At Minamata, the amount of accumulated mercury in the bay area within. 2 km from the coastal source was about 200 tons in 1963 at which time the discharge ...
Journal of the Oceanographical Vol. 34, pp. 222 to 232, 1978
Some
Society
Regular
Patterns
Contamination Yasushi
Abstract:
of Japan
in the
in the
Coastal
HIRAIZUMI**, Takehiko
Observations
of sediment
When the pollutant concentration regular pattern is observed in the
Distribution
of Sediment
Waters
along
Japan*
MANABE*** and Hajime NISHIMURA**
contamination
is divided quantitative
along
the
coast
of Japan
were
analyzed.
by the fine particle fraction in the sediment, a relationship among the degree and the area of
contamination and the discharge rate of pollutant released continuously into the water along the coast. This regularity was observed with respect to COD, n-hexane soluble substances and heavy metals, and could be expressed by a formula. Polluted and thus dispersion
particles
were
supposed
their distribution in the in the surface water.
Introduction In coastal waters enter, contamination extending out from
to disperse surface
1.
where industrial effluents of sediments are observed the fixed sources of the
pollutants. This is known empirically to be closely related to the contamination of the aquatic ecosystem of that region. In environmental impact assessment to predict the contamination of the aquatic ecosystem, it is necessary to predict quantitatively the extent and intensity of contamination of the sediment; therefore, it would be useful to find a regular pattern of bed sediment contamination from analysis of field data. For the cases referred to in Table 1, regional dispersion of pollutants in the sediment are found to be described by the following empirical equation,
(1) where surface value, tration
C is the pollutant concentration in the of the sediment, C. is its background and S is the polluted area with concenhigher than C. The parameters n and
/3 appear to become constant for given location and pollutant, according to the above mentioned * Received
Aug .
11,
1975,
revised
Oct.
30
and
accepted Oct. 31, 1978. ** University of Tokyo , Department of Chemical Engineering, Bunkyo-ku, Tokyo 113, Japan *** Hyogo Prefectual Fisheries Experimental Station, Nakasaki-cho,
Akashi,
Hyogo
673, Japan
through
sediment
suspension
is expected
in the bottom
to become
similar
water
layer,
to effluent
observations. In this paper, we examine the general relationship between pollutant concentration, distribution in the sediment and release rate of the pollutant. 2.
Relationship among pollutant concentration in sediment, dispersed area and release rate of pollutant In the surface sediment, the distributions of pollutants released from a source are always similar irrespective of the kind of pollutant. This tendency was observed in Osaka Bay with respect to heavy metals, COD and oils (JOH et al . , 1974). From this it is inferred that essentially the same process controls the distribution of pollutants in the sediment. As for the extent of sediment contamination, the pollutant concentrations in the sediment surface were found roughly proportional to the rate of pollutant influx. Based upon this, the following equation is introduced, (2) where M is the rate of heavy metal discharge (kg (1-9, and a and n are constant parameters. Of the earlier study carried out in Osaka Bay, values of 1.56 and 0.4 were respectively obtained for a and n (NISHIMURA and KUMAGAI, 1975). We now proceed to ascertain this relationship in other offshore areas, for other pollutants. (A) COD (in this paper we use the COD as
Regular
Table
1.
Patterns
of Sediment
Studies
of sediment
Table
* (1) (2) (3) (4)
2.
Influx
rate
Contamination
223
contamination.
of COD.
