How Mercury works as a sample from Thailand
how we get dayli poisend from the one dark wather and from Mining
Â
Thammasat Int. J. Sc. Tech., Vol.5, No.2, May -August 2000
Amplification of Mercury Concentrationsin
the Marine Food Chain of the East Coast of
1. Introduction
Mercury coumpounds are utilized on a
wide scale both in industry and agriculture
Mercury from industrial and agricultural wastes
accumulatein soil and water, and is partially
transportetdo the aquatice nvironmentw, hich in
turn becomesa sourceo f contaminationo f fish
and other organisms. The ability of some
microorganismsto methylatein organicm ercury
to the moreb iologicals tablea lkyl formsa ndt he
more toxic forms further increasesth e dangero l
contamination[1 ]. The concerna boutm ercury
pollutioni n the marinee nvironments tartedi n
the 1950s with the case of Minamata in Japan
where severapl eopled iedo r became.terminally
sick after consuming fish and
’strett
fish
containing relatively high concentrationso f
methyl mercury [2]. High levels of mercury
were also found in fish from Swedish lakes and
streamsT. he principalm ercuryc ontaminatioonf
these fish was reported to be an organic form of
methyl mercury [3].
Thailand
Voravit CheevaPorn
Departmento f Aquatic ScienceB, uraphaU niversity,B angsaen,
Chonburi 20 13 1, Thailand
Imelda Velasquez
MarineS cienceIn stituteU, niversityo f theP hilippines,
Diliman,Q uezonI l0l, PhiliPPines
Piamsak Menasveta
Aquatic ResourcesR esearchIn stitute,C hulalongkornU niversify,
Bangkok I 0330, Thailand
Abstract
Threeh undreda nd ninetys ampleso f marineo rganismsw erec ollectedf rom the EastC oasto f
Thailandf or total mercurya nalysis.T he resultsi ndicatedt hat mercuryl evelso f fish and other marine
organisms from the East Coast of Thailand are within the safety limit. However, biological
ma’gnificationo f mercuryr esiduei n the marinef ood chainw as observedO. rganismso f highert rophic
levelsh ave higher mercuryr esiduet han thosei n the lower trophic levels.S tatisticaal nalysiss howed
positive linear iegression between the size of the marine organisms and mercury contents of some
specieosf marineo rganisms.
Many studies on a wide range of marine
fish have reportedp ositivec orrelationsb etween
mercury concentration and a measure of age,
weight,o r lengtho f fish [4,5,6,7,8,9]T. his may’
however, reflect the increased interest in
mercury as a potential threat to human health’
Despitet his tendencyf or mercuryt o increasein
concentrationw ith increasings izelageo f some
fish, muscle mercury levels tend to be less than
I ppm with kidney and liver levels slightly
higheIr l 0 . l l . l 2 . l 3 l .
In 1975, the total mercury contents ot
fish in the Gulf of Thailand ranged from 0 to
0.58 ppm [4]. In the same year, traces of total
mercury were found in the marine food chain of
Bang Prac oastaal reao f Chonburip rovinceI l]
which tend to increasea t highert rophic levels
and accordingto the sizeo f organisms. Since
Thailand is one of the countries where the
nationwide fish consumption is comparatively
high, further study on the contamination of
mercuryi n fish and other marineo rganismsis
essential.
A A
2. Materials and Methods
2.1 Sample collection and treatment
Samples for mercury analysis were
collected from Station A (Angsila) Station B
(Laem Chabang) subdivision of Chonburi
province and Station C (Ban Pae) subdivision of
Rayong province(Fig. l). Fish samples were
collected from the catch by otter trawl in
January 1999. The species of fish and other
organisms from which samples were taken
ranged from the lower trophic level to the higher
trophic levels. Plankton samples were collected
by a plankton net. All of the samples were
preservedin a freezera t approximately-2 0 oC.
For fish assay the samples were thawed and
dissected with a stainless steel knife, and a
portion of muscle under the dorsal fin, kidney,
liver, gill, and stomach were dried in the freeze
dryer and used for mercury determination.
