FINAL
               United States                                    ECAO-CIN-P230
               Environmental Protection                              Anrii
               Agency                                       *M» ' '.
&EPA       Research and
               Development
               HEALTH AND ENVIRONMENTAL EFFECTS PROFILE
               FOR AHTKRACEME
              Prepared for
               OFFICE OF SOLID WASTE AND
               EMERGENCY RESPONSE
              Prepared by
              Environmental Criteria and  Assessment Office
              Office of Health and Environmental Assessment
              U.S. Environmental Protection  Agency
              Cincinnati. OH  45268
                          DRAFT: 00 NOT CITE OR QUOTE
                                  NOTICE

           .,..* Uw«.uiM7ii«. is d preliminary  draft.  It has not been formally released
        by the U.S. Environmental Protection Aqency and should  not at this stage be
        construed to represent Agency policy.  It Is being circulated for comments
        an Its technical accuracy and policy Implications.

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                                  DISCLAIMER

    This report  Is  an external draft  for  review purposes only  and  does  not
constitute  Agency  policy.   Mention of  trade names  or  commercial  products
does not constitute endorsement or recommendation for use.

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                                    PREFACE


    Health  and  Environmental  Effects Profiles  (HEEPs)  are prepared  for  the
Office  of Solid  Waste  and Emergency Response  by the  Office  of Health  and
Environmental  Assessment.   The  HEEPs  are  Intended  to  support listings  of
hazardous  constituents  of  a wide  range  of  waste streams  under  Section  3001
of  the  Resource  Conservation  and Recovery Act  (RCRA),  as  well  as  to provide
health-related limits for  emergency actions under Section  101  of the Compre-
hensive  Environmental  Response,  Compensation  and   Liability  Act  (CERCLA).
Both  published  literature and  Information  obtained  from  Agency  program
office  files  are  evaluated  as  they  pertain   to   potential  human  health,
aquatic life and  environmental  effects  of hazardous  waste  constituents.   The
literature  searched  and   the  dates  of  the  searches  are  Included  In  the
section  titled  'Appendix:  Literature   Searched."    The  literature  search
material 1s current through November, 1985.

    Quantitative  estimates  are   presented   provided   sufficient   data   are
available.  For systemic toxicants,  these Include Reference  doses  (RfOs)  for
chronic exposures.   An  RfO Is  defined  as  the amount of a chemical  to  which
humans  can be  exposed  on  a  dally  basis over  an   extended  period  of  time
(usually a lifetime) without suffering  a  deleterious effect.   In the case of
suspected  carcinogens,  RfOs  are  not  estimated  1n  this  document  series.
Instead,  a carcinogenic potency  factor  of  q-|*  Is   provided.   These  potency
estimates are derived for  both  oral  and  Inhalation exposures  where possible.
In  addition,  unit  risk estimates  for air  and  drinking water  are  presented
based on inhalation and oral data, respectively.

    Reportable quantities  (RQs) based on both  chronic  toxlclty and cardno-
genlclty are derived.   The  RQ 1s  used to determine  the quantity of a hazard-
ous substance  for which notification 1s  required In the  event  of  a release
as  specified under  CERCLA.  These two RQs (chronic  toxldty  and carcinogen-
1c1ty)  represent  two of  six  scores  developed  (the remaining  four  reflect
1gn1tab1l1ty, reactivity,  aquatic toxldty and acute  mammalian toxlclty).

    The  first  draft  of  this   document  was  prepared  by  Syracuse  Research
Corporation  under  EPA  Contract  No.  68-03-3228.    The  document was  subse-
quently  revised   after  reviews   by  staff  within the  Office  of Health  and
Environmental Assessment:  Carcinogen Assessment Group,  Reproductive Effects
Assessment Group,  Exposure Assessment Group, and the  Environmental Criteria
and Assessment Office In Cincinnati.

    The HEEPs will become part of the EPA RCRA and CERCLA dockets.
                                      111

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                               EXECUTIVE  SUMMARY

     Anthracene  Is  a  colorless  solid at ambient temperatures.   It  1s  soluble
 In   a  variety  of  organic  solvents  Including ethanol,  methanol,  benzene,
 toluene  and-carbon dlsulflde  (Hlndholz,  1983), but  It  Is  almost Insoluble In
 water  (Pearlman  et   al.,  1984).   The  solubility   of  anthracene  1n  water
 decreases  slightly with  the  Increase In salt  content,  but  decreases  greatly
 with the lowering  of  water temperature  (WhHehouse,  1984).   This  compound Is
 susceptible  to  oxidation by ozone,  peroxides and  other  oxldants (MAS,  1972).
 The  commercial  production  of  anthracene 1n the United  States  Is  believed to
 have stopped  since 1982  (IARC.  1983),  although Us  U.S. production was >2-20
 million  pounds  In  1977  (U.S.  EPA,  1977).   In  1983.  30.458  pounds of anthra-
 cene was  Imported  Into  the   United States  (USITC.  1984).    Anthracene  Is
 produced  commercially from anthracene  oil,  a coal  tar fraction  boiling In
 the  range  of 270-360°C  (IARC,  1983; Hawley. 1981).   It 1s  used primarily 1n
 the  production  of dye.   Also,  small  amounts of  anthracene  are  used as  a
 component  of  smoke   screens,   as   scintillation  counter  crystals,  and  1n
 organic  semiconductor research (IARC, 1983; Hawley,  1981).
     The  fate  and  transport  of anthracene  1n aquatic  media  has received much
more attention  than  1n  any other media, because  a  raultlcompartment modeling
 program  conducted  by Nackay  et al.  (1985)  estimated  that  >95X  of environ-
mental  anthracene  will  reside  In  the  aquatic  compartment.   The  fate  and
 transport  of anthracene  In surface  waters will  depend on  the nature of  the
water.   In most waters, the  loss  of anthracene  Is  mainly  due to photolysis
and  blodegradatlon (Hackay et  al.. 1985); however.  In  a  very  shallow, fast-
 flowing  clear water,  volatilization and photolysis  will  play dominant roles
 In  determining  the  fate of  anthracene (Southworth,  1979).   In  deep,  slow
                                      1v

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flowing  and  muddy waters, m1crob1al  degradation  and adsorption may  account
for  the  major  losses  of  anthracene  from  water  (Southworth,  1979).   There-
fore,  the  half-life  of anthracene  1n  natural  surface waters will  depend  on
the  nature of  the  water bodies.   In very  shallow,  fast-flowing and  clear
water, its..half-life may be -1  hour  (Southworth.  1979;  Herbes  et  al..  1980).
On  the  other  hand,  the  half-life  may  be  as  high  as 29  days   1n  a  deep
eutrophlc pond (Zepp, 1980).
    In air,  anthracene 1s  expected  to be  present  both  1n the vapor  and  the
partlcle-sorbed state.   Over 78% of  atmospheric anthracene may be  present  In
the  vapor  state  (Thrane  and  Nlkalsen.  1981).   Both  chemical  processes
Including  CL  and   OH   radical  and  photochemical   reaction  will  degrade
            w
atmospheric anthracene (Nlessner et  al., 1985; Atkinson,  1985;  Korfmacher  et
al..  1980;  Behymer  and H1tes,  1985).  The degradation of vapor  phase atmo-
spheric  anthracene  1s  expected  to be  faster  than  partlcle-sorbed  anthracene
(Santodonato  et  al..  1981).   The  atmospheric half-life  of anthracene  may
vary  from  hours to  days  (Atkinson,  1985;  Korfmacher et al.. 1980;  Behymer
and Kites,  1985;  Lunde  and  BJoerseth, 1977).   The  long range transport  of
anthracene observed  by Lunde and  Bjoerseth (1977)  Indicates  that partlcle-
sorbed anthracene may have a  half-life of the order of days.
    The  fate and transport of anthracene In  soils  Is not well  studied.  Both
blodegradatlon  and  abiotic   processes  will  degrade  anthracene  In  soils
(Bossert et al., 1984).  The half-life of  anthracene In soil may be -1 month
(Bossert et al., 1984).  Anthracene  may  not  leach from most  soils because of
Us high K   value;  however, 1t  may leach  through  soils  that  have attained
the breakthrough capacity for anthracene sorptlon (Plet and Morra,  1979).

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    Anthracene  Is ubiquitous  In  the aquatic  environment.   Anthracene at  a
 concentration  range  of  <13-105  ng/l  was  reported  In the  effluent  from  a
 sewage  treatment  plant   In  Norway  (Kveseth  et  al.,  1982).   It  was also
 reported  In  the concentration  range  of  <0.03-0.84  yg/l   1n  the effluent
 from  coal  oven  plants  (Walters and Luthy,  1984; Grlest,  1980).   It has been
 reported  to  be  present  In several  surface waters  (Hltes, 1979;  Dewalle  and
 Chlan,  1978;  Staples   et al.,   1985).    A  maximum  concentration of 12.1
 vg/l  was  reported 1n  the water  from  Tennessee  RWer 1n  Calvert CHy,   KY
 (Goodley and Gordon, 1976).  In general,  anthracene  occurs  In  ambient  waters
 at  a  frequency  of  4% and  at  a  median  concentration  of <10 pg/l  (Staples
 et  al..  1985).    Anthracene  has  been reported  to  be present  in  groundwater
 from  a few contaminated  sites.  Bedlent  et al. (1984) reported the detection
 of  up to  168.6  yg/l  of  anthracene  In  groundwater  from  a  creosote  waste
 site  In Conroe,  IX.  The detection  of anthracene  In  drinking waters  through-
 out  the  world  have  been reported  (Williams et al.,  1982;  Kveseth et al.,
 1982; Shlnohara  et al.,  1981;  Plet  and  Morra,  1979).  The highest concentra-
 tion  of  combined anthracene/phenanthrene  at 1269 ng/l  was  reported   In
 drinking water  In Sault  Ste. Marie  (Williams et al.. 1982).   Finished waters
 from  13 different locations  throughout  the United  States, however, failed to
 show  the presence of  any anthracene (Sorrel 1 et al..  1980).
    The concentrations  of anthracene 1n ambient   air  In  some cities  1n  the
United States and around the world have  been  reported.   The mean concentra-
 tion  of anthracene 1n  the air of Los Angeles  during 1981-82 was  reported to
be  O.S4  ng/m*  (Grosjean,  1983),  whereas  Us  mean  concentration  In  Osaka,
Japan, during the same  period  was  reported to be 0.32 ng/ra»  (Hatsumoto  and
Kashlmoto, 1985).   It  has  been  demonstrated  by  Grosjean  (1983) that  the

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atmospheric  anthracene  concentrations  show both seasonal and  diurnal  varia-
tions,  with  the  anthracene concentration  higher  1n winter  and during  the
night.   Although  suitable  data were  not  available  on anthracene  for  compari-
son.  Grosjean  (1983)  estimated that  the  levels  of  other  polynuclear  aromatic
hydrocarbons  In Los Angeles  air  did  not  change  significantly  during  the last
decade.   Based  on the assumptions that  the mean level of anthracene  In U.S.
air  Is  0.54 ng/m*  (same as  concentration In  Los Angeles) and that an  adult
Individual  Inhales  20  m*  air/day,  the  average dally  Intake of  anthracene
from  Inhalation Is 11 ng.
    Anthracene  has  been   reported  to  be  present  In smoked  foods,  liquid
smoke,  charcoal-broiled steaks  and  edible aquatic  organisms  collected from
certain  contaminated waters  (Fazio and Howard,  1983; Galloway  et al..  1983).
For example,  the  concentrations  of anthracene  1n charcoal-broiled steaks and
barbecued  Mbs  were  reported  to be 4.5 and  7.1  ugAg,  respectively  (Fazio
and Howard,  1983).  The U.S.  National  Mussel watch program  collected mussels
from  >100 sites on the East.  West  and Gulf coasts  (Galloway  et al..  1983).
The  concentration  of  anthracene  In  these  mussel  composites  was  7.9-32
ug/kg  (Galloway et al.,  1983).   Until  data  on the level  of this  compound
In food  composites  used by an Individual 1n the United States are available.
It  Is  not  possible  to  estimate the  human  Intake  of anthracene  through
consumption of foods 1n the United States.
    There  Is  relatively  little  Information  concerning  the  toxlclty  of
anthracene  to aquatic  organisms.   Acutely toxic  concentrations  range from
1.9  wg/l  for  Oaohnla  pulex  (Allred  and  Glesy,  1985;   Orls  et  al.,   1984)
to  3030  vg/1  for  Daphnla  magna  (Bobra et   al..  1983).   Some  of  this
variability  may  be  explained  by  the   fact   that   anthracene   toxlclty  Is
affected  by  lighting  conditions,   with  toxlclty  Increased  under  natural

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 sunlight  and ultraviolet  radiation  rather  than  fluorescent  lights  (Allred
 and  Glesy,  1985;  Bowling et al.,  1983;  Kagan  et  al.,  1985).  Reported  toxic
 concentrations  for  aquatic plants were  also highly  variable.   Hutchlnson  et
 al.   (1980)  reported  that  photosynthesis   was   Inhibited   1n  Chlamydomonas
 anqulosa   at  239  yg/l,  while   G1dd1ngs   (1979)   found   that  Selenastrum
 caprlcornutum  was  unaffected  by  a  100%  saturated  solution.  Reported  BCF
 values  ranged  from  47-132 for Chlronomus rlparlus (Gerould  et  al..  1983)  to
 16,800  for  Pontoporlla  hoyl  (Landrum,  1982).   These  species  also represent
 the extremes In the ability to metabolize and eliminate anthracene.
    Limited  Information   1s  available  regarding  the  pharmacoklnetlc  profile
 of  anthracene.   Gastrointestinal  absorption   may   be  poor,   as  53-84%  of
 anthracene administered  by diet  or stomach  tube  was  eliminated In the feces
 by  rats 1n  2-3  days  (Chang,  1943);  however,  urinary and  biliary excretion
 were  not  measured.   Radioactivity from single  Intratracheal Instillations of
 1*C-anthracene  was  cleared  from  the  lungs  1n  a  blphaslc  manner  with
 half-times of  0.1  hours  (99.7% of dose) and 25.6 hours  (0.3% of  dose) (Bond
 et al., 1985).  The distribution  of  anthracene to tissues  does not appear to
 have  been  Investigated.   Metabolites  resulting from  epoxldatlon  at  the
 1.2-bond or  oxidation  at the 9- and 10-posHlons have been Identified In in
 vivo  and  .In  vitro studies  with  rats  (S1ms.  1964;  Akhtar et  al.,  1979).
Trans-1,2-d1hydroxy-l,2-d1hydroanthracene and  sulfate  and  glucuronlde conju-
gates consistent with the formation  of anthracene-1,2-ox1de appear to be the
major products.   Orally  administered anthracene  appears to be eliminated by
rats  primarily  (53-84%)  1n  the  feces  (Chang,  1943).  Metabolites of orally
administered anthracene have been detected 1n  the urine of  rats (S1ms, 1964).

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    Administration  of  diets  that  supplied  a  total  dose  of  4.5  g/rat  of
anthracene over  78 weeks  produced  tumors  1n  2/28  rats  (a  liver sarcoma and a
uterine  adenocardnoma)  that  were  observed for  life (Schmahl,  1955).   A
control group was not  used  and  the  tumors  were  not  ascribed  to treatment.  A
single  Intrapulmonary  Injection of 0.5 mg anthracene  In  beeswax-trlcaprylln
mixture did  not  Induce local neoplastlc  responses  1n  rats after 4-55 weeks
of observation (Stanton et al..  1972).
    Twice or  thrice  weekly  skin applications of anthracene for  life did not
produce local  tumors  In  mice  (Bachmann et  al.,  1937;  Uynder and  Hoffmann,
1959;  Hlescher,  1942),   but   contradictory  results   were  obtained  when
anthracene was applied  to mouse skin with concurrent or  directly  subsequent
ultraviolet  Irradiation  (Heller",  1950;  Forbes  et  al..  1976).   Mouse skin
Initiation-promotion assays using  croton  oil (Salaman  and Roe,  1956) or TPA
(ScMbner, 1973) as  the promoter did not  Indicate  a tumor  Initiating effect
of anthracene.   Weekly subcutaneous Injections of  anthracene  1n rats for 6
weeks  to  life  (PolHa.  1941;  Schmahl.  1955;  Boyland and  Burrows. 1935).
weekly 1ntraper1toneal  Injections   In rats  for  33  weeks  (Schmahl. 1955)  or
brain  or  eye  Implants In  rabbits  for  4.5  years  (Russell,  1947) did not
produce local tumors,  but these findings should be regarded as  Inconclusive
because of  Inadequacies In experimental design.  Taken together,  the avail-
able human and animal  data for  cardnogenlcHy are Inadequate,  EPA Group  0,
to make an assessment of human  carcinogenic activity.
    Anthracene has been tested  In  numerous mutagen1c1ty and  other  short-term
assays with primarily negative  results  (IARC,  1983; Langenbach et  al..  1983;
Lubet et  al..  1983;  Ved  Brat et al.,  1983;  Hamber et al.,  1984;  Qulllardet

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et al.,  1985).   These Include ONA damage, mutation,  cytogenlcHy and trans-
formation  assays  with bacteria,  yeast  'and mammalian  cells J_n  vitro  and Jji
vivo.   Exogenous  metabolic activation  systems  were  used  In most  of  the j_n
vitro assays.
    Pertinent  data  regarding  chronic  or  subchronlc  toxic  effects,  terato-
genlclty or other reproductive effects  of  anthracene  could not be  located In
the available literature as dted In the Appendix.
    Data  were   Insufficient  to  derive   an RfO,  q *   RQ  or  F  factor,  and
thus, a hazard ranking 1s precluded.

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                              TABLE  OF  CONTENTS
1.   INTRODUCTION	    1

     1.1.   STRUCTURE AND CAS NUMBER	    1
     1.2.   PHYSICAL AND CHEHICAL PROPERTIES 	    1
     1.3.   PRODUCTION DATA	    2
     1.4.   USE DATA	    3
     1.5.   SUMMARY	    3

2.   ENVIRONMENTAL FATE AND TRANSPORT PROCESSES	    5

     2.1.   WATER	    5

           2.1.1.   Photodegradatlon	    5
           2.1.2.   Chemical Reactions	    6
           2.1.3.   81odeqradat1on	    6
           2.1.4.   Volatilization	    9
           2.1.5.   Adsorption	   10
           2.1.6.   Bloconcentratlon	   10
           2.1.7.   Overall  Removal Processes 	   12

     2.2.   AIR	   15
     2.3.   SOIL	   17
     2.4.   SUMMARY	   19

3.   EXPOSURE	   21

     3.1.   WATER	   21
     3.2.   AIR	   23
     3.3.   FOOD	   25
     3.4.   SUMMARY	   27

4.   PHARMACOKINETCS	   31

     4.1.   ABSORPTION	   31
     4.2.   DISTRIBUTION	   31
    4.3.   METABOLISM	   31
    4.4.   EXCRETION	   32
    4.5.   SUMMARY	   32

5.  EFFECTS	   34

     5.1.   CARCINOGENICITY	   34
    5.2.   WTAGENICITY	   38
    5.3.   TERATOGENICITY	   39
    5.4.   OTHER REPRODUCTIVE EFFECTS 	   39
    5.5.   CHRONIC AND SUBCHRONIC TOXICITY	   39
    5.6.   OTHER RELEVANT INFORMATION 	   40
    5.7.   SUMMARY	   41

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                           TABLE  OF  CONTENTS (cont.)