COD influx was estimated
on basis of SS (suspended solids) influx . Economic Planning Agency, Japan (1966): Observation on Water Quality in Coastal Waters of Otake, Iwakuni. 217 pp. Japan Aquatic Resources Conservation Society (1971): Investigation on Environmental Pollution in Eastern Hiuchi-nada. 34 pp. Economic Planning Agency, Japan (1970): Observation on Water Quality in Coastal Waters of Mishima, Kawanoe. 79 pp. Conference on Utilization and Development of the Seto Inland Sea (1972): Analysis on Pollutant Influx to the Seto Inland Sea. ed. by Chugoku Areal Business and Finance Association. 92 pp.
an index for organic pollutants): Distributions of organic pollutants in the sediment were studied in Osaka Bay, the eastern part of Hiuchi-nada, and the offshore region of OtakeIwakuni district. Release rates of COD in these areas are shown in Table 2. Based upon observational results with respect to COD as shown in Fig. 1, the parameters a and n of Eq. (2) were found to be 1.5 and 0.75 respectively. Here C is expressed in mg g-1, M in ton d-1 and S in km2. (B) n-hexane soluble substances (oils): The distributions of oils in the sediment were studied in Osaka Bay, the area off Otake-Iwakuni and off Yokkaichi. The rates of oils discharge in these waters are shown in Table 3. The observational results shown in Fig. 2 give 2.4 and 0.55 respectively for the values of a and n. However, we must note the fact that, not every n-hexane soluble substance in the sediment is attributable to oils. In Osaka Bay, which is
Fig.
1.
divided
Relationship by influx
between rate
of COD
the concentration in bottom
sedi-
ment and its dispersed area based on COD influx summarized in Table 2. Symbols are explained in the
table.
IIIRAIZUMI, MANABE and NISHIMUIZA
224
Table
(5)
3.
Influx
of n-hexane
soluble
substances.
NAGAI, U., K. KAWAMURA, S. NAKANISHI and K. FUKATSU (1964): Special Survey Report on Fishes Tainted with Oils. pp. 70-85. Science and Technology Agency, Japan. Table
(6)
rate
Environment
4.
Influx
rate
of heavy
metals.
Agency, Japan (1973): Inspection on Environmental
Contamination
by Mercury
in Japan.
Fig. 3. Relationship between the concentration divided by influx rate of heavy metals in bottom sediment
Fig.
2.
divided
Relationship by influx
between rate
the
concentration
of n-hexane
soluble
and
dispersed
area
based
summarized in Table in the table.
4.
Symbols
X,
correlation line shima Bay.
of
distributions
of distributions
sub-
data
in
Mizu-
stances in bottom sediment and dispersed area based on data summarized in Table 3. Symbols
Y,
correlation
are explained
Z,
Osaka Bay. expected correlation
line on basis
of heavy
metals
in fine particle
fraction
in the table.
Chain
a correlation line for the distribution fraction of oil in sediment.
line indicates of the net
line
on
are explained
concentration
of sediment.
mainly
of
Regular
Patterns
of Sediment
always affected by severe organic pollution, 50-80 % of the n-hexane soluble substances in the sediment were observed to be elementary sulfur or sulfide (JoH et al., 1974). In addition, the waters of chronic oil pollution in the present paper are also affected by chronic organic pollution. We will assume that the net concentration of oils in the sediment accounts for approximately half of the n-hexane soluble substances, and we therefore find the value of 1.2 to a in Fig. 2. (C) Heavy metals : Horizontal distributions of heavy metals have been studied in detail for Osaka Bay (JoH et al., 1974); for the eastern part of Hiuchi-nada (YANAGI, 1973); and for the waters off Mizushima, Niihama and Tokuyama by the Environment Agency of Japan (Table 4). We now consider the relationship between these distributions and the discharge rates of heavy metals. First, the discharge rates of pollutant heavy metals are given in Table 4. From these data, relationships can be obtained between the concentration divided by influx rate of heavy metals and the area of the heavy metals distribution on the surface of the sediment (Fig. 3). In this figure, the slope of the correlation line is large for the case of Mizushima (X), and small for the cases of Osaka Bay and eastern Hiuchi-nada (Y). The difference may be explained as follows. In the inner part of Mizushima Bay the water is relatively stagnant, while at the entrance it flows faster due to the tidal current. This results in pollutant particles settling more densely
Fig.
4.
