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Diss Factsheets

Ecotoxicological information

Toxicity to aquatic plants other than algae

Administrative data

Endpoint:
toxicity to aquatic plants other than algae
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2018

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 221 (Lemna sp. Growth Inhibition Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Reaction mass of Chromate(1-), [2-(3-chlorophenyl)-2,4-dihydro-4-[[2-hydroxy-5-(methylsulfonyl)phenyl]azo]-5-methyl-3H-pyrazol-3-onato(2-)][methyl [7-hydroxy-8-[[2-hydroxy-5-(methylsulfonyl)phenyl]azo]-1-naphthalenyl]carbamato(2-)]-, sodium and sodium bis[2-(3-chlorophenyl)-2,4-dihydro-4-[[2-hydroxy-5-mesylphenyl]azo]-5-methyl-3H-pyrazol-3-onato(2-)]chromate(1-) and sodium bis[methyl [7-hydroxy-8-[[2-hydroxy-5-mesylphenyl]azo]-1-naphthyl]carbamato(2-)]chromate(1-)
EC Number:
915-704-1
Molecular formula:
C36H28ClCrN7O10S2.Na / C34H26Cl2CrN8O8S2.Na / C38H30CrN6O12S2.Na
IUPAC Name:
Reaction mass of Chromate(1-), [2-(3-chlorophenyl)-2,4-dihydro-4-[[2-hydroxy-5-(methylsulfonyl)phenyl]azo]-5-methyl-3H-pyrazol-3-onato(2-)][methyl [7-hydroxy-8-[[2-hydroxy-5-(methylsulfonyl)phenyl]azo]-1-naphthalenyl]carbamato(2-)]-, sodium and sodium bis[2-(3-chlorophenyl)-2,4-dihydro-4-[[2-hydroxy-5-mesylphenyl]azo]-5-methyl-3H-pyrazol-3-onato(2-)]chromate(1-) and sodium bis[methyl [7-hydroxy-8-[[2-hydroxy-5-mesylphenyl]azo]-1-naphthyl]carbamato(2-)]chromate(1-)
Test material form:
solid
Details on test material:
Appearance
- physical state. solid
- color: brown
Specific details on test material used for the study:
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: The test substance was stored at ambient temperature.

Sampling and analysis

Analytical monitoring:
no

Test solutions

Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
The test substance is a poorly water soluble mixture; therefore a water accommodated fraction (WAF) was prepared following general guidance provided in OECD 23. Each test solution was prepared separately (differential loading) by directly adding test substance to test medium according to the loading rate described in the table below and stirring for about 2 days. Undissolved test substance was removed by centrifugation (approximately 20 min at about 17700 G). After centrifugation, undissolved test substance was still observed and the Tyndall effect was positive. Then filtration with a membrane filter (Nalgene, pore width 0.2 µm) was done. The first 50-100 mL of filtered solution was discarded (used to condition the filter). After filtration, no undissolved test substance was observed. In the filtered solution the Tyndall effect was negative, only in the two highest test solutions a positive Tyndall Effect was observed. The aqueous fraction of the test solution, after separation of the undissolved material, is considered the water saturated fraction (WSF) in test media.
Fresh test solutions were prepared on day 1 for renewal on day 3 to maximize the exposure to all soluble components of the test substance.
The control and the lowest test solution (1 mg/L) were visibly colorless and clear.
The test concentrations 3.2 and10 mg/L were visibly clear, beige and brown over the exposure period. The test concentrations 32 and100 mg/L were visibly clear, beige and dark brown with foam on the surface.

Test organisms

Test organisms (species):
Lemna gibba
Details on test organisms:
TEST ORGANISM
- Common name: Gibbous duckweed
- Strain: Clone G3
- Source (laboratory, culture collection): The stock culture was obtained from BASF SE, Crop Protection Ecology and Environmental Analytics, Speyerer Strasse 2, 67117 Limburgerhof, Germany.
- Age of inoculum (at test initiation): An inoculum culture of Lemna gibba (7-10 days old at 24 °C ± 2°) is used to initiate the test (study day 0).
- Method of cultivation: A culture is maintained continuously at the test facility. Before the exposure an inoculum culture is prepared with sufficient colonies of Lemna transferred aseptically into fresh sterile 20X AAP media. The inoculum culture is incubated under test conditions for 7 days prior to test initiation.

