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PFOS: A DIETARY LC50 STUDY WITH THE MALLARD
WILDLIFE INTERNATIONAL LTD. PROJECT NO.: 454-102 3M REQUEST NO. U2723
U.S. Environmental Protection Agency Series 850 - Ecological Effects Test Guidelines (draft)
OPPTS Number 850.2200
FIFRA Subdivision E, Section 71-2
OECD Guideline 205
AUTHORS: Sean P. Gallagher Courtney S. Casey Joann B. Beavers Raymond L. Van Hoven
STUDY INITIATION: April 21, 1999
STUDY COMPLETION: April 26, 2000
AMENDED REPORT DATE: March 23, 2004
SUBMITTED TO
3M Corporation Environmental Laboratory
935 Bush Avenue St. Paul, Minnesota 55144
Wildlife International, Ltd.
8598 Commerce Drive Easton, Maryland 21601
(410) 822-8600
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PROJECT NO.: 454-102
GOOD LABORATORY PRACTICE COMPLIANCE STATEMENT
SPONSOR: 3M Corporation
TITLE: PFOS: A Dietary LC50 Study with the Mallard
WILDLIFE INTERNATIONAL LTD. PROJECT NO.: 454-102
STUDY COMPLETION: April 26,2000
AMENDED REPORT DATE: March 23, 2004
This study was conducted in compliance with Good Laboratory Practice Standards as published by the U.S. Environmental Protection Agency, 40 CFR Part 160 and 792, 17 August 1989; OECD Principles of Good Laboratory Practice, (OCDE/GD(92) 32, Environment Monograph No. 45, Paris, 1992); and Japan MAFF, 59 NohSan, Notification No. 3850, Agricultural Production Bureau, 10 August 1984 with the following exception:
At the time the test was conducted the test substance was not characterized in accordance with full GLP compliance; however, the characterization was performed according to 3M Standard Operating Procedures and Methods, and all raw data are being maintained in the 3M archives. The test substance was recharacterized in accordance with GLP standards following study completion.
The stability of the test substance and reference standard under conditions of storage at the test site was not determined in accordance with Good Laboratory Practice Standards.
Analyses of liver and sera samples conducted by 3M Corporation were not performed in accordance with GLP standards and results of these analyses are being reported separately.
STUDY DIRECTOR:
JlU jC *
_________________ DATE
Sean P. Gallagher
r
Senior Biologist, Avian Toxicology
SPONSOR'S REPRESENTATIVE
DATE
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QUALITY ASSURANCE STATEMENT
This study was examined for compliance with Good Laboratory Practice Standards as published by the U.S. Environmental Protection Agency, 40 CFR Part 160 & 792, 17 August 1989; OECD Principles of Good Laboratory Practice, (OCDE/GD(92) 32, Environment Monograph No. 45, Paris, 1992); and Japan MAFF, 59 NohSan, Notification No. 3850, Agricultural Production Bureau, 10 August 1984. The dates of all audits and inspections and the dates that any findings were reported to the Study Director and Laboratory Management were as follows:
ACTIVITY
DATE CONDUCTED
Matrix Fortification, Test Substance Prep., Analytical Sampling
April 22, 1999
Feed Consumption and Analytical Sampling April 27, 1999
Necropsy, Blood Collection,
Liver Weights and Bile
Collection
May 14, 1999
Analytical Data and Draft Report
July 7, 8, and 9, 1999
Biological Data and Draft Report
Aug. 30, 31, Sept. 1, 1999
Final Report
April 18, 2000
Amended Final Report
March 19, 2004
DATE REPORTED TO: STUDY DIRECTOR MANAGEMENT
April 22, 1999 April 27, 1999
April 23, 1999 May 4, 1999
May 14, 1999
May 21, 1999
July 9, 1999
July 16, 1999
September 1, 1999 April 18, 2000
September 3, 1999 April 19,2000
March 19, 2004
March 19, 2004
S.JU Arxn ( 7 \. Susan L. Coleman
Senior Quality Assurance Representative
DATE
04
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AMENDED REPORT APPROVAL
SPONSOR: 3M Corporation
TITLE: PFOS: A Dietary LC50 Study with the Mallard
WILDLIFE INTERNATIONAL LTD. PROJECT NO.: 454-102
3M LAB REQUEST NO.: U2723
STUDY DIRECTOR:
P.
Sean P. Gallagher
i
Senior Biologist, Avian Toxicology
0A Date
CHEMISTRY PRINCIPAL INVESTIGATOR:
i s /*+*?*+ ^
r"^
Raryiliona L. Van Hoven, Ph.D
Scientist, Analytical Chemistry
\jn Date
REPORT APPROVED BY:
Linda R. Mitchell Manager of Ecotox Operations
Director of Chemistry
Z 3 /J+'ci* Date
M i __
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TABLE OF CONTENTS
TITLE PAGE...........................................................................................................................Page 1
GOOD LABORATORY PRACTICE COMPLIANCE STATEMENT....................................Page2
QUALITY ASSURANCE STATEMENT................................................................................ Page3
REPORT APPROVAL............................................................................................................... Page4
TABLE OF CONTENTS............................................................................................................Page5 Tables and Appendices............................................................................................................. Page6
SUMMARY................................................................................................................................ Page7 INTRODUCTION...................................................................................................................... Page8
OBJECTIVE............................................................................................................................... Page8
MATERIALS AND METHODS................................................................................................Page8
Test Substance.......................................................................................................................... Page8 Treatment Groups..................................................................................................................... Page9 Duration of the Test.................................................................................................................. Page9 Test Birds...................................................................................................................................Page9 Animal D iet................................................................................................................................Page10 Diet Preparation.................................................................................................................... Page 10 Diet Sampling........................................................................................................................Page 10 Analytical Method..................................................................................................................... Page10 Housing and Environmental Conditions....................................................................................Page13 Observations.............................................................................................................................. Page13 Animal Body Weights/Feed Consumption................................................................................Page14 Gross Necropsy.......................................................................................................................... Page14 Statistical Analyses............................................................................................................... Page 14
RESULTS.................................................................................................................................... Page14
Diet Analysis............................................................................................................................. Page14 Mortalities and Clinical Observations..................................................................................Page 15 Body Weight and Feed Consumption........................................................................................Page16 Gross Necropsy.......................................................................................................................... Page17
CONCLUSION............................................................................................................................ Page18
REFERENCES............................................................................................................................ Page19
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TABLE OF CONTENTS - continued -
TABLES AND APPENDICES
TABLE 1: TABLE 2: TABLE 3: TABLE 4: TABLE 5:
Cumulative Mortality from a Mallard Acute Dietary Toxicity Study with PFOS............................................................................................ Page 20
Mean Body Weight (g) from a Mallard Acute Dietary Toxicity Study with PFOS............................................................................................ Page 21
Mean Feed Consumption (g/bird/day) from a Mallard Acute Dietary Toxicity Study with PFOS.....................................................Page 23
Gross Pathological Observations from a Mallard Acute Dietary Toxicity Study with PFOS...............................................................Page 25
Cumulative Mortality (Estimated Cumulative Dose, mg/kg) from a Mallard Acute Dietary Toxicity Study with PFOS...................................... Page 26
APPENDIX I: Certificate of Analysis.................................................................................... Page27
APPENDIX II: Diet Formulation.............................................................................................Page28
APPENDIX III: Analytical Methods and Results.................................................................... Page29
APPENDIX IV: Diet Preparation..............................................................................................Page43 APPENDIX V : Cumulative Mortality by Pen from a Mallard
Acute Dietary Toxicity Study with PFOS....................................................Page44
APPENDIX VI: Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS............................................. Page 45
APPENDIX VII: Feed Consumption (g/bird/day) by Pen from a Mallard Acute Dietary Toxicity Study with PFOS..................................... Page60
APPENDIX VIII: Changes to Protocol........................................................................................Page64
APPENDIX IX: Personnel Involved in the Study.................................................................... Page65
APPENDIX X: Revised Study Summary.................................................................................Page66
APPENDIX XI: Report Amendment.................................................................................... Page 71
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PROJECT NO.: 454-102
SUMMARY SPONSOR: 3M Corporation TEST SUBSTANCE: PFOS WILDLIFE INTERNATIONAL LTD. PROJECT NO.: 454-102 STUDY: PFOS: A Dietary LC50 Study with the Mallard
RESULTS :
The dietary LC50 value for Mallards exposed to PFOS was determined to be 628 ppm a.i. with a 95% confidence interval of 448 ppm a.i. to 958 ppm a.i. The slope of the concentration-response curve was 3.67 and the chisquare value was 2.13. The no mortality concentration was 146 ppm a.i. Based upon reductions in body weight gain at the 73.2 ppm a.i. test concentration, the no-observed-effect concentration was 36.6 ppm a.i.
TEST DATES:
Hatch - April 13,1999 Acclimation - April 14-22, 1999 Experimental Start -April 22, 1999 Experimental Termination - May 14,1999
NOMINAL TEST
CONCENTRATIONS: 0, 9.1, 18.3, 36.6, 73.2, 146, 293, 586, and 1171 ppm a.i.
TEST ANIMALS:
Mallard (Anasplatyrhynchos)
AGE TEST ANIMALS: 10 days of age at test initiation
SOURCE TEST ANIMALS:
Whistling Wings, Inc. PO Box 1-A 113 Washington St. Hanover, IL 61041-3512
STUDY COMPLETION: April 26, 2000
AMENDED REPORT DATE: March 23,20041
1See Appendix X for the revised nominal test concentrations and results based upon the reanalysis of the test material following study completion.
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PROJECT NO.: 454-102
INTROD1JCTION This study was conducted by Wildlife International Ltd. for 3M Corporation at the Wildlife International Ltd. toxicology facility in Easton, Maryland. The in-life portion of the test was conducted from April 22, 1999 to May 14, 1999. Raw data generated at Wildlife International Ltd. and a copy of the final report are filed under Project Number 454-102 in archives located on the Wildlife International Ltd. site.
OBJECTIVE The objective of this study was to evaluate the toxicity of a test substance to the mallard (Anas platyrhynchos) administered through the diet for five days. An LC50 value will be calculated, if possible.
MATERIALS AND METHODS The methods used in conducting this study are based upon procedures specified in the U.S. Environmental Protection Agency Series 850 Ecological Effects Test Guidelines OPPTS Number 850.2200 (1) Section 71-2 of the Environmental Protection Agency's Registration Guidelines, Pesticide Assessment Guidelines, FIFRA Subdivision E, Hazard Evaluation: Wildlife and Aquatic Organisms (2); OECD Guideline 205, Guideline for Testing of Chemicals, Avian Dietary Toxicity Test (3); and upon ASTM Standard E857-87, "Standard Practice for Conducting Subacute Dietary Toxicity Tests with Avian Species" (4).
