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EC number: 237-384-6 | CAS number: 13768-67-7
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Long-term toxicity to fish
Administrative data
- Endpoint:
- adult fish: sub(lethal) effects
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 2002
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- significant methodological deficiencies
- Remarks:
- - The species of Yb3+ introduced as the test item is unknown. - No analytical monitoring despite the fact that "water-soluble" rare earth compounds do not dissolve easily in typical aquatic media used for ecotoxicological tests; which results in actual concentrations that are often well lower than nominal concentrations. - Not enough information about the statistical significance of the differences among treatments; thus not possible to derive NOEC for the different enzymatic endpoints. - This is a chronic study as it lasted 40 days. However, No data on the classically investigated chronic endpoints. The publication indicates that at the end of the exposure, the fish were measured but the corresponding body length data are not reported.
Data source
Reference
- Reference Type:
- publication
- Title:
- Physiological Responses of Carassius auratus to Ytterbium exposure
- Author:
- Guo Hongyan et al.
- Year:
- 2 002
- Bibliographic source:
- Ecotoxicology and Environmental Safety 53, 312}316 (2002) Environmental Research, Section B
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- - Principle of test: The purpose of the present study was to investigate the physiological responses of Carassius auratus to Yb3+ solutions of different concentration following long-term exposure. Glutamate-pyruvate transaminase (GPT), involved in body nitrogen metabolism, was studied. Antioxidant defense (SOD, CAT) and detoxifying (GST, GST-Px) enzymes were also tested so as to describe the influence of low Yb3+ exposure on C. auratus liver and to indicate the most sensitive biomonitor index of Yb3+ in aquatic ecosystems.
- GLP compliance:
- no
Test material
- Test material form:
- not specified
- Details on test material:
- No information are available.
- Specific details on test material used for the study:
- The Yb3+ compound used for the exposure is unknown. However, because HNO3 was used to maintain the pH in all test solutions, it can be suspected that fish were exposed to ytterbium trinitrate.
Sampling and analysis
- Analytical monitoring:
- no
Test solutions
- Vehicle:
- not specified
Test organisms
- Test organisms (species):
- Carassius auratus
- Details on test organisms:
- TEST ORGANISM
- Common name: Goldfish
- Source: purchased from a local aquatic research institute
- Age at study initiation (mean and range, SD): unknown
- Length at study initiation (length definition, mean, range and SD): The average body length was 8.0 cm
- Weight at study initiation (mean and range, SD): The average weight was 11.0 g
- Feeding during test: yes
- Food type: crumbled commercial assorted feed
- Frequency: once a day
ACCLIMATION
- Acclimation period: 10 days
- Acclimation conditions (same as test or not): normal conditions
- Type and amount of food: crumbled commercial assorted feed
- Feeding frequency during acclimation: once a day
- Health during acclimation (any mortality observed): mortality rate was below 1%
Study design
- Test type:
- semi-static
- Water media type:
- other: aerated test solution
- Remarks:
- composition not reported
- Limit test:
- no
- Total exposure duration:
- 40 d
Test conditions
- pH:
- pH of all test solutions was maintained at 6.7 +/- 0.2 with 0.5% HNO
- Dissolved oxygen:
- Test solutions were aerated, but no data is available on dissolved oxygen levels
- Nominal and measured concentrations:
- nominal: 0, 0.01, 0.05, 0.1, 0.5 and 1.0 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Glass aquarium filled with 10 L of test solution
- Aeration: Yes
- Type of flow-through (e.g. peristaltic or proportional diluter): not a flow-through, but a semi-static design
- Renewal rate of test solution (frequency/flow rate): 50% of the solution was renewed daily
- No. of organisms per vessel: 6
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
- Biomass loading rate: 6.6 g/L (considering 6 fish of a mean weight of 11 g in 10 L of exposure medium)
TEST MEDIUM / WATER PARAMETERS
No data
OTHER TEST CONDITIONS
- Adjustment of pH: Yes, pH of all test solutions was maintained at 6.7 +/- 0.2 with 0.5% HNO
EFFECT PARAMETERS MEASURED:
Some enzymatic activities were measured at the end of the 40-day exposure. For further details, see in the field "Any other information on materials and methods incl. tables".