                                                                        Page

 6.  AQUATIC TOXICITY	   43

     6.1.   ACUTE	   43
     6.2.   CHRONIC	   45
     6.3.   PLANTS	   45
     6.4.   RESIDUES	;	   45
     6.5.   SUMMARY	   47

 7.  EXISTING GUIDELINES AND STANDARDS 	   48

     7.1.   HUMAN	   48
     7.2.   AQUATIC	   49

 8.  RISK ASSESSMENT	   50

 9.  REPORTABLE QUANTITIES 	   52

     S.I.   REPORTABLE QUANTITY (RQ) RANKING BASED ON CHRONIC
            TOXICITY	   52
     9.2.   WEIGHT OF EVIDENCE AND POTENCY  FACTOR (F=1/ED10)
            FOR CARCINOGENICITY	   52

10.  REFERENCES.		   55

APPENDIX: LITERATURE SEARCHED	   81

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                               LIST OF TABLES

No.                               Title                                Page

2-1     Removal of Anthracene by Volatilization from Hater
        Bodies at 25aC	   11

2-2     BCFs for Anthracene In Different Aquatic Organisms	   13

2-3     Contributions of Major Processes In Removal of Anthracene
        from Water at 25°C During Midsummer	   14

3-1     Ratios of Anthracene to Benzo(e)pyrene, Benzo(a)pyrene to
        Benzo(e)pyrene and the Concentrations of Benzo(a)pyrene
        from Various Sources of Emm1ss1on 	   24

3-2     Ambient Atmospheric Concentrations of Anthracene  In
        Various Locations 	   26

3-3     Anthracene Levels 1n Different Foods	   28

5-1     Dermal. Injection amd Implantation Carc1nogen1c1ty
        Assays of Anthracene	   35

6-1     Acute Tox1c1ty of Anthracene to Aquatic Animals  	   44

6-2     Bloconcentratlon Data for Anthracene In Aquatic Organisms  .  .   46

9-1     Anthracene: Minimum Effective Dose (MED) and Reportable
        Quantity (RQ)	   53

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                             LIST OF ABBREVIATIONS

ADI                     Acceptable dally Intake
BCF                     B1oconcentrat1on factor
CAS                     Chemical Abstract Service
ONSO                    Dimethyl sulpoxlde
DNA                     Deoxyrlbonuclelc add
ECso                    Concentration effective to 50% of recipients
GC                      Gas chromatography
HGPRT                   Hypoxanthlne-guanlne phosphorlbosyl transferase
Koc                     Soil sorptlon coefficient standardized
                        with respect to organic carbon
Kow                     Octanol/water partition coefficient
LD5Q                    Dose lethal to 50% of recipients
MED                     Minimum effective dose
PAH                     Polynuclear aromatic hydrocarbon
ppb                     Parts per billion
ppra                     Parts per million
RQ                      Reportable quantity
TLV                     Threshold limit value
TPA                     Terephthallc add
TWA                     Time-weighted average
                                      x1v

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                               1.   INTRODUCTION
1.1.   STRUCTURE AND CAS NUMBER
    The  chemical  commonly  known as  anthracene  1s  also known by the synonyms
paranaphthalene,  green oil  and  tetra  olive  NZG  (U.S.  EPA,   1986a).   The
structure,  empirical  formula,  molecular weight and  CAS  Registry  number for
this chemical are as follows:
Empirical formula:  C..H..
Nolecular weight:  178.22
CAS Registry number:  120-12-7
1.2.   PHYSICAL AND CHEMICAL PROPERTIES
    Anthracene  Is  a colorless crystalline compound at ambient  temperatures.
It  Is  almost  Insoluble  In  water but  1s soluble  1n  a  variety  of  organic
solvents  Including  ethanol,  methanol,  benzene, toluene and  carbon  dlsulflde
(Ulndholz.  1983).   Some  of  the  relevant  physical  properties of anthracene
are listed below.
Melting point:
Boiling point:
Density at 27/4*C:
Water solubility:
216'C
340-C

1.25
  Distilled water at 25'C:  0.041-0.080 mg/t
                            0.066 mg/t (average)
                at 2S.3*C:  0.044 mg/t
                 at 4.6*C:  0.010 mg/l
  Distilled water with
  36.SX salinity at 25.3'C: 0.032 mg/t
Santodonato et al.,
1981
Santodonato et al.,
1981
Ulndholz, 1983
                          Pearlman et al.. 1984
                          Pear loan et al.. 1984
                          UhUehouse. 1984
                          UhUehouse, 1984
                          UhUehouse, 1984
0867p
        -1-
                11/17/86

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 Log  Kow:                    4.45-4.63                 Ruepert et al., 1985;
                                                      Readman et al., 1982;
                                                      Ogata et al.,  1984;
                                                      Yalkowsky and  Valvanl,
                                                      1979
 Vapor  pressure:             7.65xlO~» mm Hg at 20°C   Grayson and Fosbraey,
                                                      1982
                            5.65x10"* to 8.48x10"*    Sears and Hoplce, 1949;
                            mm Hg at 25°C             McEachern and  Sandoval,
                                                      1973; Etzweller et al.,
                                                      1984
 Henry's Law constant:       3.64x10"' atmos»m»/mol    Webster et al., 1985

     It can be  concluded  from  these  data  that  the solubility of anthracene In
 water  decreases  slightly with  the  Increase  of  salt content,  but  the  solu-
 bility  1s  greatly dependent  on  the  temperature  of the  water.  Chemically,
 polycycllc aromatic  hydrocarbons  are reasonably  reactive.   They can undergo
 substitution  and  addition  reactions.    In   addition,  these   compounds  are
 susceptible to oxidation by ozone, peroxides and other oxldants  (NAS, 1972).
 1.3.   PRODUCTION DATA
    According  to the  nonconfldentlal portion  of  the  TSCA  production file
 (U.S.  EPA, 1977), Koppers  Co.,  Inc., reported production  of a total of 2-20
million pounds  of anthracene at  two  sites In 1977, and  DuPont Co.  produced
<1000  pounds  of  the chemical during the same  year.   Allied  Chemical also
reported production  of  anthracene In 1977 but did  not  report  the production
volume.  The  commercial production  of  anthracene   1n  the United  States  Is
believed to  have stopped  since  1982 (IARC,  1983).   In 1983,  the  amount of
anthracene Imported to the United States was 30.458  pounds  (USITC. 1984).
    Anthracene  1s commercially   produced  from  anthracene  oil, a  coal-tar
fraction boiling 1n  the range  of  270-360'C.   Crude anthracene 1s obtained
from anthracene  oil  either by crystallization or by distillation of  the oil.
0867p                               -2-                              02/11/87

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 The  crude  product  Is purified by washing with appropriate  solvents  followed
 by  sublimation.   Pure crystals of  anthracene  are  obtained by  zone  refining
 of  solid  anthracene.   Commercial  anthracene Is -90-95% pure by weight.   The
 major  Impurities  In  commercial anthracene are:   carbazole  (3%  max),  pyMdlne
 (0.2%  max)r- Iron  (0.03% max),  phenanthrene  and chrysene  (IARC,  1983;  Hawley,
 1981).
 1.4.   USE  DATA
    Anthracene Is used primarily  as  an  Intermediate  In  dye production;  1t 1s
 no longer  used In the United  States  for the commercial  production of anthra-
 qulnone  for dye  usage.   Anthracene  1s  also  used  as a  component of  smoke
 screens,  as  scintillation  counter  crystals,  and  In organic  semiconductor
 research (IARC, 1983; Hawley,  1981).
 1.5.   SUMMARY
    Anthracene Is a  colorless  solid at ambient  temperatures.   It  Is  soluble
 In  a  variety of  organic  solvents  Including  ethanol,  methanol,  benzene,
 toluene and  carbon dlsulflde  (Wlndholz, 1983), but  1t Is  almost Insoluble In
water  (Pearlman   et   al.,  1984).   The  solubility   of  anthracene  In  water
decreases  slightly with  the  Increase In salt  content,  but  decreases  greatly
with the lowering of  water temperature  (HhHehouse.  1984).   This  compound 1s
susceptible  to oxidation by ozone,  peroxides  and other  oxldants (NAS, 1972).
The commercial production of  anthracene In the  United  States  Is  believed to
have stopped since 1982  (IARC, 1983),  although Us  U.S.  production was >2-20
million pounds 1n 1977 (U.S.  EPA, 1977).   In  1983,  30.458 pounds of anthra-
cene  was   Imported  Into  the   United States  (USITC.  1984).    Anthracene 1s
produced commercially from  anthracene  oil, a coal  tar fraction  boiling In
the range  of  270-360'C (IARC,  1983; Hawley,  1981).   It  1s used primarily In
0867p                               -3-                              02/11/87

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 the  production of  dye.   Also,  small  amounts  of  anthracene  are  used  as  a
 component  of  smoke  screens,   as   scintillation  counter  crystals,  and  In
 organic semiconductor research (IARC, 1983; Hawley,  1981).
0867p                                -4-                               11/17/86

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                2.  ENVIRONMENTAL FATE AND TRANSPORT PROCESSES
 2.1.   HATER
 2.1.1.    Photodegradatlon.   The  photolysis  of  anthracene   In   water   was
 studied  by Zepp and  Schlot2hauer  (1979).   It was observed by  these  authors
 that   photoreactlons   are   more   efficient   In   water   than   In  hydrocarbon
 solvents.   Besides  the  Intensity  of  solar  radiation,  which  depends on  the
 season of  the  year,  the  time of  day and the latitude of the site, the photo-
 reaction  rate  also  depends  on the  depth and turbidity of  the  water  bodies.
 In  turbid  waters,  the  photodegradatlon  rate   1s  slower because of  light
 attenuation, which  1s due  to scattering, and the  partitioning  of anthracene
 between  water  and sediment.  The  portion  of anthracene  that  may be  present
 1n  the  sediment as  a  result of  adsorption will not  photodegrade because of
 the  Inability  of light  to  reach  the  bottom.   Zepp and  Schlotzhauer (1979)
 computed  the  near-surface  half-life for direct  photochemical transformation
 of  anthracene  at 40°N latitude  by mid-day, midsummer  sun  to be -1  hour.
 Because  of  the attenuation of solar radiation,  the  average  half-life In the
 top 35 m  of water from the middle of  the Gulf of Mexico was computed to be 6
 hours.   Since  the coastal  water  near Tampa, FL,  was more turbid,  the com-
 puted average  half-life  was >1 day (Zepp and Schlotzhauer,  1979).   Besides
 direct photoreactlon,  the  Indirect photooxldatlon of  anthracene mediated by
 singlet oxygen  was  also  studied  by Zepp and Schlotzhauer (1979).  The half-
 life for  this  photosensitized oxidation  of  anthracene was computed to be 200
 hours.  Therefore, photosensitized  oxidation 1n  natural waters was concluded
 to be too slow to compete with direct photolysis.
    The  photolysis  of anthracene  1n  distilled  water  was  also  reported by
 Southworth  (1979).   Exposure of  anthracene solution  (-10  ppb) to midsummer
mid-day  sunlight  at  35°N  latitude  rapidly   degraded  anthracene  with  a


0867p                               -5-                               02/11/87

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 half-life  of  35 minutes.  Under  average  winter and summer  solar  conditions
 at  the  same  latitude,  this  corresponds  to photolytlc  half-lives  of  4.8 hours
 and  1.6  hours,  respectively.   In  most  natural  waters,  the  absorption  of
 light by  dissolved  and suspended matter and  the depth of  water  would  act  to
 reduce  photolysis  rates  considerably.   Thus,  the  photolytlc  half-lives  of
 anthracene  In natural waters  with  decadlc light absorption coefficients  of
 0.020 and  0.100, which Is due to an Increase 1n turbidity, were estimated to
 Increase by factors  of 4 and  19, respectively,  compared  with distilled water
 photolysis (Southworth, 1979).
 2.1.2.   Chemical Reactions.   The  rate  constant for the  reaction  of anthra-
 cene  with  singlet   oxygen  {*&  )   1n  benzene  at  25'C  was reported  to  be
 0.15x10*  M"1   sec"1   (Stevens  et al.,  1974).   Assuming  the  rate  constant
 In  aquatic media to  be similar and  the  concentration of  singlet  oxygen  1n
 natural water to be  10~la N  (Mill et al.,  1982),  the  half-life .for  this
 reaction can  be estimated to  be >50 days.   Therefore,  this reaction  1s not
 likely  to  be  environmentally  significant.   The reaction  of anthracene  with
 ozone,  which  may be  environmentally significant 1f  ozonatlon  1s  used  as a
method  of  disinfecting drinking  water,  was  studied  by  Kuo and  Barnes (1985).
The reaction  between anthracene and  ozone  In aqueous solution  was found to
be  extremely   fast and the  estimated  half-life was  less  than  a  few  milli-
 seconds;  however,  the  products  of  the ozonatlon  were  not reported  by  the
authors.
2.1.3.   B1odt$radat1on.   The   blodegradabHUy  of  anthracene   has  been
studied  wltlt  pure   cultures   of microorganisms,   mixed   microorganisms   and
natural  water.  Several  pure  cultures  of  microorganisms  Including  Flavo-
bacterlum  sp.,  Pseudomonas  aeruqlnosa.   Pseudomonas  putlda.   Nocardla   sp.
 (Fuhs,  1961;  McKenna,  1977),  Beljerlnckla  sp.  (Gibson,  1977), Vibrio sp.,
0867p                               -6-                               02/11/87

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 Bacillus  sp., Candida  sp.,  Arthrobacter  sp.  (Bhosle and  Mavlnkurve.  1980)
 and  Aleallgenes  faecalls  (Klyohara  et al.,  1982)  were shown  to  blodegrade
 anthracene.   Although these pure  culture studies  are  far  removed  from  the
 natural  conditions  for  blodegradatlon,   they  are  useful  In  establishing
 blodegradatlon  pathways  of  chemicals.   The  proposed pathway  for  bacterial
 catabollsra  of anthracene Is  as follows (Cernlglla,  1981; Ribbons  and Eaton,
 1982; McKenna and  Kalllo,  1965;  Subramanlan  et al., 1978;  Van der Linden and
 Thljsse, 1965):
    anthracene -» l.2-d1hydroxyanthracene -» 2-hydroxy-3-naphthaldehyde -»
    2-hydroxy-3-naphtho1c acid -» 2.3-d1hydroxynaphthalene -» salicylic acid
    The blodegradabHlty of  anthracene with  mixed microorganisms was studied
 by  several  authors.   Thorn  and  Agg   (1975)   reported  that  anthracene  Is
 biodegradable  1n   sewage treatment  plants provided  suitable  acclimatization
 can be achieved.   UUh  settled  domestic wastewater  as m1crob1al Inoculum and
 a  static-culture  flask-screening procedure,  43% of anthracene  was  found to
 be  biodegradable  In 7 days  at  an Initial concentration  of 5  ppm.   After 7
 days of acclimatization, the same  solution showed 70% degradation In 7 days.
 The corresponding  degradation  was only 26 and  30%  at  an  Initial anthracene
 concentration  of  10  ppa (Tabak  et  al.,  1981).  Lutln et al.  (1965)  used
 activated sludge from three  municipal  treatment plants as  ralcroblal  Inoculum
 and the Warburg  method as a  means for estimating  the  rate of  b1oox1dat1on.
 Anthracene  was  reported to  be  appreciably  resistant  to  blodegradatlon with
 activated sludg*  from two municipal  plants,  and degradable  with  the third
activated sludg*.   Freltag et  al.  (1985) reported only 0.3% CO.  formation
 (relative  to  applied dose)  on  Incubation  of  anthracene  for  5  days  with
activated sludge.
0867p                               -7-                               11/17/86

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     The  blodegradabllHy of  anthracene  with  natural  sediments  (Gardner  et
 al.,  1979;  Bauer and  Capone,  1985;  Schwall and  Herbes,  1979;  Herbes,  1981;
 Herbes  and  Schwall, 1978;  Lee  and  Ryan, 1983) and  natural  estuarlne  waters
 (Loe  and  Ryan,  1983;  Lee,  1977)  has  been   studied  by  several  authors.
 Several  conclusions can  be reached  from these studies.   The  blodegradatlon
 of  anthracene  1n  aquatic  media  Is  controlled  by  the  temperature,  oxygen
 content   and   accl1mat1zat1on/nonacc11mat1zat1on   of  the   microorganisms.
 Higher blodegradatlon  rates were  observed at 30°C than  at 20 and 10°C (Bauer
 and  Capone,  1985).   The  blodegradatlon  process was found to  be aerobic and
 higher oxygen  concentration up  to a  certain optimum value tended to Increase
 the  oxidation  rates  (Bauer  and  Capone,  1985).   Similarly, the blodegradatlon
 rates were reported  to be faster  with acclimatized microorganisms (Bauer and
 Capone,  1985;  Herbes and Schwall, 1978;  Lee and Ryan, 1983;  Lee, 1977).  The
 Incubation of  anthracene with  Intertldal sediment  slurries  for a reasonable
 period of  time (-1  month)  not  only produces  the mineralization product CO.
 but also produces  Intermediate  metabolites.  A large portion  of the Initial
 material  or   Us  Intermediate  metabolites   (which  could  not  be Identified
 because  14C  counting of  the  combustion  products  of  residue was used  as the
 method of  quantification)  remained  cellular  bound  (Bauer and  Capone.   1985;
 Schwall  and   Herbes,   1979).    For  example,  Incubation  of  anthracene  with
 petroleum-contaminated   sediments  for  5  days   at  12*C  produced  '42%  of
 extractable  unaltered  anthracene,  4% of CO-   and  4% of  polar  metabolites;
•30% remained  cellular bound (Schwall  and  Herbes,  1979).   The residual 20%
of  the  original  anthracene  remained  unaccounted  for.   The  half-lives  of
anthracene In  waters  and sediments  are  generally expressed  as  the complete
mineralization  half-life and  the half-life for the disappearance of Initial
0867p                               -3-                               02/11/87

