&EPA
United States
Environmental Protection
Agency
Office of Chemical Safety
and Pollution Prevention
(7101)
EPA712-C-008
January 2012
        Ecological Effects
        Test Guidelines

        OCSPP 850.4400:
        Aquatic Plant Toxicity
        Test Using Lemna spp

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                                     NOTICE

     This guideline is one of a series of test guidelines established by the United States
Environmental Protection Agency's Office of Chemical Safety and Pollution Prevention
(OCSPP) for use in testing pesticides and chemical substances to develop data for
submission to the Agency under the Toxic Substances Control Act (TSCA) (15 U.S.C. 2601,
et seq.), the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA) (7 U.S.C. 136, et
seq.), and section 408 of the Federal Food, Drug and Cosmetic (FFDCA) (21 U.S.C. 346a).
Prior to April 22, 2010, OCSPP was known as the Office of Prevention, Pesticides and Toxic
Substances (OPPTS). To distinguish these guidelines from guidelines issued by other
organizations, the numbering convention adopted in 1994 specifically included OPPTS as
part of the guideline's  number.  Any test guidelines developed after April 22, 2010 will use
the new acronym (OCSPP)  in their title.

     The OCSPP harmonized test guidelines serve as a compendium of accepted scientific
methodologies and protocols that are intended to provide data to inform regulatory decisions
under TSCA, FIFRA, and/or FFDCA. This document provides guidance for conducting the
test, and is also  used  by EPA, the public, and the companies that are subject to data
submission requirements under TSCA, FIFRA, and/or the FFDCA.  As a guidance
document, these guidelines are not binding on either EPA or any outside parties, and the
EPA may depart from  the guidelines where circumstances warrant and without prior notice.
At places in this  guidance, the Agency uses the word "should."  In this guidance, the use of
"should" with regard to an action means that the action is recommended rather than
mandatory. The procedures contained in this guideline are strongly recommended for
generating the data that are the subject of the guideline, but EPA recognizes that departures
may be appropriate in specific situations. You may propose alternatives to the
recommendations described in these guidelines, and the Agency will assess them for
appropriateness on a  case-by-case basis

     For additional information about these test guidelines and to access these guidelines
electronically, please go to http://www.epa.qov/ocspp and select "Test Methods &
Guidelines" on the left side navigation menu.  You may also access the guidelines in
http://www.regulations.gov grouped by Series under Docket ID #s: EPA-HQ-OPPT-2009-
0150 through EPA-HQ-OPPT-2009-0159, and EPA-HQ-OPPT-2009-0576.

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OCSPP 850.4400: Aquatic plant toxicity test using Lemna spp.

(a) Scope—
       (1) Applicability. This guideline is intended to be used to help develop data to submit to
       EPA under the Toxic Substances Control Act (TSCA) (15 U.S.C. 2601, et seq.),  the
       Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) (7 U.S.C. 136, et seq.), and
       the Federal Food, Drug, and Cosmetic Act (FFDCA) (21 U.S.C. 346a).
       (2) Background.  The source materials used in developing this harmonized OCSPP test
       guideline include OPPT guideline under 40 CFR 797.1160 Lemna Acute Toxicity Test;
       the OPP Non-target Plants:  Growth and Reproduction of Aquatic Plants - Tiers 1 and 2
       Standard Evaluation Procedure; OPP  122-2 Growth and Reproduction of Aquatic Plants
       (Tier 1), OPP 123-2 Growth and Reproduction of Aquatic Plants (Tier 2)  (Pesticide
       Assessment  Guidelines  Subdivision  J—Hazard Evaluation: Nontarget Plants); OPP
       Pesticides Reregi strati on  Rejection Rate  Analysis: Ecological  Effects; and  ASTM E
       1415-91, Standard guide for conducting static toxicity tests with Lemna gibba G3.

(b) Purpose.  This guideline is intended for use in developing data on the toxicity of chemical
substances and mixtures ("test chemicals" or "test substances")  subject to environmental  effects
test regulations.  This guideline prescribes test procedures and conditions using the freshwater
vascular aquatic plants Lemna gibba or Lemna minor to develop data on the phytotoxicity of test
substances. The Environmental Protection Agency will use data from these tests in assessing the
hazard and risks a test substance may present in the aquatic environment.  This guideline  should
be used in conjunction with  OCSPP 850.4000 (Background and  special  considerations  for
conducting ecological effects  tests with  terrestrial  and aquatic  plants,  cyanobacteria,  and
terrestrial soil core microcosms), which  provides general information and overall guidance for
the  plant test  guidelines and  OCSPP 850.1000 (Background and  special  considerations  for
conducting ecological effects  tests with  aquatic and sediment-dwelling fauna and  aquatic
microcosms), which  provides general  information for conducting toxicity tests in an aqueous
matrix.

(c) Definitions. The definitions in OCSPP 850.1000 and OCSPP 850.4000 are applicable to this
guideline. In addition, the more specific definitions in this paragraph also apply:

       Colony is an aggregate of mother and daughter fronds attached to each other.

       Frond is a single Lemna "leaf-like" structure.

       Frond mortality refers to dead  fronds which are identified by a  total  discoloration
       (yellow, white, black, or clear) of the entire frond.

(d) General considerations—

       (1) Summary of the test. Organisms of a particular species of duckweed (Lemna gibba
       or Lemna minor}  are maintained in test vessels containing  nutrient medium  alone and
       nutrient medium to which the test substance has been added.  Over an exposure period of
       7 days,  data  on population growth are obtained  on a regular  basis.   In addition to
       measurements of effects on frond  number,  effects on frond size (dry weight or frond area)

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are determined.   The test is designed to determine the quantity of test substance that
results in a 50 percent inhibition (1C50) in yield and average growth rate based on number
of fronds  and yield, and average growth rate based on frond size (dry weight or frond
area), and to  determine the no  observed effect concentration (NOEC) for these  effect
measures.  The results are used to establish toxicity levels, evaluate hazards or risks to
aquatic vascular plants, and to  indicate  if further testing at a higher tier  is necessary.
Note historically in OCSPP pesticide and industrial chemical guidelines the term ECX was
used to cover both the current OCSPP 850.4000 definition of ECX (concentration where x
percent (x%) of the population exhibit the effect (e.g., mortality)) and ICX (concentration
resulting in an x% decrease or inhibition effect on an attribute of the population (e.g.,
growth rate)).

(2) General test  guidance.  The general guidance in  OCSPP 850.4000 and OCSPP
850.1000  applies to this guideline except as specifically noted herein.

