Abstract
Malaysia is a developing country in Southeast Asia, with rapid industrial and economic growth. Speedy population growth and aggressive consumerism in the past five decades have resulted in environmental pollution issues, including products containing polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs). PCBs and PBDEs are classified as persistent organic pollutants (POPs) by the Stockholm Convention due to their persistence, bioaccumulation in the environment and toxicity to humans and wildlife. These compounds are known to cause liver dysfunction, thyroid toxicity, developmental neuro-toxicity and possibly cancer. PCBs in air, mussels, pellets, seawater, fresh water, and human breast milk samples were analyzed in Malaysia, while studies on the pollution level of PBDEs in Malaysia were conducted on mussels, soils, leachate and sediment samples. PCBs in breast milk collected from Malaysia was the highest among Asian developing countries, with mean concentration of 80 ng/g lipid weight. On the other hand, the mean concentration of PCBs in mussels collected from Malaysia recorded the second lowest, with 56 ng/g and 89 ng/g lipid weight in two studies respectively. The concentrations of PBDEs in mussels taken from Malaysia fall in the range of 0.84–16 ng/g lipid weight, which is considerably low compared to 104.5 ng/g lipid weight in Philippines and 90.59 ng/g in Korea. Nevertheless, there are limited studies on these compounds in Malaysia, particularly there is no research on PBDEs in breast milk and sediment samples. This review will summarize the contamination levels of PCBs and PBDEs in different samples collected from Asian countries since 1988 until 2010 with a focus on Malaysia and will provide needed information for further research in this field.
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Keywords
- Polychlorinated biphenyls (PCBs)
- Polybrominated diphenyl ethers (PBDEs)
- Persistent organic pollutants (POPs)
- Mussel
- Human breast milk
- Sediment
- Status
- South Asia
- Malaysia
- Review
- Developing country
- Consumerism
- Economic growth
- Human health
- Ecotoxicology
- Environmental
- Contaminants
- Bioaccumulation
- Trend
- Mussel watch
- Survey
- Pellet watch
- Dumpsite
- River water
- Landfill leachates
1 Introduction
The monarchy of Malaysia consists of peninsular Malaysia, located between Singapore, Thailand and Indonesia, and states of Sabah and Sarawak on the island of Kalimantan (Borneo). Malaysia has a total landmass of 329,758 km2 and is almost as diverse as its culture (Fig. 1).
Since 1970s the leading sector of development has been a range of export orientated manufacturing industries such as textiles, electrical and electronic goods, rubber products, while Malaysia became the world’s largest producer of oil palm in the 1970s (Drabble 2001). Due to the current policy of achieving high income status by 2020 and transform Malaysia into a multi-sector economy, Malaysia is attempting to move farther up in the value-added production chain by shifting its focus on high tech industries (Central Intelligence Agency 2015). Thus, 34.7 % of the total Gross Domestic Product (GDP) generated in Malaysia in 2014 was from industrial sector, followed by agriculture and other service industries which accounted for 9.3 % and 56 % respectively. In which, the electrical and electronic contributing 35 % of country’s total exports between January to May 2015 (Department of Statistics Malaysia 2015).
Polychlorinated biphenyls (PCBs) are aromatic, synthetic chemicals with a chemical formula C12H10−nCln, where n ranges from 1 to 10 (Fig. 2). PCBs consist of 209 congeners which exhibit wide differences in their chemical characteristics and biological effects (Kannan et al. 1989). PCBs were used widely in electrical equipments like capacitors and transformers and in hydraulic fluids, heat transfer fluids, lubricants, and plasticizers. PCBs have been used commercially since 1929 (De Voogt and Brinkman 1989) but its presence in the environment was not recognized until 1966, when Jensen identified PCBs in human and wildlife samples (Jensen 1966).
PCBs are well known environmental contaminants with persistence, bioaccumulation and human health problems (Safe 1994). Approximately two million tonnes of PCBs have been produced commercially and about 10 % of which still remains in the environment today (WHO 2003). Besides, potentially toxic coplanar PCBs have been determined in humans, rats, dogs, cats, rhesus monkeys (terrestrial), finless porpoise, Dall’s porpoises, Baird’s beaked whales, striped dolphins and killer whales (marine) (Kimbrough et al. 1975; Kannan et al. 1989, 1993; Golub et al. 1991; Kannan 2000). Mono- and non-ortho coplanar PCBs that persist in the environment and in animals cause reproductive dysfunction (Barsotti et al. 1976; Golub et al. 1991; Kannan et al. 1988). The Stockholm Convention entered into force in 2004 and recommended that all equipment containing PCBs are eliminated by the year 2025 and then manage the rest with environmentally sound policies until 2028. In fact based on the Stockholm Convention website, Malaysia has only signed the Stockholm Convention but that the country has not ratified the Convention to date, therefore Malaysia has yet to develop a National Implementation Plan on POPs. Recently, the International Agency for Research on Cancer (IARC) has classified PCBs as carcinogen Group 1 (carcinogenic to humans), which further underline the significance of PCBs monitoring (IARC 2015).
Polybrominated diphenyl ethers (PBDEs) (Fig. 3) have been widely used as flame retardants (BFRs). PBDEs like PCBs are hydrophobic, lipophilic and thermally stable and are capable of bioaccumulating in food chain (Rahman et al. 2001; de Wit 2002; Kannan et al. 2005). Furthermore, the similarity between the structures of PCBs and PBDEs suggests similar toxicity to animals and humans (Ogata et al. 2009; Hong et al. 2010). The higher proportion of lower brominated PBDE congeners in the brain tissues of little brown bats compared to fat tissues indicated that lower brominated PBDE congeners could cross the blood-brain barrier more efficiently than the higher brominated PBDE congeners (Kannan et al. 2010). Studies carried out by McDonald (2002), Fowles et al. (1994), Zhou et al. (2002) and Branchi et al. (2002) show that PBDEs in humans disrupt thyroid hormones, cause neurobehavioral deficiency and possibly cause cancer. Hence in 2009, Stockholm Convention has listed commercial Penta-BDE and Octa-BDE as POPs.
Although PCBs-containing electrical equipment and other applications are not manufactured in Malaysia, they have been imported for a while until they were banned in June 1998 (Hashim 2003; Ibrahim 2007). PCBs have been used in heat exchangers and hydraulic systems while PBDEs were commonly used as flame retardants in a series of applications including textiles, television sets, plastics and wire insulation. Waste motor and transformer oils are considered as a main source of PCBs emission into the environment in Malaysia (Jahromi et al. 2014). There is still approximately 15 % of known PCBs residing in developing countries including Malaysia, mostly as a result of shipments of wastes from industrialized countries (Abel and McConnell 2009).
2 PCBs and PBDEs in E-Waste in Malaysia
Solid waste is a major environmental problem in Malaysia. In 2008, 23,000 tons of waste were produced each day in Malaysia with less than 5 % being recycled and approximately 19 % of waste being ended up in the drains, polluting the environment including PCBs and PBDEs (Wu et al. 2008; Tue et al. 2010; Desa et al. 2012).