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 anthracene.   Although  the  former  method  correctly  predicts  the  mineraliza-
 tion  half-life.  It does  not  reflect the loss  of  anthracene that  Is  due  to
 formation  of  Intermediate  metabolites.   Therefore,  It  always  overestimates
 the  half-life for  blodegradatlon of  anthracene.   The  latter method,  on  the
 other  hand,  may  underestimate the  blodegradatlon  half-life because  of  the
 Inability  of the quantification method  to  determine the amount  of starting
 material  1n  the  cellular  bound  part and  to  obtain  a  complete  material
 balance  for the starting material.   The  mineralization  half-life of anthra-
 cene has been reported  to be  57-210 days  In unaccllmatlzed sediments and 5-7
 days  1n oil  treated sediments  (Lee  and Ryan.  1983).   The  mineralization
 half-life  of anthracene  was  also  reported  to be  -200  days  In  oil-treated
 water and  -20-fold  higher 1n uncontamlnated water  (Lee,  1977).   The overall
 blotransformatlon   (both   CO.   and   Intermediate   metabolite   formation)
 half-life  of anthracene  In  petroleum-contaminated   sediment was  reported  to
 be -12  days (Herbes  and Schwall, 1978).  In  pristine  sediments,  the overall
 blotransformatlon half-life was  -10-fold higher  (Herbes  and Schwall, 1978).
 The overall  blotransformatlon half-life  of anthracene  In sediments contami-
 nated with  a  coal-coking  wastewater  was  -2  days.   The  anthracene transforma-
 tion rate was -20 times lower In the water (Herbes,  1981).
 2.1.4.   Volatilization.   The rates of  volatilization   of  anthracene  from
 bodies  of  water were  studied by  several Investigators.  Besides  the water
 temperatures,  the  rates  of volatilization are  dependent  on  the depth of the
water,  the  current  of the  flowing  water, the  wind  velocity above the water
and  the  nature  and  amount  of  suspended  solids  present  1n   the  water
 (Southworth,  1979).   Decreases  1n  water depths.  Increases  In  current and
wind velocity  and  decreases In absorption onto suspended particles  1n water
are expected to Increase  the volatilization  rates.  None  of  the  available
0867p                               -9-                               02/11/87

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 estimation  methods  for  the determination of evaporative half-life of anthra-
 cene   In  water  bodies,   however,  Incorporates  the  effect   of   sorptlon  on
 volatilization.   The estimated  evaporative  rate  constants,  half-lives  and
 percent  loss  that   1s  due  to evaporation  from different  water bodies  as
 estimated  from  gas and  liquid  phase  exchange  constants  and   Henry's  Law
 constant are  shown  In Table 2-1.
 2.1.5.   Adsorption.  The adsorption  of a compound  to  suspended  participate
 matter  and  sediments can  be  predicted from  Us K    value,  which 1s -26,000
 for anthracene  (Karlckhoff et a!., 1979).  This  Is  Indicative of the possi-
 bility  of  strong  adsorption of  anthracene  onto  suspended particles  and
 sediments 1n  water.  Several  Investigators  have estimated, however,  that the
 removal  rate  of  anthracene  from  water  that  1s  due to adsorption  Is  small
 compared with other  removal  processes.   Depending on the nature of the water
 body,  the percent of anthracene removal  from water  may vary from negligible
 to  18%.   The percent  removal by  adsorption  was  estimated  to be maximum 1n
 deep,  slow  moving,  muddy  water bodies  (Southworth,  1979).   Depending on the
 characteristics  of  water   bodies,  Herbes et  al.  (1980) also  estimated that
 between  2.8 and  19% of  anthracene  removal  will  take  place  by  adsorption.
 The EXAMS computer  modeling  of a  2 m  deep  eutrophlc pond  and 3 m deep river
with  an  Input  K   value  of   26,000  estimated  that  -3.3  and  0.4X,  respec-
 tively, of anthracene will be  removed by sedimentation  (Zepp, 1980).
 2.1.6.   Bloconcentratlon.   The  bloconcentratlons .of  chemicals   In  aquatic
organisms are  dependent  on  the  overall   uptake  and  elimination kinetics.
Unless an equilibrium  Is  attained between  these  two opposing processes, the
bloconcentratlon  factors  are expected  to vary.   With the  possible exception
of  the  results   of  Freltag et al.  (1982),  BCFs  for  anthracene   In different
0867p                               -10-                              02/11/87

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                                   TABLE  2-1
      Removal of Anthracene by Volatilization from Water Bodies at 25°C*
Water Velocity Wind Velocity
(ra/sec) (in/sec)
0.1 4
0.1 0.1
1.0 4.0
0.5 1.0
1 4
Depth
5 m
5 m
1 m
1 ra
25 cm
% Loss of Total
Half-Life Due to
Volatilization
14 days
29 days
16.5 hours
62 hours
4 hours
2-3
3
21
7.7
35
'Source: Southuorth. 1979; Heroes et al.. 1980
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-11-
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 aquatic  organisms  given In  Table  2-2 were obtained  under  apparent  equilib-
 rium  conditions.   Additional  data  regarding  BCFs  are presented In Chapter 6.
 McCarthy  (1983)  pointed out that  the uptake  of  PAHs Including anthracene Is
 greatly  reduced  with  sorbed  chemical   compared  with  Us  uptake  from  the
 dissolved  state.   Therefore,  natural  waters containing  anthracene   In  the
 suspended  organic  matter  1n  the sorbed state are  likely to  show  BCFs  that
 differ  from those  obtained  1n laboratory experiments  with partlculate-free
 water.   In the  case of anthracene,  the  differences  may not  be pronounced
 because  the  removal  rate of anthracene  from  water  that 1s due to adsorption
 1s  small compared  with  other  removal  processes  (see Section 2.1.5.).   It can
 be  concluded  from  Table 2-2  that anthracene moderately  bloconcentrates In
 aquatic organisms.
 2.1.7.   Overall  Removal Processes.  While   the  rate of  uptake  by  fish Is
 faster  than the  rate  of  uptake  by  partlculates,  a high  concentration of
 suspended  particles  In  water  may  offset this rate  difference.   Thus, under
 conditions  of  high concentration  of  suspended  particles, BCF  values  may be
 lower.   The removal  of anthracene from  aquatic media  will  depend  on the
 nature of  the aquatic media.   The  predicted  contributions of major processes
 In  the removal of  anthracene  from  different  aquatic media are given 1n Table
 2-3,  which indicates that,  In most  water  bodies,  photolysis  and mlcroblal
 degradation will play Important  roles  1n the loss of anthracene.  There  Is  a
 large difference,  however.  In the  predicted  half-life  of anthracene  between
 the Southworth  (1979) Investigation and the  Zepp (1980)  Investigation.  The
 former's values  are probably  underestimated  because they were derived with-
out full consideration  of  effects  of  sorptlon  on volatilization, photolysis
and mlcroblal degradation.  The  values  derived  by Zepp (1980), using  similar
 Input parameters but  using EXAMS computer model,  may not be accurate.   In  a


0867p                               -12-                              04/23/87

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                                  TABLE 2-2
              BCFs for Anthracene In Different Aquatic  OrganUrns
               Species
          BCF
    Reference
Alga (Oedoqonluro cardlacum)
Snail (Physa sp.)
Fish (Gambusla afflnls)
Golden orfe (Leuclscus Idus melanotus)

Goldfish (Carasslus auratus)
Zooplanker (Daphnla pule*)
           670
          2714
          1029
           910

           162
           917
Lu et al.t 1978
Lu et al.. 1978
Lu et al., 1978
Freltag et al.,
1982
Ogata et al., 1984
Southworth et al.,
1978
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           11/17/86

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                                                                          lABLi  2-3



                                Contributions  of Major  Processes  In Removal of Anthracene  fron Mater at  25*C During Hid*
o
cy
.^ Water Characteristics
Deep, slow and
soaewhal turbid


Deep, slow and Middy



Deep, slow and clear



Shallow, fast and clear


1
Very shallow, fast
and clear


2 • deep.
eu trophic pond


3 • deep, river



Shallow, rapidly
flowing clear strea*

Process
volatilization
adsorption
photolysis
•Icroblal degradation
volatilization
adsorption
photolysis
•Icroblal degradation
volatilization
adsorption
photolysis
•Icrobtal degradation
volatilization
adsorption
photolysis
•Icroblal degradation
volatilization
adsorption
photolysis
•Icrobtal degradation
volatilization
water borne export
photolysis
•Icroblal degradation
volatilization
waterborne export
photolysis
•Icrobtal degradation
volatilization
adsorption
photolysis

X Contribution
3
0
5
91
3
18
0
79
2
1
22
74
21
4
44
31
35
6
47
12
2.4
2.9
89
6.1
4.7
38
56
0.5
7.5
20.4
71.4

Overall Half-life Reference
(hours)
10.5 Southworth. 1979



21.6 Southworth. 1979



8.5 Southworth. 1979



3.5 Southworth. 1979



1.4 Southworth, 1979



696 Zepp. 1980



62 Zepp. 1960



1 Heroes et al.. I960

                                       •Icroblal degradation
                                                                               0.7
00

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 eutrop.hlc  pond where algae  growth will  prevent  light  penetration  into  the
 Interior  of  water,  -90%  photodegradatlon  of  anthracene  appears  to  be  an
 overestimate.
 2.2.   AIR
    The  fate  and  transport  of  anthracene  In  the  atmospheric  media  has
 received much less  attention  than In aquatic media,  because  a  multlcompart-
 ment  (six)  modeling  program conducted by  Mackay et  al.  (1985) estimated that
 >95X  of  environmental  anthracene will  reside  In  water  and <1.4  1n  atmo-
 spheric media.
    The  reactivity  of  atmospheric anthracene  will  be  largely  dependent  on
 the  state   1n  which  1t exists  In the  atmosphere.   The reactivity  of  vapor
 phase  anthracene Is  expected  to be different from Us  reactivity  In  the
 adsorbed state (Santodonato et  al..  1981).  Considering  the vapor  pressure
 of anthracene (see  Section 1.2.), the compound  Is  expected  to  exist both In
 the  vapor  and  the  partlcle-sorbed  phase  In  the  atmosphere  (Elsenrelch  et
 al., 1981).   The  experimental results of  Thrane and Hlkalsen (1981) Indicate
 that  from  78-98% of anthracene  collected from the atmosphere  exists  1n the
 vapor phase.   The reactivity  of  anthracene  with atmospheric  oxldants Includ-
 ing  OH  radical.  (L  and  NO.  has not  been  studied  comprehensively.   The
 heterogeneous  reaction  of  gas  phase 0-  and  NO-  with  anthracene  coated on
 sodium chloride was  studied by  Nlessner  et  al.  (1985),  who reported that the
 heterogeneous  reaction  of  anthracene  was  negligible with NO-  but reaction
with 03  was significant.   Both  anthrone  and anthraqulnone  were reported to
be the products of  this  reaction.  Although this  experiment points out the
possibility  of  0.   reaction  with  anthracene  1n  the atmosphere,   1n  the
absence  of  rate  data  H  cannot be used for  predicting  quantitatively the
 fate of  anthracene   In  the ambient  air  that  Is  due  to  this reaction.  The
0867p                               -15-                              04/23/87

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 rate  constant  for the reaction of gaseous  anthracene  with  hydroxyl  radicals
 at  52°C  Is  reported  to  be  112xlO~la  cra3/molecule-sec   (Atkinson,  1985).
 If  the concentration of OH  radical  1n the  atmosphere  Is  assumed to  be  10*
 radicals/cm*  (U.S.  EPA, 1980a),  the half-life of  this  reaction at  52°C  Is
 ~2  hours.  In  the troposphere  where  the  average  temperature Is <52°C  and
 part  of  the anthracene  will  exist  In  the partlcle-sorbed phase, the half-
 life may  be longer than the value estimated at 52°C.
    Based on Us  fate 1n aquatic  media,  photodegradatlon  1s expected to be a
 significant  process  1n  the  atmosphere  as  well.   The  photoreactlon  of
 partlcle-sorbed anthracene was  shown to  be  substrate-dependent  (Behymer  and
 H1tes,  1985).   For example,  when anthracene was  adsorbed onto  silica  gel,
 alumina,  fly  ash and  carbon  black  and  Irradiated  with  light from  a medium
 pressure  mercury  arc  1n a rotary  photoreactor,  the corresponding half-lives
 were  2.9, 0.5, 48  and  310 hours.   Thus.  1t appears  that both  fly  ash  and
 carbon  black stabilize  anthracene  1n the  atmosphere and  may facilitate their
 transport  from  combustion  sources.   Similar  conclusions were reached  by
 Korfmacher  et  al. (1980),  who  reported  that anthracene adsorbed on fly ash
 was resistant  to photodecoraposHlon.   Photoreactlon of anthracene  that  has
 been dispersed  Into  atmospheric partlculate matter was also  reported by Fox
 and  Olive  (1979).   These  authors  concluded  that  photodegradatlon  In  the
 atmosphere  1s a more  Important  fate  process than ozonatlon.  When anthracene
adsorbed  onto  atmospheric  partlculate  matter was  exposed  to  bright  sunshine
 for 4  days, -10% of  the compound  disappeared.   The  authors  concluded that
besides  oxidation products  (anthrone, anthraqulnone),  photolysis  may also
produce polymeric condensed  products.   Therefore,  the following conclusions
can be  reached  regarding  the  photoreactlon  of anthracene  1n  the atmosphere:
1) the majority of  anthracene that will  be  present 1n the atmosphere 1n  the


0867p                                -16-                              04/23/87

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 unadsorbed  gas  phase  will  photodegrade  by  atmospheric  sunlight  with  a
 half-life of  a few hours, as  1n  the  case  of solution phase anthracene  (see
 Section  2.1.1.  and  Korfmacher   et   al.,   1980);   2)  the   relatively   small
 fraction  of  atmospheric  anthracene  that  will exist  In  the partlcle-sorbed
 state will be  more  resistant to photodegradatlon and may degrade  by sunlight
. with a half-life of days.
     Atmospheric anthracene can also  be removed  by physical processes.  The
 removal of atmospheric  anthracene  In  the  Great Lakes ecosystem was  reported
 by Elsenrelch  et al.  (1981).   Both dry deposition  of  the  vapor  and  particle-
 bound  anthracene   and  wet  precipitation   through   rain  and  snow  occurred;
 however, dry deposition was  found  to  be more Important than wet  deposition.
 Llgockl et al. (1985a) concluded that particle scavenging was  less  Important
 than  gas  scavenging  of  atmospheric   anthracene.   The half-lives  for  these
 physical removal mechanisms were  not  provided by either study; however,  the
 removal of atmospheric  anthracene through  these physical  mechanisms  appear
 to be  less significant  than  Us  removal  through blotlc processes.   Finally,
 Lunde  and  Bjoerseth  (1977)  reported  that   the  concentration  of  anthracene
 that  originated  from trajectories  from Western Europe  contained  -4  times
 more  anthracene  than  samples  with   trajectories   from  northern  Norway  or
 stationary air from southern Norway.   This  result  suggests that at  least  a
 part of atmospheric anthracene Is  stable  enough 1n  the atmosphere  to travel
 long  distances.   Perhaps  the part  of  anthracene  1n the atmosphere  that
 existed 1n the partlcle-sorbed phase,  remained nonreactlve towards  abiotic
 processesr and was not  removed  by  physical processes  underwent  this  long
 distance transport  1n the  atmosphere.
 0867p                               -17-                             04/23/87

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 2.3.    SOIL
    The fate of anthracene  In  soils  Is studied even  less  than Us  fate  In
 the atmosphere.  Its  fate  In  soil  can  be  predicted,  however,  from  the knowl-
 edge  of Us fate  In  aquatic  media.   The  three processes that  are  Important
 1n  the  loss  of anthracene from aquatic media  are  photolysis,  blodegradatlon
 and volatilization.   Because  of  light  attenuation  and  scattering,  photolysis
 cannot  be  an  Important   process  for  the  loss   of  anthracene  beyond  the
 surflclal  layer  of soils.  It has been shown  by  Bossert et al. (1984)  that
 oily  sludge  containing anthracene and other  polynuclear aromatic  compounds
 when  Incorporated  1n  a sandy loam soil underwent  loss  of anthracene.  Since
 multiple applications  of  sludge  to soil were made  at  a certain Interval  with
 an  Intervening  nonappHcatlon  period,   1t  1s   difficult   from   the  data
 presented  to  estimate the degradation  half-life of  anthracene 1n  the soil.
 On  the  basis of the  decay  of the.chemical  after   Us  first  application,  the
 half-life  1s  -32   days.    The   authors concluded  that  blodegradatlon  and
 abiotic  processes   accounted  for  observed   decreases  In the  concentration.
 The undefined  abiotic  processes  were  responsible  for  <50%  of the  loss  of
 anthracene  from the  soil.   Some  of  the   loss was speculated  to  be  due  to
 volatilization.
    The possibility of leaching  of anthracene from soil to  groundwater  will
depend  on  soil type.   The K    value  for  anthracene  Is -26,000  (KaHckhoff
et al., 1979).   This  Indicates  that anthracene will  be adsorbed  strongly to
soil and the compound  may  degrade  before  K  reaches  groundwater.   Filtration
of  polluted surface  water containing anthracene  through  sandy  soil  at  a
residence  tine  of  -100 days  did  not  completely eliminate anthracene 1n the
filtered water  (P1et   and  Morra,  1979).  The  passage  of anthracene  through
the soil  was  explained as a breakthrough  of the  chemical  because  of the
saturation of active sorptlon sites.

