vvEPA
               Unrted States
               Environmental Protection
               Agency
               Office of Water
               Regulations and Standards
               Cntena and Standards Divwion
               Washington DC 20460
EPA «0 5-60-062
October 1980
Ambient
Water  Quality
Criteria for
Heptachlor

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      AMBIENT WATER QUALITY CRITERIA FOR

                HEPTACHLOR
                 Prepared By
    U.S. ENVIRONMENTAL PROTECTION AGENCY

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

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

        Carcinogen Assessment Group
             Washington, D.C.

    Environmental Research Laboratories
             Corvalis, Oregon
             Duluth, Minnesota
           Gujf Breeze, Florida
        Narragansett, Rhode  Island

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                              DISCLAIMER
      This  report  has been reviewed by the  Environmental  Criteria  and
Assessment Office, U.S.  Environmental  Protection  Agency,  and approved
for publication.   Mention of trade names or commercial products does not
constitute endorsement or recommendation for use.
                          AVAILABILITY NOTICE
      This  document is available  to  the public  through  the National
Technical Information Service,  (NTIS), Springfield, Virginia  22161.
                                  ii

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                               FOREWORD

     Section  304  (a)(l)  of the Clean Water  Act  of 1977 (P.L. 95-217),
 requires  the Administrator of the Environmental  Protection  Agency to
 publish  criteria for water  quality accurately  reflecting  the latest
 scientific knowledge on the kind and  extent  of all identifiable effects
 on  health and  welfare  which may  be  expected  from  the presence of
 pollutants in any body of water, including ground water.  Proposed water
 quality criteria  for  the  65  toxic pollutants  listed  under section 307
 (a)(l)  of the Clean  Water Act were developed  and  a notice  of  their
 availability was  published for public comment on March 15, 1979 (44 FR
 15926), July 25, 1979 (44 FR 43660),  and  October  1, 1979 (44 FR 56628).
 This  document  is a revision  of those proposed  criteria  based upon a
 consideration of  comments  received from  other  Federal  Agencies,  State
 agencies,  special interest  groups,  and  individual  scientists.   The
 criteria contained in  this document replace any previously published EPA
 criteria  for the 65 pollutants.    This criterion  document  is  also
 published in satisifaction of paragraph  11 of the Settlement Agreement
 in  Natural  Resources Defense  Council, et.  al.  vs. Train.  8 ERC  2120
 (0.0.C. 1976), modified, 12 ERG 1833 (D.D.C. 1979).

    The term "water  quality criteria" is used  in two  sections of the
 Clean Water Act, section 304 (a)(l) and section 303 (c)(2). The term has
 a different  program  impact in each section.  In section 304,  the  term
 represents a non-regulatory,  scientific  assessment of ecological ef-
 fects. The criteria presented in  this  publication are such  scientific
 assessments.    Such  water  quality  criteria associated  with  specific
 stream uses when adopted as State  water quality  standards under section
 303  become  enforceable  maximum  acceptable levels of  a  pollutant in
 ambient waters.   The water quality criteria adopted in the State water
quality standards could  have the same numerical  limits as the  criteria
developed under  section  304.  However, in  many situations States may want
 to adjust  water  quality  criteria developed under section 304  to reflect
 local  environmental   conditions   and  human  exposure   patterns before
 incorporation into  water  quality standards.    It is  not  until  their
adoption as part of the  State water quality  standards that the  criteria
become regulatory.

    Guidelines to assist  the States in  the modification  of  criteria
presented  in this  document,  in  the development of water quality
standards, and in other  water-related programs of this Agency, are  being
developed by EPA.
                                    STEVEN SCHATZOH
                                    Deputy Assistant Administrator
                                    Office of Water Regulations and Standards
                                   111

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    c  t:*e Toxicology

 '^ii 11 i an1 A.  Brunqs.  EcL-f-:
 U.S.  Environmental  Protection Agency

-.nalian  Toxicology an£ Human Health Effects:

 'n.  Sn.ice Peiranc (author)  HE°L


 Ter^n:^ N Gracy 'ace. mgr.} ECAO-Cin
 U.S.  Environmental  Protection Agency

 Donna  Sivulka (doc.  mgr.)  ECAC-Cin
 U.S.  Environnental  Protection Agency

 Si  Duk  Lee.  ECAC-Cin
 U.S.  Environnental  Protection Agency

 Shane  Que Hee
 University of Cincinnati
                                                  [Javid J. harser.,  E-I.-Gulf Breeze
                                                  U.S. EnvTronmenr..;1  Protect-,on
                                                 Roy E. Albert,  GAG*
                                                                      • -i - o ."-•-'  ^ -
                                                  John  Do'jll
                                                  University  of  Kansas

                                                  Kris  Khanna,  CDW
                                                  U.S.  Environmental  Protection  Agenc

                                                  Fumio Matsunura
                                                  Michigan  State University

                                                  Joseph Santodonato
                                                  Syracuse  Research Corporation
Technical Supoort Services  Staff:   D.J.  Reisman,  M.A.  Garlough,  B.L.  Zwayer,
?.f\. Daunt, K.S. Edwards, T.A.  Scandura,  A.T.  Pressley,  C.A.  Cooper,
M.M. Oenessen.

Clerical Staff:  C.A. Haynes,  S.J.  Faehr,  L.A.  Wade,  D.  Jones, B.J.  Bordicks,
B.J. Quesnell, P- Gray, R.  Swantack.
*CAG Participating Members:   Elizabeth  L.  Anderson,  Larry Anderson, Ralph Arnicar,
Steven Bayard, David  L.  Bayliss,  Chao W.  Chen,  John  R.  Fowle III, Bernard haberman,
Charaiingayya hiremath,  Chang S.  Lao, Robert McGaughy,  Jeffrey Rosenblatt,
Dnarrr V. Singh, and Todd  W.  Thorslund.
                                    IV

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                           TABLE  OF  CONTENTS
 Criteria  Suawry

 Introduction                                                       A-l

 Aquatic Life Toxicology                                            B-l
     Introcution                                                    B-l
     Effects                                                        B-2
        Acute Toxicity                                             B-2
        Chronic Toxicity                                           8-6
        Plant Effects                                              8-8
        Residues                                                   8-9
        Miscellaneous                                              B-12
        Summary                                                    B-14
     Criteria                                                       B-15
     References                                                     6-37

Mammalian Toxicology and Human Health Effects                      C-l
     Exposure                                                       C-l
        Ingestion from Water                                       C-l
        Ingestion from Food                                        C-2
        Inhalation                                                 C-7
        Dermal                                                      C-9
    Pharmacokinetics                                               C-10
        Absorption and Distribution                                C-10
        Metabolism and Excretion                                   C-12
    Effects                                                        C-19
        Acute,  Subacute, and Chronic Toxicity                      C-19
        Mutagenicity                                               C-25
        Teratogenicity                                             C-25
        Synergism and/or Antagonism                                C-26
        Carcinogenicity                                            C-27
    Criterion  Formulation                                          C-42
        Existing Guidelines and Standards                          C-42
        Current  Levels of Exposure                                 C-42
        Special  Groups at Risk                                     C-43
        Basis  and Derivation of Criteria                           C-44
    References                                                      C-48
Appendix                                                           C-60

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                               CRITERIA SUMMARY
                                  HEPTACHLOR
CRITERIA
                                 Aquatic Life
    For heptachlor  the criterion to  protect  freshwater aquatic life  as  de-
rived using the Guidelines  is  0.0038  ug/1  as  a 24-hour average, and the con-
centration should not exceed 0.52 ug/1 at any time.
    For heptachlor  the criterion  to  protect  saltwater  aquatic life  as  de-
rived using the Guidelines  is  0.0036  ug/1  as  a 24-hour average, and the con-
centration should not exceed 0.053 u9/l at any time.

                                 Human Health
    For the maximum protection of  human  health from  the  potential carcino-
genic effects due to  exposure  of heptachlor through Ingestion of contaminat-
ed water and  contaminated  aquatic organisms,  the ambient water concentration
should  be  zero  based  on   the  non-threshold   assumption  for  this  chemical.
However, zero  level may not be  attainable at  the present time.  Therefore,
the levels which may  result in incremental increase of  cancer risk over the
lifetime  are   estimated   at  10,  10"6,   and   10~7.   The  corresponding
                             co          g               Q
recommended criterion  are  2.J4 ng/1, 0.2F ng/1, and  0.02£ ng/1, respective-
ly.   If the  above  estimates  are made  for consumption  of aquatic  organisms
                                                         Q*4           C
only, excluding consumption of water, the  levels  are 2.£5*  ng/1, 0.2J ng/1,
and O.OZ^ong/l, respectively.
                                       vi

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                                  INTRODUCTION

     Heptachlor is a  broad spectrum insecticide  of  the group  of  polycyclic
 chlorinated hydrocarbons called cyclodiene  insecticides.   It  was  introduced
 in  1948 as a  contact  insecticide  under  the  trade names E  3314  and  Velsicol
 104.   During  the period  from  1971 to  1975 the most important  use of  hepta-
 chlor  was  to control  soil  insects  for corn  cultivation and other crop  pro-
 duction.   Since 1975  both  the  applications  and production volume of  hepta-
 chlor  have undergone  dramatic changes  resulting from  the sole  producer's
 voluntary  restriction of  domestic use,  and the  subsequent issuance  by  the
 U.S. Environmental Protection  Agency of  a  registration  suspension  notice  for
 all  food  crops and  home  use of heptachlor, effective  August  1,  1976.  How-
 ever,  significant commercial  use  of  heptachlor  for termite  control  or  in
 nonfood  plants  continues  and  numerous  formulation   plants  and  packaging
 facilities have remained in operation.
    Pure heptachlor  is a  white crystalline solid  with a  camphor-like  odor
 having  the molecular formula  C10H5C17,  a  molecular  weight   of  373.35,  a
melting point  of  95*C and a vapor  pressure  of  3  x 10~* mm Hg  at  25*C (Met-
calf, 1955; Martin,  1972;  Wlndholz, 1976).  It  has a solubility in  water  of
0.056 mg/1  at  25  to  29*C and  Is  readily soluble  1n  relatively nonpolar  sol-
vents (Metcalf,  1955).  The chemical  name for  heptachlor  1s  1,4,5,6,7,8,8-
heptachloro-3a,4,7,7a-tetrahydro-4,7-methano1ndene.  It  is  produced  by means
of  a  D1 els-Alder  addition  reaction which  joins cyclopentadlene  to  hexa-
cMorocycTopentadlerie  (VMndholz, 1976).
    Technical  grade  heptachlor has  the  typical composition of approximately
73  percent  heptachlor, 21  percent  trans(gamma)  chlordane, 5  percent nona-
chlor,  and  1 percent  chlordene  isomers  (Martin, 1972).   Technical  heptachlor
 is  a tan,  soft,  waxy solid with  a melting point  range  from 46  to 74*C.   It
                                      A-l

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has  a  vapor pressure  of  4 x  10   mm Hg  at 25*C and  a  density of 1.65 to
1.67 g/ml at 25*C.
     In  general,  heptachlor is  quite stable  to chemical  reactions  such as
dehydrochlorination, autooxldation,  and  thermal decomposition.   However, in
the  environment,  heptachlor undergoes numerous microbial, biochemical, and
photochemical reactions.
     Conversion  of  heptachlor  to  heptachlor epoxide  has been  reported in
microorganisms (Miles, et al. 1969), in  plants  {Gannon  and Decker,  1958), in
soils (Lichtenstein, 1960, Llchtenstein, et  al.  1970,  1971;  Nash and  Harris,
1972),  and  in mammals  (Oavidow and Radomskl,  1953a,b).   It represents the
principal metabolite of heptachlor.
    The  photodecomposition  Of  heptachlor to  photoheptachlor  has been  demon-
strated  in  various solvent  solutions  using  ultraviolet  lamps,  and as  thin
films  using  natural   sunlight   (Benson,  et  al.  1971).   Although  numerous
photoisomers  are   produced,  photoheptachlor  (III)  appears  to  predominate.
Heptachlor  epoxide has  also  been  shown  to  undergo  photodecomposition  to
photoheptachlor epoxide (IIIB)  when  exposed  to  UV light or sunlight (Graham,
et al. 1973).
    Heptachlor  can also  be  biologically  converted  to  chlordene,  3-chloro-
chlordene,  1-hydroxychlordene,  chlordene epoxide, l-hydroxy-2,   3-epoxycnlor-
dene, and 2-chlorochlordene.
    Tbt  persistence of heptachlor and heptachlor  epoxide  in the environment
1s M»11 -known.  Heptachlor  also has  been shown to be  converted  to  the meta-
bolite,  heptachlor epoxide,   1n  various  soils  (Gannon  and Bigger,  1958;
Lichtenstein,  1960; Llchtenstein, et «1.   1971; Nash  and Harris,  1972} and
plants  (Gannon and  Decker, 1958).
                                      A-2

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                                  REFERENCES

 Sensors,  W.R., et  al.  1971.   Photolysis of  solid  and  dissolved  dieldrin.
 Jour.  Agric,  Food  Chem.   19: 65,

 Davidow,  8,  and J,U  Radomskis   1953a«   Isolation of  an  epoxide  metabolite
 from   fat  tissues  of dogs  fed  heptachlor.   Jour.  Pharmacol.  Exp.  Ther.
 107: 259.

 Oavidow,  B.  and J.L.  Radomski.   1953b.  The  metabolite of  heptachlor,  its
 estimation, storage, and  toxicity.  Jour. Pharmacol. Exp. Ther.  107: 266.

 Gannon, N. and  J.H. Bigger.  1958.  The  conversion of  aldrin and heptachlor
 to their epoxides  in soil.  Jour. Econ. Entomol.  51:  1.

 Gannon, N. and  G.C. Decker.  1958.  The  conversion of  aldrin to dieldrin on
 plants.  Jour. Econ. Entomol.  51: 8.

 Graham, R.E., et al.   1973.  Photochemical  decomposition of heptachlor epox-
 ide.  Jour. Agric. Food Chem.  21: 284.

 Lichtensteln, E.P.  1960.  InsecticidaT  residues  1n  various  crops  grown in
 soils  treated  with abnormal rates  of aldrin  and heptachlor.   Jour.  Agric.
 Food Chem.  8: 448.

 Lichtensteln, E.P.,  et al.  1970.   Degradation of aldrin  and heptachlor in
field soils.   Jour. AgHc. Food Chem.  18: 100.
                                      A-3

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Lichtenstein, E.P., et al.   1971.   Effects  of  a  cover  c     /ersus  soil  cult-
ivation on the fate of vertical  distribution of  insects  e residues  in  soil
7 to 11 years after soil  treatment.  Pestic. Monitor.     -.   5:  218.

Martin,  H.,   (ed.)   1972.   Pesticide Manual,  3rd  (ed.).   Br.  Crop  Prot.
Counc., Worcester, England.

Metcalf,  R.L.   1955.  Organic  Insecticides.   Interscience Publishers,  John
Wiley and Sons, Inc., New York.

Miles,  J.R.H.,  et al.  1969.  Metabolism  of  heptachlor and  its  degradation
products by soil microorganisms.  Jour. Econ.  Entomol.   62:  1334.

Nash,  R.6.   and  W.G.  Harris.   1972.   Chlorinated hydrocarbon  insecticide
residues in crops and soil.  Jour. Environ. Qual.  2:  269.

Windholz, M.,  (ed.)   1976.  The  Merck  Index.   Merck  and Co.,  Inc.,  Rahway,
Mew Jersey.
                                      A-4

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 Aquatic  life  Toxicology*
                                  INTRODUCTION

     Heptachlor  is a chlorinated hydrocarbon pesticide  that  has  had wide us-
 age  in  the  United States  as  a crop insecticide.   It has been widely used for
 such  purposes as  fire  ant  and general insect control  in  much  of the United
 States.   It has  been  shown  to  be toxic to  aquatic life,  to  accumulate  in
 plant and animal  tissues, and to persist  in aquatic  ecosystems.
     Earlier studies  reported toxicity of this material  to freshwater organ-
 isms.  More recently,  pertinent studies have been completed that demonstrate
 acute and chronic toxicity  and b1oaccumulat1on potential to saltwater organ-
 isms.  Most of  these studies,  however, were  carried out under static condi-
 tions with  results based on  unmeasured rather than measured concentrations.
 In most  instances  tests used  technical  grade  heptachlor  as  the  toxicant.
Technical grade  heptachlor  usually consists of  72  percent heptachlor and 28
percent  impurities;  these   impurities are  primarily  trans-chlordane,  cis-
chlordane, and nonachlor.   There  are  insufficient data to evaluate the rela-
tive toxicitles  of  the  various grades of  heptachlor and the  Impact of the
 impurities on the toxicity  determinations.   Because of the unknown contribu-
tion of  the Impurities,  all  data Included In this  document are reported 1n
concentrations of the actual  material  used for  testing.   Some authors used
technical material  in testing and  then calculated concentrations as  100 per-
cent heptachlor  for  data reporting.   These data  were converted back to con-
*The reader  1s  referred to the  Guidelines  for Deriving Water Quality  Crite-
ria for  the  Protection of Aquatic  Life  and Its Uses  1n  order to better un-
derstand the  following discussion  and  recommendation.  The following  tables
contain  the  appropriate data that were  found  In the  literature,  and at the
bottom of  each  table are calculations  for  deriving various measures of  tox-
icity as described in the Guidelines.
                                      B-l

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centrations of technical grade heptachlor  in this document.
     Some  reported studies  have examined  the  impact  of water  hardness  and
temperature  on acute  toxicity of  heptachlor.   Variable results  were  found
regarding  the effect  of  temperature on  heptachlor toxicity,  whereas  water
hardness  had  little  effect on  toxicity  to  fathead  minnows  in a  single
comparison.
     Heptachlor  epoxide is  the most commonly found degradation  product  of
heptachlor.   Both heptachlor  and  heptachlor epoxide  have  been  reported  in
fish  residues.   There are  few  data on the  relative toxicity to aquatic or-
ganisms of  these  two materials.  What  data  are available  suggest  that the
epoxide is not more  toxic than heptachlor  itself.
                                    EFFECTS
Acute Toxicity
     In  all  but one  case  (Macek, et al.  1976)(Table  6),  freshwater  data on
acute  toxicity were obtained  in static  tests,  and in every case  exposure
concentrations were  unmeasured.  Values for standard tests with fish and in-
vertebrate species are reported  in  Table  1, and some additional acute toxic-
ity  data  are given  in  Table 6.  Ten freshwater  invertebrate and eight fish
species have been tested.
    Many of  the  authors  cited in Table 1 reported values for  numerous other
pesticides  in  addition to  heptachlor.   No clear relationship regarding the
toxicity of heptachlor compared  to  other pesticides was found.  For example,
heptachlor 1$  substantially less toxic  to the scud, Gammarus  fasciatus, than
DOT  and endrln;   for the  freshwater glass shrimp,  however,  there 1s little
difference 1n  toxicity among the three pesticides  (Sanders, 1972).   For the
stonefly, Pteronarcys  californica,   heptachlor 1s  less toxic than endrin and
more  toxic  than  DOT  (Sanders  and  Cope,  1968).   Katz  (1961)  found  with
chinootc  salmon and  coho  salmon  that  DDT  and  endrln  are  more  toxic than

                                      B-2

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 heptachlor,  whereas with rainbow  trout,  heptachlor is more  toxic  than DDT.
 It is difficult to determine  how  many of the variations  in  results  are due
 to differences  in species  sensitivity  and  how much  to  test  variability.
 However,  it  seems  probable  that species sensitivity varies considerably with
 different  pesticides.   It  is also  apparent  from the  data in Table  1 that
 heptachlor  is  generally  highly toxic  in an acute exposure.
    LC50  values for  invertebrate  species  range  from 0.9  ug/l  for  a 96-hour
 exposure  with  the  stonefly,  Pteronarcella  badia, to 80  ug/1 for  a 48-hour
 exposure  with  the cladoceran,  Simocephalus serrulatus  (Table 1).   Larvae of
 the Fowler's toad were  tested by Sanders (1970)(Table 6); the 96-hour LC5Q
 is 440 i»g/l.
    Freshwater  fish species are generally less  sensitive to heptachlor than
 are  invertebrate  species  (Table  1).   Ninety-six-hour  IC5«  values  for fish
 species range   from 10.0 ug/1  for rainbow  trout to  320  ug/1  for goldfish
 (Table 1).
    The Freshwater Final Acute  Value for heptachlor, derived  from the spe-
cies mean  acute values  listed in Table  3 using the procedure  described in
 the Guidelines,  is 0.52 ug/1.
    There is little information  regarding the possible  effect of water hard-
ness  on  the toxicity of heptachlor.  The 96-hour  LC50  values  for fathead
minnows exposed  to  technical  grade heptachlor in soft and hard water are 130
and 78 wg/1. respectively (Henderson, et  al.  1959).  It  is difficult to for-
mulate any  conclusions  regarding  hardness-related effects  on the  basis of
these tests.
    Bridges  (1965Lfound that  toxicity to redear sunflsh Increased at  higher
temperatures  (Table 6).   Twenty-four-hour ECgQ values  decreased   (toxicity
 increased) from 92 wg/l  at  45*F to  22 Pg/l  at  85*F.  Macek,  et  al.  (1969)
 found essentially  no  difference in toxicity  to  rainbow trout when tested at