2.2 Mercury analysis
Total mercury levels in fish and other
organismsw ere determinedb y meanso f Colc
Vapor analysist echniquesO. ne gram of tissue
was digested in 20 ml of I :1 conaentratecr
redistilled HNO3 and concentratedH zSOq, and
further oxidized with 10 mL of saturated
KzSzOs solution. Excess oxidizing agents and
mercury ions were reduced by l0 mL of
reducing solution (3%NaBHa in l% NaOH) in
hydride generatora pparatus,a nd then mercury
was vaporized and measured in the flamelesss
atomic absorption spectrophotometer.
A Perkin-Elmer 3300 atomic absorption
spectrophotometer (The Perkin-Elmer
Corporation, Norwalk, CT) equipped with a
MHS-I0 mercury hydride system was used to
determine the total mercury concentration of
each sample. The accuracy of these
determination was verified with a standard
reference material DOLT-1 (dogfish liver :
0.225 + 0.057 ppm Hg) of the National Research
Council of Canada. Results of analysis are
within the range of + 10 %.
ThammasaInt t.J . Sc.T ech.V, ol.5,N o.2,M ay- August2 000
3. Results and Discussion
One hundred and seventy samples of 5
species of fish, one hundred and eight samples
of2 specieso fcrustacean,f ifty-four sampleso f
I species of shellfish, fifty-four samples of I
species of squid and four samples of plankton
from the East Coast of Thailand were analysed
for total mercury. Results showed that total
mercury concentrations ranged from 0.002 -
0.714 ppm (dry weight) with the mean value of
0.118 ppm. While those found in 1975 in the
adjacent area ranged from 0-0.58 ppm [4]. Of
the total of 390 samples analysed, 20 %
contained less than 0.05 ppm of total mercury,
79 %o had a total mercury content between 0.05 -
0.5 ppm and I o/o contained over 0.5 ppm.
According to Menasveta t 1] , these
concentration can be regarded as a natural
background of mercury for fish in general. It
should be noted that only 3 samples were found
having total mercury levels above the United
States Food and Drug Administration tolerance
limit of 0.5 ppm.
Table 1 gives the mean and standard
deviationo f total mercury concentrationsin the
four trophic levels. The mean values of total
mercury for the first and second trophic levels
( compositeds pecieso f plankton) from station
A (Angsila) and B (Laem Chabang) were 0.004
and 0.007 ppm, respectively. The mercury
residue concentration in the third trophic level
was higher than the first and second trophic
levels.T he meanv aluesw ere0 .068.0 .1 12,a nd
0.053 ppm for station A, B, and C respectively.
The mean values of the fourth trophic level
have higherm ercuryr esidueth ant hosei n third
trophic level as shown in Tablel. Student’t'test
showed significant difference in total mercury
concentrationbse tweentr ophicl evelsI + ll and
trophic level III and between trophic levels III
and IV ( p < 0.5 ). The lowest mercury residue
( 0.002 ppm ) was detected in the composite
specieso f planktonw hile the highestm eroury
residue (0.714 ppm) was detected in Loligo
formosana (Splendid squid). This species was
categorized in trophic level IV
25
ThammasaItn t..J.S c.T ech.,V ol.5,N o.2, May August2 000
Table l: Total mercury contents (ppm) in different trophic levels from three sampling stations
( Angsila, Laem Chabang, and Rayong )
A) Angsila station
Trophic levels No. of samples standardd eviation
I
B) Laem Chabang station
Trophicl evels No. of samples standardd eviation
C) Rayong station
Trophicl evels No. of samples standardd eviation
Based on the above analysis, it can be
concluded that there is a biological
magnification of mercury residue in the marine
food chain of the East Coast of Thailand’ Fish of
higher trophic levels contain higher mercury
residue than those in the lower trophic levels
(Fig. 2). This suggests that mercury may be
concentratedin the same mannera s an organic
compounds uch as organochlorinec ompounds,
i.e., passed through and amplified by the food
chain. The concept also conforms to the the
datap resentedb y Johnelse t al. [3], Scott[ 15] ‘
andM enasveta[l ].
Statisticala nalysiss howed positivel inear
resression between the size of the marine
organisms (weight) and mercury contents of
some species of marine organisms. Figure 3
gives the exampleo f the linear regressionin
Peneausm erguiensis( White shrimp), Portunus
pelagicus (Blue swimming crab), Mytilus edulis
( Green mussel), Sillago maculata (Trumpeter
sillago), and Atule mate (Banded crevalle)
collected from stationB. (Laem Chabang)’
However, the results showed different
correlation between size and mercury contents
in different sampling stations for other
organisms. The positive linear regression
between agelor weight and mercury contents of
fish is welldocumentedb y Scott[ 15].