0867p                                -18-                              04/23/87

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 2.4.   SUMMARY
    The  fate  and transport  of anthracene 1n aquatic media  has  received  much
 more  attention  than  In any  other media, because a  mu HI compartment  modeling
 program  conducted  by  Hackay  et  al.  (1985)  estimated  that >95%  of  environ-
 mental  anthracene  will  reside  1n  the  aquatic  compartment.    The  fate  and
 transport  of  anthracene 1n  surface waters  will  depend on  the  nature  of  the
 water.   In most waters, the  loss  of  anthracene Is mainly  due  to photolysis
 and blodegradatlon (Hackay  et al.,  1985);  however. In a  very  shallow, fast-
 flowing  clear  water,  volatilization and photolysis will  pla-y  dominant roles
 In  determining   the  fate  of  anthracene  (Southworth,   1979).   In deep,  slow
 flowing  and  muddy  waters,  mlcroblal  degradation and  adsorption  may  account
 for   the  major  losses  of   anthracene  from  water   {Southworth,   1979).
 Therefore, the  half-life of anthracene  1n natural  surface waters will  depend
 on  the nature  of the water  bodies.   In  very  shallow,  fast-flowing  and clear
 water, Us half-life may be -1 hour  (Southworth.  1979; Herbes  et al.,  1980).
 On  the   other  hand,  the  half-life may  be  as  high  as  29 days  In  a  deep
 eutrophlc  pond   (Zepp,   1980).  Anthracene  will  moderately  bVpconcentrate In
 aquatic organisms.
    In air,  anthracene Is  expected to  be  present  both 1n  the  vapor  and the
 partlcle-sorbed  state.  Over  78% of atmospheric  anthracene may be present In
 the  vapor  state  (Thrane   and  Mlkalsen.   1981).   Both  chemical  processes
 Including  0.   and  OH radical  and   photochemical  reaction   will  degrade
atmospheric anthracene  (Nlessner et al., 1985;  Atkinson,  1985; Korfmacher et
al.,  1980; Bthyaer  and HHes, 1985).   The degradation  of  vapor phase atmo-
spheric  anthracene 1s  expected to be  faster  than  partlcle-sorbed anthracene
 (Santodonato  et al.,  1981).   The  atmospheric  half-life  of  anthracene may
0867p                               -19-                             04/23/87

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 vary  from hours  to  days  (Atkinson,  1985;  Korfmacher et  al.,  1980;  Behymer
 and  Hltes,  1985;  Lunde  and BJeorseth,  1977).   The  long  range  transport  of
 anthracene  observed  by  Lunde  and Bjoerseth  (1977)  Indicates  that partlcle-
 sorbed anthracene may have a half-life of the order of days.
    The  fate  and  transport of  anthracene In soils Is not well studied.  Both
 blodegradatlon  and  abiotic  processes  will  degrade  anthracene  1n  soils
 (Bossert  et al.,  1984).   The  half-life of  anthracene 1n soil may be -1 month
 (Bossert  et al.,  1984).   Anthracene  may  not leach from most soils because of
 Us!high K   value; however.  It may  leach  through  soils  that  have attained
 the breakthrough capacity  for anthracene sorptlon (P1et and Horra, 1979).
0867p                                -20-                              02/11/87

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                                 3.  EXPOSURE
 3.1.   WATER
    Anthracene  Is  ubiquitous  In   the   aquatic  environment.   It  has  been
 detected  1n Industrial effluents,  1n  run-off waters,  In  surface water  and
 sediments.  In  groundwater,  and 1n drinking water.  The  Industrial  effluents
 that  are most  likely  to  contain  polynuclear  aromatic compounds  Including
 anthracene  are wastewaters  from  the   synfuel  Industry,  shale oil  plants,
 petroleum processing  plants, other  Industries  using coal  derived  products,
 wastewater  treatment  plants  and aluminum reduction  plants  (Bjoerseth  et al.,
 1978;  Gammage,  1983;  Kveseth  et   al..  1982); however,  anthracene has  been
 reported  1n effluents from  only a few  Industries.   Anthracene at  a  concen-
 tration  range  of  <13-105  ng/i was  reported  In the  effluent From a  sewage
 treatment plant In Norway  (Kveseth et  al.. 1982).  Other  Investigators have
 reported  anthracene  at  a  concentration  range  of  <0.03-0.84 yg/i   In  the
 effluent from coke oven plants  (Walters  and  Luthy.  1984; Grlest,  1980).  The
 detection of anthracene was  also  reported In urban run-off  waters.   Cole et
 al. (1984)  monitored  run-off waters from 15 U.S.  cities  and detected an 8%
 frequency of  anthracene and a concentration range of  1-10  ug/l.   Anthra-
 cene  was  detected  at  trace  levels  1n  the water of  a   small  segment  of the
 Delaware  River,   north  of  Philadelphia  (Kites,  1979).   Dewalle and Chlan
 (1978) analyzed water  from the Delaware  River and  Us  major tributaries and
 detected  anthracene  at  a   concentration  of >1  i»g/i  with  a frequency of
 3X.   Samples  of water  taken from  the  Tennessee  River   In  Calvert  City, KY,
were  reported  to  contain  anthracene  at  a  concentration  of  12.1   vg/l
 (Goodley  and  Gordon,  1976).   Since 1980,  U.S.  EPA  collected  776   ambient
water  samples   for  the  analysis  of  anthracene  (Staples  et al.,   1985).
0867p                               -21-                              04/23/87

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 Anthracene  was  detected In  4%  of  the samples and at  a  median concentration
 of  <10  vg/l.   Anthracene  was  also  reported  In  surface  wastes  in  England
 (Fielding  et  al..  1981) and  In Germany  (Malle.  1984).   A  number of  Investi-
 gators  reported the detection of  anthracene  In  surface water  sediments.   A
 few  authors  used  the  sediment  analysis  to  establish  the  source of  these
 compounds  1n  the  environment  and  the  mode  of this  transport  In  aquatic
 environment  (Windsor and  HUes,   1979;  Eadle et  al.,  1982;  Tan and  HeU,
 1981;  Sporstol  et  al.,  1983;  Boehm  and  Farrlngton,  1984).   Unseparated
 anthracene/phenanthrene at  a  concentration as  high as  6.4  mg/kg was  reported
 In a  sediment  sample from an estuary between  England and Hales (John et al.,
 1979).
    Anthracene  has  been  reported  1n groundwater   from  a  few  contaminated
 sites.   For  example. Rostad  et al.  (1985) reported the  quantitative detec-
 tion  of  anthracene  In groundwater  from a coal  tar  waste aquifer In St. Louis
 Park,  HN.   Bed lent  et  al.   (1984)  reported   the  detection  of  up  to  168.6
 tig/I   of  anthracene   In   groundwater   from  a  creosote  waste   site  In
 Conroe, TX.
    The  detection  of  anthracene  In Canadian  drinking  water  derived  from
 Great Lakes was reported by Williams et  al.  (1982).   The combined concentra-
 tion  of  anthracene/phenanthrene (unseparable)  in these waters  ranged between
 0.6 and  1269  ng/l.  The highest  concentration was  obtained In  a water from
 Sault  Ste.   Marie collected during  the summer.  Anthracene  has also been
 reported to be present  1n  Nordic   drinking water at  a  concentration  range of
0.04-9.7  ng/t   (Kveseth   et  al.,   1982).    In  Japanese  drinking  water,
Shlnohara  et  al.  (1981)  reported  the  detection  of  1.7  vg/l  of   combined
anthracene and  phenanthrene.  P1et  and  Horra (1973)  reported the detection
of a  maximum  of   30 yg/l  of anthracene  1n  bank-filtered  tapwater  In the


0867p                                -22-                              02/11/87

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Netherlands.   Finished  waters  from  13  different  locations  throughout  the
United  States  were  analyzed for anthracene (Sorrell et al.,  1980).   Anthra-
cene was not detected  In any of these drinking water samples.
3.2.    AIR
    The sources  of  PAHs Including  anthracene  In  the  atmosphere have  been
reported  extensively  (Santodonato  et  al.,   1981;  Oalsey  et  al.,  1986;
Gammage,  1983).   Some of  the  conventional  sources are vehicular  emissions,
coal  burning,  oil  burning,  wood  combustion,  coke plants, aluminum  plants.
Iron  and  steel works,  foundries,  ferro-alloy plants and  municipal  Inciner-
ators.  Some of  the more common modern  sources  of PAHs  Including anthracene
are  synfuel plants  and  oil  shale  plants.   The ratios  of  anthracene  and
benzo(a)pyrene to benzo(e)pyrene and the concentrations  of benzo(a)pyrene In
partlculate from various sources are given 1n Table 3-1.
    The concentration  of  anthracene In municipal  fly ash was  reported  to
vary  between  4  and  380  vg/kg  (EIceman  et  al.,  1981).    The  workroom
atmospheric concentration  of anthracene  1n  an aluminum reduction  plant has
been  reported  to  be  as   high  as  33.1  yg/m*  (Bjoerseth  et  al.,  1978).
Personnel   monitoring  of  an anode plant  showed  that  the concentration  of
partlculate anthracene varied  from none detected  for pitch dust  sweepers to
1.9  yg/ra*   for  pitch  bin   workers  (BJoerseth  et al..  1978).    The  concen-
trations  of  atmospheric  combined  anthracene  and  phenanthrene  Inside  a
solvent refined  coal pilot plant  facility  was reported to vary  between 1.8
and  43.2  wfl/B*  (Ganmage.   1983).   Personal  air  samples  taken  In  the coal
preparation area  of  the solvent  refined  coal  pilot  plant  showed  combined
anthracene/phenanthrene  concentrations  of   none  detected  to  15.7   ug/m'
(Gammage,   1983).    The  simulated  Incineration  of  poly(v1ny1  chloride)  at
850°C was  qualitatively shown  to  produce anthracene  (Hawley-Fedder  et al..


0867p                                -23-                              04/23/87

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00
o»
                                                       TABLE  3-1

                       Ratios of Anthracene to Benzo(e)pyrene. Benzo(a)pyrene to Benzo(e)pyrene
                      and the Concentrations of Benzo(a)pyrene from Various Sources of Emission*
1
ro
.»
1
Ratios and
Concentration
Anthracene to
benzo(e)pyrene ratio
Benzo(a)pyrene to
Tunnel
2.2
1.2
Residential
Coal-Burning
0.4-7.5
0.6-2.0
Residential
Oil-Burning
0.6
0.9
Coke Oven
0.2-6.9
1.0-2.3
Auto
Exhaust
6.9-17
0.3-1.4
Wood
Combust Ion
1.1-20
0.5-3.0
     Benzo(a)pyrene
     concentrations  In
     parttculate matter
     from various  sources.
     ppra (mg/kg)
66-500
10-600
NR
1400-5BOO
NR
3-870,900
      'Source:  Datsey et  al.,  1986

      NR = Not reported
CD

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 1984).   The concentrations of  PAHs  1n the  air  of  three different  types  of
 wood-heated  saunas  were reported by  Hasanen  et  al.  (1984).   The  anthracene
 concentrations  1n sauna air varied from 0.3-25.2  pg/m3.
    The  concentrations  of anthracene  In  ambient air  In some cities  In  the
 United  States  and  around  the world  have  been reported by  several  Investi-
 gators.   Table 3-2  shows  the ambient atmospheric  concentrations  of  anthra-
 cene  In  various  locations.   It  1s  evident  from Table 3-2  that  the  atmo-
 spheric  concentrations  of anthracene (even  after  consideration  of  phenan-
 threne  contribution) measured  for  Osaka,  Japan,  In  1977-1978  are  substan-
 tially  higher   than  the  other  reported  values.   Since the  authors used  a
 small packed (6 ft.) GC column  and  flame  1on1zat1on detecter for quantifica-
 tion  of  compounds,   It  Is  likely  that complete  separation  of  some compounds
 was not  achieved  by this  analytical  technique.  Grosjean (1983)  demonstrated
 that  the  atmospheric   anthracene  concentrations  showed  both  seasonal  and
 diurnal  variations,  with anthracene concentrations  higher  In  winter  and
 during  the  night.   Although   suitable  data  were  not  available on  anthracene
 for comparison, Grosjean  (1983) estimated  that  the  levels  of other  PAHs In
 Los Angeles air did  not significantly change during the last decade.  If one
 assumes  that  the mean  level  of  anthracene  Is  similar to Los  Angeles  air
 (mean  of 0.54  ng/m»)  and that  an  adult  Individual  Inhales  20 m»  air/day.
 the average dally Intake of anthracene from Inhalation Is 11 ng.
 3.3.   FOOD
    The  levels  of anthracene  In different  foods  have been studied much  less
 extensively than the levels of  some  other PAHs,  such as benzo(a)pyrene.  The
 lack  of  evidence   for  carclnogenlcHy  of  the   compound   (IARC,  1983)  and
analytical  difficulty  In  quantifying anthracene  may  have  contributed to the
 lack of  data pertaining to Its  level  1n foods.  Anthracene has  been  reported


0867p                               -25-                              02/11/87

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                                  TABLE 3-2
     Ambient  Atmospheric Concentrations of Anthracene 1n Various  Locations
    Location
  Year
 Sampled
   Anthracene
  Concentration
     (ng/mj)
      Reference
Columbia, SC
Savannah River
Plant, SC
Gainesville, FL
Jacksonville, FL
Portland, OR
Los Angeles. CA
Budapest. Hungary
Singapore
Osaka, Japan

Osaka, Japan
1981-1982    0.3->4.2
1982-1983    0.09->0.2
NRa
1984
1981-1982
1971-1972
1.0
6.0
2.8
0-4.82 (0.54)b
4.4-618 (61.5)b
1983         <0.1
1981-1982    0.17-0.57 (0.32)°

1977-1978    52.1-294.5C
Keller and Bldleman.
1984
Keller and Bldleman,
1984
Kerkhoff et al., 1985
Kerkhoff et al., 1985
L1gock1 et al., 19855
Grosjean. 1983
Kertesz-Sarlnger and
HorUn, 1975
Ang et al.. 1986
Matsumoto and
Kashlmoto. 1985
Yamasakl et al.. 1982
aThe year  of sampling was  not reported  by  the authors,  but appears  to  be
 1982.
bThese  are the wan concentrations.
cThe  reported  concentrations  were   for  the   combined   concentrations   of
 anthracene and phenanthrene.
0867p
               -26-
                                   11/17/86

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 to  be  present \r\ smoked foods,  liquid  smoke,  charcoal-broiled  steaks  (Fazio
 and  Howard,  1983)  and In  edible  aquatic  organisms  collected  from  certain
 contaminated  waters.   The  levels of anthracene In different  foods  are  given
 In Table  3-3.
     It  Is evident from Table  3-3  that data regarding the  levels  of  anthra-
 cene  In a  few  foods  have  been  reported,  but no data  on the level  of  this
 compound  In food composites used  by  an Individual  In the  United  States  are
 available.   Until  such data  are available.  It  Is  not possible  to estimate
 the human Intake of anthracene through consumption of foods.
 3.4.    SUMMARY
    Anthracene  Is  ubiquitous  In the  aquatic  environment.   Anthracene at  a
 concentration  range of  <13-105 ng/i  was  reported  In the  effluent  from  a
 sewage  treatment  plant 1n Norway  (Kveseth  et  al.,  1982).  It  was  also
 reported  1n  the concentration  range  of  <0.03-0.84  wg/l  In  the  effluent
 from coal oven  plants  (Halters and Luthy,  1984;  Grlest,  1980).   It has been
 reported  to be  present 1n  several  surface waters (HHes,  1979;  Dewalle  and
 Chlan,  1978;  Staples   et   al.,  1985).    A  maximum  concentration  of  12.1
 tfg/l was  reported  In  the  water from  Tennessee  River 1n  Calvert  City,  KY
 (Goodley and  Gordon. 1976).   In  general,  anthracene  occurs  In ambient waters
 at  a  frequency  of  4%  and  at  a median  concentration  of <10  vg/i (Staples
 et al..  1985).   Anthracene  has  been  reported  to be present  In  groundwater
 front a  few  contaminated sites.   Bed lent  et al.  (1984) reported the detection
 of  up   to  166.6 v
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                                  TABLE 3-3

                     Anthracene Levels In  Different  Foods
              Food
    Anthracene
   Concentration
  '  Reference
Electric broiled
Japanese horse mackerel

Gas broiled Japanese
horse mackerel

Charcoal-broiled steaks
Barbecued ribs
Mussel composite (U.S.)
(M. edulls and M. callfornlanus)

Nigerian-preserved
freshwater fish

Mussel 1 (Greece)
(H. galloprovlnclalls)

Fish (U.S.)

Clam (Australia)
(Trldacma
     0.2-1.9


     2.0-2.3


     4.5


     7.1


     7.9-32*


     0.20-30.1


     8-9


     <20-100*

     <3.2
Fazio and Howard,
1983

Fazio and Howard,
1983

Fazio and Howard,
1983

Fazio and Howard,
1983

Galloway et al.,
1983

Afolabl et al..
1983

loslfldou et al.,
1982

Devault, 1985

Smith et al.. 1984
•These are values for combined anthracene/phenanthrene concentrations.
0867p
-28-
           11/17/86

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drinking water  In  Sault  Ste.  Marie  (Williams  et  al.,  1982).   Finished  waters
from  13 different  locations  throughout  the  United  States,  however,  failed  to
show  the presence of any anthracene (Sorrel 1 et al.,  1980).
    The concentrations  of anthracene  In  ambient air  In  some cities  In  the
United States  and  around the world have been  reported.   The  mean  concentra-
tion  of anthracene In the air  of Los Angeles during  1981-1982  was  reported
to  be  0.54  ng/m*  (Grosjean,   1983),  whereas  Its  mean  concentration  In
Osaka,  Japan,  during  the  same  period  was  reported  to  be  0.32   ng/m3
(Matsumoto  and  Kashlmoto.   1985).   It  has  been  demonstrated  by  Grosjean
(1983) that  the  atmospheric  anthracene  concentrations  show both seasonal  and
diurnal variations,  with the anthracene  concentration higher  In  winter  and
during the  night.   Although  suitable data  were  not available  on  anthracene
for comparison,  Grosjean (1983) estimated  that  the  levels of  other PAHs  In
Los Angeles  air  did  not  change  significantly  during  the  last decade.   Based
on  the  assumptions that  the mean  level  of anthracene  1n  U.S. air Is  0.54
ng/m*  (same  as concentration  In Los Angeles)  and that  an adult  Individual
                                                               ^
Inhales 20  m*  air/day,   the  average dally Intake  of  anthracene from Inhala-
tion  1s 11  ng.
    Anthracene  has been  reported  to  be  present  In  smoked  foods,  liquid
smoke, charcoal-broiled  steaks   and  edible  aquatic organisms  collected  from
certain contaminated waters  (Fazio  and  Howard,  1983;  Galloway et al.,  1983).
For example, the concentrations  of  anthracene In charcoal-broiled steaks and
barbecued ribs  were  reported  to be  4.5  and 7.1  yg/kg.  respectively  (Fazio
and Howard,  1983).  The  U.S.  National  Mussel  watch program collected mussels
from  >100 sites  on the  East, West  and  Gulf coasts (Galloway  et al., 1983).
0867p                               -29-                              02/11/87

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 The  concentration   of  anthracene   In  these  mussel  composites  was  7.9-32
 vg/kg (Galloway  et  al.,   1983).   Until data  on the  level  of  this  compound
 In  food  composites  used by an Individual  in  the  United  States  are  available,
 It   Is  not  possible  to   estimate  the  human  Intake  of  anthracene  through
 consumption  of  foods In the  United  States.
0867p                                -30-                              02/11/87