Solid
lines
Cd concentration (MANABE, tours for fraction
indicate
contours
in sediment
1974a). Broken Cd concentration
of sediment.
ppm
for overall
in Harima-nada lines indicate conin fine particle in dry
mud.
Contamination
225
in the nearshore region of the inner bay than at the entrance. In contrast, for Osaka Bay and Hiuchi-nada, the average sediment particle size is larger at the inner regions and smaller at the entrance, far offshore, reflecting the difference of the water depth. This explains why the pollutants are more liable to settle and accumulate offshore and at the center of the bay than at the interior region and near the shore. If the sediment particle size distribution were uniform over the whole area, the pollutant particles would not be liable to settle and accumulate locally, and the slopes of the correlation lines would be identical for any region. As for the case in Fig. 3, the scattered points of data are expected to approach a single correlation line (Z), provided that the areal variance of the sediment size distribution could be cancelled. Thus the correlation line may give 0.9 and 0.6 respectively for the values of a and n. Here C is in lig M is in kg c1-1 and S is in km2. 3.
Effect of particle size distribution on sediment contamination 3.1. Distribution of pollutant in surface sediment As mentioned briefly in the previous section, the horizontal distribution of pollutant in the surface sediment appears to be greatly influenced by geographical and topographical features, current and tide. In the northern part of Hiuchi-nada, the distribution of heavy metals in the sediment is seen to extend out from the sources on
Fig. 5. Solid lines indicate contours for overall Cr concentration in sediment in Harima-nada (MANABE, 1974a). Broken lines indicate contours for Cr concentration in fine particle fraction in sediment.
HIRAIZUMI,
226
the
northern
coast,
located
in
where
an
there
A
is
similar with
no
source
and
KUMAGAI,
to
be
and
size
tween
the
the
in
1972a).
of
sediment
of
in nated
Bay with
In
PCB
addition,
is
generally
of
the
each
where
particle
pollutants
sediment.
in
particle
true
for
PCB
contamidata).
heavy
metals
particle in
fraction
the
findings
at
content
in
metals of
the
and
sediment
(3) where
Ca
is the
pollutant
concentration
in the
was
KUMAGAI,
divided
cations
where
the
1975;
offshore
fine
occupies
sediment
than
in
apparently
in
an
tration
in
the
We
now
between
a
proceed
to
It
is
the
size
remains that
fine
particle of
area, pollutant
consider
the
the
coastal
the
and
this
concen-
fine
in
Harima-nada that
source particle
constant the
contamifound
distribution
on
the
an of
with
coast in
when the
area. the
an
pollutant
decreases
fraction over
in as
the
sediment
the
relationship
water
relationship out
the
from of
lo-
example,
percentage
noteworthy
in
distance
the
that carried
concentration the
At
for
higher
and
studies
example.
fraction.
surrounding
particularly
earlier
net concen-
sediment.
offshore
nation,
total
stagnant,
higher
the
"the
for
Harima-nada,
fraction
fraction
define
particle is
assumed
particle
here
water
of
be
fine
pollutant"
by the
results
generally the
We of
tration
suggests
fine
heavy
in
concentration
ment
the
may
concentrated
the
far
also
pollutant concentration in the fine particle fraction of the sediment will reflect the actual process of pollutant dispersion in the sediment. Of the previously mentioned studies at Harimanada, we now describe the distribution of pollutant with the concept of "the net concentration of pollutant", which corresponds to assume that the pollutant concentrates almost entirely in the fine particle fraction of the sediment (particle diameter less than 50 pm). We then obtain distribution patterns shown by the broken lines in Figs. 4 and 5 that indicate sediment contamination by the heavy metals d, Cr-Stretching far south offshore -Cfrom the northern coast at Harima-nada. Applying the same method to the distribution of the other heavy metals, the following equation is obtained for describing the distribution of pollutant in the fine particle fraction in the sediment (Fig. 6),
1977).