26
Figure 4. showed the mean values of
mercury content in various marine organisms
collected from 3 sampling stations. The results
indicated that Portunus pelagicus ( Blue
swimming crab)(0.240 ppm), Loligo formosana
(Splendids quid)(0.325p pm) and Atule mate
(Bandedc revalle)( 0.387p pm) havet heh ighest
mercury content among other marine organisms
colfected from Angsila, Laem Chabang, and
Rayong respectively. However, the average
mercuryc ontento f thesem arine’organismfsr om
the East Coast of Thailand were lower than the
United States Food and Drug Administration
tolerance limit of 0.5 ppm.
The mercury contents in various tissues
such as kidney, stomach, gill, muscle, and liver
of Epinephelus corallicola (Grouper) collected
from station b. ( Laem Chabang) were analysed.
Highest mercury residues were found in kidney
and liver respectivel(y Fig. 5 ). This is probably
due to their high affinity for sulphur containing
ligands such as sulhydryl (-SH) group in
metallothionine in fish’s kidney and liver as
described by De [6]. Similar results were
reported by Thongra-ar [7] in 1988.
The resultso f this studyi ndicatedth att he
average mercury content of fish and other
marine organisms from the Eastern Coast of
Thailand was lower than the United States Food
and Drug Administraton tolerance limit of 0.5
ppm. The mean value of 0.118 ppm for total
mercury is only one-fourth of this tolerance
limit. However it is probably not practical to
consider this recommended level without
correlatingi t to the frequencyo f consumptionI.t
was estimated that the fish/sea food
consumption rate among Thai people is 20
kg/person/year[8 ]. This level is equal to 55
g/person/dayI.f the mean total mercury content
of fish and other marine organisms is 0.118
ppm, it can be calculated that the daily intake of
mercury through fish/seafood consumption is
6.49 pglperson/day for Thai people. This value
is greater than 4 pglperson/day as reported from
Sweden [19]. The Joint FAO/WHO Expert
Committee on Food Additives proposed that the
provisional tolerate-weekly intake (PTWI) of
mercury for man be set at 0.0033 mg/kg bodyweight
for methyl mercury. This value is equato
to PTWI of 0.2 mg. mercury as methyl
mercury, for an average body-weight of 60 kg
The daily mercury intake of 6.49 pglpersonlday
ThammasaItn t. J. Sc.T ech.,V ol.5,N o.2, May -August 2000
which we derived from this study, would
contribute to weekly intake of 0.045 mg/person.
This level is only one-fourth of PTWI of
mercury ( assuming that all mercury contributed
by fish and other marine organisms is in the
form of methyl mercury). It is therefore, the
mercury levels of fish and other marine
organisms from the East Coast of Thailand are
within the safety limit for consumption.
4. Conclusions
The resulto f this study indicatest hat the
mercury levels .of fish and other marine
organisms from the East Coast of Thailand are
within the safety limit. However, the situation
may changei n the future,b ecausea t presento ur
country is still at developing stage. Modern
agriculturatle chniquesi,n cludinge xtensiveu se
of pesticides, coupled with industrial
developmentw, ill probably increaset he amount
of mercury in the environment in the future.
Hence, the plan for monitoring, proper
protection and control of mercury residue in
Thailand’s environment should be formulated
andi mplementewd ithoutd elay.
5. Acknowledgements
This investigationis financiallys upported
by The Thailand Research Fund (TRF). The
authors thank Mrs. Rattana Cheevaporn, Ms.
WannaK osillawatf or theirt echnicaal ssistance.
6. References
tl] MenasvetaP, ., Total Mercury in the Food
Chain of Bang Pra Coastal Area Cholburi,
J. Sci.Soc. Thailand, Yol. 2, pp.1l7-126,
1976.
l2l Kurland,L., The Outbreak of Neurological
Disorder in Minamata, Japan, and Its
Relationshipto the Ingestiono f Seafood
Contaminated by Mercuric Compounds,
WorldN eurol,V ol. 1,pp.3703- 95, 1960.
t3l Johnels,A .G., WestermarkT, ., Berg, W.,
PerssonP, .I.,a nd SjostrandB, ., Pike( Esox
lucius L.) and Some other Aquatic
Organisms in Sweden as Indicators of
Mercury Contamination in the
Environment, Oikos, Vol.18, pp.323-333,
1967.