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                             4.  PHARHACOKINETICS
 4.1.   ABSORPTION
     Excretion  data  suggest  that  gastrointestinal  absorption of  anthracene
 may  be relatively  low.   As  detailed  1n  Section 4.4., 53-84% of  anthracene
 Ingested  from diets  containing  0.2-1.0%,  and 64-74%  of  anthracene  adminis-
 tered  by  stomach tube at 200 ing/rat were  eliminated  1n the  feces  by rats  In
 2-3  days  (Chang,  1943);  urine was  not  analyzed and biliary excretion was not
 measured.  The amount  of  anthracene  In the feces was  determined  gravimetric-
 ally.  No  Information was available for low-dose 1ngest1on of anthracene.
     [9-14C]Anthracene  (1  ntnol  suspended  In  10%  OMSO In  0.9%  saline)  was
 administered  to  24 female F344/CM rats 1n a  single  Intratracheal Instilla-
 tion  (Bond et a!., 1985).  Groups of  3 rats  were sacrificed after  1,  3,  6,
 12,  24,  48,  72  and 96  hours  for determination  of  amount  of 14C remaining
 1n the lungs.  Clearance of 14C from  the lungs was  Diphasic, with  99.7 and
 0.3%  of  the  administered  radioactivity cleared with half-times  of  0.1 and
 25.6  hours,  respectively.  PAHs,  In general,  are  highly llpld  soluble and
 are  absorbed  readily  from  the  gastrointestinal  tract and  lungs  (U.S.  EPA,
 19805).
 4.2.   DISTRIBUTION
    Pertinent  data regarding  the distribution of anthracene  could  not  be
 located In the available literature as cited 1n  the Appendix.
 4.3.   METABOLISM
    Metabolites  resulting  from  monooxygenase  attack at  the  1,2-bond  of
 anthracene have been  Identified  In  the  urine  of  rats  and rabbits  treated
 with anthracene  1n diet  (Sims,   1964;  Boyland  and  Burrows,  1935;  Boyland and
 Levl.  1935) and  1n ht vitro  studies  that  Incubated anthracene with  rat  liver
mlcrosomes (Akhtar  et  al., 1979).   The 1,2-d1hydrod1ol of anthracene  appears


 0867p                                -31-                              04/23/87

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 to  be the major  metabolite  (Akhtar  et al.,  1979).   Products  resulting from
 oxidation  at the 9- and  10-posltlons  of  anthracene were  also  Identified  In
 rat  urine In  the in vivo  study  (Sims,  1964),  but  not j_n  vitro  (Akhtar  et
 al.,  1979),  suggesting  possible nonhepatlc  origin;  these metabolites Include
 3,lO-d1hydrod1ol   and   2,9,10-trlhydroxyanthracene.    The   metabolites  are
 excreted at  least In part as glucuronlde or sulfate conjugates (S1ms, 1964).
 4.4.   EXCRETION
    Groups of  four  male  white  rats  were fed diets that contained 0.2, 1.0 or
 1.0%  anthracene In  two  1-hour feedings  during  the same  day.  (Chang, 1943);
 total  Intake  was  270,  605  and  830  mg  anthracene,  respectively.   Feces
 collected  during  the 2  days  Following administration  contained S3,  82  and
 84% of  the Ingested anthracene, respectively.   Anthracene In  aqueous starch
 suspension was  administered to  two male white rats  by stomach tube at a dose
 of  200  mg  (Chang.  1943).   Feces  collected during  the  3 days  after dosing
 contained  64  and  74% of  the  anthracene administered;  the amount  of anthra-
 cene  1n  the  feces  In  the  above experiments,  however,  was determined gravl-
 metrlcally and  the urine was not analyzed.
    Guinea  pigs  Injected  Intravenously  with  a  colloidal  suspension  of
 anthracene  showed  uncharacterlzed  fluorescent  materials   In  the  bile  and
 urine within 1  hour  (Peacock,  1936).   A secondary review of this study (U.S.
 EPA,  1981) Indicated  that  additional  Information  regarding  this  study was
 not available.
4.5.   SUNKABY
    Limited  Information  1s available  regarding  the  pharmacoklnetlc  profile
of  anthracene.   Gastrointestinal   absorption  may   be  poor,   as   53-84% of
anthracene administered  by  diet or stomach  tube was  eliminated In  the  feces
by rats  In 2-3 days (Chang,   1943);  however, urinary  and biliary  excretion


0857p                               -32-                              04/23/87

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were  not  measured.   Radioactivity from single Intratracheal Instillations of
14C-anthracene  was  cleared  from  the  lungs   In  a  blphaslc  manner  with
half-times  of  0.1  hours (99.7% of dose) and  25.6 hours  (0.3% of dose) (Bond
et  al.,  198S).  The  distribution  of  anthracene to tissues does not appear to
have  been  Investigated.   Metabolites  resulting  from   epoxldatlon   at  the
1,2-bond  or  oxidation  at the 9- and  10-posHlons  have  been Identified In hj_
vivo  and .In  vitro  studies  with  rats  (S1ms,  1964; Akhtar  et  al..  1979).
Trans-1,2-dlhydroxy-l,2-d1hydroanthracene and  sulfate  and glucuronlde conju-
gates consistent with  the  formation  of anthracene-1,2-oxlde appear to be the
major products.   Orally administered anthracene  appears  to be eliminated by
rats  primarily  (53-84%) In  the  feces (Chang, 1943).  Metabolites of orally
administered anthracene have been detected In  the urine of  rats  (Sims, 1964).
0867p                                -33-                              04/23/87

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                                  5.   EFFECTS
 5.1.    CARCINOGENICITY
    A  group of  28 fourteen-week-old  801  or  BOIII  rats  of unspecified  sex
 were  given  diets   that  Initially contained  5  mg,  and  later  (not  further
 specified)  15  mg of  "highly  purified"  anthracene  In oil  on 6  days/week  for
 78 weeks  (Schmahl,  1955).   The  total  dose  was 4.5  g/rat and the animals  were
 observed  for life.   Mean  survival  time was  700  days.  Tumors developed  In
 2/28  rats and consisted  of a  liver  sarcoma  after  18  months  and  a  uterine
 adenocardnoma after  25  months.  A control group was  not  used  In  this  study
 and the tumors were not ascribed to treatment.
    Single  direct  Injections  of heat-liquified  beeswax-trlcaprylln  (1:1)
 mixture  containing 0.5  mg  anthracene  Into  the lungs  of  3- to  6-month-old
 female  Osborne-Mendel  rats  did  not  Induce keratlnlzlng  squamous  metaplasia
 or epldermold carcinomas at the pellet  site after  4-16 weeks (8 rats).  17-29
 weeks  (1  rat)  or 43-55 weeks  (28 rats)  (Stanton et  a!.,  1972).   Nonspecific
 granulomatous  reactions  occurred  In  all  of  these  animals.   Treatment  of
 several  groups  of  rats  with  5-200  yg  3-methylcholanthrene under the  same
 experimental conditions  produced pulmonary epldermold  carcinomas  within the
 first year.
    Anthracene has  also  been  tested for cardnogenldty  by skin  application
with and  without ultraviolet  radiation  In  nice.  In skin Initiation-promotion
assays with «1c»,  by  subcutaneous and  Intraperltoneal  Injection In rats, and
by Implantation  Into  the brain  or eyes  In rabbits  (Table 5-1).  The results
of the  skte*app11cat1on studies  with  anthracene do not  provide  evidence of
cardnogenldty, but  contradictory results were  obtained  when anthracene was
applied to  skin  together with exposure to  ultraviolet radiation.   Initiating
activity  was  not  Indicated In  the mouse  skin  Initiation-promotion assays.


0867p                                -34-                             02/11/87

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                                                                                TABU 5-1

                                                 Dermal. Injection and Implantation Carclnogentclly Assays of Anthracene
o
CD
       ioute
                    Species/     No.-/Sex
                                               Purity
                                   Treatment
                                                              Duration
                                                                                                                       Effects/Cements
                                                                                                                                                      Reference
     Skin
     Skin
     Skin
     Skin
     Skin
en
 1    Skin
     Skin
     Skin
                   mouse/NR      100/NJ
                   •ouse/NR      41/ltt
                   mouse/NR       SO/MR
                   mouse/Swiss    S/f
                   •ouse/NR
                   •ouse/NR
                   •ouse/NR
                     ouse/NR
                                  44/NR
44/NR
100/NR
                                 NR/NR
NR



NR




NR


NR




NR



NR




NR



NR
^   Skin
-u
^
_j
^j
v.
CD	
                   mouse/Skh:     24/mtxed
                   hatrless-1
                                             NR
dose and number of appltca-       NR
ttons not specified; 4OX solu-
tion In lanolin

dose and number of appllca-       life (133
ttons not specified; unspect-     days average)
fled solutions In water.
beniene or sesame oil

dose not specified; 0.3X solu-    732 days
tlon In beniene twice weekly

dose not specified; IOX solu-     life
tlon In acetone 3 times/week      (10-20 months)
on the back
dose not specified; 5* solu-      life
tton In petroleum jelly-olive     (II months)
oil 3 times/week on the ear

treatment as above but with       life
ultraviolet radiation (>320 nm)   (10 months)
for 40 or 60 minutes. 2 hours
after skin application

treatment as above but mice       life
received ultraviolet radiation    (10 months)
for 90 minutes

dose and number of appllca-       NR
ttons not specified; 10X solu-
tion In petroleum Jelly-olive
oil followed by unspecified
exposure to ultraviolet
(320 405 nm) alone or with
visible light
                         0 or 4 Mg tn methanol once        36 weeks
                         dally, followed by ultraviolet
                         (>290 nm) for 2 hours. & days/
                         week
                                                                             No skin tutors; 45 and 6 alee  sur-
                                                                             vlved >6 Months and >160-days.
                                                                             respectively

                                                                             No skin tumors; dlbeni(a.h]anthra-
                                                                             cene was tumor tgentc In same study
No skin tumors; 34 and 16 alive at
6 months and 1 year, respectively

No skin tumors; benio(a]pyrene
Induced high Incidences of skin
paplllomas and carcinomas under
the same conditions

No skin tumors; 1/44 alive after
II months; primary report not
available

No skin tumors; 5/44 alive after
7 months
No skin tumors; 7/100 alive after
7 months
•High Incidence* of skin tumors.
Including many carclnonas. was
observed after 5-8 weeks; no lumors
tn controls treated with anthracene.
ultraviolet or ultraviolet with
visible light; primary report  not
available; unusually short latency
and Inadequate hlstopathology
reporting noted by IARC (1993)

Incidence of skin tumors not sig-
nificantly Increased tn treated
group; survival was 20/24 and  19/24
In controls and treated groups
                                                                                                                                                    Kennaway.
                                                                                                                                                    1924a,b
                                                                                                                                                    Pollta. 1939
                                                                                                                                                    Bachiuann
                                                                                                                                                    et  al..  1937

                                                                                                                                                    Uynder  and
                                                                                                                                                    Hoffmann.  1959
                                                                                                                   Hlescher.  1942
                                      Hlescher. 1942
                                                                                                                                                    Mlesther,
                                                                                                                                                    Heller. 1950
                                                                                         iorbes el a)..
                                                                                         1976

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                                                                            TABLE  S-l (conl.)
g     Route
                    Species/     No.'/Sex     Purity
                                                 Treatment
                                                              Duration
                                                                                                    Effects/Cooaenls
                                                                                                                                                      Reference
     Sktn
MOuse/S
20/NR
                                              NR
     Skin
aouse/CD-1
30/f
o«
i
     i.e.
rat/NR
10/NR
                                              chromato-
                                              graphlc-
                                              ally
                                              purified
                          MR
                   rat/Utstar     5/NR
      i.e.
ral/BOJ
and BOH I
                                  10/NR
                   rat/BOl or     10/NR
                   BOI1I
            highly
            purified
                          highly
                          purified
two applications (0.3 ml of
0.5X solution In acetone per
application) with a 30-*tnule
Interval 3 times /week for a
total of 20 applications (30
•g/anlaal total); 18 weekly
applications of croton oil In
acetone (0.3 n) consisting of
1/0. in. 2/O.OBSX and 15/0. 17X
croton oil. beginning 25 days
after the first anthracene
application; controls received
the same treatment with croton
oil only.
single application of 10
(I7B2 tig) In beniene followed
I week later by S >*ol IPA
twice weekly for 34 weeks;
controls received the same
treatment with TPA only

weekly Injections of 2 ml of
O.OSk suspension In water for
life (103 •g/anlaal •axkma
total dose)
                                       S *g In sesame oil. once
                                       weekly for 6 or J weeks
                                                           20 *g In  unspecified oil  once
                                                           weekly for  33 weeks
                         20 «g In unspecified oil once
                         weekly for 33 weeks
                                                                                            25 weeks
                                                                                            35 weeks
                                                                         >18 Months
                                                                                            10 Months
                                                                                            life
                                                                                             life
                                                                                             (aean -2 years)
                                                                                                              Incidence of skin tuaors not sig-
                                                                                                              nificantly Increased In treated
                                                                                                              groups; survival was 19/20 and
                                                                                                              17/20  In the control and.treated
                                                                                                              groups, respectively
                                                                                                                                 Salaman and
                                                                                                                                 Roe.  1956
Incidence of skin paptlloaas was
4/26 (14X) In treated and 1/30 (3X)
In controls
No subcutaneous sarcomas; survival
was 7/10 after 12 Months and 8/10
after 18 Months; dlbeni(a.h]-
anthracene was tuMorlgenlc under
the sane conditions

No tunors; examinations apparently
Included viscera; dtbeni(a.h]-
anthracene Induced subcutaneous
tumors In 2/5 slMllarly treated rats

Injection site tuaors (fibromas
with sarcoMalous areas) In 6/9
rats, mean latency. 26 months; no
controls, but rats treated simi-
larly with naphthalene In oil did
not develop local tuaors

Tuaor In one rat (spindle-cell
sarcoma In abdoalnal cavity); no
control group
Scrlbner. 13)3
                                                                                                                                                    Boyland and
                                                                                                                                                    Burrows. 1935
                                                                                                                   Pollla,  1941
                                                                                                                                 Schmahl.  I'm
                                                                                                                                                    Schmahl.
oo

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                                                                            TABLE  5-1  (conl.)
S
Route
Cerebral
cortei
t*plant
Cerebellar
laplant
Optic
k ftp Ian t
Species/
rabbi t/NR
rabbU/NB
rabblt/HR
No.' /Sex
S/NR
2/NR
2/Ni
Purity
NR
NR
NR
Treatment
10 og (1 rabbit) or 20 «g
(4 rabbits) pellets
12 *g pellets
4 or 5 *g pellets
Duration
4.S years
4.5 years
4.5 years
Effects/foments
No tunors; survival was 4/5 after
4 years and 2/5 at 4.5 years
No tunors; survival was 2/2 at
4.3 years
No tunors; survival was 2/2 at
4.5 years
Reference
Russell.
Hussell.
Kussell.
m;
1947
194/
     •Muofcers In treatment and control (\t used) group(t) unless specified otherwise.


     NR - Not reported; s.c. • subcutaneous; I.p. • Intraperltoneal
 -J
 V.
 CD

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 The  Injection and  Implantation  studies  do  not provide evidence  of  carctno-
 genlcHy,  but  these  results  cannot  be  regarded  as  conclusive  because  of
 Inadequacies  In  experimental  design  (e.g.,  small numbers  of  animals,  limited
 number  of exposures, Inadequate controls).
    Three cases  of  eplthelloma (hand,  cheek and wrist) were  reported  In  men
 engaged  1n~ handling 40X crude  anthracene In an alizarin  factory  (Kennaway,
 1924a.b).   Two of  these  workers  had  worked  for  30 and  32 years with  the
 crude  anthracene  and  had never  worked  with any other  tar  product.   Workers
 In  the same  factory who  had  contact with  only purified anthracene  did  not
 develop  tumors  or  other   skin  lesions  (acne,  keratoses,  telanglectases,
 pigmentation)  that  affected those who  had  contact  with  the  crude  material.
 The  crude  anthracene  was  not  characterized  and  additional  Information
 regarding these observations was not reported.
 5.2.   MUTAGENICITY
    Anthracene has  been tested 1n numerous  mutagenlclty and other short-tern
 assays  with  negative  results.    IARC  (1983)  has   reviewed many  of  these
 studies, which  Include  such assays with  prokaryotes as  DMA  damage/repair In
 EscheMchla  coll  and   Bacillus  subtlHs.   reverse  mutation   1n  Salmonella
 typhlmuMum   Including  strains  TA1535,  TA1537,  TA1538,  TA98  and  TA100;
 various  assays  In  fungi   Including  mltotlc  recombination  In  Saccharomyces
cerevlslae:  assays  1n mammalian  cells jr»  vitro, unscheduled ONA synthesis 1n
primary rat hepatocytes and HeLa cells,  mutation 1n  Chinese hamster V79 and
mouse  lyapluw, LS178Y  cells,  sister   chromatld  exchange and/or  chromosome
breaks 1n Chinese hamster 06  or rat  liver epithelial cells, cell transforma-
tion 1n mouse 8ALB/3T3, gu1nea-p1g fetal  or Syrian  hamster embryo cells; and
mammalian cells  In vivo,  sister  chromatld exchange and  chromosome aberra-
tions  1n  Chinese  hamsters,  mlcronuclel  In mice.   Anthracene  also produced


0867p                               -38-                             04/23/87

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 negative  responses  In mutagenlclty and short-term assays  that  were  reported
 In  the more  recent  literature,  Including Induction of  prophage  (Inductest)
 (Mamber  et al.,  1984)  and  sMA  gene  (SOS  Chromotest)  (Qulllardet  et  al.,
 1985)  In  E.. coll, mutation  at  the  HGPRT locus  and sister chromatld exchanges
 In  rat liver  epithelial  cells  .In vitro (Ved Brat et al..  1983),  mutation  to
 6-th1oguan1ne  resistance  1n Chinese  hamster  V79 cells In  vitro  (Langenbach
 et  al., 1983),  ONA  single  strand breaks 1n rat hepatocytes 1n vitro  (S1na  et
 al.,  1983)  and  neoplastlc  transformation  In C3H/10T1/2 Clone 8 cells  (Lubet
 et  al.,  1983).   Exogenous  metabolic activation systems were-used  1n most  of
 the  aforementioned  Jji vitro assays.   Many  of  the  assays were  Included  In
 validation studies, where anthracene was presumed to be noncardnogenlc.
    Although most of  the available  data Indicate unequivocal  nonmutagen1c1ty
 of  anthracene,  weak mutagenldty was  recently  demonstrated 1n the Ames assay
 with  a new tester  strain  (TA97)  of  S.  typhlmuMum  (Sakal  et  al.,  1985).
 Mutagenlc  activity  was  expressed  only  In  the  presence  of  S-9 metabolic
 activation preparation, and  was not  observed with  strains  TA98  or TA100 with
 or without metabolic activation.
 5.3.   TERATOGEMICITY
    Pertinent  data  regarding the  teratogenldty  of anthracene could  not  be
 located In the available literature as cited 1n the Appendix.
 5.4.   OTHER REPRODUCTIVE EFFECTS
    Pertinent  data  regarding other reproductive  effects  of anthracene could
 not be located  In the available literature as dted 1n the Appendix.
 5.5.   CHMUC AND SUBCHRONIC TOXICITY
    Pertinent data  regarding toxic  effects of chronic or  subchronlc oral  or
 Inhalation  exposure to  anthracene  could not  be  located In  the  available
0867p                               -39-                             04/23/87

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 literature  as  cHed  In  the  Appendix.   Information regarding  nonneoplastic
 effects  was  not  reported  In  the  only oral cardnogenlclty study of  anthra-
 cene  (Schmahl, 1955) (see Section 5.1.).
    Holland  et  al.  (1980)  administered uncharacterlzed oil shale containing
 polycycllc  aromatic  hydrocarbons,  Including  anthracene,  to  Syrian  golden
 hamsters  by  Inhalation of  50 mg resplrable  shale  dust/m* for 4 hours/day,
 4  days/week.  The  authors reported  Interim  results  Indicating  that  shale
 dust  caused  little pulmonary  epithelial  or  flbrotlc  reaction,  but  that
 retorted  shales caused Inflammation accompanied by  flbrosls. '  Because of  the
 uncharacterlzed nature of  the test  material.   It Is not possible  to  quantify
 these or  future data from this study for  use 1n risk assessment.
 5.6.   OTHER RELEVANT INFORMATION
    The  abstract of a  Russian  study  Indicated  that  single  oral doses of 1.47
 or  2.44  g/kg of  commercial  grade anthracene  or  17 g/kg  of pure  anthracene
were not  lethal to  mice  (Nagornyl,  1969).   Toxic  effects  reportedly  Included
 fatlgablllty, adynamia,  hlstologlcal  hyperemla  In  the kidney, liver,  heart
and lungs, "llpld dystrophy" In the liver and leukocytosls  with neutrophllla.
    Daily  Intragastrlc administration of  100  mg/kg anthracene In olive  oil
 for  4  days  produced  a  small  (3-fold)   Increase  1n  mean  liver  cytosollc
aldehyde  dehydrogenase  activity  1n  a   group  of  five   male  Ulstar  rats
 (Torronen et al.,  1981).  Treatment-related effects on aldehyde  dehydrogen-
ase activity In the liver  nlcrosomes  or  postraltochondrlal  fractions  of small
 Intestinal aucosa or effects on liver/body weight ratios were not observed.
    Salanorw tt  al.  (1381)  reported that  the single-dose   1ntraper1toneal
ID., for  nice  Is  >430 rag/kg.   Gerarde (1960) found that  9/10 mice   survived
dally  IntraperUoneal  Injections of  500  mg/kg  anthracene  for 7 days with
depressed weight gain.