                                      B-3

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1.6, 7.2,  and  12.7'C  (Table 1).   Naqvi  (1973)  found 100 percent mortality of
tubificid  worms,  Sranchiura sowerbyi.  at 2,500  ug/1  when tested at 4.4  and
32.2*C  (Table  6);  at  21.0'C no mortality occurred.   Sanders  and Cope  (1966)
found  that with  the  cladoceran,  Simocephalus  serrulatus,  the  48-hour  ECgo
values for heptachlor were 47 ug/l at 60*F and 80 ug/l at 70*F (Table 1).
    Only  one  acceptable freshwater study was  found that compared  the  rela-
tive  toxicity  of  heptachlor  to its  common  degradation  product,  heptachlor
epoxide.   Frear  and Boyd  (1967),  using  an  unspecified grade of material,  de-
termined  the   26-hour  LC^Q for Daphnia  magna  to be  52  ug/1  for  heptachlor
and 120 ug/1 for heptachlor epoxide (Table 6).
    Many  authors  reported LC5Q  values for  freshwater  fish  species  after
24, 48,  and 96  hours  of  exposure to heptachlor.   In  general,  toxicity  in-
creased  slightly with  time,  although  considerable variation  existed  among
species.   The  ratios  of  96-hour/24-hour  and  96-hour/48-hour LC50  values
ranged from 0.45 to 0.97  and  0.57 to 1.00, respectively.   The relationship
of  LCgg  values  to  exposure time  was more  dramatic and  variable  for  inver-
tebrate  species.   The  range  of  values for  the  ratio of  96-hour/24-hour
LCg0 values was 0.06 to  0.56.   Exposure time,  therefore,  can significantly
affect ICgQ values for  invertebrate species exposed to heptachlor.
    Heptachlor has been shown  to  be acutely toxic  to  saltwater fish and in-
vertebrate  species.   Many  of  the  saltwater  toxicity  tests  with  heptachlor
have used  technical  grade material containing  approximately  65 percent hep-
tachlor, with  the remaining 35  percent  being a mixture of trans-chlordane,
cis-chlordane,  nonachlor,  and  related  compounds.   There  are insufficient
saltwater  data to  evaluate relative toxicity  of  heptachjor  and heptachlor
epoxide.  However, the  data available suggest  that toxicity of the  technical
material is mostly attributable to heptachlor  and  that toxicitles of hepta-
chlor and heptachlor  epoxide are  similar (Schlmmel, et al.  1976a).  The  tox-

                                      B-4

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 fcity of the several  chlordane isomers 1s discussed in the criteria document
 for   that  compound and  is,  in  general,  2  to  7  times  less  than that  of
 heotachlor.
     Saltwater  invertebrate species seem to be more  sensitive  than fish spe-
 cies  to heptachlor and  heptachlor epoxide and demonstrate  a  greater  varia-
 bility   in  sensitivity  between  species  (Table   1).   Of  the   seven  species
 tested,  the commercially  valuable  pink:  shrimp is especially  sensitive with
 96-hour  I_C50  values  as  low  as  0.03  wg/l  (Schimmel,  et al.  1976a).   Other
 species,  such  as the blue  crab  and American  oyster, are 2,100  to 950 times
 less  sensitive,  respectively,  than the pink  shrimp (Butler,  1963)(Tables 1
 and  6).   Ninety-six-hour  LC50 values derived front static exposures  or  ex-
 posures  based  on  unmeasured  concentrations  probably  underestimate toxicity
 of heptachlor  and heptachlor  epoxide  to  Invertebrate  species.  For example,
the 96-hour  LC5Q  of  heptachlor  for the  grass shrimp  based on  a  static  ex-
posure using unmeasured  concentrations  is 440 gg/1 (Eisler,  1969),  whereas
the result  from  a flow-through  test with measured concentrations  is 1.06
ug/l   (Schimmel,   et  al.   1976a).    A  similar   relationship  is  true for  the
American oyster.   Test results from  a flow-through  exposure with unmeasured
concentrations  (Butler,  1963) were 27 and 30 ug/l and,  using flow-through
procedures and measured  concentrations,  Schimmel,  et  al.  (1976a) determined
a 96-hour  ECgg  of 1.5 yg/1.   Generally toxicity data  obtained from static
tests  or those  1n which   concentrations  were not  measured  yielded  higher
 acute  values  for  heptachlor  than other  tests.   The  range of  LCg0  values
for saltwater  Invertebrate  species  is  from 0.03 to 440 ug/l.
    The  96-hour  LC50 values  (Table 1) derived from flow-through  .tests with
four  saltwater fish species range from 0.85 to 10.5 ug/l  (Korn and Earnest,
 1974; Schimmel,  et al. 1976a; Hansen  and Parrlsh,  1977).   Results of  static
 exposures  of  eight  fish  species  are more  variable  and  yield  higher LC^g

                                      8-5

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values  than those  from  flow-through  tests;  i.e.,  0.8  to  194  ug/l  (Katz,
1961;  Eisler,  1970a).   LC50  values   derived  from  tests  using  aeration,
static test  procedures,  or unmeasured  concentrations  probably underestimate
the toxicity of heptachlor (Schimmel, et al. 1976a; Goodman, et al. 1978).
    The Saltwater Final  Acute  Value  for heptachlor,  derived from the species
mean  acute values  listed in  Table  3  using  the procedure described  in  the
Guidelines, is 0.053 ug/1-
Chronic Toxicity
    The only  available  freshwater  chronic study  on  heptachlor  was  that  of
Macek, et  al.  (1976)  using  the fathead  minnow  (Table 2).   This life-cycle
test  lasted  40 weeks  during which  growth,  survival,  and  reproduction  were
monitored.   Concentrations  tested  were  1.84,  0.86,  0.43,  0.20,  and  0.11
ug/l.  All  fish  exposed  to  1.84 ug/l  were  dead after 60  days.   No adverse
effects on parental  fish or  their offspring  were  noted at concentrations of
0.86  ug/l  or  lower.  Analytical  difficulties  were encountered  during  the
last 10 weeks of the 40-week  exposure  period.  However, all effects found in
the study occurred  during the  first  60 days, and so the  analytical difficul-
ties did not affect the  reported chronic  endpolnt values.   The chronic lim-
its of heptachlor  for fathead  minnows  are 0.86 and  1.84 ug/l.   Data on the
acute toxicity of  heptachlor  to  fathead minnows  indicate  that this species
is generally somewhat  less sensitive than other fish species.  There are no
direct  comparisons   between  the  chronic  results  for  fathead  minnows  and
96-hour LC50  values from tests conducted  by the same  author.   However, by
using the species mean acute value  for  fathead minnows, an acute-chronic ra-
tio of 80 can be calculated for fathead minnows  (Table  2).
    No valid  chronic  test data were  available  for  any  freshwater  inverte-
brate species.  However, 1n  general, invertebrate acute values are  consider-
ably  lower  than  fish  acute  values  (Table 1);  Indeed, some  LC5Q values for

                                      B-6

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 Invertebrate  species  were lower than  the  chronic  value for fathead minnows.
 It  is reasonable  to  expect,  therefore,  that  some  freshwater invertebrate
 chronic  values would  be  lower  than  the  available  freshwater  fish  chronic
 value.
     Insufficient  data are available to  calculate  a Freshwater Final  Chronic
 Value for  heptachlor.
     A  28-day life-cycle  toxicity  test (Table 6) was  completed with  a salt-
water mysid shrimp, Hysidopsis  bahia  (U.S. EPA, 1980).   Mortality of mysid
shrimp exposed  to measured  concentrations  of 0.17,  0.64,  1.3, and 3.1 ug/1
was significantly greater than  that  in the control.  Mortality of  animals at
an intermediate low  concentration  of 0.33 ug/1  was not significantly differ-
ent from controls.   Because  of  this  anomaly  in  the data,  the more conserva-
tive estimate of effect  on mortality is used (0.64 i»g/l).  Statistical anal-
ysis of  data on cumulative  number of offspring  per female per day  did  not
reveal significant  differences  between  the control  and  any  test  concentra-
tion.  Therefore, cumulative mortality of  test  animals  exposed to 0.64 ug/l
heptachlor  was  the  most  sensitive effect.   Because  this  effect  is based on
anomalous data, test results are included in Table  6  rather than Table 2.
    The  chronic  toxicity of technical  heptachlor  to  the sheepshead minnow
was measured  in  an  18-week  partial  life-cycle  exposure begun with juveniles
(Hansen and  Parrish,  1977).   Survival was  affected at concentrations of 2.8
ug/l and  greater  (Table  6).   Embryo production was  significantly decreased
at the lowest  concentration  tested,  0.71,  and  at  test concentrations of 1.9
to 5.7 iig/1.   An  Intermediate  test  concentration,  0.97 yg/1,  did not cause
reduced embryo production significantly different from controls.   Because of
this anomaly 1n the  data, test  results were  Included 1n  Table 6 rather than
Table 2.
                                      B-7

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    The  chronic  toxicity of  technical  heptachlor to sheepshead  minnows  was
also measured  in  a  separate 28-day early  Tife-stage  test.   Hatching  was  un-
affected,  but  survival  of  fry was significantly  reduced from that  of con-
trols  at  measured  concentrations  of  2.24  to  4.3  ug/1   (Goodman,  et  al.
1978).   Comparison of these data  with  that from the early life-stage  portion
of the  partial life-cycle exposure  (Hansen and  Parrish,  1977)  shows survival
of  fry was reduced  at  a similar  concentration  in both  exposures  (2.24  and
2.8 ug/1,  respectively).  Growth  of fry in the early life-stage  test (Good-
man, et  al.  1978) was  significantly  reduced  at  concentrations of  2.04  ug/l
and above.  No detrimental  effects were observed  at  1.22  ug/1.   If observed
decreases  in embryo  production in  the  partial  life-cycle  test at  0.71  ug/l
are an  anomaly,  then the results from  the  embryo-fry  exposure  predict  the
results of a life-cycle toxicity test rather accurately.
    Chronic  values   for saltwater  species can be  obtained  from only  the
sheepshead minnow early  life-stage test  (Table   2)  and not  the  life-cycle
tests on  this  fish  species and mysid shrimp  (Table 6).   The  chronic  value
from the  early life-stage  test is  1.58  ug/1,  and the acute-chronic ratio is
3.9.   If  effects  observed  in  the sheepshead  minnow  partial  life-cycle  test
at 0.71  ug/l  and in the mysid shrimp life-cycle  test at  0.17  ug/l are con-
sidered anomalies, the  acute-chronic  ratios calculated  using these two tests
are 4.6  and  7.6, respectively.  The range  1n acute-chronic ratios  for  the
three tests 1s  remarkably narrow, less than a factor of  two.
Plant Effects
    Two 96-hour tests with  a  freshwater algal  species,   Selenastrum capricor-
nutum,  have  been conducted (Table 4).    The  ECgg values  obtained are  39.4
and 26.7  ug/1.   It should be  noted that the exposure concentrations  of hep-
tachlor rapidly  diminished  during  the  course  of  the tests,  and  substantial

-------
 amounts of  hydroxychlordene  were present and  may have contributed signifi-
 cantly to  the toxic effect  (Call  and  Brooke^  1980).
     Information on the sensitivity of saltwater aquatic plants is limited to
 effects on  five species of  unicellular  algae,  or dinoflagellates  and  one
 study on a natural  phytoplankton  community (Tables 4 and 6).
     Effects of heptachlor on  three species of marine unicellular algae, Iso-
 chrysis galbana, Porphyridium cruentum, and Skeletonema costatum, are fairly
 similar.   The  96-hour ECgo  values   range from  93  to  273  wg/l.   The EC5Q
 for  a fourth  species,  Dunaliella  tertlolecta.  is  8 to 24 times higher  (Table
 4).
     Toxicity  tests with  the  marine  dinoflagellate,  Exuviella baltica. show
 effects of heptachlor  at  a  concentration  of 50 ug/1  (Table  6).  Cell densi-
 ty,  chlorophyll  a^ per  unit  volume  of  culture,  * C  uptake   per  cell,  and
carbon  fixation  per unit  of chlorophyll £ were reduced at this concentration
after  seven days.   The  natural  phytoplankton  community study was  a 4-hour
exposure at  a single exposure  concentration  of 1,000  ug/1.   This concentra-
tion  of heptachlor caused  a  94.4 percent decrease  in  productivity (Butler,
1963)(Table 6).
Residues
    The only  appropriate  residue  studies on  freshwater  species are those re-
oorted by Velth, et al.  (1979).  These studies used 32-day exposures of fat-
head  minnows  to heptachlor and heptachlor epoxide (Table 5).   Bioconcentra-
tion  factors  (BCF)  are  9,500  for  heptachlor  and 14,400  for  heptachlor
epoxide.
    Andrews,  et  al. (1966)  reported  the  results  of tests 1n which bluegills
held  in plastic pools were fed  food containing  heptachlor at either 25.0,
10.0, 5.0,  or  0.0  mg/kg/day (Table 6); tests were run  1n duplicate.  Effects
on survival,  histopathology,  and  growth were monitored.  In general, adverse

                                      B-9

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effects were found  at  a  feeding rate of 10 mg/kg/day.  In order to determine
a maximum dally  dietary  Intake  level for wildlife, a value  of  7.1  mg/kg/day
(the geometric mean of 5 and 10 mg/kg/day) was calculated.
    Data on  the bioconcentration of heptachlor  and heptachlor epoxide  from
water  Into  the tissues  of  saltwater organisms  are given 1n Tables 5  and  6.
The only  8CF  values available  at steady-state for  heptachlor  and  heptachlor
epoxide are those for fish species (Table 5).
    The three  studies  (Schlmmel,  et  al.  1976b;  Hansen  and Parrish,  1977;
Goodman, et al.  1978)  listed  1n Table 5 used technical  heptachlor containing
65 percent heptachlor,  22 percent trans-chlordane,  2  percent cis-chlordane,
2  percent  nonachlor, and  9 percent  other  unidentified  compounds.   Goodman,
et al.  (1978)  and  Hansen and  Parrish  (1977)  measured  both  heptachlor  and
trans-chlordane  1n  the  exposure water.   Schlmmel, et al.  (1976b)  measured
only heptachlor  1n  the  exposure water.  Each study  measured concentrations
of heptachlor, heptachlor  epoxide,  trans-chlordane, and  c1s-chlordane in ed-
ible tissues  or  whole fish.   Therefore, several calculations  of  8CF values
are possible, and these  are given In Table 5.
    Spot exposed  for 24 days to technical  grade material  reached  a  maximum
concentration of heptachlor  1n  whole body after three days  (Schimmel, et al.
1976b).   In  the  same  exposure,  maximum levels  of heptachlor epoxide  were
reached 1n whole fish  after 17  days.  Whole body residues were generally 1.6
times higher than residues  1n edible portions of fish.   After a 28-day peri-
od of  depuration,  less  than  10 percent of  the  maximum  amount of heptachlor
remained  1n  tissues;  1t  was  either  lost  or  metabolized  to the  epoxide
(Schimmel, et al. 1976b).
    Juvenile sheepshead  minnows exposed 1n two  separate  exper-    ts for  28
days to  technical  grade material had  similar  BCF values,  I.e.,  4,667  and
5,700  (Hansen  and  Parrish,  1977; Goodman,  et al.  1978).   Adult sheepshead

                                      B-10

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 minnows  exposed to technical grade  material  for  126 days accumulated hepta-
 chlor and heptachlor  epoxide to  a  much  greater  extent, an  average 37,000
 times that 1n the exposure water  (Hansen  and Parrish, 1977).  The BCF values
 derived  in  the  above studies are from effect,  as  well as  safe concentra-
 tions, and they appear similar.
     The  only BCF values considered  appropriate for  heptachlor  for the deri-
 vation  of a  Final  Residue  Value  were those based  on  the  concentration  of
 heptachlor in water  and  the total  concentration of heptachlor and heptachlor
 epoxide  in tissue.   Dividing a  BCF value  by  the  percent lipid  value for the
 same  species  provides a BCF  value adjusted  to  1  percent lipid content; this
 resultant  BCF value is  referred  to  as the  normalized bioconcentration fac-
 tor.  The  geometric mean of the  appropriate normalized  BCF values for hepta-
 chlor for  freshwater and saltwater aquatic life is 5,222  (Table 5).
    Dividing  the  U.S. Food  and  Drug  Administration (FDA) action  level of 0.3
mg/kg for  edible  fish  and  shellfish  by the  geometric  mean  of normalized BCF
 values (5,222)  and by  a percent  lipid value  of 15  for freshwater species
 (see  Guidelines)  gives  a freshwater residue value  of 0.0038 »g/l  based on
marketability  for human consumption  (Table  5).   Dividing  the  FDA action
 level (0.3 mg/kg) by the geometric mean  of normalized BCF values  (5,222) and
by a  percent  lipid value of  16  for  saltwater species (see Guidelines) gives
a saltwater  residue  value  of 0.0036 gg/1.  Also based  on  marketability for
human consumption,  using the FDA  action  level  and  the highest  appropriate
BCF for edible portion of a consumed species (3,435 for  spot for  saltwater),
a  saltwater  residue  value  of   0.087  wg/l  1s  obtained   (Table   5).   No
appropriate BCF value for  edible portion  of  a  consumed species  Is available
for  freshwater.   The  Freshwater  Final  Residue Value  1s 0.0038 u9/L   The
Saltwater  Final  Residue Value  is  the  lower of  the  two calculated residue
                                     8-11

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values  and  is  0.0036 ug/l.  It  should  be  pointed  out that the Final  Residue
Values  may  be too  high because  the  average concentration  in a high  lipid
species will be at the FDA action level.
Miscellaneous
    Macek,  et  al.   (1976)  reported  an  incipent   LC5Q  of  7.0  ug/l  for  a
10-day  exposure  of  the  fathead minnow  (Table  6).  This  incipient LC50  was
derived  using  flow-through testing procedures  by  determining when no  addi-
tional  significant mortality  (less  than 10 percent) was  observed at any con-
centration during a  48-hour  period.  A linear regression equation was calcu-
lated by converting  test  concentrations and corresponding  mortalities  into
logarithms and probits,  respectively.   This equation was then used to deter-
mine  the incipient  LC5Q.   Due  to  analytical  difficulties,  however, actual
concentration measurements were not made;  rather,  concentration values were
based on nominal values.
    Andrews,  et  al.  (1966)  studied  the  impact of a single  application of
technical grade heptachlor in  several  earthen ponds (Table 6).  Initial con-
centrations as technical grade heptachlor  in the test ponds ranged from 17.4
to 69.4  ug/l.  Residue  levels  measured in  stocked  bluegills were not propor-
tional  to  dosage.   Time  to  peak residue   levels  depended  on concentration,
with  the  lower  concentrations  peaking  within 24  hours.   Residue concentra-
tions at all  test levels decreased to  below detectable  limits by the end of
84 days.   Although  the  data  were not  usable for  calculating  8CF  values in
this  document,  maximum  BCF  values, based  on peak  residue  levels  for total
heptachlor, heptachlor  epoxide, and  related compounds, compared  to  initial
dose  concentrations  of  technical grade  heptachlor,  ranged  from 638 to 1,326
ug/l.   The highest  BCF value  was for  fish in one  of  the  intermediate level
ponds.
                                      B-12