Most be
distribution
pm
of
fraction
the were
unpublished
(NISHIMURA
KUMAGAI,
(a
strongly
shown
the
size
determined
of
in as
Bay
is
region
highest
ƒÊ
in
the 10
concentration
sediment,
Beppu
to than
(HIRAIzuMI,
the
50
Hiuchi-nada
this
where
than (MANABE,
chlorophyll-a)
closely less
beand
pheophytine-a
and
Apparently
Beppu
to
Bay
sediment
found metals
(less
of of
Beppu
diameter.
was
Harima-nada
degradation
fine
sediment.
particles
at
corresponding the
relationship
heavy
distributions
of
found
in
fine
off heavy
concentration
of
of
to
clear
relationship
sediment
Also,
product
A
concentration
the
and and
respect
distribution
percentage
m)
1977),
pollutant
linear
Beppu
(NisHimuRA
with
1972).
a
5). at
data),
also
between
particle Recently
and
metals
unpublished
expected
offshore,
KUMAGAI,
Hiuchi-nada (YANAGI,
can
4
NISHIMURA
in the sediment is controlled by the mixing and diffusion processes of the pollutant in the fine particle fraction. This means that the pollutant distribution in the sediment described by the
being
far
observed
heavy
1975;
(HIRAIzuMI,
Kannonji,
pattern
(Figs. was
respect
metals
another position
situation
Bay
PCB
with
isolated
MANABE and
sediThis
pollutant
Fig. 6. Relationship between trations in fine sediment dispersed
areas
concentration.
bounded
heavy metals concenin Harima-nada and by
the contour
of that
Regular Table
5.
Estimated
released nada.
from
influx the
rate
Patterns
of heavy
northern
coast
of Sediment
Contamination
227
metals
of Harima-
These influx rate figures were originally estimated by the authors from material balance calculations and observations fine
particle
is
the
of urban
fraction
of
background
equation
to
constant
always
be
take of The
of
the
same and
in
fine
and
patterns at Harima-nada and of Osaka Bay. In summary, it was found that the distribution of pollutant in sediment can be generally expressed as
pollutant
rate
of
pollutant
discharge In
Section
for
the is
that
not
may
be
the
generally
area
We
may
from in as
concentration
of
estimated
on
The
between
which
is
pollutant
concentration
is
in
shown
used
for
bution
along
above in of
(JOH
is in
a
coastal
be
calcu-
background is
earlier
reasonably findings
and
The
the
a
the
fine
in same
3, fine
1974).
Osaka
area
of
decreases In
Fig.
distriBay.
than
7
The of
99
%
the
bay
to
about we
4. was
fraction
show
where Ca is the net pollutant concentration in the fine particle fraction f in the sediment (mg kg-1), c/f, Ca,00 is the background pollutant concentration in the fine particle fraction of the sediment (mg kg-1), S is the contaminated area bounded by the contours for equal pollutant concentration Ca (km2) and M is the rate of pollutant discharge (kg d-1). The average value of the power n is about 0.65 and n ranges between 0.4 and 0.9 for heavy metals and oils. The corresponding n for COD is greater than this average value probably because of biodegradation. The average value of aa is 1.5 and it ranges between 0.5 and :3. The correlation coefficient for these data is 0.98 for the empirically determined equation shown in Fig. 7.
of
sediment,
procedure
particle
small
the
contour
pollutant for
higher
it
and
by
mentioned
coast :al.,
(Ca -Ca,•‡)/M
Fig.
generally
very
the et
7.
the
percentage
but
the
The
bounded Ca
Fig.
pattern
sdiment
to
metals of
at
pollutant
features.
relation S,
of
can 5.
basis
even
features
rate sources
heavy
the
geological
area
regular
Table
(2)
pollutant
sediment.