Test Substance
The test substance was received from 3M Corporation on October 29, 1998 and was assigned
Wildlife International Ltd. Identification Number 4675 upon receipt. The test substance was white powder identified as: FC-95; Lot No.:217. The reported purity of the test substance was 98.9%, with an expiration date of 2008. Following test termination, the test material was reanalyzed. The results of reanalysis indicate a test substance purity of 90.49%. All test concentrations have been adjusted to reflect the purity reported on the new Certificate of Analysis (Appendix I)1. The test substance was stored under ambient conditions.
The internal standard was received from 3M Corporation on July 2, 1998 and was assigned Wildlife International Ltd. identification number 4526 upon receipt. The internal standard, a granular
1Following study completion, the test material was recharacterized in accordance with GLP standards and the results o f reanalysis indicate a purity of 86.9%. While test concentrations have not been adjusted to reflect the newest purity, the revised study summary in Appendix X summarizes the effect o f the change in purity.
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material, was identified as: 1H, 1H, 2H, 2H Perfluorooctane Sulfonic Acid, Chemical Abstract Number: 27619-97-2. The standard was stored under ambient conditions
Treatment Groups The test consisted of a geometric series of eight test concentrations and a control group. Thirty
mallard ducklings were assigned to the control group and ten mallard ducklings were assigned to each of the treatment groups. Birds were sorted by weight, then chosen indiscriminately from within each represented weight class for placement into control and treatment groups. The birds were housed in brooding pens containing five ducklings each. On Day 0, following experimental start, the Sponsor requested the addition of a 10 ppm test concentration. Birds from the same lot that remained after test initiation were used for the additional test concentration. Nominal dietary concentrations used in this study were 0, 9.1, 18.3, 36.6, 73.2, 146, 293, 586 and 1171 parts per million active ingredient (ppm a.i.). The dietary concentrations were established based upon known toxicity data and information supplied by the Sponsor.
Each group was fed the appropriate test or control diet for five days. During the exposure period the control group received untreated feed. Following the five-day exposure period all groups were given untreated basal diet for three days. On Day 8, half of the treatment and control birds were euthanized and liver weight and tissue, blood, and bile samples collected for analysis. The remaining birds were fed basal ration until Day 22. On Day 22, these birds were sacrificed and also sampled for liver weight and tissue, blood, and bile.
Duration of the Test The primary phases of this test and their durations were:
1. Acclimation - 9 days. 2. Exposure - 5 days. 3. Post-exposure observation - 3 or 17 days
Test Birds All mallard (Anas platyrhynchos ) were 10 days of age and appeared to be in good health at
initiation of the test. The birds were obtained from Whistling Wings Inc., Hanover, IL. and were hatched on April 13, 1999. Birds ranged in weight from 96 to 204 grams at test initiation. The birds used in this study were immature and could not be differentiated by sex. All birds were from the
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same hatch, pen-reared and phenotypically indistinguishable from wild birds. All birds were acclimated to the caging and facilities from the day after hatch until initiation of the test.
Animal Diet Throughout acclimation and testing all test birds were fed a game bird ration formulated to
Wildlife International Ltd.'s specifications (Appendix 11). Water from the town of Easton public water supply, and feed were provided ad libitum during acclimation and testing. The birds received no form of antibiotic medication during acclimation or testing.
Diet Preparation The test substance was mixed directly into the ration. Mixing was done with a Hobart mixer
(Model Number AS200T). All dietary test concentrations were adjusted to 100% PFOS based upon the reported purity of the test substance. All dietary concentrations and the LC50 value are reported as ppm a.i. in the diet. Nominal dietary test concentrations used in this study were 9.1, 18.3, 36.6, 73.2, 146, 293, 586 and 1171 ppm a.i. (Appendix IV).
Diet Sampling Samples of the test diets were collected to verify the test concentrations administered and to
confirm the stability and homogeneity of the test substance in the diets. Homogeneity of the test substance in the diet was evaluated by collecting six samples from the 9.1 ppm a.i. a.i. and six samples from the 1171 ppm a.i. a.i. test diets at preparation on Day 0. Homogeneity samples were collected from the top, middle and bottom of the left and right sections of the mixing vessel. The homogeneity samples also served as verification samples. One verification sample was collected from the control diet and two verification samples were collected from each remaining treatment group at preparation on Day 0. At the end of the exposure period (Day 5), one sample was collected from the control and two samples were collected from each treatment group to determine stability of the test substance in the diet. The stability samples were collected from feed remaining in the feeders after being at ambient test pen conditions for five days. Samples were transferred immediately to Wildlife International Ltd. analytical chemistry.
Analytical Method The method used for the analysis of the avian diet samples was based upon methodology
developed at Wildlife International Ltd. and entitled "Method Outline for the Determination of PFOS
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in Avian Feed". Avian diet samples were extracted with methanol. Methanol was added to a requisite quantity of feed contained in a French-square glass bottle. Bottles were capped and shaken on a shaker table. Samples were vacuum filtered using qualitative filter paper. The retained feed was rinsed three times with methanol into the filtrate. The filtrate was transferred to a volumetric flask and brought to volume with methanol. As appropriate, samples were further diluted with methanol. Each sample then was diluted with a 50% methanol : 50% NANOpure water solution containing 0.100 mg 4H PFOS (internal standard)/L and 0.05% formic acid (v/v) so they fell within the calibration range of the PFOS methodology. A method flowchart is provided in Appendix 111, Figure 1.
Concentrations of PFOS in the standards and samples were determined by reversed-phase high performance liquid chromatography using a Hewlett-Packard Model 1100 High Performance Liquid Chromatograph (HPLC) with a Perkin-Elmer API 100LC Mass Spectrometer equipped with a PerkinElmer TurboIonSpray ion source. HPLC separations were achieved using a Keystone Betasil C|g analytical column (100 mm x 2 mm I.D., 3 pm particle size). The instrument parameters are summarized in Appendix III, Table 1.
Calibration standards of PFOS prepared in a 50% methanol : 50% NANOpure water solution containing 0.100 mg 4H PFOS (internal standard)/!, and 0.05% formic acid (v/v), ranging in concentration from 0.00229 to 0.0457 mg a.i./L were analyzed with the samples. The same and most prominent peak response for PFOS was utilized to monitor PFOS in all calibration, quality control, and study samples. No attempt was made to quantify PFOS on the basis of individual isomeric components. Linear regression equations were generated using peak area response ratios (PFOS : internal standard) versus the respective concentration ratios (PFOS : internal standard) of the calibration standards. A typical calibration curve is presented in Appendix III, Figure 2. The concentration of PFOS in the samples was determined by substituting the peak area response ratios into the applicable linear regression equation. Representative ion chromatograms of low and high calibration standards are presented in Appendix III, Figures 3 and 4, respectively.
The method limit of quantitation (LOQ) for these analyses was set at 1.15 ppm a.i. calculated as the product of the lowest calibration standard analyzed (0.00229 mg a.i./L) and the dilution factor of the matrix blank samples (500).
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Two matrix blank samples were analyzed to determine possible interferences. No interferences were observed at or above the LOQ during sample analyses (Appendix III, Table 2). An interference in the feed appeared at approximately the same retention time as the peak of interest but it was well below the LOQ. A representative chromatogram of a matrix blank is presented in Appendix III, Figure 5.
Avian diet was fortified at 4.57, 183 and 1830 ppm a.i. and analyzed concurrently with the samples to determine the mean procedural recovery (Appendix III, Table 3). Sample concentrations were not corrected for the mean procedural recovery of 94.7%. A representative chromatogram of a matrix fortification is presented in Appendix III, Figure 6.
An example calculation is presented for sample number 454-102-2, nominal concentration of 18.3 ppm a.i. in avian diet.
Initial Weight: 10.0 g Final Volume: 200 mL Dilution Factor: 100 (intermediate dilution factor x final dilution factor) PFOS Peak Area: 113568 Internal Standard Peak Area: 413160 Peak Area Ratio: 0.2749
Calibration curve equation. Slope: 2.77397 Intercept: 0.01894 Curve is weighted (1/x).
PFOS (mg a.i./L) at instrument
(Peak area ratio - (Y-intercept)) x I.S. Concentration Slope
(0.2749 - 0.01894) X 0.100 mg/L __
Note: I S. = internal standard.
= 0.00923 mg a.i./L
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PFOS (ppm a.i.) in sample
PFOS (mg a.i./L) at instrument x Final Volume (L) x Dilution Factor Initial Weight (Kg)
0 .0 0 9 2 3 x 0 .2 0 0 x 100
<koi
= 18.5 ppm a.i.
Percent o f Nominal Concentration
PFOS (ppm a.i.) in sample = --------------------------------------- x 100
PFOS (ppm a.i.) nominal 18.5
------x 100= 101%
18.3
Housing and Environmental Conditions During acclimation and testing, all birds were housed indoors in batteries of thermostatically
controlled brooding pens manufactured by Safeguard Products, Inc. Each pen had floor space that measured approximately 62 X 90 cm. Ceiling height was approximately 25.5 cm. External walls, ceilings and floors were constructed of galvanized steel wire and sheeting. Birds were sorted by weight, then chosen indiscriminately from within each represented weight class for assignment to pens. Each group of birds was identified by pen number and test concentration. Individual birds were identified by wing bands.
During the test the average temperature in the brooding compartment of the pens was 38C 2C (SD). Average ambient room temperature for this study was 25.2C 0.7C (SD) with an average relative humidity of 53% 18% (SD). The photoperiod (maintained by a time clock) was sixteen hours of light per day during acclimation and throughout the test. The light source was fluorescent lights which closely approximate noon-day sunlight. The birds were exposed to an average of approximately 207 lux of illumination. Housing and husbandry practices were based on guidelines established by the National Research Council (5).
Observations During acclimation all birds were observed daily. Birds exhibiting abnormal behavior or physical
injury were not used. Following test initiation and continuing until termination, all birds were
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observed at least once daily. A record was maintained of all mortality, signs of toxicity, and abnormal behavior.
Animal Body Weiehts/Feed Consumption Individual body weights were measured at the initiation of the test, on Day 5, on Day 8 for all
birds, and on Days 15 and Day 22 for all remaining birds. Average feed consumption values during the exposure period (Days 0-5) and the post-exposure observation period (Days 6-8) were determined by pen for each treatment group and the control group. Additionally, feed consumption was determined for Days 8-15 and 15-22 for the remaining half of the treatment and control birds. Feed consumption was determined by measuring the change in the weight of the feed presented to the birds over a given period of time. The accuracy of feed consumption values may have been affected by the unavoidable wastage of feed by the birds.
Gross Necropsy All test birds that died during the course of the test and all birds remaining at the termination were
subjected to a gross necropsy. Additionally, liver weight and liver tissue, serum and blood solids, and bile were collected from birds euthanized on Day 8 and 22, and when possible from those that died during the course of the study.
Statistical Analyses Mortality data were analyzed using the computer program of C.E. Stephan (6). The program was
designed to calculate the LC50 value and the 95% confidence interval by probit analysis, moving average method or the binomial probability method (7, 8, 9). In this study the LC50 value was determined by the probit method. The slope of the concentration-response curve and results of the goodness of fit test are reported. Body weight data were compared by Dunnell's test using TOXSTAT software (10,11). No statistical analyses were applied to feed consumption data.
