| QUERY NAME: All Endpoint Result Information, TABLE NAME: V_TEST_RESULT_EZ |
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Alkalinity |
The acid-neutralizing (i.e., proton accepting) capacity of water; the quality and quantity of constituents of water that result in a shift in the pH toward the alkaline side of neutrality. |
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Analytical Monitoring Ind |
An indicator whether or not instrumental analyses were used to detect the precise exposure amount of the chemical exposed to the organisms throughout the experiment. |
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Animals at Final Sacrifice |
The number of animals examined at the final sacrifice. |
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Animals at Interim Sacrifice |
The number of animals examined at the interim sacrifice. |
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Basis for Concentration |
Indication of whether the concentration is measured or nominal. |
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Biodegradability Indicator |
Qualitative indicator of whether biodegradation was observed in the study, and if so whether the test substance was readily or inherently biodegradable. |
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Biodegradation Value |
The numeric results as described in the Robust Summary. |
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Biodegradation Value Description |
A mathematical symbol to further describe the measured or estimated endpoint test value. |
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Biodegradation Value Lower Range |
The measured or estimated lower numeric value of the range for the endpoint property or effect. |
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Biodegradation Value Units |
Unit of measure used for the given Test Value or range for the endpoint. |
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Biodegradation Value Upper Range |
The measured or estimated upper numeric value of the range for the endpoint property or effect. |
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Biotransformation Type |
The type of biotransformation observed. |
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Body Fluids Sampled |
All bodily fluids monitored by the study. |
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Boiling Indicator |
An indicator specifying whether or not the substance boils or decomposes during the boiling point test. |
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Boiling Point Pressure Units |
The units of measure for the given boiling point test pressure. |
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Boiling Point Pressure Value |
The pressure level at which the boiling point was determined. |
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Breakdown Products/Metabolites |
A description of the partial degradation products or metabolites that are stable enough and formed in sufficient amounts to be detectable analytically. If possible provide both identities and percentages relative to the starting concentration. |
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Carcinogenic Effect |
An indicator of the carcinogenicity of the chemical tested. |
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CAS Number |
A standardized number assigned by the Chemical Abstracts Service (CAS) to identify a chemical (e.g., 10595-60-5). |
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Category Chemical |
The system generated ID for the category chemical for which the study is being performed. |
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Challenge Exposure Period |
Duration of the challenge portion of the test. |
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Challenge Exposure Period Units |
Time units represented by the exposure period value. |
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Challenge Frequency of Treatment |
Description of the administration of doses to the test animals during the challenge phase of the test (e.g., n doses per per week). |
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Chemical Category Name |
The name of the chemical category. |
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Clinical Observations |
Additional information that may be needed for an adequate assessment of data reliability. Provide, at a minimum, qualitative descriptions of observations indicating dose-related effects:
1. Body Weight
2. Food/Water Consumption
3. Identity, Severity, Time of Onset (e.g., date/time of day, days after exposure) and Duration of Clinical Signs
4. Clinical chemistry (e.g., hematology, urinalysis), if possible
5. Other examination, e.g., Enzyme Induction, Cell Proliferation, Reversibility of Effects |
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COD |
Chemical oxygen demand (COD) is the amount of oxygen that is consumed when the test substance is oxidized by a strong chemical oxidant, such as potassium dichromate, according to standard procedures; units mg O2 per mg of test substance. It is often substituted for ThOD when the latter cannot be calculated. |
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COD Units |
The units of measure for COD. |
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Concentration Percentage |
Percentage of test test subjects impacted by the observed concentration. |
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Concentration Result Type |
An indicator signifying whether the value reported is a lethal concentration of an effective concentration. |
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Concentration Units |
The unit of the concentration of the substance in water during the pH determination, preferably in mg/L. |
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Concentration Upper Value |
The upper concentration value. |
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Concentration Value |
Concentration that causes the indicated effect on the indicated percentage of the test subjects. |
