Sediment oxygen consumption in semi-closed Korean coastal bays during summer

We used an oxygen microsensor for high-resolution measurements of pore water oxygen concentration in semi-closed coastal bays of the South Sea of Korea during summer. The oxygen penetration depths ranged from 0.60 to 3.65 mm. Oxygen consumption rates were estimated to be 9.1 to 59 mmol m^?2 d^?1 (average: 22.8 mmol m^?2 d^?1). At the sediment-water interface, the oxidation rates of organic carbon were estimated to be 84–545 mg C m^?2 d^?1 (average: 211 mg C m^?2 d^?1). Approximately 38% (～211 mg C m^?2 d^?1) of pelagic primary production was regenerated in the surface sediment, indicating the tight benthic-pelagic coupling in the coastal sea of the South Sea of Korea.     

A study on the preparation of fine and low soda alumina

A simple process to produce fine and low soda α-alumina (α-Al₂O₃) from a commercial grade aluminium trihydroxide (gibbsite, Al(OH)₃) produced by KC Corporation Ltd was developed. There are two options for this process with the first one producing low soda α-alumina (< 0.05% Na₂O) having a mean particle size of 50 μm. The second option yields a fine product with a mean size of less than 10 μm. In the first option, a plant aluminium trihydroxide containing 0.20% Na₂O was first fluidized with nitrogen at 400–600 °C to yield an amorphous activated alumina. This intermediate product was then treated with acetic or oxalic acid, washed with water and heated to 1200 °C to form calcined α-alumina, having a Na₂O content of less than 0.05%. A 20 min leaching using 0.2 M acetic or oxalic acid could yield an alumina product containing 0.04% Na₂O. In the second option, a new technique for the preparation of fine and low soda α-alumina was evaluated using an attrition mill working also as a leaching vessel at 80 °C. Fine (< 10 μm in mean particle size) and low soda (< 0.04% Na₂O) alumina was produced by a 20 min leaching step with 0.2 M acetic acid and concurrent attrition milling.     

Distribution of Cs and Pu in the surface waters of the East Sea (Sea of Japan)

Surface and subsurface water samples for ¹³⁷Cs and ^239,240Pu analysis were collected in the East Sea (Sea of Japan) during August 1993. The ¹³⁷Cs levels of the surface waters are quite homogeneous in the East Sea (average = 3.1±0.2 mBq kg⁻¹). The ^239,240Pu levels vary from 6 to 10 μBq kg⁻¹ in the surface. ^239,240Pu to ¹³⁷Cs ratios in the surface water are within 0.002 to 0.003. The East Sea may be regarded as a part of the North Pacific Ocean in terms of ¹³⁷Cs dispersal in the surface, where the ¹³⁷Cs contents of the surface seawater seem to be controlled primarily by the atmospheric input. However, since our sampling was made just two months prior to the widely publicized Russian dumping incident on the 17th October 1993, our measurements may provide background data to assess the immediate impact of the Russian dumping on the levels of ¹³⁷Cs and ^239,240Pu in the East Sea.     

Identification of groundwater recharge sources and processes in a heterogeneous alluvial aquifer: results from multi‐level monitoring of hydrochemistry and environmental isotopes in a riverside agricultural area in Korea

We evaluated sources and pathways of groundwater recharge for a heterogeneous alluvial aquifer beneath an agricultural field, based on multi‐level monitoring of hydrochemistry and environmental isotopes of a riverside groundwater system at Buyeo, Korea. Two distinct groundwater zones were identified with depth: (1) a shallow oxic groundwater zone, characterized by elevated concentrations of NO₃^? and (2) a deeper (>10–14 m from the ground surface) sub‐oxic groundwater zone with high concentrations of dissolved Fe, silica, and HCO₃^?, but little nitrate. The change of redox zones occurred at a depth where the aquifer sediments change from an upper sandy stratum to a silty stratum with mud caps. The δ¹⁸O and δ²H values of groundwater were also different between the two zones. Hydrochemical and δ¹⁸O? δ²H data of oxic groundwater are similar to those of soil water. This illustrates that recharge of oxic groundwater mainly occurs through direct infiltration of rain and irrigation water in the sandy soil area where vegetable cropping with abundant fertilizer use is predominant. Oxic groundwater is therefore severely contaminated by agrochemical pollutants such as nitrate. In contrast, deeper sub‐oxic groundwater contains only small amounts of dissolved oxygen (DO) and NO₃^?. The ³H contents and elevated silica concentrations in sub‐oxic groundwater indicate a somewhat longer mean residence time of groundwater within this part of the aquifer. Sub‐oxic groundwater was also characterized by higher δ¹⁸O and δ²H values and lower d‐excess values, indicating significant evaporation during recharge. We suggest that recharge of sub‐oxic groundwater occurs in the areas of paddy rice fields where standing irrigation and rain water are affected by strong evaporation, and that reducing conditions develop during subsequent sub‐surface infiltration. This study illustrates the existence of two groundwater bodies with different recharge processes within an alluvial aquifer. Copyright © 2009 John Wiley & Sons, Ltd.     