RESULTS
Diet Analysis Avian diet samples were collected from the 9.1, 18.3 and 1171 ppm a.i. test concentrations and
analyzed to evaluate homogeneity of the test substance in the avian diet. The analysis of these samples also served as verification of test substance concentrations. Resulting mean measured
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concentrations, standard deviations and coefficients of variation (CV) for these test concentrations were 9.8 0.969 ppm a.i. (CV = 9.94%), 19.5 2.13 ppm a.i. (CV = 10.9%) and 1196 70.2 ppm a.i. (CV = 5.87%), respectively (Appendix III, Table 4). Control avian diet samples collected during the test showed no interferences above the LOQ. Samples collected during the test to verify the 36.6, 73.2, 146, 293 and 586 ppm a.i. test substance concentrations had mean measured concentrations of 40.2, 74.5, 174, 291 and 537 ppm a.i., respectively. These values represented 110, 102, 119, 99.3 and 91.6% of the nominal concentrations, respectively (Appendix III, Table 5). Analysis of avian diet samples collected from feeders after being held at ambient temperature for five days averaged 119, 97.4, 130, 104, 94.3, 101, 101 and 95.0% of the Day 0 values for the 9.1, 18.3, 36.6, 73.2, 146, 293, 586 and 1171 ppm a.i. test substance concentrations, respectively (Appendix III, Table). A representative chromatogram of a test sample is shown in Appendix III, Figure 7.
Mortalities and Clinical Observations No mortalities occurred in the control group, and all birds were normal in appearance and
behavior throughout the test. There were no treatment-related mortalities or overt signs of toxicity in the 9.1, 18.3, 36.6, 73.2, or 146 ppm a.i. treatment groups (Table 1 and Appendix V). However, there was 20% (2 of 10) mortality in the 293 ppm a.i. treatment group, 30% (3 of 10) mortality in the 586 ppm a.i. treatment group and 90% (9 of 10) in the 1171 ppm a.i. treatment group.
In the 293 ppm a.i. treatment group single mortalities were noted on the mornings of Day 7 and Day 8. Signs of toxicity were first observed on the morning of Day 4 and continued until termination for those birds sacrificed on Day 8 and until the afternoon of Day 8 for those birds sacrificed on Day 22. All birds in this treatment level displayed signs of toxicity. These included reduced reaction to stimuli (sound and motion), loss of coordination, ruffled appearance, lethargy, and lower limb weakness. All remaining birds appeared to have recovered and were normal in appearance and behavior from the morning of Day 9 until test termination.
At the 586 ppm a.i. treatment level there were three treatment-related mortalities, one each noted on the morning of Day 5, Day 6, and Day 7. Signs of toxicity were first observed on the morning of Day 3 and continued until termination for those birds sacrificed on Day 8 and until the afternoon of Day 8 for those birds sacrificed on Day 22. All birds in this treatment level displayed signs of toxicity. These included reduced reaction to stimuli (sound and motion), ruffled appearance, lower
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limb weakness, and lethargy. All remaining birds appeared to have recovered and were normal in appearance and behavior from the morning of Day 9 until test termination.
In the 1171 ppm a.i. treatment group there were nine treatment-related mortalities. The first two mortalities were found on the morning of Day 4, followed by four mortalities on Day 5, two mortalities on Day 6 and the final mortality on Day 7. Overt signs of toxicity were first observed on the morning of Day 2 and the single surviving bird continued to display signs of toxicity through the afternoon of Day 8. Signs of toxicity observed among birds in the 1171 ppm a.i. treatment group included reduced reaction to stimuli (sound and motion), loss of coordination, prostrate posture, depression, convulsions, ruffled appearance, lower limb weakness, and lethargy. The one surviving bird appeared to have recovered and was normal in appearance and behavior from the morning of Day 9 until test termination.
Body Weight and Feed Consumption When compared to the control group, there were no apparent treatment related effects on body
weight among birds in the 9.1, 18.3, or 36.6 ppm a.i. treatment groups. There was a statistically significant (p<0.05) reduction in weight gain at the 9.1 ppm a.i. level for the Day 0-5 period that was reflected in significantly lower (p< 0.05) mean Day 5 body weight. When compared to the control group, reductions in weight gain were also statistically significant (p<0.05) for the Day 5-8 period, resulting in a significantly (p<0.05) lower Day 8 mean body weight. However, differences from the control group at the 9.1 ppm a.i. level appear to be due to a lower mean Day 0 body weight for the 9.1 ppm a.i. level and were not dose responsive. Therefore, these differences were not considered treatment related.
There was a marked, treatment-related, concentration-responsive effect on body weight in the 73.2, 146, 293, 586, and 1171 ppm a.i. treatment groups during the exposure period (Days 0-5) (Table 2 and Appendix VI). These reductions were statistically significant at p<0.05 for the 73.2 ppm a.i. level and at p<0.01 at the 146, 293, 586 and 1171 ppm a.i. levels. During the Day 5-8 post-exposure period, weight gain continued to be reduced for surviving birds in the 293, 586 and 1171 ppm a.i. treatment groups. These reductions were statistically significant at p<0.01 for the 293 and 586 ppm a.i. levels. Differences at the 1171 ppm a.i. level were marked but could not be statistically compared. Body weight losses and reductions in weight gain at the 293, 586 and 1171 ppm a.i. levels were reflected in significantly (p<0.05 or p<0.01) lower mean body weights on Days 5, 8, 15, and 22
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of the test. At the 146 ppm a.i. level mean body weights on Days 8 and 22 were also significantly (p<0.05) lower than the control group. During the Day 8-15 and Day 15-22 post-exposure periods, body weight gain appeared comparable among all groups.
When compared to the control group, there was a marked reduction in feed consumption in the 293, 586, and 1171 ppm a.i. treatment groups during the exposure period (Days 0-5). A reduction in feed consumption continued to be observed through Day 15 in the 293, 586 and 1171 ppm a.i. treatment groups.
Gross Necropsy During the course of the test, all birds that died were subjected to a gross necropsy. Necropsy
results for birds found dead were similar. Common observations included thin condition, loss of muscle mass, altered spleen color, empty crops, and empty gastrointestinal tracts. Findings were considered to be treatment related. Details of the necropsy findings are presented in Table 4.
Half of the surviving birds were subjected to gross necropsy on Day 8 and the remaining birds on Day 22, following test termination. The necropsy results for birds euthanized on Day 8 and Day 22 from the 18,3, 146 and 1171 ppm a.i. treatment groups were unremarkable. One bird in the control group and one bird in the 36.6 ppm a.i. treatment group were noted with retained yolk sacs during necropsy of birds on Day 8. A single bird in the 9.1 ppm a.i. treatment group necropsied on Day 8 was noted as small, with a lack of muscle mass. In the 73.2 ppm a.i. treatment group one bird necropsied on Day 8 was small, with a lack of muscle mass, and had a 2 x 0.5 cm abscess containing caceous necrotic material on the right side of the abdominal wall. Due to the nature of the lesions observed in birds, and the isolated incidence of occurrence, the findings listed above in euthanized birds from the 9.1, 36.6, and 73.2 ppm a.i. treatment groups were not considered to be related to treatment. In addition, all remaining birds in the control, 9.1, 36.6, and 73.2 ppm a.i. treatment groups were non remarkable.
In the 293 ppm a.i. treatment group, one bird euthanized on Day 8 was noted with an incidental finding of a retained yolk sac. A second bird in the 293 ppm a.i. group, necropsied on Day 8, was noted as emaciated with a lack of muscle mass. This loss of muscle mass was consistent with reduced weight gain for the level and was considered treatment related. Another bird in the 293 ppm a.i. treatment group, euthanized on Day 22, was noted with 2 cm cysts containing yellow fluid on the
000707
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PROJECT NO.: 454-102
anterior portion of the left lobe of the liver. Due to the nature of the cysts and the isolated incidence of occurrence, this observation was not considered treatment related.
Three birds in the 586 ppm a.i. treatment level were euthanized on Day 8. At necropsy, they were noted to be thin and lacking muscle mass. One bird was noted with a slightly pale liver. These findings are considered to be treatment related. Four birds in the 586 ppm a.i. treatment level survived until Day 22. Necropsy results for these four birds were not remarkable.
CONCLUSION
The dietary LC50 value for Mallards exposed to PFOS was determined to be 628 ppm a.i. with a 95% confidence interval of 448 ppm a.i. to 958 ppm a.i.. The slope of the concentration-response curve was 3.67 and the chi-square value was 2.13. The no mortality concentration was 146 ppm a.i.. Based upon reductions in body weight gain at the 73.2 ppm a.i. test concentration, the no-observedeffect concentration was 36.6 ppm a.i..
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PROJECT NO.: 454-102
REFERENCES
1 U. S. Environmental Protection Agency, 1996. Series 850- Ecological Effects Test Guidlelines {draft), OPPTS Number 850.2200: Avian Dietary Toxicity Test.
2 U.S. Environmental Protection Agency. 1982. Pesticide Assessment Guidelines, F1FRA Subdivision E, Hazard Evaluation: Wildlife and Aquatic Organisms, subsection 71-2, Environmental Protection Agency, Office of Pesticide Programs. Washington, D.C.
3 Organization for Economic Cooperation and Development. 1984. Avian Dietary Toxicity Test. OECD Guideline for Testing of Chemicals. Guideline 205. Paris.
4 American Society for Testing and Materials. 1987. Standard Practice for Conducting Subacute Dietary Toxicity Tests with Avian Species. ASTM Standard E857-87. Annual Book of ASTM Standards, Vol. 11.04. Philadelphia, PA.
5 National Research Council. 1996. Guide fo r the Care and Use o f Laboratory Animals. Washington, D.C. National Academy Press. 125 pp.
6 Stephan, C.E. 1977. Methods for Calculating an LC50. Pages 65-84 In Aquatic Toxicology and Hazard Evaluations, American Society for Testing and Materials. Pub. No. STP 634. Philadelphia, PA.
7 Stephan, C.E. 1978. U.S. EPA, Environmental Research Laboratory, Duluth, MN. Personal Communication.
8 Finney, D.J. 1971. Statistical Methods in Biological Assay, 2nd ed., Griffin Press, London.
9 Thompson, W.R. 1947. Bacteriological Reviews, Vol 2, No.2: 115-145.
10. Dunnet, C.W. 1955. A Multiple Comparison's Procedure for Comparing Several Treatments with a Control. Jour. Amer. Statis. Assoc. 50:1096-1121.1
11. Gulley, D.D. 1990. TOXSTAT Release 3.2. The University of Wyoming.
000V09
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PROJECT NO.: 454-102
TABLE1 Cumulative Mortality from a Mallard Acute Dietary Toxicity Study with PFOS
Experimental Group
(ppm a.i.)