Harima-nada in
Eq. the
of
The
terrestrial
shown
sediment,
fraction,
size
6).
northern
use
particle
these
(Fig.
waters
the
fine
observe
concentrated the
fraction. we
varying
frac-
discussion,
in
if
(4)
area
particle
more
particle
the
with
Harima-nada discharge
are
stated in
the
fine
hold
the
previous
fraction
coarse
to in
the
the
pollutants
concentration
lated
of
particle
in
ascertained
pollutant
From
fine
and
was
distribution
seen
the
for
(2) of
uniform.
was
in
Eq.
distribution
where tion it
2.,
the
pollutant by influx dispersed pollutant
of
condition.
between
sediment
but almost
irrespective
bed
Fig. 7. Relationship between the net concentration in fine sediment divided rate of pollutant (Ca-Ca.00)/M and area S bounded by the contour of concentration Ca.
.
This
Eq.(1), may
value sea
Ca,
Ca.
to here
relationship
content
and
similar n
area
effluent.
sediment
parameter
differences 3.2.
the
concentration
appears
the
and industrial
the
there, bottom 50
% the
Discussion Here we give a physical interpretation for the results of the preceeding section. 4.1. Processes controlling contamination of bed sediment in coastal waters The following processes are supposed to be the mechanisms controlling the contamination pattern of sediment: 1) The discharged pollutant, for the most part,
228
HIRAIZUMI,
MANABE
settles in an area comparatively close to the site of pollutant release. 2) The settling fine particles mix and disperse in a dense suspension of grain-fluid mixture just above the bottom. 3) The fine sediment particles settle and deposit to form contamination patterns in the bed sediment. 4) The deposited pollutant fine particles are stirred again, mixed in a dense suspension above the bottom and redispersed in the sediment by a shear stress strong enough to cause movement. Let us investigate these proposed processes. (A) Sedimentation of pollutant particles: First let us describe the sedimentation pattern. Suspended solids (SS) discharged from paper mills is observed to disperse as far as 1 km from the source. At a distance beyond 1 km a sharp decrease in concentration in the surface water is observed. Vertically, at the
Fig. 8. Horizontal distribution pattern of SS in each layer in coastal waters. ** off Iwakuni coast -June 15, 1965-(based on JEPA, 1966) Al, ebb tide, surface 0.75 m depth layer; layer; B2, flood tide, ** off Tagonoura -Nov.
layer; A2, ebb tide, Bl, flood tide, surface 0.75 m depth layer. 22, 1970-
Cl, surface layer; C2, 2 m depth layer; C3, 5 m depth layer.
and NISHIMURA
front of distribution, the layer of highest concentration of SS shifts from the surface layer to the middle, and finally may descend to the bottom (Fig. 8). Most SS are deposited on the sea bed within 5 km from the discharge source on the coast. At Minamata, the amount of accumulated mercury in the bay area within 2 km from the coastal source was about 200 tons in 1963 at which time the discharge from the source had already ceased (HANYA et al., 1973). This was about 50 % of the total released mercury. At Tokuyama, within the bay area, the accumulated mercury in the sediment was estimated to be 15 tons in 1972 (NAKANISHI et al., 1973), which is 15,-20 % of the total estimated discharge. These examples suggest that a fair amount of the discharged mercury settles and deposits in the area near the source. The average diameter of polluted particles in the sediment appears to be 50 pm or less (NISHIMURA and KUMAGAI, 1974), the settling velocity of which is around 18 mor less. However, most of the finer particles seem to settle rapidly to the bottom, by agglomeration of particles. The above situation may be explained in this way. (B) Motion and depositing process of the pollutant on the sea bed: The horizontal distribution of the contaminated suspension is formed as the result of the interaction of two processes, referred to above as 2) and 4). Then the horizontal distribution of contaminant in the sediment is governed by process 3). The horizontal and settling velocities of the sediment control these processes. The critical velocity for initiating sediment movement has been studied by many researchers. In this paper, we select certain contributions and review the relationship between particle size, critical velocity and settling velocity (Fig. 9). From this figure the behavior of sediment particles can be devided into four categories, according to the region defined by water velocity and particle size. Region 1: After erosion, sediment is suspended again. Region 2: Sediment rolls or saltates on the bottom without being suspended again. Region 3: Suspended matter settles and de-