2′7
t4l Menasveta, P. and Siriyong, R., Mercury
Content of SeveralP redaciousF ish in the
Andaman Sea. Man Pollut. Bull., Vol.l9,
pp.80,1977.
t5] Rivers, J.B., Pearson, J.E., and Shultz,
C.D., Total and Organic Mercury in Marine
Fish, Bull. Environ. Contam. Toxicol.,
Vol.8,p p.2571, 972.
t6l Shultz, C.D. and Ito, B.M., Mercury and
Selenium in Blue Marlin Makaira
Nigricans from the Hawaiian Islands, Fisft.
Bull, Y ol.1 6, pp.872, 197 9.
Ul Thomson,J .D., Mercury Concentrationso f
the Axial Muscle Tissues of Some Marine
Fishes of the Continental Shelf Adjacent to
Tasmania, Aust. J. Mar. Freshwater Res.,
Vol. 36, pp.509,1979.
t8l Walker, T.1., Effects of Species, Sex,
Length and Locality on the Mercury
Content of School Shark Galeorhinus
Australis (Macleay) and Gummy Shark
Mustelus antarticus Guenther from South-
Eastern Australian Waters, Aust. J. Mar.
FreshwateRr es.,V ol. 27, pp.603,1 979.
t9l Watling, R.J., McClurg, T.P., and Stanton,
R.C., Relation between MercurY
Concentrationa nd Size in the Mako Shark,
Bull. Environ. Contam. Toxicol., Yol. 26′
pp.352, 1979.
[10] Chvojka, R. and Williams R’J., Mercury
Levels in Six Species of Australian
Commercial Fish, Aust. J. Mar. Freshwater
Res.V, ol.3l, pp.4691, 980.
[11] Greig, R.A. and Krzynonek. J., Mercury
Concentrationsin Three Specieso f Tunas
Collected from Various Oceanic Waters’
Bull. Environ. Contam. Toxicol., Yol. 22,
pp.120,1979.
ThammasaItn t. J. Sc.T ech.,V ol.5, No.2, May -August 2000
[12] Kai, N., Ueda, T., Takeda, M., and
Kataoka, A.., On Mercury and Selenium in
Tuna Fish Tissues. VIII. Thelevels of
Mercury and Selenium in Albacore from
the Indian Ocean, J. Shimonoseki Univ.
FisheriesV, ol.3l, pp.69,1 983.
[3] Lyle, J.M., Mercury and Selenium
Concentrations in Sharks from Northern
Australian Waters, Aust. J. Mar.
FreshwateRr es,V ol.37, pp.309,1 983.
[4] National Marine Science Committee, Third
Pollution Survey ( GuU of Thailand), The
National Research Board of Thailand,
19′76.
[15] Scott, D.M., Mercury Concentration of
White Muscle in Relation to Age, Growth
and Condition in four Species of Fishes
from Cfay Lake, Ontario, J. Fish. Res.
Board.C an,Y ol.3l, pp.1723-l’ 729,1 976.
[6] De,A.K., Environmental Chemistry, Wiley
EasternL imited,N ew Delhi, 1994.
[17] Thongra-ar,W ., Mercury Contentsi n Some
Economic Fish from the Eastern Coast of
Thailand, Research Report No. 3412531,
Marine Science Institute, Burapha
UniversityT, hailand,1 994.
[18] Man, J.C.,C omplemenC, . and Murdoch,
W.R., Thailand;F isheryD evelopmenat nd
Management Policies, Programmes and
Institutional Anangements TINDP/FAO,
South China Sea Fisheries Development
and Coordinating Programme, Manila,
Philippines1, 994.
[9] Nilsson, T., Skerfving, S. and Svensson,
P.G.,C onsumptiono f Fisha ndE xposureto
Methylmercury Through Fish in Swedish
Males.P ollutionA bst,Y o1.5,p p.90,1 972.
28
Thammasaltn t. J. Sc. Tech.,V ol.S, No.2, May -August 2000
Figure5 Averagem ercuryc ontenitn variousti ssueso f Epinephelucso rallicola
( Grouper)
Epinephelus corallicola
Â
Â
Â
Comments off