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     In vitro measurements  of the effect of heptachlor on biochemical activi-
 ty have also been  reported by several  authors (Table 6).  The value of these
 data  for  criteria derivation  is  limited,  however, since  no environmental
 dose relationships  were tested  or derived.
     A  study  by  O'Kelley  and Deason  (1976)  Investigated the  effect  of hep-
 tachlor  on  the  growth  of 20 algal  species isolates from Black Warrior River,
 Alabama  (Table  6).   Exposures were  conducted in FW-1 algal media spiked with
 10,  100 and  10,000  «g/l  heptachlor.   Effects  on growth were  determined by
 comparison  with  control  values  after  two weeks  of  exposure.   Variable spe-
 cies responses were found.  At all   three  concentrations  the majority of the
 species  exhibited  51  to  110  percent growth  compared to controls.  At 10 and
 100  ug/1  there  were no  species that  grew at  less  than 50  percent  of con-
 trols.   At  1,000 wg/1  two  species  grew at less than 50 percent of controls,
 but there was also  one species  that grew at 151  to  190 percent of controls.
 The values for particular species were  not specified.
    Other saltwater BCF data  (Table  6)  available  for heptachlor  and hep-
 tachlor  epoxide are   based  on  short-term  exposures  and  are  probably  not
 steady-state  values (Wilson, 1965;  Schimmel, et  al.  1976a).   These values
 are  also measured  at  effect exposure concentrations.  Two shrimp species,
 pink shrimp  and  grass  shrimp,  showed  less bioconcentration in 96-hour expo-
 sures  to technical  heptachlor  than did  another Invertebrate  species,  the
 American oyst«r  (BCF  values ranged  from  200 to 700 for the shrimp and from
 3,900  to 8,500  for  oysters).  A BCF  of  17,600  was obtained  in a separate
 10-day exposure  of oysters to  technical  heptachlor  (Wilson, 1965).  The BCF
 values for  three fish species  exposed for  96  hours to technical heptachlor
 ranged from 2,800 to 21,300.
    Exposure  to  heptachlor  as the technical  material and to analytical grade
heptachlor  (99  percent pure  heptachlor)  gave comparable  BCF  values for two

                                     B-13

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species  tested.   The pink shrimp  had  BCF values of 200 to  300  when  exposed
to  technical  material  and from 300 to  600 when exposed to  analytical  grade
heptachlor.   The spot had  BCF values  from  3,000  to 13,800 when  exposed  to
technical material,  as compared  to 3,600 to 10,000  1n  an  exposure to analy-
tical material.
    Table 6  contains no  saltwater  effect data at  lower  concentrations  than
those summarized  in  previous  tables,  except for the work  of Hansen  and  Par-
Msh (1977) and U.S. EPA  (1980), which were discussed earlier.
Summary
    Acute  toxidty  data  are  available  for  18 freshwater  invertebrate  and
fish species.   Species mean acute values  range from 0.9  to 78  ug/l  for  in-
vertebrate  species  and  from  13.1  to  320 ug/l  for fish   species.   A single
life-cycle  test  has been  conducted  with  the  fathead minnow,   providing  a
chronic  value of 1.26 pg/1  and an acute-chronic  ratio of  80 for this  spe-
cies.  No chronic data are available for  any freshwater Invertebrate species.
    Steady-state  bioconcentration  factors for  fathead  minnows  are 9,500 for
heptachlor and  14,400  for heptachlor epoxlde.   Adverse effects  on bluegills
were observed at a  feeding  rate of 10 mg/kg/day.  EC5g   values  of  39.4 and
26.7 ug/l  are  available  for  a  freshwater algal  species,  although  hydroxy-
chlordene was present  1n  the  test solutions and may have  contributed signif-
icantly to the observed toxlcity.
    Acute  toxidty  data  are  available  for 19 species of  saltwater organ-
Isms.  The range of  species mean  acute  values  1s from 0.04 to  194 wg/l.   The
96-hour  LC--  values for  pink shrimp  from flow-through tests with  measured
concentrations  are  0.11  ug/l  using technical  heptachlor  and 0.03 ug/l using
99  percent  pure  heptachlor.   Three  saltwater chronic toxidty  tests  have
been conducted, but the  only acceptable one  was an  early life-stage test
with the sheepshead minnow  which resulted  1n a  chronic  value  of 1.58 ug/l

                                     8-14

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 and  an acute-chronic ratio  of 3.9.   If  the  acute-chronic ratio for penaeid
 shrimp is  similar to that of  the  tested  species,  then chronic effects might
 be expected to  occur  at concentrations  less  than 0.008  ug/1.   EC5Q values
 for  four saltwater  algal  species range from 93 to 2,260  ug/1.
     The  saltwater  bioconcentration  data show  that uptake of  heptachlor is
 fairly rapid,  reaching  a maximum in one  study  in  three  days.  However, hep-
 tach^or  is  readily metabolized in fish  to  heptachlor  epoxide.   The relative
 amount of  heptachlor epoxide  in  tissues increased with  length  of exposure,
 with the maximum amount  occurring  by day 17.   After a 28-day depuration, ap-
 proximately  90 percent  of  the heptachlor was either  eliminated or degraded
 to heptachlor  epoxide.
    Freshwater and  Saltwater  Final  Residue  Values  of 0.0038 and 0.0036 pg/1,
 respectively,  were  derived.   However, these Final  Residue Values  may be too
high because the average concentration  1n a  high lipid  species  will  be at
FDA action levels.
                                   CRITERIA

    For heptachlor  the  criterion  to  protect  freshwater aquatic  life  as de-
rived  using  the  Guidelines  is 0.0038 ug/1 as  a 24-hour  average, and the con-
centration should not exceed 0.52  wg/l  at any time.
    For heptachlor  the criterion  to  protect  saltwater  aquatic  life  as de-
rived  using  the  Guidelines  is  0.0036  tfg/l  as a  24-hour average,  and the
concentration should not  exceed 0.053  ug/1 at any time.
                                      B-15

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Tab la 1.  Acwta wlaaa  for haptadtlor
Spaclaa
H**oa«
C^.cal
U34/H30
Spaclaa Maaa
Anita Valwa
two/D Hafaraaca

FRESHWATER SPECIES
Cladooaraa,
Capital* jjgjm
Cladooaraa,
Dapaala put ax
Cladocaran,
Slaocaphalu* *arrulatu»
Cladocaran,
Slaocaphalu* *amil*tus
Scud,
GaaMTu* faaclatu*
Scud,
Gaaa»ru* ta*clatu>
Scud.
Gaamaru* lacu»trl»
CraylUh,
Ola** ahrlap.
Stoaaf ly.
S tonal ly.
Stonatly,
Ptaronarcy* call torn lea
Coho calami,
Oncorhynchu* M*utch
Chinook *alaon,
Oocorhyachtj* t*ha»yt*cha
S, U
S, U
S, 0
s. u
s. u
s, u
s, u
s. u
s, u
s. o
s, u
s, u
s, u
s, u
Haptachlor (99f)
UntpaclHad
grada
Uncpaciflad
grada
grada
Tachnlcal
haptachlor (72$)
Tachnlcal
haptachlor (72$)
Tachnlcal
haptachlor (72$)
Tachnlcal
haptachlor (72|)
Tachnlcal
haptachlor (72$)
Tachnlcal
haptachlor (72$)
Tachnlcal
haptachlor (72$)
Tachnlcal
haptachlor (72$)
Tachnlcal ••
haptachlor (72$)
Tachnlcal1*
haptachlor (72$)
70
42
47
00
96
40
29
7.6
1.6
2.0
0.9
I.I
01.9
24.0
70 MacaK. at al. 1976
42 Sandar* 1 Copa, 1966
Sandar* 1 Copa, 1966
61.3 Sandars 1 Copa, 1966
Sandar*, 1972
47.3 Sandar*, 1972
29 Sandar*, 1969
7.0 Sandars, 1972
1.0 Sandar*, 1972
2.0 Sandar* t Copa, I960
0.9 Sandars 4 Copa, I960
I.I Sandar* & Copa, 1966
01.9 Kotz, 1961
24.0 Katl. 1961
                  B-16

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TabU I.   (Continued)
Speclaa
Rainbow trout,
Salao palrafrarl
Ralnbov trout.
Selao oalrdnerl
Rainbow trout.
Satan oalrdnerl
Rainbow trout,
Salao oalrdnerl
Goldfish.
Carats lu> auratus
Fathead •lnno«,
Plawphalae proa* las
Fathead •Innow,
Plaaohales proMlas
Guppy,
Poacllla ration lata
Blueglll.
LapOB.lt aacrodilrus
Raoaar sun fish,
Lapoals •Icrolophus
Aawrlcan oymtar,
Crassoatraa vlralnlca
A*arlcan oystar,
Crassostraa virgin lea
A«arlcan oystar.
Crassoctraa vlrglnlca
Mathod*
s. u
S. U
S. U
S. U
S. U
S. U
S. U
S. U
S. U
S. U
FT. U
FT. U
FT. M
Chaailcal
Technical"
hapt settlor (72J)
Tachnlcal"*
haptacMor (12%)
Tachnlcal"*
haptachlor (72|)
Tachnlcal •••
haptachlor (72|)
Tachnlcal
haptachlor (721)
Tachnlcal
haptachlor (72|)
Tachnlcal
haptachlor (72|)
Tachnlcal
haptachlor (72<)
Tachnlcal
haptachlor <72f)
Tachnlcal1"
haptachlor (72
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Tabla I.   (ContlMtW)
Spaclas
Mysld thrlap,
Mysldopsls kali 1 a
Sand shrlap,
Crangon saptaasplnosa
Hara.lt crab,
Pagurus longl carpus
Koraan shrlap,
Palaaann a*crodactylu»
Grass shrlap,
Palaaannatat vulgar Is
Grass shrlap,
PalaasKMiatas vulgar Is
Pink shrlap.
Panaaus duoraruat
Pink shrlap.
Panaaus duoraruai
Pink shrlap.
Panaaus duoraruai
Aaarlcan aal,
Angullla rostrata
Shaapshaad •Innm,
Cyprlnodon varlagatus
Shaapshaad stlnnov,
Cyprlnodon yarlagatus
MuMlohog,
Fundulus hataroclltus
Strlpad kllllHsh,
FT, M
S, U
S. U
S, U
S, U
FT, M
FT, M
FT. M
FT, M
S, U
FT, M
FT. M
S. U
S, U
Chaailcal
tteptachlor
Haptachlor1*
Haptach lor6
Haptachlor
H»ptachlorb
Tachdlcaic
haptach lor
Tachnlcalc
haptach lor
Haptachlor
Haptachlor
apoxlda <99J>
Tachnlcalc
haptach lor
Tachnlcalc
haptach lor
Haptach tor"
Itoptochlor6
Spaclas Maan
LC90/ECM Acitta Valua
(Kfl/l) (ug/l) Rafaranca
3.4
e
55
14.5
440
1.06
0.11
0.03
0.04
10
3.66
10.3
50
32
3.4 U.S. tPA. I960
a ElsUr, 1969
55 tlsler. 1969
14.5 Schoattgar. 1970
Elsler, 1969
1.06 SchlaMal, at al.
I976a
SchlaMl, at al.
I976a
0.057 SchlaMal, at al.
I976a
0.04 SchlaMal, at al.
I976a
10 El«lar, I970a
SchlaMal, at si.
I976o
6.22 Hansan 1 Parrlsh,
1977
SO Elstar, I970a
32 Els tar, I970a
Fundulut  aajalIt
                                                         B-18

-------
Table I.  (Coatlaued)
Species
Atlantic silver*! da,
Menldla BMNIf
Threesplne stickleback,
Gasteroateus aculeatus
Threesplne stickleback,
Gasteroateus aculeatus
Striped bass.
Moron* saxatllls
Plnflsh.
Laaodon rhoatooldes
Spot.
LelostoMis xanthurus
Spot.
LelostOMis xanthurus
Bluatwad.
TKallassoMi bltasclatuai
Striped Millet.
Muflll caohalus
Norther n puffer,
Sphaeroldaa a*culatus

Method*
S, U
S, U
s, u
FT, U
FT, M
FT. M
FT, M
s, u
S, U
S, U
Cfcemlcal
Heptachlor6
Technical
heptachlor (72|)
Technical
heptachlor (72J)
Heptachlor
Technical0
heptach lor
Technical0
heptach lor
Heptachlor
Heptachlor1*
Heptach tor b
LC9Q/EC30
(Nfl/D
3
III. 9
II 1.9
3
3.77
0.85
0.86
0.8
194
188
Species Meaa
Acute Value
(Hfl/O
3
112
3
3.77
0.86
0.8
194
188
Reference
Elsler. I970a
Katz, 1961
Kati, 1961
Korn A Earnest, 1974
Schliaael, at al.
I976a
SchleMl, at al.
I976a
SchlaMel, et al.
I976a
Elsler, I970a
Elsler, I970a
El star. (970a
•  S - ctatlc, FT • flow-through, U • umMasured, M * •aatored

•• Author converted fro* technical grade (72|) to lOOf active  Ingredient.  For the purpose of this criterion
   docuMnt, LC50 was converted beck to technical (rede.

•••Authors converted fro» technical grade of unspecified percent heptachlor to lOOf active Ingredient.  For this
   criterion document It Mas assuned that the technical grade DBS 72f and LC50 values «ere converted back to
   technical grade.

•  ECM:  aaount of cheacal estlnated to reduce shell growth by 50|.

b  Entowol. Soc. fm> reference standard.

c  Technical Material:  65| heptachlor. 22$ trans-chlordana, 2% cls-chlordane. 1% nonnchlor. and 9$
   unidentified compound*.
                                                            B-19

-------
                                  Ta»U 2.  ChrtMlc walMM for haptccftlor
                                                                      Chromic Valw
                                                                          (m/O
                                             FRESMMTEfi SPECIES
Fathaad •Innow,               LC           Haptachlor      0.66-1.64        1.26         MAC**, at at. 1976
       laa proa»la»

                                              SALTMATER SPECIES
           •InnoH.            ELS           Tachfllcal"    1.22-2.04        1.56         Good»an, at al.  1976
• LC • Ufa cycla or partial  Ufa eye I a.  ELS - aarly Ufa
            •atarlali  65J Itaptachlor.  221 traa»-chlordaoa,  2| cl»-chlorQ/|)     Ratio
                   Fattwad •InnoH,                101          1.26        60
                                                   6.22       1.56         5.9
                   Cyprlftodoa varlagatut
                                                    B-20

-------
Tab I* 3.  Specie* Man acute vejlue* a*d acute-cfcroftlc ratio* tor he*tech lor
R«ik«
Specie*
C**,lc.l«
Specie* Mae*
Acute Value
(WO/I)
Specie* Meee
Acute-Chronic
Ratio
FRESHWATER SPECIES
te
17
16
14
13
12
11
10
9
a
7
6
Goldfish,
Carasslut auratus
Guppy,
Poecllla retlculata
Fathead winnow.
Coho talaon,
Oncorhynchu* 1(1 tut ch
Cladoceran,
Oaphnla eagna
slZote^^;, terrolatu*
Scud,
GaaMarus tasclatu*
Cladoceran,
Scud,
Gaawww* lacu»trls
Blueglll,
lefKwl* MBcrochlrus
Chinook *al«on,
Oncorhynchu* t>ha»yt»cha
Redear sunflth.
tepceilt alcrolophus
Ralntxw trout,
SatMo oalrdnerl
Technical
heptach lor
Technical
heptachlor
Technical
heptachlor
Technical
heptachlor
Technical
heptach lor
Technical
heptachlor
Technical
heptachlor
Technical
heptachlor
Technical
heptachlor
Technical
heptachlor
Technical
heptach lor
Technical
heptachlor
Technical
heptachlor
320
146
101
81.9
76
61.3
47.3
42
29
26
24
23.6
13.1
60
                                 B-21

-------
TafcU 5.   (Co*tlMw4)
ft«**
«***MBM*^
5
4
3
2
1
19
18
17
16
14
13
12
CraytUh.
Orconactas nals
Stonaf ly.
Claassanla sabulosa
Glass shrlap.
Stonaf ly.
Ptaronarcys calif or a lea
Stonaf ly.
Ptaronarcall* bad la
Strlpad aullat.
Mug II capnalus
Northarn put far,
Sphaaroldaa ••culatus
Thraasplna stlcklaback.
Gastarostaus aculaatus
Har«lt crab.
PaguTMS loaglcarpus
Mavldiog,
Fuadu 1 us hataroc 1 1 tus
Strlpad kllllflsli,
Fundulus Mjalls
KoraM sir lap.
PalaajKM atscrodactylus
African aal.
Cha.le.1"
TachAlcal
haptadtlor
Technical
lM0t«d»lor
TacMtlcal
haptacti lor
Technical
haptacfclor
Tachnlcal
haptacklor
SALTWATER SPCCIES
Haptadilor*11
HaptachlorttlB
Tachnlcal
haptachlor
Haptachlor*"
Haptachlor""
Haptachlor"*
Maptachlor
Haptachlor»M
Sfaclas Naaa
AcMt* Val«M
lHfl/1)
7.8
2.8
1.8
I.I
0.9
194
188
112
55
50
32
14.5
10
AcHta-Cnroalc
Ratio
-
          Angullla rottrata
                                      B-22

-------
Table 5.  CContlMied)
Raafc*

  It


  10


   9


   •


   7


   6


   5


   4


   3



   2


   I
Sand shrlep,
Crangon sept*
fcplnosa
Sheapshead »lnnow,
Cyprlnodon varleoatus

PinfisJi.
lagodon rhoaboldes

Mysld *hrl«p.
           bahla
Atlantic
Myiljla •anldla

Strlp*d bass.
Horonm saxatllls

Aawrlcan oystar,
Crassostraa vlrglnlca

Grass shrlap,
Palaaannata* vulgarts
Spot,
Lalostcwus xanthurus
Bluatwad,
Thallassoaa blfasclatu*

Pink shrlap,
Pacwwis duorarua
Haptacttlor'1*


 Tachnlcal*""1
haptach lor
                 haptach lor

                 Haptach lor
                 Haptach lor««*
                 Haptacltlor
                  Tachnlcal
                 haptach lor

                 Haptachlor****
                 Haptach lor""
               (Both technical
                  and
                 Haptach lor**"
                 Haptachlor*•»•
               (Both technical
                  and
                                   Specie* Mean
                                   Acute Value
                                       related co*pounds unless noted otharnlse.

