Desalinatio~~. 30(1979)411424 OElsevierScientif~cPublishingCompany~ Am&dam-PdntedinTheNetherlands
ECOTOXICOLOGY
F.
KORTE
OF
(ref.
Institut
EV @
BELGARD
1)
fiir Chemie
der
und
Weihenstephan,
Technischen
Institut
fur
Universitit
bkologische
Miinchen,
Cbemie
der
Freising-
GSF,
Neuherberg
(G.F.R.)
DUring
the
last
only
in
occur
not
or
overregionally
in
unintended food
andeven all
to
the
- and
a test
and
the
in
the
ecosystem for
the
to
ecotoxicological
to
the-following possible
to
developed.
simulate
substance
an
select
follow
the
parameters ecological
to
ecotoxicological, in
the
still
ecosystem in
These
agreed subjected
area
of
Corresponding
are
parameters
assessment.
practical
be
in
test
the
ecotoxicological
in question
and
including
should
procedures
for
globally
unexpected
internationally
products
ecotoxicology
also
an
physico-chemical,
are
chemicals
everywhere,
it was
approaches to
first,
under
of
two
in
chemicals
Evaluation
area
but
results
- new
includes
industrial
application
Therefore,
new are
that
This
being
toxicology
secondly,
decided
their
and
the
or,
investigated We
which
namely,
investigate
time
questions.
There
procedures
body.
the
procedure
development_
of
environmental
human
physico-chemistry
and
of
for
toxicological
procedures
areas
shown
distribution.
presence
that
it was
decade,
as
such
stage
small
as
a simulated
which
can
parameters
of
screening
be
possible mini-
interpreted
should
then
be
conditions. second be
route
and
determined
conditions
have,
under
(ref_
2,
3,
therefore,
conditions
selected
as
close
as
4):
1) Persistence 2)
Dispersion
3) Conversion Apart ally
from it
these
on
under
use
biotic
parameters
is necessary
4) production 5)
tendency
for
level
an
and to
be
abiotic
conditions
determined
ecotoxicological
(including
the
experimentally, evaluation
composition
of
to
additionknow
technical
(ref.
pattern.
The
determination
of
persistence
the
degradability
of
a chemical 411
in
the
substance
environment in
results
ecosystems.
The
5)
product),
in
data
dis-
412
KORTE
persion like
tendency
biotic
water,
is
and and
soil,
conversion
with
of
screening,
reliable
any
environmental type
of
the
for
of
of
of
each
methods in
test model
these
or
is
of
as
air,
and the
abiotic
industrial A sound
would
in question.
investigation
need
substances
chemicals,that
biotic
parameters
chemical
for
factors in
significance.
reliability
systems
of
derivatives
environmental
limits
feasible
a test
been
system
developed
behaviour whole
and
for
of
6,
this
and
are
and
be
For
a
a
necessary
interpretability.
either
calibration
should
be
for
interpreted
a comparative
known as
evaluation
a
of
set
of
environmental is made
comprise
simulated
the
individual attempt
substances
tests
ecotoxicological in
no
designed
These
ted
but
is being
of
Profile
Analysis
screening tests
is
and
has the
assessed
as
a
7).
chemical
viour
Ecotoxicological
chemicals
scheme,
controlled tests
called
comparative
tested
(ref.
In
a)
for
feasible
data
determination on
includes
phenomena
chemicals.
Thus,
of
The
and
transport
determination
have
ranking
parameter
indications
research
however,
necessarily
Therefore,
chains.
gives
extensive
complex
accumulation,
a potential
scientifically
which
food
products
chemicals
subject
a rather
abiotic
to
(Fig.
aerobic
conditions simulate
information various
are
simulated
ecosystems. regarding
environmental
A series the
beha-
conditions.