Study design

Test type:
semi-static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
7 d

Test conditions

Test temperature:
24 ± 2°C
Nominal and measured concentrations:
Test groups: 0 (control), 1, 3.2, 10, 32, 100 as loading rate based on test substance mass without a correction for purity or composition
Details on test conditions:
TEST SYSTEM
- Incubation chamber used: yes (Infors HT Multitron Pro controlled climate cabinet)
- Test vessel: Glass petri dishes covered with glass plates (nominal volume 300 mL) / (colorless glass with a minimum water depth of 20 mm)
- Test volume: 160 mL
- Aeration: No
- Renewal rate of test solution (frequency/flow rate): : In order to insure constant exposure conditions this study was conducted as a static-renewal exposure. The renewal was done at day 3.
- Initial colonies:11 fronds/ test vessel at the start of exposurey:
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 6

GROWTH MEDIUM
- Standard medium used: yes (synthetic fresh water (20X AAP))

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: The test medium (20X AAP medium) was prepared as described in OECD Guideline for Testing of Chemicals, No. 221 Lemna sp. Growth inhibition Test, Mar 2006, Annex 4.
Growth medium intended for testing was prepared at least 2 days before use to allow the pH to stabilize. The pH of growth medium was checked prior to use and readjusted if necessary by the addition of 1 M HCl.

OTHER TEST CONDITIONS
- Sterile test conditions: yes (The test media was sterilized after preparation and prior to inoculation.)
- Adjustment of pH: The pH of growth medium was checked prior to use and readjusted if necessary by the addition of 1 M HCl.
- Photoperiod: Continuous
- Light intensity and quality: 8522 lux (±15%) at a wave length of 400 - 700 nm
- Illumination: Artificial light, type universal white (OSRAM L 25), permanent illumination. To minimize the potential effect of slight variations in illumination.

TEST INITIATION, MAINTAINANCE AND TOC MEASUREMENT
Colonies consisting of 2 to 4 visible fronds were transferred from the inoculum culture and randomly assigned to the test vessels under aseptic conditions. Each test vessel should contain a total of 9 to 12 fronds. The number of fronds and colonies were the same in each test vessel. The test vessels were impartially distributed in an incubator and continuous illumination. Vessel positions were altered after each assessment. The temperature was monitored within the incubator and in a separate vessel filled with deionized water. At the end of the test, the pH was measured in all replicates of the control and treatment groups; the pH at test initiation was measured in the respective bulk solutions.
The TOC values of all the test solutions were measured at the start and end of one renewal interval as an additional water quality parameter.

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
Frond number
The frond number in the test vessels were counted at the start of the test, after day 3, day 5 and after end of exposure the total number of fronds was counted in each replicate. Every frond visibly projecting beyond the edge of the parent frond was counted. Observations on the appearance of the fronds included necrosis, chlorosis, changes in plant size or shape and root growth were documented. The TOC values of all the test solutions were measured at the start and end of one renewal interval as an additional water quality parameter.
Dry weight
The biomass based on dry weight was determined at the start of exposure from a sample of the inoculum culture representative of what was used to begin the test, and at the end of the test with the plant material from each treatment and control vessel. All colonies were collected from each of the test vessels and rinsed with deionized water. They were blotted to remove excess water and then dried at 60°C for 3 days to a constant weight. Any root fragments were included.

RANGE-FINDING STUDY
According to the test guidelines, at least 5 concentrations in a geometric series with a separation factor of ≤3.2 should be used.
The test concentrations were selected on the basis of a range finding test (experimental conduct in accordance with GLP but without a GLP Status). The results of the 7 days range finding test were (as nominal concentrations):
ErC50 = between 10 and 100 mg/L
The test concentrations were selected on the basis of range finding tests (experimental conduct in accordance with GLP but without a GLP Status). The results of the 7 day range finding tests can be found below (as nominal concentrations based on frond number):
Reference substance (positive control):
yes
Remarks:
3,5 Dichlorphenol

Results and discussion

Effect concentrationsopen allclose all
Duration:
7 d
Dose descriptor:
EL10
Effect conc.:
1.31 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
growth rate
Duration:
7 d
Dose descriptor:
EL50
Effect conc.:
45.2 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
growth rate
Duration:
7 d
Dose descriptor:
EL10
Effect conc.:
1.54 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
growth rate
Duration:
7 d
Dose descriptor:
EL50
Effect conc.:
63.2 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
growth rate
Duration:
7 d
Dose descriptor:
EL10
Effect conc.:
1.98 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
biomass
Duration:
7 d
Dose descriptor:
EL50
Effect conc.:
6.03 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
biomass
Duration:
7 d
Dose descriptor:
EL10
Effect conc.:
0.895 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
biomass
Duration:
7 d
Dose descriptor:
EL50
Effect conc.:
8.07 mg/L
Nominal / measured:
nominal
Conc. based on:
other: loading rate
Basis for effect:
biomass
Details on results:
VALIDITY CRITERIA
This test was fully compliant with all the following validity criteria required by the corresponding test guidelines and is considered valid.
• The doubling time of frond number in the control was 1.4 days (<2.5 days).
Results with reference substance (positive control):
In order to verify that the Lemna cultures are responding normally to toxic stress, tests with a reference substance (3,5 Dichlorphenol) are conducted. Reference substance tests are conducted according to OECD 221 guidelines and in accordance with GLP, but without a GLP status. The results from the reference substance test are compared to 3,5 Dichlorphenol EC50 values published in OECD Guideline, which represent the typical response range for the Lemna species tested.
The EC50(7d) of the reference substance 3,5 Dichlorphenol was 10.3 mg/L (experiment date: 03 Apr 2017, project number: 63E0308/02E014).
This result is within the range of 5.9 – 13.3 mg/L and indicates that the culture of Lemna gibbqa used in this study is responding normally to toxic stress.

