xvEPA
              United States
              Environmental Protection
              Agency
              Office of Water
              Regulations and Standards
              Criteria and Standards Division
              Washington DC IJ0460
ErM 440/5-80-068
October. 1980
Ambient
Water Quality
Criteria for
Polychlorinated  Biphenyls

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     AMBIENT WATER QUALITY  CRITERIA FOR

         POLYCHLORINATED 8IPHENYLS    !
                Prepared By
    U.S. ENVIRONMENTAL PROTECTION AGENCY

 Office of Water Regulations and  Standards
      Criteria and Standards Division
              Washington, O.C.         I

     Office of Research and Development
Environmental Criteria and Assessment Office
              Cincinnati, Ohio

        Carcinogen Assessment  Group
              Washington, D.C.

     Environmental Research Laboratories
              Corvalis, Oregon
              Duluth,  Minnesota       i
            Gulf Breeze, Florida      •
         Narragansett, Rhode Island   •!

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                               FOREWORD
    Section 304  (a)(l) of  the  Clean Water Act of  1977  (P.L.  95-217),
requires the Administrator of  the Environmental  Protection Agency  to
nuhlish criteria for water  quality accurately reflecting  the  latest
nus  cr
Sclitlflc ^knowledge on the  kind  and extent of all identifiable effects
on  health and* Sare which  may be  expected  from  the presence  of
on   ea    an
Snutants in any body of water, including ground water. | Proposed water
auaitv criteria  for the 65  toxic  pollutants  listed under section 307
(a)(l) of  the Clean Water Act were developed and  a notice  of their
ava  lability was  published for public comment on Merch 15. 1979 (44 FR
15926), July 25, 1979 (44 FR  43660),  and  October 1, 1979 (44 FR 56628).
This  document  is a revision  of  those proposed criteria  based upon a
consideration of  comments received  from  other Federal  Agencies, State
agencies,  special interest  groups,  and  individua   scientists.   The
criteria contained in this document replace any previously  published EPA
criteria  for the 65  pollutants.    This  criterion  document  is  also
published in satisif action of  paragraph  11 of the Sett lianent Agreement
in  Natural  Resources Defense  Council, et. , al . vs.  Traon,  8 ERC 2120
(D.O.C. l^b), modified, 12 EEC im (D.IJ.C.  MM).    ,
    The  term  "water quality criteria" is  used  in two • sections i of the
Clean Water Act, section 304 (a)(l) and section 303 (c) 2).  The term Jias
a different program impact in each section.  In sectioin 304,  the term
represents  a  non -regulatory, scientific assessment  of ecological ef-
fects. The  criteria presented in this publication are such scientific
assessments.   Such  water quality criteria associated  with   specific
stream uses when adopted as State water quality  standards under section
303  become enforceable maximum acceptable  levels  of a  pollutant in
ambient  waters.  The water quality criteria adopted  in the State water
quality  standards could have  the same numerical  limits as the  criteria
developed under section 304.   However, in  many situations States may want
to adjust water quality criteria developed under section  304 to reflect
local  environmental  conditions  and  human exposure  patterns before
incorporation  into water  quality standards.   It is  mot  until their
adoption as part of the State water quality standards that  the criteria
become regulatory.

     guidelines  to  assist  the States  in  the modification of  criteria
presented  in  this  document,  in  the development  of  water quality
standards,  and in other water -related programs of this Agency,  are  being
developed  by  EPA.
                                     STEVEN SCHATZOW
                                     Deputy Assistant Administrator
                                     Office of Water Regulations and Standards
                                   iii

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                             ACKNOWLEDGEMENTS
Aquatic Life Toxicology

   Charles E. Stephan, ERL-Duluth
   U.S. Environmental Protection Agency


Mammalian Toxicity and Human Health Effects

   Jonathan Ward  (author)
   University of Texas

   Steven D. Lutkenhoff (doc. mgr.), ECAO
   U.S. Environmental Protection Agency

   Bonnie Smith (doc. mgr.), ECAO-Cin
   U.S. Environmental Protection Agency

   Patrick Durkin
   Syracuse Research Corporation

   Alfred Garyin
   University of Cincinnati

   Betty Hemdon
   Midwest Research  Institute
    Steven D. Lutkenhoff, ECAO-Cin
    U.S. Environmental Protection Agency

    Anne Trontell
    Energy Resources Co., Inc.
    Robert Wllles
    Health and Welfare
    Canada
David J. Hansen, ERL-Duluth        C
U.S. Environmental Protection Agency^
Karen Blackburn, HERL
U.S. Environmental Protection Agency

Norman Clarke. HERL
U.S. Environmental Protection Agency

Diane Courtney- ECAO-RTP
U.S. Environmental Protection Agency

Larry Fradkin, ECAO-C1n
U.S. Environmental Protection Agency

Rolf Hartung
University of Michigan

Larry Lowry
National Institute of Occupational
     Safety and Health

Albert E. Munson
Medical College of Virginia

Walter Weigel
National Institute of Occupational
     Safety and Health

Roy E. Albert*
Carcinogen Assessment Group
U.S. Environmental Protection Agency
 Technical  Support Services  Staff:   D.J.  Reisman,  M.A.  Garlough, B.L.  Zwayer,
 P.A. Daunt,  K.S. Edwards, T.A.  Scandura, A.T.  Pressley,  C.A.  Cooper,
 M.M. Denessen.

 Clerical  Staff:  C.A.-Haynes, S.J.  Faehr, L.A. Wade,  D.  Jones, B.J. Bordicks,
 B.J. Quesnell.

 *CAG Participating  Members:
    Elizabeth L.  Anderson, Larry Anderson, Dolph Amicar, Steven  Bayard,
    David L.  Bayliss, Chao W. Chen, John R. Fowle III, Bernard Haberman,
    Charallngayya Hiremath, Chang S. Lao, Robert McGaughy, Jeffrey Rosen-
    blatt, Dharm V.  Singh, and Todd W. Thorslund.
                                    iv

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                          Human Health
     For the maximum protection of human health from the potential
carcinogenic effects due to exposure  of polychlorinated biphenyls
through  ingestion  of contaminated water  and  contaminated aquatic
organisms, the ambient water concentration should be zero based on
the  non-threshold  assumption  for  this  chemical.    However,  zero
level may not be  attainable at the present time.   Therefore, the
levels which may result in  incremental increase of cancer  risk over
the  lifetime  are  estimated at 10"5,  10"6,  and 10"7.   The corre-
sponding recommended criteria are 0.79 ng/1, 0.079 ng/1, and 0.0079
ng/1, respectively.  If  the above  estimates are made for consump-
tion of aquatic organisms only, exluding consumption of water, the
levels are 0.79 ng/1, 0.079 ng/1, and 0.0079 ng/1, respectively.
                              VII

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A.
                                               TABLE OF CONTENTS
                Criteria Summary

                Introduction

                Aquatic Life Toxicology
                    Introduction
                    Effects
                         Acute Toxicology
                         Chronic Toxicology
                         Plant Effects
                         Residues
                         Miscellaneous
                         Summary
                    Criteria
                    References

                Mammalian Toxicology and Human Health Effects
                    Summary
                    Exposure
                         Ingestion from Water
                         Ingestion from Food
                         Inhalation
                         Dermal
                    Pharmacokinetics
                         Absorption
                         Distribution
                         Metabolism
                         Excretion
                    Effects
                         Acute, Subacute, and Chronic Toxicity
                         Synergism and/or Antagonism
                         Teratogenlcity
                         Mutagenicity
                         Careinogenicity
                    Criterion Formulation
                         Existing Guidelines and  Standards
                         Current Levels of  Exposure
                         Special Groups at  Risk
                         Basis and Derivation of  Criterion
                    References
                Appendix
                                                                                  Page
A-l

B-l
B-l
B-2
B-2
B-4
B-7
B-7
B-10
B-12
B-13
B-38

C-l
C-l
C-2
C-3
C-5
C-16
C-19
C-20
C-20
C-21
C-25
C-27
C-32
C-32
C-59
C-59
C-60
C-62
C-76
C-76
C-77
C-79
C-79
C-87
C-114

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                        CRITERIA DOCUMENT
                    POLYCHLORINATED BIPHENYLS
CRITERIA
                           Aquatic  Life
     For polychlorinated biohenyls the criterion to protect fresh-
water aquatic life as derived using the Guidelines  is 0.014 ug/1 as
a 24-hour average.  The concentration of  0.014  ug/1 is probably too
high because  it  is based on  bioconcentration  factors  measured in
laboratory studies, but field studies apparently produce factors at
least  ten  times  higher for  fishes.   The  available data indicate
that acute  toxicity to freshwater  aquatic life probably will only
occur at concentrations above 2.0 ug/1 and  that the 24-hour average
should provide adequate protection against acute toxicity.
     For polychlorinated biphenyls the criterion to protect salt-
water aquatic life as derived using the Guidelines is 0.030 uq/1 as
a 24-hour average.  The concentration of 0.030  ug/1 is probably too
high because it  is  based  on bioconcentration  factors  measured in
laboratory studies, but field studies apparently produce factors at
least  ten times  higher  for  fishes.   The  available data  indicate
that acute  toxicity to saltwater  aquatic  life probably will only
occur  at concentrations  above 10 ug/1 and  that the 24-hour average
criterion  should  provide  adequate protection against  acute  tox-
icity.

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                          INTRODUCTION
     Polychlorinated biphenyls  (PCBs) are  the  chlorinated deriva-
tives of a class of  aromatic organic compounds called biphenyls and
are manufactured  by the direct chlorination of  the biphenyl ring
system.  The commercial products are complex mixtures of chlorobi-
phenyls and are marketed for  various  uses according  to the percent-
age of chlorine in  the  mixture.   Currently there is no production
of PCBs  in  the United States  but  the sole  producer of PCBs  in the
United States previously marketed four mixtures containing 21 per-
cent, 41 percent, 42 percent, and 54 percent chlorine for use only
in closed  electrical systems under  the  registered trademark Aro-
clor.  Prior to 1971, mixtures containing up to 68 percent chlorine
were  used  in  a  number  of other applications,  including plasticiz-
ers,  heat transfer  fluids, hydraulic fluids, fluids in vacuum pumps
and compressors,  lubricants,  and  wax extenders.
      in 1974  approximately 65 to  70  percent of domestic sales were
to manufacturers  of capacitors and the remainder to  manufacturers
of  transformers  while  approximately 450,000  pounds  of  PCBs were
imported primarily for use  in  non-closed  systems.    Production  in
the  United States appeared  to be  one-half  of the world total.
      As a  result  of the long  life of many products containing PCBs,
 it is believed that a substantial portion  of' the PCBs manufactured
 before 1971 are still in service and thus  represent potential pol-
 lution through possible future discharge  into the environment.
      During  the  period 1972  to 1974, domestic  production  of PCBs
 averaged approximately 40 million pounds  per year with  33  million
                                 A-l

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 pounds representing the annual domestic marketed consumption during
 that period.
      Although the environmental  behavior and biological activity of
 a number of individual chlorobiphenyl isomers have been studied in
 recent years, it is still difficult to evaluate the potential tox-
 icity of the complex mixtures  actually  found in  the  environment
 since their composition often changes.  In making this evaluation
 it is necessary to weigh carefully the results of studies  of indi-
 vidual compounds, and to compare  critically  the  environmental and
 toxicological properties of  the  commercial mixtures.
      A further  complication  is that several commercial PCB  mixtures
 have  been reported to contain small quantities of  highly toxic con-
 taminants,  polychlorinated  dibenzofurans (PCDFs).  Certain  of the
 toxic effects observed in animals and humans exposed to  PCBs  appear
 to  be attributable to PCDFs, while  others  appear to be caused  by
 PCBs  themselves.  There is also some evidence  that small quantities
of PCDFs may  be formed from PCBs  while in service  or as  a result  of
metabolic changes  in certain organisms.
      PCBs consist of a mixture of  chlorinated  biphenyls which  con-
tain a varying number of substituted chlorine  atoms on the  aromatic
rings.  The biphenyl molecule has  a total of ten  sites  where chlo-
rine  substitution can be accommodated as shown  in the following
structure:
                               A-2

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The  potential  positions  for  chlorine  substitution  are numbered
according  to  the  American  Chemical  Society  standard notation.
Chlorinated biphenyIs having the same number ;of  chlorine atoms per
molecule  are  referred  to as a specific class of  chlorobiphenyls,
with  a suitable numerical prefix  to define the number of  substi-
tuted chlorines.  Hence, there are classes varying from monochloro-
biphenyls to decachlorobiphenyls.   All compounds within the  same
class  have  the same molecular  weight and  are  structural isomers  of
each  other.  They differ only  in terms of the location of the chlo-
rine  atoms in  the  biphenyl ring.   The  ten  classes  of  chlorobi-
phenyls,   comprising   209   possible  isomers,  are  summarized  in
Table l.                                     |
      Chlorobiphenyls with  five or more chlorine atoms are referred
to as -higher  chlorobiphenyls.-  This distinction  is made in recog-
nition of the fact that the former group of compounds is much more
persistent in the environment than the latter  group.   The tetra-
chlorobiphenyls are intermediate in persistence.
      The physical  properties of  individual  chlorinated biphenyls
 are  known  (Cook,  1972).   The physical  properties of the Aroclor
 mixtures are  summarized in Table 2.   Lower  chlorinated Aroclors
 (1221, 1232,  1016, 1242, and  1248)  are colorless  mobile oils.   In-
 creasing chlorine content  results in mixtures taking on the  consis-
 tency of viscous liquids  (Aroclor  1254)  or sticky resins  (Aroclors
 1260 and 1262).  Aroclors 1268 and 1270 are of white powders.  With
 the  exception of  Aroclors 1221 and 1268,  Aroclors do not  crystal-
 lize upon heating or cooling  but at a specific temperature,  defined
 as a "pour point," change into a resinous state.
                                 A-3

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                              TABLE 1

            Empirical Formulation,  Molecular Weights,
                 and Chlorine Percentage in PCBsa
Empirical Formula
Chlorobiphenyls
C12H10
C12H9C1
C12H8C12
C12H7C13
C12H6C14
C12H5C15
C12H4C16
C12H3C17
C12H2C18
C12H1C19
C12C110
Molecular
Weight0
154
188
222
256
290
324
358
392
426
460
490
PercentK
Chlorine0
0
18.6
31.5
41.0
48.3
54.0
58.7
62.5
65.7
68.5
79.9
No. of
Isomers
1
3
12
24
42
46
42
24
12
3
1
 Source:   Hutzinger,  et al. 1974
"'Based on Cl
                             A-4

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     It is known from the studies of pesticides that soil moisture
and evaporation  of  water have a  strong influence on  the  rate of
chlorinated hydrocarbon volatilization from soils and sand.  Haque,
et al.  (1974) demonstrated  that  the periodic evaporation of water
from Ottawa sand enhanced the total  volatilisation of  Aroclor  1254
but reduced the degree of differentiation  in  the  volatility of the
higher  chlorinated  biphenyls  (1,  6,  and 5  chlorine aroms)  from the
tetrachlorobiphenyls..  However,  when  Aroclor 1254  was heated  in
water at  100°C the  total volatilization of this Aroclor was reduced
compared  to equivalent dry isothermal conditions, but the differen-
tiation  in volatility  between  the higher  and   lower  chlorinated
biphenyls was increased  (Bowes,  et al.  1975).
      Mackay  and Wolkoff (1973) calculated theoretical evaporation
rates  for various  Aroclors  from water and  predicted  very  rapid
volatilization rates.  Under laboratory conditions,  PCBs appear to
volatilize fairly  rapidly  from  water  in  aquaria (Uhlken, et al.
 1973) and even from flasks plugged with glass wool  (Oloffs, et al.
 1972).    Under  the same conditions,  volatilization  was  markedly
 reduced  in the presence of sediments (Oloffs, et al.  1973).  Hence
 in natural waters,  it  would seem likely  that absorption to   sedi-
 ments would  limit  the rate of volatilization.
      Solubilities  of the individual chlorinated  biphenyls in  water
 have been studied by  several  workers  and  an inverse  correlation
 between  solubility and degree  of  chlorination  has been reported
  (Wollnofer,  et al.  1973;  Haque  and Schmedding, 1975;  Metcalf,  et
 al.  1975).   The problem in obtaining  true solution  equilibria data
  for  PCBs in  water  has been explained by Schoor (1975) who has given
                                 A-7

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 evidence  that  solutions  of  PCBs in water are in fact stable emul-
 sions of  PCS aggregates and  that the true  solubility  of Aroclor
 1254 is less than  0.1  yg/1  in fresh water and 0.04 ug/l in marine
 water.
      Chlorobiphenyls  are freely  soluble  in relatively  nonpolar
 organic solvents (Hutzinger, et al. 1974) and lipids in biological
 systems (Metcalf,  et al.   1975).   Metcalf, et  al.  have reported
 octanol/water  partition  coefficients  in the range  of 10/000  to
 20,000 for representative tri-,  tetra-,  and pentachlorobiphenyls.
 Partition  coefficients with  this biphasic solvent system have been
 found to correlate  well  with ecological magnification  factors  in
 aquatic  organisms (Metcalf,  et. al. 1975).
      PCBs  are strongly adsorbed on solid  surfaces,  including  glass
 and .metal  surfaces  in  laboratory  apparatus (Schoor,  1975) and
 soils,  sediments, and particulates  in the environment  (Haque,  et
 al. 1974;  Oloffs, et al.  1973;  Crump-Wiesner, et  al.  1974; Dennis,
 1976; Munson, et  al.  1976; Pfister,  et al.  1969).
      In  aquatic environments, PCBs  are associated  with sediments
 and are  usually found at much higher concentrations in sediments
 than  in  water  in contact with  them (Young,  et  al.  1976; Crump-
Weisner, et al. 1974;  Dennis,  1976).  As  with  other chlorinated
hydrocarbons, PCBs  are probably  associated particularly strongly
with  micro-particulates  of  0.15 urn  diameter  or  less (Pfister, et
al. 1969).
     PCBs  are commercially  produced  by  the chlorination of the
biphenyl ring with anhydrous chlorine  in  the presence of iron fil-
ings  or  ferric  chloride  as  the catalyst.   The  crude  product is
                               A-8

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purified to remove the color and traces of  the by-product  hydrogen
chloride, and the catalyst by treatment with  alkali  and  subsequent
distillation.   The purified  product is  a  complex mixture of  the
chlorobiphenyls,  the  precise composition depending  on  the condi-
                                                !
tions  under which the chlorination  occurred.    j
     It  has been  reported  that  foreign  PCB  mixtures  are  similar in
composition  to one of the 10 Aroclor products previously manufac-
tured  in  the U.S.   Gas  liquid  chromatograms  of  Phenoclor  DP6
 (France),  Clopen A60 (Germany), and Aroclor  12(50  (U.S.),  all mix-
tures  containing  60  percent chlorine,  show that these mixtures are
virtually identical (Tas and de Vos, 1971).   Jensen and Sundstron
 (1974) have shown that Clophen  A60  and A50  (Germany) are very simi-
 lar in isomer composition  to Aroclors 1260  and 1254  (U.S.), respec-
 tively.   Table 3 lists the  distribution  of the  various  classes of
 chlorobiphenyls  in  seven  major  Aroclor mixtures as reported by
 Mieure,  et al.  (1976), Webb and McCall  (1973), and Hirwe,  et al.
 (1974).   The small  difiEerences in analytical results reported for
 Aroclors 1242 and 1254 may reflect  either differences  in analytical
 methods or variations in sample constitution,  j
       Certain  substitution patterns are  believed  to influence the
 biological  activities of  chlorobiphenyls.   The presence  of two
 adjacent carbon  atoms without  chlorine substitution in  one or  both
 rings is believed to facilitate metabolism  because  it  oermits the
 formation of arene oxide intermediates (Safe, et al. 1975).   Essen-
 tially  all chlorobiphenyls with five or fewer;chlorine atoms have
 at least one pair of adjacent  unsubstituted  carbon atoms because of
  the rarity of 3,5-substitution in the natural mixtures.
                                 A-9

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A-10

-------
     Jensen and Sundstrom (1974) presented evidence that chlorooi-
phenyls with three or  Cour  chlorine atoms in the ortho- positions
(2-  and  *- positions)  are  more  easily metabolized by humans  than
those with only one  or two  ortho-chlorines.   Compounds with three
or four ortho- substituted chlorines are virtually absent from  Aro-
clors  1016 and 1242 but  are fairly well represented in  Aroclors
1254 and 1260  (Clopens A50  and  AbO,  respectively).
     McKinney  (1976) has suggested that chlorobiphenyl isomers  witn
chlorine  substitution in both  the  4-  and 4' positions  tend to be
biologically  active  and well retained in tissues.  The  number and
proportion of  these  isomers increase with increasing chlorination.
     McKinney, et al.  (1976) have shown an association between bio-
logical  activity  and substitutions in the 3,4- or 3,4,5- positions
on one or  both rings.  The  first pattern  is frequently found in PCB
mixtures but  the second  is  found only as part of the 2,3,4,b-patr-
 tern which is found in only trace amounts in PCBs.
      Toxic materials  other than  chlorinated biphenyls  have   been
 found in  commercial PCB  mixtures.   Vos, et  al.  (1*70) , Bowes, et
 al.  (1975), Roach  and Pomerantz  (197*),  Nagayama,  et al.  (1976),
 and Kuratsune, et al.  (1976) have detected polychlorinated dibenzo-
 furans  (PCDFs) in a number of domestic and  foreign PCB  mixtures at
 levels of 0.8 to 33 mg/kg.  While 119 structurally  different PCDF
 isomers  are  possible, only two have been precisely  identified  to
 date,  the  2,3,7,8-tetrachloro- and  the  2,3,4,7,8-pentachlorodi-
                                               j
 benzofurans  (Bowes, et  al. 1975).
                                 A-11

-------
      Polychlorinated naphthalenes (PCtts) have also been identified
 in small quantities in Clopen A60 and Phenochlor DP 6 (both corre-
 sponding to Aroclor 1260), Aroclor 1254, and KC-400 (corresponding
 to Aroclor  1248)  (Vos, et  al.  1970;  Roach and  Pomerantz,  1974;
 Bowes,  et al.  1975).
      There appear  to be no authenticated reports of polychlorinated
 dibenzo-p-dioxins  (PCDDs)  in commercial PCBs (Bowes,  et al. 1975).
 The presence of potentially toxic compounds other than polychlori-
 nated biphenyls  in commercial PCB mixtures complicates both analyt-
 ical and toxicological evaluation of such mixtures.
      PCBs are  considered  to be inert to almost all of the  typical
 chemical reactions.   PCBs  do not  undergo oxidation,  reduction,
 addition,  elimination,  or  electrophilic  substitution reactions
 except  under  extreme conditions.   Chlorines can  be replaced  by
 reductive dechlorination  with any metal hydride  such as  lithium
 aluminum hydride but temperatures  of 245°C  or greater  are  required
 to effect chlorine displacement.
     The reactions of environmental  importance that PCBs appear  to
 undergo   include alkali-  and  photochemically-catalyzed   nucleo-
philic substitutions and photochemical  free radical substitutions,
all of which occur with alkali and water.
     Photolysis  generally  has been found to give one type  of pro-
duct under environmental conditions  (Hutzinger, et al. 1972, 1974;
Ruzo, et al.  1972,  1974;  Ruzo  and  Zabik,  1975;  Herring,  et al.
1972).  Chlorine is  replaced by hydroxy groups in aqueous systems.
     A marked  increase  in  rate of PCB photolysis was observed when
solvents  were  degassed prior to irradiation (Ruzo,  et al. 1974).
                               A-12

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Oxygen  is  known to  act as a  free radical quencher  by accepting
energy  from  free radicals before  any chemical  change  can occur.
This increase in rate therefore implies that a free radical process
is occurring and in the  environment these photochemical  transforma-
tions will be enhanced  under anaerobic conditions.
     The photochemical  behavior  of higher chlorobiphenyls appears
similar  to  that  of  the  tetrachlorobiphenyls  (Hutzinger,  et  al.
1972; Herring,  et  al. 1972).   Irradiation  of  Aroclor  1254  in  aque-
ous  solution gave rise to dechlorinated and  hydroxylated  products
 (Hutzinger,  et  al.  1972).   Hexa- and octachloirobiphenyls  are more
photochemically reactive  than tetrachlorobiph«nyls,  so that  under
 irradiation  the higher  components of Aroclor  1254  are  selectively
degraded  (Hutzinger,  et al.  1972;  Herring, et al.  1972).
     The creation of  free  radicals by sunlight allows the  environ-
mental  replacement of chlorines  by hydroxy groups from water  with-
out  the intervention of  alkali.  When  this  occurs  at  the  ortho-
 position  (found  to  be the most preferred foe  chlorine loss)  the
 resulting  2-hydroxychlorobiphenyl is perfectly positioned  to allow
 oxygen  to bond to an ortho- position of  the  other ring.  This re-
 sults in the creation  of  potentially the most  important  class of
 contaminant in commercial mixtures of PCBs, the chlorodibenzofurans
                       1                        I
 (CDFS).                                       j
      Irradiation studies on either Aroclor 1254  or  2,5,2',5'-tetra-
 chlorobiphenyl (Hutzinger, et al.  1972)  in hydtoxylic solvents  have
 shown  the  formation of phenolic  compounds,  carboxylic compounds,
 and polymers along with  dechlorination.   Activation of the  phenyl
 rings  by  metals  or  metallic salts  make  them more  susceptible  to
                                A-13

-------
 hydroxylation.   Thus,  in the  environment,  either heat, light, or
 metals and metal salts in water could  theoretically  accelerate the
 transformation of PCBs to PCDFs.  The ultraviolet component of sun-
 light is sufficiently energetic to generate  free  radicals from both
 phenols and PCBs.  The energies required to  break the Ar-Cl bond to
 form hydroxy-PCBs  in  a hydroxylic solvent and ArO-H bond  to form
 CDPs correspond  to wavelengths near 360  to 320  nm, respectively.
 These wave lengths are clearly within the sunlight region.
      Irradiation  experiments  with  five  pure   2-chlorinated  bi-
 phenyls  as  5  mg/1  aqueous suspensions,  showed  that traces  of
 2-chlorodibenzofuran  were  detectable  although  only  the  2,5-di-
 chloro- and the  2,5,2',5•-tetrachlorobiphenyls provided identifi-
 able amounts or approximately  a 0.2  percent  yield during  a seven-
 day  irradiation (Crosby,  et al. 1973; Crosby  and Moilanen, 1973).
 The  environmental  significance of this  is  fourfold:   (1) ortho-
 chlorobiphenyls can be hydroxylated  by radiation similar  to  sun-
 light when  they are suspended in aqueous media;  (2)  the product(s)
 are  converted  to CDFs;  (3)  rates of CDF formation by this  process
 are  approximately;the same as  their  rates of  degradation,  leading
 to an approximately steady concentration;  and (4)  decomposition of
 2,8-dichlorobenzofuran  was found to oe very slow in aqueous  suspen-
 sion but  dehalogenation did  not take place to form the relatively
 photolytically  stable  2-chlorodibenzofuran  (Crosby  ana Moilanen,
 1973) .
     In addition  to photochemical  and metallic salt  formations of
PCDFs from  PCBs,  a  third  route of formation  has been  suggested.
Kanechlor KC-400  (analogous  to Aroclor 1248)  having  an intitial ^
                               A-14

-------
PCDF content  of  20 mg/kg, was  shown  to undergo conversion as  the
heat transfer  fluid  in a heat exchanger  to  give PCBs with a  PCDF
content of 4,975 to ' 11,76b mg/kg  (Nagayma, et  al.  197b;  Kuratsune,
et al. 1976).  This material was identified as the agent which  poi-
soned  a  large number  of Japanese in 1968.   A  general disadvantage
of PCBs  in many of their  applications  including electrical capaci-
tor  and  transformer  uses as well as  heat transfer  uses  is  their
tendency to decompose under the action of heat or electrical arcing
to rorm  potentially moice  toxic products (Broadhurst, 1972).
                                A-15

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                             REFERENCES

 Bowes, G.W., et al.  1975.  Identification of chlorinated dibenzo-
 furans in American polychorinated biphenyls.  Nature.  256: 305.

