. The paper also reports important progress in Chinese human geography over the past 30 years through the institutional lens of the NSFC, revealing major characteristics and trends in the discipline. The paper concludes by calling for further collaboration between the research community and the NSFC for the development of a locally suitable and globally influential Chinese human geography. 相似文献
Central Asian countries are located in the heartland of the Eurasian Continent. Their geographic location puts their energy flows under tremendous geopolitical pressure from the countries along their limited number of pipelines. With energy trade data from the United Nations Comtrade Statistics Database in the period from 2005 to 2016, this paper evaluates energy security of Kazakhstan and Turkmenistan (exporter) and Kyrgyzstan (importer) using three standards: correlativeness, diversity, and the impact of international relations. It concludes that Kazakhstan and Turkmenistan’s oil markets are balanced in terms of correlation and diversification, and thus less subject to geopolitical pressure. Turkmenistan’s gas markets, on the other hand, still have tremendous exposure to geopolitical risks for lack of diversification. Kyrgyzstan, as an energy importer, could rely on a few neighboring countries for energy supply. We found out that the three Central Asian countries’ energy security is largely determined by four political factors: the relationship with Russia, the new “great game” in Eurasia, the rise of China, and Central Asian regional geopolitical configuration. 相似文献
The use of shale gas is commonly considered as a low-cost option for meeting ambitious climate policy targets. This article explores global and country-specific effects of increasing global shale gas exploitation on the energy markets, on greenhouse gas emissions, and on mitigation costs. The global techno-economic partial equilibrium model POLES (Prospective Outlook on Long-term Energy Systems) is employed to compare policies which limit global warming to 2°C and baseline scenarios when the availability of shale gas is either high or low. According to the simulation results, a high availability of shale gas has rather small effects on the costs of meeting climate targets in the medium and long term. In the long term, a higher availability of shale gas increases baseline emissions of greenhouse gases for most countries and for the world, and leads to higher compliance costs for most, but not all, countries. Allowing for global trading of emission certificates does not alter these general results. In sum, these findings cast doubt on shale gas’s potential as a low-cost option for meeting ambitious global climate targets.
POLICY RELEVANCE
Many countries with a large shale gas resource base consider the expansion of local shale gas extraction as an option to reduce their GHG emissions. The findings in this article imply that a higher availability of shale gas in these countries might actually increase emissions and mitigation costs for these countries and also for the world. An increase in shale gas extraction may spur a switch from coal to gas electricity generation, thus lowering emissions. At the global level and for many countries, though, this effect is more than offset by a crowding out of renewable and nuclear energy carriers, and by lower energy prices, leading to higher emissions and higher mitigation costs in turn. These findings would warrant a re-evaluation of the climate strategy in most countries relying on the exploitation of shale gas to meet their climate targets. 相似文献
A series of natural omphacites from a wide range of P, T occurrences were investigated by electron microprobe (EMP), infrared (IR)-, Mössbauer (MS)- and optical spectroscopy in the UV/VIS spectral range (UV/VIS), secondary ion mass spectrometry (SIMS) and single crystal structure refinement by X-ray diffraction (XRD) to study the influence of hydrogen loss on valence state and site occupancies of iron. In accordance with literature data we found Fe2+ at M1 as well as at M2, and in a first approach assigned Fe3+ to M1, as indicated by MS and XRD results. Hydrogen content of three of our omphacite samples were measured by SIMS. In combination with IR spectroscopy we determined an absorption coefficient: εi,tot = 65,000 ± 3,000 lmolH2O?1 cm?2. Using this new εi,tot value, we obtained water concentrations ranging from 60 to 700 ppm H2O (by weight). Hydrogen loss was simulated by stepwise heating the most water rich samples in air up to 800°C. After heat treatment the samples were analyzed again by IR, MS, UV/VIS, and XRD. Depending on the type of the OH defect, the grade of dehydration with increasing temperature is significantly different. In samples relatively poor in Fe3+ (<0.1 Fe3+ pfu), hydrogen associated with vacancies at M2 (OH bands around 3,450 cm?1) starts to leave the structure at about 550°C and is completely gone at 780°C. Hydrogen associated with Al3+ at the tetrahedral site (OH bands around 3,525 cm?1, Koch-Müller et al., Am Mineral, 89:921–931, 2004) remains completely unaffected by heat treatment up to 700°C. But all hydrogen vanished at about 775°C. However, this is different for a more Fe3+-rich sample (0.2 Fe3+ pfu). Its IR spectrum is characterized by a very intense OH band at 3,515 cm?1 plus shoulder at 3,450 cm?1. We assign this intense high-energy band to vibrations of an OH dipole associated with Fe3+ at M1 and a vacancy either at M1 or M2. OH release during heating is positively correlated with decrease in Fe2+ and combined with increase in Fe3+. That dehydration is correlated with oxidation of Fe2+ is indirectly confirmed by annealing of one sample in a gas mixing furnace at 700°C under reducing conditions keeping almost constant OH? content and giving no indication of Fe2+-oxidation. Obtained data indicate that in samples with a relatively high concentration of Fe2+ at M2 and low-water concentrations, i.e., at a ratio of Fe2+ M2/H > 10 dehydration occurs by iron oxidation of Fe2+ exclusively at the M2 site following the reaction: \( {\left[ {{\text{Fe}}^{{{\text{2 + [ M2]}}}}{\text{OH}}^{ - } } \right]} = {\left[ {{\text{Fe}}^{{{\text{3 + [ M2]}}}} {\text{O}}^{{{\text{2}} - }} } \right]} + {\text{1/2}}\;{\text{H}}_{{\text{2}}} \uparrow . \) In samples having relatively low concentration of Fe2+ at M2 but high-water concentrations, i.e., ratio of Fe2+ M2/H < 5.0 dehydration occurs through oxidation of Fe2+ at M1. 相似文献