 •** Entoeol.  Soc. A*, reference  standard.
                                              B-23

-------
T«*i« 5.   iCMf i
             Mt«rl«l>  69% h*pt«* tor.  22J tr«*s-otilor
-------
                                Tab la 4.  Plant valua*  for  kaptachlor
Sjpaclas
Mga,
SaTanaftrwji caprlcornutua)
AIM.
SalaMCtruB caprlcornutua)
Alga,
Ow«a Malta tartlolacta
Alga.
Itochrysls galbana
Porphyrldlu* cruantua)
Alga.
Sfcatatonaa* costatua

Chaailcal
Haptachlor
Haptachlor
Haptachlor
Maptach lor
(99|)
Haptachlor
i99t)
Haptach lor
(99*)
Effact (fig/I} Rafaranca
FRESHWATER SPECIES
96-hr EC50, 39.4« Call & Brooka, I98O
growth Inhibition
96-hr EC50, 26.7" Call t Brooka, 1980
growth Inhibition
SALTWATER SPECIES
EC5O, raductlon 2,260 U.S. EPA. I960
In growth a*
•aasurad by
abcorbanca
EC50, raductlon 157 U.S. EPA, I960
In growth as
•aacurad by
absorbanca
ECSO, raductlon 273 U.S. EPA, I960
In growth as
•aaaurad by
aborbanca
EC50, raductlon 93 U.S. EPA, 1900
In growth as
•aasurad by
absorbanca
• Ta*t solutions of haptachlor oontalnad froai 6 |ig/l hydroxychlordana  In  tha  lowact fast  concantratIon
  of S.6 Mfl/l to 29 Mfl/l hydroxydi lordana In tha hi ghat t tattad conoantrat Ion of 37 pa/1.
                                                          B-25

-------
TabU 9.   RaaldMM  tor feeetachlor
Fathead Minnow,
PlMOhale* proa* la*
Fathead elnacw,
Pleaphele* nroMlat
Sheepxhaad •JAAOV
(Juvenile),
Cyprlnodon varlegattt»
Sheep t heed Minnow
(Juvenile).
Cyprlnooon verleoetu*
Shaepshead minmau
(Juvenile),
(Juvenile).
Cyprlnodon varlegetut
SheepBhead a)lnnon (adult).
(Juvenile).
Cyprlnodon verleoatu«
Spot,
Spot.
Lelostoew* xanthurw*
Spot.
lelo»t
-------
TafeU 9.  (Co»tlawa«1>
tlpld
Spacla* Tlssua (f)
Spot, Whola body 1. 1b
Lalostosws xanthurus
Spot, Edlbla tlssua
La lot tOWft Xaathuntt
Spot, Whola body l.lb
LaloStOM* XMthurttft

Bloconoaatratlon
Chaalcal Factor
Technical 3.744
haptach lor**
Technical 4,686
haptach lorc
Tachnlcal B.282
h»ptachlorc
Duration
(days) Kafwanc*
24 Schl«Ml, at
19766
24 ScMaaal, at
I976b
24 Schl*Ml, at
19766
al.
al.
al.
•  Concantratloft  of  toataclilor  In  tlttua dlvldad by coocantratlon of haotacMor In vatar.
" ConoantratloM  of  haptachlor  and baptachlor  apoxlda In tlttwa dlvldad by conoantratIon of haptacnlor In Matar.
•••Concantratlon  of  haptachlor  and trant-cnlordana In tltsua dlvldad by coocantratlon of haptachlor and trans-chlordana In «atar.
*  Concentration  of  haptacftlor, haptachlor  apoxlda, trans-en lordana and cl«-cMordana In tl»»ua dlvldad by concantratlon of
   haptachlor and tran»-chlordana  In vatar.
5  Paroant  llpld  data  fro* Hainan. I960.
c  Coflcaatratlon  of  haptachlor, haptachlor  apoxlda, trans-chlordana and clt-chtordana In tUwta dlvldad by conoantratlon of
   haptachlor  I*  vatar.
                                             Hmxlmm Pamilnlbla TUwa Concantratlon
                                                                  ConcantratIon
                                      Action Laval  or  Elfact        (aaAg)        Hafaranca
                                      Fl«h  and •hallfish              0.3          U.S.  fDA Gbldallna
                                                                                    7420. Oft, 1919
                                      Raducad  survival,                7.1          Afidraws, at al.  1966
                                      Bluaglll.
                                      Lapo»l«  aacrochlrus
                                                                     B-27

-------
T«*U 9.
                 B«OMtrlc MM of appro?flat* norMllzwJ BCf  v«luM  (*•• t«xt) • 9.744/1.1 • 5,222
MtrMtablllty for (MM oontuaptloni  FDA action Uv*l for M*h  MM) itwlltlth - 0.3 ««Ag
                                     PM-cwit llpld valu* for  frMlMatcr if«c)M («M Guld«lln»») - 1
                                     f>«rc*nr llald val«M for  HltMfar *p*cl«* <»•• Guld*lln«) « 16
                                «ri     0.3     • 0.0000038  a«Ag - 0.0038
                                     5,227 * 15
                        S«ltw«t«r;      0.3     - 0.0000036  a«Ag - 0.0036
                                     5.222 xTF
                                     Us 1*0 MghMt approprlat* BCF  for •dlbl* portion of  • coMuacd tp*cl*s
                        S«ftw«t«rf   Spot - 4.6M (ScfclMMl, «t •!. I976b)
                                      0.3  - 0.000087 •vAg - 0.087 w/l
                                          *
Fr«HHat«r FlMl  AMldu* V«lu« - 0.003*
                               0.0036
                                                                  B-28

-------
                                       Table 6.  Other 4ate for heptacMor
Twenty river *l9»l
•pecle* Isolate*
HuMirou*
Mlsceili
Invertebrate*
Cladooeran,
Tublficld worm.
Tublfield VOTM,
Branchlor*
Tufal field worm,
CniytUfc,
            clarfc.ll
                                 ChMlcal
                                H»ptach lor
                                H*pt«cft lor
                                H»pt*chlor
                                HaptKhlor
                                                 Duration
                                                                   Effect
                                                                                  ftectilt
"RESHMATEft SPECIES
2 ttfcS
171 days
26 hr*
26 hr*
72 hr*
72 hr*
72 hr*
Variable
Reduction in growth
in naptachlor-
splked FU-I algal
Media
tOOf mortality In
24 hr*; returned
to norMi popula-
tion level* by
day 14
LC50
l£50
lOOf Mortality
at 4.4 C
Of Mortality at
21.0 C
VMt Mortality
•t 32.2 C
Tie* to death
70| of O'Kal ley i
specie* 1976
are* to
51-901 o»
controls
10 119/1
52.1 Andrews, <
52 frear 4 ft
120 Frear A &
2,500 Naqvl, 191
2,500 Naqvi, 191
2,500 Nftqvl, 191
2
                                                              after  con MM Ing
                                                              oontaMlnatad
Crayfish,
            clarkt '
                                                      B-29

-------
Tabla 6.   (CoatlMiad)
Glass shrlap.
PalaaMonataa MdJafcansU

Fowlar's toad (larva),
Burp woodhousll tow jar I

Bullfrog (larva).
Ran* cataabalana
Rainbow trout,
Sal MO flalrdnarl
Rainbow trout,
Sal MO oalrdnarl

Atlantic salMon  (juvanlla),
Sal MO salar

Fathaad Minnow,
PlMaphalaa prostala*

Motqultoflsh,
GaMbusIa afflnls
MosqultofIsh,
GaMbuila afflnls
     lt «*crochlru»
LapoaU MacrocMrus
Heptachlor


Haptachlor


Haptachlor





Haptach lor


Haptachlor


Haptach lor


Haptach lor


Haptach lor





Haptach lor


Haptach lor


Haptachlor
Duratloa

 24 hr*


 96 hrs


 46 hrs





 19 Mln


 19 Mln


 24 hrs


 10 days


 48 hrs





 36 hrs
                                                                    Effact
                                                                                              Rafaranca
                                                               LC50


                                                               LC50
                                                                                      40.6


                                                                                     440
                                Haqvl
                                1970
        Farguson,


Sandars. 1970
                                                               eof Mortality  In       0.9      Hulla, 1963
                                                               cagas  sub*argad      Ibc/acra
                                                               ponds  dosad with
                                                               aaulslflabla
                                                               concantrata
67| Inhibition     37,350
of NaK-ATPasa

3I| Inhibition      3,735
of Mg-ATPasa
                                                                                              Davis, at al. 1972


                                                                                              Davis, at al. 1972
                                                              Changa  In taMpar-  No affact    Patarsoo. 1976
                                                              atura salactlon    up to 29
                                                               loci pi ant LOO
                        7.0    Macek.  at  al.  1976
                                                              64f Mortality  In       0.5      Nulla. 1963
                                                              cagas subMargad In  Ibs/acra
                                                              ponds dosad with
                                                              aaulslflabla
                                                              concantrata
                                                              LOO
                                                                                     70
                               Boyd  & Karguson,  1964
                                                 171 days*    >90f Mortality
                                                  171 days*    Growth and
                                                              reproduction
                                                                                     69.4     Andrews, at al. (966
                   No affact    Andrews, at  al.  1966
                   whara  fish
                   survl vad
                                                             B-30

-------
T«bl« «*   (CMtfMMd)
^Iti.
Bluaglll.
Laooal* ewjcrochtru*
Blueglli,
Lapoals •acrodilrM
Bluaglll,
Lepaatls aacrochlruk
Bluaglll.
Bluaglll.
LapoaiU eecrocMrus
filueglll.
Bluagl It.
Lepoftls •ecrochlru*

Cfcealcal Ouretlo* Effect
Haptachlor 171 days* Tissue accuw-
latloa
Haptachlor 17 1 days" increased
aortal Ity
Heptachlor 171 days** Dose-related
growth d»creasa
Heptachlor t71 days** Tissue
eccuw let Ion
H^tachlor 29 eln 69-691 Inhi-
bition of NeK-
Haptechlor 29 eln 49-47* Inhi-
bit Ion of HaK-
Heptachlor 96 hrs LC90 of Kepta-
chlor as eeulsl-
Mable concen-
trate U soft
water
Heptadi lor 96 hrs LC90 of hepta-
chlor es •«ul*l-
Mable concen-
trate In herd
4tML/lft BaTi 0 a^f ^^^~»*t
Max leu* Andrews, et el.
of 1.326*
Initial dose
concentration;
return to
Aoreel efter
M days
10 Andrews, et aU
9 to 29 AAdrews. et al.
AccueMlatlon Andrea* , et al.
DA^Ile"^ Mid
subsequently
declined to
undetectabla
levels by
dey 112
19.600 Cutkoap. «t al.
16.200 Cutkoep. et el.
11 Handarson, et el
I960
IB tender son, et el
I960
1966
1966
1966
\966
1971
1971
                                                  B-31

-------
Tabla 6.   (Coatlauad)
SpaclM

Blueglll,
            odtlrua
Bluaglll,
Lapoali •acrochlru*
Blueglll,
lapojiU aacrochtru*
Bluaglll,
            octilrus
Bluaglll,
Lapoals Mcrochlrua
Redaar suntUh,
Lapoaili •Icroloptim

Radaar tunflfh.
       wntlslt,
        •lcrolophu»
Radaar tunflsh,
Lapo»l> •Icroloahus
        «lcrolot>hu»
Natural phytoplankton
coMwnltlas
Chaalca)
Haptach lor
Haptachlor
Haptach lor
Haptachlor
Haptach lor
Haptachlor
Haptachlor
Haptach lor
Haptachlor
Haptach lor
Duration
Unspecified
Unspecified
Unspecified
Unspecified
Untpeclfled
24 hr»
24 hr»
24 hr»
24 hr»
24 hr»
Effact
67| Inhibition
of 02 utiliza-
tion by «lto-
chondrla
29J Inhibition
of P04 utiliza-
tion by *lto-
chondrla
50< Inhibition
of Mitochondria)
Mg-ATPasa
50f Inhibition
of brain
MaK-ATPate
50* Inhibition
of brain
NaK-ATPa»a
EC50 at 45 F
BC50 at 59 F
EC50 at 65 F
EC50 at 75 F
EC50 at 85 F
RasulT
370,000
370,000
6,790
16,434
6,179
92
64
47
34
22
Reference
HI Itlbran. 1974
Hlltlbran, 1974
Yap. at
Yap. ef
Yap. et
Bridges,
Bridges,
Bridges,
Br 1 dges ,
Br 1 dges ,
al. 1975
al. 1975
al. 1975
1965
1965
1963
1965
1965
SALTWATER SPECIES
Technical
heptachlor""
4 hrs
94. 4< dacraasa In
productivity
J.OOO
But ler.
1963
                                                           B-32

-------
Tafel* 6.  (CmtlMM4>
Olnoflagallata,
Exuvlalla sf'tlca
AaOTtcM oystar,
Crassoatraa vlrgUIca
AswrlcM oystar,
Crassoatraa virgin lea
Mysld shrlap,
Hysldopsls bahU
Grass shrlap,
Pataaaxmatas vulgarls
Grass shrlap,
Palsaacnstas vulgar Is
Grass shrlap,
Palsaaunstas vulgar Is
Grass shrlap,
PalaaMonatas vulgar Is
Palaaaanstas vuloarls
Grass shrlap,
£?alo£iat'vulgarls
Grass shrlap,
Cha.lcal
Tachnlcal
haptachlor""
Technical
haptachlor11"*
Tachnlcal
haptachlor"1"'
Haptachlor
Haptachlor*
Haptachlor*
Haptachlor*
Haptachlor*
Hsptach lor*
Hitachi or*
Ouratloa
7 days
10 days
96 hrs
28 days
48 hrs
48 Irs
48 hrs
48 Irs
48 Irs
48 hrs
48 hrs
48 hrs
tffact
Rsduoad call dan-
slty, chlorophyll a
psr unit yolua* of
cultura, '*C
uptaka par call and
carbon fixation par
unit of chlorophyll
B loconcantrat Ion
factor " 17,600°
B loconcantrat Ion
factog • 3,900 to
Raducad survival
50-751 Mortality
12 gAg salinity
25-501 Mortality
18 gAg salinity
29-901 Mortality
24 gAg salinity
29-901 Mortality
30 gAg salinity
29-501 Mortality
36 gAg salinity
0-291 Mortality
IOC
Of Mortality
19 C
29-50| Mortality
Raault

-------
Tabla 6.  (Coatlauad)
Spaclas
Grass shri«a,
PalaaSKMataa Mllgar Ift
Grass shrlap,
Palaaannatas vulgar l»
Grass shrlap,
Paliaannataa vulgar Is
Pink shrlap.
Panaaus duorarust
Pink shrlap,
Panaaus duoraru*
Pink shrlap,
Panaaus duoranm
Pink shrlap,
Panaaus duorarusi
Blua crab (juvanlla),
Calllnactas sapldus
Shaapshaad Minnow,
Cypf Inodon varlagatus
Shaapshaad Minnow,
Cypr Inodon varlaaatus
MuMMlchog.
Fundulus hataroclltus
MuMlchog.
Fundulus hataroclltus
MuMlchog,
Fundulus hataroclltus
MuMlchog.
Fundulus hataroclltus
Cltastlcal
Haptachtor*
Haptach lor'
Tachnlcal
haptachlor11***
Technical
naptachlor***
Tachnical
haptachlor****
Haptach lor
(99f)
Haptach lor
apoxlda (99%}
Tachnical
haptach !«-•*•
Tachnical
naptachlor1"1"
Tachnical
naptachlor****
Haptach lor*
HaptacMor*
Haptach lor"
Haptach lor"
Duration
48 hrs
48 hrs
96 hrs
48 hrs
96 hrs
96 hrs
96 hrs
48 hrs
96 hrs
1% days
96 hrs
96 hrs
96 hrs
96 nrs
ftaault
CHact 
Elsler, I970b
                                                 B-34

-------
Tafcla 6.  (ContlMia*)
Spaclaa
Mummlchog,
Fundulus hataroclltus
Mumalchog,
Fundulus hatarocl Itus
Mummlchog.
Fundulus hataroclltus
MuaMlcfcog.
Fundulus hataroclltus
Muajmlchog,
Fundulus hataroclltus
Mwmlchog,
Fundulus hataroclltus
Mummlchog,
Fundulus hataroclltus
Plnflsh,
Lagodo* rhomtoldM
Spot.
Lalostomus KMthurus
Spot,
Caloatomus xanthurus
Mhlta mullat (Juvwtlla).
Mugll curama

Cmamlcal
Haptachlor4
Haptachlor*
Haptachlor*
Haptachlor*
Tachnlcal
haptachlor*"*
Haptachlor
(99f|
Tachnlcal
haptachlor***
Duration
96 hrs
96 hrs
96 hrs
96 hrs
96 hrs
96 hrs
240 hrs
96 hrs
96 hrs
96 hrs
48 hrs
Cf fact
25-SOf mortality
36 gAg salinity
Of mortality
IOC
0| mortality
ISC
0-25| mortality
20 C
50-751 mortality
25C
0-23* mortality
30 C
LCSO
Bloconcantrat Ion
factor - 2,800 to
7,700b
B loconoantrat Ion
factor - 3,000 to
I3,800b
6 loconoantrat Ion
factor • 3,600 to
IO,000C
LCSO
CHfl/l ) R*f aran
90 Elslar,
SO Elslar,
90 Elslar,
50 Elslar,
SO Elslar,
90 Elslar,
II Elslar,
Schlama
I976a
SchlMM
I976a
I976a
3 But tar.
c*
19706
I970b
19706
19706
19706
19706
19706
1. at al.
1, at al.
1, at al.
1963
•   Tastad  In poods, dosad on day  I only.  Authors  dosad with tachnlcal  grada haptachlor and report ad as tig/1
    actlva  Ingradlant.  For  tha purpose of this  documant, valuas ara r«port«d as |ig/< tachnlcal  grada haptachlor.

••  Tastad  In small pools.   Tachnlcal grada  haptachlor  Mam Incorporated  Into fish food only and  fad (or duration
    of  tast.
                                                           B-35

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Tafcle t.
••* Technical Material:  contains  741 heptachlor  and  26%  otter  chemicals.  Including  trans-eftlordane, cls-ch lor dene,
    nonacMlor, end other*.

••••Technical Mterlal:  contains  65* Iwptachlor, 22| trans-chIonian*. 2$  cls-chlordan«, 2} nonachlor, and 9t
    othw».

•   Haptachlor; Entoawl. Soc. Aau  r«(«raoc«  standard.

**   ConcantratIon of NaptacMor  In vhol* body  divided  by  concentration of  naptachlor In Matar.  Ck-ganls* «Mpo«ad
    to technical iMptachlor  <65J Iwptachlor, 22$  trans-chlordana,  2f  cU-chlordana.  and 2f nonAchlor).

c   Concentration of Iwptachlor  In whole body  divided by  concentration of  heptacnlor In water.  Organise exposed
    to •Mlytlcal-flrad* neptachlor (99t heptachlor).

4   Concentration of heptachlor epoxlde In whole  body  divided  by concentration  of  heptachlor apoxlde In water.
    Or0MlM exposed to heptachlor epoxlde (99J)
                                                            B-36

-------
                                   REFERENCES

 Andrew,  A.K.,  et  al.   1966.   Some effects of heptachlor on bluegills (Lepom-
 is  macrochirus).   Trans. Am. F1sh. Soc.  95: 297.

 Boyd,  C.E.  and D.E. Ferguson.  1964.   Susceptibility  and  resistance of mos-
 quito  fish  to  several  insecticides.  Jour. Econ. Entomol.  57: 430.

 Bridges,  W.R.   1965.   Effects  of Time  and  Temperature on  the  Toxicity  of
 Heptachlor  and Kepone  to Redear Sunfish.  In:  C.M.  Tarzwell  (ed.),  Biologi-
 cal Problems in Water  Pollution,  3rd Seminar 1962.  U.S.  Publ.  Health  Serv.
 999-WP-25.  p. 247.

 Butler, P.A.   1963.  Commercial fisheries Investigations,  pesticide-wildlife
 studies:  A  review  of  F1sh  and  Wildlife  Service  Investigations  during
 1961-1962.  U.S. Oept.  Inter. F1sh and WUdl. C1rc.  167: 11.

Call, D.J. and L.T. Brooke.  1980.  Memorandum to R.C.  Russo.  July 17.

Cutkomp, L.K., et  al.   1971.  ATPase activity 1n fish  tissue homogenates and
 inhibitory effects  of  DOT  and related compounds.  Chew. Blol. Interactions.
3: 439.

 Davis, P.W., et al.  1972.  Organochlorlne  Insecticide, herbicide and  poly-
chorlnated blpnenyl  (PCB)  Inhibition of NaK-ATPase  In  rainbow trout.  Bull.
Environ. Contam. Toxlcol.  8: 69.
                                     B-37

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Eisler, R.   1969.   Acute toxlcitles of insecticides to marine decapod crus-
taceans.  Crustaceana.  16: 302.

Eisler, R.   1970a.   Acute  toxlcitles  of organochlorine  and  organophosphorous
insecticides  to estuarine  fishes.   U.S.  Oept.   Inter.   Bur.  Sport Fish.
Wild!. Tech. Pap.  46.

Eisler, R.   1970b.   Factors  affecting  pesticide-induced  toxicity in an es-
tuarine fish.  U.S.  Dept. Inter. 8ur. Sport Hsh.  Wild!. Tech.  Pap.   45.

Frear, O.E.H.  and O.E.  Boyd.   1967,  Use  of  Daphnia magna  for the  microbio-
assay of  pesticides.   I.  Development of standardized techniques  for  rearing
Daphnia and preparation of  dosage-mortality  curves  for pesticides.   Oour.
Econ. Entomol.  60:  1228.

Goodman,  L.R.,  et.  al.   1978.  Effects of  heptachlor and toxaphene  on  labo-
ratory-reared  embryos  and fry  of the sheepshead  minnow.   Proc. 30th  Annu.
Conf. Conf. S.E. Assoc. Game Fish Conm.  p. 192.

Guilbault,  G.G., et  al.   1972.  Effect of  pesticides on  cholinesterase  from
aquatic species: Crayfish, trout and fiddler crab.  Environ. Lett.  3: 235.

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

Hansen, D.J.  and  P.P.  Parrlsh.   1977.   Suitability  of Sheepshead  Minnows
(Cyprinodon  varlegatus)  for  Life-Cycle Toxlctty  Tests.  In:  F.L.  Meyer  and
J.L. Hamelink  (eds.).  Toxicology and Hazard  Evaluation.   ASTM  STP  634,  Am.
Soc. Test. Mater,  p.117.

                                     B-38

-------
 Henderson,  C., et  al.   1959.  Relative  toxicity of ten  chlorinated  hydro-
 carbon  Insecticides  to  four species of fish.  Trans. Am. F1sh. Soc.  88: 23.