 Broadhurst, M.G.  1972.  Use and replaceability of polychlorinated
 biphenyls.  Environ. Health Perspect.  2: 81.

 Cook, J.w.   1972.   Some chemical aspects of  polychlorinated bi-
 phenyls (PCBs).   Environ. Health Perspect.  1:  1.

 Crosby,  D.G.,  et al.   1973.  Environmental generation and degrada-
 tion of dibenzodioxins  and dibenzofurans.   Environ. Health  Per-
 spect.   5:  259.

 Crosby, D.H. and K.W. Moilanen.  1973.  Photodecomposition of chlo-
 rinated biphenyls  and dibenzofurans.   Bull. Environ.  Contam. Toxi-
 col.  10: 372.

Crump-Wiesncr, H.J.,  et al.  1974.  Pesticides in water: A study of
the distribution of polychlorinated biphenyls in the  aquatic envi-
ronment.  Pestic. Monitor.  Jour.  8:  157.

Dennis,  D.S.   1976.    Polychlorinated biphenyls  in  the surface
waters  and  bottom  sediments of  the  major  basins of  the United
States.   Proc.  Natl. Conf. on Polychlorinated Biphenyls.  p. 193.
                               A-16

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Haque, R. and D.  Schmedding.   1975.  A method of measuring  the water
solubility of hydrophobia chemicals:  Solubility of five polychlori-
nated biphenyls.  Bull. Environ. Contain. Toxicol.  14: 13.
                                            i
                                            i
Haque, R., et al.  1974.  Aqueous solubility,  adsorption,  and vapor
behavior of  polychlorinated  biphenyl Aroclor  1254.   Environ. Sci.
Technol.  8:  139.                           j

Herring, J.L., et al.  1972.   UV irradiation of Aroclor 1254.  Bull.
Environ. Contain. Toxicol.  8:  153.
                                       chroroatography-
Hirwe, S.N., et al.   1974.  Gas-liquid
metric characterization of  Aroclor  1242 and
Environ. Contam. Toxicol.  12: 135.
         -mass spectro-
1254 components.  Bull.
Hutzinger,  O.,  et al.   1972.   Photochemical degradation of chloro-
biphenyls  (PCBs).  Environ.  Health Perspect.  1:  15.
                                            r
Hutzinger,  O.,  et al.   1974.   The Chemistry of  PCBs.   CRC Press,
Cleveland,  Ohio.                            ;

Jensen,  S.  and  G. Sundstrom.  1974.  Structures and levels of most
chlorobiphenyls in two technical PCS products and in human adipose
 tissue.   Ambio.  3: 70.
                                            i
 Kuratsune,  M.,  et al.  1976.  Some of the  recent findings concern-
 ing Yusho.   Proc. Natl. Conf. on Polychlorinated Biphenyls.  p.  15.
                                A-17

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Mackay,  D.  and A.W.  Wolkoff.  1973.   Rate of evaporation on low-  ^
solubility contaminants from water bodies  to  atmosphere.  Environ.
                                                                    f
Sci. Technol.   7: 611.

McKinney,  J.D.  1976.   Toxicology of  selected symmetrical hexa-
chlorobiphenyl isomers: Correlating biological  effects with chemi-
cal  structure.  Proc.  Natl. Conf. on Polychlorinated Biphenyls.
p. 99.

McKinney,  J.D., et al.   1976.    Toxicology of hexachlorobiphenyl
isomers  and  2,3,7,8-tetrachlorodibenzofuran  in chicks.   I.  Rela-
tionship of  chemical parameters.  Toxicol.  Appl.  Pharmacol.    (In
press)

Metcalf, R.L., et al.  1975.  Laboratory model ecosystem studies of
the degradation and  fate  of radiolabeled tri-, tetra-/ and penta-
chlorobiphenyl compared with DDE.  Arch. Environ. Contam. Toxicol.
3: 151.

Mieure,  J.P.,  et  al.  1976.   Characterization of polychlorinated
biphenyls.     Proc.  Natl.  Conf.  on  Polychlorinated  Biphenyls.
p. 112.

Munson, T.O.,  et al.  1976.  Transport of  chlorinated hydrocarbons
in the Upper Chesapeake Bay.  Proc. Natl.  Conf. on Polychlorinated
Biphenyls.  p.  223.
                               A-18

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Nagayama, J., et al.  1976.  Determination oil chlorinated dibenzo-
furans in Kanechlors and "Yusho Oil".  Bull. Environ. Contam. Toxi-
                                            i
col.  15: 9.
                                            't

Oloffs, P.C., et al.  1972.  Fate and behavior of five chlorinated
hydrocarbons  in  three   natural waters.    Can.   Jour.  Microbiol.
18: 1393.                                   I

Oloffs, P.C., et al.  1973.  Factors affecting the behavior  of  five
chlorinated  hydrocarbons in  the two natural waters  and  their sedi-
ments.  Jour. Fish.  Res.  Board Can.   30:  1619.

Pfister,  R.M.,  et  al.    1969.   Microparticulates:  Isolation  from
water  and  identification of   associated  chlorinated  pesticides.
Science.   166:  878.                         I

Roach,  J.A.G. and  l.H.  Pomerantz.   1974.  The  finding of  chlori-
nated  dibenzofurans in  a Japanese polychlorinated biphenyl  sample.
                                            j
Bull.  Environ.  Contain.  Toxicol.  12: 338.

Ruzo,  L.O.  and M.J,  Zabik.    1975.   Polyhalogenated  biphenyls:
Photolysis of hexabromo  and hexachlorobiphenyls in methanol solu-
 tion.   Bull. Environ. Contam. Toxicol.  13: 181.

 RUZO,  L.O., et al.  1972. Polychlorinated biphenyls: Photolysis of
 3,4,3',4'-tetrachlorobiphenyl and  4,4'-dichlorobiphenyl  in  solu-
 tion.  Bull. Environ.  Contam.  Toxicol.   8: 217.
                                A-19

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 Ruzo,  L.O., et al.  1974.   Photochemistry  of  bioactive compounds:
 Photo-products and kinetics of  polychlorinated biphenyls.   Jour.
 Agric.  Food Chem.   22:  199.

 Safe/  S., et  al.   1975.   The mechanism of chlorobiphenyl metabo-
 lism.   Jour.  Agric. Food  Chem.   28:  851.

 Schoor,  W.P.   1975.  Problems associated with  low-solubility com-
 pounds  in aquatic  toxicity tests:  theoretical model  and solubility
 characteristics of Aroclor 1254  in water.   Water Res.   9:  937.

 Tas, A.C.  and R.H. deVos.   1971.   Characterization  of  four  major
 components  in  a technical polychlorinated biphenyl mixture.   Envi-
 ron. Sci. Technol.  5:  1216.

 Tucker, E.S.,  et al.  1975.   Migration of polychlorinated biphenyls
 in  soil induced by percolating  water.   Bull. Environ.   Contarn.
 Toxicol.  13:  86.

 Uhlken, L.D.,  et al.  1973.   Apparent volatility of PCBs as used in
 continuous flow bioassays.   PCS Newsletter.  5: 4.

Versar,  Inc.   1976.   Final  Report.   PCBs in  the  United States:
 Industrial  use and environmental distribution.   Report  to U.S.
Environmental Protection Agency.   Task I.  Contract No. 68-01-3259.
                               A-20

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Vos, J.G., et al.  1970.  Identification and toxicological evalua-
tion of chlorinated benzofuran  and  chlorinated naphthalene in two
commercial  polychlorinated  biphenyls.    Food  Cosmet.  Toxicol.
8: 625.                                      ;
                                             i
Webb, R.G. and A.C. Mcqall.  1973.  Quantitative PCB standards for
electron  capture  gas  chromatography.    Jour.  Chromatog.    Sci.
11: 366.                                     I
Wollnofer,  P.R.,  et al.   1973.   The  solubilities  of twenty-one
chlorobiphenyls in water.  Analabs Research Notes.  13: 14.
Young, D.R.,  et  al.   1976.  Marine  inputs of
phenyls off southern California.  Proc. Natl
nated Biphenyls.  p. 197.
                               A-21
 polychlorinated bi-
Conf. on Polychlori-

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Aquatic Life Toxicology*                             .
                                 INTRODUCTION
    Most  data  for polychlorinated  biphenyls  (PCBs) ifound  in  the  literature
are from  studies  concerned with tissue  levels  in fish, mammals,  and  birds,
without  correlation  with  source or  exposure  concentrations.   Many  studies
dealing with various  physiological  parameters  are also available but,  again,
are such  that they are  of little  use here.  Also,  PCBs often do  not  appear
to be  very acutely toxic to juvenile and  adult  freshwater fish and inverte-
brate  species  in  static tests due to  low solubility, and this can  lead to
erroneous  judgments as to  the  actual  toxicity of  the compounds.
    PCBs  occur as mixtures of  chemical  isomers  that differ in the amount of
chlorination  of the biphenyl  structure;  they  have  been treated herein  as  a
single entity.   Polychlorinated biphenyls were  manufactured  by  the  direct
chlorination  of  biphenyl;  production in  the  United  States  has now ceased.
These  mixtures were  identified under  the trade names  Aroclo?® and capaci-
toi®,  and  sold  on the  basis  of percentage chlorine  (e.g.,  21,  42,  54,  and
60 percent).   Because each component of the mixtures  differs  slightly in  its
physical,  chemical,  and  biological  properties,  and  because  a possible  209
different  chlorobiphenyls may be  produced, the  evaluation of the potential
 impact of the various mixtures on  the environment is complicated.
     PCBs  are  highly  lipophilic and bioconcentrate to high concentrations  in
 tissue  from  concentrations   in  water   that  are  often below   the   usual
 SrttSi  of  each table are calculations  for  deriving various measures of tox-
 icity as described  in the Guidelines.               ;
                                       B-l

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detection limits.  When  an  evaluation of the  impact  of  PCBs  on the environ-
ment is performed, it is- necessary  to  relate  the data gathered in laboratory
experiments with relatively pure mixtures to  what happens  to  the mixtures in
nature.  There is evidence that percentages of chlorine  change with time and
location ,as the mixtures are  transported through the  environment.  For exam-
ple,  the proportion  of major  peaks  of Aroclo® 1254  in  shrimp  and  fish
captured from Escambia Bay, Florida,  differed from each  other (Nimmo, et al.
1971).  The major  peaks  in these organisms and in organisms  from laboratory
studies (Hansen, et al.  1971) also  differed from the  standard used to calcu-
late the amounts of the  chemical  in tissues.   Results of environmental moni-
 t
toring  by  Butler  and  Schultzmann  (1978)  showed  that PCBs  Identified  in
fishes, Pacific staghorn sculpin and  English  sole from the Ouwamish River in
the  state  of  Washington,  during  the period  of fall 1972  to  spring 1976,
changed  from those  resembling Aroclor® 1254  to those resembling Aroclor®
1260 and, later, Aroclor^ 1242.
                                    EFFECTS
Acute Toxicity
    The  acute toxicity  data  base  for freshwater  invertebrate species  con-
tains 12 values  for three species.   These  values were from  both static and
flow-through  tests;  the flow-through  tests   showed  an  LC5Q range  from 10
ug/l for scud,  Gammarus fasciatus, to 400  wg/l  for  the damselfly,  Ischnura
vertical is.
    Six  96-hour LCgo  values  (Table   1)  are  available  for  four  freshwater
fish species;  all  of  these are from flow-through tests with measured  concen-
trations.   Newly  hatched  rainbow trout were  the  most  sensitive  species
tested,  with  a 96-hour LC5Q  of  2.0  wg/l  for  Capacitoi® 21  (21  percent
chlorine);  largemouth  bass  were  almost equally  sensitive  with  a  96-hour
                                      B-2

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LC,
LC
  50
     of  2.3  u9/l  (Birge,  et al.  1979).   The  fathead  minnow had  a  similar
     of  7.7  ug/l  for  Aroclor® 1254  (Nebeker, et  al, 1974).   All  of  the
acute values for fish species are  for  newly hatched  fishes,  reflecting  their
much greater sensitivity as compared to the other fish life stages.
    The  toxicity of  PCBs appears  to  be similar for  both  fish  and inverte-
brate freshwater species if  test methods  are considered.   The lowest species
mean acute value is 2.0 wg/l for rainbow trout  (Table 3).
    The  LC5Q  or  EC50  values  for  saltwater  invertebrate  species  range
from 10.2  to  60 ug/l (Table 1).   The available data show little  difference
in  the  acute toxicity  of  different  Aroclor©   This  low  variability in
species  sensitivity  and small  difference  in  acute  toxicity  of  the  Aro-
clors£> tested could  be  real.   However,  it is  likely  that this  is  a  func-
tion of  the small  number of  species tested and that the solubilities of  PCBs
are less than their  acute toxicities.                  ;
    Acute  toxicity tests of PCB mixtures  to saltwater, fish species have not
produced data that  can  be  used to obtain  96-hour  LCgo  values because  con-
centrations  tested were not sufficiently high  (Table ,6),,  Pinfish were not
affected  in  48  hours  by  100 wg/l   Aroclot® 1254  (Duke,  et  al.  1970).
Eighteen percent  of  the pinfish  died  after 96 hours  in  water to which 100
ug/l  Aroclor® 1016  was added,  compared  to 2 percent of the control  fish,
 (Hansen, et  al.  1974a).   Additional   tests  with  saltwater  fish  species  at
 slightly higher concentrations might have given data sufficient  to calculate
 96-hour LC50 values.   However,   possible problems could exist  in  validity
 of acute tests  with PCBs  because  of  their low solubility  in  water  (Schoor,
 1975; Wiese and Griffin, 1978).                       :
     There are  too few data for  PCBs  and  freshwater cir  saltwater species  to
 calculate a  Freshwater  or  Saltwater Final  Acute.Value,*  according to the pro-
                                       B-3

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 cedures  described  in  the   Guidelines.    Species   mean   acute  values   are
 summarized in Table 3.
 Chronic Toxlcity
     Results from  six  chronic tests  with  three freshwater  Invertebrate  spe-
 cies, Daphnla magna, Gammarus pseudolimnaeus,, and the midge, Tanytarsus  dis-
 simHls, are shown  in  Table  2.   The chronic values  for Daphnla magna of 4.3
 ug/1  for  Aroclor®,1248 and  2.1 »g/l  for Aroclor® 1254, were  from flow-
 through tests with measured concentrations  (Nebeker  and Puglisl,  1974).   The
                                                (S\
 value of  0.8 wg/l  for the  midge with Aroclory 1254, and the  two chronic
 values of  4.9  wg/l for Aroclor® 1242 and 3.3  ug/l for  Aroclor® 1248  for
 Gammarus pseudollmnaeus,  were  also  from  flow-through  tests  with measured
 concentrations.
     Five freshwater  flow-through  tests with  measured  concentrations   have
 been conducted with  two fish  species, four with fathead minnows and one  with
                                                  Ob
 brook  trout  (Table 2).  The  most  toxic  Aroclor*' to  fathead minnows  was
 Aroclor® 1248 which gave  a  chronic value of 0.2 i»g/l  (Defoe,  et al. 1978);
 chronic   values   for  Aroclor®  1242,   Aroclor®  1254,   and  Aroclor®   1260
 were 9.0,  2.9,  and 2.3  ug/1.  respectively (Nebeker, et al. 1974; OeFoe, et
                                                      /R\
 al.  1978).   A chronic  value  of  1.0  wg/l  for  Aroclory 1254 was obtained by
 Mauck, et al. (1978) for the brook trout.
     Two  geometric  mean  acute-chronic ratios are  calculable; these  are  6.4
 for  the  fathead  minnow  and 11  for the  scud, Gammarus  pseudollmnaeus (Table
 2>-
     No chronic tests have  been reported in which saltwater  Invertebrate spe-
 cies were exposed to PCBs.
     In an  early-life-stage test  (Table 2) with the sheepshead  minnow,  fer-
tilization was  not affected  by  Aroclor®  1254,  but  significantly fewer  ero-
                                      8-4

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bryos survived to hatching  in a measured concentration  of  3.48 ug/l  (Schim-
mel  et al. 1974).  Survivial of fish during  the  two weeks following hatching
was significantly less in 0.16  ug/l, but  not different from controls in 0.06
                                                       i
ug/l.                                                  1
    In a  study to determine the effect of PCBs  in fish embryos on survival,
Hansen, et al.  (1973)  exposed adult  sheepshead minnows for  four weeks  to
Aroclor® 1254 (Table  6).   Adult fish  exposed to  5.6 ug/l died,  but those
in 1.1 ug/l or lower  apparently were not affected.   Embryos  from adult fish
exposed to concentrations  as low as 0.14 wg/l were placed in PCB-free flow-
ing  saltwater and observed for four  weeks.  Fertilization success  was not
affected  by PCBs in embryos,  but survival   of embryos and  the resulting fry
was reduced  (Table 6).  Fry from embryos containing 7,,0  wg/g  or more of PCB
began dying a few hours after hatching.  The concentration in embryos calcu-
lated to  be lethal to 50 percent  of the fish was  6.1 wg/g.   If PCB  affects
other species similarly, then  other fish species with  equally high  concen-
trations  of Aroclor® 1254 in  their embryos may be  endangered.
    The  effect  of  another  PCB,  Arocloi® 1016,  in waiter  on  fry, juvenile,
or adult  sheepshead  minnows was determined  in a 4-week exposure  (Hansen, et
al.  1975)(Table  2).   Survival of  all  three  life stages was  reduced in 15
ug/l  but  not in  3.4  Mg/l  or less.   Unlike Aroclor^ 1254,  as  much as 77
ug/g  of  Aroclof® 1016 in embryos apparently  did  not affect  survival  of
embryos  and fry in water free of this  PCB.             j
     Concentrations of  Aroclor^ 1016  and 1254  affecting sheepshead  minnows
 in chronic  exposures differed  markedly (7.14  and  0.098  ug/l);  similarly,
 life-cycle tests  with  the fathead minnow  and  Aroclors*' 1242,  1248,  1254,
 and 1260  yielded chronic  values  of 0.2 to 9.0  ug/l  (Table 2).  Degree  of
 chlorination  in  these tests  using  a freshwater  fish  species   appears
 unrelated to  extent of  chronic  toxicity  and suggests that additional chronic
                                       8-5

-------
 data  on saltwater  species  for other Aroclors*5' may be needed to  demonstrate
 adeauately the presence of a relationship between  degree of  chlorination  and
 chronic toxicity.
    Chronic  exposure  of  saltwater  fish  species  to  Aroclors®  produced
 pathological  effects  not observed in acute tests.  Hansen, et al.  (1971)  re-
 ported  signs of poisoning  in pinfish exposed  to 5 ug/1  Aroclor*'1254, such
 as  fungus-like  lesions on  the  body,  hemorrhagic  areas  around  the mouth,
 ragged  fins etc.;  and 41 to 66 percent mortality occurred.   Signs  of poison-
 ing in  adult sheepshead  minnows  exposed to 10 ug/1  Aroclor"'1254 and juve-
 nile  sheepshead minnows exposed  to 0.16 ug/1  or greater included lethargy,
 fin rot,  and reduced  feeding (Hansen,  et al.  1973;  Schimmel,  et al. 1974);
 decreased  survival  occurred  at concentrations  where these signs of poisoning
 were observed (Table 6).
    Spot  exposed to  5 ug/1  AroclorS' 1254  for  two  weeks  or  longer showed
 fatty changes in their livers (Nimmo, et al.  1975).   In  intermediate stages
 of liver  pathogenesis in fish  species  exposed  to  Aroclor**' 1254,  there were
 extreme fatty changes  characterized by  the  presence of large vacuoles within
 hepatocytes  and disorientation  of  liver  cord  distribution.   In advanced
 stages  of  pathogenesis in moribund fish, there were  intracellular PAS-posi-
 tive  bodies (ceroid),  congestion of blood  sinuses, and  severe vacuolation
 (Table 6).
    Chronic  toxicity  tests,  including  early-life-stage  tests  with  fishes,
demonstrate that the toxicity of PCBs  increases with  increased duration  of
 exposure.  Because  data on the acute toxicity  of PCBs to saltwater organisms
 are limited,  the relationship between  acute and chronic toxicity is poorly
understood.  Available  data  (Tables 2 and 6)  from  chronic  tests demonstrate
                                      B-6

-------
 that  Aroclorv1254 affects  saltwater  organisms at  concentrations  as low as
 0.14  v9/l  and  Aroclor^ 1016  affects  pinfish  at  15 u'3/1.   No effects have
 been  observed  at  0.06  yg/1  for  Aroclor-' 1254  and  at  3.4  ug/1  for Aro-
 Plant  Effects                                          ;
     No appropriate freshwater plant effects data are available, but  informa-
 tion which  has  been found for plants is given  in  Table  6.  Information con-
 cerning  the sensitivity of saltwater plant  species  is  restricted to unicel-
 lular  algae (Table 4).  Fisher and  Wurster  (1973) found  that  the growth of
 the  diatom,  Rhizosolenia  setigera,  was  reduced in a medium to which  0.1 wg/1
 Arocloi® 1254  was  added.    Likewise,  Fisher,  et  al,   (1974)  demonstrated
 that 0.1 vg/1  Arocloi® 1254  added  per liter  of water  changed  the species
 ratio  of the  alga, Dunaliella  tertiolecta, and  the diatom,  Thai ass iosira
 pseudonana.  Fisher, et al; (1974) also showed  a  decrease in species diver-
 sity and species  ratio  change in  natural  phytoplanktcm  communities  at 0.1
 ug/l Aroclor-' 1254.  In summary,  some  data suggest  that unicellular plants
 are  affected by concentrations of PCBs similar to concentrations  that are
 chronically  toxic  to animals.  Unfortunately,  no data using measured concen-
 trations were  presented, and it  1s  difficult  to interpret the  ecological
 significance of these studies.
 Residues
    Table  5  contains   the  results  of 21  appropriate  freshwater  residue
studies  as  defined by the  Guidelines.   The studies  include  only  laboratory
data for  invertebrate  and fish species and show a wide  range  of  bioconcen-
tratlon  factors  (8CF).   Freshwater   field  studies  were  placed  in  Table  6
rather than  Table  5 because it could not be shown that the PCS concentration
 in water was constant for a long  period of time over the range of territory
                                      B-7