No further data. - Reference substance (positive control):
- not specified
Results and discussion
- Details on results:
- - Glutamate-pyruvirate transminase (GPT) enzime activity: Exposure to less than 0.01 mg/L Yb3+ solutions had no effect on GPT activity. However, exposure to low concentrations of Yb3+ solutions stimulates GPT activity in liver (P=0.05); the activation rate reached 15.2% at 0.05 mg/L Yb3+ solution. On exposure to high concentrations of Yb3+ solutions, liver GPT activity was depressed about 9% (P=0.05), occurring at 0.1 mg/L Yb3+ and remained unchanged in solutions containing more than 0.1 mg/L Yb3+.
- Superoxide dismutase (SOD) activity was stimulated when goldfish were exposed to Yb3+ solutions, and SOD activity reached the maximum of 35% (P=0.05) at 0.05 mg/L, the stimulation ratio was decreased with an increase in Yb3+ concentration.
- Catalase (CAT) enzime activity in C. auratus livers was strongly inhibited after 40 days of Yb3+ exposure; activity decreased about 30% (P=0.05) on exposure to 0.01 mg/L Yb3+.
- Glutathione peroxidase (GSH-Px) activity was stimulated about 45% at 0.05 mg/L Yb3+, whereas at Yb3+ concentrations greater than 0.1 mg/L, GSH-Px activity was reduced and not signifcantly different from that of control.
- Glutathione S-transferase (GST) activity in C. auratus liver was stimulated at low concentration and inhibited at high concentration; 0.01 mg/L Yb3+ had no effect on GST activity. A maximum increase of 38% and maximum inhibition of 30% was observed at 0.05 and 1.0 mg/L respectively. - Reported statistics and error estimates:
- Indication about the statistical significance of the differences among treatments is not always available (sometimes mentioned in the publication text, but not in the figures); thus not possible to derive NOEC for the different enzymatic endpoints.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- not applicable
- Conclusions:
- Glutamate-pyruvate transaminase (GPT) activity in goldfish liver was stimulated at 0.05 mg/L Yb3+ and inhibited at higher Yb3+ concentrations. Activity of the antioxidant enzyme superoxide dismutase (SOD) was stimulated at Yb3+ higher than 0.05 mg/L, and catalase (CAT) activity was strongly inhibited after 40 days of exposure. Detoxifying enzymes glutathione S-transferase (GST) and glutathione peroxidase (GSH-Px) were stimulated at 0.05 mg/L and inhibited at 0.1 mg/L after 40 days of exposure. Among the parameters determined, CAT in goldfish liver was most sensitive to Yb3+, indicating that CAT might be considered a potential tool in the biomonitoring of exposure to Yb3+ in an aquatic ecosystem.
- Executive summary:
Carassius auratus (six fish per concentration) were exposed to Yb+3 concentrations of 0, 0.01, 0.05, 0.1, 0.5 and 1.0 mg/L (nominal). After 40 days, they were sacrificed with a scalpel. Goldfish livers were carefully isolated from adipose tissue and pancreas for analysis. The following enzyme activities were measured: glutamate-pyruvate transminase, catalase, superoxide dismutase, glutathione S-transferase and glutathione peroxidase.
Glutamate-pyruvate transaminase (GPT) activity in goldfish liver was stimulated at 0.05 mg/L Yb3+ and inhibited at higher Yb3+ concentrations. Activity of the antioxidant enzyme superoxide dismutase (SOD) was stimulated at Yb3 + higher than 0.05 mg/L, and catalase (CAT) activity was strongly inhibited after 40 days of exposure. Detoxifying enzymes glutathione S-transferase (GST) and glutathione peroxidase (GSH-Px) were stimulated at 0.05 mg/L and inhibited at 0.1 mg/ after 40 days of exposure. Among the parameters determined, CAT in goldfish liver was most sensitive to Yb3 +, indicating that CAT might be considered a potential tool in the biomonitoring of exposure to Yb3 + in an aquatic ecosystem.
Although the results of this experiment are considered not reliable due to the significant methodological deficiencies, this publication confirms that rare earth nitrates exert toxicity on fish as already showed with other soluble rare earth trinitrates.
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