1):
technological
sludge,
supply under
to
processes
degradation
(aerobic in
degradation
garbage
pits,
with
activa-
incineration
of
waste)
b)
simulated bolism,
cl
complete
simulated
be
relative the
solvent
acceptable:
suitable
classified
to
the
selection
substance
simulated
processes
distribution
choosing
can
under
transport
solubility,
By
(excretion,
biodegradation/meta-
atmospheric
conditions
9)
water/organic
ces
processes
degradation
a,
(ref.
d)
biological
retention/bioaccumulation)
of
will
standard
be
that
standard
Obviously, compounds
low
in
reference to
suitable
the
if
accumulating,
it
the
important real
is
medium
and
soils).
test-substanbehaviour criterion
behaviour.
still
water,
systems
environmental
most
their
and
standardized
compounds
their
is
soil
-water/soil
seepage
respect
considered means,
from
in standardized systems,
with
standard.
(evaporation
A
environmentally
degradable,
and
for
413
KoR!rE
ecotoxicologically compounds, For
dichloro-biphenyl
instance,
ting,
while
Among
acceptable.
seems
dichloro-biphenyl
to satisfy
is easily
tetrachloro-biphenyl
accumulates
the widely
is much
used
organo-chlorine
the above
degraded
conditions.
and non-accumula-
less degradable
and already
in organisms.
Mammalian
Metabolism
Biodccuf lulation
stored
RATS
ALGAE
3 oral administrations
% and cont. in fish
constant
% and cont. in
0.05 mgll
equivalent
to lmglkg in diet
Atmospheric
sorbed
Fig.
1. Outline
In all these ces
are
range on
of
experiments,
of potential
the
pound
test,
and/or
radioactivity tained
the standard
Concentrations
occurrence,
released/excreted
that
unreacte
analysis
as well
of applied is ppb up
as the test-substan-
substances
to
a
few
are
ppm-
in the
Dependins
vs. the amount
of radioactivity
re-
are determined. degradation,
experimental and transport
metabolism
by rats,
upon waste
cornposting as well
with
profile
lf.
the data measured are radiolabelled C02. the parent comthe sum of conversion products. Ratios of the amount of
The standardized tion,
composting
-1. unreacted
ecotoxicological
l4 C-labelled.
=I= reacted
waste
Y. I unreactd
I-
camposting
IO mglkg standard
-‘orgonics
to silicar
incuboCon
sludge
Waste
Break-down
sunlight
accumulation
and activated
design
to provi de data
includes by
tests
for accumula-
for excretion
fish and by algae,
and
the conversion
as the determinate on of mineralization sludge.
414
KORTE of
Details
and
the
test
performance
have
been
reported
in
references
5
8. so
tests were use
far,
a set
with
additional
selected
for
homologous
The
scale
of
tested
up
to
the
acid
The
the
This
In order
to
products
in plant
residence
nificant In
summarized.
identical than
800
water
between
in
presented ducts
The
the in
(CO21
chemical under
2)
lower 4 and
different and
the
table an
its
also
low
4,
is
the
(table
impurity aryl
suc-
compound,
The
in
an
hour
results
as
The
at in
120°C. no
sig-
tests
are
compared
to
All
factor
for
accumulation and the
about whole
EV to
chemicals
of
some
the
5)
a good
200
is even by
times In
lower
1 and
(table
sludge
3)
degradation
test,
The
pro-
photoover
10%
conditions.
had
chemical
been to
designed
chemical
to
result
in order
to
in
significant
achieve
is
com-
mineralization
biomass.
in
golden
below
rats
EV is
accumulating
activated
in
Belgard factor
set.
known
fixation shows
determined.
acid.
Retention
formation
acid.
EV derived
conditions.
