Water and heat fluxes above a lowland dipterocarp forest in Peninsular Malaysia

We measured the fluxes of sensible and latent heat between a low‐land dipterocarp forest in Peninsular Malaysia and the atmosphere. No clear seasonal or interannual changes in latent heat flux were found from 2003 to 2005, while sensible heat flux sometimes fluctuated depending on the fluctuation of incoming radiation between wet and dry seasons. The evapotranspiration rates averaged for the period between 2003 and 2005 were 2·77 and 3·61 mm day^?1 using eddy covariance data without and with an energy balance correction, respectively. Average precipitation was 4·74 mm day^?1. Midday surface conductance decreased with an increasing atmospheric water vapour pressure deficit and thus restricted the excess water loss on sunny days in the dry season. However, the relationship between the surface conductance and vapour pressure deficit did not significantly decline with an increase in volumetric soil water content even during a period of extremely low rainfall. Copyright © 2009 John Wiley & Sons, Ltd.     

Contamination level of mercury in red meat products from cetaceans available from South Korea markets

Levels of total mercury (T-Hg) were surveyed in red meat (n=73) and liver (n=3) from toothed whales, dolphins and porpoises (odontocetes) sold for human consumption in the coastal cities of South Korea. High concentrations of T-Hg were found in the liver products of finless porpoises (18.7 and 156 microg/wet g) and common dolphins (13.2 microg/wet g). The T-Hg concentrations in red meat products were highest in the false killer whale (9.66+/-12.3 microg/wet g, n=9), bottlenose dolphin (10.6+/-12.6 microg/wet g, n=3) and killer whale (13.3 microg/wet g, n=1), and lowest in Cuvier's beaked whale and the harbour porpoise (0.4-0.5 microg/wet g). Thus, most of the products that originated from odontocetes exceeded the safety limit of 0.5 microg/wet g for T-Hg set by the South Korean health authorities for the fishery industry. Pregnant women and other vulnerable sectors of the population living in South Korea should therefore limit their consumption of odontocete products.     

Reliability analysis of shallow foundations in reference to design codes development

In this study, FORM analysis is carried out for shallow foundation of a typical building in order to evaluate relative magnitude of uncertainties involved in the force and the resistance sides. The distinguished feature of this study is to take into account the uncertainty of the earthquake force as much as possible. Tthis is because, the seismic design dominates major part of structural design in Japan, and without referring to this problem, no useful information of practical value is gained. The results of the FORM analysis exhibited the reliability index values between 2.0 to 3.5, which is considered to be in a reasonable range. Since the 50 year maximum earthquake force is considered in the reliability calculation, calculated reliability index values are for the period of 50 years. The sensitivity factor obtained in a case more realistic ground variability is taken into account exhibited values not very different from those obtained in the upper structures.     

A study on the interaction between ferric ion and silicic acid in hydrosphere: Si-containing ferruginous deposits formed in neutral hot spring waters

Five ferruginous deposit samples formed from neutral hot springs were analyzed to determine whether they consisted of a mixture of silica, hydrous iron oxide or iron silicate by differential thermal analysis (DTA), infrared (IR) spectroscopy, powder X-ray diffraction (XRD), and 57Fe Mssbauer spectroscopy. The Si/Fe atomic ratios of the deposits ranged from 0.25 to 0.45, and were smaller than those of hisingerite (12), but apparently close to those of siliceous ferrihydrite (0.250.5). Si was confirmed to be present as monomeric or oligomeric silicate from the Si-O stretching vibration frequencies on the IR spectra. Judging from the results of DTA, which minerals starting to produce after heating, and a relationship between Si-O stretching vibration frequency and Si/Fe atomic ratio proposed by Henmi et al. (1981), all the deposits in this study were concluded to be mixtures of various siliceous ferri-hydrites with low and high Si/Fe atomic ratios. Moreover, by comparing the chemical properties of hot spring waters, the formation conditions of siliceous ferrihydrite were also discussed.     

Decrease in anthropogenic nutrients and its effect on the C/N/P molar ratio of suspended particulate matter in hypertrophic Dokai Bay (Japan) in summer

Biologically important nutrient concentrations in Dokai Bay have declined as a result of reductions in anthropogenic inputs of total nitrogen and total phosphorus. A decrease in nutrient concentrations affects phytoplankton growth, thereby changing the biochemical characteristics of autochthonous particulate matter. We therefore investigated changes in the C/N/P molar ratio of suspended particulate matter (SPM) in the summer, when phytoplankton growth is vigorous, before environmental quality standards (EQSs) were attained (1995–1998) and afterward (2006–2009). We found that the ratio of particulate organic nitrogen (PON) to particulate phosphorus (PP) changed in conjunction with changes in the ratio of dissolved inorganic nitrogen to dissolved inorganic phosphorus (DIP) that resulted from reductions in nutrient loading. Furthermore, we suggest that because the DIP concentration in seawater was high before EQSs were attained, inorganic phosphorus was possibly adsorbed onto SPM. After the attainment of EQSs, however, the DIP concentration fell, and PON/PP was high. Phosphorus limitation of phytoplankton growth in the mouth of the bay may explain the high PON/PP ratios after EQS attainment.     