Any other information on results incl. tables

Table 3: Lemna morphology and visual signs of phytotoxicity

Signs of phytotoxicity were observed in the treatment groups 10 mg/L and higher on day 3 and in treatment groups 3.2 mg/L and higher on day 5 and 7.

 

Loading rate

[mg/L]

Replicate No.

Morphological changes, signs of phytotoxicity

Day 3

Day 5

Day 7

0 (control)

1 - 6

0

0

0

1

1 - 3

0

0

0

3.2

1 - 3

0

4, 8 (a)

4, 8 (a)

10

1 - 3

8 (a)

4, 8(a, b)

1 (+++), 4, 8(a, b)

32

1 - 3

6, 8 (a)

6, 8 (a, b)

1 (+++), 6, 8 (a, b)

100

1 - 3

4, 6, 8 (a)

4, 6, 8 (a, b)

1 (+++), 4, 6,
8 (a, b)

Explanation of abbreviations:

0:            No findings

1:            frond or root yellowing (chlorosis)

2:            fronds humped or swollen (gibbosity)

3:            small fronds

4:            shortened roots

5:            no roots

6:            plants fragmented (fronds and/or roots)

 

7:            dead white plant tissue (necrosis)

8:             plants colored (a-red, b green-grey) by test substanz (fronds and/or roots)

9:            others

(+):          slight effects

(++):       medium effects

(+++):     strong effects

Table 4: Test medium

Physical and chemical characteristics of the test medium used.

Date of preparation

pH value

pH value after adjustment

Date of measurement

15 Aug 2017

8.2

7.4

15 Aug 2017

15 Aug 2017

8.3

7.5

17 Aug 2017

 

Table 5 and 6: pH values

pH values in the test solutions after 0 and 3 days – 1st Interval

 

Loading rate

[mg/L]

pH value
after 0 daysa

pH value after 3 days

Replicate 1

Replicate 2

Replicate 3

Replicate 4

Replicate 5

Replicate 6

0 (control)

7.6

8.7

8.7

8.7

8.6

8.6

8.6

1

8.0

8.6

8.6

8.6

 

 

 

3.2

7.9

8.6

8.6

8.6

 

 

 

10

7.9

8.6

8.6

8.6

 

 

 

32

7.9

8.6

8.6

8.6

 

 

 

100

7.9

8.6

8.6

8.6

 

 

 

awithout Lemna

pH values in the test solutions after 3 and 7 days–2nd Interval

Loading rate

[mg/L]

pH value
after 3 daysa

pH value after 7 days

Replicate 1

Replicate 2

Replicate 3

Replicate 4

Replicate 5

Replicate 6

0 (control)

7.6

9.1

9.1

8.9

9.0

8.8

8.9

1

7.9

8.8

8.9

8.8

 

 

 

3.2

7.9

8.8

8.8

8.7

 

 

 

10

7.8

8.6

8.6

8.6

 

 

 

32

7.9

8.6

8.6

8.6

 

 

 

100

7.8

8.6

8.6

8.6

 

 

 

awithout Lemna

  

Table 7: TOC values

TOC values were measured over one renewal interval as an additional water quality measure.

 

Nominal concentration / Loading rate
[mg/L]

day 0 (fresh solution)

day 3 (aged solution)

0 (control)

2.2

2.8

1

2.2

2.8

3.2

2.3

3.0

10

2.8

4.2

32

6.0

5.5

100

13.9

12.7

 

The TOC in the treatment groups 10, 32 and 100 was higher than in the control test medium. The higher TOC is likely due to soluble organic components from the test substance. The TOC value confirms qualitatively that the daphnids in the WAF were exposed to soluble organic components from the test substance.

Table 8: Dissolution behavior

The following observations were recorded for the dissolution behavior of the test substance in the test water:

 

Loading rate

[mg/L]

day 0

day 3

day 5

day 7

aged test solution

fresh test solution

0 (control)

0

0

0

0

0

1

0

0

0

0

0

3.2

1

4, 5

1

4

4

10

1

2, 5

1

2

2

32

2, 7

2, 6

2, 7

2, 6

2, 6

100

3, 7

2, 6

3, 7

2, 6

2, 6

Explanation of abbreviations:

0:          no remarkable observations, clear test medium

1:          coloration caused by the test substance (beige-brown, colorless)

2:          coloration caused by the test substance (brown)

3:          coloration caused by the test substance (dark brown)

4:          coloration caused by the test substance (yellow)

5:          yellow up to brown crumbs on the bottom

6:           precipitation, undissolved test substance (brown dust) at the bottom of the test vessel

7:           other: slightly foam on the water surface

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The test substance is acutely harmful for aquatic plants.