No. Dead Per No. Exposed Exposure Period
Day 0 Day 1 Day 2 Day 3 Day 4 Day 5
No. Dead Per No. Exposed Post-Exposure Period
Day 6 Day 7 Day 8
Control 0
0/30 0/30 0/30 0/30 0/30 0/30
0/30 0/30 0/30
Treatment 9.1 18.3 36.6 73.2 146 293 586 1171
0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 1/10 0/10 0/10 0/10 0/10 2/10 6/10
0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 0/10 1/10 2/10 2/10 3/10 3/10 8/10 9/10 9/10
The LC50 value was calculated to be 628 ppm a.i. with a 95% confidence interval of 448 ppm a.i. to 958 ppm a.i. ! - No mortalities occurred in any of the treatment levels from Day 8 to Day 22.
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PROJECT NO.: 454-102
TABLE 2 Page 1
Mean Body Weight (g) from a Mallard Acute Dietary Toxicity Study with PFOS
Experimental Group
(ppm a.i.)
Exposure Period
Change1
Day 0
Day 5____ Day 0-5
Post-Exposure Period
Change1
Day 8
Day 5-8
Control
0
Mean SD
135 279 24 42
144 22
380 101 53 16
Treatment
9.1
Mean SD
119
226**
108**
14 36
23
317* 66
91 33
18.3 Mean SD
146 277 14 26
131 18
377 100 32 11
36.6 Mean SD
147 275 16 32
128 22
375 100 37 12
73.2 Mean SD
143 260 30 55
117* 33
343 82 90 42
146 Mean SD
143 242 19 37
100** 21
331 89 48 16
293 Mean SD
129 161** 32**
17 28
33
220** 55
57 44
586 Mean SD
144 137** -6**
23 27
26
175** 34
36 41
1171 Mean SD
147 112**
25 28
13
1852
-
'Mean change is calculated separately from the mean body weights using individual body weights (See Appendix VI). 2n=l, could not be evaluated statistically using Dunnett's t-test. (-) = No data available due to mortality. ''Statistically different from the control group at p < 0.05 (Dunnett's t-test). ^^Statmtican^di^fcren^fronT^the^controJ^^^ug^^at^g^^O^OI^iDumnett^sjt^t^t)^
312
-
Total Change (Day 0-8)1
245 34
198* 55
231 25
228 30
200* 73
188** 32 9 4 ** 54
39** 36
152
-
-a * C O O '.!
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TABLE 2 Page 2
Mean Body Weight (g) from a Mallard Acute Dietary Toxicity Study with PFOS
Experimental Group
(ppm a.i.)
Day 8
Post-Exposure Period
Change1
Day 15 Day 8-15
Day 22
Change' Day 15-22
Total Change'(8-22)
Control 0
Mean SD
410 640 230 30 56 47
823 183 49 24
Treatment 9.1
Mean SD
345* 33
575 32
230 20
773 198 38 15
18.3 Mean SD
384 625 241 27 42 22
811 186 81 41
36.6 Mean SD
377 620 243 33 44 40
828 208 78 34
73.2 Mean SD
364 579 216 82 97 21
782 203 135 39
146 Mean SD
293 Mean SD
332* 58
211** 49
564 56
467** 51
232 22
256 35
688* 86
701* 41
124* 90
234 35
586 Mean SD
174** 46
394** 82
221 37
613** 91
219 13
1171 Mean SD
1852 -
3732 -
1982 -
6342 -
2512 -
Mean change is calculated separately from the mean body weights using individual body weights (See Appendix VI). 2n=l, could not be evaluated statistically using Dunnett's t-test. (-) = No data available due to mortality. Statistically different from the control group at p < 0.05 (Dunnett's t-test). Statistically different from the control group at p < 0.01 (Dunnett's t-test).
413 42
427 34
427 62
451 71
418 56
356 106
490 54
439 47
4492 -
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PROJECT NO.: 454-102
TABLE 3 Page 1
Mean Feed Consumption (g/bird/day) from a Mallard Acute Dietary Toxicity Study with PFOS
Experimental Group
(ppm a.i.)
Control
0
Exposure Period Day 0-5
Mean SD
92 10
Treatm ent 9.1 18.3 36.6 73.2 146 293 586 1171
(-) = No data available due to mortality.
73 91 94 77 105 44 36 22
Post-Exposure Period Day 6-8
125 17
117 132 125 101 159 63 55 25
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PROJECT NO.: 454-102
TABLE 3 Page 2
Mean Feed Consumption (g/bird/day) from a Mallard Acute Dietary Toxicity Study with PFOS
Experimental Group
(ppm a.i.)
C ontrol
0
Mean SD
Post-Exposure Period
Day 8-15
Day 15
171 180 13 20
Treatm ent 9.1 18.3 36.6 73.2 146 293 586 1171
(-) = No data available due to mortality.
172 186 165 148 159 109 114 106
198 204 179 173 164 132 143 154
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PROJECT NO.: 454-102
TABLE 4
Gross Pathological Observations from a Mallard Acute Dietary Toxicity Study with PFOS
Birds that died during the course of the study
Finding
Crop empty Emaciated G.I. Tract, primarily empty Gizzard contents bile stained Gizzard, empty Intestinal contents, black and tar-like Keel prominent Kidneys, pale Loss of muscle mass Spleen, grey Spleen, small and pale Spleen, pale Thin
Male, Female, and Undetermined PPM A.I.
293 586 1171 N=2 N=3 N=9
027 1 14 111 024 00 1 00 1 002 00 1 225 00 1 1 12 023 1 14
GOOr
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Table 5 Cumulative Mortality (Estimated Cumulative Dose, mg/kg1) from a Mallard ____ ______________________________________ Acute Dietary Toxicity Study with PFOS_____________________________________________
Experimental Group
(ppm a.i.)
No. Dead Per No. Exposed (Cumulative Dose, mg/kg)
___________________________ Exposure Period____________________________________
Pen Day 0
Day 1
Day 2
Day 3
Day 4
Day 5
No. Dead Per No. Exposed Post-Exposure Period
Day 6 Day 7 Day 8'
C ontrol 0 0 0 0 0 0
T reatm ent 9.1 9.1
1 0/5 2 0/5 3 0/5 4 0/5 5 0/5 6 0/5
1 0/5 2 0/5
0/5 0/5 0/5 0/5 0/5 0/5
0/5 (4) 0/5 (4)
0/5 0/5 0/5 0/5 0/5 0/5
0/5 (8) 0/5 (8)
0/5 0/5 0/5 0/5 0/5 0/5
0/5(12) 0/5 (12)
0/5 0/5 0/5 0/5 0/5 0/5
0/5(16) 0/5 (16)
0/5 0/5 0/5 0/5 0/5 0/5
0/5 (20) 0/5 (20)
0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5
0/5 0/5 0/5 0/5 0/5 0/5
18.3
1 0/5
0/5 (8)
0/5(16)
0/5 (24)
0/5 (32)
0/5 (40)
0/5 0/5 0/5
18.3
2 0/5
0/5 (9)
0/5(18)
0/5 (27)
0/5 (36)
0/5 (45)
0/5 0/5 0/5
36.6
1 0/5
0/5(19)
0/5 (38)
0/5 (57)
0/5 (76)
0/5 (95)
0/5 0/5 0/5
36.6
2 0/5
0/5(16)
0/5 (32)
0/5 (48)
0/5 (64)
0/5 (80)
0/5 0/5 0/5
73.2
1 0/5
0/5(31)
0/5 (62)
0/5 (93)
0/5(124)
0/5(155)
0/5 0/5 0/5
73.2
2 0/5
0/5 (30)
0/5 (60)
0/5 (90)
0/5 (120) 0/5(150) 0/5 0/5 0/5
146
1 0/5
0/5 (74)
0/5(148) 0/5 (222) 0/5 (296) 0/5 (370) 0/5 0/5 0/5
146
2 0/5
0/5(101)
0/5 (202)
0/5 (303)
0/5 (404)
0/5 (505)
0/5 0/5 0/5
293
1 0/5
0/5 (64)
0/5 (128) 0/5(192) 0/5 (256) 0/5 (320) 0/5 0/5 0/5
293 2 0/5 0/5(126) 0/5 (252) 0/5 (378) 0/5 (504) 0/5 (630) 0/5 1/5 2/5
586 1 0/5 0/5(175) 0/5 (350) 0/5 (525) 0/5 (700) 0/5 (875) 0/5 1/5 1/5
586
2 0/5
0/5(153)
0/5 (306)
0/5 (459)
0/5 (612)
1/5 (765)
2/5 2/5 2/5
1171
1 0/5
0/5 (240)
0/5 (480)
0/5 (720)
1/5 (960)
4/5(1200) 5/5
5/5
1171
2 0/5
0/5 (207)
0/5 (414)
0/5(621)
1/5 (828)
2/5 (1035) 3/5
4/5
The LC50 value was calculated to be approximately 628 ppm a.i. with a 95% confidence interval o f448 to 958 ppm a.i.. '- Estimated cumulative dose is based upon the average body weight and feed consumption over the 5-day exposure period, and serves as a rough
approximation of the actual amount of test substance consumed. 2 - No mortalities occurred in any of the treatment or control groups after Day 8.
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PROJECT NO.: 454-102
APPENDIX I
Certificate O f A nalysis
FC-95, Lot 217
March 9,2000
Richard M. Payfer
Tfaia sample was analyzed using LC/MS, 'H-NMR, i9F-NMR* end elem ental analyses techniquea. The results
Vi these tests show tbe.sample to contata the following weight percent composition:
__ CiFsSOiTc CSjFfiItjSSCOhiK'K4* cCWsTFlpiiSSilCOlShiTT^CT: ! CkRiSOsTC" CdiPiF,-CjjOSOTs'KK*T ______ SFiCsFisSOsTT
0.04% 0.83% U8% 31..7310%% -910.1399%% 000.53034%%% 0.35%
Additionally, the isomer distribution o fthe sanale was determined,using IJF-NMR techniques and found to contain a following mole percent composition:
CKKCFt)A- S Q ,ir (N onnsl chain, where x Is mainly 7)
C FitC FaV C PiC FjM C Fiy SCV KT (Intem d monometfajd (ranch,
w herex+y tom ainlvs. andxw Q.y ioi
(CFj)jCP-(CFiV SO* K* (Isopropyl hrancih. where x is mainly 5)
C J^i-C T C C F ,)- S O j'IC (Alpha branch, where x Is mainly 61
(CF)iC-(CFi)r S O i 'r (t-iwtvl branch, where x to mainly 4)
CF-(CFs><-C(CFiMCFa)y SOj' IT (Internal gem-dimethyl branch, where x+y
to mainly 4. and x * 01
70.5%
17.1% 10.3% 1.6% 0.2%
0.2%
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PROJECT NO.: 454-102
APPENDIX II
DIET FORMULATION WILDLIFE INTERNATIONAL LTD. GAME BIRD RATION1
INGREDIENTS
Fine Com Meal Soy Bean Meal, 48% Protein Wheat Midds Protein Base Agway Special, 60% Protein Alfalfa Meal, 20% Protein Dried Whey Ground Limestone Eastman CalPhos Methionine Premix + Liquid Vitamin and Mineral Premix (see below) GL Ferm (Fermatco)2 Salt Iodized Total
PERCENT (%)
44.83 30.65
6.50 6.00 4.00 3.00 2.50 0.90 0.60 0.35 0.32 0.25 0.10 100.00
VITAMIN AND MINERAL PREMIX
AMOUNT ADDED PER TON
Vitamin D3 Vitamin A Riboflavin Niacin
Pantothenic Acid
Vitamin B,2 Folic Acid Biotin Pyridoxine Thiamine Vitamin E Vitamin K (Menadione Dimethylpyrimidinol Bisulfite) Manganese Zinc Copper Iodine Iron Selenium
2.000. 000 I.C.U. 7.000. 0001.U.