Regular
Patterns
of Sediment
Contamination
229
To estimate the horizontal mixing of pollutant in sediment on the sea bed, the results of studies on the dispersion and stranding of radioactive labelled sand (INOUE, 1956; SATO, 1962, 1963) can be utilized. To interpret the studies, the basic equation for horizontal mixing from a radially symmetric source will be used as an analogy. For an instantaneous point release of contaminant of amount M, the general solution was given by OKUBO (1962) with diffusion coefficient K(=Arm). In case of m=1, the solution was Fig. 9. Relationship between particle size:and motion on sea bottom. Uer.(V), critical velocity after VANNONI(1964); Ucr.(W), critical velocity after WHITE (1970); Usettling, settling velocity of particles with specific density 2.5. Circle numbers indicate regions. posits to the bottom. Suspended matter is maintained in a suspension without erosion, rolling, saltation or settling. Very small particles of diameter less than 50 gm, which are now being discussed, mix and disperse in the sediment by repeating the processes of Region 1, 3 and 4, but not of Region 2. Thus the transport of pollutants in the fine sediment will go through the following process : Pollutants and polluted fine particles remain in suspension and are dispersed by water movement, stay for a long time in the water near the bottom and spread over a wide area. Once the particles settle and form a deposit, a surface contamination pattern soon appears on the bottom sediment corresponding to the contamination pattern of the floating particles in the water above. Under such conditions, removal of the deposited pollutant takes place very slowly because a velocity (Ucr in Fig. 9) greater than the critical shear is not as likely to occur as often as the condition which allows particles to float. This means that when compared with the rate of contamination process, recovery process will be slow. The above mentioned conditions may bring about formation of a highly contaminated suspension layer just above the bottom, as observed in polluted waters. 4.2. Diffusion of pollutant in sediment
(JOSEPH and SENDER, 1958) and m=4/3,
(5)
the solution was
(6)
(OZMIDOV, 1958)
Region 4:
where the
CI
is
the
distance
time, is
p the
is
the
the the
of
and
2/3 Of
the
n
results
employed
(Fig.
assumed
transition
of
From
former
power
r of
the
solution
dispersed
area
sand.
Little
value
it
may
than
an
discussed
tracer
either and
less
1956),
of
of
of
n
reasonably
1
of
can
sediment
diffusion
area
In
the
grains
and
above
than by
150ƒÊm) rolling of
area
is be
lies
around
shown
that
of
diffusion
m
the (1
experiment, so
coarse
the
sand
than
by
this
the
surface
upon
exponent
mentioned were
the
depend
the
for
the
11).
that
may and
in
(Fig.
assume
rather particles
also
tracer
employed
disperse behavior
are
other
we of
greater
The
C
(INOSE,
radioactive
the
this,
coefficient
sand
s-1).
distance
relationship
patterns of
sediment
3/4).
nth
is
the
the
when
n
and ƒÁ
1/3.
distribution
scale
of
is the
solution.
10),
that and
linear
concentration
radioactivity
difference
s-1)
relationship
linear
the
is
a
data the
r t
(cm2/3
for
experimental
the
The
1
patch,
(cm
n, the
latter
between
and
is
the
verifies
above
1/2
power, of
S;
for
analysis
S
nth
a patch,
parameter imply
logarithm
contour
of
velocity
solutions
between
in
center
dissipation
above
and
the diffusion
energy
The
concentration
from
size
and the
(diameter seemed suspension. are
classified
to
HIRAIZUMI,
230
MANABE
and NISHIMURA
Eq. (4), expressing the regular pattern controlling the contamination of coastal sediment. As was shown in the preceding, this process is similar to diffusion of pollutant in the surface water layer. Assuming that the polluted particles disperse in the nepheloid layer or in the suspension layer on the bottom of thickness H, the following equation can be derived, (7) where r is the the dispersion
distance from the source, K is coefficient, M is the rate of
pollutant discharge, C is the pollutant content in the sediment and c is the ratio of settling Fig.
