A study to determine the impact of leachate from operating and closed landfills into the surface water and groundwater systems in the state of Selangor was conducted in the year 2009. Groundwater was a major source of water for various uses in Selangor, Malaysia and was especially important for industrial purposes. The presence of high numbers of landfill sites was seen to have increased the risk of groundwater contamination. There were 20 landfill sites in the state of Selangor and seven of them were still operating and 13 closed. The landfills are classified into four categories, which were: (a) landfills operating at critical stages without controls to prevent pollution into the environment; (b) open dumpsites that have the capacity to continue to accept waste but needed to be upgraded to manage leachate and gas; (c) landfills that were closed but no safety closure plan was carried out; and (d) engineered landfills with up to date technologies. As most of the landfills were built prior to 1989, they were not subjected to the Environmental Impact Assessment requirements, hence, they were being poorly managed and were badly sited. The non-engineered sites had no proper pollution controls such as cover materials, liner materials, groundwater monitoring wells, leachate collection ponds and treatment, and methane gas collection pipes. This study revealed that the surface water and groundwater at and nearby the landfill sites were contaminated at various levels due to the landfill sites and operation. A comparison between the current quality of surface water and groundwater with their respective standards and background levels was carried out to survey the trend of the contamination. However, the limited financial resources hindered a very thorough investigation and restricted the number of samples collected and parameters analysed.
Near-shore surface sediment was collected from five stations off Redang Island located on the eastern coast of Peninsular Malaysia. Freeze-dried sediments were Soxhlet extracted and then fractionated using column chromatography into aliphatic and polar fractions. Determination of these fractions was carried out using gas chromatography mass spectrometry. The concentration of total resolved aliphatic hydrocarbons in sediments ranged from 157 to 308 ng/g. The distribution of aliphatic fraction showed the presence of n-alkanes ranging from nC15 to nC33 with a minor odd-to-even predominance exhibiting carbon maximum, depending on station, at nC17, nC26, nC29 or nC31. Calculation of Carbon Preference Index (CPI) for CPI(15-33) gave values ranging from 1.09 to 1.46. n-Alkanol in all sediment exhibits even-to-odd carbon predominance ranging from nC16 to nC28 and maximising at nC22. n-Fatty acids distribution ranged from nC14 to nC24 with a dominant maximum at nC16 and exhibiting high values of short chain fatty acids (≤nC20) to long chain fatty acids (>nC20) ratios. Unsaturated fatty acids, particularly nC16:1 and nC18:1 is also ubiquitous in all samples. Cholesterol is the most abundant compound amongst the sterol group ranging from 42.8 to 62.6% of the total sterols. β-Sitosterol, brassicasterol and stigmasterol, are also present but of relatively lower amount. These observations suggest that the aliphatic lipids and sterols in the study area originate, mainly, from biogenic sources of marine microbial with minor contribution from epiticular waxes of terrestrial plants.
The distribution of total petrogenic hydrocarbon was investigated in the subsurface water of Setiu Wetland from July to October 2008. The concentration was quantified by UV-fluorescence spectroscopy and ranged from 4 to 121 μg/L (mean 60 ± 41 μg/L). Higher total petrogenic hydrocarbon concentrations were found in area with high boating activities suggesting that the contribution is likely related to fossil fuel combustion. The present study also revealed that the total petrogenic hydrocarbon values are still lower that those reported in Malaysian coastal waters.