Department of Environment (DOE) Malaysia has defined e-wastes as wastes from the used electronic and electrical (EEE) equipment such as accumulators, mercury switches, transformers, cathode-ray tubes (CRT) or PCBs-containing capacitors (DOE 2008), which are regulated in Malaysia since 2005 and listed as scheduled wastes. According to the E-waste Inventory of Malaysia, total volume of e-waste generated in 2008 was 688,000 metric tonnes and it will reach 11.2 million metric tonnes by 2020. Currently, there are 18 full recovery facilities and 128 partial recovery facilities permitted by the DOE of Malaysia for the segregation, dismantling and treatment of e-waste. Despite the law that e-waste could only be treated and recovered by the licensed facilities in Malaysia, Environmentally Sound Management (ESM) is lacking in the collection, treatment and recovery of e-waste (Suja et al. 2014).
3 PCBs in Malaysia
3.1 PCBs in Sewage Sludge
A research conducted by Ahmad et al. (2005) on palm oil and sewage sludge revealed PCB congeners such as PCB-28, 52, 101, 118, 138, 153 and 180 in oil and PCBs congeners 28, 52 and 101 in sludge, while PCBs 118, 138, 153 and 180 were not detected (3.37–70.6 ng/g). On the other hand, Halim (2007) investigated the concentrations of PCBs in sewage sludge using two types of extraction methods. The samples were extracted using supercritical fluid carbon dioxide (SFCO2) and subcritical water extraction (SWE) and PCB-28, 52, 101, 118,138, 153 and 180 were determined using GC-ECD. The concentration of PCBs in the sludge samples extracted using SFCO2 were comparatively higher (31.2–82.0 ng/g) than samples extracted using SWE (20.2–60.1 ng/g).
3.2 PCBs in Pellet
Plastic resin pellets (0.1–0.5 cm) are found on beaches around the world. A Japanese study (Ogata et al. 2009) analyzed samples of polyethylene pellets from 30 beaches in 17 countries including Malaysia to determine the concentration of organochlorine compounds. Sampling locations in Malaysia were Langkawi, Penang and Borneo and the median concentration of the sum of 13 PCB congeners (CB-66, 101, 110, 149, 118, 105, 153, 138, 128, 187, 180, 170, 206) recorded at these places were 8 ng/g-pellet, 12 ng/g-pellet and 10 ng/g-pellet, respectively (Fig. 4).
3.3 PCBs in Air
PCBs were measured in air using Polyurethane foam (PUF) passive air samplers (PAS) in Malaysia, Japan, Vietnam and the Philippines by Kwan (2014). The air samplers were deployed at six locations in these Asian countries including Malaysia (Port Dickson) during dry and wet seasons for a month. CB-66, 101, 110, 149, 118, 105, 153, 138, 128, 187, 180, 170 and 206 were measured. Result showed that the atmospheric concentration of PCBs in Malaysia (less than 5 pg/m3) was not as high as in other countries. For example, Philippines recorded a high 80 pg/m3.
3.4 PCBs in Mussels
Bivalves such as mussels are suitable bio-indicator for monitoring trace toxic contaminants in coastal waters due to their wide distribution, sessile lifestyle, easy sampling, tolerance to a considerable range of salinity, resistance to stress and high accumulation of a wide range of chemicals (Goldberg et al. 1978). A study using green mussels (Perna viridis) was conducted in Penang, Malaysia. Mussel samples were collected from six stations on the island of Penang (Weld Quay Pier, Marine Depot, Pulau Jerejak, Permatang Damar Laut, Batu Maung and Gertak Sanggul) and three more stations in Singapore waters (Selatar, Serangoon and Ponggol). The concentration of PCBs analysed in Malaysia was in the range of 99.9–599.9 ng/g on a dry weight basis (Sivalingam et al. 1982).
Besides, Monirith et al. (2003) also examined the contamination of persistent organochlorines (OCs) including PCBs in mussels collected from coastal waters of Asian countries like Cambodia, China, Hong Kong, India, Indonesia, Japan, Korea, Malaysia, Philippines, Far East Russia, Singapore, and Vietnam. The sampling locations were at different parts of Malaysia (Kuala Penyu and Trayong of Sabah, Sangkar Ikan and Tanjung Rhu of Langkawi, Butterworth and Penang Bridge of Penang, Bagan Bridge of Selangor, Lukut and Pasir Panjang of Negeri Sembilan, Tanjung Batu of Malacca and Pasir Puteh of Johor Bahru). Generally the concentration of PCBs in Malaysia was in low range from <4.2 to 60 ng/g lipid weight. However, high concentration of PCBs was found at Pasir Puteh, Johor Bahru which recorded 230 and 250 ng/g lipid weight respectively. The mean and range of PCBs concentrations from Asian countries in two studies are shown in Table 1.
Similarly, there was another study that used mussel samples, including green mussels (Perna viridis) and blue mussels (Mytilus edulis) to measure the levels of PCBs in the coastal waters of Asian countries (Ramu et al. 2007). Mussels were collected at Port Dickson, Pantai Lido, Pasir Puteh, Sebatu and Penang in Malaysia and the concentrations of PCBs analyzed in this study were in between 25 to 160 ng/g lipid weight. PCBs concentrations in mussels collected from coastal waters of Asian countries are shown in Fig. 5.
3.5 PCBs Concentration in Sediment, River Waters and Surface Seawaters
There was only one study each on the concentration of POPs including PCBs in river waters and surface seawaters by a Japanese group. It was found out that the total PCBs concentration was 0.45 ng/L in Selangor River water, and <5.0 ng/g of PCBs in the sediment samples from the same location (Iwata et al. 1994). Whereas the surface waters at the Straits of Malacca contained 0.02 ng/L of PCBs (Iwata et al. 1993), which was similar to the POP contamination levels at South China Sea.
3.6 PCBs Contamination in Fresh Water Fishes and Marine Organisms
Muhammad (2006) analyzed six species of fresh water fishes and seven species of marine organisms. All samples were collected from the northern region of peninsular Malaysia. The PCB concentrations in these fresh water samples ranged from 7.8 to 22.5 ng/g wet weight and the more toxic PCB-126 congener was detected only in the snakehead fish at very low concentration (0.03 ng/g wet weight). PCBs concentrations in marine organisms were generally lower than in the fresh water fishes. All the fish species in both categories and PCBs concentration are listed in Table 2.
3.7 PCBs in Human Breast Milk
PCBs were analyzed in human breast milk from non-smoking, healthy primipara mothers in the age group of 23–38 who were living in Penang and Kedah, Malaysia (Sudaryanto et al. 2005). Basically PCBs were detected in all the breast milk samples and the mono-ortho coplanar PCBs, were detected with an average concentration of 11 ng/g lipid weight, followed by non-ortho PCBs with concentration of 0.062 ng/g lipid weight. The same study also showed the result of average total TEQ levels to be 0.013 ng TEQs/g lipid weight. PCB levels in breast milk from Malaysia (Total PCBs with mean concentration of 80 ng/g lipid weight) were comparatively lower than developed countries, but slightly higher than other developing countries such as India, Vietnam, Cambodia and the Philippines (Fig. 6).