Belgard
standard
maleic
degradation
maleic
compared
The
be
presented
coumarin
of
to
130°C
accumulation fusca.
as
body.
and
set
products.
and
hexachlorobenzene.
shows
at
identical
chemical
low
the
major
active
about.half
1 week
monomer
compound
is
in
the Belgard
had
is
EV
under
apFreCiable
procedure from
for
accumulation
than
as
monomeric
of
decomposition
accumulating
included
acid
the
the
stability
Belgard
to
natural
of
of
plant
Chlorella
mineralization
test
and
chemicals
500 to 5000. The labelled product 14 the C-label in the 2.3-position of
accumulation
including
mammalian
and
weight
its
assessed
been
fumaric
15%
tables
9% which
standardized
differences
50
chemicals,
contains
of
identity
of
a medium
has
contains
volatile
algae
the
(table
pounds
of
been
highest
times
system
The
characteristics,
chemical
solution
results
these
have
to
the
orfes
mg/l
I-5
1 shows
fresh
of
the
is
has
effluents,
1.2
In
molecular
analysis
chemicals
Table the
in
completed.
product
anhydride,
the
EV
amounts
a desalination
formation
25 other
small
product
in
a
tables
in a test
technical
and
establish
time
Autoclaving
screened
classes
Belgard
The
overall
profile
monomer.
been almost
physico-chemical
agent
polymaleic
for
has are
different
of
preventive
acids.
used
covering
chemicals.
hydrolysed
chemicals chemicals
series.
7% maleic
cinic
50
a variety
patterns,
some
of
a ranking.
KoKrE
415
Table
1:
Accumulation
in algae
(Chlorella
chemical
fusca)
% in algae
% in water
=24
Hexachlorohenzene
60
Hexadecanol
95
10
18 Ooo
2,4,6,2',4'-Pentachlorobiphenyl
79
15.5
11 SW
2,5,4'-Trichlorobiphenyl
67
17.5
7 700
Dodecane
69 70
17 24
8000
Aldrin
58
21
Di(2-ethylhexyl)phthalate Pentachloronitrobenzene
67 37/43
2,2'-Dichlorobiphenyl
5
24 000
5 800 5 400
38 31123
3 600 2 4w/3
700
Pentachlorophenol
35
57
1 240
Hexachlorocyclopentadiene
31
54
1 140
2,6-Di-tert-butylphenol
61
24
800
Biphenyl
14
53
540
6.5
93
140
6.5
93
140
5.8
85
135
2,4,6-Trichlorophenol
7
92
116
p-Chlorobenzoic
Belgard
ES
Coumarin n-Dodecylbenzenesulfonate
(Na)
acid
3
100
63
Hydroquinone
3
99
.63
p-tert-Butylphenol
1.7
99
35
Nitrobenzene
0.9
74
24
Monolinuron
1.0
97
15
Maleic acid p-Nitrophenol
0.7
99
14
o-5
99
11
Aniline
o-4
94-s
8
0.3
99
6
2,4-Dichlorophenoxyacetic
Amount
of algae: chemical
f24
acid
0,l g/l dry weight concentration
= 0,5 g/l fresh
in algae pg/g
fresh
= final
chemical
concentration
in water
weight
weight
@g/ml)
after
24 h
416 Table
2:
Accumulation
in fish within
3 days
chemical
average exposure
f24
(pg/l) Hexachlorobenzene
39
400
Hexadecanol
48
18
2,4,6,2*,4'-Pentachlorobiphenyl
34
770
2,5,4'-Trichlorobiphenyl
36
850
Dodecane
37
17
Aldrin
30/2
Di(2-ethylhexyl)phthalate Pentachloronitrobenzene
680/1180
20
85
33/6/0.4
250/320/380
2,2'-Dichlorobiphenyl
50
830
Pentachlorophenol
42
350
Hexachlorocyclopentadiene
48
308
2,6-Di-tert-butylphenol
37
230
Biphenyl Belgard EV
33
110
Coumarin
46
45
n-Dodecylbenzenesulfonate
(Na)
0.5 c
0.1
48
43
2,4,6-Trichlorophenol
30
80
p-Chlorobenzoic
53
acid
Hydroguinone
1.1
80
33
p-tert-Butylphenol
46
39
Nitrobenzene Monolinuron
50
Maleic
45
acid
31
0.8 -cl0
1.4
p-Nitrophenol
50
Aniline
55
1.7
50
2
2,4-Dichlorophenoxyacetic chemical f24 =
cont.