6 grams 40 grams
10 grams
8 mgs 600 mgs 64 mgs
1.2 grams 1.2 grams 20,000 I.U. 5.8 grams 102 grams 47 grams 6.8 grams 1.5 grams 51 grams 182 mgs
'The guaranteed analysis is a minimum of 27% protein, a minimum of 2.5% crude fat and a maximum of 5% crude fiber.
fermentation By-Products (Source of Unidentified Growth Factors)
0-0O'"./8
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APPENDIX III ANALYTICAL METHODS AND RESULTS
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PROJECT NO.: 454-102
INSTRUMENT:
Appendix III Table 1
Typical LC/MS Operational Parameters
Hewlett-Packard Model 1100 High Performance Liquid Chromatograph with a Perkin-Elmer API 100LC Mass Spectrometer equipped with a Perkin-Elmer TurboIonSpray ion source. Operated in selective ion monitoring mode (SIM).
ANALYTICAL COLUMN:
Keystone Betasil C)8 column (100 mm x 2 mm I.D., 3 pm particle size)
OVEN TEMPERATURE:
30C
STOP TIME:
10.0 minutes
FLOW RATE:
0.220 mL/minute
MOBILE PHASE:
72.0% Methanol : 28.0% NANOpure Water containing 0.1% Formic Acid
INJECTION VOLUME:
25.0 pL
PFOS RETENTION TIME:
Approximately 7.0 minutes
INTERNAL STANDARD RETENTION TIME:
Approximately 4.8 minutes
PFOS MONITORED MASS:
INTERNAL STANDARD MONITORED MASS:
498.6 amu 426.7 amu
ooov:-:o
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PROJECT NO.: 454-102
Appendix III Table 2
Matrix Blanks Analyzed Concurrently During Sample Analysis
Number (454-102-)
MAB-1
JSamgle
-la s
Matrix Blank
Measured Concentration of PFOS1
(ppm a.i.)
< loq
MAB-2
Matrix Blank
< LOQ
'The limit o f quantitation (LOQ) was 1.15 ppm a.i. based upon the product o f the lowest calibration standard
"kA
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Appendix III Table 3
Matrix Fortifications Analyzed Concurrently During Sample Analysis
Sample Number (454-102-)
MAS-1 A MAS-4A
Concentrations of PFOS
Fortified
4.57 4.57
Measured
4.54 4.79
Percent Recovered
99.2 105
MAS-2
183
176
96.1
MAS-5
183
162
88.3
MAS-3 MAS-6
1830 1830
1576 1716
86.1
93.7
Mean =
94.7
Standard Deviation = CV = N=
6.99
7.38
6
Note: Results and corrections for new test substance purity were generated using MacQuan version 1.5 software and manual calculations. Values have been rounded for reporting purposes.
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-33Appendix III
Table 4
Homogeneity of PFOS in Avian Diet
PROJECT NO.: 454-102
Nominal Concentration
(ppm a.i.)
9.1
Sample Number (S-454-102-)
54 55 56 57 58 59
Location Sampled in
Mixing Vessel
Top Left Top Right Middle Left Middle Right Bottom Left Bottom Right
PFOS Measured Concentration
(ppm a.i.)
9.52 9.70 9.79 8.09 10.9 10.5
Mean Measured Concentration (X) Standard Deviation (SD)
Coefficient of Variation (CV)1
x = 9.8 ppm a.i. SD = 0.969 ppm a.i. CV = 9.94%
Mean Percent of
Nominal
108
18.3 2
Top Left
3 Top Right
4 Middle Left
5 Middle Right
6 Bottom Left
7 Bottom Right
18.5 23.4 18.3 17.3 19.4 19.9
x = 19.5 ppm a.i. SD = 2.13 ppm a.i. C V = 10.9%
107
1171 18 Top Left 19 Top Right 20 Middle Left 21 Middle Right 22 Bottom Left 23 Bottom Right
1239 1221 1118 1301 1163 1133
X = 1196 ppm a.i. SD = 70.2 ppm a.i. CV = 5.87%
102
Note: Results and corrections for new test substance purity were generated using MacQuan version 1.5 software and manual calculations. Values have been rounded for reporting purposes.
1Coefficient of variation was calculated using fall precision o f mean and standard deviation results.
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-34Appendix III
Table 5
Verification of PFOS Concentrations in Avian Diet
PROJECT NO.: 454-102
Nominal Concentration
(ppm a.i.)
0.0
Sample Number (S-454-102-)
1
Sampling Interval (Day)
0
PFOS Measured Concentration1
(ppm a.i.)
< LOQ
Percent of
Nominal
-
Mean Measured Concentration
(ppm a.i.)
--
Mean Percent of
Nominal
-
9.1 -
18.3 -
36.6 8 9
-
-
0 0
- -- 9.82 1082
--
--
19.52
1072
45.7
125 40.2
110
34.6 94.5
73.2 10 11
0 0
77.8
106 74.5
102
71.2 97.3
146 12 0 13 0
76
120 174
119
172 117
293 14 0 15 0
274 93.8 291 99.3 307 105
586 16 0 17 0
550 93.9 537 91.6 523 89.4
1171 -
-
-
-
11962
1022
Note: Results and corrections for new test substance purity were generated using MaeQuan version 1.5 software and manual calculations. Values have been rounded for reporting purposes.
'The limit of quantitation (LOQ) was 1.15 ppm a.i. based upon the product of the lowest calibration standard analyzed (0.00229 mg a.i./L) and the dilution factor of the matrix
blank samples (500). 2Rcsult obtained from Table 4.
e> *\
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-35Appendix III
Table 6
Ambient Stability of PFOS in Avian Diet During the Mallard LC50 Study
PROJECT NO.: 454-102
Nominal Concentration
(ppm a.i.)
0
9.1
Sample Number (S-454-102-)
1
54-59
Day O'
Mean Measured Concentration
(ppm a.i.)
-
9.8
Mean Percent of
Nominal
-
108
Sample Number (S-454-102-)
39
60 61
Day 5
Measured Concentration2
(ppm a.i.)
< LOQ
Mean Measured Concentration
(ppm a.i.)
-
12.3 11.7 11.0
Mean Percent of
Day 0
-
119
18.3 2-7 19.5 107
40 18.2 19.0 97.4 41 19.7
36.6 8,9 40.2 110
42 47.9 52.4 1303 43 56.8
73.2 10, 11 74.5
102
44 77.6 77.8 104 45 77.9
146 12,13 174
119
46 167 164 94.3 47 160
293
14, 15
291
99.3
48 297 295 101 49 293
586
16, 17
537
91.6
50 552 541 101 51 530
1171 18-23 1196
102
52 1150 1136 95.0 53 1122
'Day 0 results obtained from Table 4 and Table 5. The limit of quantitation (LOQ) was 1.15 ppm a.i. based upon the product of the lowest calibration standard analyzed (0.00229 mg a.i./L) and the dilution factor of the matrix blank samples
(500). 3The Day 5 value is consistent with the Day 0 mean measured concentration value for this level. No analytical measuring bias is indicated.
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PROJECT NO.: 454-102
METHOD OUTLINE FOR THE ANALYSIS OF PFOS IN AVIAN DIET
Prepare matrix fortification samples in the desired avian feed stock using the dry mix technique.
4.
Dry Mix Technique
For the high-level matrix fortification sample, weigh the requisite quantity o f Wildlife International Ltd. (W1L) ration into a weigh boat.
X
Weigh the requisite quantity of test substance (PFOS) into a beaker.
X
Add 'Aof the WIL ration and the test substance to a larger beaker.
4
Rinse the beaker that contained the PFOS with small portions of the remaining ration and transfer all portions to the larger beaker.
X
Mix the contents of the larger beaker well and transfer the mixture to a Waring blender.
X
Blend the mixture for ~5 minutes stopping at l minute intervals to scrape down the sides of the blender. During the third interval transfer the fortified feed to a beaker, mix well and return the mixture to the blender to complete mixing in the specified
time.
X
Prepare the next two matrix fortification levels by serial dilutions. Follow the same procedure described for the high-level matrix fortification except weigh the appropriate quantity o f fortified matrix (high or mid-
level) rather than the test substance.
X
Weigh 10-g samples of the matrix blank, matrix fortification and test samples into weigh boats and transfer to )6-oz. French-square glass bottles. Record the weights.
X
For each sample, measure 100 mLs o f methanol with a graduated cylinder and transfer volume to the French-square bottle.
X
Cap bottles and place on shaker table. Allow the samples to shake for a minimum of 30 minutes at 250 rpm.
X
Vacuum filter each sample with qualitative filter paper and rinse retained feed 3 times with methanol into the filtrate.
X
Transfer the filtrate to a 200-mL volumetric flask and bring the tlask to volume with methanol.
X
Prepare appropriate dilution(s) to bring final concentration into the calibration range of the LCMS methodology. Use methanol for intermediate dilutions, if required
For all final dilutions use 50% methanol : 50% NANOpure water solution containing 0.100 mg 4H PFOS (internal standard)/L and 0.05% formic acid (v/v).
X
Amputate and submit samples for LC'/MS analysis.
F ig u re 1.
Analytical method flowchart for the analysis o f PFOS in avian diet.
O O O 1- Ivy
,
W il d l if e In t e r n a t io n a l , ltd
-37-
Appendix III
PROJECT NO.: 454-102
F ig u re 2.
A typical calibration curve for PFOS. Slope = 2.77397; Intercept = 0.01894; r = 0.9981. Curve is weighted (1/x).
W il d l if e In t e r n a t io n a l , ltd
-38-
Appendix III
PROJECT NO.: 454-102
intensity: 1995 cps 167
Figure 3.
A representative ion chromatogram of a low-level (0.00229 mg a.i./L) PFOS standard.
(K
W il d l if e In t e r n a t io n a l , ltd
-39-
Appendix III
PROJECT NO.: 454-102
Figure 4.
A representative ion chromatogram of a high-level (0.0457 mg a.i./L) PFOS standard.
W il d l if e In t e r n a t io n a l , ltd
-40-
Appendix III
PROJECT NO.: 454-102
Figure 5.
A representative chromatogram o f a matrix blank sample (454-102-M AB-l). The arrow indicates the retention time o f PFOS.
W il d l if e In t e r n a t io n a l , ltd
-41 -
Appendix III
PROJECT NO.: 454-102
intensity: 6238 cps 166
Scan Time
Figure 6.
