Source tracing and chemical weathering implications of strontium in agricultural basin in Thailand during flood season: A combined hydrochemical approach and strontium isotope.

87Sr/86Sr of river water are of great significance in constraining oceanic strontium (Sr) record and terrestrial climate change due to the connection of continental weathering and the adjacent ocean. This work presents the geochemical characteristics of dissolved Sr and hydrochemistry, and estimates chemical weathering rate together with elemental Sr flux during the flood season of the Mun River, the largest tributary of Mekong River. Hydrochemistry analysis indicates the dominance of Cl- and HCO3- for major anions with the average of 34.6 and 43.0 mg/L, respectively, and Na+ and Ca2+ together dominated the cationic composition with the average of 22.9 and 10.5 mg/L, respectively. The ion concentrations during flood season were lower than that in dry season, implying tremendous river runoff due to extreme rainfall. The dissolved Sr ranges 6.1-237.5 µg/L with higher contents in the upper Mun. Sr contents in flood season are lower and less fluctuated than that in dry season, whereas the divergence between up and downstream becomes larger. 87Sr/86Sr ranges 0.7100-0.7597, slightly higher than global average. Elemental molar ratio analysis partly corroborates the inference from correlation analysis, but 87Sr/86Sr does not correlate with Na/Ca, indicating additional influence except for the weathering of evaporites and silicates. Comparing to regional wastewater and rainwater, the lower reaches exhibits superimposed impact of agricultural inputs on weathering to dissolved loads, especially in downstream with more tributary convergence. Extreme rainfall during flood season and extensive agricultural production activities may interfere in altering riverine solutes. Silicate weathering rate and CO2 consumption rate are calculated as well as the yearly 87Sr in excess to the Mekong River and finally to the Pacific Ocean with a Sr flux of 1.98 × 103 tons/year, indicating significant influence on seawater strontium isotope evolution in the long run. Together with tropical climate and high-intensity precipitation, the accelerated chemical weathering process seems inevitable. Therefore, the impact of agricultural interference in the pan-Mekong River basin needs more systematic and multi-angle research to provide a comprehensive insight on better watershed management under tropical climatic conditions.

Vertical Distribution and Controlling Factors Exploration of Sc, V, Co, Ni, Mo and Ba in Six Soil Profiles of The Mun River Basin, Northeast Thailand.

Exploring the enrichment and controlling factors of heavy metals in soils is essential because heavy metals can cause severe soil contamination and threaten human health when they are excessively enriched in soils. Soil samples (total 103) from six soil profiles (T1 to T6) in the Mun River Basin, Northeast Thailand, were collected for the analyses of the content of heavy metals, including Sc, V, Co, Ni, Mo, Ba. The average contents of soil heavy metals decrease in the following order: Ba, V, Ni, Sc, Co, and Mo (T1, T3, T4 and T5); Ni, V, Ba, Co, Sc, Mo, and Ba (T2); Ba, V, Sc, Ni, Mo, and Co (T6). An enrichment factor (EF) and geoaccumulation index were calculated to assess the degree of heavy metal contamination in the soils. The EFs of these heavy metals in most samples range from 0 to 1.5, which reveals that most heavy metals are slightly enriched. Geoaccumulation indexes show that only the topsoil of T1 and T2 is slightly contaminated by Ba, Sc, Ni, and V. Soil organic carbon (SOC), soil pH and soil texture are significantly positively correlated with most heavy metals, except for a negative correlation between soil pH and Mo content. In conclusion, the influence of heavy metals on soils in the study area is slight and SOC, soil pH, soil texture dominate the behavior of heavy metals.

Occurrence of phthalate esters in the eastern coast of Thailand.

In this work, we investigated possible contamination of phthalates in seawater and sediment around the eastern coast of Thailand in the area of Chonburi, Rayong, and Chanthaburi. The main focus was on Pradu Bay east of Map Ta Phut, a well-known industrial and economic hub in Thailand. Among six selected phthalates of interest, diethyl phthalate (DEP), and benzyl butyl phthalate (BBP) were not found in any sample, while the concentrations of dimethyl phthalate (DMP) and dioctyl phthalate (DnOP) were very low or undetectable in most samples. In December 2014, the concentration of dibutyl phthalate (DBP) and diethylhexyl phthalate (DEHP) in Pradu Bay were 0.23-0.77 and 0.31-0.91 µg L-1 in seawater, respectively and non-detected (ND)-0.80 and ND-1.65 µg g-1 for 11 out of 20 sediment samples. DBP and DEHP were considered as the predominant congeners. A surface mapping system provided us an overview concentration distribution of DBP and DEHP congeners in seawater and sediment in Pradu Bay, showing a correlation between water and sediment and allowing a prediction of a possible point source. A comparison with the EU standard concentration limit in surface water confirmed that the phthalate concentration in this area was acceptable. However, continuous monitoring of phthalate congeners in the matrices should be done to detect a possible increase in their concentrations. To the best of our knowledge, this is the first study to determine concentrations of phthalates in seawater and sediment along the east coast of Thailand.

High-Throughput and Low-Cost Analysis of Trace Volatile Phthalates in Seafood by Online Coupling of Monolithic Capillary Adsorbent with GC-MS.

A simple, sensitive, and high-throughput method was developed for the determination of six volatile phthalate esters-dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), benzylbutyl phthalate (BBP), di(2-ethylhexyl) phthalate (DEHP), and di-n-octyl phthalate (DnOP)-in seafood samples by using monolith adsorbent in a capillary coupled to a gas chromatography-mass spectrometry (GC-MS) system. The freeze-dried samples were subjected to an ultrasonication with hexane, followed by vortex mixing. The liquid extract was quantitatively determined by a direct application to an online silica monolith capillary adsorbent coupled with a gas chromatograph with mass spectrometric detection. Method validation in seafood matrix gave recoveries of 72.8-85.4% and a detection limit of 6.8-10.0 ng g(-1) for bivalve samples. Reusability of the monolith capillary for trapping coextracted matrix was up to six times, allowing high-throughput analysis at the parts per billion level. When compared with the Food and Environment Research Agency (FERA) method, no significant difference in the result was observed, confirming the method was valid and applicable for the routine analysis of phthalates in seafood samples for food and environmental laboratories.