This study was conducted to determine the composition and source apportionment of surfactant in atmospheric aerosols around urban and semi-urban areas in Malaysia based on ionic compositions. Colorimetric analysis was undertaken to determine the concentrations of anionic surfactants as Methylene Blue Active Substances (MBAS) and cationic surfactants as Disulphine Blue Active Substances (DBAS) using a UV spectrophotometer. Ionic compositions were determined using ion chromatography for cations (Na(+), NH4(+), K(+), Mg(2+), Ca(2+)) and anions (F(-), Cl(-), NO3(-), SO4(2-)). Principle component analysis (PCA) combined with multiple linear regression (MLR) were used to identify the source apportionment of MBAS and DBAS. Results indicated that the concentrations of surfactants at both sampling sites were dominated by MBAS rather than DBAS especially in fine mode aerosols during the southwest monsoon. Three main sources of surfactants were identified from PCA-MLR analysis for MBAS in fine mode samples particularly in Kuala Lumpur, dominated by motor vehicles, followed by soil/road dust and sea spray. Besides, for MBAS in coarse mode, biomass burning/sea spray were the dominant source followed by motor vehicles/road dust and building material.
This study investigates the presence and distribution of organochlorine pesticides in streams and the lake in the Sembrong Lake Basin in Malaysia. The catchment of Sembrong Lake has been converted to agricultural areas over the past 30 years, with oil palm plantations and modern agricultural farming being the main land use. Surface water samples were collected from eight sites comprising the stream and lake and analysed for 19 organochlorine pesticides (OCPs). In situ measurement of temperature, dissolved oxygen, pH and conductivity were also undertaken at each site. Aldrin, endrin, δ-BHC, 4,4-DDT, methoxychlor and endosulfan were the main OCPs detected in the lake basin. The total OCP concentration ranged between 5.42 and 349.2 ng/L. The most frequently detected OCPs were δ-BHC, heptachlor and aldrin. The maximum values detected were 23.0, 43.2 and 50.4 ng/L respectively. The highest concentration of OCPs was attributed to 4,4-DDT, but such high residue was rare and only detected once. Other OCP residues were low. Significant differences in the mean values were observed between lake and stream for dichlorodiphenyldichloroethylene (DDE) and α-endosulfan concentration (p
One of the molecular chemical markers used to identify anthropogenic inputs is linear alkylbenzenes (LABs) that cause serious impacts in the bays and coastal ecosystems. The surface sediments samples collected from the East Malaysia, including Brunei bay to estimate the LABs concentration and distribution as molecular markers of anthropogenic indicators. Gas chromatography-mass spectrometry (GC-MS) was used after purification, fractionation the hydrocarbons in the sediment samples to identify the sources of LABs. The analysis of variance (ANOVA) and Pearson correlation coefficient were applied to analyze the difference between sampling stations' significance at p S, homologs C13/C12, and internal to external (I/E) congeners have used to assess the LABs degradation rates as well as the effectiveness of sewage treatment. Results of this study showed that the LABs concentration ranged between 7.1 to 41.3 ng g-1 dw, in the investigated stations. The majority of sample sites exhibited a considerable input of C13-LABs homologs, and LABs homologs differed significantly. The estimated LABs ratios (I/E), which ranged between 0.6 and 2.2, demonstrated the effluents with primary and less secondary sources are released into the bay waters. The degradation of LABs were up to 42% in the interrogated locations. The conclusion is that the wastewater treatment system needs to be improved, and that LABs molecular markers are highly effective in tracing anthropogenic sewage contamination.
Influences of river hydrodynamic behaviours on hydrochemistry (salinity, pH, dissolved oxygen saturations and dissolved phosphorus) were evaluated through high spatial and temporal resolution study of a sandbar-regulated coastal river. River hydrodynamic during sandbar-closed event was characterized by minor dependency on tidal fluctuations, very gradual increase of water level and continual low flow velocity. These hydrodynamic behaviours established a hydrochemistry equilibrium, in which water properties generally were characterized by virtual absence of horizontal gradients while vertical stratifications were significant. In addition, the river was in high trophic status as algae blooms were visible. Conversely, river hydrodynamic in sandbar-opened event was tidal-controlled and showed higher flow velocity. Horizontal gradients of water properties became significant while vertically more homogenised and with lower trophic status. In essence, this study reveals that estuarine sandbar directly regulates river hydrodynamic behaviours which in turn influences river hydrochemistry.