0867p                               -40-                              11/17/86

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    Systemlcally  administered  anthracene   (50  mg/mi  corn  oil   by  gavage)
with  ultraviolet  Irradiation  of the skin  for  1  hour,  2 hours after dosing,
produced keratHls of the exposed skin  in mice  (Dayhaw-Barker et  al., 1985).
This  effect  reportedly  was less  pronounced 1n mice exposed  only to ultra-
violet  light  alone and  not evident  In  vehicle controls.   Topically applied
anthracene  Increases  the sensitivity  of  human  and  hairless mouse  skin to
ultraviolet light (IARC, 1983; U.S.  EPA. 1981;  Kaldbey  and  Nonaka, 1984).
5.7.   SUMMARY
    Administration  of   diets  that  supplied a  total  dose  of 4.5  g/rat of
anthracene over 78 weeks produced tumors 1n 2/28 rats  (a liver sarcoma and  a
uterine  adenocardnoma) that  were   observed  for  life (Schmahl,  1955).   A
control group was not used and  the  tumors were  not ascribed  to treatment.   A
single  Intrapulmonary Injection  of  0.5 mg  anthracene  1n beeswax-trlcaprylIn
mixture did  not  Induce  local  neoplastlc responses  In  rats after 4-55 weeks
of observation (Stanton  et  al.,  1972).
    Twice or  thrice weekly  skin applications  of anthracene for  life did  not
produce local  tumors  In mice (Bachmann et al..  1937; Hynder and  Hoffmann.
1959; Mlescher.  1942),  but  contradictory  results were obtained  when anthra-
cene was applied to mouse skin  with  concurrent  or  directly subsequent ultra-
violet  Irradiation  (Heller,   1950;  Forbes  et  al.,  1976).    Mouse   skin
Initiation-promotion assays using croton oil  (Salaman  and  Roe,  1956) or  TPA
(ScMbner, 1973) as the promoter  did not Indicate a tumor Initiating effect
of anthracene.   Weekly  subcutaneous Injections of anthracene In rats for  6
weeks  to  Iff*  (PolHa. 1941;  Schmahl. 1955;  Boyland and   Burrows,  1935),
weekly  IntraperHoneal  Injections In rats  for 33 weeks   (Schmahl,  1955)  or
brain  or  eye  Implants   In  rabbits   for 4.5  years  (Russell,  1947) did  not
produce local tumors, but  these findings  should be regarded  as  Inconclusive
because of Inadequacies  1n  experimental  design.

0867p                                41-                             02/11/87

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     Although  Sakal  et  al.  (1985)  recently  obtained a weak mutagenlc response
with  activation  for  anthracene  using  a  new tester  strain (TA97) of S. typhl-
muMum.  this  represents  the only  positive  response.   Anthracene  has  been
tested  In numerous  mutagenlclty  and other  short-term assays  with  negative
results  (IARC.  1983; Langenbach et al.,  1983;  Lubet et  al.,  1983;  Ved  Brat
et  al.,  1983; Hamber et al., 1984; Qulllardet  et  al.,  1985).   These Include
ONA  damage,  mutation,  cytogenUHy and transformation  assays  with bacteria,
yeast and mammalian  cells In  vitro  and  Ui  vivo.  Exogenous metabolic activa-
tion  systems  were used In most of the .1^ vitro assays.
    Pertinent  data  regarding chronic or  subchronlc toxic  effects,  terato-
genlclty or  other reproductive  effects  of  anthracene could not be located 1n
the available literature as cited 1n  the Appendix.
0867p                               -42-                              04/23/87

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                             6.  AQUATIC TOXICITY
6.1.   ACUTE
    The  available  Information  concerning acute  toxldty of  anthracene  to
aquatic  animals  Is  presented  In  Table  6-1.  The  most  sensitive  species
tested  was Daphnla  pulex.  with a  15-mlnute EC,Q  for  Immobilization  value
of  1.2  wg/l  In  natural   sunlight  (Allred  and  Glesy,  1985;  OMs  et  al.,
1984).
    The  toxlclty  of  anthracene  1s greatly  Influenced by  lighting  conditions.
Anthracene  Is  essentially  nontoxlc  within  solubility  limits  under  normal
laboratory  fluorescent  lighting  (wavelengths >380  nm)   (Allred  and  Glesy,
1985).   Several studies, however, have  shown  that  the  toxlclty of anthracene
Is  substantially   Increased  under  natural  lighting conditions   (Allred  and
Glesy,  1985;  Bowling et al.,  1983; Kagan  et  al.,  1985;  Or1s et  al.,  1984).
Allred and Glesy  (1985) found  that anthracene was  not  toxic  to Daphnla pulex
at  30 jig/I under fluorescent  lighting,  but caused  100% Immobilization  In
2 minutes  under natural sunlight.   The available  Information  Indicates that
this  photo-enhanced  toxlclty   Is  due  to   material  associated  with  the
organisms  themselves rather  than anthracene  In  the water.   Allred  and Glesy
(1985)  found   that  Oaphnla  pulex   that  were exposed  to  anthracene,  then
transferred to  clean water  and then  exposed to  sunlight still  experienced
the toxic  effects (1mnob1l1zat1on).   Bowling et al. (1983)  demonstrated the
sane  phenomenon with bluegllls (Leponls macrochlrus).   F1sh exposed to 12.7
vg/l  In sunlight  were  killed;  however,  fish held  In the  shade downstream
from  a  sunlit area at  this  concentration did not die.   When  transferred to
clean water  and  sunlight,  previously  exposed  fish  died.  Indicating again
that  anthracene  accumulated by the  animals  was  the cause  of  the  photo-
enhanced  toxlclty.   The   Influence  of  lighting  conditions  on anthracene
toxldty may explain why some  of the acute toxldty data are quite  variable.

0867p                               -43-                              11/17/86

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CD
cr
•vj
•a
                                                                           TABtf  6-1

                                                        Acute loxlctly of Anthracene  to Aquatic  Antuls
                      Species
Concentration
                                         ((feet
                                                                                                                                     Reference
       FISH
          fathead Minnow, PlMephales  proMelas
          Bluegtll. LepoMlt iHcrpchUus
   360
    11.9
    12.7
24-hour
96-hour
Mortality
Kagan et a).. 19BS
Orls et al.. 1964
Bowling et al..  1963
       AMPHIBIANS
         frog. Rana plptens
   no
    25
24-hour
5-hour
Kagan et al.,  19US
Kagan et al..  1904
        INVfRTEBRATiS
         Hater  flea.  Daphnla aagna

         yater  flea.  Daphnla pule;
         Hasqulto, Aerie* aegyptl
         Mosquito. Culex tp.
         Brine  ihrlap. Afteala  sallna
         Hunel. HytHut edulU
    20            24-hour  ICSO
  3030            46-hour  lC$o
     1.2          IS alnute EC^Q.  lonobllliatIon.  In  natural  sunlight

     9.6          IOOX Imoblllzatton.  10 alnutes.  In natural  sunlight
   ISO            24-hour  LCjo
    26.8          24-hour  IC50
    20            24-hour  ICjo
    50-200        decreased lysosomal  stability, digestive gland
                                                          Kagan et al.. 19US
                                                          Bobra et al.. 1903
                                                          Allred and Glesey. I9B5;
                                                          Orts et al.. 1964
                                                          Allred and Glesy. 19BS
                                                          Kagan et a I.. I9BS
                                                          Orts et al.. 1964
                                                          Kagan et al.. 190S
                                                          Hoore and ferrar. 198&
       PR010ZOA
         dilate. Paraaeclua caudatua
  1000
SOX lethal. 60 Minutes
Epstein et al..  1963
CD

-------
 For  example,  LC5Q  values  of  20  and  3030  \iq/i  were  reported for  Daphnla
 tnaqna  (Bobra et al., 1983; Kagan et al..  1985).
 6.2.   CHRONIC
     Pertinent  data  regarding  chronic   toxlclty  of  anthracene  to  aquatic
 organisms  could  not be located  In  the  available  literature as cited  In  the
 Appendix.
 6.3.   PLANTS
     There  Is  IHtle  Information  regarding  the   effects   of  anthracene  on
 aquatic  plants.   Hutchlnson et  al.  (1980) reported  EC.,  values  of  239  and
 535  yg/l  for  Inhibition  of  photosynthesis  1n  Chlamydotnonas  angulosa  and
 Chlorella  vulqarls.   respectively.   G1dd1ngs  (1979)   found   that  a  100%
 saturated  anthracene solution  had  no effect  on  photosynthesis  In  Selenastrum
 caprlcornutum.
     Anthracene  toxlclty  to  aquatic  plants also  seems  to  be  Influenced  by
 lighting conditions.   Cody et al.  (1984)  stated  that growth  of  Selenastrum
 caprlcornutum  was  unaffected by  40  mg/l  under gold  fluorescent  light,  but
 was  Inhibited 30% at 8 mg/l under cool-white fluorescent light.
 6.4.   RESIDUES
     Data from  bloconcentratlon experiments with  anthracene are presented In
 Table  6-2.  The largest BCF  was  16,800  for the  benthlc amphlpod,  Pontoporcla
 hoyl  (Landrura,  1982).   The  ability to  metabolize and  eliminate  anthracene
 seems  to vary  considerably among  different species.   The fish that have been
 tested  (rainbow trout,  dolly varden  char and  blueglll)  do  not  appear  to
metabolize  anthracene  rapidly  (Under  and  Bergman,  1984;  Spade  et  al.,
 1983;  Thomas  and  R1ce, 1982).   Some  Invertebrates such as oysters,  Crasso-
 strea  vlrqlnlca  (Lee  et   al.,  1978),   and the  amphlpod,   Pontoporlla hoyl.
 (Landrum,  1982)  also metabolize  and  eliminate  anthracene  slowly,  but other
 species  such as  the  midge,  Chlronomus  vlparlus.  metabolize  and eliminate

0867p                               -45-                              04/23/87

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                                                                             TABU  6-2

                                                     Bloconcenlratlon Data tor Anthracene In Aquatic  Organises
o
OB
                      Species
Concentration
BCF
                                              Remarks
                                                                                        Reference
          FISH
            Rainbow trout.  Saljff ff
            Goldfish.  Carasslm iuratm
            Bluegtll.  Lepoplt •acrochlrus
  36               200           la  hours
  50               779           72  hours
  MR              9000-9200      estimated  steady-state BCf
  MR               162           NC
   0.7-16.6        675           estimated  steady-state BCf based on
                                 anthracene only
   0.1-16.6        900           estimated  steady-state BCF based on  total
                                 >«C accumulation
                                                            Under and Ber
-------
 anthracene  rapidly  (Gerould  et  al.,   1983).   The  presence  or  absence  of
 sediment  In  these  studies  may  also  Influence the  calculated  BCFs  because
 sediment  can  be a major source  of anthracene  uptake,  especially  for  benthlc
 organisms such  as amphlpods (Eadle et al., 1983;  Landrum and  Scavla,  1983).
     There  are  relatively  little residue  monitoring  data  for   anthracene
 compared  with other polycycllc  aromatic  hydrocarbons.   Tsujl  et  al.  (1985)
 reported  that  clams  (unspecified species)  from  Japanese  waters  contained
 O.H-0.64 ng/g.   Mallns et al.  (1985)  found  that  stomach  contents  of  English
 sole,  Parophyrys  vetulus.  from  Puget  Sound, Washington,  contained  13-460
 ng/g.   Maccubbln  et  al.  (1985)  reported  that   stomach  contents  of  white
 suckers,   Catostomus   commersonl.   from  eastern   Lake   Erie   contained
 1.97-2.17 ng/g.
 6.5.   SUMMARY
    There  Is  relatively  little  Information concerning  the   toxldty  of
 anthracene  to aquatic  organisms.   Acutely toxic  concentrations   range  from
 1.9  yg/l for  Oaphnla   pulex  (Allred  and G1esy,  1985;  OMs  et   al..  1984)
 to  3030  vg/l  for  Daphnla   maqna  (Bobra  et  al.,  1983).   Some  of  this
 variability  may  be  explained   by  the   fact  that  anthracene  toxldty  Is
 affected  by  lighting   conditions,  with   toxldty   Increased  under  natural
 sunlight  and  ultraviolet radiation  rather than  fluorescent lights  (Allred
 and Glesy,  1985;  Bowling  et  al.,  1983; Kagan  et  al.,  1985).   Reported toxic
 concentrations  for  aquatic  plants were also highly  variable.   Hutchlnson et
 al.  (1980)   reported  that   photosynthesis  was   Inhibited  1n  Chlamydomonas
 angulosa  at   239  jig/I,   while   Glddlngs  (1979)   found   that  Selenastrum
 capMcornutua  was unaffected  by  a  100%  saturated  solution.   Reported BCF
 values ranged  from  47-132  for Chlronomus Mparlus (Gerould  et  al., 1983) to
 16,800 for  Pontoporlla  hoy|  (Landrum,  1982).   These  species  also represent
 the extremes In the ability to metabolize and eliminate anthracene.

0867p                               -47-                             04/23/87

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                     7.  EXISTING GUIDELINES AND  STANDARDS
 7.1.    HUMAN
     Exposure  criteria and TLVs  have  been  developed  for  polycyclk  aromatic
 hydrocarbons  as  a  class,  as  well  as  for  several  Individual  polycycllc
 aromatic  hydrocarbons.   The  OSHA has  set  an 8-hour  TWA  concentration  limit
 of  0.2 mg/ma  for  the benzene-soluble  fraction  of coal  tar  pitch  volatlles
 (anthracene,   benzo[a]pyrene,   phenanthrene,  acMdlne,    chrysene,   pyrene)
 (OSHAt  1985).   NIOSH (1977)  recommended a  concentration limit  for  coal  tar,
 coal  tar  pitch, creosote  and  mixtures of  these  substances  of  0.1  mg/m3  of
 the  cyclohexane-extractable  fraction  of the sample,  determined  as  a 10-hour
 TWA.   NIOSH  (1977)  concluded  that these specific  coal tar products, as  well
 as  coke oven emissions, are carcinogenic  and  can  Increase  the  risk of  lung
 and  skin  cancer In  workers.   NIOSH  (1977)  also  recommended  a  celling  limit
 for exposure to asphalt fumes of 5 mg airborne partlculates/m" of air.
    Environmental  quality  criteria,   which  specify  concentration  limits
 Intended  to  protect  humans  against  adverse  health  effects,  have been recom-
 mended  for polycycllc aromatic hydrocarbons In ambient water.   The U.S.  EPA
 (1980b)  has  recommended  a  concentration  limit  of  28  ng/l  for the sum  of
 all  carcinogenic  polycycllc aromatic  hydrocarbons  In  ambient  water.   This
 value  1s  based on a  mathematical  extrapolation of  the  results from studies
with mice treated  orally  with  benzo[a]pyrene,  and acknowledges  the conserva-
 tive assumption that all  carcinogenic polycycllc  aromatic  hydrocarbons  are
 equal  1n  potency  to benzo[a]pyrene.   On   the basis  of  the  animal bloassay
data,   dally  consumption  of   water   containing  28  ng/l  of  carcinogenic
polycycllc aromatic   hydrocarbons  over  an  entire  lifetime   Is  estimated  to
keep the  lifetime risk  of  cancer development below one  chance In 100,000.
Anthracene was  not  among the PAH considered as  carcinogenic by the U.S. EPA
 (1980).

