太平洋海气CO₂通量对气候事件的响应     

李阳春  徐永福 《气候与环境研究》2013,18(5):571-582

应用一个嵌套了海洋生物地球化学循环的太平洋环流碳循环模式,分析了1960～2000年太平洋不同海区海气碳通量随时间的变化。模拟结果显示,赤道太平洋为大气CO₂的排放区,南、北太平洋(南、北纬15°至模式计算区域南、北边界)为吸收区。3个海区海气碳通量随时间均存在显著的波动,其中赤道太平洋海气碳通量年际波动最显著。3个海区海气碳通量年际波动对气候事件的响应并不一致,在El Niño年赤道太平洋冷舌的强度和总溶解无机碳(DIC)的浓度以及输出生产力均会受到上升流减弱的影响而降低,La Niña年这些海气碳通量控制要素的分布情况则正好相反,但在南北太平洋副热带以及高纬度海区,El Niño和La Niña对这些要素带来的影响却并不一定相反,对输出生产力的影响甚至是一致的。以海表温度(SST)为例考察海气碳通量与物理场之间的关系表明,在赤道太平洋上升流对DIC的影响是控制海气碳通量变化的主要因素,而在其他海区,尤其是副热带海区,由于垂直运动的年际变化较小,且生物生产力水平较低,SST的波动对海气碳通量年际变化的影响更加重要。  相似文献   

Variations of levels and composition of PM₁₀ and PM_2.5 at an insular site in the Western Mediterranean     

Jorge Pey  Xavier Querol  Andrs Alastuey 《Atmospheric Research》2009,94(2):285-299

The insular suburban site of Castillo de Bellver was selected for the study of the variability of PM levels and composition in the Western Mediterranean Basin (WMB).Mean annual (in 2004) PM₁₀ and PM_2.5 levels at this site were 29 and 20 µg/m³, respectively. These levels may be regarded as relatively low when compared with other suburban insular locations in the Eastern Mediterranean Basin (EMB), but they are higher than those recorded at most of the European suburban sites, especially in Northern and Western Europe. Seasonal variability of PM levels at this site is governed by meteorology rather than local emissions, whereas the daily cycles are clearly defined by the anthropogenic emissions, mainly coming from the urban area of Palma de Mallorca and the harbour area of the same city.Concerning the aerosol composition at this site, the main PM constituent is the mineral matter (29% in PM₁₀ and 16 % in PM_2.5), more than 50% (in PM₁₀) being attributable to African dust. The amount of secondary inorganic aerosols is also very high (27% in PM₁₀ and 34% in PM_2.5), with the predominance of fine ammonium sulphate, and in a less proportion fine ammonium nitrate (in winter) and coarse Ca and Na nitrate (with higher importance in summer). The carbonaceous particles, dominantly fine, account for 17% of PM₁₀ and 25% of PM_2.5. The elemental carbon/organic carbon (EC/OC) ratio reached a mean value of 0.17, similar to those observed at regional background sites in the WMB coast of Spain. The sea spray aerosols (mainly coarse) represented around 10% of PM₁₀, and only 4% in PM_2.5. Finally, the unaccounted fraction increased from 15% to 20% in PM_2.5, being mostly attributed to water.The concentrations of trace elements in PM₁₀ and PM_2.5 were usually in the range to those observed in regional background sites in the Iberian Peninsula, with the exception of the typical tracers of road traffic such as Cu, Sb, Zn, Sn and Ba, which presented concentrations in the range of urban sites of Iberia. Other elements such as Cr, Zr, Hf and Co have been identified as the main tracers of the harbour contributions.  相似文献   

地下水污染调查中水样无机组分检测质量控制体系 的建立和应用   总被引：1，自引：0，他引：1  

刘晓雯 《岩矿测试》2010,29(5):580-584

实验室分析全过程的质量控制,其目的是将检测误差控制在容许限度内,以保证数据在给定的置信水平内达到质量要求。国土资源部天津矿产资源监督检测中心根据地质矿产行业标准DZ/T0130—2006《地质矿产实验室测试质量管理规范》、DD2008—01中国地质调查局标准《地下水污染调查评价规范》,并参照其他行业对水质分析质量控制要求,结合水质检测的具体情况,制定了适宜的地下水分析过程的质量控制体系,使实验室质量控制和质量管理具有良好的操作性和可行性,确保检测数据的可靠性。文章从5个方面提出地下水水质无机组分检测中质量控制方法,使水质无机组分的检测质量得到有效控制。  相似文献   

非水滴定法连续测定铀矿地质样品中的无机碳和有机碳     

朱樱  康友纯  欧阳泉根 《铀矿地质》2010,26(1):55-59

研究了非水滴定法连续测定铀矿地质样品中的无机碳和有机碳的新方法,建立了优化的测定体系。无机碳回收率为99．4％～100．1％,有机碳的回收率为98．54％～103．1％,该法应用于生产,简便快速,准确可靠,结果令人满意。  相似文献   