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Concentration Value Description |
The mathematical symbol to describe the measured/estimated lethal concentration. |
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Conclusion |
Sponsor's characterization of whether the validity criteria of the test guidelines followed can be considered fulfilled for Genetic Toxicity in vitro. |
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Conclusion |
Sponsor's characterization of whether the validity criteria of the test guidelines followed can be considered fulfilled. |
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Conjunctivae (Chemosis) |
Irritation score. |
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Conjunctivae (Redness) |
Irritation score. |
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Consortium Name |
The names of the companies that belong to the consortium or partnership if applicable. |
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Control Group Type |
Describe the concurrent controls used in the study |
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Control Substance Remarks |
Information on the control substance, if any, including name, initial concentration, and degradation results. |
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Cornea Irritation |
Irritation score. |
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Degradation Indicator |
An indicator signifying whether or not degradation took place during the experiment. |
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Density Type |
An indicator specifying whether the endpoint being tested is Density, Relative Density, or Bulk Density. |
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Depuration Rate |
A description of the rate constant for the depuration phases in an experimental bioaccumulation study. |
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Details on Cytogenetic Assay |
Any details that could be relevant for evaluating this study summary or that are requested by the respective regulatory programme. Consult the programme-specific guidance (e.g. OECD HPVC, Pesticides NAFTA or EU REACH) thereof. |
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Deviations from Test Guideline Flag |
Indication that a study contains deviations from the standard test protocol. |
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Dissolved Oxygen |
The amount of soluble oxygen in water. This represents the amount necessary to sustain life in an aquatic system. |
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Dose Remarks |
Information about the Doses or Concentrations applied to the test subjects. |
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Edema |
Irritation score. |
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Endpoint Name |
The specific endpoint about which data is reported. |
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Erythema |
Irritation score. |
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Excretion Routes |
Excretion routes monitored by the study. |
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Exposure Duration |
Numeric value of exposure duration. |
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Exposure Duration |
Numeric value of No Effect Observed Concentration (NOEC) exposure duration. |
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Exposure Period |
Duration of the test. |
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Exposure Period Units |
Time units represented by the exposure period value. |
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Exposure Period Upper Value |
Upper duration of the test. |
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Exposure Period Value Description |
The mathematical symbol to describe the measured/estimated value. |
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Exposure Units |
Units of measure describing the No Effect Observed Concentration (NOEC) exposure value. |
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Exposure Units |
Units of measure. |
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Final Sacrifice Time |
The number of weeks following the initiation of the study when the final sacrifice occurred. |
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Frequency of Treatment |
Description of the administration of doses to the test animals (e.g., n doses per day, n days per week). |
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Gender |
Gender of the tested animals. |
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Genotoxic Effect |
Description of study results for each dose/concentration level. |
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Genotoxic Effect |
Description of study results for each dose/concentration level. |
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GLP |
Indicate if the study was conducted following Good Laboratory Practice standards. Enter Not Applicable for studies involving estimated values. |
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Grade |
Grade determined for the result. |
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Grading Scale |
Identify the scale/grading system used. |
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Half-Life |
Degration half-life as described in the study for the endpoint Stability in Water. |
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Half-Life |
Degration half-life as described in the study. |
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Half-Life Units |
Half-Life units of measure for the endpoint Stability in Water. |
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Half-Life Units |
Half-Life Units of measure. |
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Half-Life Value Description |
A mathematical symbol to further describe the measured or estimated degradation half-life. |
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Half-Life Value Description |