Sources of uncertainty in estimating stream solute export from headwater catchments at three sites

Uncertainty in the estimation of hydrologic export of solutes has never been fully evaluated at the scale of a small‐watershed ecosystem. We used data from the Gomadansan Experimental Forest, Japan, Hubbard Brook Experimental Forest, USA, and Coweeta Hydrologic Laboratory, USA, to evaluate many sources of uncertainty, including the precision and accuracy of measurements, selection of models, and spatial and temporal variation. Uncertainty in the analysis of stream chemistry samples was generally small but could be large in relative terms for solutes near detection limits, as is common for ammonium and phosphate in forested catchments. Instantaneous flow deviated from the theoretical curve relating height to discharge by up to 10% at Hubbard Brook, but the resulting corrections to the theoretical curve generally amounted to <0.5% of annual flows. Calibrations were limited to low flows; uncertainties at high flows were not evaluated because of the difficulties in performing calibrations during events. However, high flows likely contribute more uncertainty to annual flows because of the greater volume of water that is exported during these events. Uncertainty in catchment area was as much as 5%, based on a comparison of digital elevation maps with ground surveys. Three different interpolation methods are used at the three sites to combine periodic chemistry samples with streamflow to calculate fluxes. The three methods differed by <5% in annual export calculations for calcium, but up to 12% for nitrate exports, when applied to a stream at Hubbard Brook for 1997–2008; nitrate has higher weekly variation at this site. Natural variation was larger than most other sources of uncertainty. Specifically, coefficients of variation across streams or across years, within site, for runoff and weighted annual concentrations of calcium, magnesium, potassium, sodium, sulphate, chloride, and silicate ranged from 5 to 50% and were even higher for nitrate. Uncertainty analysis can be used to guide efforts to improve confidence in estimated stream fluxes and also to optimize design of monitoring programmes. © 2014 The Authors. Hydrological Processes published John Wiley & Sons, Ltd.     

Establishment of chemical equilibrium in the volcanic gas obtained from the lava lake of Kilauea,Hawaii

The establishment of gaseous chemical equilibrium in gases obtained from Kilauea lava lake was studied. Using Shepherd’s elaborate analytical data, we examined six chemical reactions in the gas phase and concluded that they were in equilibrium. The gases reflected the « quenched » equilibrium conditions of temperature within a range from 1,000° C to 1,200° C under 1 atmosphere. The gas samples had been collected over a period of three years in different localities of the same lava lake. Although the analytical result was varied considerably for each sample, the establishment of chemical equilibrium was confirmed in five of the six reactions, the exception being due to sulfur trioxide in the sixth.     

Phase transition of potassium sulfate,K2SO4 (II); dielectric constant and electrical conductivity

The phase transition of K₂SO₄ has been investigated by measurements of the dielectric constant and electrical conductivity, correlated with the structural point of view. Using single crystals, the temperature dependences of the dielectric constants and electrical conductivities were measured at frequencies of 0.3, 1, 3, and 5 MHz in the temperature range from 20° to 640 °C. Within this range, the dielectric constant does not reach a maximum, but near the phase-transition temperature at 587° C, the dielectric constant along the c axis shows a larger discontinuity than those along the a and b axes. The temperature dependence of the dielectric constant is consistent with the disordered structure of the high temperature form. Based on the parabolic increase of the dielectric constant in the temperature range from 582° to 587° C, it is likely that the phase transition propagates through an intermediate state. The electrical conductivity coefficients of K₂SO₄ increase with increasing temperature, exhibiting semiconducting character above the phase-transition temperature. In the high-temperature form, the electrical conductivity along the a axis exceeds that along the c axis. Since the electrical conductivity of K₂SO₄ is mainly ionic in character, the migration of K⁺ ions makes a major contribution to the conduction process.     

Chemistry of rainwaters in the south Pacific area of Russia

On the south-eastern edge of Russia, the chemical composition of rainwater is controlled by sea salts, terrestrial material, as well as volcanic (Kuril islands volcanic area) and anthropogenic emissions, mostly in the southern part of the area. The predominant major ions of the Primorye, Sakhalin and the Kuril Islands rainwaters were respectively HCO₃⁻–SO₄²⁻, Ca–Na, and of Cl–Na. Concentration of trace elements changes within 1–2 orders of magnitude but some difference in the distribution of the elements between continental and island rainwater is found. The concentration of the chemical elements in the particulate fraction varies from < 10% to 90% of the total concentration (dissolved + particulate) with the following distribution: Tl, Na, Ca, Sr, Zn, Cd (< 10%)–Be, Th, Bi, Rb, U, K, Sc (10–20%)–Cu, Mn, Mg, Mo, Se, Ba, Ni, As, Ag, Cs, Co, Y, Ga, V (20–50%)–Sb, Pb, Ge, Cr, Fe, Al (50–90%).The concentration of elements of the particulate fraction of the rainwater usually is significantly different from concentrations in the crust, including both higher and lower concentrations. The terrestrial contribution to dissolved elements was evaluated and follows the decreasing order: Fe > K, Mg, Ca > Ba, Sr > Na (65–1%). Close order was found for total (dissolved and solid) concentrations. Sea salt contribution to dissolved element concentration in the rainwater decrease in the following order: Cl, Mg > K, SO₄ > Ca > HCO₃⁻, Ba, Fe (78–0.1%). Calculation of anthropogenic and volcanic inputs for two ions (Cl⁻ and SO₄²⁻) shows that anthropogenic inputs for the Vladivostok and Yuzno-Sakhalinsk cities can be evaluated as 15–20% of Cl⁻ and up to 80–90% of SO₄²⁻. Volcanic components in the Kuril Islands, where anthropogenic inputs are absent, can reach up to 76% of SO₄²⁻ and 36% of Cl⁻.