四川省马边县六股水磷矿床的地质特征     

刘力生 《化工矿产地质》2010,32(4):201-205

六股水磷矿床赋存于下寒武统麦地坪组,包含2个磷矿层、6个磷矿体。矿体水平延伸1200～2700m,均厚1.3～4.88m,深部延深大于120m。矿石类型有块状及白云质条带(条纹)状2种磷矿石,P2O5平均品位29.42%。稀土元素总量低,分布模式呈轻稀土富集型。矿床为生物化学沉积成因,磷经历了复杂的富集过程。  相似文献   

Comparative studies of inorganic carbon utilization inEmiliania huxleyi and some non-calcifying marine microalgae     

Dong Liang-feng  M. J. Merrett  Wu Chao-yuan 《中国海洋湖沼学报》1999,17(3):219-232

Inorganic carbon utilization in the non-calcifying marine microalgae,Nannochloropsis oculata, Phaeodactylum tricornutum andPorphyridium purpureum was compared with high- and low-calcifying strains ofEmiliania huxleyi grown in artificial seawater medium aerated with either air (0.03% V/V CO₂) or CO₂-free air. For high-calcifying strain ofE. oculata andP. tricornutem, similar growth patterns were observed in air-and CO₂-free air-grown cultures.P. purpureum showed a less final cell density in CO₂-free air than in air-grown culture. However, low-calcifying strain ofE. huxleyi was able to grow only in air-grown culture, but not in CO₂-free air-grown culture. Measurements of alkalinity, pH, concentration of dissolved inorganic carbon (DIC) and free CO₂ showed different patterns of DIC utilization. WithN. oculata, P. tricornutum andP. purpureum the pattern of DIC utilization was characterized by an increase of pH and a decrease of DIC but a constant alkalinity in the cultures aerated with air or CO₂-free air, suggesting that bicarbonate utilization was concomitant with an efflux of OH⁻. Both alkalinity and pH were maintained rather constant in air-grown culture of low-calcifying strain ofE. huxleyi, suggesting that diffusive entry of CO₂ could meet the requirement of DIC for its photosynthesis and growth. High-calcifying strain ofE. huxleyi, however, showed a pattern of decrease of alkalinity and DIC but an almost constant pH, indicating that bicarbonate was the major form of inorganic carbon utilised by this organism and bicarbonate uptake is unlikely to be accompanied by an efflux of OH⁻. The final pH values reached byN. oculata, P. tricornutum andP. purpureum in a closed system were 10.75, 10.60 and 9.85 respectively, showing that bicarbonate utilisation is concomitant with an efflux of OH⁻. While the final pH of 8.4 in high-calcifyingE. huxleyi suggests that bicarbonate utilization was not accompanied by an efflux of OH⁻. Contribution No. 3557 from the Institue of Oceanology, Chinese Academy of Sciences. This work was supported by NERC grant GRE3/7853 U. K. and partly supported by Bio-Engineering Center, SSTC 96-C01-05-01.  相似文献   

Leaky savannas: the significance of lateral carbon fluxes in the seasonal tropics          下载免费PDF全文

Sarah Tweed  Marc Leblanc  Adrian Bass  Glenn A. Harrington  Niels Munksgaard  Michael I. Bird 《水文研究》2016,30(6):873-887

Globally, dissolved inorganic carbon (DIC) accounts for more than half the annual flux of carbon exported from terrestrial ecosystems via rivers. Here, we assess the relative influences of biogeochemical and hydrological processes on DIC fluxes exported from a tropical river catchment characterized by distinct land cover, climate and geology transition from the wet tropical mountains to the low‐lying savanna plains. Processes controlling changes in river DIC were investigated using dissolved organic carbon, particulate organic carbon and DIC concentrations and stable isotope ratios of DIC (δ¹³C_DIC) at two time scales: seasonal and diel. The recently developed Isotopic Continuous Dissolved Inorganic Carbon Analyser was used to measure diel DIC concentration and δ¹³C_DIC changes at a 15‐min temporal resolution. Results highlight the predominance of biologically mediated processes (photosynthesis and respiration) controlling diel changes in DIC. These resulted in DIC concentrations varying between 3.55 and 3.82 mg/l and δ¹³C_DIC values ranging from ?19.7 ± 0.31‰ to ?17.1 ± 0.08‰. In contrast, at the seasonal scale, we observed wet season DIC variations predominantly from mixing processes and dry season DIC variations due to both mixing processes and biological processes. The observed wet season increases in DIC concentrations (by 6.81 mg/l) and δ¹³C_DIC values of river water (by 5.4‰) largely result from proportional increases in subsurface inflows from the savanna plains (C₄ vegetation) region relative to inflows from the rainforest (C₃ vegetation) highlands. The high DIC river load during the wet season resulted in the transfer of 97% of the annual river carbon load. Therefore, in this gaining river, there are significant seasonal variations in both the hydrological and carbon cycles, and there is evidence of substantial coupling between the carbon cycles of the terrestrial and the fluvial environments. Recent identification of a substantial carbon sink in the savannas of northern Australia during wetter years in the recent past does not take into account the possibility of a substantial, rapid, lateral flux of carbon to rivers and back to the atmosphere. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