(3) Range-finding test.  A range-finding test is usually conducted  to  establish  the
appropriate test solution concentrations for the definitive test. In the range-finding test,
the test organisms are exposed  to a series of widely-spaced concentrations of the test
substance (e.g., 0.1, 1.0, 10, 100 milligrams  per liter (mg/L), etc.), usually under static
conditions.  The  details of the  range-finding test  do  not have to be the same as  the
definitive  testing  in that there  are no replicates,  and the number of test organisms used,
and duration of exposure may be less than in definitive testing. In addition,  the types and
frequency of observations made on test  organisms are not as detailed or  as frequently
observed  as  that of  a  definitive  test  and  results  are analyzed using  nominal
concentrations.  However,  the range-finding test will  be more useful the greater  the
similarity  between the range-finding and the definitive test.

(4) Definitive test.  The goal of the definitive test is  to determine  for Lemna sp.  the
concentration-response  curve  for yield  and growth rate,  and the  median  inhibition
concentration  (ICso) value for each of these responses (with 95% confidence interval and
standard error).  If possible the  slopes of the concentration-response curves, associated
standard  errors,  and  the  95%  confidence  intervals  of the slopes  should also be
determined.   However, at  a  minimum, the full  concentration-response  curve  (curve
between ICos  and ICgo) is determined for the most sensitive measure of effect using a
minimum of five  concentrations of the test chemical,  plus  appropriate controls.   For a
satisfactory test,  the lowest treatment  concentration is below the ICso value for all
measures  of effect.  Analytical confirmation  of test  concentrations is  performed  as
described  in OCSPP 850.1000.  A summary of test conditions is provided  in Table 2 in
paragraph (g)  of this guideline and validity elements for an acceptable definitive test are
listed in Table 3 in paragraph (h) of this guideline.

(5) Limit test. In some situations, it is  only necessary to ascertain that the 7-day ICso
value for  yield, area under the growth curve, and growth rate are above a certain limit
concentration, and that at this limit concentration there is no observable adverse effect.
For pesticides a limit test has also been referred to as a Tier I test or Maximum Challenge
Concentration test.  In a Lemna sp. limit test, at least four replicate test vessels  are
exposed to a single "limit concentration," with the same number of test vessels containing


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       the  appropriate control  solution(s).  The multiple-concentration definitive test may be
       waived if the following two conditions  are met for  all measures of effect  (yield and
       average specific growth rate based on number of fronds and frond size  (dry weight or
       frond area).  First, the "limit" treatment response is  both  statistically less than a 50%
       decrease from the control response (i.e., ICso values > limit concentration), and second,
       limit treatment responses are not significantly reduced (or inhibited) as compared to the
       control response (i.e., NOEC > limit concentration).  For most industrial chemicals 1,000
       mg/L or the limits of water solubility or dispersion are  considered appropriate as the limit
       concentration. For pesticides the limit concentration is equivalent to the maximum label
       rate (pounds of active ingredient per acre (Ibs a.i./A))  directly applied to a one acre pool
       that is 6 inches deep (21,280 cubic feet (ft3) or 602,581 liters). For example, a 1 Ib a.i./A
       (or 453,592 milligrams (mg) a.i.  per acre) application  rate and assuming a water density
       of 1 gram per milliliter would have a limit concentration of 0.75 mg a.i./L. Except for the
       number of treatment groups, an acceptable limit test follows the same test procedures, is
       the  same duration,  and  has the  same number of  controls as the multi-concentration
       definitive test (Table 3  in paragraph (h)  of this guideline). Acceptable  limit tests like
       definitive tests include analytical  confirmation of the test exposure concentration.

(e) Test standards—

       (1)  Test substance.  For industrial  chemicals, the  substance to be tested  should be
       technical grade unless the test is designed to test a specific formulation, mixture, or end-
       use  product.  For pesticides, the use of the  typical end-use  product (TEP) instead of the
       technical grade active ingredient (TGAI) is preferred  for all aquatic plant phytotoxicity
       tests.  If there is more than one TEP with the same  inert  substances, the one with the
       highest percent a.i. and/or the one most commonly used should be tested. If there is more
       than one TEP with different inert substances, a TEP representative of each different inert
       substance should be tested in the range-finding test and at a minimum the most sensitive
       one tested  in the definitive or limit test.  Adjuvants  are not used with TEP or  TGAI
       testing of algae.  OCSPP 850.1000 and OCSPP  850.4000 list the type of information that
       should be  known  about  the test substance  before testing, and  discuss methods for
       preparation of test substances.

       (2) Test duration.  The duration of the test is 7 days.

       (3) Test organism—

              (i) Species. The test species is L. gibba G3 or L. minor. L. gibba has been widely
             used for testing with pesticides and other chemicals in the United States, while L.
             minor has been used more frequently for testing of environmental  samples and in
             Europe.  The identity of the organism  should be verified using  an  appropriate
             taxonomic key and it is also desirable to  identify the  clone (see paragraph (j)0) of
             this guideline).

              (ii)  Source.   Axenic cultures may be obtained  from  laboratory  cultures or
              commercial sources.
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       (iii) Age and condition.  The plants used in testing should be from stock cultures
       that have been actively growing in growth medium under the same conditions as
       used in the test for at least eight weeks immediately preceding the start of the test.
       Plants should be aseptically transferred on a regular schedule (such as weekly) to
       fresh growth medium.  Long-term maintenance of cultures  on  a  solid medium
       containing 1%  agar  in  sterile Petrie  dishes or test  tubes may be  desirable.
       However for a satisfactory test, the plants used to initiate toxicity tests are from a
       liquid culture.  Plants used in a test should be randomly selected from cultures
       which are between 7 and  12 days old.

       (iv) Culturing procedures.  Lemna spp. cultures should be maintained in growth
       medium using the culturing procedures described in the reference in  paragraph
       (j)(l) of this guideline.   The cultures should be  maintained  under the  same
       conditions as used for testing.

(4) Administration of test substance—

       (i) Preparation of test solutions—

              (A) Stock solutions  or direct addition. Test  solutions  are prepared by
              adding the test substance directly to the nutrient medium or by addition of
              a stock solution to the nutrient medium.  Typically, a stock solution of the
              test substance is  prepared and aliquots  of  the stock solution added to
              nutrient  medium to obtain the desired test concentrations.  Guidance for
              preparation of test solutions, especially for difficult or low solubility test
              substances, is provided in OCSPP 850.1000.

              (B) Solvents.  The recommended solvent for Lemna spp. toxicity tests is
              N,N-dimethyl-formamide,  as  solvents  such  as  acetone  can  cause
              stimulation  of bacterial growth.   The  concentration  of solvent should
              preferably be the same in all test  treatments and should not  exceed 0.1
              milliliter per liter (mL/L).

              (C) Exposure  technique.