A representative chromatogram of a matrix fortification sample (454-102-MAS-1A).
4
W il d l if e In t e r n a t io n a l , ltd
-42-
Appendix III
PROJECT NO.: 454-102
Figure 7.
A representative chromatogram of a test sample (454-102-2).
0 0 ':' 'l **
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-43-
PROJECT NO.: 454-102
APPENDIX IV
DIET PREPARATION
Weight and volume of constituents used to prepare test diets:
Nominal Concentrations
(ppma.i.) 0 9.1
18.3 36.6 73.2 146 293 586 1171
Test Substance
(g)
0.0910 0.1818 0.3638 0.7282 1.4659 2.9123 5.8239 11.6483
Basal Ration
(g )....... 9000.0 8999.9 8999.8 8999.6 8999.3 8998.5 8997.1 8994.2 8988.4
Diets were prepared as follows:
5000.0 g o f basal ration was weighed into a tared Hobart mixing bowl.
The test substance was weighed in a tared weigh boat
Approximately 100 g of basal ration was taken from the mixing bowl and placed in a Waring blender.
The test substance was added to the blender and the weigh boat was rinsed with additional ration, with the rinse also being placed in the blender.
The blender contents were blended for approximately 60 seconds and transferred to the mixing bowl. The blender was rinsed with additional ration, with the rinse also being placed in the mixing bowl.
The bowl was placed on a Hobart mixer and the contents were mixed for approximately six minutes. The remaining ration as added to the bowl and the contents were mixed for six more minutes.
The diet was transferred to a labelled paper feed bag.
W il d l if e In t e r n a t io n a l , ltd
PROJECT NO.: 454-102
-44-
APPENDIX V Cumulative Mortality by Pen from a Mallard Acute Dietary Toxicity Study with PFOS
Experimental Group
(ppm a.i.)
C ontrol 0 0 0 0 0 0
T reatm ent 9.1 9.1 18.3 18.3 36.6 36.6 73.2 73.2 146 146 293 293 586 586 1171 1171
No. Dead Per No. Exposed
Pen___________________________ Exposure Period________________________
Day 0
Day 1
Day 2
Day 3
Day 4
Day 5
1 0/5 0/5 0/5 0/5 0/5 0/5 2 0/5 0/5 0/5 0/5 0/5 0/5 3 0/5 0/5 0/5 0/5 0/5 0/5 4 0/5 0/5 0/5 0/5 0/5 0/5 5 0/5 0/5 0/5 0/5 0/5 0/5 6 0/5 0/5 0/5 0/5 0/5 0/5
1 0/5 0/5 0/5 0/5 0/5 0/5
2 0/5 0/5 0/5 0/5 0/5 0/5
1 0/5 0/5 0/5 0/5 0/5 0/5
2 0/5 0/5 0/5 0/5 0/5 0/5
1 0/5 0/5 0/5 0/5 0/5 0/5
2 0/5 0/5 0/5 0/5 0/5 0/5
1 0/5 0/5 0/5 0/5 0/5 0/5
2 0/5 0/5 0/5 0/5 0/5 0/5
1 0/5 0/5 0/5 0/5 0/5 0/5
2 0/5 0/5 0/5 0/5 0/5 0/5
1 0/5 0/5 0/5 0/5 0/5 0/5
2 0/5 0/5 0/5 0/5 0/5 0/5
1 0/5 0/5 0/5 0/5 0/5 0/5
2 0/5 0/5 0/5 0/5 0/5
1/5
1 0/5 0/5 0/5 0/5 1/5 4/5
2 0/5 0/5 0/5 0/5 1/5 2/5
No. Dead Per No. Exposed
_______ Post-Exposure Period
Day 6 Day 7
Day8*
0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5
0/5 0/5 0/5 0/5 0/5 0/5
0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 1/5 0/5 1/5 2/5 2/5 5/5 5/5 3/5 4/5
0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 0/5 2/5 1/5 2/5 5/5 4/5
The LC50 value was calculated to be 628 ppm a.i. with a 95% confidence interval o f448 ppm a.i. to 958 ppm a.i. * - No mortalities occurred in any of the treatment or control groups after Day 8.
o
am.
W il d l if e In t e r n a t io n a l , ltd
-45-
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 1
PROJECT NO.: 454-102
Experimental Group
(ppm a.i.)
Bird
Day 0
Day 5
Change Day 0-5
Day 8
Change Day 5-8
Total Change (0-8)
0 1 132 302 170 404 102
2 136 292 156 381 89
3 154 319 165 415 96
4 158 319 161 429 110
5 169 309 140 418 109
Mean
150
308
158
409 101
SD 15 12 12 18 9
272 245 261 271 249 260
12
0 1 136 282 146 399 117
2 142 284 142 394 110
3 152 299 147 409 110
4 152 312 160 430 118
5 177 345 168 484 139
Mean
152
304
153
423 119
SD 16 26 11 37 12
263 252 257 278 307 271
22
0 1 125 265 140 372 107
2 134 282
148 371
89
3 149 304 155 440 136
4 154 292 138 378 86
5 166 328 162 430 102
M ean
146
294
149
398 104
SD 16
24
10
34 20
247 237 291 224 264 253
26
0
1 124 271
147 376 105
2 135 263 128 360 97
3 151 300 149 408 108
4 163 333 170 432 99
5 170 351
181 453 102
Mean
149
304
155 406 102
SD 19 38 21 38 4
252 225 257 269 283 257
22
O-OOV'^5
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APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 2
Experimental
Group
(ppm a.i.)
Bird Day 0
Day 5
Change Day 0-5
Day 8
0 1 107 222 115 298
2 126 267 141 360
3 116 203
87 266
4 107 203
96 284
5 111 248 137 348
Mean
113
229
115
311
SD 8 28 24 41
PROJECT NO.: 454-102
Change Day 5-8
76 93 63 81 100 83 15
Total Change
191 234 150 177 237 198
37
0
Group Total
1 2 3 4 5
Mean SD
Mean SD
100 100 102 108 102 102
3
135 24
235 232 233 267 210
235 20
279 42
135 335 132 328 131 317 159 383 108 299 133 332
18 32 144 380 22 53
100 96 84 116 89
97 12
101 16
235 228 215 275 197
230 29
245 34
G 0 73G
W il d l if e In t e r n a t io n a l , ltd
-47APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 3
PROJECT NO.: 454-102
Experimental
Group
(ppm a.i.)
Bird Day 0
9.1 1 123
2 118
3 151
4 108
5 119
Mean SD
124 16
Day 5
Change Day 0-5
244 121 231 113 286 135 209 101 231 112 240 116
29 13
Day 8
349 334 399 313 332 345
33
Change Day 5-8
105 103 113 104 101 105
5
Total Change (0-8)__
226 216 248 205 213 222
17
9.1
1 96 145
49
2 123 250 127
3 127 237 110
4 112 216 104 5 111 215 104
Mean SD
114 12
213 41
99 29
Group Total
Mean SD
119 14
226" 36
108** 23
` Statistically different from the control group at p < 0.05 (Dunnett's t-test). " Statistically different from the control group at p < 0.01 (Dunnett's t-test).
146
345
343
316 294
289 83
317* 66
1
95
106
100
79
76 43 91 33
50
222
216
204 183
175 71 198* 55
GOO'
W il d l if e In t e r n a t io n a l , ltd
-48-
PROJECT NO.: 454-102
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 4
Experimental Group
(ppm a.i.)
Bird Day 0
18.3 1 123
2 141
3 150
4 152
5 160
Mean SD
145 14
Day 5
Change Day 0-5
Day 8
261 138 355 297 156 421 270 120 361 286 134 390 294 134 391 282 136 384
16 13 27
Change Day 5-8
94 124 91 104 97 102
13
Total Change
232 280 211 238 231 238
25
18.3
Group
T o ta l
1 130 240 110 327
87
2 137 266 129 359
93
3 145 268 123 366
98
4 151 258 107 3 6 6 108
5 171 333 162 433 100
M ean
147
273
126
370
97
S D 16 35 22 39
8
M ean
146
277
131
377
100
SD 14 26
18 32
11
197
222
221
215
262
223 24
231 25
G 0 * v ;'
W il d l if e In t e r n a t io n a l , ltd
-49-
PROJECT NO.: 454-102
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 5
Experimental Group
(ppm a.i.)
Bird Day 0
36.6 1 131
2 132
3 142
4 160
5 179
Mean SD
149 21
Day 5
Change Day 0-5
Day 8
261 130 372 256 124 356 269 127 369 270 110 353 335 156 433
278 129 377 32 17 33
Change Day 5-8
111 100 100 83 98 98
10
Total Change
241 224 227 193 254 228
23
36.6
Group Total
1
2
3
4
5
Mean SD
Mean SD
131
136
147
151
160
145 12
147 16
230
287
263
255
324
272 36
275 32
99 316
151 402
116 379
104 344
164 427
127 374 29 44 128 375 22 37
86
115
116
89
103
102 14
100 12
185
266
232
193
267
229 39
228 30
0 0 0 f>'39
W il d l if e In t e r n a t io n a l , ltd
-50-
PROJECT NO.: 454-102
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 6
Experimental
Group
(ppm a.i.)
Bird Day 0
73.2 1 113
2 113
3 142
4 154
5 179
Mean SD
140 28
Day 5
Change Day 0-5
203 90 219 106 286 144 290 136 338 159 267 127
56 28
Day 8
281 288 390 379 480 364
82
Change Day 5-8
78 69 104 89 142 96 29
Total Change
168 175 248 225 301 223 55
73.2 1 109 222 113
2 129 254 125
3 139 243 104
4 147 196
49
5 204 352 148
Mean
146
253
108
SD 36 59 37
Group
Mean
143
260
117*
Total
SD 30 55 33
Statistically different from the control group at p < 0.05 (Dunnett's t-test).
302
332
340
175
458
321 101 343 90
80
78
97
-21
106
68 51 82 42
193
203
201
28
254
176 86
200* 73
c o o v 0
W il d lif e In ter n atio n al, ltd
-51 -
PROJECT NO.: 454-102
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 7
Experimental Group
(ppma.i.)
Bird Day 0
146 1 108
2 138
3 151
4 151
5 164
Mean SD
142 21
Day 5
Change Day 0-5
169 61 248 110 271 120 254 103 282 118
245 102 44 24
Day 8
236 330 375 341 380 332
58
Change Day 5-8
67 82 104 87 98 88 14
Total Change
128 192 224 190 216 190 38
146
1 115 204
89
2 139 219
80
3 144 229
85
4 159 261 102
5 158 285
127
Group Total
Mean
143
240
97
SD 18 33 19
Mean
143
242
100**
SD 19 37 21
` Statistically different from the control group at p < 0.01 (Dunnett's t-test).
280
287
348
358
374
329 43
331 48
76
68
119
97
89
90 20 89 16
165
148
204
199
216
186 29 188** 32
W il d l if e In t e r n a t io n a l , ltd
-52APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 8
PROJECT NO.: 454-102
Experimental
Group
(ppm a.i.)