3 x average
acid
in whole
chemical
fish
cont.
+g/g)
in water
@g/ml)
19
417
KoKrE
Table
3:
Excretion and retention applied doses)
of chemicals
chemical
by rats
total excretion
(%I
(in % of
total
storage (%I
Hexachlorobenzene
30.6
57.2
Hexadecanol
27.2
65.4
37.4
40.7
2,4,6,2',4'-Pentachlorobiphenyl 2,5,4'-Trichlorobiphenyl
107.9
Dodecane Aldrin Di(2-ethylhexyl)phthalate
19.0
12.7
68.2
29.1
100.4
7.1
Pentachloronitrobenzene
98.6
2,2'-Dichlorobiphenyl
99-I
0.2
Pentachlorophenol
87.5
1.6
Hexachlorocyclopentadiene
96.1
'2,6-Di-tert-butylphenol Biphenyl Belgard
EZV
83.3
2.9
78.4
0.4
86.9
9.1
114.9
Coumarin n-Dodecylbenzenesulfonate
(Na)
85.3
2,4,6-Trichlorophenol p-Chlorobenzoic
acid
0.6
n.d.
104.5
7.8
89.2
0.1
Hydroquinone
100.0
0.4
p-tert-Butylphenol
112.3
0.1
Nitrobenzene
74.7
2.3
Monolinuron Maleic acid
98.2 25-O
6.7
p-Nitrophenol
76.5
0.4
Aniline
83.3
0.5
2,4-Dichlorophenoxyacetic
n-d.
= =
not detectable not analysed
acid
(CO.01
102.5
%)
l-1
418
KORTE
Table
4:
Mineralization, accumulation of
chemical cone,: 50 pg/l
degradation, chemicals by
volatilization and activated sludge within
volatilization
minerafization
%
%
% degradation products in sludge
3.0
Hexachlorohenzene
Accumulation
/ water
n-d.
5 days
n-d.
f5 32
000
28.5
28.0
30
3
170
2,4,6,2’
1.2
0.2
1
27
800
2,5,4 '-Trichlorobiphenyl
0.5
n-d.
32
000
18
Hexadecanol ,4*-Pentachlorobiphenyl
71.4
38.0
Dodecane
37.0
1 300
18-8
Aldrin
1.5
11.1
n-d.
Di(Z-ethylhexyl) phthalate
1 .o
1
n-d_
Pentachloronitrobenzene
7-O
2,2'-Dichlorobiphenyl
6.6
39.2 0.1
0.8
2.3
000
3 000 4
500
6
300
Pentachlorophenol
0.5
10.6
5
7
700
Hexachlorocyclopentadiene
2.0
49
26.4
2
350
2,6-Di-tert-butylphenol
7-7
1.1
29.8
15.1
2
600
Biphenyl
9.1
8.5
7.8
8.5
Belgard
EV
Coumarin n-Dodecylbenzenesulfonate (Na)
3.1 29.5
3.5
3.0
1
29
1
260 400 140
n.d.
40
55
5.1
5.4
acid
n.d.
3.7
0.1
2,4,6-Trichlorophenol p-Chlorobenzoic
3-3 30.0
430
n-d.
170
Hydroguinone
7.6
7.5
19.7
24.4
520
p-tert-Butylphenol
4.9
0.2
3.7
n-d.
240
Nitrobenzene
1.7
0.4
n-d.
n-d.
40
Monolinuron
0.5
n.d.
8
70
acid
26.9
26.3
p-Nitrophenol
1.4
1-l
0.5
34.7
37.0
37.0
21.4
11.7
Maleic
Aniline
0.1
2,4-Dichlorophenoxyacetic acid chemical f5
n.d.
cont.
in
2
41
0.14
sludge
(r_lg/gdry
weight)
=
final
chemical
not
detectable
cont.
in
(CO,l%)
aqueous
after
phase
(pg/ml)
-
not
=
30 1 030
n-d.