4 PBDEs in Malaysia
4.1 PBDEs in Mussels
The green mussels (Perna viridis) and blue mussels (Mytilus edulis) collected from various locations in Asia by Ramu et al. (2007) were studied for PBDEs. Based on their analysis, PBDEs were detected in all mussel samples indicating widespread contamination of these compounds in the coastal waters of Asian region. The level of contamination varied among sampling locations. Lower residue levels of PBDEs were found in samples from Cambodia, Vietnam, India and Malaysia in comparison to samples from Korea, Japan, Hong Kong, China and the Philippines. The total concentration of PBDEs in mussels collected from Malaysia ranged from 0.84 (at Sebatu) to 16 ng/g lipid weight (at Pasir Puteh) with relatively higher concentration of mono- to hepta-BDEs. On the other hand, the concentration of octa- to deca-BDEs in all mussel samples were below detection limit except at Pasir Puteh, where 0.19 ng/g lipid weight was detected. All these data are summarized in Table 3 (Fig. 7).
4.2 PBDEs in Soils at Municipal Waste Dumping Sites
Huge amount of municipal waste is being disposed in open dumping sites with lack of effective management or treatment in Asian developing countries. The total municipal solid waste (MSW) generation in Malaysia has increased from 5.91 million tonnes in 2001 to 6.97 million tonnes in 2005 and is expected to increase about 2.5–3 % annually due to population and economic growth (Tarmudi et al. 2009). In Malaysia particularly, landfilling is the main option of waste disposal (90–95 %) with a recycling rate of 5–10 % despite the fact that approximately 70–80 % of the waste is recyclable (Johari et al. 2014). Eguchi et al. (2013) investigated the BFR contamination of soils from municipal waste dumping sites in five Asian developing countries (India, Vietnam, Malaysia, Indonesia and Cambodia). Soil samples in Malaysia were collected from the open dumping sites at Kuala Lumpur and Penang. A total of 14 PBDE congeners from mono- to deca-BDE were detected in all soil samples and the concentration of BDE-209 is significantly higher than other PBDE congeners in most of the samples. The levels were highest in Vietnam (mean: 95 ng/g dry weight, range: 1.2–430 ng/g dry weight), followed by Indonesia, Cambodia, India, and the lowest levels were detected in Malaysia (mean: 6.2 ng/g dry weight; range: 4.6–7.8 ng/g dry weight) (Eguchi et al. 2013). Concentration of PBDEs in soil samples from waste dumping sites of Malaysia can be found in Table 4. The higher PBDE levels in municipal waste dumping sites than those reference site also suggested that municipal waste dumping sites are a potential source of PBDEs in Asian developing countries.
4.3 PBDEs in Landfill Leachates
PBDE-containing products at landfills or municipal solid waste dumping sites (MSWDS) have been identified (Rahman et al. 2001). The concentration levels of PBDEs in the landfills were generally higher than those found in rivers and coastal waters (Kwan 2014). Among eight MSWDS from tropical Asian countries, leachate samples were collected at Tamang Beringin, Kuala Lumpur once during the wet season in 2003 and twice during the dry season in 2004. Based on her findings, the concentration of PBDEs in the MSWDS leachates from tropical Asian countries in this study were higher than those reported in other countries such as Japan, South Africa, Canada, United States of America and Sweden. Particularly Thailand, Cambodia, India, Malaysia and the Philippines were the hotspots of PBDE contamination, probably because of the rapid urbanization and industrialization (Table 5).
4.4 PBDEs in Sediments
PBDEs being lipophilic with low solubility in water tend to accumulate in sediments or particulate matter, aiding their distribution further to marine biota. Many previous studies have shown the predominance of BDE-209 in sediments probably due to high production and usage of technical deca-BDE products (Eljarrat et al. 2005; Moon et al. 2007a; Tokarz et al. 2008; Toms et al. 2008; Chen et al. 2009). This statement was further substantiated by Kwan (2014), who investigated the occurrence of PBDEs in surface sediment samples from urban areas of tropical Asian countries, including Lao PDR, Cambodia, Vietnam, India, Indonesia, Thailand, the Philippines and Malaysia. According to her analysis, nearly all the sediment samples from Lao PDR, Cambodia, Vietnam, India (Mumbai), Thailand, the Philippines and Malaysia have exhibited the predominance of BDE-209. Relative to the sediment samples from Japan (with a total PBDE geometric mean concentration (GMC) of 100 ng/g dw (dry weight)), studies from Kwan (2014) indicated the lowest total PBDE GMC in Lao PDR (9.38 ng/g dw). Compared to the GMCs of total PBDEs found in Vietnam (34.2 ng/g dw), Indonesia (42.2 ng/g dw), Cambodia (58.4 ng/g dw), India (67.3 ng/g dw), Thailand (160 ng/g dw), and the Philippines (178 ng/g dw), Malaysia (Klang river) recorded a marginally higher readings than these countries with 275 ng/g dw. In addition, Kwan (2014) has also correlated concentrations of PBDEs in the aquatic environment such as sediments to the GDP per capita and the number of MSWDS; higher population and more MSWDS will result in higher concentration of PBDEs in sediments.
5 PCBs and PBDEs in Sea Turtle
Several studies have reported that persistent organic pollutants (POPs) such as PCBs and PBDEs are found in sea turtle populations. Due to the lipophilic properties of these compounds and the mobilization of lipids by sea turtle for egg production, it is likely that POPs are transferred from nesting females to eggs and hatchlings during reproduction (Kwan 1994). van de Merwe et al. (2010) have analyzed POP contamination in a nesting population of Chelonia mydas in Malaysia, and investigated the maternal transfer of these chemicals to eggs and embryos as well as their impacts on hatchling development. Eggs and blood were collected from 11 adult female Chelonia mydas nesting at the Ma’Daerah Turtle Sanctuary, Terengganu, Malaysia in 2004 and analyzed for POP concentrations. The result showed significant correlation between maternal blood and eggs, and between eggs and hatchling, in other words, these chemicals are being transferred from nesting female Chelonia mydas to eggs and hatchlings. Additionally, this study also proved that the less lipophilic congeners tend to preferentially transfer from eggs to hatchlings, while the highly lipophilic congeners stay back with the mother. In general, hatchlings are at high risk from exposure to PCBs and PBDEs (Table 6).
6 Pan Asian Comparisons
6.1 Comparison of PCBs and PBDEs Concentrations in Human Breast Milk
By comparing the concentration of total PCBs (obtained by summing up the concentration of individually resolved peaks of PCB isomers and congeners) in human breast milk samples collected from mothers residing in Malaysia (Sudaryanto et al. 2005) to other Asian countries (Kunisue et al. 2002, 2004a, b, 2006; Sudaryanto et al. 2006; Wong et al. 2013). Malaysia recorded one of the highest level of PCBs contamination with 80 ng/g lipid weight. the highest concentration of PCBs around the same sampling year was detected at Payatas, Philippines with concentration of 92.5 ng/g lipid weight in 2004. The highest PCBs contaminated human breast milk sample since the year of 1989 until 2009 was collected at Hong Kong in 1989, followed by Dong Nai in 1991 and Chennai in 1988, with concentration of 640, 353 and 110 ng/g lipid weight respectively (Table 7).