 Henderson,  C.,  et al.   1960.   The Toxicity of Organic Phosphorus and Chlori-
 nated Hydrocarbon Insecticides  to F1sh.   l_n:  C.M. Tarzwell (ed.), Biological
 Problems  in Water  Pollution,  2nd  Seminar 1959.   U.S.  Pub!.  Health  Serv.,
 R.A. Taft  Sanitary Eng. Center, Tech. Rep. WGO-3.  p. 76.

 Hlltibran,  R.C.  1974.   Oxygen  and  phosphate  metabolism of  bluegill  liver
 mitochondria  in the presence of  some  Insecticides.   Trans.  111. State Acad.
 Sc1.  67: 228.

 Katz, M.   1961.  Acute toxicity  of some  organic Insecticides to three spe-
cies of salmonids and  to the threespine  stickleback.   Trans.  Am. Fish. Soc.
90: 264.

Korn, S. and  R.  Earnest.   1974.   Acute  toxicity of twenty  insecticides  to
striped bass, Morone saxtHis.  Calif. F1sh Game.  60: 128.

Macek,  K.J., et al.  1969.   The effects  of temperature on the susceptibility
of  bluegllls  and rainbow  trout to  selected  pesticides.    Bull.  Environ.
Contam.  Toxlcol.  4: 174.

Macek,   K.J.,  et  al.  1976.   Toxicity of  four  pesticides  to water fleas and
 fathead minnows.  EPA 600/3-76-099, U.S.  Environ.  Prot.  Agency.
                                      B-39

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Magani,  B.  et al.  1978.   Effects  of chordane and heptachlor on the marine
dinoflageHate, Exuviella  baltlca  Lohmann.   Bull. Environ. Contam.  Toxicol.
20: 1.

Mulla,  M.S.   1963.   Toxicity of organochlorine Insecticides to the mosquito
fish  Gambusi a  affinis  and  the  bullfrog  Rana  catesbeiana.   Mosq.  News.
23: 299.

Naqvi,  S.M.Z.   1973.   ToxicUy of  twenty-three  insecticides  to a  tubificid
worm Branchiura  sowerbyi  from the  Mississippi delta.   Jour.   Econ. Entomol.
66: 70.

Naqvi,  S.M.Z. and D.E. Ferguson.   1970.   Levels  of Insecticide resistance  in
freshwater shrimp, Palaemonetes kadiakensis.  Trans. Am. F1sh.  Soc.  99:  696.

O'Kelley, J.C, and  T.R.  Oeason.   1976.  Degradation of  pesticides  by  algae.
EPA 600/3-76-022, U.S. Environ. Prot. Agency.

Peterson,  R.H.    1976.   Temperature  selection of  juvenile Atlantic  salmon
(Salmo  salar)  as Influenced  by various  toxic substances. Jour.  Fish.  Res.
Board Can.  33:  1722.

Sanders,  H.O.  1969.   Toxlcity  of  pesticides  to  the crustacean  Gammarus
Tacustrts.  U.S. Bur.  Sport Fish. VlUdl. Tech. Pap.  25: 3.

Sanders, H.O.  1970.   Pesticide toxidtles  to tadpoles  of  the  western  chorus
frog  Pseudacrls  trlseriata  and  Fowler's  toad  Bufo  woodhousii   fowleri.
Copeia.  2: 246.
                                     B-40

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Sanders, H.O.   1972.   Toxicity  of  some  insecticides  to four species of mala-
costracan crustaceans.  U.S. Bur. Sport Fish. Wild!.  Tech. Pap.  66: 3.

Sanders, H.O. and  0.8.  Cope.  1966.   Toxlcities  of several  pesticides  to two
species of cladocerans.  Trans.  Am. F1sh. Soc.  95: 165.

Sanders, H.O. and  0.8.  Cope.  1968.   The relative  toxicities of several pes-
ticides  to  naiads  of  three  species  of  stoneflles.   Ltmnol.  Oceanogr.
13: 112.

Schimmel, S.C., et  al.   1976a.   Heptachlor:  Toxicity to and uptake by sever-
al estuarine organisms.  Jour. Toxicol. Environ. Health.  1: 955.

Schimmel, S.C.,  et  al.   1976b.   Heptachlor:  Uptake,  depuration,  retention
and  metabolism  by  spot,  Lelostomus  xanthurus.  Jour.  Toxicol.  Environ.
Health.  2:  169.

Schoettger,   R.A.    1970.   Fish-Pesticide  Research  Laboratory:  Progress  in
sport fishery research.  U.S. Oept.  Inter.  Bur.  Sport  Fish.  W1ldl.  Resour.
Publ.  106.

U.S.  EPA.   1980.   Unpublished   laboratory  data.  Environ. Res.  Lab., Gulf
Breeze, Florida.

U.S.  Food   and  Drug  Administration.   1979.   Administrative  Guideline No.
7420.08, Attachment G, 7/5/79.
                                     B-41

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Yeith, G.O.,   et al.   1979.   Measuring and estimating  the  bioconcentration
factor of chemicals 1n fish.  Jour. Fish. Res.  Board Can.  36:  1040.

Wilson, A.J.   1965.   Chem. assays.   Annu.  Rep.  Bur. Commercial  Fish.  Biol.
Lab., Gulf Breeze, Florida.  U.S. Bur. Cornm. Fish.  Circ.   247:  6.

Yap,  H.H.  et  al.   1975.   ^n_ vitro  inhibition of  fish brain ATPase  activity
by  cyclodiene  insecticides and  related compounds.   Bull.  Environ.  Contam.
Toxicol.   U:  163.
                                               B-42

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Mammalian Toxicology and Human Health Effects
                             EXPOSURE
Ingestion from Water
     Heptachlor  and/or  heptachlor epoxide have been  found  in the
major  river  basins  within  the  United  States.    Weaver/  et  al.
(1965)  reported  that  from  96  river sampling  points around  the
U.S., 15 showed presumptive  evidence of heptachlor residues.   They
also reported that heptachlor epoxide was not detectable in any of
the samples taken.   They  explained  the  failure  to find heptachlor
epoxide  in  their samples  by indicating that the  detection  limit
for heptachlor was  in the range  of 0.002 to 0.010  ug/1,  but was
only  0.075  ug/1  for  heptachlor epoxide.    Breidenbach,  et  al.
(1967) did  an extensive  survey  of   the  water  in  the  major  river
basins within the U.S.  and,  in instances where  they were detect-
able,  found levels of heptachlor ranging from 0.001 to 0.035 ug/1,
and heptachlor epoxide levels ranging  from 0.001  to 0.020  ug/1,
with  a  mean  concentration  for  both  of 0.0063  ug/1  (U.S.  EPA,
1976).  They added that 24 percent  of the water grab samples taken
in  1965  showed  positive  to presumptive  evidence  of  heptachlor
residues and  that heptachlor epoxide was present  in 25 percent of
their samples.   Their level of  analytical  sensitivity  was  0.001
ug/1 for both heptachlor  and heptachlor  epoxide.   Another survey
conducted by  th« U.S. Geological Survey  of 11 western U.S. streams
showed heptachlor  levels  ranging  froa  O.OOS  ug/1 to  0.015  ug/1
when  found  and  heptachlor epoxide   levels  ranging from  0.005  to
0.010   ug/1  when  found,  with  one  sample  showing  0.090  ug/1
heptachlor epoxide (Brown  and Nishioka,  1967).
                               C-l

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Ingestion front Food
     Food  can  add significantly  to man's exposure  to heptachloc
and  heptachlor  epoxide.   This  occurs  through  biomagnification of
heptachlor/heptachlor  epoxide  through  the food  chain.    For  ex-
ample,  the U.S.  EPA  (1976)  cited  data  from Hannon,  et al. (1970),
who  reported  that average  heptachlor/heptachlor  epoxide  residues
in  the  Lake  Poinsett, S. Dakota  ecosystem were:    0.006  ug/1  for
water;  0.8 ug/kg  for  bottom sediment;  1.0 ug/kg for crayfish;  1.1
ug/kg for plankton-algae; 8.0 ug/kg for fish;  and 312.0 ug/kg  for
aquatic  insects.  Additionally,  there is an approximate 10-fold to
15-fold  increase in heptachlor residues found in  body fat, milk
butterfat, and the  fat of eggs and livestock as compared to resi-
due  levels found  in normal  food rations  (U.S.  EPA,  1976).
     Since 1964,  the  Food  and Drug Administration (FDA)  has  re-
ported  pesticide residues  in  their  Total Diet  Study,  sometimes
called  the  "Market  Basket  Study"  (Johnson  and  Manske,   1977).
Their  "market  basket" of  food,  which  is collected  in  each of
several geographic  areas, represents the basic 2-week diet  of  16-
to  19-year-old  males,  statistically  the  nation's   highest  per
capita  consumers.   The foods analyzed  in  these studies were  pre-
pared  in the manner  in  which  they would be  normally served  and
eaten.   Th«  latest published  study  covers   food  collected  from
August  1974  to  July  1975   in  20  different  cities  (Johnson  and
Manske,  1977).   Their results  showed  that only  3  of the 12  food
classes  in this  study  contained detectable residues  of heptachlor
epoxide  (Table 1).    In these  three  instances,  the heptachlor
epoxide  levels were found to range  from 0.0006 to 0.003 ppm.
                                C-2

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                                         TABLE  i



                           Heptachlor  Epoxide Residues  in Food*
positive composites
Pood
I
II
VIII
Class
Dairy Products
Meat, Pish,
and Poultry
Garden Pruits
Average
Concentration
ppra
0.0004
0.001
Trace
Total
Number
11
13
1
Number
Reported
as Trace
5
4
1
Range ppra
0.0006-0
0.001-0.
Trace
.003
0003

*Source< Johnson and Nanake,  1977
                                               C-3

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     Nisbet  (1977)  calculated  the average daily  intake  of  hepta-
chlor epoxide from the FDA's Market Basket Study standardized diet
and estimated  that  the daily intake of  heptachlor  epoxide  ranged
from 1  to  3  ug/day between  1965  and  1970,  and from 0.29  to 0.64
ug/day  between  1971 and  1974.   Nisbet  questioned  the  calculated
decrease in  residue  levels  observed between  the  two time periods,
because  the  decrease  coincided with  FDA's  change  in  analytical
methodology.   Nisbet  (1977)  stated  that  there  was apparently  a
dilution effect  taking place when FDA switched  methodologies and
he regarded  the  total  Diet Survey for  heptachlor  epoxide  as only
semi-quantitative.  He stated  that  the results suggest  an overall
mean daily  intake,  in the  standardized diet,  of the  order  of  1
ug/day of heptachlor epoxide.
     The U.S. Department  of Agriculture's (USDA)  Food Surveillance
Program found heptachlor  epoxide  residues  greater than 0.03 mg/kg
in 19 percent  of red meat, 17  percent of  poultry,  and  14 percent
of dairy products in the  years  1964 to 1974  (Nisbet, 1977).
     The FDA and USDA studies address  only food sold in  interstate
commerce.  There  is  evidence that game fish may contribute to the
daily dietary exposure of heptachlor and heptachlor epoxide  in ad-
dition to that estimated  for commercially bought  fish.  A national
study by the U.S. Department of the Interior during  the spring and
fall  of 1967  and  the spring  of 1968 reported  that  heptachlor
and/or heptachlor epoxide was  found  in 32 percent of the 590 fish
samples examined  (Henderson,  et al.  1969).   Results were reported
as mg/kg  (wet weight  whole fish)  and  ranged from 0.01  to 8.33
rag/kg when  found.   It must  be  noted  that these  results  represent
                                C-4

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 the whole fish, not  just  the portions  that man eata, so it is pos-
 sible  that  much  of  the  residues  are  accumulated  in  the uneaten
 portion  (Henderson,  et  al. 1969).
     A bioconcentration factor  (BCF) relates the concentration of
 a chemical  in aquatic animals to the concentration  in the water in
 which  they  live.   The steady-state BCFs  for  a lipid-soluble com-
 pound in the tissues  of various aquatic animals seem to be propor-
 tional to the  percent lipid in the tissue.   Thus,  the per capita
 ingestion of  a lipid-soluble chemical can be estimated  from the
 per capita consumption  of fish and shellfish,  the weighted average
 percent lipids  of  consumed  fish  and  shellfish, and a steady-state
 BCF for the chemical.
     Data from  a  recent survey on fish  and  shellfish consumption
 in the United States were analyzed by  SRI International (U.S. EPA,
 1980).  These data were used  to estimate that the per capita con-
 sumption of  freshwater and  estuarine  fish  and  shellfish  in the
United States  is  6.5 g/day  (Stephan,  1980).  In  addition,   these
data were used  with  data  on the  fat  content  of the edible portion
 of the same species  to  estimate  that  the weighted average percent
 lipids for consumed  freshwater and estuarine fish and shellfish is
3.0 percent.
     Several  laboratory  studies,  in   which  percent lipids  and  a
 steady-state BCP were measured, have been conducted on heptachlor.
The mean of  the  BCP values,  after   normalization to  1 percent
 lipids,  is  3,747  (see  Table  in Aquatic  Life Toxicology, Section
 B).  An adjustment factor of 3 can be  used to  adjust  the  mean nor-
malized BCP to  the 3.0  percent lipids  that is  the weighted average
                                C-5

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for consumed fish and  shellfish.   Thus,  the  weighted  average  bio-
concentration factor for heptachlor and  the  edible  portion  of  all
freshwater and  estuarine  aquatic organisms  consumed  by  Americans
is calculated to b« 11,200.
     Infants  are exposed  to  heptachlor  and  heptachlor  epoxide
through mothers' mil*  (Savage,  1976), cows'  milk  (Ritcey,  et  al.
1972;  Johnson  and  Manske, 1977),  and commercially prepared  baby
foods  (Lipscorab, 1968).  A recent nationwide study, conducted dur-
ing 1975-1976,  indicates  that 63.1 percent  of  the 1,936 mothers'
milk samples possessed heptachlor epoxide residues  (Savage/ 1976).
The adjusted mean fat  concentration  for  heptachlor epoxide  in the
mothers' milk, with levels above the  1 ug/1  sensitivity  level, was
91,36  ug/1  with a range  of   15.24  to 2,050  ug/1.   Therefore,  it
appears that many nursing  infants  have been  exposed to  heptachlor
epoxide, and  it is  probable  that  a  certain percentage  have been
exposed to levels that exceeded  the levels in dairy products (Sav-
age, 1976).  Whole  cows'  milk and  evaporated milk did not show a
trace  of  heptachlor epoxide  in the  U.S.  FDA's  1974-1975  Market
Basket  Survey   (Johnson and  Manske,  1977),  but a  Canadian study
which  expressed the  residues  on a  fat basis,  reported  heptachlor
epoxide residue  levels of  5.00 ug/1 in evaporated  milk (Ritcey, et
al. 1972).  Commercially  prepared  baby food  was tested  by the FDA
during a period of July  1963  to June 1967,  and heptachlor epoxide
residues were found in 0.9 percent  of 684  samples  with most of the
positive samples shewing residues  in the  range of trace to 0.03
mg/kg  (Lipscorab, 1968).  Therefore,  it  appears  that infants raised
                                C-6

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 on mothers'  millc  run  a greater risk of ingesting heptachlor epox-
 ide  than  if  they  were fed cows'  milk and/or commercially prepared
 baby food.
     Ritcey, et al. (1972) investigated the effects of cooking and
 heating poultry containing 28.1 mg  of heptachlor epoxide per kg of
 tissue on  a  dry weight basis {U.S.  EPA,  1976).   They found baking
 reduced the  residue  level to 22.5  mg/kg, steaming  to 22.1 mg/kg,
 and frying resulted in no change.   They also found .that heating in
 a closed container at  350°F  for 60  to 90 minutes reduced the resi-
 due to 16.0  to 19.5 mg/kg.
 Inhalation
     Volatilization is a major  route  of loss  of  heptachlor from
 treated surfaces,  plants,  and soils (Nisbet, 1977).   It has been
 concluded  from various surveys that heptachlor  and  to lesser ex-
 tent heptachlor  epoxide  are widespread in  our ambient  air with
 typical mean concentrations  of  approximately 0.5  ng/m3  (Nisbet,
 1977).   Levels  of heptachlor and  heptachlor  epoxide  in  the air
vary both  geographically and  seasonally  (Stanley, et  al. 1971).
Higher  levels  have  been  found  generally  in  rural  agricultural
 areas where  crop  spraying  was practiced  (Stanley,   et  al.  1971;
Nisbet,  1977).  However, certain suburban  areas have exhibited  a
 substantial concentration of heptachlor in  their ambient air  {Nis-
 bet, 1977).
     Nisb«t  (1977) has  reported air  surveys  where  agricultural
 fields  have  been  treated  with technical heptachlor  (2 Ib/acre).
 The air above and  downwind from the fields showed heptachlor  con-
centrations  as  high  as  244  ng/m3  immediately  after application.
                               C-7

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After  three weeks  the  concentrations  remained  as  high  as  15.4
ng/ra3.   One survey reported  heptachlor  concentrations  as high as
600  ng/m3   in  air  over  a  treated field,  with the  field showing
high  concentrations  in the air throughout  the growing  season,  at
least  from May to October  (Nisbet,  1977).   Nisbet  (1977)  states
that  these  "high  concentrations  found  above  and  downwind  from
treated  fields  are obviously  significant  sources  of exposure for
persons  living and working  in  or  near the  treated  areas."
     Arthur, et  al.  (1976)  conducted a  3-year  study from 1972 to
1974 of  Stoneville, Miss.,  which  is  reported  as one  of  the highest
pesticide  usage  areas  of the U.S. due to intensive  cotton produc-
tion.   They found  heptachlor  in  62  percent of their monthly sam-
ples,  with an  average  level  of 0.25 ng/m3 and  a maximum concen-
tration  of 0.8  ng/m3.   Heptachlor  epoxide was  found  in 36 per-
cent  of the monthly  samples  at  an  average  level  of  0.21   ng/m3
and  a  maximum  concentration of  9.3  ng/ra3 (Arthur,  et al.   1976;
Nisbet,  1977) .
     Stanley,  et al.   (1971)  found  heptachlor in  only  two out of
nine U.S.  localities  studied,  and did not  detect  heptachlor  epox-
ide  in any  of  the localities.   The  localities   showing  residues
were Iowa  City,  Iowa  and Orlando, Florida  with maximum  heptachlor
levels  of  19.2 ng/m3 and 2.3  ng/m3,  respectively.
     Niab«t (1977) calculated  the typical  human exposure  to  hepta-
chlor  to b* 0.01  ug/individual/day  based  on  an  ambient air mean
concentration  of 0.5  ng/m3 and  breathing  20  m3   of  air per day.
He  stated  further  that  even in Jackson, Miss.,  which  has a mean
air  level  as  high  as  6.3 ng/m3,  the  average   individual   would
                                C-8

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inhale only 0.13  ug/day  of  heptachlor.   The significance of these
figures  is  dependent  upon  the efficiency  of lung  absorption  of
heptachlor and heptachlor epoxide  which  has not  been reported for
humans (Nisbet,  1977).   Based on  the  information  presented here,
it appears that  inhalation  is not  a major route for human exposure
to  heptachlor and  its  metabolites.   However,  an  experiment  by
Arthur, et al. (1975)  using rabbits,  although controversial (Nis-
bet, 1977), suggests that inhalation may be a significant route of
exposure even at  ambient levels as low as 1.86 ng/m3.
Dermal
     Limited  information is available regarding  the dermal route
of exposure to heptachlor and/or  heptachlor epoxide.  However, it
may be assumed that persons handling this  compound  would be der-
mally exposed.    Razen, et  al. (1974) found that chlordane, a com-
pound  structurally  similar  to heptachlor,  could  be  found  on   a
man's skin two years  after occupational exposure.   Gaines (1960)
found that rats dermally exposed to technical grade  heptachlor had
LDso values  of  195  tag/kg   for males  and  250 mgAg  for females,
while  the  LDsQ  values  for orally  exposed  rats  were  100 rag/kg
for males and 162 mg/kg  for females.  Xylene was  used as  the ve-
hicle to dissolve and  apply the  heptachlor/ with the solution ap-
plied at a rate  of 0.0016 ml/kg body weight.
     It is significant to  note  that  the U.S.  EPA suspended most
uses of heptachlor  effective  August 1,  1976, including  most  agri-
cultural, hone,  and garden  uses of technical  grade  heptachlor.
                                C-9