Effect of aerosol pollution on clouds and its dependence on precipitation intensity

In this study, simulations performed with a large-eddy resolving numerical model are used to examine the effect of aerosol on cumulus clouds, and how this effect varies with precipitation intensity. By systematically varying the surface moisture fluxes, the modeled precipitation rate is forced to change from weak to strong intensity. For each of these intensities, simulations of a high-aerosol case (a polluted case with a higher aerosol concentration) and a low-aerosol case (a clean case with a lower aerosol concentration) are performed. Whether or not precipitation and associated sub-cloud evaporation and convective available potential energy (CAPE) are large, liquid–water path (LWP) is larger in the high-aerosol case than in the low-aerosol case over the first two-thirds of the entire simulation period. In weak precipitation cases, reduction in aerosol content leads to changes in CAPE in the middle parts of cloud layers, which in turn induces larger LWP in the low-aerosol case over the last third of the simulation period. With strong precipitation, stronger stabilization of the sub-cloud layers in the low-aerosol case counters the CAPE changes in the middle parts of cloud layers, inducing smaller LWP in the low-aerosol case over the last third of the simulation period. The results highlight an interaction between aerosol effects on CAPE above cloud base and those in sub-cloud layers, and indicate the importance of a consideration of aerosol effects on CAPE above cloud base as well as those in sub-cloud layers. In the high-aerosol case, near the beginning of the simulation period, larger environmental CAPE does not necessarily lead to larger in-cloud CAPE and associated larger cloud intensity because aerosol-induced increase in cloud population enhances competition among clouds for the environmental CAPE. This demonstrates the importance of the consideration of cloud population for an improved parameterization of convective clouds in climate models.     

The geochemistry of aliphatic and polar organic tracers in sediments from Lake Bera, Malaysia

The molecular distributions of homologous aliphatic lipid compounds (n-alkanes, n-alkanoic acids, n-alkanols, n-alkanals and n-alkan-2-ones) were investigated in sediments of Lake Bera, Malaysia as well as in plant waxes from the vicinity using gas chromatography-mass spectrometry. In addition, triterpenoids of the oleanane, ursane, lupane and friedelane series, and their diagenetic products were also identified. Using the aquatic proxy P_aq, it was found that the n-alkanes present in surface sediments S1, S5 and S6 correspond to an input from emergent macrophytes, whereas in sediments collected from open water (S2, S3 and S4) they correspond to input from submerged/floating macrophytes. The presence of n-alkan-2-ols, a commonly found homologous series in the sediments as well as in the plant wax, is novel here. In addition, the presence of 24-methylcycloart-22-enol and 24-ethylcycloart-22-enol in sediments as well as the plant wax of Pandanus helicopus, a dominant reed around the lake, also supports the input of plant biomarkers to the sediments. The occurrence of 5-membered ring triterpenoid derivatives as major diagenetic products of the triterpenoids identified (e.g. friedelan-2,3-dione) shows that the degradation of the organic matter in the sediments occurs mainly under oxic conditions. Also, the presence of ring-A degraded triterpenoids (dihydroputranjivic acid, 3-nor-2,4-seco-friedelane, 4α- and 4β-3-norfriedelanes, A-norfriedel-10-one, and A-norfriedel-8-en-10-one) and the aromatized triterpenoid hydrocarbons (mono- and triaromatic derivatives) as minor diagenetic products indicates photochemical and microorganism-mediated alteration reactions of natural products in the sediments. Additional novel polyfunctional friedelane derivatives, namely friedelane-2,3-dione, friedelane-1,3-diol-2-one and friedel-1(10)-ene-1,3-diol-2-one were identified for the first time in this study. These novel polyfunctional triterpenoids were inferred to derive from the oxidation of the triterpenoids from higher plants in this oxic tropical environment. For future reference purposes, the mass spectra of the identified polar triterpenoids are also presented here. This study provides important data on the biogeochemistry of organic matter in a tropical lake of SE Asia.