-------
inhabited by  the organism.   Freshwater  invertebrate BCF  values  in Table  5
range from  2,700 for the  phantom  midge exposed for  14  days to 108,000  for
the scud, Gammarus  pseudolimnaeus,  exposed for 60 days.   BCF  values for  ex-
posures of fish species (Table 5) range  from  3,000 for  brook trout (fillets)
exposed  to  Arocloi® 1254  for  500  days  to  274,000  for  fathead minnows
(whole body) exposed to Aroclor^l242 for 255 days.
    The BCF values of PCBs  in saltwater  species in  laboratory tests are also
shown in  Table  5.  The diatom, Cvlindrotheca  closterium,  had  a BCF of 1,000
(Keil, et al. 1971);  Eastern oyster,  up to 101,000  (Lowe, et  al.  1972; Par-
rish, et  al.  1974); grass shrimp, Palaemonetes  puglo.  27,000 (Ninrno,  et al.
1974); and  1n the three fish species  listed,  Leiostomus  xanthurus, Cyprino-
don variegatus.  and  Lagodon rhomboides, as  high  as 43,100  (Hansen,  et  al.
1971, 1973, 1974a,  1975).   81 concentration factors for PCBs  In five  of six
species  of  freshwater fishes in  laboratory tests were generally  similar to
BCF values  for  saltwater  species.   Variation  in BCF values  among  species is
greater  than  the variation in BCF  values when one species 1s exposed to var-
ious  Aroclor®  For  example,  BCF  values in  adult sheepshead minnows  ex-
posed  under  similar  conditions  averaged  25,000  for  Arocloi® 1016  and
30,000 for  Aroc1or®1254.
    Bioconcentratlon  factors calculated from  data  from Escambla Bay,   Flori-
da, were greater than  230,000  for blue crab,  greater  than  100,000  for oy-
sters,  and  greater  than  670,000  for  speckled trout  (Duke,  et  al. 1970;
Nimmo, et al. 1975).   These data,  and field data on freshwater fish species,
suggest  that either  BCF  from laboratory studies underestimate bioconcentra-
tlon  potentials of PCBs in  the environment  or that water samples  from field
studies   Inadequately  characterized ambient  concentrations  of PCBs (Hansen,
1975).
                                       B-8

-------
     The bloaccumulatlon of PCBs  Into  aquatic  organisms;from PCSs  in food and
 1n water and the effects of PCBs on  mammals that feed on  fish  and shellfish
 are  important.   The  lowest  maximum  permissible  tissue concentration  (0.64
 ug/1) is based on the effect of  dietary PCBs on mink (Platonow and Karstad,
 1973).  Significant  effects  on  reproduction  of mink were observed at  this
 concentration but a safe concentration was not determined.
     Dividing a  BCF value  by  the percent  lipid value for the same species
 provides a  BCF  value based! on 1 percent lipid content;  this resultant  BCF
 value is  referred  to  as  the  normalized BCF.  Each  of the  BCF  values  for
 which percent lipid  data  are available  was normalized by dividing the  BCF
 value by its corresponding  percent  lipid value.   The geometric mean of  the
 normalized  BCF  values was then calculated to be 10,400!  (Table  5).  The  ac-
 tion  level  for marketability for human  consumption established by the U.S.
 Food  and Drug Administration  (FDA) for PCBs  1n  edible fish and shellfish is
 5.0 mg/kg.   Dividing the FDA action  level of 5.0 mg/kg by  the geometric mean
 of normalized BCF values  (10,400) and  by a  percent  lipid value  of  15  for
 freshwater  species  (see Guidelines)  gives  a  freshwater  residue  value  of
 0.032  jig/L   Similarly, dividing  the  FDA action level of  5.0 mg/kg by the
 geometric  mean  of  normalized  BCF values (10,400), and  by a  percent  lipid
 value of 16  for  saltwater species (see Guidelines)  gives  a saltwater residue
                                                        i
 value of 0.030 wg/1.   The highest BCF value for edible portion of a consumed
 freshwater  species  1s  9,550  for  rainbow  trout  (Branson, et  al.  1975).
 Dividing this value into the FDA action  level  of  5.0 mg/kg gives  a  fresh-
                                                        i
water residue value of 0.52  vg/1. The highest  BCF value  for  edible portion
of a  consumed saltwater species  is  the value of 101,000  for  Eastern  oyster
 (Lowe, et al. 1972).   Dividing  this  value  into  the FDA action  level of 5.0
mg/kg gives  a saltwater residue  value of 0.050 yg/1.  [These concentrations
                                      B-9

-------
are probably too high  because the average concentration  in  some edible  spe-
cies would be at the FOA action level.
    For wildlife  protection, the  lowest maximum permissible  tissue  concen-
tration is 0.64 mg/kg for mink  (Plantonow  and  Karstad,  1973),  but this level
adversely affected mink.  Dividing  this  value  by the geometric mean (45,000)
of whole-body  BCF  values for salmonids  (rainbow  trout,  46,000;  brook trout.
42,000 and 47,000) gives  a  residual value for  freshwater of 0.014 wg/l.   The
mean  BCF  of  45,000 for salmonids  is  based only on  laboratory data.   Eleven
BCF  values  for salmonids  are  available from  field studies  (Table 6).   The
highest  is  for  the  siscowet, but  the  other  10 range  from 119,000  to
2,333,000 with a geometric  mean  of .456,000.   Even  if  the concentrations of
PCBs  in water  in  these field studies are  not  documented as  well as desired,
the  total available  information strongly indicates that field BCF values for
PCBs  are  probably a  factor at 10  higher  than the  available  laboratory BCF
values.   The data from Escambia Bay indicate that similar effects  occur with
saltwater fishes  (Table 5).  The model  developed by Welniger  (1978)  provides
a possible  explanation  for this  difference  between   laboratory  and field
data.  Thus  the freshwater  and saltwater Final  Residue Values  of 0.014 and
0.030 ug/1,  respectively, are probably at least a factor of  10 too  high.
Miscellaneous
     Table 6 contains  data for other  effects  not listed in Tables 1  through
5.   The  tests conducted by Birge,   et al.  (1979)  with  Capacitor^ 21 are
 flow-through early-life-stage  tests  with measured concentrations, where em-
 bryos were  tested  from just  after  fertilization until  4  days  post-hatch
 (Table 6).   Test LC50 values  for redear  sunfish were  8  vg/l;  for  large-
                                       B-10

-------
mouth  bass 1.5 wg/1;  and  for rainbow trout 2.0  wg/l.   These low values are
very  close to the data  of Nebeker, et  al.  .(1974) and  Defoe,  et al. (1978)
for fathead minnows  (Table 2).
    Several  studies  have  shown  that tests  for PCBs lasting  longer  than 96
hours  (Table  6) provide  a  better estimate of long-term adverse effects (mor-
tality,  growth,  pathology) than lethality in  96-hour  tests.   Aroclor--'1254
killed pink shrimp at  a  concentration of 0.94  wg/l within 15 days (Nimmo, et
al.  1971).   Pink  shrimp  exposed  to 3.0 wg/1  for 7  days  were  sensitive
changes  in salinity  (Nimmo  and Bahner,  1974).  This species  also appeared
more  susceptible  to  a  viral   Infection  after  exposure  to Aroclor-^ 1254
(Couch and Nimmo, 1974a,to).                          '
                                                     i
    The growth rate  (height and  in-water weight)  of Eastern oysters was sig-
nificantly  reduced  by  exposure to  5.0  ug/1  Arocloi® 1254  for  24  weeks
(Lowe, et  al. 1972).  These  oysters also displayed general  tissue  altera-
tions  in  the  vesllcular  connective tissue  (parenchyma)  around the  digestive
diverticula of the hepatopancreas.                   ;
    Aroclor^  1254  was toxic  to  the saltwater  amphipod,  Gammarus oceanicus,
at a  nominal  concentration of 10.0  wg/1  (Table  6)^   Molting animals  were
particularly  vulnerable  to the  PCB.   Necrotlc branchla  were found  in  some
animals exposed for about 6 days to nominal concentration of 1.0 ug/1.
    Arocloi®  1254  affected  the species  composition of communities  of  es-
tuarine  animals  that  developed from planktonic  larvae  in saltwater  that
flowed for  four  months through  small  aquaria   (Table 6;  Hansen,  1974).   The
number of  arthropods  decreased  while the number  of chordates increased  in
aquaria receiving  0.6 wg/1 of the PCB.   Numbers  of phyla,  species  and  in-
dividuals were decreased by this PCB,  but there  was  no apparent  effect  on
the  abundance  of  annelids,  brachiopods,  coelenterates,  echiniderms,  or
                                     8-11

-------
nemerteans.  This  study showed  that  a PCB can  have marked effects  on com-
munity  structure  at  concentrations   not  much  different  from  those  that
produced chronic effects on single species.
Summary
    The acute toxicity of  polychlorinated  biphenyls  (PCBs)  to freshwater an-
imals has  been  measured with three  invertebrate and four  fish  species, and
the species  mean  acute values  range  from 2.0  to 283  ug/l-  The  data from
flow-through tests with measured concentrations  are  similar for  fish and in-
vertebrate species,  and probably accurately reflect  the toxicity of the com-
pounds.  The data  from static tests  are more variable, and many may not re-
flect actual  toxicity, due  to  volatility, solubility,  bloconcentration, and
adsorption characteristics  of the various PCB compounds.   Eleven life-cycle
or  partial  life-cycle  tests  were completed  with three  Invertebrate  and two
fish species; the  chronic values  range from 0.2  to 15 jig/1-
    Species mean acute values for PCBs and saltwater animals range from 10.5.
to  20 wg/1 from six  tests on three  invertebrate species.   Two chronic tests
have been  conducted on  the sheepshead minnow,  providing  chronic values for
this species of 7.14 and 0.098  ug/l.
    The freshwater residue data show that PCBs accumulate  to relatively high
levels  1n  fish  and Invertebrate tissues,  and that for  most species PCBs are
not rapidly  depurated  when  exposure is discontinued.  Bloconcentration fac-
tors for  invertebrate species range from 2,700  to 108,000.  Bloconcentration
factors for PCB  exposures  of fish species  range  from 3,000  to 274,000.
    Bloconcentration data for  PCBs  in saltwater fish  and invertebrate spe-
cies show bloconcentration factors ranging from 800  to >230,000  for  inverte-
brate species and  from 14,400 to >670,000 for fish species.
                                      B-12

-------
    The BCF values  obtained  from field data are  generally apreciabTy higher
than laboratory-derived BCF values, so  Final Residue Values based on labora-
tory-derived BCF values are probably at least a factor of 10 too high.
    Data available  for freshwater  plant species  generally indicate that they
are  less  sensitive  to  PCBs  than  are  invertebrates or fish  species.   Data
available for  saltwater  plant species  indicate  that unicellular  plants  are
affected  by  concentrations  of   PCBs   similar   to   concentrations  that  are
chronically toxic to animals.                         j
                                   CRITERIA           !
                                   •MMV^UBHV^MB           ,|
    For  polychlorinated  biphenyls  the   criterion   to  protect  freshwater
aauatic life  as  derived  using  the  Guidelines  is  0..014  ug/l  as  a  24-hour
average.  The concentration of 0.014 wg/l  is probably too high because it is
based on bioconcentration  factors measured in laboratory studies,  but field
studies apparently  produce factors at  least 10 times higher for fishes.  The
available data indicate that  acute toxicity to freshwater aquatic life prob-.
ably will only occur at  concentrations above 2.0 vg/1 and  that  the 24-hour
average, should provide adequate protection aganist acute toxicity.
    For polychlorinated biphenyls  the  criterion  to  protect saltwater aquatic
life as  derived  using the Guidelines  is  0.030  j»g/l  as a  24-hour average.
The concentration at 0.030 yg/1  is probably  too  high because  it  is based on
bioconcentration  factors  measured in  laboratory studies,  but  field studies
apparently produce  factors at least  10 times higher  for  fishes.   The avail-
able data  indicate that  acute toxicity to  saltwater aquatic  life probably
will only occur at  concentrations  above 10 u9/1  and that the 24-hour average
should provide adecruate protection against acute toxicity.
                                     B-13

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                                  REFERENCES

Addison  R.F.,  et al.  1978.   Induction of  hepatic mixed-function  oxidase
(HFO) enzymes  in  trout (Salvelinus fontinalis)  by  feeding Aroclor^ 1254 or
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Aulerich,  R.J.  and R.K.  Ringer.   1977.  Current  status  of PCB  toxicity  to
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 Birge, W.J.,  et  al.   1979.   Toxicity  of  organic chemicals to embryo-larval
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 Branson,  O.R.,  et al.  1975.  Bioconcentration of  2,  2', 4,  4'-tetrachloro-
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                                       B-38

-------
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                                                         |
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                                     B-39

-------
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                                      B-40

-------
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                                                         i
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 combined effects  of
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-------
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                                     B-42

-------
Hansen,  D.J.   1975.   PCBs: Effects  on  and accumulation by  estuarine organ-



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Hansen, D.J.  1980.  Memorandum to C.E.  Stephan.  July.






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6: 113.                                              <



                                                     ,!


Hansen,  D.J.,  et al.   1973.   Aroclor^ 1254  in eggs of sheepshead  minnows:



Effect on fertilization success and  survival of embryos and  fry.  Proc. 27th



Annu. Conf. S.E. Assoc. Game Fish Comm.   p. 420.






Hansen  O.J.,  et  al.  1974a.   Arocloi®  1016:  Toxicity to  and  uptake by  es-



tuarine animals.  Environ. Res.  7: 363.             •'
                                                     '!





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Am. Fish. Soc.   104: 584.                            :
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catfish  (Ictalurus punctatus)  and  the  selective  accumulation  of  PCB  com-


ponents.  Jour. Fish. Res. Board Can.  33: 1343.     ;
                                     B-43

-------
Harding,  L.W.,  Jr. and  J.H.  Phillips, Jr.   1978.   PolychTorinated  biphenyl
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Hogan, J.W.  and J.E. Brauhn.   1975.   Abnormal rainbow  trout fry from  eggs
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Ito,  Y.   1973.   Studies  on the  influence of PCB on aquatic  organisms-II.
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                                     B-44

-------
   Ito, y.  and  T. Murata.  1974.   Studies  on the  influence  of PCB on  aquatic
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  Ken,  J.E.,  et  al.   1971.   Polychlorinated biphenyl  (Aroclo.® 1242):  Ef-
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  Koch,  R.S.,  et  ,1.   197?:.   Polychlorinated bipohenyls: Effect  of  long-term
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 Larsson, C.M.  and J.E.  Tillberg.  1975.   Effects  of the  co^ercial  poly-
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                                     B-45

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Lowe, J.I.   Results of  toxicity tests  with fishes  and  macroinvertebrates.
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Lowe   J.I., et  al.   1972.   Effects  of the  polychlorinated  biphenyl  Aro-
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Maki,  A.W.  and H.E.  Johnson.  1975.  Effects of  PCB (Aroclor® 1254) and p,
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                                       B-46

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                                        (Rj
Morgan, J.R.   1972.'  Effects  of Aroclor^ 1242  (a  polychlorinated biphenyl)
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  In: Physiological  Re-

-------
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                                     B-48

-------
 Norstrom,  R.J.,  et al   Kne   • u-
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         .  H.B..
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                          by  Peduc1ng  phytoplanktoi,
                                                     b
                                                         and           ;
                                                                 ""ion.
                  .   1375.                                jor

                    .  Bu.,. Environ. cont». Toxicou  14= 480.
             estuar)ne anj
                                 Assoc. S.E.


Platonow,  N.S. and L.H. Karstad    IQT-J
                                 1973*
         on .ink.  Can. Jour.  Comp. Med.  37:391
          ,.  et a,.
                          Effect of
                                                     of polychlorinated
   expose,  to po,ych,or,ate, Mpheny1s  (PC8s).   z :
                                    -

                                                      kinetics.  Map.
                              B-49

-------
Roesijadi, G.f  et al.   1976b.   Osmoregulation of  the  grass shrimp  Paslae-
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                                     B-50

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                                      B-51

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Zullei,  H.  and 6. Benecke.   1978.   Application of a new bioassay to screen
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                                    B-52

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Mammalian Toxicology  and  Human  Health Effects
                              SUMMARY
     Polychlorinated  biphenyls (PCBs)  have been  used  commercially
since  1929 as dielectric  and  heat  exchange  fluids and  in  a  variety
of other applications.  They have become widely disseminated in the
environment worldwide.   Like  many organochlorine  pesticides,  they
are highly persistent and accumulate in  food  webs.   Human exposure
to PCBs  has resulted  largely  from the  consumption of  contaminated
food but also from inhalation  and  skin absorption in work environ-
ments.   PCBs  accumulate  in the fatty  tissues and skin of man  and
other mammals.  Metabolism occurs  oy hydroxylation and dihydrodiol
formation with arene oxides as probable intermediates.  The  rate of
metabolism and excretion  slows dramatically as  the chlorination of
the biphenyl  nucleus increases.   Arrangement  of chlorines which
eliminate adjacent  unsubstituted  carbons  greatly increase resis-
tance  to metabolism.   PCBs have caused  profound  toxic effects in
man and  animals,  particularly  if  repeated exposures  occur.    The
skin and liver are major  sites of  pathology,  with  the  gastrointes-
tinal tract and nervous systems also being targets.  Polychlorodi-
benzofurans which contaminate commercial PCB  mixtures  may contrib-
ute significantly  to  their toxicity.   Several studies in rodents
                                                ,f
suggest strongly that some PCBs are carcinogenic  and that they  can
                                                ;
enhance the carcinogenicity of other chemicals. , A linear  model  for
risk assessment has  been used to  estimate maximum safe   levels in
water and fish which  will establish a  level of risk for  the human
population from cancer.  A maximum level of  PCBs
                               C-i
in water  projected

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to result in no more than one cancer  in 105  individuals with life-
time exposure of 0.79 ng/1 is suggested by the analysis.
                             EXPOSURE
     The magnitude of the dispersal of these chemicals is revealed
by their  detection in  the  tissues of plants  and animals  in all
parts of the world.  PCS residues have been observed  in wildlife in
Sweden, North America, Great  Britain,  the  Netherlands, and even the
Arctic  (Risebrough and deLappe,  1972).  Because PCBs are not natu-
rally  occurring  substances,   their  dissemination  is  entirely the
result  of  human activity.   Their entry  into  the environment has
occurred by  vaporization into the atmosphere, and by spilling or
dumping into water or onto land.   It has been estimated that of the
1970 sales of PCBs in North America, only 20 percent represented a
net increase in the total amount  in service.  Estimated sources of
loss for that year were  1 -  2 x  10  tons  for evaporation; 4 - 5 x
10  tons for  leaks and  disposal  of  fluids;  and  22 x 10   tons for
disposal by  incineration and  burial (Misbet and  Sarofim,  1972).
The cumulative  input  to the  environment  between 1930 and 1970 was
                       4                      4
estimated to  be 3 x 10   tons to air, 6  x  10  tons  to  fresh and
coastal waters, and 3 x  10   tons to dumps and landfills.   In that
time, up to  one-third of the PCBs released to air and one-half of
that  released to  water were  probably degraded.   Degradation in
landfills is more difficult to estimate (Nisbet and Sarofim, 1972).
PCBs  have  been found repeatedly to  be widespread in analyses of
human  tissues.   For  example, detectable  levels  of PCBs  have been
reported in  adipose  tissue samples of up to 91 percent of  indivi-
duals sampled in a survey of  the  United States  population  (Kutz and
                                C-2

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 Strassman,  1976;  see Table 13).  This  finding  ssuggests that envi-
 ronmental contamination may be a significant source of human expo-
 sure.   Likely  routes of exposure  for  the general  population  are
 water  and  particularly  food/  while inhalation and  dermal  contact
 are likely  to be  more significant routes in occupational exposure.
 Ingestion from Water                            ;
     The solubility of  PCBs in water is very low, decreasing as  the
 percent chlorination  is raised.   Solubilities of Aroclors in water
 at  20°C vary  from 200  yg/1  for 1242  to  about  25 ug/1 for 1260
 (Nisbet and  Sarofim,  1972).   The major factors  in  the  dynamics  of
 PCB distribution  in  water  are  its  low solubility, high specific
 gravity, and its  high affinity  for  solids.  Most PCBs  discharged
 into water are found  in bottom sediments near the site  of discharge
 (Nisbet and  Sarofim,  1972).  Evaluation of PCB; levels  in  surface
 waters  and  bottom sediments  of the major  drainage basins of the
 United States  was conducted  between 1971 and 1974  (Dennis,  1976).
 The data were derived from the U.S.  Geological  Survey  (USGS)  study
 of  1971-72  (Crump-Weisn«r,  et al.  1974) and  from additional data
 collected  by  the  USGS  between 1972  and 1975  (PCB  data base
 1972-75).   It is  summarized in detail in the Criteria Document for
 PCBs (U.S. EPA, 1976a).  The highest concentrations in  both water
 and  sediment were  found in  the basins  east   of  the  Mississippi
 River.   The highest levels were  found in 1971 in the lower Missis-
 sippi basin,  with  a median concentration for the region  of 3.0 yg/l
 and positive  detections at  100  percent of  stations tested.  Over
 the time period of the  sstudy  the concentrations and incidences  of
PCBs detected in  all  basins have decreased  substantially.  By 1974
                               C-3

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the median level in the lower Mississippi basin had dropped to 0.1
Vig/1 and  the incidence  of  detection  to  2.6 percent  of stations
tested.   The levels  in sediments,  however,  have persisted at much
higher levels over  this period of time.  In 1971 median sediment
levels for the Mississippi basin were 30 ug/kg and the  incidence of
detection 100 percent.   By 1974 the  incidence  had dropped  to 9.9
percent,  and the median level was 10.5  ug/kg.
     Although PCBs are widespread in  aquatic  environments  (Peakall,
1973), their  low  solubility generally prevents them from reaching
high concentrations in drinking water supplies.  The persistence of
PCBs  and  their accumulation  in sediments,  however,  increase the
significance of water as a  source of  human exposure by providing a
reservoir of material which can  continue to  contaminate water long
after the addition of  PCBs  has ceased.  In combination with these
factors,  the lipophilicity  of PCBs results  in their continued .in-
troduction to,  and  accumulation in,   the food chain.   As a conse-
quence, fish and other foods obtained from aquatic environments may
become  important  sources of  exposure  even  if  PCB  levels  in the
water are low.
     The  ability  of  PCBs discharged  from a  manufacturing facility
to contaminate a drinking water system has  recently been, highlight-
ed.  Billings,  et al.  (1978)  determined the  levels of PCBs in the
Easley-Central  Water  District,  Pickens  County,  South  Carolina.
They observed  that  PCBs discharged  by a capacitor manufacturing
facility  12  km  upstream from the water district's  treatment plant
were entering the water  system.  Finished  potable  water  supplies
were contaminated to  levels as high  as 818  ng/1.
                                C-4

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 Ingestion from Food
      Contamination  of  food  with  PCBs  occurs primarily  by three
 mechanisms.  The first is contamination of  human food as a conse-
 quence of  accumulation  in  the food  chain. The  contamination  of
 freshwater fish as a consequence of the contamination of the aqua-
 tic environment  is  a particularly significant route  of PCB entry
 into the human diet which will be discussed in more  detail below.
 The second mechanism occurs by  the direct contamination of feeds or
 foodstuffs with PCBs.  This  may occur  as  a result of  accidental
 spills or  equipment  malfunctions  as  was the  case  in the episode  of
 rice oil contamination  in Japan which  led to the  outbreak of Yusho
 or  rice oil  disease in  1968  (Kuratsune,  et al.  1976).    in  this
 instance leaks  in a heat  exchanger  used to  process rice  bran oil
 resulted  in the  contamination  of the  oil  by the  exchanger  fluid
 (Kanechlor  400).    Discovery  of  the  contamination was  made only •
 after  numerous cases  of  chlorinated  hydrocarbon  intoxication  in
 Fukuoka prefecture,  Japan.  The oil  was found to contain  2,000  to
 3,000  ppm  Kanechlor  400 which was contaminated with polychlorodi-
 benzofurans  (1.6  to  5  ppm).    Average consumption of  PCBs among
 affected individuals was   estimated  to be 2 g  (Kuratsune, et al.
 1972).   By 1975 the  total number of known individuals affected was
 1,291.   Elevated  PCB levels  in  fat were still observed four years
 after the exposure,  and  dermatological  symptoms were found  in up to
 89 percent of a group of  72 patients examined in 1973 or 1974.  An
 example of  accidental PCBs contamination in animal feed occurred as
a result of  the use of PCBs  in silo  coatings  (Willett and Hess,
1975).   The third  significant  source  of PCBs  in foodstuffs was food
                               C-5