10.
Examination
of
dispersion
radioactive sand on sea, bed with time-at Tomakomai, 1955-count activity root
to area
8, or the
of S bounded
cube
patterns
of
portion is that
of
pollutant.
the elapse of C of radioroot
by the contour
The
boundary
condition
(7a)
or square
for count
C.
If
we
assume
(7b) The
solution
becomes
(8)
Fig. 11. Typical example showing extension of dispersion area of radioactive labelled sand on sea bed with the elapse of time-at Kashima, 11.1 m depth-based on the data of SATO (1962).
into Regions 2 and 3 of Fig. 9. For a smaller disperion range r, the coarse particles may be suspended in eddies and this dispersion seems to be controlled by eddy diffusion. For a larger diffusion range r, the sand particles probably settle before completing dispersion in the larger eddy. This suggests that even the dispersion of coarse grain sediment may partly be accounted for by eddy diffusion. 4.3. A formula describing the distribution of polluted sediment In Section 3 we found an empirical equation,
where S is the area bounded by the contour, of the pollutant concentration C, and n and A are constants. In Eq. (8), C represents the pollutant content in the sediment as a whole. Now we use Ca as a pollutant concentration in the fine sediment fraction f, and reduce Eq. (8) to the following equation, assuming that the product Af is equal to a constant parameter A' , (9) From the above discussion, the exponent of the diffusion coefficient in Eq. (7b) appears- to be in the range of 1 to 4/3 and we expect K at about the value Ar1.0 on the basis of the above analysis of Eqs. (5) and (6), and the observations. On the other hand, from the results of the preceding, Sec. 3.2., we estimated that n/2 of Eq. (9) averaged to 0.65 and ranged from 0.4 and 0.9. Therefore we know that. it ranges from 0.8 to 1.8. This result implies that
Regular
Patterns
of Sediment-
the physical processes leading to Eq. (9) are similar to those leading to Eq. (4) 5.
Conclusion Based on a treatment of the fine particle fraction, a formula has been deduced which expresses the relationship between the continuous influx of pollutant from a fixed source and the extent and the intensity of sea bed contamination. The horizontal dispersion of the contaminated sediment resembles that of the effluent from a coastal source in the surface water and a similar correlation formula could be derived for the contamination of the sediment. The behavior of the fine sediment suggests that when compared with the process of contamination, once settled sediment is supposed not to be easily suspended again, and natural elimination of the polluted sediment takes place slowly. These findings make it possible to fairly accurately predict and assess the degree of contamination of bottom sediment once the amount of pollutant discharge at the coast is known. Acknowledgement The authors wish to express their gratitude to their colleague, Dr. Mikio KUMAGAI, for his constructive criticisms and suggestions. Also, the authors wish to express sincere appreciation to Dr. Nicholas C. KRAUS, Nearshore Environment Research Center, for his helpful review of the manuscript. References HANYA, T. and T. AIZAWA (1973): Accumulation of mercury