Generally, PCBs contamination gradually decreased over the years as shown by readings at Chennai and Phnom Penh, which dropped from 110 to 34 ng/g lipid weight and from 39 to 20 ng/g lipid weight. The only exception is PCBs concentration in Bangkok which increased from 15 ng/g lipid weight in 1989 to 52 ng/g lipid weight in 1991.
However, not many studies have been carried out to examine the PBDEs contamination in breast milk samples collected from Asian countries, and none has been done in Malaysia. Among all studies on PBDEs in breast milk, China recorded the highest concentration of 8.6 ng/g lipid weight and the second highest was Philippines with 7.8 ng/g lipid weight, followed by Indonesia, Japan and Vietnam.
Studies on PCBs and PBDEs concentration in breast milk samples are important because several researches proved that persistent organochlorines (OCs) compounds such as PCBs in human breast milk will be transferred to infants through breast-feeding, especially older primiparae mothers who transfer higher amounts of OCs (Kunisue et al. 2006). Besides, breast-feeding is the primary exposure route for infants, and by examining the concentration of PCBs and PBDEs in daily milk intake, the exposure risks of infants can be estimated (Ma et al. 2012) (Table 8).
6.2 Comparison of PCBs and PBDEs Concentrations in Bivalves
Basically two major studies that analyzed the concentration of PCBs and PBDEs in mussels as part of International Mussel Watch Programme between 1994 to 2001 and 2003 to 2005 from Asian coastal waters; one was reported by Monirith et al. (2003) and another by Ramu et al. (2007). The concentration of PCBs in mussels collected from Malaysia during 1998–1999 recorded the second lowest at 56 ng/g lipid weight after Cambodia with 35 ng/g lipid weight indicating low PCBs pollution. While the highest PCBs contamination was from Japan which recorded 3000 ng/g lipid weight, followed by India with 340 ng/g lipid weight. Similarly from mussels collected during 2003–2005, the highest PCBs concentration was found in Japanese samples (83–2000 ng/g lipid weight). Again, PCBs concentration in Malaysian coastal waters was low with an average concentration of <100 ng/g lipid weight in comparison to other heavily industrialised Asian countries such as China, Hong Kong, Korea, India, Philippines and Indonesia which showed high PCBs levels in the range of 61–1500 ng/g lipid weight.
The highest concentration of PBDEs was identified in mussel samples collected at Cavite province of Philippines which is an agriculture province. Other countries that showed high level of PBDEs contamination in mussels are Korea, Hong Kong and China. Previous studies pointed out that higher level of PCBs and PBDEs were recorded at urbanised or industrialized locations; areas with shipping activities (Moon et al. 2007a). Particularly untreated effluent that directly discharged into the environment from e-waste manufacturing or treatment plant and municipal waste treatment facility has been proved as the potential source that caused high levels of PCBs and PBDEs at Hong Kong and China (Zheng et al. 2004; Shi et al. 2009). A Korean study (Hong et al. 2009) highlights a growing pollution problem in Asia and in particular a tremendous uptrend in PBDEs pollution in Korea, in comparison to more controlled discharges and releases in Western Europe (Table 9).
6.3 Comparison of PCBs and PBDEs Concentrations in Sediments
Unfortunately there were limited studies on PCBs and PBDEs contamination in Malaysia. In fact, PCBs and PBDEs were widely found in both river and marine sediments due to its persistency. There were 195 ng/g dry weight of PCBs detected at Zhujiang River, China which was also the highest PCBs concentration recorded in Asian countries. This was confirmed in a research conducted by Fang (2004) at the same region (Pearl River Delta) for PCBs. The Pearl River delta region is one of the largest electronic and telecommunication manufacturing bases in China, hence lots of studies have been implemented in the area and previous results did indicate significant level of PCBs and PBDEs pollution within this region. Apart from that, sediment samples collected at canals in lower Mekong River Basin (Laos), Ho Chi Minh city canals (Vietnam) and a sewer system in Hanoi (Vietnam) showed high PCBs contamination with 111, 81 and 104 ng/g dry weight respectively.
On the other hand, exceptionally high concentration of PBDEs (285 ng/g dry weight) was observed at Busan Bay, Korea which is much higher than PBDEs levels in sediments from Hong Kong with 95 ng/g dry weight. In surface sediments, the average ΣPBDEs levels approached that of average ΣPCBs values. However, trends observed in the sediment core suggest that this pattern will alter over time and result in higher surface sediment PBDE concentrations than PCBs in future (Hong et al. 2010). Various diffuse and point sources for PBDEs and PCBs were identified in this location. Shipping and other industrial activities were associated with PCB contamination while domestic and industrial waste discharges corresponded with PBDE contamination. Busan Bay is the largest harbor area in Korea which comprises more than four fifth of the country’s container cargo and 42 % of the domestically produced marine products, in addition to the fact that 40 % of marine export cargo processed here (Hong et al. 2005).
Despite showing low contamination levels of PBDEs in sediment samples collected from China, concentration of BDE209 in some of these samples were extremely high. The result summarized by Mai et al. (2005) showed 12.9 ng/g dry weight of total PBDEs that consisted of BDE-28, -47, -66, -99, -100, -138, -153, -154 and -183 at Zhujiang River, while the mean concentration of BDE209 was 890 ng/g dry weight (ranged from 26.3 to 3580 ng/g dry weight). Similarly studies conducted by Shi et al. (2009) on the concentration of PBDEs in sediments from Dongjiang River, showed, for the same suite of PBDEs, a PBDEs concentration of 3.94 ng/g dry weight while the concentration of BDE209 was 1190 ng/g dry weight. The main reason for high concentration of BDE209 in Pearl River Delta was due to the manufacturing of electrical and electronic products where BDE209 is the main ingredient of BFR. Such high concentration of BDE209 in the environment poses risks and concern because it may degrade to less-brominated congeners which are more volatile and easily taken up by living organism and transferred to organisms in the higher food chain and bioaccumulate in humans. Recent studies also pointed out that BDE209 can be broken down under sunlight in sediments (Mai et al. 2005).
7 Conclusion and Recommendations
Many tropical Asian countries including Malaysia have experienced a rapid economic development and population growth during the past few decades. Industrialization and urbanization caused high waste generation and release of PCBs and PBDEs into the environment. In general, the concentrations of PCBs and PBDEs in pellets, mussels, air and soil from Malaysian samples were comparatively lower than most of neighboring Asian countries; on the other hand, their levels were high in sediment and leachate samples. Similarly, high levels PCBs were recorded in breast milk samples collected from northern Malaysia. Till now, there is no research on PBDEs in breast milk in Malaysia. Unfortunately, the samples collected in these studies were from selected locations and may not reflect the national status. The previous studies on PCBs and PBDEs contamination in Malaysia were conducted by Japanese researchers. It is surprising to note that local Malaysian universities and research institutes with analytical facilities have not generated substantial national data on these important contaminants. So far there is no nationwide study (geographical distribution) or their temporal trends in Malaysia. Additionally, the spectrum of samples were limited to bivalves, sediments, breast milk and human blood only. Other media need to be studied as well. That will provide a clearer picture of contamination status of Malaysia on a global map. Trend studies will help policymakers to amend regulations accordingly. Despite the fact that concentration of PBDEs in Malaysian air is negligible, it is still needed to be monitored. The reason is that uncontrolled waste dumping occurs in southern hemisphere countries from industrialized countries and global transboundary pollution needs to be monitored (Parolini et al. 2013). In summary, more studies are needed to fully understand POPs contamination status, their transport pathways, sources and their biological impacts on developing nations in Asia, with the emphasis of further researches in Malaysia.