-------
packaging made  from  recycled  paper containing  PCBs (Jelinek and
Corneliussen, 1976).
     A special case  of  human exposure via food which must be con-
sidered  is human  breast milk.   Adverse effects have been observed
in breast fed infants of women with Yusho  (Kuratsune, et al.  1976)
and in infant Rhesus monkeys ingesting breast milk containing 7  to
16 ppm  PCBs  (fat  basis)  (Allen,  1975;  Allen and Barsotti,  1976).
Preliminary survey data indicate average PCB levels  in human  breast
milk of  1.8  ppm  (fat basis)  (42 PR 17487), and  a study of PCB ex-
posed nursing mothers in Germany  indicated average PCB levels  of
3.5 ppm (Tombergs,  1972).   The proximity  of  these values  to the
toxic levels in  infant monkeys  (7  to 16 ppm)  suggests that human
breast  milk  must  be  considered  a significant source of PCB expo-
sure.
     The extent  of contamination of the U.S.  food  supply  has been
the subject of Food and Drug Administration (FDA) and Department  of
Agriculture  (USDA)  monitoring programs  since  1969.   Results  of
these  studies have been  summarized by  Jelinek and  Corneliussen
 (1976).   The initial analysis of  15,000  food  samples  between 1969
and 1971 is  summarized in Table 1.  The results of monitoring pro-
grams   in  fiscal  years 1973,  1974,  and  1975  are summarized  in
Table  2.  Over  the monitored period  the  incidence and  levels  of
PCBs  have dropped in all  food classes.   By 1975 the only signifi-
 cant  food sources were  fish,  meat,  and  dairy  products.   Fish were
 by far  the most  significant source.   The findings for the  1969-71
 period  led  to the establishment of regulations  for  PCB  levels  in
 food (38 FR 18096).   The temporary tolerances established  at that
                                C-6

-------
                            TABLE  1
                    Summary of PCBs in Pood*
                    Nov., 1969 - June, 1971a
Pood
Commod i ty
Finfish
Oysters
Fish by-products
Cheese
Milk
Eggs
Potato
by-products
Miscellaneous
Positive
Findings
317
12
6
44
60
17
12
11
Avg. of
Positives
(ppm) ,
2.1
Trace
1.8
0.3b
2.5b;
'''race
1.1 i
|
1.9
Max. Level
(ppm)
35.3
Trace
5.0
1.0b
22. 9b
0.5
4.2
6.5
 Approximately 15,000 samples examined      i
bFat basis                                  i
 Detection limits: fish 0.5 pom, other foods 0.05 ppm
 (P.E. Corneliussen, personal communication)
*Source:  Jelinek and Corneliussen, 1976
                             C-7

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time and new tolerances recommended in 1977  (42 PR 17487) are given
in Table 3.  The enforcement of those tolerances and restriction of
PCB use in open systems after 1970 probably account for the general
decline of PCB  levels  in  foodstuffs.          l
     Comprehensive  fish,  surveys  conducted  by  the  FDA  in  fiscal
years 1973 and 1974 indicated a drop in the incidence of  PCB detec-
tion in fish from less than 30 percent in 1973 to less than 20  per-
cent in 1974.  In 1973, 3 percent contained over 1 ppm and  0.5  per-
cent contained  over  5  ppm PCBs.   The data from all  FDA  studies in
the fiscal years  1973,  1974,  and» 1975 are summarized  in Figure 1.
While the  incidence of PCBs  in  fish  dropped over the period,  the
fraction of positive fish containing over 5 ppm  PCBs  increased  from
less than  5 percent to  over 10 percent.   The  samples  containing
more than 5 ppm were from the Great Lakes.  Because  the study  in-
volved different sources  and  objectives  from year  to year,  no  con-
clusion as  to  whether  a  significant trend  existed was drawn.    It
should be noted that these surveys were conducted with fish in  com-
merce and  provide no  information  about sport  fish  per se.    The
studies indicated that: significant levels of PCBs  generally  do  not
occur in saltwater fish.                      j
     The impact of  sport  fish consumption was examined in a study
of a group of sports fishermen who consumed an average of  24 to  25
pounds of fish  annually   (highest individual exposure 180  Ibs/year
over a two-year period).   PCB residues in cooked fish ranged  from
0.35 - 5.38 ppm.  Plasma PCB levels ranged from  a  high of 0.366  ppm
in the exposed group to control levels of 0.007 ppm  (less  than  six
Ibs consumed per year)  (42 FR 17487).         i
                               C-9

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                               TABLE 3

                      FDA Regulations for PCBs*
I. Temporary
Cornmod i ty
Milk (fat basis)
Dairy products (fat basis)
Poultry (fat basis)
Eggs
Finished animal feed
Animal feed components
Fish (edible portion)
Infant and junior foods
Paper food-packaging material
without PCB- impermeable barrier
tolerances
PCB cone.
(ppm)
2.5
2.5
5.0
0.5
0.2
2.0
5.0
0.2
10. Oa
Proposed Guidelines
1977
1.5
1.5
3.0
0.3
0.2
2.0
2.0
pending

a
 Administrative guideline, pending hearing

*Source:  Jelinek and Corneliussen, 1976
          42 FR 17487
                               C-10

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  60
 50
                        FIGURE 1        i



PCBs in Pish PY 7.3, 74, 75  (Level  of detection:  0.5 ppm)



         Source:  Jelinek and  Corneliusen,  1976
                          C-ll

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     A bioconcentration factor (BCF) relates the concentration of a
chemical in aquatic  animals to the concentration  in  the water in
which they  live.   The steady-state BCFs  for a lipid-soluble com-
pound in the tissues of various aquatic animals seem to  be propor-
tional to the  percent  lipid in the tissue.   Thus, the per capita
ingestion of a  lipid-soluble chemical  can  be  estimated  from the per
capita consumption of fish and shellfish,  the weighted  average oer-
cent lipids of consumed fish and shellfish,  and a  steady-state BCF
for the chemical.
     Data from a recent survey on fish and shellfish consumption in
the United  States were analyzed  by SRI  International  (U.S.  EPA,
1980).  These  data were used to estimate that the per capita con-
sumption of  freshwater and estuarine fish  and shellfish  in  the
United States  is 6.5  g/day (Stephan, 1980).   In addition, these
data were used  with data on  the fat content of the edible  portion of
the  same  species  to estimate  that the  weighted  average percent
lipids for consumed  freshwater and estuarine fish  and  shellfish is
3.0 percent.
     Several  laboratory  studies,  in   which  percent lipids  and a
steady-state BCF were measured, have been conducted on polychlori-
nated biphenyls.   The  mean of the BCF values, after normalization
to one percent lipids,  is 10,385 (see  Table 5 in Aquatic  Life Toxi-
cology section) .   An adjustment factor of 3 can be used  to ad-just
the  mean  normalized BCF  to  the  3.0   percent lipids  that  is   the
weighted  average  for  consumed  fish  and  shellfish.    Thus,   the
weighted  average bioconcentration  factor for polychlorinated  bi-
phenyls  and the  edible  portion  of all  freshwater and  estuarine
aquatic organisms consumed by Americans is calculated to  be 31,200.
                               C-12

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     Higher BCP  values  apparently can  be  achieved in field expo-
sures  (Haile,  et al. 1975;  Norstrom,  et  al.  1976;  Duke,  et al.
1970;  Nimmo,  et al. 1975;  Veith,  1975; Veith,  et al.  1977), but
those values cannot be considered quantitative  because the exposure
of the organism cannot  be adequately documented and integrated over
a long enough period of time.          l       :
     In order  to estimate human dietary PCB  intake,  the FDA con-
ducts a continuing survey of the total  diet.  Composites of 12 dif-
ferent food categories are analyzed for PCB content.  Table 4 sum-
marizes the results of the survey from 1971 through the first half
of 1975.   While contamination  was  observed  in most categories in
1972,  the  number  of positive categories had dropped  by  1973.   In
1974 and 1975 only meat,  fish,  and poultry  were observed to contain
PCBs; fish was almost always the contributor oi: positive results in
that category  (Jelinelc and  Corneliussen,  1976) .  Most of the con-
tamination  noted in the other  categories in earlier years  was
thought  to result  from  exposure during  processing  or  packaging
                                              f
because the  raw foods  were  rarely  found  to contain  PCBs.   Total
daily  intake/  calculated from  the  composite   figures for  a young
adult  male over  the period  1971-75,  is  summarized  in  Table  5.
Total  daily  intake dropped  by  almost  50 percent over the period,
but intake  in  the  meat-fish-poultry category  changed  very little.
By 1974, almost all of the dietary  intake resulted  from the inges-
tion of  PCB-contaminated fish.  The  mea.sures  taken  in  the early
1970's  to  limit the release of PCBs  into  the environment  and to
remove them from  food  processing environments effectively reduced
direct contamination of foodstuffs to a minimum level. The persis-
                               C-13

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                           TABLE 5
               Estinuites of Daily PCB Intakes;*
              (Total Diet Study - Teenage Male)
Fiscal
Year
1971
1972
1973
1974
1975 (1st half)
Average
Total Diet
(ug/day)
15.0
12.6
13.1
8.3
8.7
Daily Intake of PCBsa
Meat- fish-poultry
Food Class (yg/day)
1 9-5
9.1
I 8-7
8.8
1 8.7
 Lower limit of quantitative reporting = 0.05 ppm with  analyt-
 ical method employed                        <
*Source:  Jelinek and Corneliussen, 1976     ;
                             C-15

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 tence of PCBs in aquatic environments and in fish has maintained a
 residual dietary exposure level.  Further reduction  of  PCB levels
 in the diet will require that entry of PCBs  into waterways be more
 tightly controlled and that monitoring of fish and other foods for
 PCB contamination  be  continued (Jelinek and  Corneliussen,  1976).
 The recently recommended reduction of allowable PCB levels in fish
 to 2.0 ppm may further reduce dietary intake (42 PR 17487).
      Two special situations which must  be  avoided to prevent  un-
 necessary PCB  ingestion should be  mentioned.   First,  accidental
 contamination of foodstuffs  or feeds with  PCBs must be  avoided.
 Although PCB  manufacture is  now  stopping  and distribution  will
 cease  in the near  future,  many PCB-containing products remain  in
 service.   Failure  to exercise  care in the maintenance and  disposal
 of  these  units  could result  in the contamination of  food or  water.
 The  tragic results of  the  episode  of  rice  oil contamination .-in
 Japan  (Kuratsune,  1972)  provides  ample evidence  of  the need  for
 care and continued surveillance of foods. Second,  although occupa-
 tional  exposure to  PCBs will decline over the next several  years,
 the possibility of  food  contamination as  a consequence of  transfer
 from workers'  tools or clothing must  be  considered  as a possible
 route of dietary exposure.
 Inhalation
     PCBs can enter the atmosphere by vaporization and may  be found
 in either gaseous form  or adsorbed  to airborne particulates.   Prior
 to the restriction of  PCB use,  substantial losses to  the  atmosphere
 resulted from evaporation of plasticizers and from improper  incin-
eration.  In 1972,  terrestrial  input  from fallout was estimated to
                               C-16

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be 1,000 to 2,000 tons/year.  Annual emission rates were estimated
                                               ;
at 1,500 to 2,500  tons  (Nisbet and Sarofim, 1972).   In 1975, a study
of PCS  content in air  in suburban areas  in  Florida  and Colorado
indicated  that  average atmospheric levels  were  approximately 100
ng/m3  (Kutz and Yang,  1976).   Rates of fallout^ along the southern
California  coast  were estimated  to average 1,800  kg/year  over  a
50,000 km  area (Young, et al. 1976).  The distribution of PCBs in
air is nonuniform, being  more  highly  concentrated in urban areas.
The aerial fallout  survey  in southern California indicated that
sectors in the urban areas around Los Angeles Had  fallout rates of
up to 180 kg/yr, while less  industrialized sectors had  rates as low
as 30  kg/yr. A study of PCB levels in  soil samples  showed that they
were rarely detectable in agricultural soils but were found in 63
percent of  urban  samples  from 19 cities  (Carey  and Gowan,  1976).
General  human  exposure to  inhaled  PCBs  probably  varies  with the-
local conditions.   In  relation  to the 9 ug/day  intake estimated
from  the diet  (Jelinelc and Corneliussen,  1976) , nonoccupational
exposures by inhalation are probably small.    j
     While  inhalation  of  PCBs  is  not and  most likely will not be a
major route of  general human  exposure, it is a highly significant
route  of  occupational  exposure.   Early  in  its  commercial  use an
association  was  observed between  occupational  exposure  to  PCB
vapors and chloracne  (Jones and Alden,  1936; Schwartz, 1936).  The
benefits of controlling leaks  from closed systems into work envi-
ronments were noted  by Meigs,  et  al.  (1954).   ;
     A study of occupational exposure  in  Japan found PCB vapors at
levels between 13 and 540 ug/m  and airborne particulates between  4
                               C-17

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and 650 ug/m  in a survey of six  industrial plants.  An additional
finding  of 6,270  pg/m  PCS  particulates was  associated  with a
spill.  Blood PCS levels of 99 exposed workers averaged 370 ppb as
compared  to  levels  in 32  controls  of 20  ppb   (Hasegawa,  et al.
1972).   Ouw,  et al.   (1976)  observed  Aroclor  1242 levels between
2.22 and  0.32 mg/m   in different  areas of an electrical equipment
manufacturing  facility in Australia.   Blood Aroclor  levels were
analyzed  by gas chromatography, and  fractions  with several reten-
tion times standardized against Aroclor 1242 were detected in ex-
posed workers.  Workers in an impregnation  room where inhalation
was a  major  mode of  exposure  had higher levels  of  PCBs  than did
workers  in another  area where exposure  was primarily  dermal.   A
series of 30  control individuals  was not found to have detectable
PCB levels.  The limit of detection in this study  was not reported;
however, Finklea, et al. (1972) reports American control population
blood levels of 0.3 to 3 ppb.
     It  is difficult to differentiate between industrial exposure
by inhalation and dermal absorption  (see  Dermal  section).  Animal
studies do indicate that animals exposed to PCB aerosols show  raoid
increases  in  liver  PCB levels.   Exposure to Pydranl A 200  for 15
minutes resulted in  the accumulation  in the liver  of 50 percent of
the PCBs  accumulated after two hours  (Benthe, et al.  1972) .   The
lung appears  to be  a good  site of absorption, and certain occupa-
tional environments  contain significant  levels  of airborne  PCBs.
The National  Institute for Occupational Safety and Health has  re-
cently proposed  an occupational exposure  limit of  1.0 ug/m  on  a
time  weighted  average  10-hour  day,  40-hour week  basis  (NIOSH,
                               C-18

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                                            2
1977) .  Assuming a  tidal  air  volume of 10 m  in an eight-hour day
and 100  percent absorption,  the  resulting dose  at  this exposure
level would be 10 yg/deiy.                      '[
Dermal                                         i
     Dermal exposure,  like  inhalation exposure, is a particularly
significant route in  the  occupational setting.   With the restric-
tion of PCS uses to sealed systems, the use of  PCBs in products to
which the public might  be exposed  has declined markedly, reducing
opportunities for general exposure.   Past uses of PCBs  in carbon-
less copy paper, printer's  inks,  and  other products probably con-
tributed to general PCB exposures.   Documented exposures  are large-
ly  occupational as  exemplified by  the  results of  Ouw, et  al.
(1976).  The authors noted that one group  of  employees was largely
exposed through skin  contact  and  had  significantly elevated blood
PCB levels.                                    :
     In a variety  of  animal studies dermal application  of several
PCB-containing materials  has  produced both local and systemic ef-
fects including  liver degeneration and death  (Miller, 1944; Pari-
bok, 1954; Vos and Beems, 1971).   In  neonatal rats treated by skin
application with PCBs,  a 5- to 10-fold increase in aryl hydrocar-
bonhydroxylase activity occurred in liver, skin, lung, and kidney,
indicating significant .distribution to these tissues  after exposure
by this route (Bickers,, 1976;  Bickers, et  al.  1975).
     The  relative  contributions of various routes of exposure can
be expected to vary widely.   Occupational  exposures are  by far the
most severe with inhalation and skin contact being the major routes
of absorption.   A  noteworthy by-product of occupational PCB expo-
                               C-19

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sure  is  the  elevated  risk  of  exposure  among  other  members of  work-
ers'  families.   An epidemiological  study in Bloomington,  Indiana
revealed significantly elevated serum PCS levels  among a group of
18 occupationally exposed workers (mean 71.7 ppb)  and a slight ele-
vation  among 19  members of their families (near 33.6  ppb)  as com-
pared to background levels  (5  to 20 ppb)  (McCloskey,  et al. 1978).
The  general  public  is widely  exposed  to PCBs but  at much  lower
levels and primarily through the diet.   Pish  living in contaminated
waters are by far the largest contributors to dietary PCBs (Jelinek
and Corneliussen, 1976).
                         PHARMACOKINETICS
Absorption
     The  efficiency of PCS absorption in  the gut of  rats  was  shown
to be between 92 to 98.9 percent (Albro and Fishbein,  1972).   Nei-
ther  the degree  of  chlorination (mono-hexachlorobiphenyl) nor the
dose ingested (5 to 100 mg/kg) markedly affected the  efficiency of
the uptake.  Matthews and Anderson  (I975b) observed a reduced  accu-
mulation of PCBs in adipose tissues of rats exposed orally as com-
pared to intravenous  (i.v.)  injection.   The differences  were more
pronounced with biphenyls of low chlorine content  and  were thought
to be related to route of  absorption  and metabolic rates, rather
than to  the  overall  efficiency of transport across  the gut.   Ab-
sorption  via  the gut  was  also very efficient in adult Rhesus mon-
keys, 90 percent of a  single  dose  of  1.5 or  3.0 g/kg Aroclor  1248
being absorbed   from  the  gastrointestinal  tract  (Allen,  et al.
1974a) .
                               C-20

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     Efficient absorption via  inhalation has been demonstrated in
rats by Benthe, et al. (1972).                j
     In humans, absorption  via the intestine has been best illus-
trated by  the Yusho  Japan  incident  in  1968. •   Among individuals
ingesting less than  720  ml  of contaminated rice bran oil  (equiva-
lent to 1.5  to 2.2 g Kanechlor 400), 39  percent developed severe
symptoms and  an additional  49 percent developed moderate  symptoms
of PCS intoxication.  The lowest  level  of PCB ingestion in an af-
fected  individual was , estimated  to  be  0.5 g:  (Kuratsune,  et al.
1972).  Absorption via the respiratory tract and  skin  is also effi-
                                              i
cient as indicated by occupational exposures where effects of PCB
exposure can be detected  even  at doses too low to produce pathology
(Alvares, et al. 1977) ..                       ;
Distribution                                  '
     PCBs given  to  rats  by  i.v.  injection  ai:e  removed  from the
blood rapidly  and  stored initially in the liver and muscle.  'With
time  they are redistributed primarily  to skin  and adipose tissue
(Matthews and Anderson,   1975b).    The  degree  to which  PCBs are
stored or excreted depends on  their  susceptibility to metabolism
and, therefore, on the degree of  chlorination and availability of
adjacent  unsubstituted  carbons.    Tissue  levels  of  mono-,  di-,
penta- and hexachlorobiphenyls in  rats given a single  injected dose
at 0.6 mg/kg were determined by Matthews and Anderson  (1975b).  The
maximum doses  accumulated  in  each tissue increased with degree of
chlorination  as did the  half-life in each  tissue.  The proportion
of- total PCBs present in tissues  as  metabolites was greatest for
the  mono-  and dichlorbbiphenyls.   Hexachlorobiphenyls in  tissues
                               C-21

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were  largely unmetabolized.   The  distribution of PCBs  in  adipose
tissue  provides  a useful example  of  the relative accumulation of
different isomers.  Tissues were examined for up to 42 days; a  sum-
mary  of the  results is presented in Table 6.
      A  similar pattern was  observed in  skin, with  up  to  22  percent
of the hexachlorobiphenyl dose being accumulated there at 1  day and
residual levels around 15 percent  remaining at  42  days.
      Single  intravenous  doses  of 0.6  or 6.0 mg/kg of  2,4,5,2',5'-
pentachlorobiphenyl were cleared from the blood in ten minutes and
initially deposited  in  liver and  muscle.   They were  subsequently
translocated  to  adipose  tissue and skin as depositories  (Matthews
and Anderson, 1975a).
      A  single   administration  of  approximately  500  mg/kg  of
2,5,2',5'-tetrachlorobiphenyl to rats resulted  in a similar  distri-
bution with adipose, skin,  and blood being the  significant  storage
depots after 24 hours (Van  Miller, et al. 1975).
      The significance of chlorine position as  well  as number was
addressed in  a  study of the pharmacokinetics  of  3,5,3'^'-tetra-
chlorobiphenyl (TCB) by Tuey and Matthews (1977).  The arrangement
of chlorines  on  this  molecule results  in the  absence of adjacent
unsubstituted sites.  The  pattern  of distribution of  the compound
following a single i.v.  injection  of 0.6 mg/kg  was similar  to  that
observed in  earlier  studies (Matthews and Anderson, 1975a,b)  with
adipose tissue and skin  becoming  the major long  term storage sites.
However, loss of 3,5,3',5'-TCB was  slower than  earlier observed for
2,4,5,2',5'-pentachlorobiphenyl (see Table 6) with  the  maximum  adi-
pose  tissue  load  reaching  52.9  percent   of  total  dose  on
                               C-22

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day 4  and  the residual on  day 7 remaining  at  45.4  percent.   The
distribution  of  several  tetrachlorobiphenyl isoraers  in 'mice -was
analyzed by Mizutani, et al. (1977).   In  all  cases the  accumulation
of the compound  was  greater in the carcass  than  in  the liver.  A
tendency for  those  isomers  with adjacent unsubstituted carbons to
be rapidly  cleared  was  observed.  2,6,2',6'-TCB  was very rapidly
cleared from carcass and liver, and 2,3,2',3'-TCB  was cleared  fair-
ly rapidly.   However, 2,4,2',4'-TCB was  more resistant to removal
than 3,5,3',5'-TCB,  which might not  be  anticipated  on structural
grounds.  The half-life in  the carcass of the former was 9.2 days
but only 2.1 days for the  latter.  The degree of  accumulation of the
isomers was assessed by  the  introduction  of an index  referred  to as
a storage  ratio  (the daily  amount entering  storage/daily oral in-
gest ion) .   By this  measure 3,5,3',5'-TCB and  2,4,2',4'-TCB  were
similar with  indices of 0.7 and 0.6,  respectively,  while the more
readily metabolized  2,3,2',3'-TCB had an index of 0.06.
     The distribution of 2,5,2',5'-TCB in infant Rhesus monkeys was
determined after a single  dose of tritiated TCB  (500  mg/kg).   At 72
hours the distribution differed from that in  rats  in  that the  label
was more widely dispersed in the monkeys.  Blood levels were  lower
than observed in rats, and  the major  storage depots  were bone mar-
row, adrenal  glands, and  skin.  Most of  the labeled material was
associated with macromolecules, although it was  largely extractable
and not covalently bound  (Hsu, et  al.  1975a).
     Distribution of PCBs in the human body has not been the  sub-
ject of  systematic   experimentation.   Data  available  from general
population  surveys  indicate that general patterns of  distribution
                               C-24

-------
are consistent  with  those  found  in other animals.  When detected in
the adipose tissue of.the general populace, PCB levels are around 1
ing/kg  (Yobs,  1972;  Kutz and Strassman, 1976; Grant,  et  al.  1976).
Plasma  levels detected  in  the general populace  are two  to  three
orders  of magnitude lower  than adipose  levels  (Finklea, et  al.
1972).   Similarly,  Yusho patients exhibited  a 100-  to  1,000-fold
greater concentration in the fat of skin, liver and in adipose tis-
sue than  in plasma.  Over several years  both  the fat and plasma
levels were  observed to decline to near normal levels  (Kuratsune,
et al. 1976).   The PCBs  found  in human  adipose  tissues in the U.S.
chromatographically  resemble Aroclor 1254 and 1260, suggesting that
less chlorinated  isomers found in  Aroclor 1248 are  preferentially
excreted  (Kutz  and Strassman,  1976).
Metabolism                                   I
••^«WM^^^^HMI^^^_MM>           , .                       I
     The metabolism of PCBs has been studied extensively  in several
organisms.   A  detailed  review of PCB  metabolism  was  written by
Sundstrom, et al.  (1976a).   Rather than attempt to treat  the  sub-
ject exhaustively, this  section will summarize the major character-
istics of PCB metabolism which relate to their distribution,  accu-
mulation, toxicity, aiid  possible mechanisms of carcinogenicity.
     The metabolism  of  PCBs depends  on theirichlorine content and
the sites of  chlorination on the  biphenyl  (Sundstrom,  et al. 1976a;
Lutz,  et  al.  1977).  While the overall  mechanisms of metabolism
appear to be similar in  most vertebrates examined, the capacity to
metabolize PCBs declines from mammals to birds to fish (Hutzinger,
et al.  1972).  Elucidation of PCB metabolism has been  made possible
by the use of individual purified isomers.  Predominantly,  the pro-
                               C-25

