Humic-like substances (HULIS) are complex mixtures that are highly associated with brown carbon (BrC) and are important components of biomass burning (BB) emissions. In this study, we investigated the light absorption, emission factors (EFs), and amounts of HULIS emitted from the simulated burning of 27 types of regionally important rainforest biomass in Southeast Asia. We observed that HULIS had a high mass absorption efficiency at 365 nm (MAE₃₆₅), with an average value of 2.6 ± 0.83 m² g⁻¹ C. HULIS emitted from BB accounted for 65% ± 13% of the amount of water-soluble organic carbon (WSOC) and 85% ± 10% of the light absorption of WSOC at 365 nm. The EFs of HULIS from BB averaged 2.3 ± 2.1 g kg⁻¹ fuel, and the burning of the four vegetation subtypes (herbaceous plants, shrubs, evergreen trees, and deciduous trees) exhibited different characteristics. The differences in EFs among the subtypes were likely due to differences in lignin content in the vegetation, the burning conditions, or other factors. The light absorption characteristics of HULIS were strongly associated with the EFs. The annual emissions (minimum–maximum) of HULIS from BB in this region in 2016 were 200–371 Gg. Furthermore, the emissions from January to April accounted for 99% of the total annual emissions of HULIS, which is likely the result of the burning activities during this season. The most significant emission regions were Cambodia, Burma, Thailand, and Laos. This study, which evaluated emissions of HULIS by simulating open BB, contributes to a better understanding of the light-absorbing properties and regional budgets of BrC in this region.

During the Vietnam War, the United States military sprayed over 74 million litres of Agent Orange (AO) to destroy forest cover as a counterinsurgency tactic in Vietnam, Laos and Cambodia. The main ingredient was contaminated by 2,3,7,8-tetrachlorodibenzo-paradioxin (TCDD). DNA methylation (DNAm) differences are potential biomarker of environmental toxicants exposure. The aim of this study was to perform a preliminary investigation of the DNAm levels from peripheral blood of the present-day Vietnamese population, including individuals whose parents, according to historical data, were exposed to AO/TCDD during the war. 94 individuals from heavily sprayed areas (cases) and 94 individuals from non-sprayed areas (controls) were studied, and historical data on alleged exposure of parents collected. 94 cases were analysed considering those whose father/parents participated in the war (N = 29) and considering the place of residence of both parents (64 living in sprayed areas versus 30 in non-contaminated areas). DNAm levels in CYP1A1 and IGF2 genes were measured (MALDI-TOF technology). The analyses showed that: 1) one CpG site in the CYP1A1 and one in the IGF2 gene showed significant differences in DNAm levels between cases and controls; 2) the CYP1A1 region resulted to be hypomethylated (in 9 out of 16 sites/units; p-val<0.01) in 29 individuals whose father/parents participated in the war in the spray zones; 3) we showed that the place of residence of both parents influenced methylation levels of the CYP1A1 and IGF2 genes (p-val<0.05). In conclusion this study indicates that past environmental exposure to dioxin (AO/TCDD) shapes the DNAm profile of CYP1A1 and that the place of living for parents in former spray zones influences DNAm of CYP1A1 and IGF2 genes. These results open the way to new applications of DNAm as potential biomarker(s) of past human exposure to dioxin.

Arsenic and other trace element concentrations were determined for tube-well water collected in the Lao PDR provinces of Attapeu, Bolikhamxai, Champasak, Savannakhet, Saravane, and Vientiane. Water samples, especially from floodplain areas of central and southern Laos, were significantly contaminated not only with As, but with B, Ba, Mn, U, and Fe as well. Total As concentrations ranged from <0.5μgL⁻¹ to 278μgL⁻¹, with over half exceeding the WHO guideline of 10μgL⁻¹. 46% of samples, notably, were dominated by As(III). Samples from Vientiane, further north, were all acceptable except on pH, which was below drinking water limits. A principal component analysis found associations between general water characteristics, As, and other trace elements. Causes of elevated As concentrations in Lao tube wells were considered similar to those in other Mekong River countries, particularly Cambodia and Vietnam, where young alluvial aquifers give rise to reducing conditions.

The potential arsenite bioteansformation activity of arsenic was investigated by examining bacterial arsenic arsenite-oxidizing gene such as aoxS, aoxR, aoxA, aoxB, aoxC, and aoxD in high arsenic-contaminated drinking water produced from the surface water of floating houses. There is a biogeochemical cycle of activity involving arsenite oxidase aox system and the ars (arsenic resistance system) gene operon and aoxR leader gene activity in Alcaligenes faecalis SRR-11 and aoxS leader gene activity in Achromobacter xylosoxidans TSL-66. Batch experiments showed that SRR-11 and TSL-66 completely oxidized 1 mM of As (III) to As (V) within 35–40 h. The leaders of aoxS and aoxR are important for gene activity, and their effects in arsenic bioremediation and mobility in natural water has a significant ecological role because it allows arsenite oxidase in bacteria to control the biogeochemical cycle of arsenic-contaminated drinking water produced from surface water of floating houses.

We investigated total daily intake of As by residents in Prey Veng province in the Mekong River basin of Cambodia. Groundwater (n = 11), rice (n = 11) and fingernail (n = 23) samples were randomly collected from the households and analyzed for total As by inductively coupled plasma mass spectrometry. Calculation indicated that daily dose of inorganic As was greater than the lower limits on the benchmark dose for a 0.5% increased incidence of lung cancer (BMDL0.5 equals to 3.0 μg d−1 kg−1body wt.). Moreover, positive correlation between As in fingernail and daily dose of As from groundwater and rice and total daily dose of As were found. These results suggest that the Prey Veng residents are exposed to As in groundwater. As in rice is an additional source which is attributable to high As accumulation in human bodies in the Mekong River basin of Cambodia.

