Implications for Neoarchaean ocean chemistry from primary carbonate mineralogy of the Campbellrand-Malmani Platform, South Africa

The precipitation of calcite and aragonite as encrustations directly on the seafloor was an important platform‐building process during deposition of the 2560–2520 Ma Campbellrand‐Malmani carbonate platform, South Africa. Aragonite fans and fibrous coatings are common in unrestricted, shallow subtidal to intertidal facies. They are also present in restricted facies, but are absent from deep subtidal facies. Decimetre‐thick fibrous calcite encrustations are present to abundant in all depositional environments except the deepest slope and basinal facies. The proportion of the rock composed of carbonate that precipitated as encrustations or in primary voids ranges from 0% to > 65% depending on the facies. Subtidal facies commonly contain 20–35%in situ precipitated carbonate, demonstrating that Neoarchaean sea water was supersaturated with respect to aragonite, carbonate crystal growth rates were rapid compared with sediment influx rates, and the dynamics of carbonate precipitation were different from those in younger carbonate platforms. The abundance of aragonite pseudomorphs suggests that sea‐water pH was neutral to alkaline, whereas the paucity of micrite suggests the presence of inhibitors to calcite and aragonite nucleation in the mixed zone of the oceans.     

Satellite-derived vegetation index and cover type maps for estimating carbon dioxide flux for arctic tundra regions

The spatial variability and co-variability of two different types of remote sensing derivatives that portray vegetation and geomorphic patterns are analyzed in the context of estimating regional-scale CO₂ flux from land surfaces in the arctic tundra. For a study area encompassing the Kuparuk River watershed of the North Slope of Alaska, we compare satellite-derived maps of the normalized difference vegetation index (NDVI) generated at two different spatial resolutions to a map of vegetation types derived by image classification of data from the Landsat multispectral scanner (MSS). Mean values of NDVI for each cover type stratum are unique (with the exception of moist acidic tundra and shrubland types). Based on analysis of semi-variograms generated for SPOT-NDVI data, most of the vegetation cover and landform features of this arctic tundra landscape have spatial dimensions of less than 1 km. Thaw lakes on the coastal plain and glacial depositional landforms, such as moraines in the foothills, seem to be the largest features, with vegetation units having dimensions no larger than 700 m. Frequency distributions of NDVI and vegetation types extracted for sampling transects flown by an aircraft sensing CO₂ flux, relative to distributions for the entire Kuparuk River watershed, suggest a slight sampling bias towards greater cover of mesic wet sedge tundra and thaw lakes and associated lower NDVI values. The regional pattern of NDVI for the North Slope of Alaska corresponds primarily to differences between the two major physiographic provinces of this region.     

钛白副产绿矾生产聚合硫酸铁的研究

本文以钛白副产品绿矾为原料,氧化后,加入聚合剂生产聚合硫酸铁。     

National carbon dioxide emissions: geography matters

This article examines the role of geographical factors as determinants of cross-country differences in per capita carbon dioxide emissions. Such differences have been explained by economists mostly in terms of per capita income. Geographical factors on the other hand have been neglected by economic analysis. We examine the effects of cold and hot climates, transportation requirements and the availability of renewable energy sources on emissions. We find that with the exception of cooling requirements as measured by hot climates, all these geographical factors are statistically significant determinants of emissions in accordance with our expectation. Furthermore, cold climates and the availability of renewable resources are also substantively important.     

Effects of sunspot cycle length and CO2 on air temperature along Qinghai-Xizang railway and air temperature''s trend prediction

There are well coherences between annual averaged air temperatures at every meteorological station along the Qinghai-Xizang railway, and its 10-year moving average correlation coefficient is 0.92. Thus, the regional averaged annual mean temperature series along the Qinghai-Xizang railway (Trw) from 1935 to 2000 are constructed. The investigation is suggested that: Trw had significant responses to the 5-year lagged sunspot cycle length (SCL) and 15-year lagged concentration of atmospheric carbon dioxide (CO2), and the correlation coefficients between them are -0.76 (SCL) and 0.88 (CO2), respectively. The future SCL is predicted by the model of average generated function constructed with its main cycles of 76a, 93a, 108a, 205a and 275a. The result shows that the SCL would be becoming longer in the first half of the 21st century, and then it could be becoming shorter in the second half of the 21st century. Based on the natural change of SCL and the effect of double CO2 concentration, Trw in the 21st century is forecasted. It could warm up about 0.50℃ in the first half of the 21st century compared with the last decade of last century. The mean maximum air temperature could be likely about 0.20℃ in July and from 0.40℃ to 1.10℃ in January. The annual air temperature difference would likely reduce 0.3-1.00℃. The probability of above predictions ranges from 0.64 to 0.73.     

Ground-Based UV Measurements of BrO and OClO over Ny-Ålesund during Winter 1996 and 1997 and Andøya during Winter 1998/99

Presented here are measurements of BrO and OClO performed by ground-based UV-visible zenith-sky viewing spectrometers developed by the Norwegian Institute for Air Research (NILU). Measurements were taken at Ny-Ålesund, Spitsbergen (79° N, 11° E), in winter and spring1996 and 1997 and at Andøya (69.3° N, 16° E) from summer 1998 until summer 1999. AM and PM differential slant column densities (DSCDs) at 90°SZA of BrO and OClO reached their maxima during polar vortex conditions in the winter months and were anti-correlated to temperature andNO₂. Comparison of BrO with a 3-D chemical transport model showed good agreement for seasonal trends and non-vortex conditions. BrO AM/PM ratios were underestimated by the model for vortex conditions, indicating the need for better quantification of BrO source and sink reaction rates. The detection of OClO above 200 K at the 475 K isentropic level indicates the possible activation of chlorine on sulphate particles. Several episodes of boundary layer ozone depletion due to marine-derived BrO were evident in our zenith-skyspectra during April 1997 in Ny-Ålesund.     