A mathematical symbol to further describe the measured or estimated degradation half-life for the endpoint Stability in Water. |
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Half-Life Value Description |
The mathematical symbol to describe the measured/estimated value for the endpoint Stability in Water. |
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Hydrolysis Indicator |
Indicator for whether the test substance contains functional groups or substructures that may be susceptible to hydrolysis under reasonably anticipated environmental conditions. |
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Incubation Condition |
Specifies whether the test method involves aerobic or anaerobic incubation. |
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Inoculum |
The source of microorganisms used in the study. |
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Inoculum Concentration |
Concentration of microorganisms (microbial biomass) or the amount of an environmental sample (e.g., soil) added to the test vessels at the start of the test. |
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Inoculum Concentration Units |
Units of the concentration of microorganisms (i.e. the microbial biomass) in the test vessels at the start of the test |
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Inoculum Remarks |
Description of the environmental sample used as inoculum, including time of collection, environmental temperature at the time of collection, conditions during transport of the sample to the lab, and basic information on the sample itself; e.g. pH and texture for soil samples. Include information on history of prior exposure to test substance, if any. |
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Interim Sacrifice Time |
The number of weeks following the initiation of the study when the interim sacrifice occurred. |
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Interpretation of Results |
Overall interpretation of or conclusions drawn from the test results. |
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Iris Irritation |
Irritation score. |
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Key Study Sponsor Indicator |
An indicator entered by the sponsor specifying whether or not the Robust Summary's test results for this endpoint are summarized from a "key" or "critical" study. |
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Kinetic vs. Steady-State |
In an experimental determination of bioconcentration factor (BCF), whether the steady-state method or kinetic method (I.e. the ratio of uptake and depuration rates) was used. |
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Lesions |
Description of lesions, if seen. |
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Light Source |
The source of light used in the photodegradation study |
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Light Source Spectrum |
Wavelength (in nm) range of the indicated light source. |
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Limit Test |
An indicator that the experiment was a limit test. |
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LOAEL/LOAEC Units |
The unit of measure descriibing the Lowest Observed Effect Concentration (LOEC) concentration. |
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LOEC |
Concentration that establishes the Lowest Observed Effect Concentration (LOEC). |
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LOEC Basis for Concentration |
Indication of whether the Lowest Observed Effect Concentration (LOEC) concentration is measured or nominal. |
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LOEC Exposure Duration |
Numeric value of exposure duration of Lowest Observed Effect Concentration (LOEC). |
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LOEC Exposure Units |
Units of measure describing Lowest Observed Effect Concentration (LOEC) exposure value. |
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LOEC Upper Range |
Upper concentration that establishes the Lowest Observed Effect Concentration (LOEC). |
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LOEC Value Description |
Mathematical symbol describing the Lowest Observed Effect Concentration (LOEC) value. |
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LOELR |
Concentration that establishes the Lowest Observed Effect Loading Rate (LOELR). |
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LOELR Basis for Concentration |
Indication of whether the Lowest Observed Effect Loading Rate (LOELR) concentration is measured or nominal. |
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LOELR Exposure Duration |
Numeric value of exposure duration of Lowest Observed Effect Loading Rate (LOELR). |
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LOELR Exposure Units |
Units of measure describing Lowest Observed Effect Loading Rate (LOELR) Exposure value. |
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LOELR Unit of Measure |
Units of measure describing Lowest Observed Effect Loading Rate (LOELR) value. |
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LOELR Upper Mean Value |
Upper concentration that establishes the Lowest Observed Effect Loading Rate (LOELR). |
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LOELR Value Description |
Mathematical symbol describing the Lowest Observed Effect Loading Rate (LOELR) value. |
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Loss by Advection (percent) |
The percentage lost by advection, derived from a level II or level III multimedia model, for the air compartment. |
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Loss by Reaction (percent) |
The percentage lost by reaction, derived from a level II or level III multimedia model, for the air compartment. |
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Mammalian Strain |
Strain of mammal tested. |
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Mass Distribution (percent) |