0867p                               -48-                             04/23/87

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    The  EPA  has  not  recommended  an  ambient  water  quality  criterion  for
 noncardnogenlc  polycycllc  aromatic hydrocarbons as  a  class.   The U.S.  EPA
 (1980b)  acknowledged  that  data suitable for quantitative risk assessment  of
 noncardnogenlc polycycllc aromatic hydrocarbons are essentially  nonexistent.
 7.2.   AQUATIC
    Guidelines  and  standards  for  the  protection of  aquatic  biota from  the
 effects  of  anthracene  In  particular  could not  be  located  1n the  available
 literature  as  cited  In  the Appendix.   U.S.  EPA (1980b) reported,  however.
 that  acute  toxldty  to saltwater aquatic  life  occurred  at  concentrations  as
 low   as  300  wg/l  of  polycycllc  aromatic  hydrocarbons  In   general,  and
 would  occur at  lower concentrations  1n  species more  sensitive than  those
 tested.   U.S.  EPA  (1980b)  concluded  that  the  available data  at  that  time
 were  Inadequate  to  recommend criteria  or make  generalizations about  chronic
 toxldty or acute toxldty to freshwater organisms.
0867p                               -49-                              11/17/86

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                              8.   RISK ASSESSMENT

     Administration  of  diets  that  Initially  contained  5 mg  and  later  (not
 otherwise  specified) IS  mg of anthracene on  6  days/week  for  78  weeks  {total
 dose of  4.5  g/rat) produced tumors  In  2/28  rats  (a  liver  sarcoma  and  a
 uterine  adenocarclnoma)   that were  observed  for  life  (Schmahl,  1955).   A
 control group was  not  used and  the tumors  were not ascribed to treatment.   A
 single  Intrapulmonary  Injection  of 0.5 mg  anthracene  In beeswax-trlcaprylln
 mixture did  not Induce  local neoplastlc  responses 1n rats after  4-55 weeks
 of observation  (Stanton et al.,  1972).
     Twice  or  thrice weekly skin applications of anthracene for  life did not
 produce  local  tumors  1n  mice (Bachmann et  al.. 1937; Wynder and Hoffmann,
 1959; Mlescher,  1942), but contradictory results were obtained  when anthra-
 cene was applied to mouse skin  with  concurrent or  directly subsequent ultra-
 violet  Irradiation  (Heller,  1950; Forbes  et  al.,  1976)  (see  Table  5-1).
 Mouse skin Initiation-promotion  assays  using  croton  oil (Salaman  and  Roe,
 1956)  or   TPA   (Scrlbner,  1973)   as   the  promoter   do  not  Indicate  a  tumor
 Initiating effect  of anthracene.   Weekly subcutaneous  Injections  of anthra-
 cene 1n  rats  for  6 weeks to  life (Pollla, 1941;  Schmahl,  1955;  Boyland and
 Burrows,  1935), weekly   1ntraper1toneal  Injections  In  rats for  33  weeks
 (Schmahl,  1955)  or  brain or eye Implants  In  rabbits  for 4.5  years  (Russell,
 1947) did  not produce  local tumors,  but  these findings should be  regarded as
 Inconclusive because of Inadequacies  1n experimental design.
    Anthracene has  been  tested  In  numerous  mutagenlclty  and other short-term
assays  with primarily  negative results  (IARC, 1983;  Langenbach et al., 1983;
Lubet et  al..  1983; Ved  Brat et  al., 1983;  Mamber et  al.,  1984; Qulllardet
0867p                               -50-                             04/23/87

-------
et  al.,  1985).   These Include ONA damage, mutation,  cytogenldty  and  trans-
formation  assays  with bacteria,  yeast  and mammalian  cells  J£ vitro  and  HI
vivo.   Exogenous  metabolic activation  systems  were  used  In  most of  the  \t±
vitro assays.
    Pertinent  data regarding  chronic  or  subchronlc  toxic effects,  terato-
genldty or  other  reproductive effects  of  anthracene  could not be located 1n
the available literature as cited In the Appendix.
    The  available  Information  provides  no  evidence  that  anthracene  Is
carcinogenic,  therefore  anthracene  Is  a  Group  D chemical according  to the
U.S.  EPA  weight of  evidence  system  (see  Section 9.2.).  Calculation  of  an
RfO  (formerly  ADI)   for  anthracene  1s  precluded  by the  lack of  relevant
toxlclty data.
0867p                               -51-                              04/23/87

-------
                           9.   REPORTABLE  QUANTITIES
 9.1.   REPORTABLE QUANTITY (RQ) RANKING BASED ON CHRONIC TOXICITY
    Pertinent  data  regarding  chronic  or  subchronlc  toxic effects,  terato-
 genlclty or  other reproductive  effects of  anthracene  could not  be  located  In
 the available literature as cited 1n the Appendix.
    Holland  et  al.  (1980) administered uncharacterlzed  oil  shale  containing
 polycycllc  aromatic  hydrocarbons.  Including  anthracene,   to  Syrian  golden
 hamsters by  Inhalation of  50 mg resplrable  shale dust/raa for 4  hours/day,
 4  days/week.  The  authors reported  Interim  results  Indicating   that  shale
 dust  caused  little  pulmonary  epithelial  or  flbrotlc reaction,  but  that
 retorted shales  caused  Inflammation accompanied  by flbrosls.   Because of the
 uncharacterlzed  nature  of  the  test  material  In  this  study.   It  1s  not
 possible to  quantify those  data  for use  In deriving  an  RQ  (Table  9-1)  to
 reflect hazard associated with exposure to anthracene (U.S. EPA, 1984).
 9.2.   HEIGHT OF EVIDENCE ANO POTENCY FACTOR (F-I/EO^) FOR CARCIN06ENICITY
    Administration  of diets  that Initially  contained  5  mg  and   later  (not
 otherwise specified)  15  mg of anthracene on  6  days/week for  78 weeks (total
 dose  of  4.5  g/rat)  produced tumors  In  2/28  rats  (a  liver  sarcoma  and  a
 uterus  adenocarclnoma)   that  were  observed  for  life  (Schmahl,  1955).   A
control group was not used and  the  tumors were not ascribed to treatment.  A
single Intrapulmonary  Injection of  0.5 mg  anthracene 1n beeswax-tMcaprylln
mixture did  not  Induce local  neoplastlc  responses In  rats  after  4-55 weeks
of observation (Stanton et al., 1972).
    Twice or thrice weekly skin applications of  anthracene for life did not
produce local  tumors In  mice (Bachmann  et al.,  1937;  Uynder  and Hoffmann,
1959;  Hlescher,  1942),  but contradictory results  were  obtained when anthra-
cene was applied to mouse  skin  with  concurrent or directly subsequent  ultra-
violet  Irradiation  (Heller,   1950;   Forbes  et  al..  1976).   Mouse  skin

0867p                               -52-                              11/17/86

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                                   TABLE  9-1
                                  Anthracene
           Minimum Effective Oose  (MED) and  Reportable Quantity  (RQ)


Route:
Oose:
Effect:
Reference:
RVd:
RVe:
Composite Score:
RQ:                     Data are not sufficient for deriving an RQ
0867p                               -53-                              11/17/86

-------
 Initiation-promotion  assays  using  croton  oil (Salaman and Roe,  1956)  or  TPA
 (ScMbner,  1973)  as  the  promoter  do  not  Indicate a  tumor  Initiating  effect
 of  anthracene.   Weekly subcutaneous  Injections  of  anthracene In rats  for  6
 weeks  to  life • (Pollla.  1941;  Schmahl.  1955;  Boyland  and   Burrows,  1935).
 weekly  IntraperUoneal  Injections   In  rats  for  33  weeks (Schmahl,   1955)  or
 brain  or  eye  Implants  In  rabbits  for 4.5  years  (Russell,  1947)  did  not
 produce  local  tumors, but these findings  should be regarded  as  Inconclusive
 because of  Inadequacies In experimental design.
    Anthracene has  been  tested  In  numerous  mutagenlclty  and  other short-term
 assays with primarily negative  results  (IARC.  1983; Langenbach  et al., 1983;
 Lubet  et  al..  1983;  Ved  Brat  et  al.. 1983; Mamber et al..  1984; Qulllardet
 et  al.,  1985).   These Include DNA  damage,  mutation,  cytogenldty and  trans-
 formation  assays  with bacteria,  yeast  and  mammalian  cells   \r±  vitro  and hi
 vivo.   Exogenous  metabolic  activation  systems  were  used  In most of  the Ui
 vitro assays.
    The  available  Information  provides   no  evidence  that  anthracene  Is
 carcinogenic.
    IARC  (1983)  reported  that there was  Insufficient  evidence  regarding the
 carcinogenic risk to  humans and experimental  animals  associated  with oral or
 Inhalation  exposure  to  anthracene.  According  to U.S. EPA  (1986b)  guide-
 lines,  there  Is  no  data for  humans  and  Inadequate evidence  for  animals.
Applying  the criteria for evaluation  of  the overall  weight  of  evidence for
 the carcinogenic  potential  for  humans of the  Carcinogen Assessment  Group of
 the U.S.  EPfr (1986b),  anthracene   1s most  appropriately designated a Group
0 -Not  Classified   chemical.   Direct  hazard  ranking  of   anthracene under
CERCLA Is therefore precluded.
0867p                               -54-                             04/23/87

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                                10.   REFERENCES

 Afolabl,  O.A.,  E.A.   Adesulu  and  O.L.  Oke.    1983.   Polynuclear  aromatic
 hydrocarbons  In  some Nigerian preserved freshwater fish  species.   J,  Agrlc.
 Food Chem.  31: 1083-1090.

 Akhtar,  M.N.,  J.G.  Hamilton,  O.K. Boyd, A. Braunsteln. H.  Se1fr1ed and D.H.
 Jerlna,   1979.   Anthracene l,2-ox1de:  Synthesis  and  role  In  the  metabolism
 of anthracene by mammals.  3. Chem. Soc. Perkln I.  p. 1442-1446.

 Allred,  P.M.  and  J.P.  G1esy.   1985.   Solar  radiation-Induced toxlclty  of
 anthracene to Daphnla pulex.  Environ. Toxlcol. Chem.   4(2): 219-226.

 Ang, K.P..  H. Gunaslngham  and  B.T.  Tay.   1986.   The distribution  of poly-
 nuclear  aromatic  hydrocarbons   In  ambient  air  partlculates   1n  Singapore.
 Environ. MonH. Assess.  6: 171-180.

 Atkinson, R.   1985.   Kinetics and  mechanisms  of the gas-phase reactions  of
 the  hydroxyl  radical  with  organic  compounds  under  atmospheric conditions.
 Cheffl. Rev.  85: 69-201.

 Bachraann, U.E.,  J.U.  Cook,  A. Dansl, et al.   1937.   The  production of cover
 by pure  hydrocarbons  IV.  Proc.  Roy. Soc.  London.   123:  343-368.    (Cited In
 PHS, 1951}

 Bauer.  J.E.  and  O.G. Capone.   1985.   Degradation and mineralization of  the
 polycycllc  aromatic   hydrocarbons  anthracene  and naphthalene  In   Intertldal
marine sediments.  Appl. Environ. Hlcroblol.  50(1):  81-90.

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 Bedlent,  P.B.,  A.C.  Rodgers,  T.C.   Bouvette,  M.B.  Tomson  and  T.H.   Wang.
 1984.   Ground  water qualHy  at  a creosote  waste  site.   Ground Water.   22:
 318-329.

 Behymer,  T.D.   and  R.A.  HHes.    1985.   Photolysis  of  polycycllc  aromatic
 hydrocarbons adsorbed  on simulated atmospheric partlculates.   Environ.  Sc1.
 Techno!.  19(10): 1004-1006.

 Bhosle, N.B. and S.  Mavlnkurve.   1980.   Hydrocarbon-utilizing  microorganisms
 from Dona Paula Bay, GOA.  Mar. Environ. Res.  4:  53-58.

 BJoerseth. A.,  0,  BJoerseth and P.E. FJeldstad.   1978.   Polycycllc  aromatic
 hydrocarbons  In  the  work   atmosphere.   I.  Determination  In  an  aluminum
 reduction plant.  Scand. J.  Work Environ. Health.   4: 212-223.

 Bobra,  A.M., W.Y.  Shlu and  D.  Hackay.   1983.  A  predictive correlation for
 the acute toxlclty of hydrocarbons and  chlorinated hydrocarbons to the water
 flea (Daphnla magna).  Chemosphere.  12(9-10): 1121-1130.

Boehm,  P.O. and  J.W.  Farrlngton.   1984.  Aspects  of  the polycycllc  aromatic
hydrocarbon geochemistry of  recent   sediments  In  the  Georges  Bank  region.
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 1982.   Laboratory  protocols  for  evaluating the fate of  organic  chemicals  In
 air  and water.   Environmental  Research Laboratory.  Office of  Research  and
 Development. U.S. EPA. Athens. GA.  EPA 600/3-82-022.

 Moore,  M.N. and S.V.  Farrar.  1985.  Effects of  polynuclear  aromatic  hydro-
 carbons  on lysosomal  membranes   In mollusks.   Mar.  Environ.  Res.   17(2-4):
 222-225.   [CA 104(13):103856d]

 Nagornyl,  P.A.   1969.   Comparative  study of toxlclty  1n  pure and commercial
 anthracene.  Gig. Tr. Prof. Zabol.  13(5): 59-61.

 MAS  (National  Academy  of Sciences).  1972.  Biologic  Effects of Atmospheric
 Pollutants.   Partlculate Polycycllc  Organic Matter.   MAS,  Washington.  DC.
 p. 63-81.

Nlessner.  R.t  0.  Klockow, F.  Bruynseels  and R.  Grleken.   1985.  Investiga-
 tion  of heterogeneous  reactions  of  PAHs  on  particle surfaces  using laser
mlcroprobe oiss analysis.  Int. J. Environ. Anal.  Chen.  22(3-4): 281-295.

NIOSH   (National  Institute  for  Occupational  Safety  and   Health).   1977.
Criteria  for   a  Recommended  Standard...Occupational  Exposure  to  Coal   Tar
Products, U.S. DHEH. PHS, CDC, Rockvllle, MO.  Publ. Mo. 78-107.


0867p                               -70-                             11/17/86

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Obana, H., S.  HoM,  A.  Nakamura  and  T.  Kashlmoto.   1983.   Uptake  and  release
of  polynuclear  aromatic  hydrocarbons  by  short-necked  clams  (Tapes  japonlca).
Water Res.  17(9): 1183-1188.

Ogata, H.,_K.  Fujlsawa,  Y.  Oglno  and  E.  Nano.   1984.   Partition coefficients
as  a  measure  of  bloconcentratlon potential  of  crude oil  compounds  In  fish
and shellfish.  Bull. Environ. Contam. Toxlcol.   33(5):  561-567.

Or1s,  J.T.,  J.P.  Glesy,  P.M. Allred,  D.F.  Grant  and  P.P. Landrum.   1984.
Photolnduced  toxlclty  of anthracene  In  aquatic organisms: An  environmental
perspective.  Stud. Environ. Sc1.  25: 639-658.   [CA 102(19):161728h]

OSHA  (Occupational  Safety  and  Health Administration).   1985.   OSHA  Safety
and Health Standards.  29 CFR 1910.1000.

Peacock,   P.R.   1936.   Evidence   regarding  the  mechanism  of  elimination  of
1:2-benzpyrene, 1:2:5:6-d1benzanthracene and anthracene  from  the  bloodstream
of  Injected animals.  Br. J.  Exp.  Pathol.  17:  164-172.   (Cited In U.S. EPA,
1981)

Pearlman, R.S.,  S.H. YalkowsM  and  S.  SanerJee.   1984.   Water  solubilities
of  polynuclear  aromatic and  heteroaromatlc  compounds.   J. Chem.  Ref.  Data.
13: 555-562.
0867p                                -71-                             02/11/87

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 Plet,  G.J. and  C.F.  Horra.   1979.   Behaviour  of  mlcropollutants  In  river
 water  during  bank  filtration.   Iri:  Oxidation  Techniques  In  Drinking  Water
 Treatment,  I.U.  Kuehn  and  H.  Sonthelmer,  Ed.   p. 608-620.   EPA 570/9-79-020.
 NTIS PB-301 313.

 Pollla,  J.A.   1939.   Investigations  on  the possible carcinogenic  effect  of
 anthracene  and  chrysene and  some  of  their  compounds.   I.  The  effect  of
 painting on the  skin of mice.  J. Ind. Hyg. Toxlcol.  21:  219-220.

 PolUa,  J.A.   1941.   Investigations  on  the possible carcinogenic  effect  of
 anthracene  and  chrysene  and some  of their  compounds.   II.  The  effect  of
 subcutaneous Injection In rats.  J. Ind.  Hyg. Toxlcol.  23: 449-451.

 Qulllardet, P.,  C.  DeSellecombe and M. Hofnung.  1985.  The SOS Chroraotest,
 a  co1or1metr1c  bacterial  assay  for  genotoxlns:   Validation  study with  83
 compounds.  Hutat. Res.  147(3): 79-95.

 Readman,  J.H.,  R.F.C. Mantoura,  M.M. Rhead  and L.  Brown.   1982.  Aquatic
 distribution  and  heterotrophlc  degradation  of  polycycllc  aromatic  hydro-
 carbons  (PAH)  1n  the Tamar  Estuary.  Estuarlne,  Coastal.  Shelf-Scl.   14:
 369-389.

Ribbons, O.I*,  and R.U.  Eaton.   1982.  Chemical  transformations of aromatic
hydrocarbons that  support  the growth  of  microorganisms.   In,: B1odegradat1on
and Detoxification  of Environmental  Pollutants. A.M.  Chakrabarty. Ed.  CRC
Press,  Inc., Boca Raton, FL.  p. 59-84.
0867p                               -72-                              11/17/86

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Rostad,  C.E.,  W.E. Perelra  and  M.F. Hult.   1985.   Partitioning studies  of
coal-tar   constituents   In   a   two-phase   contaminated   groundwater   system.
Chemosphere.  14(8): 1023-1036.

Ruepert,  C., A.  Grlnwts  and  H.  Govers.   1985.   Prediction  of  partition
coefficients  of  unsubstUuted  polycycllc   aromatic  hydrocarbons  from  C18
chromatographlc and structural  properties.  Chemosphere.   14:  279-291.

Russell,  H.   1947.  An  unsuccessful  attempt to  Induce  gllomata In  rabbits
with cholanthrene. J.  Pathol. Bacterlol.  59: 481-483.

Sakal,  H..  D.  Yoshlda  and  S.  H1zusak1.   1985.   Mutagenlclty  of  polycycllc
aromatic  hydrocarbons  and qulnones  on  Salmonella typhlmurlum  TA97.   Hutat.
Res.  156(1-2):  61-67.

Salaman.  N.H.  and  F.J.C.  Roe.  1956.   Further  tests for  tumour-Initiating
activity.  N,N-01-(2-ch1oroethyl)-p-am1nophenyl-butyr1c  add  (C81348)  as  an
Initiator  of skin tumour  formation  In   the  mouse.   Br.  J.  Cancer.   10:
363-378.

Salaraone,  M.F..  J.A.  Heddle and H. Katz.   1981.   Hutagenlc activity  of 41
compounds  In the .In. vivo mlcronucleus  assay,   in: Evaluation  of Short-term
Tests  for  Carcinogens.   Report  of  the International  Collaborative Program.
Progress  In  Nutation Research,  Vol. 1,  F.J. de  Serres and  J. Ashby,  Ed.
Amsterdam, Elsevler/North Holland,  p. 686-697.
0867q                               -73-                              11/17/86

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 Santodonato,  J.,  P.  Howard  and  0.  Basu.    1981.   Health  and  Ecological
 Assessment  of  Polynuclear Aromatic  Hydrocarbons.  Pathotox  Publishers  Inc.,
 Park  Forest, South,  IL.