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ducts of PCB metabolism at all levels of  chlorination are biphenyl-
ols,  biphenyldiols,  and  dihydrodihydroxybiphenyls, although  the
types  and  proportions of  specific metabolites  vary  in different
species.  A few biphenyltriols and  methoxy  derivatives have also
been observed  (Sundstrom, et al. 1976a).
     The structures of several  PCB metabolites support the forma-
tion of arene oxides as intermediates.  The  first evidence for the
formation of arene oxide  intermediates was  obtained  by Gardener, et
al.   (1973).      They   isolated   trans-3,4-dihydroxy-3,4-dihydro-
2,2',5,5'-tetrachlorobiphenyl as a metabolite of 2,2',5,5'-tetra-
chlorobiphenyl  in rabbits.  More direct  evidence for the formation
of arene oxides was obtained by Safe, et  al.  (1975,  1976).  In rab-
bits and frogs  the biohydroxylation  of 4-chlorobiphenyl was inves-
tigated  using  4'-2H-4-chlorobiphenyl.    The major  metabolite,
4'-chloro-4-biphenylol,  retained 79 percent of the label which is
consistent with arene oxide formation (Daly, et al.  1972)  The sub-
sequent  isomerization  of the arene oxide  results in the migration
of  the deuterium atom from the ultimate site of hydroxylation to
the  adjacent carbon,  an NIH  shift.   Daly, et al.  (1972) consider
the NIH  shift  of  labeled  hydrogens,  halogens or  alkyl  substituents
to  be  indicative  of enzymatic arene oxide  formation.   A subsequent
hydroxylation  to 4'-chloro-3,4-biphenyldiol  resulted in the  loss of
half  the remaining  deuterium,  suggesting a  direct hydroxylation
rather than a  second  arene oxide  formation (Safe, et al.  1975).
4,4'-Dichlorobiphenyl  produced  three metabolites  in  the  rabbit:
4,4'-dichloro-3-biphenylol,    3,4'-dichloro-4-biphenylol,    and
4'-chloro-4-biphenylol.   These  products  are  consistent with a mech-
                               C-26

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anism involving 3,4-arene oxide  formation  followed  by epoxide  ring
opening.  Either a 1,2-h'alogen shift, with or without halogen elim-
ination  upon  tautomerization, or  3-ol  formation after arene  ring
cleavage  would  produce the ultimate  products. (Safe, et al. 1976;
Sundstrom,  et  al.  1976a).  The  reactions  are  diagrammed  in  Fig-
ure 2.   Other examples of  PCBs for  which metabolic pathways  are
consistent with arene oxide formation include. 2,2',4,4',5,5'-hexa-
chlorobiphenyl in rabbits (Sundstrom, et al. 1976b)  and  4-chlorobi-
phenyl and 4,4'-dichlorobiphenyl in rats  (Hass,  et  al.  1977).   In-
fant  Rhesus  monkeys  fed  2,5,2',5-tetrachlorobiphenyl   excreted
dihydroxy, dihydrodihydroxy,  and dihydrotrihydroxy  derivatives  in
urine (Hsu, et al. 1975b).
     The  K  region  epoxides  of polyaromatic hydrocarbons are known
to bind  to  nucleic acids  in vitro  (Grover and  Sims, 1970) and  in
cultured mammalian cells (Grover, et al. 1975).  Furthermore,  they
are capable  of transforming  cells in  culture   (Huberman,  et   al.
1972)  although their significance  in tumor induction  in animals  is
in doubt  (Grover,  et al. 1975).   It has been suggested that arene
oxide metabolites of PCBs may react with nucleophilic sites  in  DNA
and other macromolecules and that alkylation  of  critical sites  may
be involved in the induction of  tumors  (Allen and Norback, 1977).
Excretion                                     |
     The  primary  routes of PCB excretion are  bile  (observed  in
feces) and urine.  Excretion is  closely coupled  to  metabolism.   In
rats  less than  ten  percent  of  excreted  PCBs  were  unmetabolized
(Matthews and Anderson, 1975b).  The rate  and efficiency of excre-
tion  were highly  dependent upon  the degree! of chlorination   and
                               C-27

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               urine  2.0
                          FIGURE 2
Metabolic Pathways  for  4,4'-dichlorobiphenyl in the Rabbit
             Source:  Sundstrom,  et al.  1976a
                             028

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structure.  Urinary excretion of PCBs accounted for the  removal of
59.8,  33.9,  7.6, and  0.7 percent  of  total  dose of  mono-, di-,
penta-, and  hexachlorobiphenyl,  respectively.'  Over 60  percent of
urinary excretion occurred within  the  first 24 hours and all uri-
nary excretion ceased  by the ninth and fourth days, respectively,
for penta- and hexachlorobiphenyl  (Matthews and Anderson, 1975b).
All the 2,4,5,2',5'-pentachlorobiphenyl  excreted  in urine by rats
was in the  form  of  a glucuronide  conjugate of a  metabolite  (Chen
and Matthews, 1974).  While urinary excretion usually ceases  within
a  few  days,  biliary  excretion  continues for  an  extended period.
The relative contribution of biliary excretion to the elimination
of PCBs increases with chlorination.  The kinetics of excretion of
mono- and dichlorobiphenyl are monophasic while the elimination of
penta- and  hexachlorobiphenyl is  biphasic.  Iwhile  90   percent of
PCBs up  to  pentachlorobiphenyl were excreted in  42 days or  less,
hexachlorobiphenyl  was largely retained  in  the tissues of the ani-
ma]L.   Extrapolation of  the  excretion  data indicated that only 20
percent of 2,4,5,2',4',5'-hexachlorobiphenyl would ever  be excret-
ed (Matthews and Anderson, 1975b).  The  absence of adjacent  unsub-
stituted  carbons greatly decreased excretion .as would be expected
from   the  effects  of   structure  on  storage  and  metabolism.
3,5,3',5'-Tetrachlorobiphenyl (TCB)  is excreted at about the same
rate  as  2,4,5,2',5'-pentachlorobiphenyl (Tuey and Matthews,  1977;
Matthews  and Anderson,  1975a).    While  the  half-life   in fat  for
2,5,2',5'-TCB  was  about 33  hours at  500  mg/kg  dose in rats  (Van
Miller, et al.   1975), the half-life for 3,5,3',5'-TCB was 12 to 15
days at dose levels oiE 0.6 mg/kg in rats (Tuey and Matthews,  1977).
                               C-29

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     The half-lives of the individual PCB isomers in the rat may be
approximated by the fecal half-lives/ which are 15.7 and 22.2 hours
for mono- and dichlorobiphenyl, respectively.  Penta- and hexachlo-
robiphenyls elimination  is biphasic,  with  first and second compo-
nent half-lives  of 39.2  and  211 hours for pentachlorobiphenyl and
49 and  642  hours for hexachlorobiphenyl  (Anderson,  et al. 1977).
Because only 20 percent of the hexachlorobiphenyl is ultimately ex-
creted, its half-life is  indefinite.
     Rates of elimination of  a series of  tetrachlorobiphenyls (TCB)
in mice were determined by Mizutani,  et al.  (1977).   Half-lives for
TCB  isomers in  liver and the carcass  ranged from  0.9 days  for
2,3,2' ,3'-TCB to 9.2  and 7.8 days for the  loss of 2,4,2',4'  from
carcass and liver, respectively.  Structure did not influence elim-
ination as markedly as in the rat.  3,5,3',5'-TCB had half-lives of
2.1  and 2.2 days  in  carcass and liver.   However, stimulation of
metabolism by the  addition of phenobarbitol did increase the rate
of elimination of 2,4,2',4'-TCB more than 3,5,3',5'-TCB. The auth-
ors concluded that the rate-limiting  step in the elimination of the
isomers was release from storage in the tissues of the mouse rather
than metabolism.
     Two  differences  between  the  elimination of 2,5,2',5'-TCB in
infant  Rhesus  monkeys and rats  may  be  of  interest in  evaluating
human metabolism.   Single doses of  500  mg/kg to rats  resulted in
total elimination of about 76 percent (66 percent feces, 10 percent
urine)  in 72 hours  (Van Miller, et al. 1975).  In primates  only one
percent of the same dose was  eliminated in feces and two percent in
urine after 72  hours  (Hsu, et al. 1975a).   In  addition, the major
excreted metabolite in  rats  appeared to be  3-hydroxy TCB, while a
                               C-30

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dihydrodiol TCB  predominated in monkeys (Van Miller/ et al.  1975;
Hsu, et al. 1975b).                           i
     A  final  comment on  the  pharmacokinetics  of PCBs must be  ad-
dressed to transplacental and transmammary  movement.  Transplacent-
al uptake of PCBs by a fetus has been documented in mice  (Masuda, ec
al. 1978),  rats  (Curley,  et al. 1973),  Rhesus  monkeys  (Allen  and
Barsotti, 1976), and  humans  (Yoshimura,  1974).   In mice, transpla-
cental  and  transmammary uptake of PCBs  were  approximately 0.1 to
0.2 and 20  to 35 percent of  total dose, respectively  (Masuda, et
al. 1978).  Similar values were observed in rats  (Mizunoya, et  al.
1974).   Female monkeys1, consuming 2.5 ppm Aroclor 1254  transferred
enough via breast milk  to produce  severe hyperplastic gastritis in
nursing  infants  (Allen and  Barsotti, 1976).   Recently,  a prelimi-
nary mathematical model of PCB distribution  in  rats has been pro-
posed (Lutz, et al. 1977; Anderson,  et al. 1977).
     It should be  noted that most of  the  laboratory studies dis-
cussed above have been  performed with pure isoraers, while toxicity
studies  and environmental  exposures involve Commercial  mixtures
with possible dibenzofuran contamination.  In addition, commercial
mixtures  tend  to contain  asymmetrical  polychlorinated biphenyls
(NIOSH, 1977).                                |
     The pharmacokinetics of  PCBs  can be summarized with the fol-
lowing points:                                :
                                              '[
1.   They are readily absorbed through the  gut,i  respiratory system,
     and skin.                                ;
2.   They may initially concentrate in the  liver, blood, and muscle
     mass; but long-term storage in mammals is primarily in adipose
     tissue and skin.                         i
                                              ,i
                               C-31           I

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3.   The major metabolic products of PCBs are phenolic derivatives
     or  dihydrodiols  which  may  be  formed  through  pathways  with
     arene oxide  intermediates or  by direct hydroxylation.   The
     susceptibility of  individual  PCB isomers to  metabolism  is a
     function of  the  number of chlorines present  on the biphenyl
     and their arrangement.   Biphenyls which have one or more pairs
     of adjacent unsubstituted carbons are more rapidly metabolized
     than those which do not.
4.   PCBs which are readily metabolized are also rapidly excreted
     in the urine and bile.   Excretion  in  urine  is most prominent
     for the least chlorinated, while bile becomes  the more signif-
     icant route of excretion for more highly chlorinated isomers.
5.   Those isomers which are most refractory to metabolism accumu-
     late for increasing periods of time in fatty tissues.  Highly
     chlorinated isomers are accumulated almost indefinitely.
6.   PCBs can be  transferred either transplacentally or in breast
     milk.
7.   Nonhuman  primates  may  retain  PCBs  more  efficiently  than
     rodents.
                             EFFECTS
Acute/ Subacute, and Chronic Toxicity
     Several  reviews  of the toxic effects of PCBs in animals  and
man have appeared in recent years [Kimbrough,  1974; Fishbein, 1974;
Peakall, 1975; Kimbrough, et  al. 1978; Cordle, et  al. 1978; NIOSH,
1977  (which is particularly recommended  for human  effects)].  This
section  will  attempt  to highlight  the  most significant toxic  ef-
fects observed in animals and man,  but will not  seek  to:be  compre-
hensive.
                               C-.32

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     The acute  oral  and dermal LDegS for  PCBs  in rats, mice, and
rabbits are given in Tables 7, 8, and 9.   In the classification by
the American Industrial Hygiene Association, the PCBs are slightly
toxic  or  almost  nontoxic  (Hodge  and  Sterner,  1949).    In rats,
Bruckner, et al. (1973)  observed a 14-day LD5Q :of  4.25 g/kg.  Toxic
effects of  high  doses  of Aroclor  1242  included diarrhea, chromo-
acryorrhea, loss  of  body weight,  unusual stance and gait, lack of
response to pain  stimuli, and  terminal  ataxia.   CNS deterioration
and dehydration  were thought to  be  contributing  factors.  Risto-
pathologic changes were observed only in liver and kidney.  Miller
(1944) found the guinea pig most sensitive to Aroclor 1242 followed
by the  rabbit  and rat.  In  the rat, toxicity  decreased with in-
creasing degree  of  chlorinationy however,  the  effect  was not ob-
served with rabbits  (Pishbein, 1972).         !
     The more  significant  toxic  effects of PCBss  are  observed on
repeated exposure over a period of time.   Aroclor  1254 at 1,000 ppm
in the  diet was fatal |to 75 percent of  male rats in 43 days with
total intakes of 500 to  2,000 mg/kg  being  lethal  (Tucker and Crab-
tree, 1970).   Phenoclor DP6  fed at  2,000  ppm;to rats  resulted in
marked weight loss and death between 12  and  56 days after the ini-
tiation of  treatment (Vos  and Koeman,  1970). 'Guinea pigs  treated
dermally for 11 days with a  total of 379.5 mg of a PCB with  42 per-
cent average chlorine content died  at intervals up to 21 days fol-
lowing the first application  (Miller, 1944). Aroclor 1254 at  1,000
ppm in  the  diet killed 5/10 male rats and 8/10,female  rats.  At 500
ppm  over eight  months  two  males  and  one  female died  while no
lethality  was  observed  at 100  or 20 ppm.   Aioclor 1260 was less
                               C-33

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C-34

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TABLE 8
Oral LD5Q (rat)a'b
Compound Tested
Aroclor 1221
Aroclor 1232
Aroclor 1242
Aroclor 1248
Aroclor 1260
Aroclor 1262
Aroclor 1268
(Undiluted)
(Undiluted)
(Undiluted)
(Undiluted)
(50% ssoln in corn oil)
(50% ssoln in corn oil)
(33.3% soln in corn oil)

LD50
g/kg body weight
2.000 -
1.26 -
0.794 -
0.794 -
1.26 -
1.26 -
2.5
3.169
2.0
1.269
1.269
2.0
3.16

aData of Panel on Hazardous Substances (6)
DSource:  Kimbrough,  et al. 1978
                           C-35

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                           TABLE 9

                   Skin LD5Q  (rabbits)a'b
Compound Tested
Aroclor 1221
Aroclor 1232
Aroclor 1242
Aroclor 1248
Aroclor 1260
Aroclor 1262
Aroclor 1268
(Undiluted)
(Undiluted)
(Undiluted)
(Undiluted)
(50% soln in corn oil)
(50% soln in corn oil)
(50% soln in corn oil)
L050
g/kg body weight
3.98
4.47
8.65
11.0
10.0
11.3
10.9
Data of Panel on Hazardous Substances  (6)
Source:  Kimbrough, et al. 1978
                          C-36

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toxic, with  8/10  females,  but no  males,  dying at  1,000  ppm.   No
males died at lower doses, and 1/10 and 2/10 females died at 100 and
500 ppm, respectively.  Substantial weight losses were observed at
100 and 500 ppm in both males and females  (Kimbrough,  et al. 1972).
Mink  have been shown to be unusually sensitive  to PCBs.   A mixture
of Aroclors  1242, 1248 and 1254  at 30 ppm  in  the diet for 6 months
was 100 percent lethal (Aulerich, et al. 1973),  !as  was 3.6 ppm Aro-
clor  1254  over 105 days in  another  study (Plantonow and Karstad,
19,.).   Adult  Rhesus monkeys  (Macaca  mulatta) were particularly
sensitive  to PCBs.  Aroclor  1248 at  100 or 300  ppm in the diet  for
two  to  three months resulted in  extreme morbidity  within  one month
and  almost 100 percent mortality  within  three  ;months.    Total  in-
takes for the two groups were 0.8 to 1.0  g  for 100 ppm and 3.6 to
5.4  g for 300 ppm (Allen,  1975).               !
      The most consistent pathological changes occurring  in  mammal's
after PCS exposure are in the liver.  In rats,  ;rabbits,  and guinea
pigs, Miller (1944)  observed fatty deposits after acute  injections
 and similar changes in rabbits and guinea pigs after dermal appli-
 cation,   in  feeding  experiments, marked  fatty  metamorphosis  was
 noted  in guinea  pig  liver with  intracellular hyaline bodies being
 observed in rats.  Less striking changes  were noted in  the kidneys,
 lungs, adrenals, and heart of guinea pigs.  Rats exposed  repeatedly
                                                 (Kimbrough,  et al.
                                                al. (1972) fed  rats
                                                1,000 ppm for eight
                                                luded hypertrophy  of
                                                pigment   in  Kupffer
to dietary  PCBs show  increased  liver weights
1972; Bruckner, et  al.  1973).   Kimbrough, et
Aroclor 1254 or 1260  at  levels between 20 and
months.  Light microscopic changes  observed  inc
liver  cells,  cytoplasmic  inclusions,  brown
                                C-37

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  cells,  lipid  accumulation  and,  at  higher doses,  adenofibrosis.
  Ultrastructural examination revealed an  increase in smooth  endo-
  plasmic  reticulum.   The  effect  of  Aroclor  1254  was more  pronounced
  than  that of 1260.  Porphyria was observed in the livers  and,  occa-
  sionally, other  tissues  of  animals  exposed  to either mixture.
       Rats fed 2,000 ppm Phenoclor DP6 also had enlarged livers with
  vacuolated foamy cells containing pycnotic  nuclei (Vos and Koeman,
  1970).  Vacuolization of liver cells was also noted by Bruckner, et
 al.  (1973)  after  dosing rats  with 100  mg/kg  Aroclor  for   three
 weeks, although no overt toxicity was manifest.
      Rats fed 100 ppm Aroclor 1242  (6.6 to 3.89 mg/kg/day) or Aro-
 clor 1016 (6.9  to  3.5  mg/kg/day) for periods of  up  to  ten months
 showed no signs of overt intoxication or gross liver  changes.  En-
 larged hepatocytes with  vacuolated  cytoplasms and inclusions were
 noted. Aroclor  1242  seemed  to produce more pronounced changes than
 1016.   Four  and  six  months  after the discontinuation of exposure
 hepatocytes were still  enlarged  but  cytoplasmic vacuoles and inclu-
 sions  had  diminished, suggesting a degree of reversibility of ef-
 fect.  Significant residual  levels of PCBs remained in adipose tis-
 sue,  using electron microscopy,  increased smooth endoplasmic  reti-
 culum  and lipid  vacuoles  as  well as  atypical mitochondria were ob-
 served.   NO  significant  gross changes in  other  organs were  noted
 (Burse, et al. 1974).
     Allen and Abrahamson (1973)  fed rats 1,000  ppm of either  Aro-
clor 1248, 1254,  or  1262 for  1, 3, 7, 14,  21,  or 28 days or 6 weeks.
Overt toxicity was not observed,  although weight gain was  retarded
in all treated groups.   The  effect  was  inversely proportional to
                               C-38

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percent chlorination.  Increased liver  size,  orotein,  and  RNA  con-
tent were  observed.   The magnitude of  changes increased with  the
percent chlorination.   Hypertrophy was associated with  orolifera-
tion of the  smooth  endoplasmic reticulum, formation of  membranous
arrays, and  increased lipid droplets.         ;
     The effect  of  metabolism on  toxicity  was explored by  giving
rats  large  (1.5 g/kg)   single doses  of 2,5,2',5'-tetrachlorobi-
phenyl  which  produced  high  mortality within two  to three  days
(Allen, et al. 1975).   Pretreatment  with phenobarbitol to  induce
metabolic  enzymes allowed survival without obvious ill effects fol-
lowing a 1.25 g/kg dose, while treatment with ,the microsomal  enzyme
inhibitor  SKF  525A lead to 100 percent mortality in four days.   The
ability  to metabolize and eliminate  2,5,2',5f-TCB appears to  pro-
tect  the  animal.  Dietary administration of  loo  opm 2,5,2',5'-TCB
for three  weeks  produced less liver  hypertrophy than Aroclor 1248.
      Liver pathology in mice exposed to  1.5  ing  PCB/day  was  essen-
tially  the same as  seen  in rats,  including  increased  smooth endo-
plasmic  reticulum and increased lipid droplets (Nishizumi, 1970).
      Rabbits receiving  300 mg orally  of Aroclor  1221,  1242, or 1254
for 14 weeks were examined (Roller and Zinkl,; 1973) .  Aroclor 1221
and 1242  treated rabbits gained weight at control rates while 1254
treated  rabbits  did not gain  as  much.  Livers of 1254  and  1242
 treated  animals were enlarged while livers of 1221,treated animals
were  smaller  than controls.   Gross liver lesions and small uteri
 were  apparent  in  the  1254  treated  animals  but not  the others.
 Liver pathology in  1254  treated animals  included enlarged hepato-
 cytes with  foamy  to granular  cytoplasms and1 subcapsular midzonal
                                              i
                                C-39

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 necrosis.   Aroclor  1242 produced  a liver pathology similar to 1254.
 Aroclor  1221 treated animals were free of histologic changes.
      Dermal studies with  rabbits  using Clophen A60,  Phenoclor  DP6,
 and  Aroclor 1260 indicated that the last was  the  least  toxic  (Vos
 and  Seems/  1971).  The former two  mixtures had  been shown to be  con-
 taminated  with  tetra- and  pentachlorodibenzofuran  (Vos,  et  al.
 1970).  Skin lesions produced included hyperplasia and hyperkerato-
 sis of the epidermal and follicular epithelium and were accompanied
 by pathological  changes in the  liver and  kidney.   The chlorodiben-
 zofuran  impurities  in  the PCBs  were thought to be responsible  for
 the  skin lesions.  A  comparison  of  the toxic effects of  dermally
 applied  2,4,5,2',4',5'-hexachlorobiphenyl and Aroclor 1260 demon-
 strated  that the  skin  lesions appeared sooner  and  were more severe
 after  treatment  with the  commercial mixture.   Liver  changes were
 found  in both treatment  groups with  the  pure isomer  inducing  the
more  severe effects.  From  this  study it was concluded that  the
chlorodibenzofuran  contaminants  in  commercial  mixtures  probaoly
contribute  to  the skin lesions  (chloracne),  edema formation,   and
liver  damage.   PCBs contribute  in lesser degrees to  chloracne  and
liver damage but  are primarily responsible for the hepatic porphy-
ria observed in PCB  intoxication  (Vos  and Notenboom^Ram, 1972) .
     Nonhuman primates are rather  sensitive  to PCBs.  Male Rhesus
monkeys  were  fed 300 ppm  Aroclor  1248 for  three months.  Effects
which began to appear  within a  month  included hair loss,  suocuta-
neous edema, purulent discharge from the eyes, acneform eruptions,
and liver hypertrophy  caused by smooth endoplasmic reticulum pro-
liferation.  Marked hypertrophy of the gastric mucosa was a signif-
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leant finding not usually seen in rodents.  Invasion of the submu-
cosa by the mucosal epithelium with increased cellularity and dys-
plasia occurred in the stomach.   The dietary levels used were about
10-fold greater than  the  contamination  levels  in foods during the
early 1970's,  and  the gastric changes observed were considered to
be of  particular  significance  to  human  risk  (Allen and Norback,
1973).  When fed low  levels  (2.5 and  5 ppm) of Aroclor 1248 for 52
weeks female monkeys developed periorbital edema,  alopecia, erythe-
ma and  acneform lesions.   Effects  in  males;were  less pronounced
(Barsotti  and  Allen,  1975).  The  high  sensitivity of monkeys to
PCBs has  been confirmed  and  the evaluation of the  toxic effects,
particularly  in the  gastric  mucosa,  has  been  extended  (McNulty,
1976; Bell, 1976).  The pathologic effects of PCBs in nonhuman pri-
mates have been reviewed by Allen and coworkers  (Allen,  1975; Allen
and Norback, 1976).
     The  ability  of  PCBs to induce  liver microsomal enzymes was
demonstrated by Street, et al. (1969).  Enzyme  induction by commer-
cial  PCBs has  been shown in rabbits (Villeheuve, et al.  1971a) ,
rats  (Litterst and  VanLoon, 1972),  and primates  (Allen,  et al.
1974b).   In rats  induction  is  observed  following intraperitoneal
injection (Bickers, et al. 1972) or  skin  application  (Bickers, et
al.  1975).   Dietary threshold values for enzyme induction varv be-
tween  0.5 and 25 ppm (Villenueve,  et al.  1971a;  Litterst, et al.
1972;  Turner  and Green,  1974).   The  induction  of demethylating
activity  in rats by  Aroclor  1254  was maximum in  seven  days  while
cytochrome P450  and nitroreductase  activities continued to  rise
over  four weeks  of  treatment.   Activities 'declined  slowly  after
                                C-41

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discontinuation of treatment, reaching control  levels  in  about  ten
days  (Litterst and VanLoon, 1974).  Cutaneous exposure  to PGBs  re-
sulted  in  a  maximum  induction within two to six days  (Bickers, et
al.  1972,  1975).    Degree of  induction  of  enzyme  activities  was
found  to correspond  to  increasing  chlorine content  of Aroclors
(Litterst, et al. 1972) and of di-, tetra-,  and hexachlorobiphenyl
mixtures (Schmoldt, et al.  1974).  The effects  of chlorine content
and position of  pure  isomers were  examined by Johnstone,  et  al.
(1974),  Ecobichon  (1975), and Ecobichon  and Comeau (1975).   More
highly chlorinated isomers  and  those substituted at the  4  and 4'
positions were most active in inducing enzymes associated with  the
endoplasmic  reticulum.   For less localized  enzymes,  position  was
less critical, although chlorinated compounds were more  effective
than biphenyl.
     The  effects  of  dietary  exposure to Aroclor  1254  on  enzyme
induction  were  investigated in  rats  by Bruckner,  et  al. (1977) .
Aroclor 1254 at 5 or  25 ppm  induced  dose-dependent increases in  the
metabolism of pentobarbitol, aminopyrine,  and acetanilide  after  35,
70, and 140  days of exposure.  Exposure to 1 ppm had little effect
on metabolism.   Liver  weight  and serum  triglyceride  levels  were
elevated only in animals  exposed  to 25 ppm.  In 15-day experiments
induction  of aminopyrine N-demethylation was observed  after  the
first day  of exposure at 5  and 25 ppm,  and  acetanilide hydroxyla-
tion was induced after two  days.   Aminopyrine N-demethylation  re-
turned to  normal 15  days after  the termination of exposure.   Con-
sumption of  as little  as  1  to  2  mg  of PCBs in 24 hours was suffi-
cient to stimulate acetanilide hydroxylation.
                               C-42

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               Commercial  PCBs have  been  shown  to  induce  cytochrome  ^450


*           (phenobarbitol  type)  and  cytochrome  P448  (3-methylcholanthrene


           type)  (Alvares,  et'al.  1973).   More recent studies with  purified


           isomers  indicated  that  ortho-para-substituted  PCBs  induce  P450


           while meta-para-substituted PCBs  induce P448.i Substitution  in the


           ortho-position dominates over  meta-, and no isomers were  found  to


           induce both activities;  (Goldstein,  et al.  1977) .   The  induction of


           both systems  by  commercial  preparations and some  purified isomers


           has recently  been  shown to  result from  contamination with  dibenzo-


           furans.   Even "99  percent  pure" isomeric  PCBs  containing  44  ppm


           tetrachlorodibenzofuran effectively induces P448  while more  rigor-


           ously purified  material does not  (Goldstein,;et  al. 1978).   This


           observation serves  as a  reminder  that the effects of trace  contami-


           nants must be kept  in  mind when evaluating  the  toxic effects  of


           PCBs.                                         ;


               Enzyme  inducing effects  of PCBs  have also  been  examined  in


           vivo by  the  observation of  shortened phenobarbitol  sleeping times


           in  PCB-treated animals  (Bickers, et al.  1972;  Johnstone,  et al.