8 Summary
Ever since PCBs and PBDEs were listed as persistent organic pollutant by Stockholm Convention, there are many studies around the world to study these compounds as well as their effects to human health and the environment. Despite the fact that PCBs-containing products being banned in many countries, old equipments that contain PCBs or PBDEs are still being used, especially in South Asian countries. Thus POPs will be released unintentionally into the environment from stockpiles or from waste treatment facilities or from E-waste treatment facility or area with high shipping activities. Owing to the limited research being conducted in Malaysia, the comparison of PCBs and PBDEs pollutions between Malaysia and other Asian countries were mainly focusing on mussels and human breast milk samples. PCBs in breast milk that was collected from Malaysia was the highest among Asian developing countries, while the mean concentration of PCBs in mussels in Malaysia recorded the second lowest. The concentrations of PBDEs in mussels taken from Malaysia was much lower if compared to the high concentration detected at Philippines and Korea. All in all, continual monitoring of these POPs by Malaysian researchers is needed in order to meet the target set by Stockholm Convention and assure the elimination of such compounds from the environment within the time frame.
References
Abel DC, McConnell RL (2009) Environmental oceanography: topics and analysis. Jones & Bartlett Publishers, Sudbury
Ahmad UK, Ujang Z, Zamani A, Halim A (2005) Determination of polychlorinated biphenyls in oils and sewage sludge. Malaysian J Anal Sci 9(2):280–283
Akutsu K, Kitagawa M, Nakazawa H, Makino T, Iwazaki K, Oda H, Hori S (2003) Time-trend (1973–2000) of polybrominated diphenyl ethers in Japanese mother’s milk. Chemosphere 53(6):645–654
Barsotti DA, Marlar RJ, Allen JR (1976) Reproductive dysfunction in rhesus monkeys exposed to low levels of polychlorinated biphenyls (Aroclor 1248). Food Cosmet Toxicol 14(2):99–103
Bayen S, Thomas GO, Lee HK, Obbard JP (2003) Occurrence of polychlorinated biphenyls and polybrominated diphenyl ethers in green mussels (Perna viridis) from Singapore, Southeast Asia. Environ Toxicol Chem 22(10):2432–2437
Bayen S, Wurl O, Karuppiah S, Sivasothi N, Lee HK, Obbard JP (2005) Persistent organic pollutants in mangrove food webs in Singapore. Chemosphere 61(3):303–313
Binelli A, Sarkar SK, Chatterjee M, Riva C, Parolini M, Bhattacharya BD, Bhattacharya AK, Satpathy KK (2007) Concentration of polybrominated diphenyl ethers (PBDEs) in sediment cores of Sundarban mangrove wetland, northeastern part of Bay of Bengal (India). Mar Pollut Bull 54(8):1220–1229
Branchi I, Alleva E, Costa LG (2002) Effects of perinatal exposure to a polybrominated diphenyl ether (PBDE 99) on mouse neurobehavioral development. Neurotoxicology 23:375–384
Carvalho FP, Villeneuve JP, Cattini C, Tolosa I, Thuan DD, Nhan DD (2008) Agrochemical and polychlorobyphenyl (PCB) residues in the Mekong River delta, Vietnam. Mar Pollut Bull 56(8):1476–1485
Central Intelligence Agency (2015) The world factbook, East & Southeast Asia: Malaysia. https://www.cia.gov/library/publications/the-world-factbook/geos/my.html
Chen L, Huang Y, Peng X, Xu Z, Zhang S, Ren M, Ye Z, Wang X (2009) PBDEs in sediments of the Beijing River, China: levels, distribution, and influence of total organic carbon. Chemosphere 76:226–231
De Voogt P, Brinkman UAT (1989) Production, properties and usage of polychlorinated biphenyls. In: Kimbrough RA, Jensen AA (eds) Halogenated biphenyls, terphenyls, naphthalenes, dibenzodioxins and related products, 2nd edn. Elsevier, Amsterdam, pp 3–45
de Wit CA (2002) An overview of brominated flame retardants in the environment. Chemosphere 46(5):583–624
Department of Environment (DOE) (2008) Guidelines for the classification of used electrical and electronic equipment in Malaysia. http://www.meti.go.jp/policy/recycle/main/admin_info/law/10/pdf/malaysia_eng.pdf
Department of Statistics Malaysia (2015) Top 10 major export products, 2015. http://www.matrade.gov.my/en/malaysia-exporters-section/33-trade-statistics/3816-top-10-major-export-products-2015
Desa A, Kadir N, Yusooff F (2012) Waste education and awareness strategy: towards solid waste management (SWM) program at UKM. Procedia Social Behav Sci 59:47–50
Devanathan G, Subramanian A, Someya M, Sudaryanto A (2009) Persistent organochlorines in human breast milk from major metropolitan cities in India. Environ Pollut 157(1):148–154
Doong R, Lee S, Lee C, Sun Y, Wu S (2008) Characterization and composition of heavy metals and persistent organic pollutants in water and estuarine sediments from Gao-ping River, Taiwan. Mar Pollut Bull 57(6–12):846–857
Drabble JH (2001) An economic history of Malaysia, c.1800–1900: the transition to modern economic growth. Economic History Association, EH.NET
Eguchi A, Isobe T, Ramu K, Tue NM, Sudaryanto A, Devanathan G, Viet PH, Tana RS, Takahashi S, Subramanian A, Tanabe S (2013) Soil contamination by brominated flame retardants in open waste dumping sites in Asian developing countries. Chemosphere 90(9):2365–2371
Eljarrat E, De La Cal A, Larrazabal D, Fernandez-Alba AR, Borrull F, March RM, Barcelo D (2005) Occurrence of polybrominated diphenylethers, polychlorinated dibenzo-p-dioxins, dibenzofurans, biphenyls in coastal sediments from Spain. Environ Pollut 136:493–501
Fang Z (2004) Organochlorines in sediments and mussels collected from coastal sites along the Pearl River Delta, South China. J Environ Sci 16(2):321–327
Fowles JR, Fairbrother A, Baecher-Steppan L, Kerkvliet NI (1994) Immunologic and endocrine effects of the flame-retardant pentabromodiphenyl ether (DE-71) in C57BL/6J mice. Toxicology 86:49–61
Fu J, Wang Z, Mai B, Kang Y (2001) Field monitoring of toxic organic pollution in the sediments of Pearl River estuary and its tributaries. Water Sci Technol 43(2):83–89
Goldberg ED, Bowen VT, Farrington JW, Harvey G, Martin JH, Parker PL, Risebrough RW, Robertson W, Schneider E, Gamble E (1978) The mussel watch. Environ Conserv 5:101–125