=
analyzed
800
5 days
77
K0Rl-E
Table
419 5:
Photomineralization
chemical
of org.
chemicals
concentration of chemical (rig/g silica gel)
Hexachlorobenzene 2,4,6,2*,4*-Pentachlorobiphenyl Dodecane Aldrin
organic fragments in % of applied org. carbon
17 h
CO2 in % of possible upon grant. mineralization
0.1
1.5
1 680
0.5
3.1
60
0.1
5.2
125
Hexadecanol
within
240
0.7
2.9
45
0.1
8.8
0.1
1.6
Pentachloronitrobenzene
40
0.1
43.0
Di(2-ethylhexyljphthalate 2,2'-Dichlorobiphenyl
77
o-1
Pentachlorophenol
80
0.1
3-5 62.0
Hexachlorocyclopentadiene
64
0.1
46.0
2.6-Di-tert-butylphenol
30
0.7
29.5
Biphenyl
80
0.1
2 500
0.1
12.1
250
0.1
97
0.1
59-2 3.2
Belgard
HV
Coumarin n-Dcdecylbenzenesulfonate (Na)
9.5
2,4,6-Trichlorophenol
80
0.1
65.8
p-Chlorobenzoic
30
0.1
6.3
62
0.1
57.4
100
0.1
46.8
acid
Hydroquinone p-text-Butylphenol Nitrobenzene
60
0.1
Monolinuron
65
0.1
38.3
165
0.1
17.0
p-Nitrophenol
80
0.2
39.1
Aniline
39
0.8
46.5
115
0.1
26.2
Maleic
acid
2,4-Dichlorophenoxyacetic acid
6.7
420
KORTE
Nevertheless, same
rank
The
several
since
fact
partly
that
differs
perties
or
dures.
in
this
set to
to
from
of
this of
are
to
environmental
of
chemicals
where
lable
for
ding
to
correct. the
the
the
environment
Theseare test
final
system.
final
in
The
production
level,
the
general
of
ihe
experimental
obtain
controlling
dustrial
e.g.
lease
10 -
coastal There
30 tons
is only
- thus
fore,
the
With
14%
an
need
for
not
the
priority
with
system
the
the
to
positions are
ranking
relative
test
posi-
the
the
are
and this
profile
avaiaccor-
ranking
is
predictive
allow
to
the
pathways
additional and
information, Belgard
EV
there of
of
the
To
of
the
the
individual
into
a the
chemical
knowledge
taking
and
achieve
especially
additional
seawater
standard
a reliable
chemicals_
reasonable
in
for
analysis
is necessary,
capacity
year
a
that
experiments
the
of
Provided
negligible
in-
results
assessment.
and
more
account
its
use
in
in-
desalination
and
exten-
would be no sewage treatment, 3 drinking water will rem
5000
chemically
unchanged
product
into
data
overall
evapcrate.
The
EV
standard acid
transfer
exposure which
of
the
of mammals are
product
into
results
favourable,
from
are
drinking its
use_
sufficient
for
Therethe
3).
Photochemical
maleic
Belgard
per
direct
(table
not
water.
no
standard
screening
(97%)_
With
deposition
a daily
do
knowledge
complete
Systems.
with
in
listing
pattern,
used
scale
fact
of
that
proproce-
water.
water
does
were
Cooling
a plant
more
that
The
compared
found
substance
compound
experimental
concluded
experimental
alone
system
this
procedures
for
the
additional use
the
sense.
of
environment.
one
Furthermore,
obtained
significance
the
to
sive
a relative
of
the
opportunity
were
data
results
is
by
sophisticated
it was
experiments
listing
To
and the
environmental
reasonable
from
3) have
different
possible_
an
(table
position that
factors.
problem
system,
Consequently,
is
data
respective
test
the
it is
test
different
test
excreted.