           1974; Villeneuve, et al.  1972).  PCB induction of  enzyme activities


           in other tissues has included  skin  (Bickers, et al. 1975),  placenta


           and  fetus  (Alvares and  Kappas, 1975), neonatal liver during  lacta-


           tion  (Alvares  and  Kappas,  1975),  and lung ; and kidney  (Vainio,


           1974) .                                        j
«.                                                       ;

               Other systemic effects of PCBs in mammals  include  porphyria


           (Bruckner, et al.  1974) , increased thyroxin metabolism (Bastomsky,


           1974)  and ultrastructural changes  in the  thyroid (Collins,  et al.


           1977),   inhibition  of  ATPases  (LaRocca  and :Carlson,  1975),  and
                                          C-43

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 interference with  oxidative phosphorylation  (Sivalingan, et  al.
 1973).   Alterations in steroid hormone metabolism  are  produced by
 PCBs in rats (Bitman and Cecil,  1970),  mice (Orberg and Kihlstrom,
 1973),  and other animals.   Aroclor 1254  appears to reduce  liver
 vitamin A concentrations  in  pregnant  rabbits (Villeneuve, et  al.
 1971b).   A more complete  review  of these effects can  be:  found in
 Matthews,  et al.  (1978).                                 ,
     PCBs  have been  shown  to have immunosuppressive effects in rab-
 bits  (Vos  and Beems, 1971; Street  and  Sharma,  1975),  guinea  pigs
 (Vos and van Genderen, 1973; Vos and DeRoij, 1972),  monkeys, mice
 (Thomas  and  Hinsdill,  1978) , and several  birds.   Significant  ef-
 fects were observed  in Rhesus monkeys exposed to  dietary levels of
Aroclor  1248  as low  as 5.0 ppm.
     Effects  of  Aroclor  1254 and. 1260  on reproduction in Sherman
strain  rats were investigated  (Linder,  et  al. 1974).  Dietary lev-
els  of  5 ppm Aroclor  1254 had no  effect  on reproduction in rats
exposed  through two  generations.   Liver weights  were increased  in
male and female offspring  of  the F± and F2 generations.  At 1 ppm,
Aroclor  1254  caused  increased liver weights in  F-^ male weanlings.
With Aroclor  1254 at 20  ppm,  the number of pups  in the Plb and  F2
generations was reduced,  while  100  ppm  resulted  in increased mor-
tality in Plb offspring and decreased the mating performance of  Flb
adults.  Aroclor 1260  produced  increased liver  weights in F-,  off-
spring at  5 ppm but did not affect reproduction at 100 ppm.  At  500
ppm litter sizes were reduced and survival was decreased in Fi lit-
ters.  Pregnant rats given 100 mg/kg/day Aroclor  1254 on days 7  to
15 had  grossly  normal litters  but  only 30.1 percent survived  to
                               C-44

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weaning.  Dosage  rates  of  50  mg/kg/day Aroclpr 1254 or 100 mg/kg/
day Aroclor 1260 did not affect reproduction or pup survival.
     Rabbits fed 0.1 or 1.0 rag/kg body weight Aroclors  1221 or 1254
showed no significant decrease  in number  of pregnancies or number
of fetuses per litter (Villeneuve, et al. 1971a).  No  induction of
fetal  liver  enzymes could  be detected.   However,  administration
during gestation of  600  to 2,500  ppm Aroclor ;1254 in  the diet re-
sulted  in  resorptions,  abortions, maternal  death,  and asymmetric
skulls in two fetuses (Villeneuve, et al. 1971b).
     Reproductive  effects   in  mice  were  investigated  in animals
treated  for  ten weeks  with 0.025 mg/day Clophen A60   (Orberg and
Kihlstrom, 1973).   The length  of the estrus  cycle  was  increased
from  6.6 days  in  controls to  8.7  days  in experimental animals.
Also,  the  percentage of  implanted  ova was reduced from 87.0 to
79.5.  In a second study the reproductive  effects!  of neonatal expo-
sure  to  PCBs  in milk were  examined  by  injecting  lactating female
mice  with  Clophen A60.   On the day of parturition  and at weekly
intervals for three  weeks,  the  females were  injected with 50 mg of
PCB.   When  treated male and female offspring were mated with each
other, the percent  implantation dropped from a control level of 94
percent  to 75 percent  (Kihlstrom,  et al.  1975).
      In  female  Rhesus  monkeys exposure to  25  ppm Aroclor 1248 in
the diet for two months  lead  to the  typical  effects of PCB intoxi-
cation for monkeys including edema/ alopecia, and  acne. One animal
ingesting  a total  of  450 mg  PCB died two  months  after exposure
ended  and was found  to  have hyperplastic  gastritis and bone marrow
hypoplasia.   The  remaining  five animals were  bred  three months
                               C-45

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 after treatment.  Three were thought to have  conceived but resorbed
 or aborted the embryos  in  the  first two months of pregnancy.  One
 delivered a fully developed but small infant (Allen, et al. 1974b).
      In a more developed study both male and female Rhesus monkeys
 were fed either 2.5 or  5.0  ppm Aroclor  1248  in the diet (Barsotti
 and Allen, 1975; Barsotti,  et al. 1976).   The  total intake  in the
 first six months for  the females  was 180 and 364 mg for th'e 2.5 and
 5.0 ppm  diets,  respectively.   Untreated  females bred  to  treated
 males had normal  rates  of conception  (Barsotti  and  Allen,  1975).
 Treated females bred  to normal males produced  the  following  rates
 of  conception:   control, 12/12; 2.5 ppm, 8/8;  5.0  ppm,  6/8.   Live
 births  resulting from the  conceptions  were:   control,  12/12;  2.5
 ppm,  5/8;  5.0  ppm, 1/6.   In the 2.5 ppm group,  three fetuses were
 resorbed  shortly after  conception.   In the  5.0 ppm group,  three
 pregnancies aborted at 46,  67, and 107 days of gestation, one  fetus
 was  resorbed,  one was  stillborn, and  one  normal birth  occurred.
 The  two females who failed  to conceive  were subsequently bred five
 times without conception.   The live  born  infants were of low  birth
 weight  and showed signs of PCB  intoxication  after nursing  their
 mothers for less than  two months.  Three infants died 44 to 112 days
 after birth (Barsotti, et al. 1976).   The mothers'  breast milk con-
                                                          i
 tained  0.154  to 0.397 ppm  PCBs  and  one contained  16.44 ppm  (fat
basis)  (Allen  and Barsotti, 1976).   It should  be  noted that  the
dose levels producing these  rather striking effects are  within  the
range of  contamination  of  the human diet  observed until the  mid-
1970's.
                               C-46

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     Recently, adipose tissue levels of PCBs  in  infant  Rhesus  mon-
keys exposed in_ utero and via breast milk  have been correlated  with
behavioral  effects  (Bowman,  et al.  1978) .   Three of five  infants
born to mothers exposed to 2.5 ppm Aroclor  1248  in the  diet during
pregnancy and  lactation  survived  over  four months.  PCS levels  in
fat tissue in the infants declined with a  first order rate constant
over a period  of  8  to 23 months of age.  Extrapolated  maximum PCB
levels were 21, 114,  and 123 ug/g fat.  A battery  of 11 behavioral
tests was conducted with the three  exposed animals and four  con-
trols over  this  time period and  a positive correlation  between
reduced  performance  and  PCB body  burden was observed for seven
tests.                 I                        |
     Minks  have been  found  to be  exceedingly  sensitive  to  PCB-
induced reproductive  faiilure.   A  marked increase  in kid mortality
was observed  in commercial mink in the mid-1960's  after fish  meal
derived from spawning Great Lakes  Coho  salmon WGLS incorporated  into
the  diet.    Laboratory  studies  confirmed  that  the reproductive
losses were related to the ingestion of Great Lcikes fish (Aulerich,
et al.  1971),  and  subsequent  investigation showed that PCBs  con-
taminating the fish meal were the  probable toxic  agents  (Ringer,  et
al. 1972).  when  fed 10  ppm  each of Aroclors  1242, 1248, and  1254
(30 ppm total), all 11  adult female mink died prior to the  end  of
the normal whelping  (delivery) period  (Ringer, et  al. 1972).   Aro-
clor 1254 fed at 10 ppm resulted in no  offspring  among six females.
At 5  ppm, Aroclor 1254 fed  for four months prior  to whelping de-
pressed reproduction  with only  3 of  12 females ,whelping and 3  of 9
kits born alive.  At 1 ppm Aroclor 1254, 8 of  10 females  whelped and
                               C-47

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35 of 43 kits were born alive.  Among control animals all 11 whelped
and 56 of 66 pups were  alive at birth.  The reproductive toxicity  of
Aroclor  1254 becomes  pronounced  between 1 and  5  ppm in  the  diet
(Ringer, et al.  1972) .  At  2  ppm in  a  nine  month feeding  trial,
Aroclor  1254  significantly reduced  reproduction  while  Aroclors
1016, 1221, and 1242 did not (Aulerich and Ringer,  1977).   Assuming
a food intake of  150 gm/day  (Schaible, 1970),  the  total PCB intake
in the two trials would have been 90  mg at 5 ppm  for four months  or
61 mg at 2  ppm for nine months  (Aulerich  and Ringer,  1977).
     Human exposures to PCBs resulting in toxic effects have almost
all resulted from the ingestion of rice oil contaminated with *ane-
chlor 400  in Japan or  from industrial exposure,   while absorption
through the gut was the route of exposure in the  former case, occu-
pational  exposures  occur  largely  by  inhalation or absorption
through the skin.
     Yusho, the disease resulting from the ingestion of contaminat-
ed rice  oil in  Japan,  has been  the  subject  of continuing study
since the  episode of  exposure  in 1968.  Periodically, special re-
ports on these continuing studies have  been  published in  Fukuoka
Acta Medica.   These results,  largely published  in Japanese, have
been reviewed in  English  by the Japanese investigators both early
in the  study (Kuratsune,  et al.  1972?  Kuratsune, 1972)  and more
recently  (Kuratsune,  et al. 1976).   The  cause  and  scope of the
exposure of the  Japanese  public has been described above  (see In-
gestion from Pood section).  The initial  symptoms of Yusho  included
increased  eye  discharge  and swelling of  upper  eyelids,  acneform
eruptions  and  follicular  accentuation,   and   pigmentation  of the
                               C-48

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skin.   Other symptoms  including  dermatologic problems, swelling,
jaundice, numbness of limbs,  spasms,  hearing and vision problems,
and  gastrointestinal  disturbances  were  prominent among  the com-
plaints of patients seen within the first eight months after expo-
sure  (Kuratsune, et al.   1972) .   The  first patients were seen al-
most immediately after the release of the contaminated oil in Feb-
ruary 1968.  Of a  group of  patients seen between October 1968 and
January 1969, 55 percent became ill between  June and  August.   It
was ultimately determined that as many as 63.9 percent  of those who
consumed contaminated oil became  ill.  Among a group of 146 known
users of the oil,  80  consumed less than  720 ml, and 88 percent of
these users were affected.  Among those who  used more  than 720 ml,
100 percent  were affected.   The clinical severity of  symptoms did
not differ by sex,  but the age group 13 to 29  was more affected than
others  (Kuratsune, et al.  1972).             j
                                              [
     The analysis .of  the oil  indicated that  it  contained between 2
                                        • •     i
and 3 mg/kg of Kanechlor  400  (Kuratsune, et al.;1972).   It was later
discovered  that Kanechlor  400 contained  18 ppm of polychlorinated
dibenzofurans  (PCDFs)  and that  the PCDF concentration  in  "Yusho
Oil™ was about 5 ppm (Nagayama, et al. 1975) .  The PCDF level  in the
oil was 250 times greater than would be expected based  on the level
in fresh Kanechlor 400, leading Kuratsune, et al.  (1976)  to suggest
that  the  concentration  increased with PCS use; as  a heat  transfer
                                              f-
medium.                                       J
     The  amounts of  Kanechlor 400 ingested were estimated for the
original  146 person study group.   The average amount  ingested was
estimated  to be 2  g while the minimum  amount ingested  by a patient
was about  0.5 g  (Kuratsune,  et al.  1972).
                               C-49

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     Laboratory  evaluations of  patients during  the  early period
were summarized by Kuratsune (1972).   Several changes  in  blood were
noted, including decrease  in erythrocyte count,  increase  in leuko-
cyte count,  and  increase  in serum lipids,  particularly  triglycer-
ides.   Blood  proteins,  electrolytes, and  enzyme activities were
normal in  most instances.   Some  increases  in urinary ketosteroid
excretion  were observed.    The  "cheesy"  material, from Yusho acne
contained more steric  and  oleic  acids than  did "normal acne," but
less myristic  palmitic and palmitoleic  acid.   Linoleic acid was
present in Yusho  acne  but not "normal acne."   Liver  biopsy indi-
cated hypertrophy of the smooth endoplasmic  reticulum,  reduction of
the rough endoplasmic reticulum, filamentous  inclusions, and mito-
chondrial  abnormalities.    Skin changes  included hyperkeratosis,
cystic dilatation  of the  hair  follicles,  and  marked  increase of
melanine in basal cells of the epidermis.  Decreased sensory nerve
conduction velocities were observed  in 9  of  23 patients.  Abnormal-
ities of  the eyes included hypersecretion  of the meibomian gland
and abnormal pigmentation of the conjunctiva.
     Thirteen  women,  11 with Yusho and  2 without,  but married to
men with Yusho, delivered  10  live and 2  stillborn infants between
February 15 and December 31, 1968.  Nine  of  the  10 had grayish-dark
stained skin,  and  5 had  similar  pigmentation of  the  gingiva and
nails.   Eye  discharge  was common.   A stillborn fetus had marked
hyperkeratosis, atrophy of the epidermis, and cystic dilatation of
the hair  follicle.   Increased melanin pigment  in the blood cells
and the epidermis  was  also noted.  Twelve  of the 13  fetuses were
small for date of birth.  The growth of children  affected by Yusho
                               C-50

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was significantly  lower  than Japanese  national  standards.   A de-
tailed clinical  study  of four Yusho babies  showed, that they were
small for their  age, had dark pigmentation on skin and mucous mem-
branes,  and  gingival hyperplasia.   Teeth were  erupted  at birth;
spotted  calcification  of the parieto-occipital skull, wide fonta-
nels, and saggital suture were present,  along with  facial edema and
exophthalmic eyes  (Yamashita, 1977).           '
     By  three years after the episode about  half the patients were
improving while  40 percent  were  essentially  unchanged and 10 per-
                                               i
cent were becoming more  severely affected.   Even among those said
to be  improving, many still complained of  persistant headaches,
general  fatigue, weakness  and numbness of limbs, weight loss, and
other problems (Kuratsune, et al. 1972).
     An  evaluation of the  longer  term effects  of  Yusho has been
summarized by  Kuratsune, et al.  (1976).   In 1972 Masuda  noted a
peculiar gas  chromatographic pattern  of PCB  fractions  which was
common to blood, tissues and breast milk of Yusho patients  (Koda
and Masuda,  1975) .  A pattern  seen  in about  SO  percent of Yusho
patients contained a larger amount of a late  elating peak than PCB-
containing tissues resulting from other types  of exposures.  This
pattern was referred to as type  A.  A similar pattern  seen in about
37 percent of Yusho patients was referred to as  type B.  These two
patterns  (types  A  and B) have never been  observed in individuals
(human or animal) exposed to PCBs in  other  situations.  These types
appear unique to Yusho.  Tissue  levels  of PCBs  in patients undergo-
ing surgery or who died  and  were autopsied were  followed over sev-
eral years.  Adipose tissue levels were high  (13  to 76 ppm)  shortly
                               C-51

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after the end of exposure but were substantially  lower by  the next
year.   By 1970 and  beyond,  tissue levels were  within the normal
range in the cases studied.   Blood levels were not determined until
1972 by which  time  they  were in the normal range.  Patients whose
plasma  PCS  pattern was  type A had higher  levels than those with
type B.
     The discovery  of  substantial levels of PCDF in Yusho oil has
been discussed.  Levels  of  PCDPs  in control individuals and Yusho
patients were determined.  No detectable (0.1 ppb) PCDFs were found
in controls  while  tissues of patients  who died  in  1969  and 1972
contained 0.009  and 0.013 ppm  in adipose and liver respectively.
Ratios of PCB/PCDF were 144  and  4 for  adipose  tissue and liver,
respectively.  PCDF  levels  were higher  in liver  than adipose on a
fat basis.  Although the sample was small,  the levels in whole adi-
pose tissue appeared to have dropped to about one-third of  the 1969
level by 1972.
     By 1972,  the  dermal and mucosal signs which were most marked
in the initial stages of toxicity were gradually  improving.  Symp-
toms considered  to be due  to  internal  disturbances,  such as fa-
tigue, poor  appetite,  abdominal pain,  headache,  pain and numbness
in the  limbs,  and cough and expectoration of sputum,  have become
more prominent.   Between March 1973  and  April  1974,  79 patients
were examined and blood PCBs evaluated (Koda and Masuda,  1975).  Of
patients with  type  A or B plasma  PCB  chromatographic  patterns, a
majority exhibited some or all  of  the typical  spectrum of dermato-
logical symptoms, with frequencies  in type A patients  being higher
than in type B patients.  Because  PCB levels  in type A patients were
                               C-52

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 higher than in type B,  the severity of  symptoms:was  correlated with
 blood PCB levels.                              \
                                                •i
      Serum triglyceride  levels  in males did  not decline signifi-
 cantly between  1969  and 1974 (Okumura,  et  al.l 1974).   Levels  in
 female patients declined  but  were still above normal.  The eleva-
 tion of  triglycerides  correlated with  increased  blood  PCB levels
 and the type A pattern.                        \
      Serum bilirubin in patients was lower in 121 patients than in
 257 controls,  indicating an accelerated rate of disposal (Hirayama,
 et  al.  1974).                                   j
      Long-term effects  continued to be observed;in children born to
 Yusho mothers.  Nine infants with dark brown skin pigmentation were
 born to Yusho mothers  between 1969 and  1972,  three of them  to  a
 patient between 1969 and  1971  (Yoshimura,  1974).   The  plasma  PCB
 levels  of 30 children born to 18  Yusho  mothers  were significantly'
 above control  levels but  lower  than maternal  levels  (Abe, et  al.
 1975).   Children  nursed  by their  mothers  had. ^higher levels  than
 children  who were  not breast  fed.   One case was  reported by Yoshi-
                                                h
 mura (1974)  in  which a  baby  was  thought to  have acquired  Yusho
 solely  as  a result of breast milk  intake.       j
      Masuda, et  al.  (1974)  found PCB levels in  breast  milk of  five
 Yusho women  between 0.03 and 0.06  ppm,  which  was just within the
 normal  range.   A recent study of PCB levels injthe  breast milk in
 400  Japanese "women detected  average levels of; 0.033, 0.026, and
 0.029 ppm  in three  measurements  made at  two month  intervals (Yaku-
 shiji,  et  al.  1977).  Based on these levels,  they calculated that
daily intake by  a  nursing  infant would be 24  jag/day.  This can be
                               C-53

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compared  to  an average  dietary intake  by Japanese  adults  of 21
ug/day or 9 ug/day by U.S. adults.  By April 30, 1975, 29 of 1,291
Yusho patients had died.   Among 22  who died before September, 1973,
nine deaths resulted from malignant neoplasms  (Urabe, 1974).
     The occurrence of Yusho symptoms after modest PCB intake cou-
pled with the  similarity  of  many of  the symptoms to those seen in
animals,  particularly  primates,  suggests  that  the  toxic effects
observed in animals must be considered potentially accurate models
for  humans.   The  persistence  of symptoms in  Yusho  patients is a
particular source of concern.  The  major  uncertainty  regarding tox-
icity in Yusho patients rests with the  unknown effects of  the PCDPs
present in unusually high concentrations in Yusho oils.
     Early reports of  toxic effects of  occupational PCB exposure
are not easily interpreted because a mixture of compounds  including
chloronaphthalenes was present.  A fatal  case  resulted from expo-
sure to a mixture of 90  percent chloronaphthalenes and 10 percent
PCBs (Drinker, et  al. 1937).  The subject: developed chloracne,  fol-
lowed by jaundice  and abdominal pain,  and was  found to have cirrho-
sis  of the liver  at autopsy.
     Many  studies of occupational exposure have shown varying  de-
grees of  toxicity under  different conditions.  The  following  dis-
cussion  will highlight studies which  indicate the  types of  toxic
reactions commonly observed in occupational exposures and the  lev-
els  of  sensitivity  in different situations.   A detailed  review of
occupational exposure to PCBs has recently been  prepared  (NIOSH,
1977).
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     Elkins  (1959)  found  that  average PCB  concentrations in  the
workroom air of several plants in Massachusetts ranged from 0.1 to
5.8  mg/m  while  peak  concentrations  were  between 0.2  and  10.5
mg/m .  Immediate toxic effects were  not seen; however, exposure to
10 mg/m   was  said  to be  unbearably irritating.    Three  cases of
severe chloracne were  reported in  a  work  environment in which PCB
air levels were found to be between 5.2 and  6.8 mg/m .  The workers
developing chloracne  had  been exposed for 2 to 4  years.   Altera-
tions in liver function or other  abnormalities were not found  (Puc-
cinelli, 1954).                               j
     An analysis of the health effects of PCBs on  eight laboratory
workers involved in testing dielectric fluids ,was made by Levy, et
al.  (1977).  The workers,  all males 25 to  49  years  of age, had been
employed 2.5 to 18 yecirs.   Breathing zone,  point  source,  and gen-
eral work  area samples  were collected on  three  occasions.   The
ranges observed were:  breathing zone, 0.014 to 0.073 mg/m3; point
source  (near an oven),  0.042  to  0.264 mg/m  ; and  room area, 0.013
to 0.15 mg/m .  Blood PCB concentrations were 36 to  286 ppb which is
substantially above the range in  several studies of general popula-
tions  (Pinklea,  et  al.  1972).   Workers complained of  dry  sore
throat (6/8), skin rash (3/8), gastrointestinal disturbances (3/8),
and eye irritation and  headache  (2/8).  Examination disclosed one
patient  with skin  rash,  two with nasal  irritation,  one showing
rales, and  four with  high  blood  pressure, but  no  abnormalities in
liver function.
     Toxic  effects  from  a  low-level exposure  were  reported  by
Meigs, et al. (1954).  A leaking  heat exchanger in  a chemical plant
                               C-55