 Schmahl,  0.  1955.   Examination  of  the  carcinogenic action of  naphthalene
 and  anthracene  1n rats.  Z. Krebsforsch.  60:  697-710.   (Ger.)   (Summarized
 In IARC, 1983)

 Schwall, L.R. and S.E. Herbes.   1979.  Methodology for  the  determination  of
 rates  of  mlcroblal  transformation  of  polycycllc aromatic  hydrocarbons  In
 sediments.  ASTH  STP-673.  p.  167-183.

 Scrlbner,  J.O.   1973.   Brief  communication.   Tumor  Initiation  by apparently
 noncarclnogenlc  polycycllc aromatic hydrocarbons.   J.   Natl.  Cancer  Inst.
 50: 1717-1719.

 Sears.  G.W.  and E.R.  Hopke.  1949.   Vapor pressure  of  naphthalene,  anthra-
 cene and hexachlorobenzene  In a  low  pressure  region.   J. Am. Chem. Soc.  71:
 1632-1634.

 Shlnohara,  R.,  A.  Kldo,  S. Eto,  T. Horl,  H.  Koga  and T.  Aklyama.   1981.
 Identification and determination of  trace  organic  substances In tap water by
computerized gas  chromatography-mass spectroraetry and  mass  fragmentography.
Water Res.  15:  535-542.

Sims, P.   1964.   Metabolism of  polycycllc compounds.   25.  The  metabolism of
anthracene and some related compounds 1n rats.  Blochem.  J.  92:  621-631.


0867p                                -74-                             11/17/86

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S1na,  J.F..  C.I.  Bean,  G.R.  Dysart.  V.I.  Taylor  and  M.O.  Bradley.   1983.
Evaluation  of  the alkaline  eluUon/rat  hepatocyte assay as  a predictor of
cardnogenlc/mutagenlc potential.  Mutat. Res.   113(5):  357-391.

Smith,  J.D.,  3.  Bagg  and  B.M.  Bycroft.  1984.   Polycycllc  aromatic  hydro-
carbons  In  the clam  Trldacma maxima from the great barrier  reef,  Australia.
Environ. Scl. Technol.  18: 353-358.

Sorrel!, R.K., H.J. Brass  and  R.  Reding.  1980.   A review of the  occurrences
and  treatment  of polynuclear  aromatic  hydrocarbons  In  water.   Environ.
Inter.  4: 245-254.

Southworth,  G.R.  1979.   Transport  and transformations of  anthracene  In
natural  waters.    In.:  ASTM  STP-667.   Aquatic  Toxicology,  L.I.  Harking  and
R.A.  Klmberle,  Ed.   American  Society for  Testing and Materials,  Philadel-
phia, PA.  p. 359-380.

Southworth, G.R.,  J.J. Beauchamp and  P.K. Schmleder.   1978.   Bloaccumulatlon
potential of  polycycllc  aromatic hydrocarbons  In  Daphnla pulex.   Water Res.
12: 973-977.

Spade, A.,  P.P.  landrua and  G.J.  Leversee.   1983.  Uptake,  depuration and
blotransfontttlon  of  anthracene  and benzo(a)pyrene   In  blueglll  sunflsh.
Ecotoxlcol. Environ.  Saf.  7: 330-341.

Sporstol, S., N.  Gjos, R.G.  Llchtenthaler,  et  al.  1983.   Source Identifica-
tion  of   aromatic hydrocarbons   In  sediments  using   GC/HS.  Environ.  Scl.
Technol.   17: 282-286.

0867p                               -75-                             11/17/86

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 Stanton,  M.F.,  E. Miller,  C.  Wrench  and R. Blackwell.   1972.   Experimental
 Induction  of epldermold  carcinoma  In the  lungs  of rats by  cigarette  smoke
 condensate.  J. Mat!. Cancer Inst.  49: 867-877.

 Staples,  C.A.,  A.  Werner and  T.  Hoogheem.   1985.   Assessment of  priority
 pollutant   concentrations   In   the  United   States   using  STORE!   database.
 Environ. Toxlcol. Chew.  4: 131-142.

 Stevens,  8.,  S.R. Perez and  J.A.  Qrs.  1974.   Photoperox1dat1on  of  unsatu-
 rated  organic  molecules 02'delta G acceptor properties  and  reactivity.   J.
 An. Chera. Soc.  96: 6846-6850.

 Subramanlan,  V.,   H.   Sugumaran   and   C.S.   Valdyanathan.    1978.    Double
 hydroxylatlon  reactions  1n  microorganisms.   Indian  Inst.  Scl.  J.    60:
 143-178.

 Tabatc, H.H.. S.A.  Quave.  C.I.  Hashnl  and E.F.  Barth.   1981.  Blodegradabll-
 1ty  studies with  organic  priority pollutant   compounds.   J.  Water  Pollut.
 Control Fed.  53: 1503-1518.

 Tan, Y.L.  and  N. He1t.   1981.   Blogenlc and  ablogenlc  polynuclear  aromatic
 hydrocarbons  In  sedlaents  from   two  remote  Adirondack  Lakes.   Geochlra.
 Cosmchln. Act*.  45: 2267-2279.

Thorn,  N.S.  and  A.R.  Agg.   1975.   The  breakdown  of  synthetic  organic
compounds In biological processes.  Proc. R. Soc. Lond. B.   189: 347-357.
0867p                               -76-                              11/17/86

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Thomas, R.E.  and  S.O.  R1ce.   1982.   Metabolism  and  clearance  of  phenolic  and
mono-,  d1-,  and  polynuclear  aromatic  hydrocarbons  by  Dolly  Varden  char.
Physlol. Mech. Mar. Pollut. Toxic,  p. 161-176.

Thrane.  K.E.  and  A.  Mlkalsen.   1981.   High-volume   sampling  of  airborne
polycycllc  aromatic  hydrocarbons  using glass fiber  filters and  polyurethane
foam.  Atmos. Environ.  IS: 909-918.

Torronen,  R.,  U.  Nouslalnen and  0.  Hannlnen.   1981.   Induction  of  aldehyde
dehydrogenase  by  polycycllc   aromatic  hydrocarbons  In  rats.   Chem.  Blol.
Interact.  36(1): 33-44.

Tsujl,  I.,  K.  Kolde,  H.  Morlyama,  K.  Tanabe  and  H.  Matsushita.   1985.
Detection  of  polynuclear  aromatic  hydrocarbons  In  shellfishes,  seabottom
sediments  and  sea water by high performance liquid chromatography.  Shokuhln
E1se1gaku  Zasshl.  26(1):  50-55.  [CA 104{10):81300p]

U.S.  EPA.    1977.   Computer  print-out of  non-confidential   production  data
from TSCA  Inventory.  OPTS, CIO, U.S. EPA, Washington,  DC.

U.S. EPA.  1980a.   Fate of  toxic  and hazardous  materials 1n the air environ-
ment.  Environmental  Sciences  Research Laboratory, Office  of  Research  and
Development.-  Research   Triangle   Park.   NC.     EPA    600/3-80-084.    NTIS
PB80-22194*..
0867p                               -77-                              02/11/87

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 U.S.  EPA.   1980b.   Ambient  Water  Quality Criteria Document  for  Polynuclear
 Aromatic  Hydrocarbons.   Prepared by  the  Office of Health  and  Environmental
 Assessment, Environmental  Criteria  and  Assessment  Office,  Cincinnati.  OH  for
 the   Office   of  Water   Regulations   and   Standards.   Washington,   DC.    EPA
 440/5-80-069.   NTIS  PB81-117806.

 U.S.  EPA.   1981.   Hazard  Information  Review.   Anthracene.  Prepared  under
 EPA Contract  No.  68-01-5789  for  TSCA  Interagency Testing  Committee by  Envlro
 Control, Inc.,  Rockvllle, MD.  Working Draft, IR-227.

 U.S.  EPA.   1984.   Reportable Quantity Document for Anthracene.   Prepared by
 the  Office of  Health  and  Environmental  Assessment,   Environmental  Criteria
 and  Assessment  Office,  Cincinnati,  OH  for  the   Office   of  Emergency  and
 Remedial Response, Washington. DC.

 U.S.  EPA.   1986a.  OHMTADS (011 and  Hazardous  Material  Technical  Assistance
 Data System).   On-Hne.

 U.S.  EPA.   1986b.   Guidelines  for   Carcinogenic  Risk Assessment.   Federal
 Register.  51(185):  33992-34003.

USITC  (U.S.  International  Trade Commission).  1984.   Imports  of benzenold
chemicals ami products,  1983.  USITC Publ. 1548, Washington, DC.  p. 10.

Van Der Linden, A.C. and G.J.E. Thljsse.  1965.   The  mechanism of mlcroblal
oxidations of  petroleum hydrocarbons.  Advanc. Enzymol.  27: 469-546.
0867p                               -78-                             02/11/87

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 Ved  Brat,  S.,  C.  long,  S. Telang  and  G.H.  Williams.  1983.  Comparison  of
 sister  chromatld  exchange  and  mammalian  cell mutagenesls  at  the  hypoxanthlne
 guanlne  phosphorlbosyl  transferase  locus   In  adult  rat  liver  epithelial
 cells.  Ann. ».Y. Acad. Sc1.  407: 474-475.

 Walters,  R.W.  and  R.G.  Luthy.   1984.   Liquid/suspended  solid  phase  parti-
 tioning  of  polycycllc  aromatic  hydrocarbon In  coal coking  waste  waters.
 Water Res.  18: 795-809.

 Webster. G.R.B..  K.I.  Frlesen,  L.P. Sarna and D.C.G. Mu1r.  1985.   Environ-
 mental  fate  modeling  of  chlorodloxlns.   Determination of  physical  constants.
 Chemosphere.  14: 609-622.

 WhHehouse,  B.G.    1984.   The  effects  of  temperature  and  salinity on  the
 aqueous  solubility  of polynuclear  aromatic hydrocarbons.   Mar. Chera.   14:
 319-332.

 Williams,  O.T., E.R.  Nestmann,  G.L. Lebel,  P.M. Benolt,  R.  Otson  and E.G.H.
 Lee.  1982.   Determination of  mutagenlc potential and  organic  contaminants
 of Great Lakes drinking water.  Chemosphere.  11:  263-276.

W1ndhol2,  N., Ed.   1983.   The Merck Index,  10th ed.  Merck  and  Co., Rahway,
NJ.  p.  100V

Windsor, J.G.,  Jr.  and R.A. HHes.  1979.   Polycycllc  aromatic  hydrocarbons
 In Gulf of Maine  sediments  and  Nova Scotia  soils.   Geochlm.  Cosmochlm. Acta.
42: 27-33.
0867p                               -79-                              11/17/86

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Hynder,  E.L. and  D.  Hoffmann.   1959.   A  study  of  tobacco  carclnogenesls.
VII.  The role of higher polycycllc hydrocarbons.  Cancer.  12: 1079-1086.

Yalkowsky.  S.H. and  S.C.  Valvanl.   1979.   Solubilities and  partitioning.
2. Relationships  between  aqueous  solubilities,  partition coefficients  and
molecular  surface  area  of rigid aromatic hydrocarbons.   J. Chem.  Eng.  Data.
24: 127-129.

Yamasakl,  H., K. Kuwata  and H.  Miyamoto.   1982.  Effects of ambient tempera-
ture  on aspects  of airborne polycycllc  aromatic hydrocarbons.  Environ. Sc1.
Technol.   16: 189-194.

Zepp,  R.G.  1980.   Assessing  the  photochemistry  of  organic  pollutants  In
aquatic environments.   In: Dynamics Exposure and Hazard Assessment of  Toxic
Chemicals,  R.  Haque,   Ed.   Ann   Arbor   Science,   Publ.,  Ann  Arbor,  HI.
p. 69-110.

Zepp,  R.G.  and  P.P.  Schlotzhauer.   1979.   Photoreactlvlty  of  selected
aromatic hydrocarbons  In  water.   In:  Polynuclear  Aromatic Hydrocarbons, O.U.
Jones and  P. Leber, Ed.   Ann Arbor  Science Publishers,  Inc., Ann. Arbor, HI.
p. 141-158.
0867p                               -80-                              11/17/86

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                                   APPENDIX

                              LITERATURE  SEARCHED



    This,  profile  1s  based  on  data  Identified  by  computerized  literature

searches of the following:


         GLOBAL
         TSCATS
         CASK online (U.S. EPA Chemical  Activities Status Report)
         CAS online STN International
         TOXLINE
         TOXBACK 76
         TOXBACK 65
         RTECS
         OHM TADS
         STORET
         SRC Environmental Fate Data Bases
         SANSS
         AQUIRE
         TSCAPP
         NTIS
         Federal Register


These  searches  were conducted  In  April,  1986.   In  addition,  hand  searches

were  made  of   Chemical  Abstracts  (Collective Indices  6  and 7),  and  the

following secondary sources were reviewed:


    ACGIH  (American  Conference of  Governmental  Industrial  Hyglenlsts).
    1986.   Documentation  of  the Threshold Limit Values  and Biological
    Exposure Indices, 5th ed.  Cincinnati, OH.

    ACGIH  (American  Conference of  Governmental  Industrial  Hyglenlsts).
    1985-1986.    TLVs:  Threshold  Limit   Values  for  Chemical  Substances
    and  Physical  Agents  In  the   Workroom   Environment  with  Intended
    Changes for 1985-1986.  Cincinnati.  OH.  114 p.

    Claytoiv 6.0.   and   F.E.  Clayton,  Ed.   1981.   Patty's  Industrial
    Hygiene and Toxicology,  3rd  rev.  ed..  Vol. 2A.   John  Wiley  and
    Sons, NY.   2878 p.

    Clayton. G.O.   and   F.E.  Clayton.  Ed.   1981.   Patty's  Industrial
    Hygiene and Toxicology,  3rd  rev.  ed.,  Vol. 28.   John  Wiley  and
    Sons, NY.   p. 2879-3816.
0867p                               -81-                             11/17/86

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     Clayton,  G.D.  and  F.E.  Clayton,  Ed.   1982.   Patty's  Industrial
     Hygiene  and  Toxicology,  3rd  rev.  ed.,  Vol.  2C.   John  WHey  and
     Sons, MY.   p. 3817-5112.

     Grayson,  M. and D.  Eckroth,  Ed.   1978-1983.  K1rk-0thmer  Encyclo-
     pedia of  Chemical  Technology,  3rd ed.   John  Wiley  and  Sons,  NY.   23
     Volumes.

     Hamilton, A.  and H.L.  Hardy.   1974.   Industrial  Toxicology.  3rd  ed.
     Publishing  Sciences Group, Inc.. Littleton, MA.   575 p.

     IARC  (International Agency  for  Research on Cancer).  IARC  Mono-
     graphs  on  the  Evaluation  of  Carcinogenic  Risk   of  Chemicals  to
     Humans.  WHO, IARC, Lyons, France.

     ITII  (International  Technical  Information Institute).   1982.   Toxic
     and  Hazardous Industrial  Chemicals  Safety Manual   for  Handling  and
     Disposal with Toxlclty and Hazard Data.  ITII, Tokyo, Japan.   700 p.

     Jaber,  H.M.,  U.R.  Habey, S.T.  Liu,  T.W. Chow  and  H.L.  Johnson.
     1984.  Data aqulsltlon  for environmental  transport and fate  screen-
     Ing  for  compounds   of  Interest In  the  Office of  Solid Waste.   EPA
     600/6-84-010.  NTIS PB84-243906.  SRI International. Menlo Park.  CA.

     NTP  (National Toxicology  Program).   1986.   Toxicology Research  and
     Testing   Program.    Chemicals   on   Standard  Protocol.   Management
     Status.

     Ouellette.  R.P. and  J.A.  King.   1977.    Chemical Week  Pesticide
     Register.  McGraw-Hill  Book Co.. NY.

     Sax, N.I.   1979.   Dangerous  Properties  of Industrial Materials,  5th
     ed.  Van Nostrand Relnhold Co.. NY.

     SRI  (Stanford Research  Institute).   1984.   Directory of  Chemical
     Producers.  Menlo Park, CA.

     U.S.  EPA.   1985.    Status  Report  on Rebuttable  Presumption  Against
     Registration  (RPAR)  or Special Review  Process.   Registration Stan-
    dards and the Data  Call 1n Programs.   Office of  Pesticide Programs,
    Washington, DC.

    U.S. EPA.   1985.   CSB  Existing Chemical Assessment Tracking System.
    Name  and CAS Number Ordered  Indexes.   Office of  Toxic Substances.
    Washington, DC.

    USITC  (U.S.  International  Trade  Commission).     1983.   Synthetic
    Organic  Chemicals.   U.S.   Production  and  Sales,   1982, USITC Publ.
    1422. Washington,  DC.

    Verschueren,  K.   1983.   Handbook of  Environmental  Data  on Organic
    Chemicals. 2nd ed.   Van Nostrand Relnhold  Co.. NY.
0867p                               -82-                              11/17/86

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    Wlndholz. M..  Ed.   1983.  The  Merck  Index,  10th  ed.   Merck  and  Co.,
    Inc., Rahway.  NJ.

    Worthing, C.R. and S.B. Walker,  Ed.   1983.  The  Pesticide  Manual.
    British Crop Protection Council.  695 p.


    In  addition,   approximately  30 compendia of  aquatic  toxIcUy data  were

reviewed, Including the following:


    Battelle's  Columbus  Laboratories.   1971.   Water  Quality  Criteria
    Data  Book.    Volume  3.   Effects  of  Chemicals  on  Aquatic  Life.
    Selected  Data  from the  Literature  through  1968.  Prepared  for  the
    U.S. EPA under Contract No.  68-01-0007.  Washington,  DC.   -

    Johnson.  W.W.  and M.T.  Flnley.   1980.  Handbook of  Acute  ToxIcUy
    of  Chemicals  to  Fish  and  Aquatic   Invertebrates.   Summaries  of
    ToxIcUy  Tests Conducted  at  Columbia  National  Fisheries  Research
    Laboratory.    1965-1978.   U.S.  Dept.  Interior,  Fish and  Wildlife
    Serv. Res. Publ. 137, Washington, DC.

    NcKee. J.E. and  H.W.  Wolf.   1963.  Water Quality  Criteria.  2nd  ed.
    Prepared  for  the  Resources  Agency  of  California,  State  Water
    Quality Control Board.  Publ. No. 3-A.

    Plmental, 0.   1971.   Ecological  Effects  of  Pesticides on Non-Target
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0867p                               -83-                              11/17/86

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