We investigated the potential contamination of trace elements in shallow Cambodian groundwater. Groundwater and hair samples were collected from three provinces in the Mekong River basin of Cambodia and analyzed by ICP-MS. Groundwater from Kandal (n = 46) and Kraite (n = 12) were enriched in As, Mn, Ba and Fe whereas none of tube wells in Kampong Cham (n = 18) had trace elements higher than Cambodian permissible limits. Risk computations indicated that 98.7% and 12.4% of residents in the study areas of Kandal (n = 297) and Kratie (n = 89) were at risk of non-carcinogenic effects from exposure to multiple elements, yet none were at risk in Kampong Cham (n = 184). Arsenic contributed 99.5%, 60.3% and 84.2% of the aggregate risk in Kandal, Kratie and Kampong Cham, respectively. Sustainable and appropriate treatment technologies must therefore be implemented in order for Cambodian groundwater to be used as potable water.

The grain size and heavy metals (Cu, Pb, Zn, Cr, Cd, and Hg) in 42 seafloor and eight river sediments from the Kompong Som Bay of Cambodia were analyzed to identify sediment characteristics and environmental quality. The high-value areas for all the metals were mainly distributed in the northern and central parts of the bay, occupied by fine-grained sediments. There was slightly to moderately severe enrichment of Pb, Cd, and Hg in the southern and western coastal areas of Sihanoukville. Although the current ecological environment risk was relatively low, the coastal areas of Sihanoukville had low to moderate pollution of Pb, Cd, and Hg, which were closely related to pollutant emissions from the industrial production from power plants and oil refineries. It is recommended to establish a normalized monitoring mechanism and control the discharge of coastal pollutants to ensure the sustainable development of the coastal environment.

Climate Change solutions include CO₂ extraction from atmosphere and water with burial by living habitats in sediment/soil. Nowhere on the planet are blue carbon plants which carry out massive carbon extraction and permanent burial more intensely concentrated than in SE Asia. For the first time we make a national and total inventory of data to date for “blue carbon” buried from mangroves and seagrass and delineate the constraints. For an area across Southeast Asia of approximately 12,000,000 km², supporting mangrove forests (5,116,032 ha) and seagrass meadows (6,744,529 ha), we analyzed the region's current blue carbon stocks. This estimate was achieved by integrating the sum of estuarine in situ carbon stock measurements with the extent of mangroves and seagrass across each nation, then summed for the region. We found that mangroves ecosystems regionally supported the greater amount of organic carbon (3095.19Tg Cₒᵣg in 1st meter) over that of seagrass (1683.97 Tg Cₒᵣg in 1st meter), with corresponding stock densities ranging from 15 to 2205 Mg ha⁻¹ and 31.3 to 2450 Mg ha⁻¹ respectively, a likely underestimate for entire carbon including sediment depths. The largest carbon stocks are found within Indonesia, followed by the Philippines, Papua New Guinea, Myanmar, Malaysia, Thailand, Tropical China, Viet-Nam, and Cambodia. Compared to the blue carbon hotspot of tropical/subtropical Gulf of Mexico's total carbon stock (480.48 Tg Corg), Southeast Asia's greater mangrove–seagrass stock density appears a more intense Blue Carbon hotspot (4778.66 Tg Corg). All regional Southeast Asian nation states should assist in superior preservation and habitat restoration plus similar measures in the USA & Mexico for the Gulf of Mexico, as apparently these form two of the largest tropical carbon sinks within coastal waters. We hypothesize it is SE Asia's regionally unique oceanic–geologic conditions, placed squarely within the tropics, which are largely responsible for this blue carbon hotspot, that is, consistently high ambient light levels and year-long warm temperatures, together with consistently strong inflow of dissolved carbon dioxide and upwelling of nutrients across the shallow geological plates.

Polybrominated diphenyl ethers (PBDEs) were measured in surface sediment samples collected from urban canals or rivers in Lao PDR, Cambodia, Vietnam, India, Indonesia, Thailand, the Philippines, Malaysia and Japan. The total PBDE concentrations in the sediments ranged from 0.83 to 3140ng/g dry wt. BDE-209 was predominant, ranging from 43% to 97% of total PBDEs, followed by nona-BDEs and some detectable concentrations of BDEs 47, 49, 99, 100, 153, 154 and 183. Sedimentary PBDE levels in Malaysia, Cambodia, the Philippines and Thailand were generally higher than those reported for highly industrialized countries. Spatial distribution of PBDEs indicated that inland sources may impact coastal areas. The presence of BDE congeners which are not contained in technical mixtures and the higher proportions of nona-BDEs relative to BDE-209 in the sediments were identified as indicators of debromination. BDE-209 was possibly debrominated under anaerobic conditions in some of the sediment samples.

We analyzed 68 green and blue mussels collected from Cambodia, China, Hong Kong, India, Indonesia, Japan, Korea, Malaysia, Philippines, Vietnam and the USA during 2003 and 2007, to elucidate the occurrence and widespread distributions of emerging pollutants, synthetic musks and benzotriazole UV stabilizers (BUVSs) in Asia–Pacific coastal waters. Synthetic musks and BUVSs were detected in mussels from all countries, suggesting their ubiquitous contamination and widespread distribution. High concentrations of musks and BUVSs were detected in mussels from Japan and Korea, where the levels were comparable or greater than those of PCBs, DDTs and PBDEs. Significant correlations were found between the concentrations of HHCB and AHTN, and also between the concentrations of UV-327 and UV-328, which suggest similar sources and compositions of these compounds in commercial and industrial products. To our knowledge, this is the first study of large-scale monitoring of synthetic musks and BUVSs in Asia–Pacific coastal waters.