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discharged PCB vapors.  No employees worked routinely at the point
of leakage, but breathing- zone  levels  in work areas were found to
be 0.1 mg/m3.  The  period of exposure  was 19 months.  Seven of 14
exposed workers developed mild to moderate chloracne  after exposure
durations of  5 to 14 months.   Liver  function tests showed normal
serum bilirubins,  24- and 48-hour  cephalin  f locculations,  thymol
turbidities,  and  serum alkaline phosphatase  activities  in  six of
the seven workers,  but- borderline  increases  in cephalin floccula-
tion  and  thymol turbidity  in the  seventh.   After  13  months, the
thymol turbidity but  not  the  cephalin flocculation had improved.
     A study  of PCB exposure  in six Japanese  industrial plants has
been  reported (Hasegawa, et  al. 1972;  Kara, et  al. 1974,  1975).
Although  the  original  publications are  in  Japanese,  a detailed
description in English is available (NIOSH,  1977).   PCBs were manu-
factured  in one plant,  used in manufacturing  capacitors  in  four
plants, and  had been  used in a fifth plant until one month before
the study  began.   The  sixth  plant  used biphenyls,  not PCBs.   PCB
concentrations in  air as both  vapor  and particulates were deter-
mined.  The lowest levels in one plant were 13 to 15 wg/m vapor and
        particulate while the highest levels in a single plant were
95  to  965  yg/m3  vapor,  73  to 650  ug/m3  particulate.   Except  in  the
instance of  a spill,  vapor  concentrations always exceeded particu-
late concentrations.   Blood PCB levels  in 99 workers were found to
average 370* ppb as compared to values  in 20 controls averaging 20
ppb.   A correlation  between duration of  exposure and blood level
could  not  be  found in data from three of the  plants.  Dermal effects
found  were chromodermatosis of the  dorsal joints of the hands  and
                                C-56

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fingers  and  of the nail bed,  and acneform exanthema.  Dermal  ef-
fects  seemed  unrelated to blood  levels,  suggesting that  they  re-
sulted directly  from .skin contact. .. Changes  in  fat  metabolism  and
mild disturbances  in  liver  function were found.  The  consequences
of  termination of  PCB exposure were examined by  following  38 cur-
rent and 80 former  workers from 1972 to 1975 who were from  the plant
which had discontinued PCB use.  During the oeriod of PCB  exposure,
17 capacitor immersion process workers had blood levels of 7 to  300
ppb, which  were closely  related  to years  of ^exposure.   One year
after  cessation  of exposure,  blood PCB  levels  decreased but  not
uniformly.  The average decrease was about 75 percent of the oriqi-
nal value.  The blood  half-lives  of PCBs  were determined  and found
to be related  to the number of  years of exposure,,  For one  year of
exposure, T*s = 3 months, while for 10  to  15  years  exposure,  T% = 30
months.   The  investigators concluded  that  blood served only as .a
PCB carrier while  fat  served as the depot tissue.  Many of  the  em-
ployees  complained of  blackheads, acne,  and  skin irritation while
working with PCBs;  however,  these  conditions cleared  markedly after
exposure  ceased.   Serum triglyceride  levels in workers were ele-
vated in correlation with blood PCB levels.   j
     A study in Australia by Ouw,  et al.  (1976);  examined two grouos
of workers with different levels  of exposure in a capacitor manu-
                                              t
facturing facility.   One group (inside)  worked in an  impregnation
process where exposure to heated (70°C) Aroclor  1242  occurred.   The
second group  (outside) assembled  cool Arodor-dipped components in
a location separate from the first group.   The entire group had an
average  blood PCB  level near 400  ppb.  The  distribution of  indivi-
                               C-57

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dual Aroclor components  differed between the groups with the out-
side workers  being low  in  early eluting  (on  gas chromatography)
fractions but  elevated in late  eluting  fractions relative to the
inside group.   Abnormalities in liver function  were not observed
but skin irritation and eczematous rashes were  observed.  One work-
er had chloracne but  no  systemic effects.   The severity of dermal
effects was not clearly  correlated  to blood PCB level.  Breathing
zone air concentrations  in  the  impregnation room varied from 2.22
to 0.32 mg/m  .   To bring conditions within government guidelines,
improved exhaust ventilation was installed  and  workers were encour-
aged to wear  impervious gloves  to  reduce  skin absorption.  These
actions  reduced atmospheric PCB  levels  to  0.75 to  0.08 mg/m  .
After two months, new blood  samples  were  taken  which  indicated that
a  slight  increase in blood  levels  had occurred.   Failure to wear
gloves  was  the reason  cited  for  the  failure  to  improve  blood
levels.
     A recent study of liver function in  Aroclor  1016-exoosed work-
ers illuminates the sensitivity of  the liver to exposure  (Alvares,
et al. 1977).   Antipyrene clearance was  determined  in  five workers
who had been occupationally exposed to PCBs for at least  four years
and Aroclor 1016 for at least two years.  Mone of the workers showed
any manifestations of PCB toxicity.  When compared to five  controls
matched  for sex, age, and  smoking  and drinking habits, the anti-
pyrene half-life was  about  two-thirds of the control level (10.8  +
0.7  experimental vs.  15.6 + 1.0 control).  The  increased rate  of
antipyrene clearance was taken  to be an indication of higher  levels
of metabolic  enzymes  in  the livers  of the exposed workers.
                               C-58

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      Data from this limited review of occupational studies indicate
 that symptoms  much lilee those seen  after  PCS ingestion can  occur
 after  atmospheric  or dermal exposure.   Air PCS concentrations  as
 low as 0.1 mg/m3 can produce toxic effects  (Meigs, 1954) and  expo-
 sure to  levels producing no overt toxicity can affect liver  func-
 tion (Alvares, et al.  1977).  Recovery after termination of  expo-
 sure occurs but is slow and depends upon the amount of PCBs stored
 in adipose tissue (NIOSH, 1977).               ;
 Synergism and/or  Antagonism                   '•
      It appears that the  synergistic antagonistic  effects of PCBs
 result  from  their  ability  to  induce mixed  function oxidases  in
 liver  and other  tissues,  although the effects of  the accelerated
 metabolism of drugs,  such as  phenobarbitol  or  hormones, such  as
 ketosteroids  and  thyroxin, have been discussed above.   The  conse-
 quences of the  PCB  induced metabolism of carcinogenic agents  such
 as benzene hexachloride or aflatoxin will be discussed below in the
 section on carcinogenicity.                    •
 Teratogenicity                                 1
     The  reproductive effects of PCBs in animals and man  have  been
 discussed above.  It is clear that  PCBs readily Across the  placental
 barrier and accumulate  in fetal tissues.   Primate infants exposed
 to PCBs in utero are typically  retarded in growth during  gestation
 (Barsotti and Allen,  1975),  and reproductive failures (abortions,
stillbirths)'are common  (Linder,  et al.  1974)j  Live  born animal
and human infants  often display  symptoms of  toxicity common for the
species (Kuratsune, et  al.  1976;  Linder,  et  al. 1974).   However,
indications of  structural malformations  or  genetic changes  have
                              C-59

-------
  been rare.  Villeneuve,  et al.  (I971b)  noted asymetric skull for-
  mation in two  rabbit fetuses exposed  to high  levels of Aroclor 1254
  in  utero.   A  written communication by P.L.  Earle  (as  cited  in
  NIOSH,  1977) reported  unspecified terata  in canine  pups  born  to
  females exposed to 48 or  200 ppm but not 20 ppm dietary equivalent,
  and  in  piglets  from sows fed the equivalent  of 50 ppm.   Mo I addition-
  al information  was given.
  Mutagenicity
      The mutagenicity of different PCB preparations has  been evalu-
  ated in several test systems.   The single  isomer 4-chlorobiphenyl
 was  found  to be highly mutagenic  in Salmonella typhimurium strain
 TA1538  after liver microsomal enzyme activation  (Wyndham,  et al.
 1976).   The products formed under these activation conditions were
 4-chloro-4'-biphenylol  and  4'-chloro-3,4-biphenyldiol,   which,  as
 previously  discussed,   are   indicative  of  arene  oxide  formation
 (Safe, et al. 1975) .  m the same study, Aroclor 1221 was less muta-
 genic while  Aroclor  1254, 1268 and  2,5,2",5'-tetrachlorobiphenyl
 were  essentially inactive.  Mutagenic activity decreased with  in-
 creasing chlorination.
      Recent attempts to repeat the experiment with different cul-
 tures of the same  tester  strain  have not  detected any  mutagenic
 activity (S.  Safe,  personal  communication).
     Also,  4-chlorobiphenyl  was  toxic  but  not  mutagenic  to  S.
 typhimurium  TA1538  with  or without activation by Aroclor 1254  (S.
Rinkus,   personal communication).   4-Chlorobiphenyl has been shown
to induce unscheduled DNA  synthesis,  an indication of  DNA repair,
in Chinese hamster ovary cells (S.  Safe, personal communication).
                              C-60

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      The Japanese Ministry of Health and Welfare-supported mutage-
 nicity screening program investigated Kanechlors 300 and 500 (Oda-
                                               i
 shima, 1976).   Both compounds were negative in the Salmonella sys-
 tem but Kanechlor  300  was listed as  positive; in a  bacterial  DNA
 repair assay and a  cytogenetic analysis with Yoshida sarcoma cells.
 Kanechlor  500  was positive in a  mouse bone marrow cell cytogenetic
                                               i
 analysis.
      Heddle  and Bruce  (1977) reported Aroclor
S.  typhimurium/  the micronucleus  test,  and
assay.  Aroclor 1254 administered to rats at 50
1254 as negative in
a  sperm morphology
ing/kg/day  for seven
days  produced  no chromosomal abnormalities in 'sperm  (Dikshith,  et
al.   1975).                                    |
                                               s
      The effects of Aroclor 1254 and 1242 on bone marrow cells were
evaluated in Osborne-Mendel rats (Green, et al.;1975a).   Animals  in
groups  of eight were  given single doses of Aroclor 1242 at  1,250-,
2,000,  or 5,000 mg/kg or  multiple doses of 500' mg/kg/day for four
days.   Aroclor  1254  was  given  for  five days at  75,  150,  or 300
mg/kg/day.  Aroclor 1242 was more toxic than 1254.  Mitotic indices
were  not reduced by Aroclor 1242 treatment and no increase in chro-
mosomal abnormalities  was  observed.   Aroclor 1254 reduced the mi-
totic index of bone marrow cells at 150 and 300 mg/kg/day but not at
the low dose.   Again,  no increase in chromosomal abnormalities was
seen.  Cytogenetic abnormalities were found in spermatogonial cells
of animals treated at  5,000 mg/kg or  500  mg/kg/day  Aroclor 1242 but
not in statistically significant numbers.
     A dominant  lethal  test with Aroclor  1242
performed in  Osborne-Mendel  rats  (Green,  et  al.  1975b).   Aroclor
                               C-61
 and 1254 was  also

-------
1242 was given in single doses of 625, 1,250, or 2,500 mg/kg or five
doses of 125  or 250 mg/kg/day.  Aroclor 1254 was given in five doses
of 75, 150, or 300 mg/kg/day.  Treated males were bred to untreated
females for the following  10 to  11  weeks.   No significant effect of
treatment was observed on  embryo implantation or lethality with any
treatment.
     In  summary,  the only  marked  genetic  effect  observed  at any
level was  with the  single isomer 4-chlorobiphenyl.  Kanechlor 300
and 500 produced  cytogenetic effects  in different  systems but Aro-
clor 1242 and 1254 did not.   Despite the apparent weak mutagenicity
of most  PCBs in  the systems used,  the fact that most animals can
metabolize many  PCS  isomers  through an  arene oxide intermediate
indicates  that the mutagenic potential of PCBs should not be casu-
ally dismissed.
Carcinogenicity
     The  carcinogenic effects of PCBs have been evaluated  in  sev-
eral  animal  studies.   The first evidence  of carcinogenic potential
in  PCBs  was  reported  by Nagasaki,  et al.  (1972) and in more detail
by  Ito, et al. (1973) . Male dd  mice were given Kanachlors 500,  400,
and 300 mixed in standard diets at  500, 250, and 100 ppm  for  32
weeks.  Of 12 mice surviving in the group  fed 500 ppm Kanachlor  500,
seven (58.3  percent)  had grossly  observable  nodular  hyperplasia,
with microscopically observable hepatomas  in  five (41.7  percent).
Tumors were not observed  in the groups treated with lower  doses of
 Kanechlor 500,  in any dose  of  the other  Kanechlors,  or  in the six
 control animals.  Kimbrough and Linder (1974)   treated Bald/cJ mice
 with Arochlor 1254.  Mice  were exposed  to 300 ppm in the  diet for
                                C-62

-------
six or 11 months.   The mice exposed for  six  months  were  fed control
diets  for  the  remaining  five  months,  and  all the  animals were
killed and examined at the same time.  All the  animals surviving 11
months' exposure had enlarged livers and adenofibrosis/ while 9/22
(41 percent) were observed  to have hepatomas.   Of  the 24 mice sur-
viving six months'  exposure/ most showed some changes  in liver cell
morphology,  and a  diffuse  interstitial fibrosis  was observed in
about  two-thirds  of them.   One hepatoma  (0.3 ; cm  diam.)  was ob-
served.   The details  of  the mouse experiments are summarized in
Table 10.  Kimbrough and Linder  (1974) reported subcutaneous  abcess
formation  in  some  mice and one sweat gland adenoma.  Neither Ito,
et al. (1973) nor  Nagaski, et al. (1972)  commented  on  any pathology
other  than  in the liver.                        :
     Studies  with  rats  have  been  reported  by  Kimura  and Baba
(1973),  Kimbrough,  et al.  (1972,  1975),  and  Ito,  et al.  (1974).*
Kimura and Baba (1973) examined the effects of  Kanechlor 400  on the
livers of Donryu strain rats.  Ten male  and  ten female animals were
exposed, in  a complex  protocol,  to amounts  of  Kanechlor 400  start-
ing at 38.7  ppm in food  and  increasing  to  616 ppm as  the animals
increased  in weight.   Total amounts ingested ; varied from  450 L.O
1,500  mg over exposure periods  of 159  to  560  days.  Five control
animals  of  each sex were  used.   Fatty degeneration was  observed in
the livers  of all  experimental  animals  and  two females  in  the con-
trol  group. - Adenomatous  nodules  were  observed in all of the fe-
males  which had a cumulative intake of more than 1,200 mg  Kanechlor
400.   Nodules were seen  in none of the males.  ' A  number  of  histo-
pathological findings were noted in spleen, lung,  adrenal  cortex,
and  brain, but no  neoplastic changes outside  ;the  liver  were  men-
tioned,                                         j
                               C-63             ;

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     I to,  et  al.  (-1974)  examined the  effects  ;of Kanechlors  500,
400, and 300 on  male Wistar  rats.  Animals  were exposed  to  dietary
levels of  1,000, 500, and 100 ppm of feach preparation  for 27  to  52
weeks, then killed and examined for  pathological changes. No  hepa-
tocellular  carcinoma  was observed,  but cholangiofibrosis  (adeno-
fibrosis)  was  seen  at  the highest dose of all  three agents  (Table
11).  Nodular  hyperplasia was observed  in animals  treated with all
three agents.   The highest  incidence  was  observed with Kanechlor
500.  Significant  changes were  not  observed in organs  other  than
the liver.                                      S
     Kimbrough,  et  al.  (1975)  exposed Sherman  strain  rats  to Aro-
clor 1260  at dietary  levels  of  100  ppm for 21  months.   Hepatocel-
lular carcinomas were  observed in 26/184 experimental animals but
in only one of the controls  (1/173) .  Tumors weire  observed  in sev-
eral other tissues of  both  experimental and  control  groups, but.
they were  of  low incidence  and  frequencies were  similar  in both
groups.   In an earlier  study, Kimbrough, et al.s(1972) fed Aroclor
1254 and 1260  to male  and female rats for eight: months.  Adenofi-
brosis was observed in animals  fed  100  and 500 ppm Aroclor  1254,
with the highest incidence in females.   Aroclor  1260 was  associated
with a  much lower  incidence of  adenofibrosis  even in animals fed
1,000 ppm.  A single bladder  tumor was observed  in  a treated animal
but was probably not the result  of PCB exposure (Kimbrough, et al.
1975).  The details of  the experiments with rats are summarized  in
Table 11.                                       1
                                                t
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trial Bio-test Laboratories Inc.   A  brief summary of the  report was
                               C-65

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presented  at the National Conference  on  Polychlorinated Biphenyls
 (1976),  and  a  more  detailed  analysis was  presented by the U.S.  EPA
                                               t
 (1976a).   One  thousand  Charles River  rats were divided  into  ten
treatment  groups.   Fifty male and 50 female rats served as a common
control  group.  Each of nine treated groups contained 50 animals of
each sex.  Groups were fed  1, 10 and 100 ppm of Aroclors 1242,  1254,
and 1260,  respectively,,  Treatment was initiated with 4- to 6-week-
old animals and continued for a  total of 24 months.  Five animals of
each sex were sacrificed at 3,  6,  and 12 months,  leaving 35 animals
in each  group  at the beginning of  the second year.   In  addition,
mortality  was high, leaving only 6  to  21  animals  remaining in each
treatment/sex  subgroup by  the  end of  the experiment.   As seen  in
the previously described studies,  the  principal  effects were  ob-
served  in  the  liver.   Vacuolar changes  and  hyperplasia were  the
major  abnormalities originally  noted  in  the  treated animals.   In
addition, chromophobe adenomas of  the pituitary were found  in  eight
of nine treated groups but not  in  the controls. In  1975  the origi-
nal liver  slides were re-evaluated  with rather different  results.
The combined results for animals treated  with  100 ppm of all  three
Aroclors included 11 hepatomas,  5 cholangiohepatomas> and  28  nodu-
lar hyperplasias.  Hepatocellular carcinomas were not observed.
     Recently,  a bioassay  for the possible carcinogenesis of Aro-
clor  1254  has  been conducted  by  the Nationcil  Cancer Institute
(1978) .  in -this study, 24  Fischer 344  rats of  each  sex were orally
                                               ji
administered Aroclor  1254  at 25,  50,  or  100  ppm  for  104 to 105
weeks.   Matched  controls consisted  of  24 untreated  rats  of each
sex.  Mortality  among the  treated  males was s
                               C-69
ignificantly higher

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than among the controls and related to dose  (P  0.001) but was not
different among the females (P   0.05).  Interstitial-cell tumors of
the testes in males and leukemias of either granulocytic or lympho-
cytic  type  were observed  frequently  in both  control and treated
animals.  Tumors  were observed in several other tissues but their
presence did not  correlate with treatment.  Proliferative lesions
of the  liver were common  in treated animals but were not found in
controls.   The types and  frequencies  of  lesions  are detailed in
Table 11.  They included nodular hyperplasia in all treated groups
increasing  in  frequency with dose, adenomas  (one  male,  three fe-
males) and hepatocellular  carcinoma  (three males,  no  females).  In
addition, adenocarcinomas  of the stomach,,  jejunum  or  cecum of two
treated  males  and  two  treated  females  but no  controls  were ob-
served.  Statistical analysis of the frequencies of tumors and pro-
liferative lesions indicated that the combined incidences of leuke-
mia and lymphoma  in  treated males  were  significant  by  one test
(Cochran-Armitage  test for positive dose-related trend) but not by
a more stringent test (Fisher exact test).   The tumors of the liver
and gastrointestinal  tract were not statistically significant; how-
ever, the occurrence  of nodular  hyperplasia  appeared  to be related
to treatment.  The study concluded that Aroclor 1254 was not carci-
nogenic  in Fischer 344 rats.   However, the high frequency of hepa-
tocellular  proliferative  lesions was considered to be a result of
treatment,  and the carcinomas  of  the gastrointestinal tract also
were  considered possibly  associated with the treatment.
      The tumors observed  in rodent experiments with PCBs were pre-
dominantly  adenofibrosis   (cholangiofibrosis),  neoplastic  nodules,
                               C-70

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and hepatocellular carcinomas.   Stewart  and  Snell (1957)  concluded
that  adenofibrosis cannot be considered  to be a  pre-malignant  le-
sion, while Reuber  (1968)  proposed  that  cholangiofibrosis might be
a  precursor  to cholangiocarcinoma.   Neoplastic  nodules  have been
observed  before the  appearance of carcinomas  in several  studies
with  known carcinogens  (Kimbrough,  et al.  1975).  Well-differenti-
ated  mouse  hepatomas  have been shown to be potentially malignant,
with  a  proportion being  transplantable  and  capable of metastasis
(Andcrvant and Dunn,  1952).                    :
     Several conclusions  can be drawn from the results of  the  ro-
dent  studies.   A correlation between degree  of  chlorination  and
tumor  inducing  potential was observed  in  mice
(Ito,  et al. 1973)
and rats (Ito, et al.  1974)  with the most  highly chlorinated prepa-
rations being  most  potent.   However,  Aroclor 1254 was more potent
than Aroclor 1260 in rats.  Where examined,  female rats were found
to be more sensitive than males  (Kimura and  Baba, 1973; Kimbrough,
et al. 1972).  No comparisons  of sex-related effects were made in
mice.                                          ;
                                               'i
     It should be noted  that none of  these studies was a lifetime
study.  In  all cases, animals  were  treated for  fixed  times then
killed and examined.   No lifetime studies with PCBs were found in
this  survey.   Such studies,  if available,  might  indicate  more
clearly the  significance of the potentially preneoplastic lesions
induced by PCBs in the studies described here. '
     Data on  the possible  carcinogenicity of PCBs  in  humans  are
sketchy at  this  time.    The largest  group  of  exposed individuals
followed longitudinally  are the "Yusho"  patients.   By late 1973,
                               C-7.1

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two of  1,291  patients had died, nine  of  them with malignant neo-
plasms (two stomach cancer,  one stomach and liver cancer, one liver
cancer with cirrhosis, one lung cancer, one lung tumor, one breast
cancer, and one malignant lymphoma)  (Urabe, 1974; Kuratsune, et al.
1976).  The authors did  not have sufficient  information to make a
detailed  epidemiplogical analysis  but concluded that  9/22 deaths
from cancer may represent an excess of deaths.
     Two cases of malignant melanoma were  reported  in a group of 31
industrial workers  exposed "heavily" to Aroclor 1254 in the process
of its manufacture.  Based on a person-year analysis and the use of
the Third National  Cancer Survey incidence rates (NCI, 1978), 0.04
malignant melanomas would have been expected making these data sig-
nificant  at  the O.OOJ. level.   In  addition, one of 41 workers ex-
posed  to  lower levels of Aroclor 1254 developed a malignant mela-
noma  (Bahn, et al.  1976).
     Although  these studies  involve  small  numbers of individuals
and  provide little  information about exposure  or other  relevant
factors,  they  do suggest that human exposure to PCBs may  be associ-
ated with increased risk of neoplasia.
      In addition to  the carcinogenic effects observed with PCBs,
they  have been shown to have a significant effect on the  carcino-
genic  properties of other substances  found in the environment.  The
co-carcinogenic properties  of  the PCBs result from their  ability  to
 induce the'mixed function oxidases, particularly in liver, as  dis-
cussed in the Acute, Subacute, and Chronic  Toxicity section.   Ito,
et al.  (1973)  observed that  dietary levels  of 250 ppm  Kanechlor
 500  markedly promoted hepatocellular  carcinoma  and nodular  hyper-
                                C-72

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plasia  in mice  exposed to benzene hexachloride at levels o€ 100 or
250  ppm in the diet.  Kanechlor  400  at 10 or;100 ppm  in  the diet
failed  to promote cervical  carcinoma or  progression  toward  it in
mice exposed to  20-methylcholanthrene saturated  thread  imclanted
in  the  cervix  and  uterus (Uchiyama/  et al.  1974) .   Ito, et  al.
(1978)  observed a pronounced increase  in  the  incidence  of preneo-
plastic,  hyperplastic  nodules   in  N-2-fluorenylacetamide  treated
rats.   The animals were  fed  1,000 ppm PCB  (type  not specified)  for
e   .t weeks  following two weeks exposure  to the carcinogen.   This
increase  in  preneoplastic lesions over a short period  was  taken to
be a significant  indicator of carcinogenic activity.  The ability
of Aroclor 1254 to  initiate  (as opoosed to promote) tumors in  the
two-stage mouse skin system was  recently examined by DiGiovanni, et
al.  (1977).  Aroclor 1254 proved to be a weak initiator of  papillo-
mas  when  a 100  ug treatment  of skin was  followed by  32  weeks  o.f
treatment with the promoter 12-0-tetradecanoyl»phorbol-13'  acetate.
When used  in combination  with the potent initiator dimethylbenzan-
thracene Aroclor 1254  slightly  increased the  incidence of  paoillo-
mas.  Aroclor 1254 also  failed  to promote  skin tumors  initiated  bv
dimethylbenzanthracene  in the  same  system  (100  ug  Aroclor  1254
applied twice weekly  for  30 weeks)  (Berry, et  al.  1978) .
     Kanechlor  500 promoted  heoatocellular carcinoma initiated  by
diethylnitrosamine  (DENA)  in male Wistar  rats  (Nishizumi, 1976).
Promotion was observed when  PCB treatment  was begun one week fol-
lowing the end of DENA treatment.  The number  of  tumors was signif-
icantly higher in rats treated with DENA and  PCB  than DENA  alone  or
DENA and  phenobarbital,  although a  promoting  effect was  observed
with the latter drug  as well.   .               J
                                               ,1
                              C-73            ;