                    (1) For pesticides, this test  should be conducted using the  static
                    renewal exposure  technique.  For industrial chemicals, this test
                    may be conducted using a  static, static  renewal,  or flow-through
                    with guidance  on the   selection  of the appropriate exposure
                    technique based on the stability of the test substance as provided in
                    OCSPP 850.1000.  To conduct tests with duckweed using the flow-
                    through exposure technique see the references in paragraphs (j)(2),
                    (j)(4) and  (j)(13) of this guideline, which may be necessary when
                    testing  volatile industrial test substances.

                    (2) Static  renewal  of test solutions.  For  static renewal tests, the
                    plants should be transferred to fresh test solutions of initial test
                    concentration levels  at  intervals  necessary to maintain the test

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              concentrations (for example, on days 3 and 5 or on days 2 and 4).
              Transfer should be done using aseptic technique in a clean, draft-
              free area as quickly as possible to minimize contamination of the
              colonies.

              (3) When a substance is know to have a tendency to vaporize,
              closed  test flasks  with increased  head-space  may  be used.
              Attempts should be made to determine the amount of the substance
              which remains dissolved  in   solution,  and extreme  caution  is
              advised when interpreting  results of test with volatile chemicals
              using closed systems.

(ii) Treatment levels. At a minimum five test solution concentrations are tested
for multi-concentration definitive testing, plus  the  appropriate  control(s).   A
range-finding test   can  be  used  to  establish  the  appropriate  test  solution
concentrations for the definitive  test (see paragraph (d)(3) of this  guideline).  For
scientifically sound estimates of a given point estimate (e.g., ICso), test substance
concentrations should immediately bracket the point estimate(s) of concern.  The
concentrations should be a twofold geometric progression (e.g., 0.1,  0.2, 0.4, 0.8,
and  1.6 milligrams per liter (mg/L)).  While a twofold progression is  preferred,
threefold and fourfold progressions are acceptable.  If a fourfold  or  higher series
progression  is  used,  the  rationale  for using  this large  an interval  between
concentrations  and the effect on the accuracy  and reproducibility  of the point
estimate and NOEC  should be provided. For an acceptable study, the lowest test
treatment level  should be lower than the ICso  values for yield and average specific
growth  rate based on number of fronds and frond size. The lack of a NOEC for
an effect  measure is not critical as long as the response-curve for the effect
measure is acceptable for calculation of the 5% inhibition concentration (ICos).  It
is recommended that one or two additional test concentrations in the lower tail  of
the concentration-response  curve  of the  most  sensitive endpoint  be added  to
insure bracketing of both the most  sensitive ICso value and the most  sensitive
NOEC  (or ICos) value. For a limit test, there is single treatment concentration,
plus the appropriate control(s). Guidance on the limit concentration is provided in
paragraph (d)(5) of this guideline.

(iii) Introduction of test organisms.

       (A)  In  preparation for the  test, containers are filled with appropriate
       volumes of nutrient medium  and/or the test solutions.  The test is initiated
       by introducing Lemna sp. fronds into each of the test vessels within 30
       minutes of addition of test substance to test solutions. Plants should be
       placed in the test vessels using a sterile inoculating loop or hook, Nitex
       screen,  or other aseptic technique.  The  plants should be impartially  or
       randomly  distributed among the test vessels in such  a manner that test
       results show no significant bias from the distributions.  The test vessels are
       then immediately placed  in a growth chamber or the controlled laboratory
       environment.
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              (B) Test vessels within the testing area are positioned in a random manner
              or in  a way in which  appropriate  statistical analyses can  be used to
              determine the variation due to placement.
(5) Controls.
       (i) Every test includes a negative control treatment consisting of the same nutrient
       medium, number of test organisms, environmental conditions, and procedures as
       the treated test vessels except that none of the test substance is added.  In addition,
       vehicle  (solvent) controls are  also  included if a solvent  is used to dissolve or
       suspend the test substance.

       (ii)  At  test termination the  control coefficient of variation for yield should
       generally be less than 20% and substantially less than 20% for growth rate, which
       is a logarithmically-transformed variable.

       (iii) For a satisfactory test the doubling time of number of fronds in the control
       should be less than 2.5 days (60 hours),  corresponding to approximately a seven-
       fold increase in seven days and an average specific growth rate of 0.275  per day
       (d-1).

(6) Number of test  organisms and replicates.

       (i) The minimum number of replicates per treatment and  control(s) is four, each
       containing three to five plants (consisting of three to four fronds per plant). Plants
       of similar size and appearance should be selected, and the number of plants and
       number of fronds should be identical in each test vessel. A total of at least 12,  but
       no more than 16 fronds, per test vessel are recommended (e.g. three 4-frond plants
       and one 3-frond plant could be  used, for a total of 15 fronds).

       (ii) For determination of initial dry weight of fronds at test initiation, an additional
       control set of replicates are created at test initiation using plants of similar size
       and appearance as those selected for the  test. The number of replicates should be
       equivalent in number to that used for the test.

(7) Facilities, apparatus and supplies—

       (i) Containers for culturing and testing.  Glass beakers (250 - 1000  milliliters
       (mL)), 250 mL flat-bottomed  test tubes, and Erlenmeyer  flasks (250 - 500 mL)
       have been used successfully.   For a satisfactory test, test vessels should be  large
       enough  to hold  the Lemna colonies without crowding (i.e.,  space and nutrient
       availability should not be growth  limiting factors) for the duration of the test.
       Test vessels  should be covered to keep out extraneous contaminants and to reduce
       evaporation  of test solutions.   Containers  and  covers  that may  contact  the test
       solution should be chosen to minimize sorption of test substances, and not contain
       substances that can be leached or dissolved into aqueous solutions in  quantities
       that can affect the test results.  Beakers  may be covered with a clear watch  glass
       while Erlenmeyer flasks may  be covered with foam plugs, stainless  steel  caps,

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Shimadzu enclosures, glass caps or screw caps. (The acceptability of foam plugs
should be investigated prior to use because some brands have been  found to be
toxic). For a satisfactory test, all test vessels and covers in a test are identical.

(ii) Growth chamber or laboratory environment.

       (A)  A controlled environment growth chamber or an enclosed laboratory
       area capable of maintaining the specified number of test vessels and  able
       to maintain the air temperature,  light intensity rate, and  photoperiod
       specified in this guideline.

       (B) Facilities should be well ventilated and free of fumes that may affect
       the test  organisms.   Construction  materials  and  equipment  that  may
       contact the stock solution, test solution, or nutrient medium should be
       chosen to minimize sorption of test  substances and not contain substances
       that can be leached or dissolved into aqueous  solutions in quantities that
       can affect  the  test results.   Refer  to  OCSPP 850.1000 for additional
       information on appropriate construction materials.

(iii) Environmental monitoring equipment.  Equipment for determination of
test environmental conditions (e.g., pH meter,  photosynthetically active radiation
(PAR) light sensor, etc.)