Bird Day 0
293 1 115
2 139
3 140
4 155
5 112
Mean SD
132 18
Day 5
Change Day 0-5
Day 8
142 27 179 119 -20 165 156 16 217 187 32 291 134 22 203 148 15 211 26 21 49
Change Day 5-8
27 -20 16 32 22 15 21
Total Change
64 26 77 136 91 79 40
293 1 123
2 120
3 151
4 106 5 124
Mean
125
SD 16
Group
Mean
129
Total
SD 17
(-) = No data available due to mortality.
205
183
139
158
185
174 26 161** 28
82
63
-12
52
61
49 36 32** 33
289
273
-
223
138
231 68
220** 55
82
63
-12
52 61
49 36 57** 44
166
153
-
117
14
113 69 94** 54
W il d l if e In t e r n a t io n a l , ltd
-53-
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 9
PROJECT NO.: 454-102
Experimental
Group
(ppm a.i.)
Bird Day 0
586 1 122
2 135
3 152
4 154
5 165
Mean SD
146 17
Day 5
Change Day 0-5
Day 8
105 -17 126
143 8 209
160 8 217
129 -25
-
195 30 143
146 1 174 34 22 46
Change Day 5-8
21 66 57
-52 23 54
Total Change
4 74 65
-22 30 47
586
1 105 114
9
2 120 130
10
3 149 - -
4 153 128 -25
5 182 128 -54
Mean
142
125
-15
SD 30
7 31
Group
Mean
144
137**
-6 **
Total
SD 23 27 26
(-) = No data available due to mortality. "Statistically different from the control group at p < 0.01 (Dunnett's t-test).
159
185
-
185
-
176 15
175** 34
45
55
-
57
-
52 6
36** 41
54
65
-
32
-
50 17 39** 36
OOO'
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-54APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 10
PROJECT NO.: 454-102
Experimental Group Bird Day 0
1171 1 124
2 140
3 145
4 150
5 166
Mean SD
145 15
Day 5
Change Day 0-5
88 -39 --
96 -49 118 -32
-100 -40
17 9
Day 8
.
-
-
Change Day 5-8
-
-
Total Change
.
-
-
1171
1 128
87 -41
2 110 - -
3 145 132 -13
4 157 - -
5 200 154 -46
Group Total
Mean SD
Mean SD
148 34
147 25
124 34
112**
28
-33 18 -37** 13
(-) = No data available due to mortality. `No mortalities occurred in any of the treatment or control groups after Day 8. J^StatisticaH ^difT ereni^tonnh^ontroljjroM ^atj^O ^H ^D unnett^rtest^^
-
-
-
185
185
-
18?
-
-
-
-
31
31
-
31J
-
-15 -15
152
-
W il d l if e In t e r n a t io n a l , ltd
PROJECT NO.: 454-102
-55 -
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 11
Experimental Group
(ppm a.i.)
Bird Day 8
Day 15
Change Day 8-15
Day 22
Change Day 15-22
Total Change (8-22)
0 1 404 721 317 895 174
2 381
633 252 780
147
3 415 685 270 861 176
4 429 692 263 822 130
5 418 679 261 847 168
Mean
409
682
273
841
159
SD 18 32 26 43 20
491 399 446 393 429
432 40
0 1 399 606 207 810 204
2 394 604 210 791
187
3 409 638 229 819 181
4 430 543 113 730 187
5 484 752 268 924 172
Mean
423
629 205
815
186
SD 37 77 57 70 12
411 397 410 300 440
392 54
0
Group Total
1 372 583 211 779 196
2 371 613 242 823 210
3 440 636 196 859 223
4 378 594 216 794 200
5 430 627 197 816 189
Mean
398
611
212
814
204
SD 34
22
19 31
13
Mean
410
640 230
823
183
SD 30 56 47 49 24
407 452 419 416 386 416
24
413 42
OOO'
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-56APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 12
PROJECT NO.: 454-102
Experimental
Group
Change
(ppm a.i.)
Bird Day 8 Day 15 Day 8-15 Day 22 Change
9.1 1 349 602 253 821 219
2 334 549 215 730 181
3 399 616 217 802 186
4 313 562 249 767 205
5 332 546 214 744 198
Mean
345*
575
230
773
198
SD 33 32 20 38 15
Total Change
472 396 403 454 412 427
34
Experimental
Group
Change
Change
(ppm a.i.)
Bird Day 8 Day 15 Day 8-15 Day 22 Day 15-22
18.3 1 355 611 256
2 421 693 272
3 361 578 217
4 390 626 238
5 391 618 231
Mean
384
625
242
SD 27 42 22
Statistical!)' d if f e r e n t fr o m th e control group at p < 0.05 (Dunnett's t-test).
811 938 713 794 799
811 81
200 245 135 168 181
186 41
Total Change
465 517 352 404 408 427
62
W il d l if e In t e r n a t io n a l , ltd
-57-
PROJECT NO.: 454-102
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 13
Experimental
Group
Change
Change
(ppm a.i.)
Bird Day 8 Day 15 Day 8-15 Day 22 Day 15-22
36.6 1 372 677 305 942 265
2 356 607 251 817 210
3 369 613 244 793 180
4 353 559 206 746 187
5 433 642 209 840 198
Mean
377
620
243
828 208
SD 33 44 40 73 34
Total Change
570 461 424 393 407 451
71
E xperim ental G roup
(ppm a.i.)
B ird
Day 8
D a y 15
Change D ay 8-15
D ay 22
Change D ay 15-22
73.2
1 281 482 201 648 166
2 288 480 192 646 166
3 390 636 246 864 228 4 379 599 220 796 197
5 480 699 219 955 256
M ean
364
579
216
782 203
SD 82 97 21 135 39
T o ta l Change
367 358 474 417 475 418
56
W il d l if e In t e r n a t io n a l , ltd
-58-
PROJECT NO.: 454-102
APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 14
Experimental
Group
(ppma.i.)
Bird Day 8
146 1 236
2 330
3 375
4 341
5 380
Mean SD
332* 58
Day 15
Change Day 8-15
Day 22
475 239 659 569 239 739 631 256 738 570 229 754 576 196 550 564 232 688*
56 22 86
Change
184 170 107 184 -26 124* 90
Total Change
423 409 363 413 170 356 106
Experimental
Group
Change
Change
(ppm a.i.)
Bird Day 8 Day 15 Day 8-15 Day 22 Day 15-22
293 1 179 447 268
2 165 415 250
3 217 526 309
4 291 516 225
5 203 430 227
Mean
211**
467**
256
SD 49 51 35
` Statistically different from the control group at p <:0.05 (Dunnett's t-test).
` Statistically different from the control group at p < 0.01 (Dunnett's t-test).
731 646 748 704 676 701*
41
284 231 222 188 246 234
35
Total Change
552 481 531 413 473 490
54
W il d l if e In t e r n a t io n a l , ltd
-59APPENDIX VI
Individual Body Weights (g) from a Mallard Acute Dietary Toxicity Study with PFOS Page 14
PROJECT NO.: 454-102
Experimental
Group
(ppm a.i.)
Bird Day 8
586 1 126
2 209
3 217
4-
5 143
Mean SD
174 46
Day 15
Change Day 8-15
Day 22
Change Day 15-22
308 182 525 217 469 260 706 237 460 243 675 215
- - -340 197 546 206 394 221 613 219
82 37 91 13
Total Change
399 497 458
403 439
47
Experimental
Group
Change
Change
(ppm a.i.)
Bird Day 8 Day 15 Day 8-15 Day 22 Day 15-22
1171 1
--
2--
-
4
5 185 383 198
Mean
18?
38?
1982
SD - - -
zn=l, could not be evaluated statistically using Dunnett's t-test.
634
6342
-
251
25?
-
Total Change
-
449 4492
-
W il d l if e In t e r n a t io n a l , ltd
-60APPENDIX VII
PROJECT NO.: 454-102
Feed Consumption (g/bird/day) by Pen from a Mallard Acute Dietary Toxicity Study with PFOS Page 1
Experimental Group (ppm a.i.)
Pen
Exposure Period Day 0-5
Post-Exposure Period Day 6-8
Control
1 2 3 4 5 6 Mean SD
109 92 85 93 82 94 92 10
145 140 117 132 100 116 125 17
ra G O O 1'
W il d l if e In t e r n a t io n a l , ltd
-61 APPENDIX VII
PROJECT NO.: 454-102
Feed Consumption (g/bird/day) by Pen from a Mallard Acute Dietary Toxicity Study with PFOS Page 2
Experimental Group (ppm a.i.)
Pen
Exposure Period Day 0-5
Post-Exposure Period Day 6-8
9.1 1 73
2 72
Mean
73
130 104 117
18.3 1 90
2 91
Mean
91
135 128 132
36.6 1 103
2 85
Mean
94
129 120 125
73.2 1 79
2 74
Mean
77
109 94 101
146 1 89
2 121
Mean
105
102 217 159
293 1 28
2 59
Mean
44
61 65 63
586 1 40
2 32
Mean
36
43 67 55
1171 1 23
2 22
Mean
22
25 26 25
W il d l if e In t e r n a t io n a l , ltd
-62APPENDIX VII
PROJECT NO.: 454-102
Feed Consumption (g/bird/day) by Pen from a Mallard Acute Dietary Toxicity Study with PFOS Page 3
Experimental Group (ppm a.i.)
Pen
Control
1
2
3
Mean SD
Exposure Period Day 8-15
185 161 166 171 13
Post-Exposure Period Day 15-22
159 182 199 180 20
GOOV^'k
W il d l if e In t e r n a t io n a l , ltd
-63 APPENDIX VII
PROJECT NO.: 454-102
Feed Consumption (g/bird/day) by Pen from a Mallard Acute Dietary Toxicity Study with PFOS Page 4
Experimental Group (ppm a.i.)
Pen
Exposure Period Day 8-15
Post-Exposure Period Day 15-22
9.1 1 172
198
18.3 1 186
204
36.6 1 165
179
73.2 1 148
173
146 1 159
164
293 1 109
132
586 1 114
143
1171 1 106
154
i*S :/k J
(
W il d l if e In te r n a tio n a l, ltd
-64APPENDIX VIII
PROJECT NO.: 454-102
CHANGES TO PROTOCOL
This study was conducted in accordance with the approved Protocol with the following changes:
1. The protocol was amended to add an additional test concentration of 10 ppm a.i..
2. The protocol was amended to indicate that bile will be collected from all study birds. The protocol was clarified to indicate the collection of liver from birds that died during the course of the study.
3. The protocol was amended to change the test concentrations from 0, 10, 20, 40, 80, 160, 320, 640 and 1280 ppm a.i., to 0, 9.1, 18.3, 36.6, 73.2, 146, 293, 586 and 1171 ppm a.i. Test concentrations were changed to reflect the test substance purity given in the new certificate of analysis.
4. Individually numbered wing bands were used to uniquely identify each duckling. The protocol required leg bands to be used to identify the birds.