in Minamata Bay. In, Mechanism of Water Pollution, ed. by Kyoritsu Publ. Co., Tokyo, pp. 92-117 (in Japanese). HIRAIZUMI,Y., T. MANABE, M. TAKAHASHI,K. NISHIDA, H. JOH and H. NISHIMURA (1975): Analysis of PCBs contamination of sediment in the coastal waters of the Seto Inland Sea. La mer, 13, 163-169. HIRAIZUMI,Y. (1976): PCBs pollution in the Seto Inland Sea-Its pathways and influxes-Kagaku (Science, Japan), 46, 314-322 (in Japanese). INOSE, Y. (1956): Observation on stranded sand
Contamination
231
using radioactive tracer. Proceeding of 2nd Coastal Engineering Conference, Tokyo, pp. 163-167. JOH, H., S. YAiviocHi and T. ABE (1974): Condition of heavy metal pollution in Osaka Bay. Bull. Osaka Fish. Exper. Stat., No. 4, pp. 1-41 (in Japanese). JOSEPH, T. and H. SENDER (1958): ilber die horizontale Diffusion im Meere. Dt. Hydrogr., 2., 11, 49. KUMAGAI, M. (1977): A Study on the pollution of coastal marine environment. Doctoral dissertation, Department of Chemical Enginnering, University of Tokyo, Japan, 257 pp. . MANABE, T. and T. TAKESUE (1974): Contamination of bed sediment in Harima-nada. Bull. Fish. Exp. Stat. of Hyogo-ken. No. 14, 61-67 (in Japanese). MANABE, T., H. SAKAGUCHI and T. TAKESUE (1974): Observation about heavy metals distribution in sediment of Harima-nada. Annual Report of Hyogo Fisheris Experimental Station, No. 48, 281-286 (in Japanese). NISHIMURA, H. (1973): Pollution in Seto Inland Sea-Oil pollutionKagaku (Science, Japan), 43, 171-179 (in Japanese). NISHIMURA, H. and M. KUMAGAI (1974): Heavy metals pollution in Seto Inland Sea. Kagaku (Science, Japan), 44, 103-109 (in Japanese). NAKANISHI, H., M. UKITA and K. MAEDA (1973): Mercury accumulation in sediment of Tokuyama Bay. Effluent Treatment Technology, 14, 915925 (in Japanese). OKUBO, A. (1962): Review of theoretical model for turbulent diffusion in the sea. J. Oceanogr. Soc. Japan, 20th anniversary vol., 286-320. OZMIDOV, R. V. (1958): On the calculation of horizontal turbulent diffusion of the pollutant patches in the sea. Doklady Acad. Nauk SSSR, 120, 761. SATO, S. (1962): Environmental setting of Kashima Industrial Port. vol. 2, ed. by Ministry of Transportation, Tokyo, 201 pp. (in Japanese). SATO, S. (1963): Observation and analysis of stranding sand by isotope technique. Technical Note of Port and Harvour Technical Res. Inst., No. 5, 1-200 (in Japanese). VANNONI, V. A. (1964): Measurement of critical shear stress. Calif. Inst. Tech. Rep., No. KH-R-7. WHITE, S. J. (1970): Plain bed thresholds of fine grained sediments. Nature, 228, p. 152. YANAGI, T. (1973): Current and sediment of Hiuchinada. Research Note on Coastal Oceans, 11, 8-11 (in Japanese).
HIRAIZUMI,
232
MANABE
and NISHIMURA
日本 沿 岸 に お け る 底 質 汚 染 分 布 の 規 則 性 平泉
泰*,真 鍋武彦**,西 村
肇*
要 旨:日 本 沿 岸 に お け る 底 質 汚 染 の 観 測 結 果 を 解 析 し
染 負 荷 量 の 間 の 定 量 的 関係 に規 則 性 が 見 出 され た.こ の
た.微 細 泥 比 率 を入 れ て,底 質 の 汚 染 を 表 示 す る と,汚
規 則 性 はCOD,n-ヘ
染 の 強 度,汚 染 面 積,継 続 的 に 沿 岸 水 域 に放 出 され る 汚
認 め られ,共 通 の 関 係 式 で表 示 され た.
*東 京 大 学 工 学 部 化 学 工 学 科 〒113東 京 都 文 京 区本 郷7-3-1 **兵 庫 県 水 産 試 験 場 〒673兵
庫 県 明石 市 中 崎 町
キサ ン可 溶 物 質,重 金 属 に関 し て
汚 染 粒 子 は底 層 水 中 を懸 濁 しなが ら拡散 す る と考 え ら れ,そ
して 底 質 に お け る汚 染 粒 子 の分 布 過 程 は表 層 水 に
お け る汚 染 粒 子 の 分 散 過 程 に類 似 す る.