(iv) Cleaning and sterilization. Apparatus for sterilizing glassware,  preparing
sterile nutrient media, and maintaining aseptic technique  during culturing and
testing. All glassware and equipment used in Lemna spp. culturing or testing  is to
be cleaned and sterilized prior to use.  The Nitex screen or inoculating loops used
for transferring the Lemna sp. should be discarded after use or thoroughly cleaned
and sterilized before reuse.

(v) Nutrient media and diluent. Different media are recommended for culturing
and testing L. gibba and L. minor.

       (A) Medium  for  L.  gibba.  20X-AAP medium  is recommended for
       maintaining L. gibba cultures and for use as the diluent in the preparation
       of the various test solution concentrations.  Medium is sterilized by
       autoclaving or filtering (0.22 micrometer (jim) filter).  Preparation  of this
       medium is described under paragraph (j)(l) of this guideline and in Table
       1.   Water used for preparation of nutrient  medium should be of reagent
       quality (e.g., ASTM  Type I water).  If prepared  in  advance,  medium
       should be stored under refrigeration in the dark at 4 degrees Celsius  (°C).
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                        Table 1.—Preparation of 20X-AAP Medium
Add 20 ml of each of the macronutrient stock solutions and 20 ml of the micronutrient stock solution
listed in this table to approximately 800 ml reagent grade water and then dilute to 1 liter (L).	
Macronutrient stock solutions are made by dissolving the following chemicals into 500 ml of reagent
grade water:
  Sodium nitrate (NaNO3) -12.750 grams (g)
  Magnesium chloride hexahydrate (MgCI2 • 6H2O) - 6.082 g
  Calcium chloride dihydrate (CaCI2 • 2H2O) - 2.205 g
  Magnesium sulfate  heptahydrate (MgSO4 • 7H2O) - 7.350 g
  Potassium phosphate (K2HPO4) - 0.522 g
  Sodium bicarbonate (NaHCO3) - 7.500 g	
The micronutrient stock solution is made by dissolving the following chemicals into 500 ml of reagent
grade water:
  Boric acid (H3BO3) - 92.760 milligrams (mg)
  Manganese chloride tetrathydrate (MnCI2 • 4H2O) - 207.690 mg
  Zinc chloride (ZnCI2) -1.635 mg
  Ferric chloride hexahydrate (FeCI3 • 6H2O) - 79.880 mg
  Cobalt chloride hexahydrate (CoCI2 • 6H2O) - 0.714 mg
  Sodium molybdate dihydrate (Na2MoO4 • 2H2O) - 3.630 mg
  Copper chloride dihydrate (CuCI2 • 2H2O) - 0.006 mg [Typically must be prepared by serial dilution].
  Ethylenediaminetetraacetic acid disodium salt dihydrate (Na2EDTA • 2H2O) -150.000 mg	
Adjust pH to 7.5 ± 0.1 with 0.1 Normal (A/) or 1.0 N sodium hydroxide (NaOH) or hydrochloric acid (HCI).
Filter the media into a sterile container through a 0.22 urn membrane filter. Store medium in the dark at
approximately 4 degrees Celsius (°C) until use.	
                     (B) Medium for L.  minor.  A modification of the Swedish  standard
                     (Standardiseringen I Sverige (SIS)) Lemna spp. medium is recommended
                     for culturing and testing with L. minor.  Preparation of this  medium is
                     described in references in paragraphs (j)(5) and (j)(8) of this guideline.

              (vi) Equipment  to observe plants.   A lighted magnifying  lens, dissecting
              microscope, or other device may be used to facilitate observations of the fronds.

       (8)  Environmental conditions.  Environmental conditions during the test should be
       maintained as follows:

              (i) Temperature.  Test solution temperature should be 25 ± 2 °C throughout the
              duration of the test.

              (ii) Lighting and photoperiod.  Continuous lighting should be used to provide a
              light intensity in the range of 57 -  90 micromoles per meter square  per second
              (|imol/m2/s). For cool-white fluorescent lighting, this is approximately equivalent
              to 4200 to 6700 lux.  Warm-white or cool-white fluorescent lighting has been
              used for testing with Lemna spp. Additional information on the use of lighting in
              plant toxicity tests can be found in the references given in OCSPP 850.4000.

              (iii) Nutrient medium pH. Prior to use, the pH of the nutrient medium should be
              adjusted to 7.5 ±0.1. Adjustment of pH can be accomplished by adding acid or
              base prior to the addition of the test substance.  The pH may be adjusted in stock
              solutions to match the pH of the nutrient medium if pH change does not affect the
              stability of the test substance in the  stock  solution or test solution. Hydrochloric


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       acid  (HC1) and sodium  hydroxide (NaOH) may be used for this adjustment if
       warranted.  The pH should not be adjusted after addition of the test substance or
       stock solution into the test medium.  Test solution pH may vary from the nutrient
       medium after the addition of the test substance and/or vehicle (if used).  Any such
       changes  should  be  recorded  but  not  adjusted.   Chelating agents,  such as
       ethylenediamine-tetraacetic  acid, are present in the 20X-AAP medium to ensure
       that trace nutrients will be available to the L. gibba fronds.
(9) Observations—
       (i) Measurement of test substance.  Analytical confirmation of dissolved test
       concentrations is performed  at test initiation and at  test termination and as
       described for renewal tests in OCSPP 850.1000.  Samples for analysis should be
       collected as described in OCSPP 850.1000, with the following exception: if there
       is insufficient volume at test termination to perform the analysis, the contents of
       the replicate test vessels may be pooled after the plants have been removed for
       observations. The analytical  methods used to measure the amount of dissolved
       test substance in a sample are validated before beginning the test, as described in
       OCSPP 850.1000.

       (ii) Test solution appearance. Observations are made daily on test substance
       solubility (e.g.,  surface slicks, clarity,  precipitates, or material adhering to the
       sides of the test vessels) and recorded.

       (iii) Dilution water  quality.   The dilution  water source used to prepare media
       should be periodically analyzed  to document and  characterize the hardness,
       alkalinity,  pH,  conductivity,  total organic  carbon (TOC) or chemical oxygen
       demand magnitude and variability, and to ensure that pesticides, PCBs and toxic
       metals are not present at concentrations that  are considered toxic.  See OCSPP
       850.1000 for guidance on dilution water.

       (iv) Environmental conditions—

             (A) Temperature.  It is impractical to  measure the temperature of the
             solutions in  the  test vessels while maintaining  axenic   conditions.
             Therefore, one or two extra test vessels may be prepared for the purpose of
             measuring the solution temperature during the test.  Alternatively, hourly
             measurements of the  air  temperature (or daily measurements  of the
             maximum and minimum) are acceptable.  Because the vessels are placed
             in an environmental chamber or incubator, the air temperature is more
             likely to fluctuate than the water temperature.