Influential factors on the exchange rate of dissolved inorganic nutrients at the sediment-water interface in Jiaozhou Bay, China   总被引：1，自引：0，他引：1  

WANG Xiulin  JIANG Fenghua  SHI Xiaoyong  ZHU Chenjian  HAN Xiurong 《中国海洋湖沼学报》2007,25(3)

Incubation experiments are carried out to study the exchange rates of dissolved inorganic nutrients including silicate, phosphate, ammonium, nitrite, and nitrate (vSiO3-Si, vPO4-P, vNH4-N, vNO2-N and vNO3-N) at the sediment-water interface in the Jiaozhou Bay. Major factors influencing the exchange rates are discussed in detail, which include the dissolved inorganic nutrient concentrations in porewater (Cpw), water and clay contents, and grain size of the sediments (CH2O, Cclay and GSsed). The results may provide insight into the dynamics of nutrient transport and the environmental capacity of nutrients in Jiaozhou Bay, and should be beneficial to solving the problems caused by excessive nutrient input this area.  相似文献   

A geochemical model for evaluating theories on the genesis of Florida''s sedimentary phosphate deposits     

Martha W. Gilliland 《Mathematical Geology》1976,8(3):219-242

Present ionic concentrations of Ca ⁺⁺,HCO ₃ ^- ,and HPO ₄ ⁼ in surface and groundwater runoff in Florida indicate that phosphorus is being concentrated in rock through dissolution and reprecipitation, with calcium phosphate increasing at the expense of calcium carbonate. Analog computer simulation of a systems model of this process suggests that significant enrichment can occur in 20 million years. The degree of enrichment depends on the supply of new phosphorus to Florida through rain and oceanic exchange processes. If the calcium phosphate content of original rock is 0.5 to 1.0 percent (0.52 to 1.05 percent P ₂ O ₅),a formation with 10 to 20 percent calcium phosphate (CaPO ₄ or 10.5 to 21.0 percent P ₂ O ₅)as in the Hawthorn Formation (Miocene)may result. Nutrient upwelling along the continental slope coupled with transport to the estuaries by lateral eddy diffusion can supply an additional 400 mg P|m ² |yr which, if deposited, would result in a sediment with a 4.3 percent CaPO ₄ (4.5 percent P ₂ O ₅)content. If this is enriched later by resolution, 40 percent CaPO ₄ (42 percent P ₂ O ₅)results. Through geologic time, the ocean may be considered as a source of phosphorus to the land through rain or estuarine sediment.  相似文献   

The role of hydrogen bonding in the thermal expansion and dehydration of brushite,di-calcium phosphate dihydrate     

P. F.?SchofieldEmail author  K. S.?Knight  J. A. M. van der?Houwen  E.?Valsami-Jones 《Physics and Chemistry of Minerals》2004,31(9):606-624

The unit-cell and atomic parameters of perdeuterated brushite have been extracted from Rietveld analysis of neutron powder diffraction data within the temperature range 4.2 to 470 K. The thermal expansion of brushite is anisotropic, with the largest expansion along the b axis due principally to the effect of the O(1)···D(4) and O(3)···D(2) hydrogen bonds. Expansion along the c axis, influenced by the Ow1···D(5) interwater hydrogen bond, is also large. The high temperature limits for the expansion coefficients for the unit-cell edges a, b and c are 9.7(5) × 10^–6, 3.82(9) × 10^–5 and 5.54(5) × 10^–5 K^–1, respectively, and for the cell volume it is 9.7(1) × 10^–5 K^–1. The angle displays oscillatory variation, and empirical data analysis results in = 1.28(3) × 10^–6sin(0.0105 T) K^–1, within this temperature range. The evolution of the thermal expansion tensor of brushite has been calculated between 50 T 400 K. At 300 K the magnitudes of the principal axes are ₁₁ = 50(6) × 10^{–6 K–1}, ₂₂ = 26.7(7) × 10^–6 K^–1 and ₃₃ = 7.0(5) × 10^–6 K^–1. The intermediate axis, ₂₂, is parallel to b, and using IRE convention for the tensor orthonormal basis, the axes ₁₁ and ₃₃ have directions equal to (–0.228, 0, –0.974) and (–0.974, 0, 0.228) respectively. Under the conditions of these experiments, the onset of dehydration occurred at temperatures above 400 K. Bond valence analysis combined with assessments of the thermal evolution of the bonding within brushite suggests that dehydration is precipitated through instabilities in the chemical environment of the second water molecule.  相似文献