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                         PHARMACOKINETICS
Absorption and Distribution
     Heptachlot  and/or heptachlor  epoxide  are  both  readily  ab-
sorbed  from  the gastrointestinal  tract  (Radomski  and  Davidow,
1953; Mizyukova  and  Kurchatov,  1970;  Matsumura and Nelson, 1971).
Mizyukova  and Kurchatov  (1970)  showed pure heptachlor reaches all
organs  and tissues  of female  rats  within  one-half  to  one  hour
after  a  single  dose   (120  mg/kg)  of  heptachlor  was  delivered
directly  into the stomach.   After  four hours  the metabolite  of
heptachlor (heptachlor epoxide) was  found  in  the  blood, liver, and
fatty tissue.  After a  few days the  concentration  of  heptachlor in
all organs and  tissues decreased, while  at  the same tine  there was
a rapid  increase in  heptachlor epoxide levels.  By  the end of one
month, only traces  of  heptachlor  could be found in  the fatty tis-
sue, chiefly  in  the  form of  its metabolic  products.   Heptachlor or
its metabolites  could  not  be found in the blood or  kidneys.  How-
ever, a small amount of heptachlor  epoxide  was found in the liver.
After three to  six months  the  level  of  heptachlor  epoxide  in  fatty
tissues became  stabilized.
     Radomski  and Davidow  (1953)  used  both  dogs and rats.   In
rats, after two  months on  a diet of  30  to 35  mg/kg  of heptachlor,
the highest  concentration  of  heptachlor's metabolite  (heptachlor
epoxide) vaa  found  in  the  fat, with markedly  lower  amounts in the
liver/ kidney and muscle,  with none  being  detected  in the  brain.
Female dogs,  dosed at  1 mg/kg daily  for  a period  from  12 to 18
months/ showed  the same heptachlor  epoxide distribution as did  the
rats, except  the dog  livers appeared  to  contain  more heptachlor
                                010

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epoxide  than  the  kidneys  and muscles.   The lowest detectable con-
centration  of heptachlor epoxide in this study was 0.6 mg/kg.
     The  degree  to which  heptachlor or heptachlor  epoxide  is ab-
sorbed  by  inhalation  has  not generally  been  reported  (Nisbet,
1977).   Arthur, et al.  (1975)  conducted  a now controversial study
where they  exposed white rabbits to the ambient air of Stoneville,
Miss., an area  of high  pesticide  use.   Their controls were  housed
indoors  at  Mississippi  State University,  an  area of low pesticide
use.   They  found that  between July  1972  and  October  1972  the
heptachlor  epoxide  level   in   the  rabbits'   adipose   tissue  from
Stoneville  was  0.039 mg/kg, while  only  0.016 mgAg  was  found  in
the same  tissue in rabbits  from Mississippi State.  The heptachlor
epoxide  level  in air  at  Stoneville  was  reported   to  be  1.86
ng/m3, while  the  Mississippi  State University  level was  so low
that they did not take air samples.   The level  of heptachlor in
the air  at  both  geographic locations was not given.   They also
stated that  no heptachlor  epoxide  residues  were  detected  in the
feed of either group.   They calculated the average daily respira-
tory  intake of heptachlor   for  rabbits  in  Stoneville,  Miss,  as
0.002 ug/day.   These  data,  even  though  controversial,  indicate
that heptachlor  epoxide can  be absorbed  to  a significant  degree
after inhalation, as determined  by  rabbit  adipose  tissue resi-
dues.
     Several studies released  in the late  1960's  indicate that the
human placenta does  not provide adequate protection against chlo-
rinated hydrocarbon  pesticides such as heptachlor epoxide  (Selby,
et al. 1969;  Zavon,  et  al.  1969; Curley, et al. 1969).  Selby, et
                               Oil

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al.  (1969)  found  that women who had  high  levels  of  heptachlor or
heptachlor  epoxide  in  their  blood  also had high levels of both in
their placenta.   They also  reported  heptachlor epoxide distribu-
tion between  the  placenta and maternal blood  in  a ratio of 5.8:1
(placenta ppbrmaternal blood ppb)  based  on the geometric means of
54  placental  and  53 maternal  blood   samples.   Polishuk,  et  al.
(1977b) has shown that heptachlor  epoxide was higher  in the  ex-
tracted lipids  of fetal  blood  and placenta  than  in the maternal
blood and  uterine muscle lipids.   Zavon,  et  al.  (1969) reported
that fetal  or neonatal tissue  taken  from stillborn or soon  dead
children showed that heptachlor epoxide levels  paralleled the  con-
centrations found  in adults.  Curley, et  al. (1969) conducted an
extensive study using  stillborn and soon dead  infants,  along  with
the  cord  blood of  live   neonates,  and found  that   the  heptachlor
epoxide levels  in  the  various tissues and cord blood  sampled  var-
ied greatly,  but were within the range observed in adults.   There-
fore,  any   exposure  of heptachlor or  heptachlor epoxide  to  the
mother will also expose the  fetus  to  heptachlor epoxide.
Metabolism  and Excretion
     Early  studies  (Radomski and Davidow,  1953;  Davidow and Radom-
ski, 1953)  show * that both the rat and the dog  metabolize  ingested
heptachlor  rapidly by epoxidation  (Figure 1) and that heptachlor
epoxide accumulates  primarily  in fat  tissue.  They also reported  a
positive relationship  between the  amount of  heptachlor in the  diet
and  the amount of heptachlor epoxide in  the fat tissue.   In  this
study, the  female  rats accumulated approximately six times  as  much
heptachlor  epoxide  in  their  fat tissue as  did the males.
                                C-12

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              CO 3
HEPTACHLOR
HEPTACHLOR EPOXIDE
               FIGURE 1
                        013

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     Matsumura  and  Nelson  (1971)  fed  four male  albino rats  10
mg/kg of 99 percent  pure  heptachlor  epoxide for  30  days (approxi-
mately  5  mg heptachlor epoxide/rat/30  days)  and found  that  they
excreted 950  ug of  a  fecal metabolite  (Figure  2),  and 66 ug  of
heptachlor epoxide  in  the feces in  the  30-day period.   Mizyukova
and  Kurchatov   (1970)  found  that the  excretion  of  the  nonstored
heptachlor and  its metabolites  occurs  within  the  first five days,
chiefly through the  gastrointestinal tract  and to a smaller extent
in the urine.
     One very important route  of  excretion  of  heptachlor and  hep-
tachlor epoxide  in  females is  through  lactation  (Jonsson,  et al.
1977).   This  study  indicates  that milk  is  a  primary excretory
route for  heptachlor and  its  metabolites.   Generally,  heptachlor
epoxide concentration  in  mothers' milk is  a good indicator of the
body burden of  heptachlor  epoxide stored in the lactating mothers'
body {Jonsson,  et al.  1977;  Strassman  and  Kutz,  1977).  Polishuk,
et al.  (1977a)  found that overweight women  excreted lower quanti-
ties of pesticides,  such  as heptachlor  epoxide, in their milk than
did women  of normal  weight.   They also  found that women front ages
20 to 29 years  old excreted higher pesticides levels in  their milk
than did  women from the  ages  30  to 39, even  though  the younger
women had  lower pesticides levels in their  plasma.
     In *  human milk study of 53 samples collected from two  Penn-
sylvania  regions during   1970,  Kroger  (1972)  found  all  of the
samples contained  heptachlor epoxide  at an average concentration
of 0.16 mg/1.   Savage, et al.  {1973} performed a  similar survey  in
Colorado  in  1970-1971 with  40  human  milk  samples,  and found  25
                                014

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  CI
    \
   HEPTACHLOR
FECAL METABOLITE
    FIGURE 2
        015

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percent  of  the  samples  contained  heptachlor  epoxide at  levels
ranging  from trace  amounts to 5 ug/1.   Strassman  arid  Kutz  (1977)
conducted  a  study  in Arkansas and Mississippi  in  1973-1974  of  57
milk samples and found heptachlor epoxide residues in 35.1 percent
of the samples with at  least a trace  amount of heptachlor epoxide
in 64.9  percent  of  the  samples.  The  levels  in this study  ranged
from trace to 0.03  mg/1 and  the mean concentration was 0.004 mg/1.
They also  found  trace to  quantifiable  amounts of trans-nonachlor,
which indicates exposure  to  heptachlor or chlordane.
     Savage  (1976)  reported  the results  of  an extensive study con-
ducted  during  1975  involving  1,436   human   milk  samples  from
selected sites within  the continental U.S.   He found  that  only 2
percent  showed  heptachlor  residues/   but   63.1  percent  of   the
mothers' milk  samples  showed  heptachlor epoxide residues  ranging
from 15.24 to 2,050  ug/1  on  a  fat adjusted  basis,  with a  mean con-
centration of  91.36 ug/1.   Savage  also found  that  11 percent of
the high residue group of  women were either occupationally  exposed
or lived in  households  where a member was  occupationally exposed.
Jonsson, et  al.  (1977)  reported that  24 percent of  51 human milk
samples  collected  from  St.   Louis  in  1977 contained  an  average
heptachlor epoxide  level  of  0.0027 mg/1. Other studies concerning
                                     p
heptachlor  epoxide   in  human  milk  from  other  countries include:
Ritcey,  «t al.  (1972);  Polishuk,  et  al.  (1977a);  and Bakkan  and
Seip (1976).
     One major problem with  the excretion of  heptachlor epoxide in
mothers' milk  is  that  it  becomes a major vehicle  for  exposing  the
neonate  (Strassman  and  Kutz/ 1977).   This  exposure  is an addition
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 to  the  body  burden which already exists due  to  exposure  _in utero
 (PolishuX, et  al.  1977b;  Zavon, et al. 1969;  Selby,  et  al. 1969;
 Curley, et al. 1969).
     Residues  of  heptachlor epoxide  in  adipose  tissue  and other
 tissues and  fluids are indicative  of  the  body burden and  of  the
 exposure  to heptachlor and heptachlor epoxide  (Kutz, et al. 1977).
 Biopsied  human  adipose tissue was  used  by Burns  (1974)  to study
 the  heptachlor  epoxide levels in 302 hospital patients  from 1969
 to 1972 in the lower Rio Grande Valley in Texas.   During the study
 period,  he  found  98  percent  of   the  adipose  samples  possessed
 heptachlor epoxide residues with a  mean  value of 0.11 mg/ kg.   An
 extensive  survey  of  human adipose  tissue levels  for heptachlor
 epoxide has  been  published by Kutz, et al.  (1977).   Tissues were
 collected during postmortem examinations,  and from surgical exci-
 sions and  rejected  samples collected from patients  known or sus-
pected  of pesticide poisoning,  cachectic patients,  and patients
 institutionalized for  extended periods.  The  samples were obtained
within the coterminous 48 states, and the sampling sites were ran-
domly selected  to  be representative of the  U.S. populations.  The
 5-year study showed  that  heptachlor epoxide  can be  found in over
 90 percent  of  the U.S. population  at approximate  mean  levels of
 0.08 to 0.09 mg/Xg (Table 2).
     In addition  to the  storage of  heptachlor  epoxide  in human
 adipose tissue, a minor component  (trans-nonachlor)  of both tech-
 nical  heptachlor  and   technical  chlordane   has  also  been found
 (Sovocool and Lewis, 1975).  They studied  nine composite  human  fat
 samples from nine  census  divisions  of the U.S. and found eight  of
                               C-17

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                           TABLE 2



     H«ptachloc Epoxide Residues in Human Adipose Tissue*
Survey Year
(fiscal)
1970
1971
1972
1973
1974
Sample
Size
1412
1615
1913
1095
898
Percent
Positive
94.76
96.22
90.28
97.72
96.21
Geometric
Mean (mgAg)
0.09
0.09
0.08
0.09
0.08
Maximum
Value tag /kg
10.62
1.53
1.21
0.84
0.77
*Source: Kutz, et al. 1977
                                C-18

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 the  nine  samples  possessed trans-nonachlor.   Also found in lesser
 amounts were cis-nonachlor and  "early-eluting" nonachlor.  Five of
 the  nine  composite  samples were also positive for heptachlor epox-
 ide  and oxychlordane.   These data indicate that nonachlors may be
 more  resistant to  metabolism  than heptachlor,   and  occurrence of
 the  nonachlors in human tissues  appears  to  be  strong evidence of
 exposure  to  heptachlor  or   chlordane  pesticides   (Sovocool  and
 Lewis, 1975) .
     Several other  researchers  (Curley,  et al. 1973; Wasserman, et
 al.  1974;  Abbott, et al.  1972;  Wasserman, et al.  1972)  have re-
 ported  heptachlor  epoxide residues  in  human  adipose  tissue in
 other countries.
                             EFFECTS
Acute, Subacute, and Chronic Toxicity
     Heptachlor  and  its  metabolites  have   LD5Q  values  ranging
 from  6  mg/kg   to  531 rag/kg  (Table 3)  depending upon  the animal
species, toxicant used,  and  the mode  of administration.   Radomski
and Davidow (1953)  were  the  first to report that heptachlor epox-
 ide  is  two  to four  times  more toxic  than  heptachlor itself  when
given intravenously  in  mice.  Buck, et  al.  (1959)  later  observed
 heptachlor  epoxide  to be  approximately 10  times  more toxic  than
 heptachlor  in  dairy  calves  when given  orally.   The  most  toxic
metabolite  is  photoheptachlor  epoxide  [III  B]   (Ivie,   et  al.
 1972), which is formed by  exposure  of  heptachlor epoxide  to  ultra-
violet light or  sunlight  in the  presence of a photosensitizer on
 plants.   Ivie, et  al.   (1972)  reported  the LD50  values   for  male
Swiss-Webster  mice  to be 18 mgAg for  heptachlor epoxide;  36 mg/kg
                               C-19

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                                            TABLE 3

                           Heptachlor  and Heptachlor Metabolites 1.050
Organism
Sex fc Strain
Mouse
(Swiss-Webster)
Mouse
(Swiss-Webster)
Mouse
(Swiss-Webster)
Rat (M-Sherman)
Rat (F-Sher»an)
Rat (M-Sherman)
Rat (P-Sherman)
Rat (M-Sprague-
Dawley)
Rat (N-Sprague-
Dawley)
Mouse
Rat
Hamster
Compound
Heptachlor
epoxide
Phot o-heptach lot
epoxide II
Photo-heptachlor
epoxide (III B)
Heptachlor
Heptachlor
Heptachlor
Heptachlor
Heptachlor
Heptachlor
Heptachlor
Heptachlor
Heptachlor
Route
of
Administration
i .p.
i.p.
i.p.
oral
oral
dermal
dermal
i.p.
I.p.
oral
oral
oral
(rag/kg)
IB
36
6
100
162
195
250
71*
531*
70
105
100
Reference
Ivie, et al. 1972
Ivie, et al. 1972
Ivie, et al. 1972
Gaines, 1960
Gaines, 1960
Gaines, 1960
Gaines, 1960
Harbison, 1975
Harbison, 1975
Gak, et al. 1976
Gak, et al. 1976
it
Gak, et al . 1976
* - assumed to be rag/kg  body weight
M - male
F - female
N - neonate
i.p. « intraperitoneally
                                                C-20

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 for  the  intermediate  photo  metabolite  photoheptachlor  epoxide
 [II];  and 6 mg/kg  for photoheptachlor  epoxide [III  B].   Gaines
 (1960)  conducted acute  ^050 studies  using  oral doses  of hepta-
 chlor  in  the  Sherman  strain  of  rat  and found  L&SO  values  of
 100  mg/kg in males  and 162 mg/kg in females,  while the acute der-
 mal  LDso  of  heptachlor  in  males  was  195  tag/kg  and  250  tug/kg
 for  females.    Harbison  (1975)  used  neonatal  and  adult  (120  to
 150  g)  Sprague-Dawley rats  to  show  that the  newborn  rat  is more
 resistant to  heptachlor  than  the  adult.   The   intraperitoneal
 LDso  for the adult  male rats  was  71  mg/kg*,  but  was 531 mg/kg*
 for  newborn  rats.   Gak, et al. (1976)  reported  heptachlor ^050
 values for the  mouse,  rat,  and hamster to be 70 mg/kg, 105 mg/kg,
 and  100 mg/kg of  body  weight,  respectively.
     Heptachlor  is generally classified  as a  neurotoxin  because  it
produces  abnormal stimulation  of the  central nervous system when
animals are exposed  to high  doses.   In an  attempt to  elucidate the
 toxic action of heptachlor/  numerous  studies have  taken  place  to
demonstrate  the biochemical  changes  induced  by  heptachlor.   St.
Omer (1971) studied  the  convulsions  produced  by heptachlor in rats
and  found that  the  intensity of the convulsions was  directly cor-
 related  with  the rise  in brain ammonia,  and the periods  between
 seizures  were  associated with  decreased levels of brain  ammonia.
 St.  Omer and Ecobichon  (1971)  reported that acute administration
 of heptachlor  to rat«  significantly elevated  their  brain acetyl-
 choline  content,  with  some  decrease  in acetylcholine  concentration

 *Assumed  to be mg/kg  body weight.
                                C-21

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        the  period of  severest  seizure activity.   They suggested
that these changes in  the brain level  of ammonia and acetylcholine
during heptachlor exposure may be part of the mechanism of convul-
sion  induction.    Hrdina,  et  al.  (1974) administered  heptachlor
chronically for 45 days  to  rats  and  found  the acetylcholine level
in  the  cerebral  cortex to  be  decreased and  the  serotonin (5-HT)
level significantly  increased  in  the  brain-stem.   They  also found
that an  acute  dose of heptachlor (200 rag/Xg)  produced  body hypo-
thermia.
     Changes in  the  energy  linked  functions  of  the mitochondria
have been studied by Pardini, et al.  (1971) and Settlemire, et al.
(1974).   Pardinir et al. (1971) reported that  heptachlor  (1 umole/
flask)  depressed  the  mitcchondrial  succinoxidase system  to 5.8
percent  of  the level of uninhibited  controls and that heptachlor
epoxide  did  not  depress the  system  at all.   Heptachlor  also de-
pressed  the mitochondrial activity  of NADH-oxidase to 8.6  percent
of  uninhibited controls, while again heptachlor epoxide  had no
effect.   They  speculated that  since heptachlor did not  interact at
any step in the  electron transport chain after  cytochrome C, the
site of  heptachlor interaction may  be either at complex III or at
complex  I  and  II  of the mitochondrial  electron  transport chain.
Settlemire, et al. (1974} found  that lower concentrations  of  hep-
tachlor  caused dramatic  changes  in the membrane  of mouse  mitochon-
dria.   They stated that the increase  in respiration  (oxidation of
succinate), observed when ADP  and heptachlor  were  added,  was  prob-
ably caused by increased permeability of  membranes  to succinate,
                                022

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 or  by  confornational changes of such a  nature  that the  intrinsic
 activity  of  the  respiratory  chain was increased.
     Induction of  liver  raicrosomal  enzymes  by heptachlor and hep-
 tachlor  epoxide  has  been  reported  by Kinoshita  and  Kempt  (1970)
 and Den Tonkelaar  and Van Esch  (1974).  Kinoshita and Kempf  (1970)
 found  heptachlor and heptachlor epoxide  to  be very persistent in-
 ducers  in rats  of  phosphorothioate detoxification, o-demethylase,
 and N-demethylase  in a  dose  related manner.   They also found that
 male rats were more  sensitive to heptachlor while female  rats were
 more sensitive to  heptachlor epoxide.   Den  Tonkelaar and Van Esch
 (1974) found that  dietary heptachlor significantly  induced aniline
 hydroxylase, aminopyrine demethylase,  and hexobarbital oxidase in
 rats at levels of  2  to 50 mg/kg, 2  to 50 mgAg, and 5 to  50  mg/kg,
 respectively.  Both  groups  reported that approximately  1 mgAg of
 heptachlor  showed   no   effect   on  the   induction  of  microsomal
 enzymes.
     Krampl  (1971) reported  that heptachlor  caused an increase in
 the enzymes glutamic-pyruvic  transaminase (GPT) and aldolase (ALD)
 in the serum of  rats.   Histologic  examinations  of  the  livers re-
vealed  that  maximum alteration  in hepatic  morphology  coincided
with the  days  on which  hepatic and serum GPT  and  ALD activities
were different from  normal.   They stated  that the  increased  enzyme
 activity  was probably  related  to  altered  membrane permeability,
 which allowed intracellular  enzymes to pass out of  cells  that were
 damaged but  not  necrotic.   Welch,  et al. (1971) found  that  hepta-
 chlor  stimulated  the  metabolism of  estrone by  liver  microsomal
enzymes  and  inhibited  the   increase  in  uterine  wet   weight   in
 treated female rats.
                               C-23