             (B) Light intensity. Light intensity should be monitored at test initiation
             at the approximate level of the test solution  at each test vessel  position in
             the growth chamber or laboratory.  If it is suspected that light intensity has
             changed  by  15%  or  more, monitoring of  light intensity  should be
             conducted daily.  A  photosynthetically active radiation  (PAR)  sensor
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       should be used  to  measure light  quality.   The  light intensity at  each
       position should  not differ by more than 15% from the selected  light
       intensity. Because illumination may vary at different positions, and since
       this environmental  parameter  has  an important influence on duckweed
       growth, it is recommended that the test vessels be  randomly re-positioned
       on a regular schedule (e.g., daily) to minimize spatial differences.

       (C) pH. The pH in the control(s) and test solutions should be measured.
       This measurement is made on the bulk test solutions at the beginning of
       each renewal period and at the end of each renewal  period on samples of
       pooled replicates of each  test treatment provided none of the replicates
       appear to be "outliers" with respect to growth.  In the case  of outlier
       growth response  individual pH measurements should be made in each test
       vessel.  For a flow-through test  for industrial  chemicals  see OCSPP
       850.1000 for guidance on frequency and sampling scheme for pH.

(v) Measures of effect—

       (A) Frond number. Using a dissecting microscope or lighted magnifying
       lens the number of fronds in each test vessel is determined and recorded at
       least every three  days during the test and at test termination (e.g. days 3, 5,
       and 7 or days 2, 4, and 7).  A frond is counted regardless of size as long as
       it is visible adjacent to the parent frond.  Any  bud which is visible when
       viewed under a hand lens or dissecting microscope should be counted as a
       frond.

       (B) Frond size.  Acceptable indicators of frond size include determination
       of dry weight and/or measurement of frond area.  Frond size determined
       using dry weight, is  made at test initiation and test termination. Frond size
       determined using frond area is determined at a minimum at test initiation
       and termination.

              (1) Dry weight. Dry weight is a destructive procedure. In order to
              evaluate the  increase in dry weight over the course of the test,  a
              representative  sample  of  fronds  at   test initiation  should be
              processed (see  paragraph  (e)(6)(ii)  of this guideline),  using the
              same  drying method as used at test termination, to establish the
              treatment and control mean dry weight of fronds at test initiation.
              To determine  dry  weight,  the  plants  (including  roots  and root
              fragments) for a test vessel (replicate)  are removed from the test
              solution, rinsed with distilled or deionized water, blotted to remove
              excess water, and placed  in previously dried, tared weighing pan
              for that replicate.  The plants  should be dried at approximately 60
              °C, cooled in a dessicator, and weighed to the nearest 0.1 milligram
              (mg).   The  drying process is repeated until  constant  weight is
              obtained.
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                            (2)  Frond area.   Frond  area for a test vessel (replicate)  is
                            determined at a minimum at test initiation and test termination but
                            may also be determined at various intervals during the test.  Frond
                            area can be determined using image  analysis, in which an image of
                            each plant  in a test vessel  (replicate)  is  captured using a video
                            camera  and  then   digitized.   An  alternative  procedure is  to
                            photograph the test vessel (replicate)  from the top,  cut  out the
                            silhouette of the plants, and determine the area  using a leaf area
                            analyzer or graph paper.

                     (C) Appearance  or condition.    The  appearance or  condition  (e.g.,
                     decrease  in  size,  necrosis,  chlorosis,  sinking of  fronds,  or  other
                     abnormalities) of plants in each  test vessel (replicate) is determined  at
                     least every three days during the test and at test termination (e.g. days 3, 5,
                     and 7 or days 2, 4, and 7).

                     (D) Phytostatic and phytocidal  effects.  At test termination,  it may be
                     desirable to determine phytostatic and phytocidal effects, e.g. whether  or
                     not plants  that were inhibited during the exposure period  are  able  to
                     resume growth when  transferred to test  substance-free medium.  This
                     optional procedure may be conducted as  described in the reference  in
                     paragraph (j)(6) of this guideline.

(f) Treatment of results—

       (1)  Determination of crowding.  For  each treatment and control vessel (replicate)
       calculate the dry weight per frond (wfrond) at test termination using Equation 1. If nutrient
       availability or space was limiting to growth, the dry weight per frond may be observed to
       increase as the number of fronds decreases.


                                      w frond = Wtotal/l                            Equation 1

              where:

              wtotal = total dry weight biomass in  a test vessel at test termination; and

              n = the number of fronds in the test vessel at test termination.

       (2) Response variable calculations.  There are  two response variables calculated from
       number of fronds and frond size: yield and average specific growth rate.

              (i) Yield  calculations.   For each treatment and  control test vessel (replicate)
              calculate the yield by subtracting the initial number of fronds, frond area, or dry
              weight from  the number of  fronds, frond  area,  or dry  weight,  respectively,
              obtained at test termination (Equation 2).
                                      Page 11 of 22

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                                Y = bl-b0                            Equation 2

             where:

             7= yield of observed biomass (number of fronds or dry weight or frond
             area)

             bo = biomass (number of fronds or dry weight or frond area, respectively)
             at test initiation

             b\ = biomass (number of fronds or dry weight or frond area, respectively)
             at test termination

       (ii) Average specific growth rate calculations.  Average specific growth rate
       (sometimes called relative growth rate) is the rate of growth over a given time
       interval.  The growth rate for number of fronds,  frond area, and dry weight for
       each test vessel (replicate) over a given time interval is  calculated as given in
       Equation 3.  At a minimum, the average specific growth rate is calculated for the
       time interval between test initiation and termination.

                                  Info,)-Info.)
                            r,-j = —^	—                        Equation 3


             where:

              ri-j= average specific growth rate per day  (day"1) of observed biomass
             (number of fronds or dry weight or frond area) from time / toy.

             b[ = observed biomass (number of fronds or dry weight or frond area,
             respectively) at beginning of the observation interval, time /'

             &j = observed biomass (number of fronds or frond area or dry weight,
             respectively) at end of the observation interval, timey

             t = time period from /' toj in days

(3) Summary statistics—

       (i) Environmental conditions.  Calculate descriptive statistics (mean, standard
       deviation, coefficient of variation, minimum, maximum)  by treatment level for
       temperature and pH.  Calculate descriptive statistics (mean, standard deviation,
       coefficient  of variation,  minimum, maximum) by test vessel  position for light
       intensity.