addressed
experience
evaluate those
rat
reveals
chemicals
test
the
tests
test
factors
ranklng
differ
in
quantitatively
test
biological
and
tions
are
from
According
listing
chemicals
they
molecular
Furthermore, reactions system
in the
is really
weight
product
500
to
incineration occur
showed
mineralized.
of
in
the
5000 is
water
the
almost
confirmation
is
itself
quantitative
surface
a photomineralization
some
product
or of
in
sea-
12%_
With
necessary
whether
KORTE
421
Confirmatory with
experiments
tropospheric
tions
of
BV up
demonstrated TABLE
and
Belgard
mineralization
(table
in
the
52%.
aqueous
'hemical
elgard
Analysis
Concentration carrier EV
show
concentra-
tropospheric
mineralization
could
,X nm
The
also
be
>290
the
>290
17
4
165 rig/g Silica gel (standard)
>290
17
16.5
80 rig/g Silica gel
>290
88
71
which
was
Belgard
the
which
is,
of
degrading
to
in
added
this
substantiated
was
the may
the
with salt an
the
content
intentional
when same
within
fresh
experiment
great
3 and high of
sludge
from
implant
17 days
binding
the
to
chemical
freshwater
a desalination in
inoculum,
no mineralization
sludge
were from
2.5
test, plant
resulting
products
46 days_
as
elimination
seawater
is of
in desalination
between
as well
activated
degradation
However,
product
occur
varied
context, to
normal
to
they
exposure
using
volatile
incubation.
as
mineralization
carried-out
Without
10) was
for
Additionally
diluted
formation
be
7),
definite
were
EV_
of
potential
concentrations
in
water.
experiments
7.3
52
(table
biomass
__-_-------__--_ 72
67
in
EV
12.1
>290
effluents
the
17
-G90
Belgard
% co2
60
Using
resulted
Irradiation time in h
72
microbial
and
of
>230
portance-
could
different
gel,
- Photomineralization
and
2,500 rig/g Silica gel (standard) _---.-----1 mg/g Silica gel
aleic cid
(ref.
irradiation
solution.
Profile
450 ng/ml aqueous solution
days
and
silica
Additionally,
4,950 rig/g Silica gel
or
sunlight
absorber
long-term
6
Ecotoxicological
from
including
stratospheric
on
to
61,
found the
a degradation
mg/l
within North to
35 Sea
about
20%
422
TABLE
7
Ecotoxicological
b:y Aquatic
Profile
- Mineralization
Analysis
Test duration days
I noculum Concentration ug/lit& sludge 990 970 1150 990
Accum. biomass
1
fish
TABLE
n-d.
system
was
(table
does
not
include
on
the
bioaccumulation
included
8).
that
20
-
knowledge
From
there
and
the
is
1 67.1
46
standard
concluded
2480 2780
38
broader species
1260
17
Staawater from dcasalination + sludge P lant 2500 L
varied
Ev
4 3.3
1400
5’ 13
from S eawater dlesalination P lant 2500
The
Belgard
% co2
in
A ctivated
obtain
of
Microorganisms
exposure
marine
no
as
factors
bioaccumulation
In
test
f3d
=
to
seawater
duration
obtained
(PCP,
order
a
potential,
as well
concentration
organisms.
it
were
can
be
1,100).
8
Ecotoxicological
Profile
I Fish golden
Exposure pg/liter
:
orfes
Analysis
- Accumulation
f3d
f13d
45 1080
1.6 3.3
2.5
50 1000
3-l O-4
l-4
of
Belgard
Ev
in Fish
I dascyllus I Analogous algae and
(table
two
marine
concentration after
24
hours
confirmatory 9).