5. Blood samples were collected on Day 8 and Day 22 in non-heparinized 5 ml borosilicate glass test tubes. The protocol indicated that heparinized vacutainers would be used.
6. The final temperature from one brooder unit on Day 8 and all brooder units on Day 22 were not recorded.
7. The afternoon observations were inadvertently not recorded for birds in a single brooder unit on May 8, 1999.
8. Observations for control birds from two brooder levels were inadvertently not recorded on Day 6 of the test. Temperatures for these brooder levels were also not recorded on this day. Observations for control birds from one brooder level were inadvertently not recorded on Day 22 of the test.
,riiV 'K A
J t V ' O JL
W il d l if e In t e r n a t io n a l , ltd
-65 APPENDIX IX PERSONNEL INVOLVED IN THE STUDY
PROJECT NO.: 454-102
The following key Wildlife International Ltd. personnel were involved in the conduct or management of this study:
(1) Mark Jaber, Wildlife Toxicologist (2) Joann B. Beavers, Director, Avian Toxicology (3) Sean P. Gallagher, Senior Biologist (4) Courtney Casey, M.S., Senior Biologist (5) Willard B. Nixon, Ph.D., Manager, Analytical Chemistry (6) Tim Kendall, Supervisor, Analytical Chemistry (7) Raymond L. Van Hoven, Ph.D., Scientist (8) Ellen Mank, Chemist
W il d l if e In t e r n a t io n a l , ltd
-66APPENDIX X
REVISED STUDY SUMMARY
PROJECT NO.: 454-102
This study was reported using a test substance purity of 90.49%. The test substance characterization was revised on 9/7/00, following study completion, and the purity was determined to be 86.9%. The Sponsor requested that the results of this study be revised to reflect the most recent purity analyses. The results previously presented were simply corrected by the ratio of the two purities or a factor of 0.9603. No attempt was made to recalculate analytical standard concentrations or measured concentrations from original raw data. As such, minor errors due to rounding may be present. Attached is the revised summary page from the final report and the most recent certificate of analysis.
AMENDED
W il d l if e In t e r n a t io n a l , ltd
PROJECT NO.: 454-102
-67-
REVISED STUDY SUMMARY BASED ON A PURITY OF 86.9%
SPONSOR:
SPONSOR'S reppresentative:
LOCATION OF STUDY, RAW DATA AND A COPY OF THE FINAL REPORT:
3M Corporation Ms. Susan A. Beach
Wildlife International Ltd. Easton, Maryland 21601
WILDLIFE INTERNATIONAL LTD. PROJECT NUMBER: TEST SUBSTANCE: STUDY: NOMINAL TEST CONCENTRATIONS: TEST DATES:
LENGTH OF TEST: TEST ORGANISM: SOURCE OF TEST ORGANISMS:
AGE OF TEST ORGANISM S:
454-102
PFOS (Perfluorooctane Sulfonic Acid Potassium Salt)
PFOS: A Dietary LC50 Study with the Mallard
0, 8.8, 17.6, 35.1,70.3, 141, 281, 562 and 1125 ppma.i.
Experimental Start - April 22, 1999 Biological Termination - May 14,1999 Experimental Termination - May 14, 1999
22 days
Mallard (Anus platyrhynchos) Whistling Wings, Inc. Hanover, IL 61041-3512 10 days at test initiation
LC50:
95% CONFIDENCE LIMITS:
NO MORTALITY CONCENTRATION:
NO-OBSERVED-EFFECTCONCENTRATION:
603 ppm a.i. 430 and 919 ppm a.i. 141 ppm a.i. 35.1 ppm a.i.
AMENDED
W il d l if e In t e r n a t io n a l , ltd
-68-
PROJECT NO.: 454-102
Centre Analytical Laboratories, Inc
3048 Research Drive State Loiags. RA1W 1
www.oentrelab.oom
Phone (814) 231-8002
ft*: (814)231-1283 of (814) 231-1580
INTERIM CERTIFICATE OFANALYSIS
Revision 3
Centre Analytical Laboratoriei COA Reference f: 023-OI8A
3M Product: PFOS, Lot 217
Reference#: SD-018
_________ _________ Parity: 8t.% ______________ _____
T ntN iw
SpedQeatlofu
Parity*
Remit 8.%
Appearance Identification
NMR
! White Crystalline Powder
donforms Positive
iE | |1 1 1 1 J 1 iilliill J S .........................
1
B g a n ffM fl& a i
Total % Impurity
1
(LOWS)
Total Vs Impurity
(GC/MS)
Related Compounds -
POAA
Residual Solvent* (TOA )
"Purityby DSC
Inorganic Anions (iC)
1. Chloride
2. Fluoride
3. Bromide
4. Nitrate
5. Nitrite
6. Phosphate
7. Sulfate*
Organic Acida *(it)
1. TFA Z. PFPA
3. HFBA
4. NFPA
Elemental Anilyiii4:
1. Carbon
2. Hydrogen
3. Nitrogen
4. Sulftzr
1
5. Fluorine
|
1. Theoretical Value-17.8%
2. Theoretical Value - 0% 3. Theoretical Value - 0% 4. Theoretical Value-5.95% 5. Theoretical Value ==60%
1. O.Q05 wtArt.% 2. 0.001 wtywt.% 3. 1.439 wtywt.% 4. *49 wtTwty. s. o.ooi vxJw .% 6. 0.005 wtywt.% 7. 0.001 wtiwt*/.
I.M wt./wt.% 8.41 wt7wt.%
None Detected
0.33 wtywt.% Note Detected Not Applicable'
1. <0.015 wUwtV. 2. 0.59 wtywt.% 3. 0 .0 4 0 wL/wtW 4. 0 .009 wtTwtii 5. 0 .0 0 wc/wt.% 6. 0 .007 wtTwtH 7. 8.76 wtTwt.%
1. <0. J wtVwt% 2. 0 .1 wtArt.% 3. 0.10wt7wL% 4. 0.28 wt7wt%
1. 12.48 wtywt.% 2. 0.244 wt.i*wt.% 3. 1.74 wtywt.% 4. 8.84 wtywt.% 5. 54.1 wt.Zwt.%
CQA023-0I8A
Page 1of3
AMENDED
W il d l if e In t e r n a t io n a l , ltd
-69-
PROJECT NO.: 454-102
Centrc Analytical Laboratories, Inc
does R m a n lt Drive s ta tt ellegs, PA 18801
www.eantraleb.ooni
PUMI*: (814) 231-8032
Fax; (814) 231-1283 or (814) 231-1580
INTERIM CERTIRFevICisioAnT3E OFANALYSIS
Centre Analytical Laboratories COA Reference #: 023-018A
Date o f Laat Analysis: 08/31/00
Expiration Date; 08/31/06
Storage Conditions: Frozen <-10C
Re-assessment Date: 08/31/06
'Purity " 100% - (sum o f metal impurities, 1.45% +LC/MS impurities, 8.41%+Inorganic Fluoride, 0.59%+NMR impurities, 1.905%+organic acid impurities, 0.38%+POAA, 0.33%)
Total impurity from all tests _ 13.07% Purity - 100% -13.07% - 86.9%
'Potassium Is expected in this salt form and is therefore not considered an imparity.
'Purity by DSC is generally not applicable to materials o f tow purity. No endotherm was observed for this sample
`Sulfur in the sample appears to be converted to SO, and hence detected using the inorganic anion method conditions. The anion result agrees well with the sulfur determination in the elemental analysis, lending confidence to this interpretation. Based on the results, the SO, is not considered an impurity.
STFA HFBA
NT?A
PFPA
Trifluoraaoetic acid Hcptailuorobutyric acid
Nonafluoropentanoic acid
Pentafluoropropanoic acid
`Theoretical value calculations based on the empirical formula, CtFnSOjX* (MW-=538)
This work was conducted under EPA Good Laboratory Practice Standards (40 CFR 160).
COA023-016A
Prgc 2 of 3
AMENDED
GOO*' 9
W i l d l i f e In t e r n a t i o n a l , ltd
-70-
PROJECT NO.: 454-102
Ccntre Analytical Laboratories. Inc
304s Rasearch Drive Stale College, M <6801
www.eentrelab.coni
Phone: (314) 23141032
Fax: (814) 231-1253 or (814) 231-1580
INTERIM CERTIFICATE OF ANALYSIS
Revision i Centre Analytical Laboratories COA Reference #; 023-018A
LC /M S Purity Profile:
Im purity
C4
a
C6
1
Total
vnjy/i. %
l55
1.33
75
1.14
8.41
Note: The C4 and C6 values were calculated using the C4 and C6 standard calibration curves, respectively. The C5 value was calculated using the average result from the C4 and C6 standard curves. Likewise, the C7 value was calculated using the avenge result from the C6 and C8 standard curves.
Prepared By: Scientist, Centre Analytical Laboratories
Dale
Reviewed By: O L &
p /* /e(
Jhni FFlliaherty
/
Date
' Laboratory Manager, Centre Analytical Laboratories
COA023-O18A
Fsg* 3 of 3
AMENDED
W il d l if e In t e r n a t io n a l , ltd
-71 APPENDIX XI
PROJECT NO.: 454-102
Report Amendment
1. Original Report: Amended Report: Reason:
2. Original Report: Amended Report: Reason:
3. Original Report: Amended Report: Reason:
4. Original Report: Amended Report: Reason:
5. Original Report: Amended Report: Reason:
6. Original Report: Amended Report: Reason:
7. Original Report: Amended Report: Reason:
Title Page The amended report date was added. The total number of pages was changed from 65 to 72. To indicate that the report was amended and note change in pagination.
Page 2 The amended Teport date was added and the exceptions to the compliance statement were revised. To show the amended report date, provide new signatures and dates for the amended report and to update the compliance statement.
Page 3 The audit dates for the amended report were added. To show the amended report audit dates and to provide a new signature and date for the amended report.
Page 4 New signatures and dates were affixed and a title change was made. To provide signatures and dates of approval for the amended report and to update a manager's title.
Page 6 Appendix X, Revised Study Summary, and Appendix XI, Report Amendment, were added to the Table of Contents. To revise the Table of Contents to include the revised summary and report amendment.
Page 7 A footnote and the amended report date were added to the Summary page. To direct the reader to Appendix X, which contains the revised study summary and to show the amended report date.
Page 8 A footnote was added to the Tcst Substance text. To direct the reader to Appendix X, which contains the most recent Certificate of Analysis.
t r.
AMENDED
COO^
W il d l if e In t e r n a t io n a l , ltd
-72APPENDIX XI
Report Amendment (continued)
PROJECT NO.: 454-102
8. Amended Report: Reason:
9. Amended Report: Reason:
Pages 66-70, Revised Study Summary, were added to the report. To provide additional information.
Pages 71 and 72, Report Amendment, were added to the report. To provide details of changes made to the original report.
AMENDMENT SIGNATURES:
Study Director
Wildlife International, Ltd. Management
REVIEWED BY:
S j u ^ olq ( . d c u n Ql
Quality Assurance
Date A 3 A L ^ ^ (-^ Date
3-33-04
Date
AMENDED
V xj t Hmt