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     Several studies have  been conducted concerning the effects of
heptachlor on  glucose  hoiueostasis in the  rat  (Kacew  and Singhal,
1973; Kacew  and  Singhal,  1974;  Singhal and Kacew,  1976).   it was
reported  that  heptachlor,  administered   either   in  small  daily
amounts over a prolonged  period  of  time or in a single oral dose,
caused  significant  increases  in  the  activities  of  renal  and
hepatic  pyruvate carboxylase,  phosphoenolpyruvate carboxykinase,
fructose  1,6-diphosphatase,  and  glucose  6-phosphatase,  an eleva-
tion of  blood  and  urinary glucose and  serum  urea levels,  and  a
depression  of  liver glycogen.    They  also found  that heptachlor
caused a  rise  in the  level of endogenous cyclic AMP and augmented
the activity of  hepatic  and  renal adenylate cyclase.   They stated
that their data  support the  hypothesis  that the heptachlor-induced
alterations  in  glucose   homeostasis  are  related  to  an   initial
stimulation  of the cyclic AMP-adenylate  cyclase  system  in  liver
and kidney cortex.
     Dvorak  and  HalacJca  (1975)  studied  the  ultrastructure of  the
liver cells  of pigs after the administration of small doses  (2 to
5 mg/Xg of body  weight) of heptachlor and  found a  marked depletion
of  glycogen,   morphological  changes  in the  granular endoplasmic
reticulum, and  increases  in the amount  of  agranular endoplasmic
reticulun.  With higher doses and a longer duration of administra-
tion of  heptachlor/ a greater   occurrence of  liver lysosomes  was
also observed.
     Reuber  (1977a) found that  C3fi male  and female  mice fed 10
mg/kg of  heptachlor or heptachlor  epoxide developed hepatic  vein
thrombosis.   Heptachlor  caused  IS  percent of  the females and  10
                                C-24

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percent  of  the  males  to develop thrombi, while heptachlor epoxide
caused  11  percent of  the females and  7 percent of  the males to
develop  thrombi.   He  also stated that 7 mice of the 39  that exhi-
bited hepatic vein thrombosis also possessed recent thrombi in the
atria of the  heart,  while no thrombi were  found  in any organs of
the  control mice.   Liver cirrhosis  was  also occasionally present
in addition to  liver carcinomas.
Mutagenicity
     Marshall,  et al.  (1976)   reported  that both  heptachlor and
heptachlor epoxide were  not  mutagenic when tested with  Salmonella
typhimurium in  the Ames  assay.   Cerey, et al.  (1973)  found  that
heptachlor in oral doses  of  1 to 5 mg/kg given  to male  rats caused
dominant lethal changes  as  demonstrated by a  statistically  sig-
nificant  increase in  the number  of resorbed  fetuses  in  intact
pregnant rats.   They  confirmed  this  by  finding a significant  in-
crease  in  the  incidence  of abnormal  mitosis,  abnormalities of
chromatids, pulverization, and  translocation of chromosomes  in  the
bone marrow cells  of  their  experimental  animals.   They  concluded
from the  results mentioned  above that  rat fetuses  in early  and
late stages of  embryonic development could be adversely  affected
by heptachlor.   Ahmed,  et al.  (1977) used SV-40 transformed  human
cells (VA4) in  culture to show  that  both heptachlor and heptachlor
epoxide  induced  unscheduled DNA  synthesis in this  system  when
metabolically activated with homogenized rat liver  supernatant.
Teratogenicity
     Mestitzova (1967)  found that heptachlor administered to  rats
in food  at 6 mg/kg  body weight  caused a marked decrease in  litter
                                C-25

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size, both in several litters of one generation as we-ll as in suc-
cessive generations.  The author also stated that the life span of
suckling rats was significantly shortened, with the death rate be-
ing highest during the first 24 to 48 hours.  In long-term feeding
studies with  heptachlor  the same author  observed  the development
of  cataracts  of the  lens,  both in  the  offspring and  the  parent
rats.   Prolonged feeding  of  heptachlor  increased  the  chances of
cataracts  occurring  in  the  parents, while  the cataracts  in the
offspring were  observed  shortly after  their  eyes  opened.   Mestit-
zova stated  that the sequence of occurrence  of the cataracts ex-
cluded the possibility of  recessive  genetic  traits  or a vitamin a
deficiency as the causative factor.
Synergism and/or Antagonism
     It has been reported that the protein content  in the diet can
affect  the  acute  toxicity of  heptachlor  in  male  weanling rats
(Webb and Miranda,  1973; Miranda, et al.  1973; Miranda and  Webb,
1974).  These  workers found that with a  10  percent dietary  level
of protein,  heptachlor  was less acutely  toxic  in  rats  fed  an un-
supplemented gluten  diet than in animals pair-fed diets containing
gluten plus  supplemental amino  acids  or  casein  plus 0.2 percent
DL-methionine.   When the dietary  protein level was  raised   to 18
percent,  heptachlor  was  twice  as toxic  to  rats  pair-fed  casein
diets, as  compared  to rats fed unsupplemented  gluten.   They also
found that weight gain,  microsomal proteins,  and heptachlor  metab-
olism were significantly reduced  in  the animals fed  unsupplemented
gluten and that animals  pair-fed  the casein  diet had  higher  hepta-
chlor epoxidase activities  than those  fed  the gluten  diet.   There-
                                C-26

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 fore,  they suggested  that low  protein  diets  impaired  or slowed
 metabolism  of  heptachlor  to  the  more  toxic  heptachlor  epoxide.
 Weatherholtz,  et al.  (1969)  reported  that  rats fed protein defi-
 cient diets were less  susceptable  to heptachlor toxicity and also
 suggested  that this observation may  have  been due  to reduced  i_n
 vivo conversion of  the pesticide to  the  epoxide form.
     Miranda  and Webb also  studied  the effects  of phenobarbital
 and  SKF525-A  on  these  protein  deficient  diets  (Miranda,  et  al.
 1973; Miranda  and Webb,  1974).  Their studies suggested an inter-
 action of protein inadequacy with drug metabolism and  with  inhibi-
 tion of  heptachlor  metabolism,  but  they believed further  studies
 should be carried out to clarify their findings.
     Harbison  (1975) studied  the effects of phenobarbital  (PB) on
 neonatal rats.   He  found  that PB potentiates the toxicity  of hep-
 tachlor  in newborn rats.    For heptachlor,  LD$Q  values  for   a
 newborn  rat,  for a newborn  pretreated with PB,  and  for an adult
male untreated  rat, were  531  mg/kg»  133 mg/kg,  and  7 mg/kg,  re-
spectively .
 Carcinogenicity
     Various  studies  regarding  the  carcinogenicity of  heptachlor
and  heptachlor epoxide when administered  to  rats and  mice have
 been conducted by  the Kettering Laboratory,  the  FDA, Cabral,  et
 al.  1972,  International  Research   and  Development   Corporation
 (IRDC)  sponsored by V«lsicol,  and  the  National  Cancer  Institute
 (NCI).   Two extensiv* reviews  of the«« studies  have been conducted
                               C-27

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by Epstein  (1976)  and by  the  U.S.  EPA (1977) and  should  be con-
sulted for more  specific  information  on each  study.  Tables 4 and
5 present summary data reported by Epstein (1976), and include the
original  authors's  conclusions, any  independent  histological re-
evaluation  of  the  studies  which have  been  conducted,  and  Dr.
Epstein's comments on each study.
     The  1955 Kettering study  on  heptachlor  in rats was  an unpub-
lished  study  by the  Kettering Laboratory  under  contract  to the
Velsicol  Corporation.   The U.S.  EPA  (1977-)  review  of  this  study
stated  that  the oral  dosages  of  heptachlor   administered  in the
diet were  0,  1.5,  3.0, 5.0,  7.0, and 10.0 rag/kg.   These dosages
were administered  to  a total of  120  male  and 120 female Carvorth
Farm strain  rats.   The length of dietary  administration  was 110
weeks with a 57 percent mortality rate in  the  male  groups and a  43
percent mortality rate in the  female groups.   The  reviews of the
report  state  that  the  majority of the deaths were  due  to  inci-
dental  diseases,  particularly  respiratory  diseases  (U.S.  EPA,
1977; Epstein,  1976).   Tumors  were found  both in controls and  in
exposed animals and the original  authors  interpreted  their data  as
indicating  no  significant difference  between  the  incidence   of
tumors  in test  and control  groups  (Epstein,   1976) .   Based  on  an
independent  statistical  analysis of  the data  from  this  study,
Epstein  (1976)  concluded  that "the  data  in  fact  demonstrated  a
statistically  significant  incidence  of  multiple  site  and  other
tumors in the higher  level  female test groups."
     Another Kettering  study  was  conducted for the Velsicol  Corp.
in 1959 by Witherup,  et al. (1959).  This  investigation evaluated
                                C-28

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        TABLE 4



of Carcinogenlclty Data in Bata*
Author*
fcetterliig,
1955
Ketterlnq,
1»S»
Strain foramlation Concentrations (ppa)
BepUchlor (H)| H HE C
•pox Id* (HE)j
CfclordM* (C)
cr n at u*j*p*ciried i.5» J.DJ
nitity &.O> l.Oi
10.0
CMI HE ot unspecified - Of 0.5) -
purity 2.5| S.0|
I.Sl 10.0
Carcinogen! city
Authors
Concluaiona
TUMOT lncld«nc«
"propox t ionat* ly*
dlatrlbut*d in
all ttmtm »mt
contKOl qroupa
Tuaor Incldenc*
•unrelated* to
H8 content In
diet*. ••€•••
hepatoaaa In teat
animal* !• «c-
knowled9«d, but
dtacount*d. Alao
unueual •ali9nant
tu*)or» in *ale*
and (••*!*•
Independent
Hiatologlcal
Me-evaluatlon
Not undertaken
Hapatocarcino-
9«nic and «Hil-
tlple alte Ma-
lignant tuaiora
Ccewenta
1. T«at diet* prepared
crudely *nd etudy
poorly docuaianted.
2. Author'* data deoon-
•trate atatlaticAlly
•l^niftcant increaae
in «ali9nant *nd any
tu*>or* in Multiple
• Ite* in acne fe*i*l«
teat group*.
1. T*et diet* prepared
crudely and atudy
poocly docutMnted.
2. Kettering data »tatl«
tlcally algnit leant, -
for incidence of tota
tuaor- bear ing anl>al*l
and for liver and pi-
tuitary tuator*.
J. Hlatologlcal re-eval-
uation *howed hepato-
carcinomaa.
4. ttepatocarcinogenlcity
•t*tl*tlcally algnl-
                                                     cant.
Ketterinq,
1*4*




CD Ntxtur* of 25%
HI (»«.»» pure).
and 75% N f»t.0%
pure >


S.Oi 1.5| 10) 12, S - Incidence of tu- Hot undertaken
•or* 'qualita-
tively *nd quan-
titatively •!•!-
lar* in te*t «nd
control*.
1. Study poorly docu-
mented *nd Methodolog
cally unaoundi featalel
rata only tea ted.
2. Unacceptable a* car-
• cinogeniclty teat.
        C-29

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                                                    TABLE 4 (Continued)
Author*
Cabral, at
al. 1972
NCI, 1977
Strain torMilation
Heptacnlor (H);
epoilde (HBh
Chlordane (C)
Hlatar H Analytic Grade
96. •% pure
Oaborne- Technical Hi
Mendel conaiating of
741 H and ca
24% alpha C
Concentration* (pp*i)
H MB C
Total
doeage
50 »g/kg
Halea 3i.9j
77.9.
Peaialea
25. 7| 51. 3
Carcinogenic Ity
Author*
Conclusion*
Mot carcinogenic
Carcinogenic
under condi-
tlona of
aaeay"
Independent
Hletologlcal
Re-evaluation
Not undertaken
Not undertaken
Coaaienta
1. Perinatal doaage only.
2. Author 'a data deaon-
atrate atatlatlcally
aignlf leant increase
in endocrine tumor »
in nalea and rare
•HpoBatoua" renal
tuMor* in 2 teat fe-
•alea.
1. Relatively Mall num-
ber negative control*)
uncertainties in doe-
agei high Mortality
in high doaage test
group*.
2. NCI data shows eiceas
hepatic nodules in
•ales and femalea.
* Sourcei Kpatein, 197*
•*The concluaion* oC NCI atate that there la no clear evidence of carcinogenic effect of  heptachlor.
                                                        030

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                                                         TABLE S

                                         SuMary of Carclnogenlcity Data In Nice*
Author*
Davla,
IfDA),
Strain formulation
Meptachlor (H),
ipoalde (H£)t
Cblordane (C)
C3N H «nd HI of un-
•peclfled purity
Concentration* fppai) Carclno^enicity
H HE C Author*
Concluaion*
10 10 - 'Benign" hepa-
toma* induced
by H And HI
Independent
Hiatological
He-evaluation
H and He both
bepetocarclno-
9«nlc

1.
2.
3.
4.
COJMent*
PDA data poorly docu-
••nted.
rPA data •tatietl-
cally •Igniftcaiit for
ttMtor incidence*.
Miatotoglcal re-eval-
uation demonstrated
hepatocarcinogeniclty
HepAtocarcinogantc
                                                                                                         algnlftcant.
I BBC,
1973
NCI, 1977
CD-I Hiiture of 25%
H *nd 75%
B6C3P1 Technical Hi
of 74% H,
and ca, 2»«C
1.0| 5.0i 10.0
Hale* t.l| -
13. •
re»alea
».0i !•
Dose related
nodular hyper-
plaaia at 5.0
and 10.0 pp*i
Carcinogenic
under condi-
tion* oC
•••ay
Hapatocarcino- 1. I HOC data et*tl>tl-
ganic cally •ignlflcant
exceaa of nodular
hyperplaaiaa.
2. Hlatological re-eval-
uation found hepato-
carcinoaiaa.
3. Hepatocarcinogenicity
•tatiatlcally •Ignl-
flcant.
Not undei taken 1. Relatively wall nu»-
ber negative control*
non-concurrent eipet 1 -
•ent*i uncer talntiea
                                                                                                         JUvlaed  data  atatln
                                                                                                         tlcally  *i9nificant
                                                                                                         (or  tMp»Voc»rcint>-
                                                                                                         g*r»lcity.
*8ourc«i Bpateln, 1»7«
                                                         C-31

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heptachlor epoxide at dietary levels of 0, 0.5, 2.5, 5.0, 7.5, and
10 rag/kg administered to CFN (Carworth Farms, Nelson^ rats for 108
weeks.   Each dosage group  consisted  of  25 males  and  25 females.
Mortality in males  ranged  from 32 percent for  the  controls  to 52
percent  at  2.5  mgAg of diet,  and in the females  ranged  from 24
percent  in  controls to  52 percent  at 7.5 mg/kg  of diet.   They
stated,  however,  that  the  increased  mortality in  the  groups fed
heptachlor  epoxide  was  not significant.   They  also  stated the
earliest  tumor  was  discovered  during  the 13th month  and animals
dying before  that were  examined, but were not included among the
numbers capable of bearing  tumors.  The authors concluded that the
tumor incidence was unrelated to the heptachlor epoxide  content in
the diet, although they acknowledged an excess  of  hepatomas  in the
test animals (Epstein, 1976).   An  independent  statistical analysis
of this data indicated that all the heptachlor  epoxide  dose  levels
except the  0.5  mg/kg level in  the males,  were significant  at the
p » 0.55 probability level.
     Re-evaluation  of  tissue  slides by Dr. Melvin  D.  Reuber of  a
1959 unpublished Kettering study indicated  that  there  was  an in-
crease in hyperplastic  nodules  and carcinomas of the liver  in the
treated animals when compared to control  animals  (U.S.  CPA,  1977).
He also  found a greater  incidence  of  carcinomas  in females  than  in
males, as the Kettering  data  had also indicated.   In addition,  he
found highly malignant  tumors  in brain,  thyroid,  adrenal,  kidney,
lung,  bone, and genital organs.   Reuber concluded that  because
carcinomas  of the liver  in the  untreated  rats  were infrequent,  the
presence  of 28  liver carcinomas  among 213 treated  rats indicated
                                C-32

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 that   heptachlor   epoxide   is   carcinogenic  in  rats  at   P<10~8
 (U.S.  EPA, 1977).
     Dr. Williams  (U.S. EPA, 1977) also re-evaluated  the Kettering
 tissue slides and  concluded  that the  study demonstrated  an in-
 creased  incidence  of cancer in the livers  of  treated rats and an
 increase in  hyperplastic nodules  in the males only at the  10 mg/kg
 level.   He considered  the  seven liver malign«fncies in the  treated
 animals  versus no  malignancies  in controls  to be strongly  sugges-
 tive of  a  carcinogenic effect  (U.S.  EPA,  1977).   Williams, like
 Kettering and Reuber,  also diagnosed  a range of unusual malignant
 tumors in treated  animals  (Epstein, 1976).
     The slides  were re-evaluated by  three other independent pa-
 thologists (Drs. Stewart,  Squire, and Popper)  and all three diag-
 nosed  a  higher  incidence  of carcinomas than  that reported  by the
 Kettering workers  who  found  only two  (U.S. EPA,  1977;   Epstein,
 1976).
     In  1966,  the  Kettering Laboratory  produced  another  unpub-
 lished  report dealing  with the administration  of  a  mixture of 75
 percent heptachlor  and  25  percent heptachlor epoxide to female CD
 rats at  doses  of  0, 5.0,  7.5,  10.0,  and 12.'5 mg/kg  in   the diet
 (Jolley,  et  al.  1966).   After  104  weeks  of  exposure,   various
lesions in the pituitary gland,  adrenal  gland,  mammary gland, and
the liver were found, but  considered  by the  original  investigators
to be  "spontaneous"  because the lesions were  found in both control
and  treated  groups.   The  lesions of  the  pituitary and  adrenal
glands were  considered hypertrophies  rather  than neoplasms.  The
 lesions of the mammary gland  were diagnosed as adenomas or fibro-
                                C-33

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adenomas of mammary glands.  The liver lesions were referred to as
•clusters of enlarged hepatic cells*  (Epstein (1976) calls it cen-
trilobular  hepatocytomegaly)  with  cytoplasmic  degranulation  and
clusters of enlarged  irregular  vacuolated  cells  which were filled
with  lipid  and distributed  randomly in  the  lobules.   They  con-
cluded  that the experimental  diet  caused  the  changes  in the liver
which were qualitatively  similar  to, but quantitatively different
from  lesions  in control  rats.   Epstein  (1976)  suggested  that a
re-evaluation  of   the liver  histology  in  all  test  and  control
groups  is  necessary  before  the significance  of these  and other
possible lesions can  be assessed.
     In  1965,  FDA completed  a 2-year  study  of  heptachlor   and
heptachlor epoxide fed  to C3Heb/Pe/J  mice  (Davis,  1965). Three
groups  of 100  males and  100  females per group  were  fed 10 mg of
heptachlor per kg  of diet,  10  mg  heptachlor  epoxide  per  kg of
diet, or a control diet.   During the 2-year period, survival rates
of 34 percent,  30  percent, and 9.5  percent were reported for  the
control group  and  the heptachlor and  heptachlor epoxide fed  ani-
mals, respectively.   Over the test period,  30  control mice  had
benign  tumors  and 21  controls  had  malignant tumors;  heptachlor-
treated mice had 51  benign tumors  and 10 malignant tumors; hepta-
chlor epoxide  treated mice had 85 benign  tumors and  13 malignant
tumors.  Statistics were  not  performed on  this data by PDA  because
of incompleteness  in  the  number of samples and  the "arbitrariness
of microscopic diagnoses"  (Davis,  1965).   Davis  stated that  the
incidence of hepatic  hyp^rplasia and benign hepatomas was  approxi-
mately  doubled  in  the test groups,  but concluded  that heptachlor
                                034