       (ii) Test substance concentration.   For each treatment level compare the test
       substance concentration at the start and end of each renewal period.  For a stable
       test substance calculate the time-weighted average concentration. For  industrial
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       chemicals if the test substance was unstable calculate a rate of decline  and the
       associated time-weighted mean concentration (e.g.,  exponential decay calculate
       the  area under  the exponential decay concentration  curve  divided by the  total
       exposure days).  Calculate descriptive statistics such as the time-weighted mean,
       standard deviation, minimum, maximum, and coefficient of variation for each test
       vessel  and  treatment  level.   For  pesticides  under  unstable  test  substance
       conditions, use the mean test substance concentration in solution measured at test
       initiation and in bulk renewal solutions for calculating concentration-response and
       NOEC-LOEC values.  Such an approach is used rather than the exponential time-
       weighted averaged because of the exposure estimate currently used by OPP for
       calculating risk estimates.

       (iii) Number of fronds. For each treatment level and observation time calculate
       the  mean, standard deviation, and coefficient of variation for number of fronds.
       Calculate  the mean treatment yield and average specific growth rate based on
       changes in number of fronds from test initiation to test termination.

       (iv) Frond size —

              (A) Dry weight. Calculate the mean treatment yield and average  specific
              growth rate based on changes in dry weight from test initiation to test
              termination.

              (B) Frond area. For each treatment level and observation time calculate
              the mean, standard deviation, and coefficient of variation for frond  area.
              Calculate the mean treatment yield and average specific  growth rate based
              on changes in frond area from test initiation to test termination.

       (v) Appearance and condition. Morphological symptoms of plant injury should
       be summarized  in tabular form by time of observation, treatment, and replicate.
       Definition of any index values used for morphological  symptoms, indicating the
       severity of the symptom(s), should be provided.

(4) Percent inhibition.  For yield and average specific growth rate for each response
variable calculate the percent inhibition (%I) at each treatment level using Equation 4.

                                                                       Equation4
       where:

       C = the control mean response value (yield or average specific growth rate); and

       X = the treatment mean response value (yield or average specific growth rate,
       respectively). Stimulation is reported as negative %I.
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(5) Doubling time of control.  The doubling time (Td) of the number of fronds in the
control is calculated using Equation 5.

                              Td = ln(2)/                              Equation 5
                                     / T 'Control

       where:

       r control = mean of the control average specific growth rate test vessel values from
       paragraph (f)(l)(ii) of this guideline.

(6) Limit test—

       (i) ICso  values.  To ascertain that the yield and average specific growth rate ICso
       values,  based  on number of fronds  and frond size, occur above the "limit"
       concentration,  a one-sided  test which compares  the  difference  between two
       sample  groups to a fixed value (or difference) is performed for each of these
       response measures.  For a comparison of sample means, the difference defining
       the ICso compared to controls is operationally defined as a 50% reduction or
       inhibition from the control sample mean (Equation 6).  The null hypothesis (Ho)
       stated in terms of true population parameters is that the difference  of the "limit"
       treatment response (|iiimit) from the control mean response (^control) is greater than
       or  equal to a 50% inhibition or reduction,  compared to the control (i.e., HQ: |icontroi
       - Hiimit > So). The alternative hypothesis (HA) is that this difference is less than a
       50% reduction, compared to the control (HA:  Hcont-oi - Hiimit < So).  An example of a
       parametric two-sample comparison test of this is the Student's t-test. If the null
       hypothesis is rejected, the inhibition level  for the given response  measure (i.e.
       yield and average specific growth rate based on frond number and size) in the
       limit treatment as compared to the control is declared to be less than 50% (i.e.,
       ICso >  limit concentration).   If  the null hypothesis is  not rejected, the limit
       treatment as compared to the control response is declared to be 50% or greater
       (i.e., ICso < limit concentration).
                                                                       Equations

              where:

              So = difference between two parameters,  defined  in this case as  a p%
              reduction from the control sample mean;

              ^control = control sample mean response (e.g.,  yield and average  mean
              biomass); and

             p = percent reduction from the control sample mean, which is 50 in the
              case of the ICso.
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       (ii) NOEC.  To ascertain that there is no observable effect at the limit treatment
       (i.e., NOEC > limit  dose)  for a  given response measure  (yield and  average
       specific growth rate based on frond number and size), the limit treatment response
       is compared to the control treatment response using a  one-sided two-sample
       parametric or  nonparametric test,  as  appropriate (see OCSPP  850.4000).  The
       minimum significant difference detectable by the test or a  similar estimate of the
       sensitivity of the test should be determined and reported.

       (iii) Multiple-concentration definitive testing.

              (A)  A  multiple-concentration  definitive  test is  performed if either the
              effect or inhibition level for one or more response measures (i.e., yield and
              average specific growth rate based on frond number and size) in the limit
              treatment as compared  to  the control response at test termination are
              declared to be 50% or greater  effect (i.e., the null hypothesis is not
              rejected) or the NOEC is less than the limit concentration.

              (B) Multiple-concentration definitive testing may be waived if at test
              termination the "limit"  treatment response is both statistically less than a
              50%  decrease  from the control response and  there is no observable
              adverse effect from  the control response for all measures of effect (yield
              and average specific growth rate based on frond number and size).

(7) Multiple-dose definitive test—

       (i) Concentration-response curve, slope and  ICso.   For  dose-response tests
       statistical procedures are employed to  calculate the ICso value (standard error and
       95% confidence interval) for yield and growth rate based on number of fronds and
       frond size (dry weight or frond area)  at test initiation and test termination. If a
       concentration-response curve model was fit to the data to determine an ICso value,
       the model parameters  (e.g., slope)  and their uncertainty estimates (e.g., standard
       error) should be recorded.  The response values for each test vessel, not the mean
       response  for each treatment level, should be used in fitting  the model.  Where the
       concentration-response range tested does not result in the determination of a
       definitive ICso  value for a given response measure, test and  document that the ICso
       value is above the highest treatment level tested (see the  statistical guidance in
       paragraph (f)(6) of this guideline).  Such an event may arise if one of the  other
       response  measures is much more sensitive, and while the full response curve for
       that  response  measure is captured too  many  additional  treatments  would  be
       needed to capture the full response relationship for the other less sensitive
       response measure(s).

       (ii)  NOEC.  The 7-day NOEC for yield and growth rate based on number of
       fronds and frond size (dry weight or frond area) are determined (see OCSPP
       850.4000).  If a 7-day NOEC value can not be determined for  a given response
       measure,  the concentration at which there is a 5% inhibition (i.e., an ICos value for
       yield or growth rate)  is estimated  and used in place of the given NOEC.  The
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              standard error and 95% confidence interval should also be calculated for the ICos
              value. For industrial chemicals, the specific ICX used in place of a NOEC that can
              not be determined will vary, consult with the Agency.  Methods, assumptions, and
              results of the statistical approaches used should be recorded.