This paper presents a preliminary result carried out in the Besut River basin, Terengganu, Malaysia to determine the selected trace metal concentrations. Concentrations of dissolved Pb, Cu, and Fe during the present study were in the range of 3.3-8.3 microg/L Pb, 0.1-0.3 microg/L Cu, and 1.1-12.3 microg/L Fe. For the particulate fraction concentrations of Pb, Cu, and Fe ranged from 1.0 to 3.6 microg/L, 0.3 to 2.8 microg/L, and 114 to 1,537 microg/L, respectively. The concentrations of metals in this study area, in general, were lower than those reported for other study areas. Higher metal concentrations measured in the wet monsoon season suggest that the input was mainly due to terrestrial runoff.
Analytical study of the influence of both the pumping well discharge rate and pumping time on contaminant transport and attenuation is significant for hydrological and environmental science applications. This article provides an analytical solution for investigating the influence of both pumping time and travelling time together for one-dimensional contaminant transport in riverbank filtration systems by using the Green's function approach. The basic aim of the model is to understand how the pumping time and pumping rate, which control the travelling time, can affect the contaminant concentration in riverbank filtration systems. Results of analytical solutions are compared with the results obtained using a MODFLOW numerical model. Graphically, it is found that both analytical and numerical solutions have almost the same behaviour. Additionally, the graphs indicate that any increase in the pumping rate or simulation pumping time should increase the contamination in groundwater. The results from the proposed analytical model are well matched with the data collected from a riverbank filtration site in France. After this validation, the model is then applied to the first pilot project of a riverbank filtration system conducted in Malaysia. Sensitivity analysis results highlight the importance of degradation rates of contaminants on groundwater quality, for which higher utilization rates lead to the faster consumption of pollutants.
The distribution of aliphatic hydrocarbons in three sediment cores from Brunei Bay was investigated in order to understand their sources and the biogeochemical processes of these hydrocarbons. The total concentrations of C15 to C37n-alkanes ranged from 0.70 to 16.5 μg g-1. Traces of hopanes with C29-C31 carbon homologs were detected in the study area. The carbon preference index (CPI15-37) ranged from 1.23 to 3.42 coupled with the natural n-alkane ratio (NAR19-32) ratios (1.52 to 5.34), and the presence of unresolved complex mixtures and hopanes, suggested slight contamination by anthropogenic hydrocarbons, presumably derived from activities along the coasts. The presence of C27 trisnorhopene and diploptene, as well as their association with long-chain and short-chain n-alkanes, revealed a depositional environment of organic matter in the sediment cores.
The objective of this study was to identify the spatial and temporal variabilities of selected nutrients in the Setiu Wetlands Lagoon (SWL), Malaysia. Water samples were collected quarterly at ten monitoring sites. This study presents results from a 10-year field investigation (2003 to 2010 and 2014 to 2015) of water quality in the SWL. For the spatial pattern, four clusters were identified with hierarchical cluster analysis. Analysis of the temporal trend shows that the high total suspended solid loading in 2010 was due to large-scale land clearing upstream of the SWL. The enrichment of ammonium after 2010 could plausibly be due to land-based aquaculture diffuse discharges. In 2005-2007, expansion of oil palm plantations within the Setiu catchment had doubled the phosphorus concentration in the SWL. The natural and anthropogenic alterations of the lagoon inlets profoundly influenced the spatial distribution patterns of nutrients in the SWL. These results suggest that intense anthropogenic disturbances close to the SWL accounted for the water quality deterioration.
This study determines the bulk surface water (BSW) dissolved inorganic nutrients of nitrogen (DINi) and phosphate (DIP) during the upwelling season off the east coast of Peninsular Malaysia, South China Sea. BSW samples were analysed for DINi and DIP by using a standard automated colorimetric method. BSW DINi and DIP concentrations varied between 0.11 and 2.55 μM (mean 1.12 ± 0.63 μM), and below detection limit, and 0.29 μM (mean 0.11 ± 0.08 μM), respectively. The spatial distribution of higher concentrations between DINi and DIP was distinct. However, the highest concentrations of DINi and DIP were mostly recorded in the month of peak upwelling (July and August), where colder BSW temperatures were also encountered during field sampling. This study provides new evidence on the presence of BSW nutrients of DINi and DIP during upwelling season peak in July and August before their decline in September.