Golub MS, Donald JM, Reyes JA (1991) Reproductive toxicity of commercial PCB mixtures: LOAELs and NOAELs from animal studies. Environ Health Perspect 94:245–253
Halim AA (2007) Analysis of polychlorinated biphenyls in sewage sludge using supercritical carbon dioxide and subcritical water extraction. Thesis, Faculty of Science, Universiti Teknologi Malaysia, pp 18–23
Hashim R (2003) PCBs situation in Malaysia. PCB Symposium 2003 in Malaysia. http://tabemono.info/report/former/pcd/2003/malaysia/e_1.html
Hoai PM, Ngoc NT, Minh NH, Viet PH, Berg M, Alder AC, Giger W (2010) Recent levels of organochlorine pesticides and polychlorinated biphenyls in sediments of the sewer system in Hanoi, Vietnam. Environ Pollut 158(3):913–920
Hong SH, Yim UH, Shim WJ, Oh JR (2005) Congener-specific survey for polychlorinated biphenyl in sediments of industrialized bays in Korea: regional characteristics and pollution sources. Environ Sci Tech 39:7380–7388
Hong SH, Munschy C, Kannan N, Tixier C, Tronczynski J, Héas-Moisan K, Shim WJ (2009) PCDD/F, PBDE, and nonylphenol contamination in a semi-enclosed bay (Masan Bay, South Korea) and a Mediterranean lagoon (Thau, France). Chemosphere 77:854–862
Hong SH, Kannan N, Jin Y, Won JH, Han GM, Shim WJ (2010) Temporal trend, spatial distribution and terrestrial sources of PBDEs and PCBs in Masan Bay, Korea. Mar Pollut Bull 60(10):1836–1841
Hung C, Gong G, Jiann K, Yeager KM, Santschi PH, Wade TL, Sericano JL, Hsieh H (2006) Relationship between carbonaceous materials and polychlorinated biphenyls (PCBs) in the sediments of the Danshui River and adjacent coastal areas, Taiwan. Chemosphere 65(9):1452–1461
IARC (2015) IARC monographs on the evaluation of carcinogen risks to humans. Polychlorinated and polybrominated biphenyls, Vol 107. http://monographs.iarc.fr/ENG/Monographs/vol107/mono107.pdf
Ibrahim SM (2007) Chapter 14: Persistent organic pollutants in Malaysia. In: Li A et al (eds) Development in environmental science, vol 7. Elsevier, Amsterdam, pp 629–655
Inoue K, Harada K, Takenaka K, Uehara S, Kono M, Shimizu T, Takasuga T, Senthilkumar K, Yamashita F, Koizumi A (2006) Levels and concentration ratios of polychlorinated biphenyls and polybrominated diphenyl ethers in serum and breast milk in Japanese mothers. Environ Health Perspect 114(8):1179–1185
Ip HMH, Phillips DJH (1989) Organochlorine chemicals in human breast milk in Hong Kong. Arch Environ Contam Toxicol 18(4):490–494
Isobe T, Amano A, Chang K, Maneja RH, Zamora PB, San Diego-Mcglone ML, Siringan FP, Prudente M, Miller TW, Tanabe S (2010) Retrospective assessment of environmental pollution by PBDEs and HBCDs using sediment core from Manila Bay, the Philippines. In: Isobe T, Nomiyama K, Subramanian A, Tanabe S (eds) Interdisciplinary studies on environmental chemistry—environmental specimen bank. TERRAPUB, Tokyo, pp 61–65
Iwata H, Tanabe S, Sakai N, Tatsukawa R (1993) Distribution of persistent organochlorines in the oceanic air and surface seawater and the role of ocean on their global transport and fate. Environ Sci Technol 27:1080
Iwata H, Tanabe S, Sakai N, Nishimura A, Tatsukawa R (1994) Geographical distribution of persistent organochlorines in air, water and sediments from Asia and Oceania, and their implications for global redistribution from lower latitudes. Environ Pollut 85:15
Jahromi FA, Kannan N, Zakaria MP, Aris AZ (2014) Persistent contaminants in waste oils: a short review on PCBs and PAHs as main contaminants. In: From sources to solution: Proceedings of the international conference on environmental forensic 2013. Springer, Singapore, pp 107–110
Jensen S (1966) Report of a new chemical hazard. N Scientist 32:612
Johari A, Alkali H, Hashim H, Ahmed SI, Mat R (2014) Municipal solid waste management and potential revenue from recycling in Malaysia. Modern Appl Sci 8(4)
Kannan N, Tanabe S, Tatsukawa R (1988) Toxic potential of non-ortho and mono-ortho coplanar PCBs in commercial PCB preparations: “2,3,7,8-T4 CDD toxicity equivalence factors approach”. Environ Contam Toxicol 41(2):267–276
Kannan N, Tanabe S, Ono M, Tatsukawa R (1989) Critical evaluation of polychlorinated biphenyl toxicity in terrestrial and marine mammals: increasing impact of non-ortho and mono-ortho coplanar polychlorinated biphenyls from land to ocean. Arch Environ Contam Toxicol 18:850–857
Kannan N (2000) Non-ortho and mono-ortho substituted PCBs, Chapter 6. In: Paasivirta J (ed) The handbook of environmental chemistry, vol 3, Anthropogenic compounds. Springer, Berlin, pp 127–156
Kannan N, Hong SH, Oh JR, Yim UH, Li DH, Shim WJ (2005) PYE [2-(1-pyrenyl)ethyldimethylsilylated silica] column HPLC and HR-GC-(micro) ECD in the accurate determination of toxic co-planar PCBs and polybrominated diphenyl ethers (PBDEs). Bull Korean Chem Soc 26(4):529
Kannan K, Tanabe S, Borrell A, Aguilar A, Focardi S, Tatsukawa R (1993) Isomer-specific analysis and toxic evaluation of polychlorinated biphenyls in striped dolphins affected by an epizootic in the Western Mediterranean Sea. Arch Environ Contam Toxicol 25(2):227–233
Kannan K, Yun SH, Rudd RJ, Behr M (2010) High concentrations of persistent organic pollutants including PCBs, DDT, PBDEs and PFOs in little brown bats with white-nose syndrome in New York, USA. Chemosphere 80(6):613–618
Kimbrough RD, Squire RA, Linder RE, Strandberg JD, Montalli RJ, Burse VW (1975) Induction of liver tumor in Sherman strain female rats by polychlorinated biphenyls aroclor 1260. J Natl Cancer Inst 55(6):1453–1459
Kueh CSW, Lam JYC (2008) Monitoring of toxic substances in the Hong Kong marine environment. Mar Pollut Bull 57(6–12):744–757
Kunisue T, Watanabe M, Someya M, Monirith I, Minh TB, Subramanian A, Tana TS, Viet PH, Prudente M, Tanabe S (2002) PCDDs, PCDFs, PCBs and organochlorine insecticides in human breast milk collected from Asian developing countries: risk assessment for infants. Organohalogen Comp 58:285–288