       (iii) Statistical methods. Statistical procedures for modeling continuous toxicity data are
       available and should be used (see references in paragraphs (j)(3), G)(7) and (j)(12) of this
       guideline).  Additional discussion about endpoints and statistical procedures is found in
       OCSPP 850.1000 and OCSPP 850.4000.

(g) Tabular summary of test conditions.  Table 2 lists the important conditions that  should
prevail during  the definitive test. Except for the number of treatment levels, Table 2 also lists the
important conditions that should prevail during a limit test.  Meeting these test conditions will
greatly increase the likelihood that the completed test will be acceptable or valid.

       Table 2.—Summary of Test Conditions for the Lemna sp. Toxicity Test
Test type
Test duration
Test matrix
Temperature
Light quality
Light intensity
Photoperiod
Test vessel size
Age of inoculum
Size of inoculum
Number of replicate test vessels per concentration
Test concentrations
Test concentration preparation
Measures of effect (measurement endpoints)
Static renewal (pesticides)
Static, static renewal, or flow through (industrial
chemicals)
7 days
Synthetic growth medium
25 ± 2 °C
Warm-white or cool-white fluorescent
57 - 90 umol/m2/s
Continuous
Sufficient to prevent crowding (e.g., 250 - 1000 mL
beakers or flasks)
From healthy stock cultures 7-12 days old
12-16 fronds total, with the same number of plants
and fronds in each test vessel
Four (minimum)
Unless performing limit test, minimum of 5 test
concentrations plus appropriate controls
Aqueous solutions prepared by adding test
substance to synthetic nutrient medium, directly or
via vehicle
IC50 and NOEC (or IC05) values for yield, and
average specific growth rate based on frond
number
IC50 and NOEC (or IC05) values for yield and
average specific growth rate based on frond size
(dry weight or frond area)
(h) Test validity elements. This test would be considered to be unacceptable or invalid if one or
more of the conditions in Table 3 occurred or one or more performance objectives in Table 3
were not met.  This list should not be misconstrued as limiting the reason(s) that a test could be
found unacceptable or invalid.  However,  except for the conditions listed in Table  3 and in
OCSPP 850.4000 and OCSPP 850.1000, it is unlikely a study will be rejected when  there are
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slight variations from guideline environmental conditions and study design unless the control
organisms are significantly affected, the precision of the test is reduced, the power of a test to
detect differences is reduced, and/or significant biases are introduced in defining the magnitude
of effect on measurement  endpoints as compared  to guideline conditions.   Before departing
significantly from this guideline, the investigator should contact the Agency to discuss the reason
for the departure and the effect the change(s) will have on test acceptability. In the test report, all
departures from the guideline should be identified, reasons  for these changes given, and  any
resulting effects on test endpoints noted and discussed.

       Table 3.—Test Validity Elements for the Lemna Toxicity Test
1.  All test vessels and closures were not identical.

2.  The duckweed plants were not impartially or randomly assigned to the test vessels.

3.  A medium (untreated) control [and solvent (vehicle) control, when a solvent was used] was not
included in the test.

4.  For testing with industrial chemicals, a surfactant or dispersant was used in the preparation of a stock
or test solution.

5.  The concentration of solvent in the range used affected growth of the test species.

6.  A minimum of five test concentrations were not used in the definitive test.

7. Controls were contaminated with the test substance.

8.  Temperature and light intensity were not measured as specified during the test.

9. The doubling time of number of fronds in the control exceed 2.5 days.

10. The lowest test concentration level was not less than the 7-day yield and average specific growth
rate IC50 values based on number of fronds and frond area (dry weight or frond area).

(i) Reporting—

       (1) Background information.   Background information to be supplied in the report
       consists at a minimum of those background information items listed in paragraph (j)0) of
       OCSPP 850.4000.

       (2) Guideline deviations.  Provide a statement of the guideline or protocol followed.
       Include a description of any deviations from the test guideline or any occurrences which
       may have  influenced the results  of the test,  the reasons  for these changes, and  any
       resulting effects on test endpoints noted and discussed.

       (3) Test substance.

              (i) Identification of the test  substance:  common name, IUPAC and CAS names,
              CAS  number, structural  formula, source, lot or batch number,  chemical  state or
              form  of the test  substance,  and its  purity (i.e.  for  pesticides, the identity  and
              concentration of active ingredient(s)).
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       (ii) Storage conditions of the test chemical or test substance and stability of the
       test chemical or test substance under storage conditions if stored prior to use.

       (iii) Methods of preparation of the test substance and the treatment concentrations
       used in the range-finding and definitive test, or limit test.

       (iv) If a vehicle (solvent) is used to prepare stock or test  substance provide: the
       name and source of the vehicle, the nominal concentration(s) of the test substance
       in the vehicle in stock solutions or mixtures, and the vehicle concentration(s) used
       in the treatments and solvent control.

(4) Plant test species.

       (i) Scientific and common name, plant family, and strain.

       (ii) Source and  method of species and strain verification.

       (iii) Culture practices, including culturing media used, and conditions.

       (iv) Acclimation period, if applicable.

       (v) Age (stage) of inoculum at test initiation.

(5) Test system and conditions.  Description of the test system and conditions used in
the definitive or limit test, and any preliminary range-finding tests.

       (i) Description  of the incubator, growth chamber, or laboratory location, type of
       lights and aeration or agitation of test vessels.

       (ii) Description of the test container used: size, type, material, fill volume.

       (iii) Number of fronds per plant  and number of plants  and fronds added to each
       test vessel at test initiation.

       (iv) Number of test vessels (replicates) per treatment level and control(s).

       (v) Description of the preparation of the synthetic growth media used including
       the preparation date, concentration of all constituents, the  initial  pH, and storage
       conditions and duration prior to use in test.

       (vi) Description of the dilution water and  any water pretreatment: source/type;
       pH; total  organic carbon content; particulate matter content;  metals, pesticides,
       and  chlorine concentration.  Describe the frequency  and  sample date(s)  for
       documenting dilution water quality.

       (vii) Methods used for treatment randomization and assignment  of plants to test
       vessels.

       (viii) Date of introduction of test organisms to test solutions and test duration.

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       (ix) Exposure technique and frequency of renewal if static renewal and flow rate
       if flow-through.

       (x) The photoperiod and light source.

       (xi) Methods and frequency of environmental monitoring performed during the
       definitive or limit study for temperature, light intensity, pH.

       (xii) Methods  and frequency of measuring test substance to confirm  exposure
       concentrations.

       (xiii) Methods and frequency  of measuring number of fronds, frond  size (dry
       weight or frond area), and any other symptoms.

       (xiv) For the definitive and  limit  test, all  analytical  procedures should  be
       described.  The  accuracy  of the  method, method detection limit, and limit of
       quantification should be given.
(6) Results.
       (i) Tabulation of test substance analytical results by test vessel and treatment
       (provide  raw  data)  and descriptive  statistics  (time-weighted mean,  standard
       deviation, minimum, maximum, coefficient of variation).