冷浸-氟硅酸钾法测定矿石中的二氧化硅

以氢氟酸、硝酸、过氧化氢混合溶剂冷浸过夜的方式分解样品 ,然后在 3mol/ L硝酸溶液加入氯化钾生成氟硅酸钾沉淀 ,经过滤、洗涤后以沸水水解 ,所生成的氢氟酸用氢氧化钠标准溶液滴定 ,来测定二氧化硅的含量。方法操作简便 ,易于掌握。经标样验证 ,结果吻合     

论大气二氧化碳温室效应的饱和度

利用最新版本的大气分子吸收光谱资料HITRAN2000，用精确的逐线积分算法，计算了大气CO₂浓度变化后产生的辐射强迫。在此基础上，研究了CO₂温室效应的饱和度以及影响CO₂辐射强迫的各种因子。主要结论如下：地面温度愈高，一般辐射强迫也愈大，但辐射强迫并不完全取决于地面温度，它还受大气温度廓线的强烈影响；研究的 6种模式大气中，吸收带重叠对热带大气的CO₂辐射强迫影响最大，对亚极冬季大气的影响最小；与长波辐射强迫相比，短波辐射强迫的贡献很小；CO₂的温室效应在15μm带中心等波段确实已经达到饱和，但在其它（15μm带两翼，10μm，5.2μm带等）波段远未达到饱和，在最近的将来也不会达到饱和。     

The carbon isotopic ratio of atmospheric carbon dioxide at Tsukuba,Japan

To find out the secular and seasonal trends of the ¹³C value and CO₂ concentration in the surface air and the determination of the ¹³C in the atmospheric CO₂ collected at Tsukuba Science City was carried out during the period from July 1981 to October 1983. The monthly average of the ¹³C value of CO₂ in the surface air collected at 1400 LMT ranged from -7.52 to \s-8.45 with an average of -7.96±0.25 and the CO₂ concentration in the air varied from 334.5 l 1^-1 to 359 l 1^-1 with an average of 347.2±6.3 l 1^-1. The ¹³C value is high in summer and low in winter and is negatively correlated with the CO₂ concentration. In general, the relationship between the ¹³C and the CO₂ concentration is explainable by a simple mixing model of two different constant carbon isotopic species but the relationship does not always follow the model. The correlation between the ¹³C value and the CO₂ concentration is low during the plant growth season and high at other times. The observed negative deviation of the ¹³C value from the simple mixing model in the plant growth season is partly due to the isotopic fractionation process which takes place in the land biota.     

Airborne measurements of dimethylsulfide,sulfur dioxide,and aerosol ions over the Southern Ocean South of Australia

Vertical distributions of dimethylsulfide (DMS), sulfur dioxide (SO₂), aerosol methane-sulfonate (MSA), non-sea-salt sulfate (nss-SO₄ ^2-), and other aerosol ions were measured in maritime air west of Tasmania (Australia) during December 1986. A few cloudwater and rainwater samples were also collected and analyzed for major anions and cations. DMS concentrations in the mixed layer (ML) were typically between 15–60 ppt (parts per trillion, 10^–12; 24 ppt=1 nmol m^–3 (20°C, 1013 hPa)) and decreased in the free troposphere (FT) to about <1–2.4 ppt at 3 km. One profile study showed elevated DMS concentrations at cloud level consistent with turbulent transport (cloud pumping) of air below convective cloud cells. In another case, a diel variation of DMS was observed in the ML. Our data suggest that meteorological rather than photochemical processes were responsible for this behavior. Based on model calculations we estimate a DMS lifetime in the ML of 0.9 days and a DMS sea-to-air flux of 2–3 mol m^–2 d^–1. These estimates pertain to early austral summer conditions and southern mid-ocean latitudes. Typical MSA concentrations were 11 ppt in the ML and 4.7–6.8 ppt in the FT. Sulfur-dioxide values were almost constant in the ML and the lower FT within a range of 4–22 ppt between individual flight days. A strong increase of the SO₂ concentration in the middle FT (5.3 km) was observed. We estimate the residence time of SO₂ in the ML to be about 1 day. Aqueous-phase oxidation in clouds is probably the major removal process for SO₂. The corresponding removal rate is estimated to be a factor of 3 larger than the rate of homogeneous oxidation of SO₂ by OH. Model calculations suggest that roughly two-thirds of DMS in the ML are converted to SO₂ and one-third to MSA. On the other hand, MSA/nss-SO₄ ^2- mole ratios were significantly higher compared to values previously reported for other ocean areas suggesting a relatively higher production of MSA from DMS oxidation over the Southern Ocean. Nss-SO₄ ^2- profiles were mostly parallel to those of MSA, except when air was advected partially from continental areas (Africa, Australia). In contrast to SO₂, nss-SO₄ ^2- values decreased significantly in the middle FT. NH₄ ⁺/nss-SO₄ ^2- mole ratios indicate that most non-sea-salt sulfate particles in the ML were neutralized by ammonium.