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     Hepatocarcinogenesis  initiated by 3'-methyl-4-dimethylamino-
azobenzene (3'-Me-DAB) in female Donryu strain rats was promoted by
oral administration of PCBs following initiation.  Tumor incidences
in animals treated  with 3'-Me-DAB + PCS,  3'-Me-DAB  alone,  or PCB
alone  were  64 percent,  13  percent, and  0 percent,  respectively.
PCB treatment  preceding or simultaneous  with 3'-Me-DAB treatment
did not produce tumors  (Kimura, et  al.  1976).
     By contrast  to  the  hepatic  co-carcinogenic effects  of PCBs
observed by  Kimura, et al.  (1976),  Nishizumi (1976),  and Ito, et
al. (1973, 1978), other  investigators  have observed an inhibition
of tumor formation  or growth in the presence  of PCBs.  Makiura, et
al. (1974) fed male Sprague-Dawley rats  3'-Me-DAB,  2FAA,  DEN, or
pair-wise combinations of them  for  20 weeks followed by four weeks
on a stock diet.  Incidence of  hepatocellular  carcinoma ranged from
65.2 to 92.3 percent, and nodular hyperplasia reached 100 percent
in animals fed pairs  of carcinogens.  The  addition of 50 ppm Kane-
chlor  500  to the diet  resulted in a large decrease  in the tumor
incidence  and liver  weight as  compared  to  carcinogen treatment
without PCBs.  PCBs alone induced no tumors or hyperplastic nodules
but did result in an increased liver weight.   The principal differ-
ence between this study and those of Ito,  et  al.  (1978), Nishizumi
(1976), and  Kimura, et  al.  (1976) using the same chemicals is that
PCB exposure was delayed  until  after  the initiating treatment in
the latter "studies.   This suggests  that the  induction  of mixed
function oxidases by PCB  at  the  time of  carcinogen treatment re-
sults  primarily  in  the inactivation of the chemicals and that the
promoting  effects  observed  with sequential  exposure  result  from
                               C-74

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some other mechanism.  The co-carcinogenesis of PCBs with simulta-
neous exposure to BHC may reflect a  difference  iir  the liver metabo-
                                             I
lism of this compound.                       j
     In rainbow trout, Salmo gairdnerii,  100 ppm Aroclor  1254 added
to the diet  reduced  the size and frequencies  of  liver tumors in-
duced by  6 ppm  aflatoxin B^ after a one year exposure (Hendricks,
et al. 1977).                                '
     In addition to the inhibition of tumor  induction by  some chem-
icals, PCBs were also1shown to  inhibit the  growth of  experimental
tumors in  rats.   Sprague-Dawley  rats  were  inoculated  with Walker
256 Carcinosarcoma cells and the effects of PCBs determined.  Both
dietary  (Kerkvliet  arid Kimeldorf,  1977a) and  injected  (Kerkvliet
and Kimeldorf, 1977b)  Aroclor 1254 reduced the  size of  solid tumors
and increased animal life span.  Total dietary PCB intake of 1,100
to 2,000  mg/kg over a 40-day period reduced tumor weight to 60 to 40
percent of control in both male and  female rats.  Aroclor 1254 in-
jected intraperitoneally reduced the efficiency of tumor  takes when
10  tumor cells were injected from 81.3 in control to  50.0 percent
in animals receiving 200 mg/kg/day.  Mean tumor sizes  were reduced
and  lifespans increased  by PCBs  in animals;;  inoculated  with 10
tumor cells.  Administration of PCBs for five days preceding tumor
inoculation or  the  first five days after inoculation  was more ef-
fective than administration between  days 5 and  10.
                               C-75


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                      CRITERION FORMULATION
Existing Guidelines and Standards
     The  Toxic  Substances  Control Act  (TSCA)   (P.L.  94-469)  was
signed  into  law  October  11, 1976.  Provisions  in  section 6(e)  of
the law specifically regulate the manufacture, sale, distribution,
and disposal of  PCBs,  Manufacture,  sale,  or distribution of PCBs
was restricted to sealed systems as of October 11, 1977.  Manufac-
ture was  banned  as  of -January 1,  1979 and all processing and dis-
tribution  in commerce  ceased July 1,  1979.  Allowance for certain
exemptions is provided in the law.  The proposed  rules  to  implement
the terms of section 6(e) of TSCA were released June  7, 1978  (43 FR
24802).   Proposed rules on  the disposal of PCBs were released Feb-
ruary  17, 1978   (43  FR 7150).  The  U.S.  Environmental Protection
Agency has proposed a water quality criterion for the protection of
freshwater  and  marine life of 0.001  ug/1  (U.S.  EPA, 1976b) .  The
Food and  Drug Administration  established tolerance levels in foods
in  1973  (38 FR  18096)  and  proposed  new  tolerance levels further
restricting levels  in 1977  (42 FR 17487).   Both the current allowed
levels  and  the proposed  levels were presented  in Table 3.
     The  occupational  exposure limits adopted  in 1968  are based on
the  recommendations  of  the  American Conference  of  Governmental
Industrial  Hygienists (ACGIH, 1968).   They set the time-weighted
average eight-hour  exposure limits to 1.0 mg/m  for mixtures con-
taining 42 percent  chlorine and 0.5 mg/m  for mixtures  containing
54  percent chlorine.  The newly recommended  standard proposed  by
NIOSH  (1977)  is 1.0 ug/m3  air TWA over a 10-hour day and  40-hour
work  week.
                               C-76

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Current Levels o£ Exposure
     Human exposure  to PCBs in the  United  States has been broad.
Several studies of tissue  and  plasma levels of PCBs have detected
them in a high percentage of randomly chosen subjects.  Yobs (1972)
detected PCBs  in  31.1 percent of  637 human ^adipose  tissue.   The
National Human  Monitoring Program for Pesticides in fiscal years
                                             i
1973 and 1974 found  PCBs in 35.1  and 40.3 percent of adipose tis-
sues tested  (Kutz and Strassman,  1976).    Table  12 indicates the
distribution of PCB  concentrations  in the population.   A study of
Canadian human adipose tissue PCB levels  found 1  ppm or more in 30
percent of 172  samples  (Grant, et  al.  1976);.  The eastern prov-
inces,  particularly  Ontario,  had  the highest incidences.  Average
adipose tissue PCB levels were just  below 1 mg/kg  (ppm) with males
having slightly higher accumulations  than females.  The same study
found human  breast milk  to contain  about 1  mg/kg on a fat basis.
PCBs were detected ini8 of 40 samples of breast milk in Colorado at
levels between  40 and 100  ppb  (whole milk) ,i
described earlier found average levels in 400
30 ppb (Yakushiji, et al.  1977).  PCB levels in plasma  in U.S. popu-
lations  were  detected  in  43 percent  of  723
positive samples ranged from 1.5 to 29 ppb with a mean  around 2 to 3
ppb.   White populations had  higher  levels than black populations
(Finklea, et al. 1972).
     As discussed in the section on exposure,
  The Japanese  study
milk samples of  about
 samples.   Levels  in
the median water lev-
els of PCBs are around 0.1 to 0.3 ug/1 in positive samples with 0 to
20  percent of  samples  being  positive  around  the  U.S.   (Dennis,
1976).  Average PCB  intake  in  food was estimated in  the mid-1970fs
                               C-77

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                              TABLE  12
                Levels of Polychlorinated Biphenyls
                      in  Human Adipose  Tissue*
Data
Source
Yobs,
1972
FY 1973
Survey
FY 1974
Survey
Sample
Size
683
1,277
1,047
Percent
Nondetected
34.2
24.5
9.1
Percent
1 ppm
33.3
40.2
50.6
Percent
1-2 ppm
27.3
29.6
35.4
Percent
2 ppm
5.2
; 5-5
4.9
*Source:  Kutz and Strassman, 1976
                                C-78

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 to be about  9 ug/day with fish being the major dietary source.  Am-
 bient air concentrations  are  around  100  ng/m3  (Kutz  and  Yang,
 1976).                                        :
 Special  Groups  at Risk                        i
      The preceding discussion  of human  exposure  makes clear  the
 fact  that  a  high  percentage  of  the U.S. population has  been  and is
 exposed  to low levels of PCBs in food, water, and air.  Those  groups
 at particular risk  for  PCB exposure  include  industrial workers  ex-
 posed in the workplace, individuals consuming large amounts of con-
 taminated  fish, such as sport fisherman  (42  FR 17487), and nursing
 infants  who,  per  kg body weight, may accumulate  significant body
 burdens  from  the  levels in  human breast milk.|  With the cessation
 of manufacture of PCBs by Monsanto in 1977 and  the  great decline in
 its use which should result  from the  implementation of section 6(e)
 of  TSCA,  industrial exposure should decline substantially.  Since
 many  PCB-containing sealed   systems  can  be  expected  to  remain  in
 service  for  many  years, continuing vigilance will be necessary  to
minimize accidental  pollution  of waterways or
 air and to  prevent
further occupational exposure.
Basis and Derivation of Criterion
     In arriving  at a criterion for  PCB  levels in ambient waters
several factors must be taken into  account.  First, PCBs are highly
persistent  in  the environment and accumulate  to  a high degree in
food webs. - As discussed in the section  Ingestion from Foods, an
average bioaccumulation factor for PCBs in all
shellfish of 31,200  has  been determined.   As
leave the environment very  slowly  once they have entered it.   Not
                               C-79
 freshwater  fish and
a consequence, PCBs

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only do PCBs persist  and  accumulate in the environment but in man
as well.  The current environmental levels are not producing obvi-
ous acute  ill  health  in the general population.  However, several
animal studies report that PCBs  produce a carcinogenic  response and
that  they  may enhance  the carcinogenic activities  of other sub-
stances.
     Although  other  adverse effects of PCB exposure could be used
as a  basis for  formulating a criterion,  carcinogenicity will be
used for a variety of reasons.  The most extensive chronic studies
                                                         !
with PCBs have  identified carcinogenicity  as the malor end point.
Although no carcinogenicity studies have been extended to more than
one generation and firm data exist only for the female  rat, a cred-
ible carcinogenic response to PCBs has been demonstrated and cannot
be  ignored.    Kimbrough,  et al.  (1972)  observed an incidence of
hepatocellular  carcinoma  of  26/184  in  treated  rats  compared to
1/173  in controls.   The  National  Cancer  Institute  (NCI) bioassay
observed a lower percentage of  hepatocellular  carcinoma at a simi-
lar dose level which  was  statistically not significant  because the
number  of  animals  was low.  In addition,  a  number of  nonmalignant
proliferative  processes observed  in  liver at high  frequencies in
the PCB-treated animals in these studies were also observed in both
rats  and mice  in other  studies  (Ito,  et al.  1973, 1974; Kimura and
Baba  1973; Kimbrough,  et al.  1972;  Kimbrough and  Linder,  1974).
PCBs  were  classified as  carcinogenic by  the  International  Agency
for  Research on Cancer (IARC,  1974).   Evidence  from human popula-
tions suggests but does not confirm an increase in cancer frequency
due  to PCB exposure  (Kuratsune, et al. 1976; Bahn, 1976).  Finally,
                               C-80

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 a theoretical basis  exists for the  quantitative  extrapolation of
 carcinogenic effects  in  treated animals to human populations.  Var-
 ious models, such as the  one  used  below,  can provide quantitative
 risk estimates based on animal data  and certain  assumptions about
 the induction of neoplasia  (e.g. one-hit  or  multi-hit induction).
 No basis .exists  for  extrapolation with  mathematical models  from
 animals to man for many  other  kinds of biological  effects.
     Although the criterion established  below! is based on  animal
 carcinogenicity  data, it  should also be noted that  other  adverse
 effects have been observed in mammals  at levels  below the  dose
 which  produces tumors in  rats.   The carcinogenic effect was  ob-
 served  in rats consuming an average of 4.9 mg/kg/day.   Dietary  lev-
 els at  2.5 ppm produced adverse reproductive effects in Rhesus  mon-
 keys (Allen and Barsotti,  1976).  If  a food intake of 350 g/day is
 assumed,  the  PCB  dose is  146  yg/kg/day  in 6  kg animals.  At  this
 time no data are available  to indicate the minimal  level   in  the
 diet at which PCBs produce toxic effects in Rhesus monkeys.
     In mink, ingestion of as  little  as 61 mg of Aroclor 1254 over
 nine months or 90 mg  of Aroclor over four months resulted in  sharp-
ly reduced  reproduction  (Aulerich and Ringer,
1977).   Assuming  a
weight of 1 kg  for  adult  mink  and a food intake of 150 g/day, the
PCB dose at 2 ppm was about 300 ug/kg/day, which is similar to the
level producing reproductive toxicity in monkeys.
     These data can be used in one approach to developing an ambi-
ent water  quality  criterion.   If  300  yg/kg/day is  taken  as the
lowest-observable-effect-level  (LOEL),  then  an Acceptable  Daily
                               C-81

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Intake (ADI)  can be calculated for a 70  kg man using an uncertainty
factor of 100:
                     7£ = 210 yg/day
     Assuming that exposure to PCBs is based on the consumotion of
2 liters of  drinking water,  6.5 g  (0.0065  kg)  of fish and shell-
fish, and  a  bioconcentration factor of 31,200; then the following
calculation can be made:
          X  [(2 1) +  (0.0065 x 31,200)] = 210  ug         ;
                                      X = 1.03 ug/1
     As will be seen  later, the carcinogenicity criterion  is  lower
and presumably more cautionary.
     An assessment of carcinogenic  risk will be, made by  extrapola-
tion from animal data using a linearized multistage (non-threshold)
model,  The  extrapolation  used  takes  into account the  bioaccumula-
tion of PCBs in fish  and shellfish.   It  is  assumed that  an average
of 2 I/day of water are consumed along with  6.5 g of fish taken from
that water source.   Exposures  from  other  food  sources, air, or oc-
cupational exposure  are not  included  in the criterion level derived
by this model.
     Among the  studies reviewed in  this  document, only one appears
suitable  for use  in  the cancer risk assessment.   None  of the  mouse
studies  involved  feeding  for most or all of a  lifetime  and  are
therefore unsuitable.  Of the rat  studies, the only one involving
long term exoosure and adequate numbers of animals is the study of
Sherman  rats by Kimbrough, et al.  (1975).
      This study has  some drawbacks  in that  it  lacks any  evidence of
a dose-response  (due to the use  of only  one  dose level) ;  it tests
                                C-82

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 only  one  sex -of  the  species, and only  one commercial mixture of
 PCBs.  Yet the experimental design is a good one  in many ways:  the
 treatment was given over a long portion of the  life span;  there was
 an appropriate route  (food)  and  distribution of exposure  (uniform
 dose  over  time) ;  the  authors provided good documentation of the
 actual intake dose;  a  sufficiently large number of experimental and
 control animals  were   used  to detect  a  statistically significant
 increase in  tumors; and  there was a thorough  and  well documented
 description of the  pathology (hepatocellular carcinoma).   The NCI
 study (1978)  was the only other  study  involving  a  long-term expo-
 sure  and was  suggestive of a  carcinogenic  effect; however, the lack
 of  an adequate number  of animals  renders  it  unsuitable as a study
 upon  which  to base an  estimate of carcinogenic  risk.
      Under  the Consent, Decree in NRDC v.  Train,  criteria  are to
 state "recommended  maximum  permissible concentrations  (including
 where appropriate,  zero)  consistent with  the protection of aquatic
 organisms,  human health, and  recreational activities."   PCBs are
 suspected of  being human carcinogens.  Because  there is no  recog-
 nized  safe  concentration for  a  human carcinogen, the  recommended
 concentration of PCBs  in water  for  maximum protection  of human
 health is zero.
     Because  attaining a zero concentration level may be infeasible
 in some cases and  in order  to assist  the Agency and States  in the
possible future development of water  quality  regulations,  the con-
centration of PCBs corresponding  to  several incremental   lifetime
cancer risk levels  have been  estimated.  A cancer risk level pro-
vides  an estimate of the additional incidence of cancer that  may be
                               C-83

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expected in an exposed population.   A risk  of  1
-------
 (2)  Approximately  99  percent  of  the PCB exposure results from the
     consumption of aquatic organisms which exhibit an average bio-
     concentration  potential of 31,200-fold.   The remaining 1 per-
     cent of  PCB exposure  results from  drinking  water.
     Concentration  levels  were derived assuming a lifetime exposure
 to  various  amounts  of  PCBs,  (1)  occurring from  the consumption  of
 both drinking water and aquatic life grown in Waters containing the
 corresponding  PCBs  concentrations,  and  (2)  occurring solely  from
 consumption of aquatic life grown in the waters containing the cor-
 responding PCB concentrations.   Although total exposure  information
 for  PCBs  is discussed  and an estimate  of the  contributions  from
 other sources of exposure  can  be  made,  this data will not  be  fac-
 tored into  ambient  water quality criteria formulation until  addi-
 tional analysis can be made.  The  criteria presented,  therefore,
 assume an incremental  risk from ambient  water  exposure only.
     These criteria are  exceedingly low.  Although sharp  restric-
 tion of open PCB use in 1970 resulted in notable declines  in water
 PCB levels  in the next several years (Dennis, J1976), the  residual
 levels remaining are still two to three orders,  of magnitude above
the criterion indicated by this extrapolation.
PCBs in water  today is probably not new effluents from industrial
or  domestic  sources,  but  the  PCB-containing  sludges underlying
waterways which typically contain 100- to 1,000-fold  higher concen-
trations than  the water  itself  (Dennis,  1976).   Efforts to reduce
water levels significantly by eliminating current pollution sources
will probably  have  little effect on  average  water PCB concentra-
tions.
                               C-85
The major source of

-------
     The very low limits suggested by this  risk estimate are due in
large  part  to  the  very  large  bioaccumulation   factor  in  fish
(31,200).  This  figure  is an average for  a  wide  variety  of salt-
water and freshwater organisms  (see Ingestion from Food section).
     As possible  strategies  to  reduce human exposures to PCBs are
considered,  the relative  contributions of  ingested water  and fish
should be kept in mind.  At the assumed consumption rate of 2 liters
of drinking water and 6.5 g of fish/day, 99 percent of the dietary
PCBs will be obtained from fish.  Strategies which focus separately
on the reduction of PCB levels in water and fish for human consump-
tion might be more practical and productive  than  a single standard
for water which takes bioaccumulation in fish into account.
     A  final comment about the  risk level derived from this study
is that  it  is based  on animal data in which a dose-response rela-
tionship  was not demonstrated.    The weight of evidence indicates
that PCBs  are carcinogenic in rodents.   However,   the  carcinogenic
                                                         i
activities of these compounds are not great.  An acceptable  noncar-
cinogenic level could be established with greater  certainty  if bet-
ter  quantitative data on carcinogenicity  were available.   Studies
with larger  numbers of animals designed to measure relatively small
effects are needed.   Also, the rat appears  to be much less sensi-
tive  to the  acute and subacute effects of  PCBs  than man  or non-
human  primates.  . Further investigation  of the effects of  PCBs in
Rhesus monkeys, particularly with reference to  the gastric  lesions
produced,  would be useful.
                                C-86

-------
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                              C-101

-------
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                               C-102

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                               C-104

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                              C-105

-------
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                               C-110

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                              C-113
:ine pesticides  in
6: 28.
                                               Polychlorinated  Si-
                                             Conf. Polychlor.  Bi-
                                               560/6-75-004.  Off.
                                         Washington, D.C.

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                             APPENDIX                                    *?•
                                                                       Mi
                                                                        t
    Summary  and  Conclusions  Regarding  the Carcinogenicitv of
                    Polychlorinated  Biohenyls*
                                                          i
     Polychlorinated biphenyls (PCBs) are prepared by  the chlorina-
tion of  biphenyl and  are  complex mixtures  containing  isomers of
chlorobiphenyls with different chlorine content.
     Because of  the widespread  industrial use of PCBs,  their  long
half-life, and the documented disease-oroducing capability of these
compounds  in several  species,  regulations  have  been promulgated
banning most of  the manufacturing, processing,  and distribution of
PCBs in the United States  (44 PR  106).
     Human studies concerning the possible carclnogenicitv of  PCBs
have involved small numbers  of  individuals and provide little in-
formation about  exposure.  Although  these studies are only marginr-
ally useful  in  describing the carcinogenic!ty of PCBs,  the inci-
dence of malignant neoplasms in  "Yusho"  patients and  in  industrial
workers  exposed to Aroclor  1254 suggests that human exposure to
PCBs is associated with  an increased risk of neoplasia.
     In  two separate  studies,  PCBs have been reported  to  induce
hepatocellular  carcinomas  in both  mice and  rats  (male  mice fed
Kanechlor  500  at 500  ppm and female Sherman rats fed Aroclor  1260
at  100 ppm).
 *This summary  has  been orepared  and approved by  the Carcinogens
  Assessment Group of EPA on June 15, 1979.
                               C-114

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       in an NCI  bioassay,  Aroclor 1254 was not carcinogenic in Fis-
  cher  344 rats,  but the high frequency of hepatocellular prolifera-
  tive  lesions  was  considered to be the result of treatment and car-
  cinomas of  the gastrointestinal  tract  possibly  associated  with
  treatment.   In  one other mouse study and  three other  rat studies,
  various PCBs induced proliferate lesions of the  liver which  might
  be  indicative of  carcinogenicity.  The most commonly  seen  lesions
  were adenofibrosis  (cholangiofibrosis)  and neoplastic  nodules.
      A  correlation between degree of chlorination and  tumor induc-
  ing potential was observed in both mouse and  rat species.  The most
 highly  chlorinated preparations  were  also the most  potent tumor
 inducers with the  exception  of  Aroclor  1254  which  was more potent
 than Aroclor  1260  in one rat study.  where  examined,  female  rats
 were found to be more sensitive than males.  No comparisons of sex
 related effects  were made in mice.            |
     PCBs have been reported to be co-carcinogens,  initiators, and
 promoters in  both  mouse and rat species.
     The mutagenicity of different PCB preparations has been evalu-
 ated in several  test systems  with  conflicting results.   in  one
 study,  the  single  isomer 4-chlorobiphenyl was reported to be highly
 mutagenic   in  Salmonella  typhimurium  strain  TA1538  after liver
 microsomal  activation, while Aroclor 1221 was Reported  to be  less
 mutagenic  and Aroclors  1254,  1268,  and  2,5,2-,5'-tetrachlorobi-
 phenyl  were" inactive.  The fact that mutagenic  activity decreased
 with increasing chlorination  is  consistent withi  the characteristic
 insensitivity  of  the  Ames  test to chlorinated  hydrocarbons.   in
other test  systems, Kanechlor 300  inhibited  bacterial DNA repair
                              C-115

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deficient cells  and induced cytogenetic  abnormalities in Yoshida
sarcoma cells.  Kanechlor 500 tested positive  in a mouse bone mar-
row cytogenetic analysis.
     in summary,  carcinogenic  responses have been induced in mice
and  rats.    These results,  together  with positive  mutagenic  re-
sponses and  suggestive  epidemiologic evidence,  constitute  substan-
tial evidence  that  PCBs are  likely  to  be  human carcinogens.
     The  water quality criterion  for  PCBs  is based  on  the Kim-
brough, et al. (1975) study on the induction of hepatocellular car-
cinomas  and neoplastic  nodules  in  female Sherman strain  rats  fed
100 ppm Aroclor 1260.   It is concluded that the water concentration
of PCBs  should be less  than  0.79  ng/1  (-0.8 ng/1) in order to keep
 the lifetime cancer risk below 10
                                  ,-5
                                C-116
                                                                        f*
                                                                        «k.
                                                                         a

-------
                    Suiranary  of  Pertinent Data

     The water quality criterion for PCBs is derived from the hepa-
tocellular  carcinoma and  neoplastic  nodule ^response  of  Sherman
strain  female  rats  fed  Aroclor 1260 at  a nominal  dietary  level of
100 ppm (Kimbrough, et al.  1975).   A time-weighted average dose of
88.4 ppm  (i.e., the dose varied between  70  and  107 ppm  in  the Kim-
orough,  et  al.  study)   was   administered   for'  approximately  21.5
months  and  the animals were  ooserved  for an additional six  weeks
before  terminal sacrifice.   The criterion  is calculated  from the
following parameters where the adjustment factor of 0.05 represents
the fraction of food consumed in relation to  body  weight:
             Dose
           (mg/kg/day)
           0
           4.42
     (i.e., 88.4 ppm x 0.05)

    le = 645 days
    Le = 730 days
    L  = 730 days
          Incidence
  (No. responding/No, tested)
             il/173
           170/184
       w = 0.400 kg
       R = 31,200 I/kg
     With  these parameters  the  carcinogenic; potency  factor  for
humans is 4.3396  (mg/kg/day)
                            -1
The resulting water concentration
of  PCBs  calculated  to keep  the individual  lifetime cancer  risk
below 10~5 is 0.79 ng/1.                      !
                              C-117

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•*•

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