The spatial and temporal distributions of trace metals in dissolved forms mainly result from anthropogenic and lithogenic contributions. Surface water samples (∼0.5 m) were collected monthly at respective stations from Setiu Wetland. In this study, the behaviour of trace metals in the dissolved phases along the water column from sampling sites in the Setiu Wetland, Malaysia was investigated. In addition, dissolved organic carbon (DOC) and physical parameters such as salinity, temperature, pH and dissolved oxygen (DO) of the surface water were measured in order to evaluate the relationship between trace metals fractionation with different water quality parameters. Size fractionation study of dissolved trace metals using ultrafiltration technique were also carried out and analysed using inductively coupled plasma mass spectrometry (ICP-MS). Correlation of trace metals with other measured parameters was made to furthermore understand the dynamics of trace metals and its fractionated components in this area. The concentration of dissolved trace metals was in the range of 0.001-0.16 μg/L for Cd, 0.12-2.81 μg/L for Cu, 0.01-1.84 μg/L for Pb, 3-17 μg/L for Fe and 1-34 μg/L for Zn, suggesting the input of anthropogenic sources for trace metals such as municipal, industrial, agricultural and domestic discharge. The periodic monitoring and evaluation of trace metals in wetlands and protected tropical areas is highly recommended.
Terrestrial anionic surfactants (AS) enter the marine environment through coastal region. Despite that, in general limited knowledge is available on the coastal AS transfer pathway. This paper aims to assess the distributions and exchange of AS in the Peninsular Malaysia coastal environments, adjacent to the southern waters of South China Sea and Strait of Malacca. An assessment case study was conducted by a review on the available data from the workgroup that span between the year 2008 and 2019. The findings showed that AS dominated in the sea surface microlayer (SML, 57%) compared to subsurface water (SSW, 43 %). AS were also found to have dominated in fine mode (FM, 71 %) compared to coarse mode (CM, 29 %) atmospheric aerosols. SML AS correspond to the SSW AS (p < 0.01); however, highest enrichment factor (EF) of the SML AS was not consistent with highest SSW AS. Direct AS exchange between SML and FM and CM was not observed. Furthermore, the paper concludes AS mainly located in the SML and FM and could potentially be the main transfer pathway in the coastal environment.
A study has been conducted to determine the composition of surfactants in runoff water in the semi-urban area of Bandar Baru Bangi, Selangor, Malaysia. Runoff samples were collected from five different locations with contrasting functional activities and the colorimetric method was used to analyze the concentrations of surfactants as methylene blue active substances (MBAS) for anionic surfactants and as disulphine blue active substances (DBAS) for cationic surfactants. The results showed that the highest surfactant concentrations of MBAS and DBAS in runoff water were recorded in the samples collected at the residential area, with the concentrations of 3.192 ± 0.727 and 0.170 ± 0.028 μmol/L, respectively. Anionic surfactants as MBAS were found to dominate the concentration of surfactants in both runoff and rainwater. The concentrations of both anionic and cationic surfactants in runoff water were recorded as being higher than in rainwater.
This study aims to determine the levels of methylene blue active substances (MBAS) and ethyl violet active substances (EVAS) as anionic surfactants and of disulphine blue active substances (DBAS) as cationic surfactants in the surface microlayer (SML) around an estuarine area using colorimetric methods. The results show that the concentrations of surfactants around the estuarine area were dominated by anionic surfactants (MBAS and EVAS) with average concentrations of 0.39 and 0.51 μmol L⁻¹, respectively. There were significant between-station differences in surfactant concentrations (p<0.05) with higher concentrations found at the stations near the sea. The concentration of surfactants was higher during the rainy season than the dry season due to the influence of runoff water. Further investigation using total organic carbon (TOC) and total organic nitrogen (TON) shows that there is a significant correlation (p<0.05) between both anionic and cationic surfactants and the TON concentration.
