An Improved 20-Year Arctic Ocean Altimetric Sea Level Data Record     

Yongcun Cheng  Per Knudsen 《Marine Geodesy》2013,36(2):146-162

For ocean and climate research, it is essential to get long-term altimetric sea level data that is as accurate as possible. However, the accuracy of the altimetric data is frequently degraded in the interior of the Arctic Ocean due to the presence of seasonal or permanent sea ice. We have reprocessed ERS-1/2/Envisat satellite altimetry to develop an improved 20-year sea level dataset for the Arctic Ocean. We have developed both an along-track dataset and three-day gridded sea level anomaly (SLA) maps from September 1992 to April 2012. A major improvement in data coverage was gained by tailoring the standard altimetric editing criteria to Arctic conditions. The new reprocessed data has significant increased data coverage with between 4 and 10 times the amount of data in regions such as the Beaufort Gyre region compared with AVISO and RADS datasets. This allows for a more accurate estimation of sea level changes from satellite altimetry in the Arctic Ocean. The reprocessed dataset exhibit a mean sea level trend of 2.1 ± 1.3 mm/year (without Glacial Isostatic Adjustment correction) covering the Arctic Ocean between 66°N and 82°N with significant higher spatial coherency in the ice-covered regions than the RADS and DUACS datasets.  相似文献   

Coordination chemistry and hydrolysis of Fe(III) in a peat humic acid studied by X-ray absorption spectroscopy   总被引：2，自引：0，他引：2  

Torbjörn Karlsson  Per Persson 《Geochimica et cosmochimica acta》2010,74(1):30-9557

The speciation of iron (Fe) in soils, sediments and surface waters is highly dependent on chemical interactions with natural organic matter (NOM). However, the molecular structure and hydrolysis of the Fe species formed in association with NOM is still poorly described. In this study extended X-ray absorption fine structure (EXAFS) spectroscopy was used to determine the coordination chemistry and hydrolysis of Fe(III) in solution of a peat humic acid (5010-49,200 μg Fe g⁻¹ dry weight, pH 3.0-7.2). Data were analyzed by both conventional EXAFS data fitting and by wavelet transforms in order to facilitate the identification of the nature of backscattering atoms. Our results show that Fe occurs predominantly in the oxidized form as ferric ions and that the speciation varies with pH and Fe concentration. At low Fe concentrations (5010-9920 μg g⁻¹; pH 3.0-7.2) mononuclear Fe(III)-NOM complexes completely dominates the speciation. The determined bond distances for the Fe(III)-NOM complexes are similar to distances obtained for Fe(III) complexed by desferrioxamine B and oxalate indicating the formation of a five-membered chelate ring structure. At higher Fe concentrations (49,200 μg g⁻¹; pH 4.2-6.9) we detect a mixture of mononuclear Fe(III)-NOM complexes and polymeric Fe(III) (hydr)oxides with an increasing amount of Fe(III) (hydr)oxides at higher pH. However, even at pH 6.9 and a Fe concentration of 49,200 μg g⁻¹ our data indicates that a substantial amount of the total Fe (>50%) is in the form of organic complexes. Thus, in environments with significant amounts of organic matter organic Fe complexes will be of great importance for the geochemistry of Fe. Furthermore, the formation of five-membered chelate ring structures is in line with the strong complexation and limited hydrolytic polymerization of Fe(III) in our samples and also agrees with EXAFS derived structures of Fe(III) in organic soils.  相似文献