Algal
species in
algae
the
experiments concentration were is
and
included.
reached
concentration
were
For
already declines
made
for
exposure this after again-
accumulation
levels
product
varied
a steady
5 hours The
were
in
state
exposure
factors
shown
and
KmrE
423
seem to demonstrate real bioaccumulation. However,-data, especially_ -. In this test, strongly depend on the experimental conditions. Adsorbed amounts
cannot
the cells
be differentiated
in nutrient
L between
significantly
TakLng
conditions.
medium,
this
algae
is as by fish,
TABLE
9
Ecotoxicological
from
a factor
in the cells.
concentration
of S to 200 depending
into account,
that means
Profile
those
the product
accumulation
Upon washing
is reduced on washing
of Belgard
EV by
insignificant_
- Accumulation
Analysis
of Belgard
EV in Algae
I
Exposure ug/liter Freshwater Chlorella O-1 g/l 1 g/l 0.1 g/l 1 g/J
fld dry weight
66: 1020 1300
Seawater Dunaniella 0.1 g/l
700 3960 1500 3200
140 790 300 650
800 330
160 66
877:
Seawater from desalination plant Dunaniella 0.1 g/l
2500
420 250
Tetraselmis 0.1 g/l
2500
690 543
+
=
washed There
- e.g.
twice
via
irrigation
systems.
the product firmation in a much
water
is retained showing
higher
that
138
110+
waste
test on uptake under
could
be exposed
the product
composting
in the matrix
that
uptake
soil
containing
The standard
an additional
out,
84 50+
seawater
is some possibility
cooling
carried
with
fld fresh weight
and not highly by plants
conditions
than
in nature
in soil and not significantly
taken-up
from
test had
this
which
industrial shown
mobile.
(table
that For con-
10) was
definitively
product
by plants.
to the product
is mainly
result fixed
424
KORTB
TABLE
10
Ecotoxicological from
Profile
- Uptake
Analysis
of
Belgard
EV
by
plants
soil
Duration days
Exposure
Soil 0.16
Uptake barley %
Non-extractable from soil %
0.17
81
13
pg/g
.
+ From
the
discussed
investigations Belgard
it can
EV will
be
ecotoxicologically In
this
general,
used priate
for
ranking
for
whole be
example of
data
from
that
no
in organisms
according
shows
chen;icals,
confirmatory
of
concluded
present safe
set
to
that can
the
the easily
standard
effective
and
that
it
presently
special
levels
Of
is, used
test-system, be
and
extended
consequently, concepts.
originally where
appro-
evaluation.
REFERENCES The investigations reported in this paper have been carried out in collaboration with D_ Freitag, S. Gab, H. Geyer, W. Klein, R. Kloskowski, D. Kotzias, A. Rraus, and E. S. Lahaniatis, F. Korte, OEPP/EPPO Bulletin, 4 (1972) 27. F. Korte, W. Klein, and B. Drefahl, Naturw. Rdsch., 23, 11 (1970) 445-457. W. G. Appleby, IUCN 11th Techn. Mtg., New Delhi, 1969, 1, Morgues, Switzerland, 1970. in F. Coulston and F. Korte (Eds), Environmental N. A. Iliff, Quality and Safety, Vol. 2, Global Aspects of Chemistry, Toxicology and Technology as Applied to the Environment, Georg Thieme Publ., Stuttgart, 1973, pp. 64-71. F_ Korte, D. Freitag, H. Geyer, W. Klein, A-G. Kraus, and E_ Lahaniatis, Chemosphere, 1 (1978) 79-102. F. Korte, in W-J_ Hunter and J.G.P.M. Smeets (Eds.), Proceedings of the Int. Colloquium The Evaluation of Toxicological Data for the Protection of Public Health, Luxembourg, December 1976, Pergamon Press, Oxford, 1977, pp. 235-246. hb, SJ.Schmitzer, H-W. Thamm, H. Parlar and F. Korte, Nature, 270 (1977) 331-333. D. Kotzias, W. Klein, F. Lotz, S. Nitz and F. Korte, Chemosphere, 5 (1979) 301-304. 10 The collection and supply of sludge by Dr. Ernst, Institut fiir Meeresforschung, Bremerhaven, is acknowledged_