Results from the present study in Kuala Terengganu, Malaysia indicated a significant spatial variation but generally the total suspended particulate concentrations (mean = 17.2-148 microg/m(3)) recorded were below the recommended Malaysia guideline for total suspended particulate (mean of 24-h measurement = 260 microg/m(3)). Some of the elemental composition of particulate aerosol is clearly affected by non crustal sources, e.g. vehicular emission sources. Based on correlation and enrichment analyses, the elements could be grouped into two i.e. Pb, Cd and Zn group with sources from vehicular emission (r > 0.6; enrichment factor > 10) and Al, Fe, Mn and Cr group that appears to be of crustal origin (r > 0.6; enrichment factor < 10). It can also be concluded that the mean levels of Pb (1 ng/m(3)), Cd (0.02 ng/m(3)) and Zn (2 ng/m(3)) in the study area are generally lower than other urban areas in Malaysia (Pb < 181 ng/m(3); Cd < 6 ng/m(3); Zn < 192 ng/m(3)).
This study determined the effect of monsoonal changes on the composition of atmospheric surfactants in coastal areas. The composition of anions (SO4(2-), NO3(-), Cl(-), F(-)) and the major elements (Ca, K, Mg, Na) in aerosols were used to determine the possible sources of surfactants. Surfactant compositions were determined using a colorimetric method as methylene blue active substances (MBAS) and disulphine blue active substances (DBAS). The anion and major element compositions of the aerosol samples were determined by ion chromatography (IC) and inductively coupled plasma mass spectrometry (ICP-MS), respectively. The results indicated that the concentrations of surfactant in aerosols were dominated by MBAS (34-326pmolm(-3)). Monsoonal changes were found to significantly affect the concentration of surfactants. Using principal component analysis-multiple linear regressions (PCA-MLR), major possible sources for surfactants in the aerosols were motor vehicle emissions, secondary aerosol and the combustion of biomass along with marine aerosol.
Heavy metal pollution in an aquatic environment has become of the main concern to the world due to their non-biodegradable properties, toxicity, persistence, and their ability to adsorb into food chains. With rapid industrialization and development nowadays, heavy metals are introduced continuously into the estuaries and coastal region through rivers, runoff, and land-based point sources. These heavy metals may degrade the aquatic environment and harm the living organisms and toward human indirection through secondary contact. The dataset provided is to give an overview of the spatial and temporal distribution of the heavy metals concentration in Merang River surficial sediment collected from September 2017 to July 2018, subsequently every two months dataset. Sediment samples were collected in 44 stations along the river and 20 stations in the coastal area, which total up to 64 stations. Teflon Bomb closed digestion method with mixed acid was used to digest the sediments. The concentration of heavy metals in the sediment were analysed by using Inductively Coupled Plasma Mass Spectrometer (ICP-MS). The spatial distribution of heavy metals shows the effect of monsoon and wet and dry seasons in the sampling area. Thus, this dataset reveals six months of information on natural and anthropogenic sources intrusion at the Merang River and may also help in monitoring the pollution in the area.
Seasonal variations in total mercury concentrations [Hg] and trophic transfer through the food web were assessed using stable isotopic tracers for the Setiu Wetlands, Terengganu. The [Hg] measured in surface sediments and biota varied inversely between wet and dry seasons. Increased rainfall and water disturbance during the wet season are suggested as the main factors releasing Hg from surface sediments and enhancing the bioavailability of Hg to biota. The elevated Hg levels associated with the leaf stage suggested that litterfall and atmospheric deposition may be the main Hg inputs into mangrove food webs. The positive relationships between log [Hg] and δ15N provided evidence for Hg biomagnification, however low trophic magnification slopes in both seasons indicated that the ecological risk of Hg in the wetland would be negligible. The [Hg] in fish and commercial crabs were below the permitted limits for human consumption.