The predicted percentage of the test substance, derived from a multimedia model, at equilibrium (level I and II models) or steady state (level III model), in the air, water, soil, and sediment compartment. |
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Mass Distribution -- Sediment |
The predicted percentage of the test substance, derived from a multimedia model, at equilibrium (level I and II models) or steady state (level III model), in the sediment compartment. |
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Mass Distribution -- Soil |
The predicted percentage of the test substance, derived from a multimedia model, at equilibrium (level I and II models) or steady state (level III model), in the soil compartment. |
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Mass Distribution -- Water |
The predicted percentage of the test substance, derived from a multimedia model, at equilibrium (level I and II models) or steady state (level III model), in the water compartment. |
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Measurement Period |
Measurement time applicable to the test result value. |
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Measurement Period Units |
Time units represented by the measurement period value. |
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Melting Indicator |
An indicator specifying whether or not the substance melts, sublimes, or decomposes during the melting point test. The melting, decomposition or sublimation temperature is entered in the test value. |
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Metabolic Activation |
Indicate whether metabolic activation was applied or not. Select "not applicable" for mammalian cell lines when no exogenous metabolic system is required for Genetic Toxicity in vitro. |
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Metabolic Activation |
Identify use of mammalian metabolism in non-mammalian (in vitro) experiments. |
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Metabolites Excreted |
List all the excreted metabolites. |
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Metabolites in Body Fluids |
List all the metabolites found in sampled body fluids. |
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Metabolites in Tissues |
List all the metabolites found in sampled tissues. |
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Method/Guideline Description |
Description of the test protocol, guideline or estimation method used in the study, if other than an OECD, USEPA, or other published test guideline. |
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Method/Guideline Followed |
The name of the Method or Guideline followed in performing the study. |
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Model Concentration -- Air |
The predicted concentration derived from a multimedia model for the air compartment. |
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Model Concentration -- Sediment |
The predicted concentration derived from a multimedia model for the sediment compartment. |
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Model Concentration -- Soil |
The predicted concentration derived from a multimedia model for the soil compartment. |
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Model Concentration -- Water |
The predicted concentration derived from a multimedia model for the water compartment. |
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Model Inputs: Chemical Properties: Henry's Law Constant |
The Henry's Law constant value used as input to run a multimedia model, or (if applicable) estimate one of the other transport/distribution endpoint subtypes. Provide a reference in the Results Remarks. |
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Model Inputs: Air Emissions |
A description of the Emissions used in the multimedia model, in kg/hr, for air. |
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Model Inputs: Chemical Properties: log KOW |
For Transport/Distribution, the log KOW value used as input to run a multimedia model, or (if applicable) estimate one of the other transport/distribution endpoints such as KOC. For bioaccumulation, log KOW can assist in interpretation of the measured or estimated BCF value; it may also be used to estimate BCF from chemical structure. Provide a reference in the Results Remarks. |
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Model Inputs: Chemical Properties: Melting Point |
The melting point value used as input to run a multimedia model, or (if applicable) estimate one of the other transport/distribution endpoint subtypes. Provide a reference in the Results Remarks. |
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Model Inputs: Chemical Properties: Vapor Pressure |
The vapor pressure value used as input to run a multimedia model, or (if applicable) estimate one of the other transport/distribution endpoint subtypes such as Henry's Law constant (Hc). Provide a reference in the Results Remarks. |
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Model Inputs: Chemical Properties: Water Solubility |
The water solubility value used as input to run a multimedia model, or (if applicable) estimate one of the other transport/distribution endpoint subtypes such as Henry's Law constant (Hc). Provide a reference in the Results Remarks. |
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Model Inputs: Half-Life |
Reaction half-lives (with units) required to run a level II, III or IV multimedia model. Provide a reference in the Results Remarks. |
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Model Inputs: Sediment Half-Life |
Reaction half-lives (with units) required to run a level II, III or IV multimedia model. Provide a reference in the Results Remarks. |
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Model Inputs: Soil Emissions |
A description of the Emissions used in the multimedia model, in kg/hr, for soil. |
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Model Inputs: Soil Half-Life |
Reaction half-lives (with units) required to run a level II, III or IV multimedia model. Provide a reference in the Results Remarks. |