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 and  heptachlor epoxide  do not  have  a significant  effect on  the
 incidence  of malignant  tumors.
     The  tissue slides  from the  1965  FDA study were  re-evaluated
 by Dr.  Reuber.  He  found  liver carcinomas in  64  of 87 male mice
 (74  percent) and  57  of  78  female mice (73 percent)  ingesting hep-
 tachlor;  in 73 of 79 male mice (92 percent) and  77 of 81 female
 mice  (95  percent)  ingesting heptachlor  epoxide;  and  in  22 of 73
 control male mice  (30 percent)  and in 2 of 53  control  female mice
 (4  percent) (Reuber, 1977b).    He  also stated  that the  affected
 treated animals often had  three to four carcinomas  per liver with
 a  size of  3 to 5 on, while affected control animals  had only  soli-
 tary carcinomas of  a size 5 nun or less.   Reuber  concluded that
 heptachlor  and heptachlor  epoxide diets caused the  development of
 a  highly  significant incidence of carcinomas  of  the  liver  which
 were capable of invasion and metastasis.
     Four  other independent  pathologists  (Drs.  Stewart,  Squire,
Williams, and  Sternberg) were  asked to review  slides  from  19 ani-
mals that Reuber had diagnosed  as  having  hepatic carcinomas.  Drs.
Stewart, Squire, and Sternberg  agreed with Dr.  Reuber  that the 19
animals had hepatic carcinomas (U.S.  EPA,  1977).   Dr.   Williams
diagnosed  eight carcinomas/ 10 nodules  or  hyperplastic  nodules,
 and  one  dysplastic  area.   However,  Dr.  Williams   considers that
 hyperplastic nodules are induced only  by  carcinogens,  therefore he
 considers  them evidence  of a  carcinogenic  effect  on the  liver
 (Epstein, 1976).
     Cabral, et al.  (1972) conducted  a study using  95  Wistar  rats
 force fed  heptachlor in corn  oil by  gastric intubation.  Hepta-
                                C-35

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chlor was administered  at  a level of 10 rag/kg of body weight five
times on alternating days  beginning  at  10 days of age.  It was ob-
served that the incidence  of  tumors  in  males  occurred at different
sites and was  not reproducible, while  the  tumors  in females were
in  the adrenal, thyroid,  and  pituitary  glands and were comparable
in  both control and  treated groups.   In the  treated females, 9 of
28  rats developed 12 tumors in  various  organs, including five mam-
mary  tumors and  two  renal  lipomatous  tumors.    In  the  control
group, 4  of 27 females  developed four  tumors,  two  of  which were
located in  the  breast.   They concluded that  "in view of the dif-
ferent locations  of  the tumors  and the  lack  of  reproducibility of
the findings among  males, the  results  are  not considered as evi-
dence of  carcinogenicity  of  heptachlor under the present experi-
mental conditions."   Epstein (1976)  on the  other hand, concluded
that  the  Cabral,  et  al.  (1972)  study  does  show a  statistically
significant incidence of endocrine tumors  in  males.
     In  1973,  the  IRDC completed an  unpublished  18-month  study
using CD-I  mice  on  a  treatment  diet containing a  mixture  of 75
percent heptachlor  epoxide and 25 percent  heptachlor.   The  study
was designed using one  negative control, one  positive dietary con-
trol of 2-acetamidofluorene at  250 mg/kg,  and three  dietary  treat-
ment group* of 1.0, 5.0,  and  10.0 mg/kg, respectively.  Each group
contained 100  males and  100  females.  After six months  on  these
treatments  10   males  and  10  females  were  sacrificed  from each
group.  It  was found that  the liver  weights were significantly  in-
creased in  the 5.0 and  10.0 mg/kg treatment groups  in males  and  in
the 10.0 mg/kg treatment group  in females  (IRDC, 1973).   Also,  the
                                C-36

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livers  from males  fed  the 1.0, 5.0, and 10.0 mg/kg diets and  from
females fed the 5.0 and  10.0 mg/kg  diets showed  a dose  related  in-
cidence and severity  of  hepatocytomegaly.   A large number of  com-
pound  related liver  masses (nodular  hyperplasias) were  seen  in
mice that died during  the study period or  that were sacrificed  at
the end of  the  test period.   These masses  were  thought to be  ex-
tensions of  the  hepatocytomegaly lesions (IRDC,  1973).  The  mice
fed  the 1.0 mg/kg  diet  were  considered  to be  free  of compound-
related nodular hyperplasia, since  the  incidence  of the lesion  was
similar to  the untreated controls.   No lesions were found sugges-
tive of a compound  effect in any tissue other than the liver,  and
no mention  was made of  any  carcinomas  in  any heptachlor epoxide/
heptachlor test group.
     Reuber also  re-evaluated   the  histological  material from  the
IRDC study (U.S EPA, 1977; Epstein, 1976).   His  findings indicated
a significant  increase in the  incidence  of liver  cancers  induced
by the  heptachlor  epoxide/heptachlor mixture  in males  in the  5.0
mg/kg group and in both  males  and females in the 10.0  mg/kg  group.
The incidence in these groups  was comparable to  or  higher  than the
incidence  in  the  positive  (2-acetamidifluorene,  250  mg/kg}  con-
trols.  It  has  been indicated  that the majority of lesions  diag-
nosed as nodular hyperplasias  by IRDC,  were diagnosed  by Reuber as
carcinomas (Epstein, 1976).  It is  interesting to note that  though
both IRDC and Reuber diagnosed  a similar  number of carcinomas in
the  positive  controls,  the discrepancies   in  the diagnoses  seem
largely restricted to the  test groups at  th« 5.0 and  10.0  mgAg
        (Epstein, 1976).
                                C-37

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     Five  additional pathologists  reviewed  slides  from  the IRDC
study  (two of the  pathologists were consultants  to the Velsicol
Corporation), and  found  that the IRDC study  had substantially un-
derdiagnosed  the  number  of  carcinomas  present  (Epstein,   1976).
Epstein  (1976) concluded  that  the IRDC study demonstrated the hep-
tachlor  epoxide/heptachlor  mixture  induced  a  dose-related  inci-
dence  of nodular hepatic  hyperplasias,  and  also demonstrated the
hepatocarcinogenicity  of  heptachlor  epoxide/heptachlor  as evi-
denced by  the histological  re-evaluations.
     The NCI  released  a preliminary report  on  the  Gulf South Re-
search Institute  study  on  heptachlor  in 1975.   These  preliminary
findings were reviewed  by both Epstein (1976) and  the  U.S. EPA
(1977).  In 1977,  the NCI  released  a final  report which reported
on contract work conducted first by  the  Gulf South  Research Insti-
tute and more currently  by Tracer  Jitco Inc.  (NCI,  1977).  Both
Osborne-Mendel  rats and  B6C3F^ mice were  used to  test  the pos-
sible carcinogenicity of  technical-grade heptachlor.
     Groups of  50  rats  of each sex were administered low and high
doses of heptachlor for 80  weeks and  then  observed for 30  weeks.
The  doses  of heptachlor  to  both  males  and  females were  lowered
several  times during the  study due  to toxic  effects,  and  the time-
weighted average doses  used were 38.9  and 77.9  rag/kg  of heptachlor
in the diet for male rats  and 25.7  and 51.3  mg/kg  for  female rats.
Matched  controls  consisted  of  10  untreated  rats  of each  sex and
pooled controls consisted  of 50 untreated  male and 50  untreated
female rats  from similar  bioassays  of five  other  compounds.  All
surviving  rats  were  killed  at  110 to  111  weeks  and  no  hepatic
                                C-38

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 tumors were  observed.   Neoplasms  were  found  in  test  animals  at  in-
 creased  frequency  when  compared  to control groups, but  the nature,
 incidence, and  severity of the  lesions  observed provide no  clear
 evidence  of  a carcinogenic effect of heptachlor  in  Osborne-Mendel
 rats as  reported by  the pathologists.
     In  the  second  part of the  NCI  study,  groups  of  50 mice  of
 each sex were administered heptachlor  at  low  and high doses  for  80
 weeks and  then  observed for 10 weeks.   The dose  for males was  re-
 duced once,  while  the  dose for  females  was  reduced twice due  to
 toxic effects.  The  time-weighted average dosages in the diet were
 6.1 and  13.8 mg/kg of heptachlor  for male mice,  and  9 and 18  rag/kg
 of heptachlor  for  female mice.   Matched  controls consisted  of  10
 of each  sex  of  untreated mice and pooled controls consisted  of  90
 untreated male  and 70 untreated  female mice  from similar bioassays
 of five  other compounds.  Results of hepatocellular carcinomas  in
 both male and female mice were found to  show a  highly  significant
dose-related  trend.   Twenty-six  percent  of  matched male controls
 and 20 percent  of  matched  female controls  developed hepatic car-
 cinomas;  18  percent  of   the pooled  male  controls and 4  percent  of
pooled female controls  developed  hepatic  carcinomas; 24  percent  of
 the low dose males and  6 percent  of the  low  dose females developed
 hepatic carcinomas>  and 72 percent of  the high dose males  and  71
 percent of the  high  dose females  developed hepatic carcinomas.   It
was concluded that heptachlor  is  carcinogenic in mice livers under
 the conditions  of  this  assay  at  the high  dosages given.
     Epidemiological  studies  conducted to date have uncovered  no
evidence  of  increased  cancer  mortality  among workers  occupation-
                                C-39

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ally exposed in the manufacture of chlordane and heptachlor (Shin-
dell,  1977; Wang  and  MacMahon,  1979a,b).    Wang  and  MacMahon
(1979a)  investigated  mortalities  in  a  cohort  of  professional
pesticide  applicators.    There  were  311  deaths  between  1967  and
1976 in the  population  of 16,126  males, giving a standard mortal-
ity  rate  (SMR)  of 84.   SMRs for  cancers  of  the lung,  liver  and
bladder did  not differ significantly  from  100 at  the  95 percent
confidence  level.   In  fact,  SMRs for  termite control operators,
exposed routinely to heptachlor and chlordane, were soraehwat lower
than SMRs  for general  pesticide operators,  who received much less
exposure to heptachlor  and chlordane.
     Wang  and  MacMahon  (1979b)   reported   on  1,403  white  male
workers who  were  employed for at  least three  months  in the manu-
facture of chlordane  and heptachlor  in  two  U.S.  plants between
1946 and  1976.    Their  study observed  113  deaths  from  the study
group, compared  to 157 expected,  giving  a  standardized mortality
ratio  of 72.  They  also observed no  overall excess of deaths from
cancer, even  in workers  followed  for  20  or  more years from entry
into the occupation.  A small nonsignificant increase  in  lung can-
cer  deaths was  seen  (12 observed,  9.0 expected), which was  not
distributed  by duration of exposure  or  latency in any  pattern sug-
gesting an etiologic  role.   Unfortunately,  cigarette  smoking data
were not available for  this  exposed  population.  The Wang  and Mac-
Mahon  (1979b) data would  indicate that chlordane and heptachlor do
not  increase the  cancer mortality  among these workers,  but  the
                                C-40

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authors express  that "the study  population is  too  small and  the
period  of  followup too short  to translate  this  into a  statement
that there is no excess risk of  cancer associated with exposure  in
man."
                                   C-41

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                           CRITERION FORMULATION
Existing Guidelines and Standards
    Source
Published Standard
      Reference
Occup. Safety
 Health Admin.

An. Conf. Gov.
 Ind. Hyg.

Fed. Republic
 Germany

USSR
World Health
 Organ.**
U.S. Pub. Health
 Serv. Adv. Cooun.
500 ug/m3*


500 ug/m3 inhaled
 (TLV)

500 ug/m3 inhaled
10 ug/m3 ceiling
 value inhaled

0.5 ug/kg/day accept-
 able daily intake in
 diet

Recommended drinking
 water standard (1968)
 18 ug/1 of heptachlor
 and 18 ug/1 heptachlor
 epoxide
Natl. Inst. Occup.
 Safety Health, 1977

Am. Conf. Gov. Ind.
 Hyg., 1971

Winell, 1975
Winell, 1975
Natl. Acad. Sci.,
 1977
Natl. Acad. Sci./
 1977
*  Time weighted average
** Maximum residue limits in certain foods can be found in Food
   Agric. Organ./World Health Organ. 1977, 1978


 Current Levels of Exposure

      Various  investigators  have  detected heptachlor and/or hepta-

 chlor epoxide  in  the  major  river basins of the United States at a

 mean concentration  of 0.0063  ug/1 (U.S. EPA,  1976)  for  those in-

 stances of  detection.  Food can  be a  significant  factor in man's

 exposure to heptachlor and metabolites  through bionagnification in
                                C-42

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 the  food  chain.    The  FDA  showed  that  in  their  "market  basket
 study"  covering  August 1974 to July 1975  for  20  different cities
 (Johnson  and  Manshe,  1977), 3 of 12 food  classes contained resi-
 dues  of heptachlor  epoxide ranging  from trace  amounts in the gar-
 den fruits class  to 0.0006 to 0.003 ppm in the dairy products and
 the meats, fish, and  poultry classes,  respectively.   A national
 study by  the  U.S.  Department of  Interior  in  1967  to 1968 reported
 that heptachlor and/or heptachlor epoxide were found  in 32 percent
 of the  590 fish samples  examined  (Henderson,  et al.  1969),  with
 whole fish  residues from 0.01  to 8.33 mg/kg.
     Nisbet (1977) calculated  the typical human exposure to hepta-
 chlor to  be 0.01 ug/individual/day, based  on a  mean ambient air
 concentration  of 0.5  ng/m3  and  a  respiratory  volume  of  20  a3
 of air  per day.   He  states further that even  in Jackson, Miss.,
which has  a mean  air  level as high as  6.3  ng/m3, the average in-
dividual would  inhale only 0.13 ug/day of heptachlor.   The sig-
 nificance  of  these figures is dependent  upon  the  efficiency  of
lung  absorption, which does not appear to have  been reported for
humans  (Nisbet/  1977).   Based on  this research,  it appears that
 inhalation  is not a major  route for human exposure to heptachlor.
Special  Groups at Risk
     Infants have been exposed to  heptachlor  and heptachlor epox-
 ide through mothers'  milk  (Savage/ 1976), cows'  milk {Ritcey,  et
 al. 1972),  and commercially prepared  baby foods  (Lipscomb, 1968).
 It appears  that infants raised on mothers1 milk run  a greater risk
 of ingesting  haptachlor  epoxid«  than if  they were  fed cows' milk
 and/or commercially prepared  baby  food.  Nisbet  (1977) found that
                               C-43

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persona living and working in or near heptachlor treated areas had
a particularly high inhalation exposure potential. =
Basis and Derivation of Criteria
     Heptachlor  has  been shewn to  exhibit  numerous toxicological
effects  in  animal systems.   Heptachlor and  its  metabolites  have
LD5Q  values  ranging   from  6  to  531  mg/kg  depending  upon  the
animal  test  system.    Heptachlor   is  generally  classified   as  a
neurotoxin because it  produces abnormal stimulation of the central
nervous system when animals  are exposed to  high doses.  Other ef-
fects  on  animal enzyme  systems  are  referenced  throughout the
literature.   Mutagenicity  was not demonstrated  with Salmonella
typhimurium  in  the  Ames assay; however,  oral doses of heptachlor
caused dominant  lethal changes  in  male rats as demonstrated  by an
increase  in the  number of  resorbed  fetuses  in  intact  pregnant
rats.  Heptachlor administered to rats  caused a marked decrease in
litter size, both in  several litters of one  generation as well as
in successive generations.
     Studies concerning  the  carcinogenicity of  heptachlor and hep-
tachlor epoxide  when  administered  to rats and mice have been con-
ducted by the Kettering Laboratory, the FDA,  Cabral, et al.  1972,
the IRDC, and the NCI.   Heptachlor  or  its metabolites  have  induced
hepatocellular carcinomas  in  three  chronic  feeding  studies  in mice
and heptachlor  epoxide has produced  the  same response in one rat
study,  although no response  was  observed  in four additional rat
studies.
     The  weight of evidence  for  carcinogencity  is sufficient to
conclude  that heptachlor is likely  to  be a human carcinogen.  As
                                C-44

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 carcinogens  are  generally  assumed  to have  a  nonthreshold dose/
 response  characteristic,  the carcinogenic effect is the most sig-
 nificant  exposure effect from which  to estimate an ambient water
 quality  criterion value.  A  linearized multistage  model,  as dis-
 cussed  in the Human Health  Methodology Appendices  to the October
 1980  Federal Register notice  which  announced the  availability  of
 this  document,  is used  in estimating  human  health risks  associated
 with  the  ingestion of  heptachlor.   Using the described  model,  the
 concentration  of heptachlor  in  water  may  be calculated from  the
 incidence  data  for  hepatocellular  carcinoma*  in  the  NCI  B6C3F]_
 mouse study, by  assuming an  additional individual lifetime  risk  of
 1/100,000, the  daily  ingestion of  2 liters of water and 6.5 grams
 of  contaminated fish products,  and  a weighted  average  biocconcen-
 tration factor  of 11,200.
     Under the  Consent Decree  in  NRDC v.  Train,  criteria are  to
state  "recommended maximum  permissible concentrations  (including
where appropriate, zero) consistent  with  the  protection  of  aquatic
organisms, human  health, and  recreational  activities."   Heptachlor
is  suspected of  being  a human  carcinogen.   Because  there  is  no
recognized safe concentration for  a human carcinogen/  the  recom-
mended concentration of  heptachlor  in water for  maximum  protection
of human health  is zero.
     Because  attaining  a zero  concentration  level  may  be  infeas-
 ible  in BOM cases and  in order  to  assist the Agency and States in
 the possible  future  development of water quality regulations,  the
concentrations  of heptachlor corresponding to several  incremental
lifetime  cancer risk levels  have  been estimated.   A cancer  risk
                                C-45

-------
level provides  an  estimate of the  additional  incidence  of cancer
that may  be expected  in  an exposed  population.   A risk  of  10~5
for  example,  indicates a  probability of  one  additional  case  of
cancer  for  every  100,000  people  exposed,  a  risk  of  10~6  indi-
cates one additional  case  of cancer  for every million  people ex-
posed, and  so forth.
     In the Federal  Register notice  of  availability  of  draft am-
bient water quality criteria, EPA stated that  it  is considering
setting  criteria  at  an  interim  target  risk  level  of  10~5,
10~^, or 10"^ as shown in  the table below.
                                         Risk Levels
Exposure Assumptions      	and Corresponding Criteria  (1)	
     (per day)
                           0        IP"7           10~6       10~5
2 liters of drinking      0    0.02^0ng/1    0.2^ng/1    2.^€ ng/1
water and consumption                                      ^o
of 6.5 grams fish
and shellfish. (2)
Consumption of fish       0    0.02Jf/ng/l    0.2#ng/l    2.J« ng/1
and shellfish only
(1)  Calculated by applying  a linearized multistage model as
     described above to  the  animal  bioassay data presented in
     the Appendix.   Since the extrapolation  model is  linear
     at  low  doses,  the  additional  lifetime  risk is directly
     proportional  to  the water  concentration.    Therefore,
     water concentrations corresponding to other risk  levels
     can  b«  derived by  multiplying or dividing one  of  the
     risk levels and corresponding  water concentrations shown
     in  the  table  by factors such  as  10,  100, 1,000,  and so
                                C-46

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 (2)  Ninety-seven percent  of  the heptachlor exposure results
     from  the consumption  of  aquatic organisms which exhibit
     an  average bioconcentration  potential  of  11,200-fold.
     The remaining  3 percent of heptachlor exposure results
     from  drinking water.
     Concentration  levels  were  derived assuming a  lifetime expo-
 sure to various amounts  of heptachlor, (1)  occurring from the con-
 sumption of  both  drinking  water and aquatic  life  grown in waters
 containing  the corresponding heptachlor  concentrations  and  (2)
 occurring  solely  from  consumption  of aquatic  life grown  in  the
waters containing the corresponding heptachlor concentrations.
     Although  total exposure information for heptachlor  is  dis-
cussed and an estimate  of  the contributions from other sources of
exposure can be made, these data will  not be  factored  into  ambient
water quality criteria  formulations until additional analysis can
be made.  The criteria presented, therefore,  assume  an  incremental
risk from ambient water  exposure only.
                                C-47

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                                C-59

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                              APPENDIX



               Derivation of Criterion £or Heptachlor



    Heptachlor fed  to  BecSF^ mice  for  nearly  a lifetime  induced



hepatocellular carcinomas wtih high frequency in  both  sexes  at two



doses  (NCI,  1977).  The data  for  males  and additional  parameters,



as shown  below,  were used to calculate the criterion:



     Dose  (rcg/kg/day)          Incidence (I responding/*  tested)



           0.0                                  5/19



           0.79                                11/46



           1.79                                34/47








     le -  546  days            w • 0.036



     Le «  630  days            R - 11,200



     L  »  630  days



     With  these  parameters  the  carcinogenic potency  for  humans,



q]_*,  is  3.37   (mg/kg/day)"1.    The   result  is  that  the  water
concentration   corresponding   to   a  lifetime  risk   of   10~J  is
          v. ^ wii   \»wkk^0£/wiiu^iJ^   w w   «  .*. A. J. %? v. .LUIC  L j. 0 /%.   wt   A. v




2.8 ng/1.
                                          « u j cx>vmmi»T PMNTWC orrici HBO -?c-o:s,«3»]
                                 C-60

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