       (ii)  Environmental  monitoring  data  results (test  solution  temperature,  light
       intensity, and pH) in tabular form (provide raw data for measurements not made
       on a  continuous basis), and  descriptive statistics (mean,  standard  deviation,
       minimum, maximum).

       (iii) For preliminary range-finding tests, if conducted, the number of fronds and
       frond  size (dry weight or frond area) at each treatment level and in the control(s).
       A description and count of visual phytotoxic effects, if recorded, at each treatment
       level and in the control(s).

       (iv) For a limit  test, tabulate for the limit concentration and the  control(s) by
       replicate, the number  of fronds  and frond size (dry weight in representative
       samples or frond area) at test initiation and termination, the number of fronds and,
       if measured, frond area in each test vessel at each observation time during the test
       (provide the raw  data).

       (v) For the definitive test, tabulation by test vessel and treatment of the number of
       fronds and frond size (dry weight or frond area) at test initiation and termination,
       and the number of fronds and, if measured, frond area in  each test vessel at each
       observation time during the test (provide the raw data).

       (vi) For the limit and definitive tests, tabulation by test vessel  and treatment of
       yield and average specific growth rate for number of fronds and frond area (dry
       weight or frond area).
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(vii) For the limit and definitive tests, tabulation of the mean treatment yield and
average  specific  growth  rate  values, treatment standard deviations for these
variables, and the treatment %I (or  stimulation) in yield and average  specific
growth rate relative to the control values.

(viii) For the limit and definitive test, tabulation of observed morphologic signs of
toxicity (chlorosis, necrosis, mortality, pigmentation, abnormal shape).

(ix)  Graphs of the concentration-response  data for yield and average  specific
growth rate based on number of fronds and frond size (dry weight or frond area).

(x) For a limit test, provide the results of hypothesis tests.

(xi)  For the limit test, provide a description of the  statistical  methods  used
including software package, and the basis for the choice of method.

(xii) For the definitive  study  and for those effect measures (yield and  average
specific growth rate for number of fronds and frond size (dry weight or frond
area)) with data sufficient to fit a concentration-response  relationship, tabulation
of the slope of the concentration-response curve and its standard error and 95%
confidence limits and any goodness of fit results.

(xiii) For the definitive test,  tabulation of ICso values  for  yield and  average
specific growth rate for number of fronds and frond size (dry weight or frond
area).

(xiv) For the definitive test, a tabulation of the NOAEC and LOAEC for each
response variable (yield and average specific growth  rate based  on number  of
fronds and frond size (dry weight or frond area)).  The ICos and 95% confidence
interval should be reported for response data  where an  NOAEC could not  be
determined.

(xv) Description  of statistical  method(s)  used for point  estimates, including
software package, for determining  ICso values, fitting  the dose-response model,
and  the basis for the choice of method.  Provide results  of any  goodness-of-fit
tests.

(xvi) Description of  statistical method(s) used  for NOAEC  and  LOAEC
determination,  including  software  package, and  the  basis  for  the choice  of
method.  If an ICos value is used in place of a NOAEC provide a description of
statistical method(s) used  for point estimates,  including  software package, for
determining ICos  values, fitting the dose-response model, and the basis  for the
choice of method. Provide results of any goodness-of-fit tests.

(xvii) If determined, report the phytostatic and phytocidal concentrations.
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(j) References.   The following references should be  consulted for additional background
material on this test guideline.

       (1) American Society for Testing and Materials.  ASTM  E 1415-91(2004).  Standard
       guide for conducting static toxicity tests with Lemna gibba G3.   In Annual Book of
       ASTM_Standards, Vol.  11.06,  West Conshohocken, PA.  Current edition  reapproved
       2004.

       (2) Bishop, W.E., and R.L. Perry, 1981. The  development and evaluation of a flow-
       through growth inhibition test with duckweed (Lemna minor), In Aquatic Toxicology and
       Hazard Assessment, ASTM STP 737, ASTM, Philadelphia, PA,  pp. 421 - 435.

       (3) Bruce, R.D. and DJ. Versteeg, 1992.  A statistical procedure for modeling continuous
       toxicity data. Environmental Toxicology and  Chemistry 11:1485-1494.

       (4) Davis, J.A.,  1981. Comparison of static-replacement and flow-through bioassays
       using duckweed, Lemna gibba G3.  EPA-560/6-81-003, U.S. Environmental Protection
       Agency, Washington, DC.

       (5) Environment Canada, 1999.   Biological Test  Method:   Test for Measuring the
       Inhibition  of Growth using  the Freshwater Macrophyte, Lemna minor. Report  EPA
       l/RM/37, Method Development and Application Section,  Environmental Technology
       Centre, Environment Canada, Ottawa, Ontario.

       (6) Hughes, J.S., Alexander, M.M., and Balu, K, 1988.  An evaluation of appropriate
       expressions of toxicity  in aquatic plant bioassays as demonstrated by the  effects of
       atrazine on algae and duckweed,  Aquatic  Toxicology and Hazard Assessment:  10*
       Volume, ASTM STP 971, W.J.  Adams, GA. Chapman and W.A. Landis, eds., ASTM,
       Philadelphia, PA, pp. 531-547.

       (7) Nyholm, N.,  P.S. Sorenson, K.O. Kusk, and E.R.  Christensen,  1992.   Statistical
       treatment of data from microbial toxicity tests, Environmental Toxicology and Chemistry
       11:157-167.

       (8) Organization for Economic Co-operation  and Development,  2006. OECD Guidelines
       for Testing of Chemicals, Test No. 221, Lemna sp. Growth  Inhibition Test, Adopted 23
       March, 2006.

       (9) U.S. Environmental Protection Agency, 1994.  Pesticides  Reregi strati on Rejection
       Rate Analysis: Ecological Effects, Office of Prevention, Pesticides and Toxic Substances,
       Washington, D.C. EPA 738-R-94-035

       (10) U.S. Environmental Protection Agency,  1986. Hazard Evaluation Division Standard
       Evaluation Procedure, Non-target Plants: Growth and Reproduction of Aquatic Plants
       Tiers 1 and 2. Office of Pesticides Programs, Washington, D.C.  EPA 540/9-86-134.
                                     Page 21 of 22

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(11) U.S. Environmental Protection Agency, 1982.  Pesticide Assessment Guidelines,
Subdivision J Hazard Evaluation: Non-target plants. Office of Pesticides and Toxic
Substances, Washington, D.C.  EPA 540/9-82-020, October 1982.

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(13) Walbridge, C.T.,  1977. A flow-through testing procedure with duckweed (Lemna
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