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Model Inputs: Water Emissions |
A description of the Emissions used in the multimedia model, in kg/hr, for water. |
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Model Inputs: Water Half-Life |
Reaction half-lives (with units) required to run a level II, III or IV multimedia model. Provide a reference in the Results Remarks. |
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MTD Indicator |
Was Maximum Tolerated Dose (MTD) reached or exceeded? |
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Multimedia Model Level |
Level of multimedia (fugacity) model: I, II, or III |
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Negative Control Substance |
Identify the negative control used in the test. |
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Neoplastic Effect |
Describe the benign or malignant neoplasm. |
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Ninth Collective Chemical Index Name |
A standardized chemical name taken from the Ninth Collective Index for the CAS Number. |
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NOAEL/NOAEC Units |
Units of measure describing the NOAEL/NOAEC value. |
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NOEC |
Concentration that establishes the No Effect Observed Concentration (NOEC). |
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NOEC Concentration Type |
Indication of whether the No Effect Observed Concentration (NOEC) concentration is measured or nominal. |
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NOEC Value Description |
Mathematical symbol describing the No Effect Observed Concentration (NOEC) value. |
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NOELR |
Concentration that establishes the No Observed Effect Loading Rate (NOELR). |
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NOELR Basis for Concentration |
Indication of whether the No Observed Effect Loading Rate (NOELR) concentration is measured or nominal. |
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NOELR Exposure Duration |
Numeric value of the exposure duration of No Observed Effect Loading Rate (NOELR). |
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NOELR Exposure Units |
Exposure units of measure for No Observed Effect Loading Rate (NOELR). |
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NOELR Units |
Units of measure describing No Observed Effect Loading Rate (NOELR) value. |
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NOELR Upper Mean Value |
Upper concentration that establishes the No Observed Effect Loading Rate (NOELR). |
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NOELR Value Description |
Mathematical symbol describing the No Observed Effect Loading Rate (NOELR) value. |
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Number of Animals per Sex and Dose Group |
Textual description of the number of animals dosed per sex and dose group |
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Number of Deaths Females |
Number of female animals that died per dose/concentration. |
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Number of Deaths Males |
Number of male animals that died per dose/concentration. |
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Number of Deaths Total |
Number of animals that died per dose/concentration. The sum of male and female deaths if reported by gender, otherwise the total number of non-gender specific deaths. |
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Number of Organisms per Dose/Concentration |
The number of organisms dosed at each dose level of the study. |
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Organism Class |
The class of organisms (fish; aquatic invertebrates; etc) to which the test organism in an experimental bioaccumulation study belongs. |
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Other Endpoint Description |
Any additional pertinent information about a non-standard Endpoint. |
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Other Endpoint Name |
The name assigned by the submitter to the Endpoint when it is not one of the existing system defined Endpoint Names. |
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Other Method/Guideline |
The name of the Method or Guideline followed in performing the study if not indicated on the pick list. |
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Other Route of Administration |
How the chemical was administered to the test animals for non-standard methods. |
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Other Species |
Identify the species tested for Genetic Toxicity in vitro. |
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Other Species |
Identify the species tested when not available from the list of standard species. |
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Other Strain |
The mammalian strain tested, when not available from the list of standard strains. |
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Other Strain |
The mammalian strain tested, when not available from the list of standard strains for Genetic Toxicity in vitro. |
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Other Vehicle Name |
Chemical identity of a non-standard vehicle. |
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Overall Irritation Score |
Total of the individual irritation measures. |
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Percent Lipid |
Percentage relative to the wet weight of the test organism that is made up of lipids. |
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Percent Lost Advection -- Sediment |
The percentage lost by advection, derived from a level II or level III multimedia model, for the sediment compartment. |
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Percent Lost Advection -- Soil |
The percentage lost by advection, derived from a level II or level III multimedia model, for the soil compartment. |