Kunisue T, Someya M, Monirith I, Watanabe M, Tana TS, Tanabe S (2004a) Occurrence of PCBs, organochlorine insecticides, tris(4-chlorophenyl)methane, and tris(4-chlorophenyl)methanol in human breast milk collected from Cambodia. Arch Environ Contam Toxicol 46(3):405–412
Kunisue T, Someya M, Kayama F, Jin Y, Tanabe S (2004b) Persistent organochlorines in human breast milk collected from primiparae in Dalian and Shenyang, China. Environ Pollut 131(3):381–392
Kunisue T, Muraoka M, Ohtake M, Sudaryanto A, Minh NH, Ueno D, Higaki Y, Ochi M, Tsydenova O, Kamikawa S, Tonegi T, Nakamura Y, Shimomura H, Nagayaman J, Tanabe S (2006) Contamination status of persistent organochlorines in human breast milk from Japan: recent levels and temporal trend. Chemosphere 64(9):1601–1608
Kwan D (1994) Fat reserves and reproduction in the green turtle, Chelonia mydas. Wildl Res 21:257–266
Kwan CS (2014) Distribution and debromination of polybrominated diphenyl ethers (PBDEs) in tropical Asian countries. Unpublished doctoral dissertation, Tokyo University of Agriculture and Technology, Tokyo
Liang Y, Wong MH, Shutes RBE, Revitt DM (1999) Ecological risk assessment of polychlorinated biphenyl contamination in the Mai Po Marshes Nature Reserve, Hong Kong. Water Res 33(6):1338–1346
Liu Y, Zheng GJ, Yu H, Martin M, Richardson BJ, Lam MHW, Lam PKS (2005) Polybrominated diphenyl ethers (PBDEs) in sediments and mussel tissues from Hong Kong marine waters. Mar Pollut Bull 50(11):1173–1184
Ma S, Yu Z, Zhang X, Ren G, Peng P, Sheng G, Fu J (2012) Levels and congener profiles of polybrominated diphenyl ethers (PBDEs) in breast milk from Shanghai: implication for exposure route of higher brominated BDEs. Environ Int 42(1):72–77
Mai B, Fu J, Sheng G, Kang Y, Lin Z, Zhang G, Min Y, Zeng EY (2002) Chlorinated and polycyclic aromatic hydrocarbons in riverine and estuarine sediments from Pearl River Delta, China. Environ Pollut 117(3):457–474
Mai B, Chen S, Luo X, Chen L, Yang Q, Sheng G, Peng P, Fu J, Zeng EY (2005) Distribution of polybrominated diphenyl ethers in sediments of the Pearl River Delta and adjacent South China Sea. Environ Sci Technol 39(10):3521–3527
Malarvannan G, Kunisue T, Isobe T, Sudaryanto A, Takahashi S, Prudente M, Subramanian A, Tanabe S (2009) Organohalogen compounds in human breast milk from mothers living in Payatas and Malate, the Philippines: levels, accumulation kinetics and infant health risk. Environ Pollut 157(6):1924–1932
McDonald TA (2002) A perspective on the potential health risks of PBDEs. Chemosphere 46:745–755
Minh NH, Minh TB, Iwata H, Kajiwara N, Kunisue T, Takahashi S, Viet PH, Tuyen BC, Tanabe S (2007) Persistent organic pollutants in sediments from Sai Gon-Dong Nai River basin, Vietnam: levels and temporal trends. Arch Environ Contam Toxicol 52(4):458–465
Monirith I, Ueno D, Takahashi S, Nakata H, Sudaryanto A, Subramanian A, Karuppiah S, Ismail A, Muchtar M, Zheng J, Richardson BJ, Prudente M, Hue ND, Tana TS, Tkalin AV, Tanabe S (2003) Asia-Pacific mussel watch: monitoring contamination of persistent organochlorine compounds in coastal waters of Asian countries. Mar Pollut Bull 46(3):281–300
Moon H, Kannan K, Choi M, Choi HG (2007a) Polybrominated diphenyl ethers (PBDEs) in marine sediments from industrialized bays of Korea. Mar Pollut Bull 54(9):1402–1412
Moon H, Kannan K, Lee S, Choi M (2007b) Polybrominated diphenyl ethers (PBDEs) in sediment and bivalves from Korean coastal waters. Chemosphere 66(2):243–251
Muhammad SA (2006) Analysis of persistent organic pollutants in fish: health risk assessment through dietary intake. M.Sc. Thesis, Universiti Sains Malaysia, March 2006
Nhan DD, Am NM, Hoi NC, Dieu LV, Carvalho FP, Villeneuve JP, Cattini C (1998) Organochlorine pesticides and PCBs in the Red River Delta, North Vietnam. Mar Pollut Bull 36(9):742–749
Ogata Y, Takada H, Mizukawa K, Hirai H, Iwasa S, Endo S, Mato Y, Saha M, Okuda K, Nakashima A, Murakami M, Zurcher N, Booyatumanondo R, Zakaria MP, Dung LQ, Gordon M, Miguez C, Suzuki S, Moore C, Karapanagioti HK, Weerts S, McClurg T, Burres E, Smith W, Velkenburg MV, Lang JS, Lang RC, Laursen D, Danner B, Stewardson N, Thompson RC (2009) International pellet watch: global monitoring of persistent organic pollutants (POPs) in coastal waters. 1. Initial phase data on PCBs, DDTs and HCHs. Mar Pollut Bull 58(10):1437–1446
Pan J, Yang Y, Xu Q, Chen D, Xi D (2007) PCBs, PCNs and PBDEs in sediments and mussels from Qingdao coastal sea in the frame of current circulations and influence of sewage sludge. Chemosphere 66(10):1971–1982
Parolini M, Guazzoni N, Comolli R, Binelli A, Tremolada P (2013) Background levels of polybrominated diphenyl ethers (PBDEs) in soils from Mount Meru area, Arusha district (Tanzania). Sci Total Environ 452–453:253–261
Phuong PK, Son CPN, Sauvain JJ, Tarradellas J (1998) Contamination by PCBs, DDTs, and heavy metals in sediments of Ho Chi Minh city’s canals, Vietnam. Environ Contam Toxicol 60(2):347–354
Poon BHT, Leung CKM, Wong CKC, Wong MH (2005) Polychlorinated biphenyls and organochlorine pesticides in human adipose tissue and breast milk collected in Hong Kong. Arch Environ Contam Toxicol 49(2):274–282
Rahman F, Langford KH, Scrimshaw MD, Lester JN (2001) Polybrominated diphenyl ether (PBDE) flame retardants. Sci Total Environ 275(1–3):1–17
Ramu K, Kajiwara N, Sudaryanto A, Isobe T, Takahashi S, Subramanian A, Ueno D, Zheng GJ, Lam PKS, Takada H, Zakaria MP, Viet PH, Prudente M, Tana TS, Tanabe S (2007) Asian Mussel watch program: contamination status of polybrominated diphenyl ethers and organochlorines in coastal waters of Asian countries. Environ Sci Tech 41(13):4580–4586
Richardson BJ, Zheng GJ (1999) Chlorinated hydrocarbon contaminants in Hong Kong surficial sediments. Chemosphere 39(6):913–923
Romano S, Piazza R, Mugnai C, Giuliani S, Bellucci LG, Huu CN, Vecchiato M, Zambon S, Hoai ND, Frignani M (2013) PBDEs and PCBs in sediments of the Thi Nai Lagoon (Central Vietnam) and soils from its mainland. Chemosphere 90(9):2396–2402
Safe S (1994) Polychlorinated-biphenyls (PCBs)—environmental impact, biochemical and toxic responses, and implications for risk assessment. Crit Rev Toxicol 24(2):87–149
Schecter A, Furst P, Kruger C, Meemken H, Groebel W, Constable JD (1989) Levels of Polychlorinated Dibenzofurans, Dibenodioxins, PCBs, DDT, and DDE, Hexachlorobenzene, Dieldrin, Hexachlorocyclohexane, and Oxychlordane in human breast milk from the United States, Thailand, Vietnam and Germany. Chemosphere 18(1–6):445–454
Schecter A, Furst P, Furst C, Papke O, Ball M, Dai LC, Quynh HT, Phoung NTN, Beim A, Vlasov B, Chongchet V, Constable JD, Charles K (1991) Dioxins, dibenzofurans and selected chlorinated organic compounds in human milk and blood from Cambodia, Germany, Thailand, The U.S.A., The U.S.S.R., and Vietnam. Chemosphere 23(11–12):1903–1912
Shi T, Chen S, Luo X, Zhang X, Tang C, Luo Y, Ma Y, Wu J, Peng X, Mai B (2009) Occurrence of brominated flame retardants other than polybrominated diphenyl ethers in environmental and biota samples from southern China. Chemosphere 74(7):910–916
Sivalingam PM, Allapitchay I, Kojima H, Yoshida T (1982) Mussel watch of PCBs and persistent pesticide residues in Perna viridis Linnaeus from Malaysian and Singapore waters. Appl Geography 2(3):231–237
Stockholm Convention (2009) PCBs overview. http://chm.pops.int/Implementation/PCBs/Overview/tabid/273/Default.aspx
Subramanian A, Ohtake M, Kunisue T, Tanabe S (2007) High levels of organochlorines in mother’s milk from Chennai (Madras) city, India. Chemosphere 68(5):928–939
Sudaryanto A, Kunisue T, Tanabe S, Niida M, Hashim H (2005) Persistent organochlorine compounds in human breast milk from mothers living in Penang and Kedah, Malaysia. Arch Environ Contam Toxicol 49(3):429–437
Sudaryanto A, Kunisue T, Kajiwara N, Iwata H, Adibroto TA, Hartono P, Tanabe S (2006) Specific accumulation of organochlorines in human breast milk from Indonesia: levels, distribution, accumulation kinetics and infant health risk. Environ Pollut 139(1):107–117
Sudaryanto A, Kajiwara N, Tsydenova OV, Isobe T, Yu H, Takahashi S, Tanabe S (2008) Levels and congener specific profiles of PBDEs in human breast milk from China: implication on exposure sources and pathways. Chemosphere 73(10):1661–1668
Sudaryanto A, Setiawan IE, Ilyas M, Soeyanto E, Riadi AS, Isobe T, Takahashi S, Tanabe S (2009) Levels of brominated flame retardants in sediments and their bioaccumulation potential in biota from Jakarta Bay and its surroundings, Indonesia. In: Obayashi Y, Isobe T, Subramanian A, Suzuki S, Tanabe S (eds) Interdisciplinary studies on environmental chemistry—environmental research in Asia. TERRAPUB, Tokyo, pp 125–131
Sudaryanto A, Isobe T, Takahashi S, Tanabe S (2011) Assessment of persistent organic pollutants in sediments from Lower Mekong River Basin. Chemosphere 82(5):679–686
Suja F, Rahman RA, Yusof A, Shahbudin M (2014) e-Waste management scenarios in Malaysia. J Waste Manage 2014:609169
Tanabe S, Gondaira F, Subramanian A, Ramesh A, Mohan D, Kumaran P, Venugopalan VK, Tatsukawa R (1990) Specific pattern of persistent organochlorine residues in human breast milk from south India. J Agric Food Chem 38(3):899–903
Tarmudi Z, Abdullah ML, Tap AOM (2009) An overview of municipal solid wastes generation in Malaysia. J Technol 51:1–15
Tokarz JA, Ahn MY, Leng J, Filey TR, Nies L (2008) Reductive debromination of polybrominated diphenyl ethers in anaerobic sediment and a biomimetic system. Environ Sci Tech 42:1157–1164
Toms LML, Mortimer M, Symons RK, Paepke O, Mueller JF (2008) Polybrominated diphenyl ethers (PBDEs) in sediment by salinity and land-use type from Australia. Environ Int 34(1):58–66
Tue NM, Sudaryanto A, Minh TB, Isobe T, Takahashi S, Viet PH, Tanabe S (2010) Accumulation of polychlorinated biphenyls and brominated flame retardants in breast milk from women living in Vietnamese e-waste recycling sites. Sci Total Environ 408(9):2155–2162
van de Merwe JP, Hodge M, Whittier JM, Ibrahim K, Lee SY (2010) Persistent organic pollutants in the green sea turtle Chelonia mydas: nesting population variation, maternal transfer, and effects on development. Mar Ecol Prog Ser 403:269–278
WHO (2003) Polychlorinated biphenyls: human health aspects. Concise international chemical assessment document 55. http://www.who.int/ipcs/publications/cicad/en/cicad55.pdf
Wong MH, Poon BHT (2003) Sources, fates and effects of persistent organic pollutants in China, with emphasis on the Pearl River Delta. Persist Org Pollut 3O:355–369
Wong CKC, Leung KM, Poon BHT, Lan CY, Wong MH (2002) Organochlorine hydrocarbons in human breast milk collected in Hong Kong and Guangzhou. Arch Environ Contam Toxicol 43(3):364–372
Wong TW, Wang AHS, Nelson EAS, Qiu H, Ku SYK (2013) Levels of PCDDs, PCDFs, and dioxin-like PCBs in human milk among Hong Kong mothers. Sci Total Environ 463–464:1230–1238
Wu J, Luo X, Zhang Y, Luo Y, Chen S, Mai S, Yang Z (2008) Bioaccumulation of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) in wild aquatic species from an electronic waste (e-waste) recycling site in South China. Environ Int 34(8):1109–1113
Wurl O, Obbard JP (2005) Organochlorine pesticides, polychlorinated biphenyls and polybrominated diphenyl ethers in Singapore’s coastal marine sediments. Chemosphere 58(7):925–933
Zheng GJ, Martin M, Richardson BJ, Yu H, Liu Y, Zhou C, Li J, Hu G, Lam MHW, Lam PKS (2004) Concentrations of polybrominated diphenyl ethers (PBDEs) in Pearl River Delta sediments. Mar Pollut Bull 49(5–6):520–524
Zhou T, Taylor MM, DeVito MJ, Crofton KM (2002) Development exposure to brominated diphenyl ethers results in thyroid hormone disruption. Toxicology 66:105–116
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Kaw, H.Y., Kannan, N. (2016). A Review on Polychlorinated Biphenyls (PCBs) and Polybrominated Diphenyl Ethers (PBDEs) in South Asia with a Focus on Malaysia. In: de Voogt, P. (eds) Reviews of Environmental Contamination and Toxicology Volume 242. Reviews of Environmental Contamination and Toxicology, vol 242. Springer, Cham. https://doi.org/10.1007/398_2016_14
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