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Percent Lost Advection -- Water |
The percentage lost by advection, derived from a level II or level III multimedia model, for the water compartment. |
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Percent Lost Reaction -- Sediment |
The percentage lost by reaction, derived from a level II or level III multimedia model, for the sediment compartment. |
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Percent Lost Reaction -- Soil |
The percentage lost by reaction, derived from a level II or level III multimedia model, for the soil compartment. |
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Percent Lost Reaction -- Water |
The percentage lost by reaction, derived from a level II or level III multimedia model, for the water compartment. |
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Percent Sensitized -- Negative Control |
Percentage of the test subjects sensitized by exposure to this dosage of the negative control substance. |
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Percent Sensitized -- Positive Control |
Percentage of the test subjects sensitized by exposure to this dosage of the positive control substance. |
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Percent Sensitized -- Test Substance |
Percentage of the test subjects sensitized by exposure to this dosage. |
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pH Value |
A measure of the acidity/alkalinity of the test medium |
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pH Value |
The pH value of the substance which represents the acidity or alkalinity of an aqueous solution; it is defined as the logarithm of the reciprocal of the hydrogen-ion concentration of a solution: pH = log10(1/[H+]). |
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pH Value |
The pH value of the substance which represents the acidity or alkalinity of an aqueous solution; it is defined as the logarithm of the reciprocal of the hydrogen-ion concentration of a solution: pH = log10(1/[H+]) for the endpoint Stability In Water. |
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pH Value Description |
The mathematical symbol to describe the measured/estimated value. |
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pH Value Upper Range |
The upper concentration value. |
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Photo (Light/Dark) |
The amount or intensity of light exposed to the subjects during control and experimental observation. |
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Photodegradation Medium |
The environmental medium to which the measured or estimated photodegradation result applies. |
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pKa - Protein Kinase |
The pKa or 'Dissociation Constant' is a measure of the strength of an acid or a base (the larger the pKa, the weaker the acid). The pKa allows you to determine the charge on a molecule at any given pH.
The propensity of a compound to donate a proton is measured as its acid ionization constant, or Ka. These Ka values cover a wide range of 1010 for the strongest acids such as sulfuric acid to 10-50 for the weakest acids such as methane. A more convenient scale of acidity is pKa, which is the negative logarithm of the Ka (pKa = -log Ka). |
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Population |
The population of test subjects in whom the referenced effect was observed. |
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Positive Control Substance |
Identify the positive control used in the test. |
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Positive, Negative and Solvent Control Substance(s) |
Indicate whether a positive, negative and solvent control substance was used in this study. If yes, please indicate the postive, negative and solvent control substance. Also describe the validity of the positive, negative and solvent control substance tests. |
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Post-Exposure Period Value Description |
The mathematical symbol to describe the measured/estimated value. |
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Post-Exposure/Depuration Period |
Observation period after last exposure to the test chemical. |
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Post-Exposure/Depuration Period Units |
Time units represented by the post-exposure period value. |
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Pre-Exposure Indicator |
An indicator for whether the microbial population in a study was deliberately pre-exposed to the test substance before the start of the test. Such a population may be acclimated or adapted to the test substance before the start of the test. |
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Pre-Exposure Procedure |
Procedure employed if any, to acclimate the microbial population by pre-exposing it to the test substance before the start of the test. |
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Pre-Mating Exposure Period for Females |
Number of days females dosed prior to mating. |
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Pre-Mating Exposure Period for Males |
Number of days males dosed prior to mating. |
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Preliminary Test |
If less than 10% of the test substance is degraded in 5 days at 50 C at pH 4, 7 or 9, the substance is assumed to have a half-life >1 year and is therefore considered stable to hydrolysis. |
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Preparation of Test Site |
Indicator whether test site was shaved or abraded. |
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Primary Irritation Index |
Note the Irritation Index score. |
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Program Flag |
Program that the submission is associated with. |
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Quantum Yield |
The reaction efficiency as calculated from the experimental measurements derived from a direct photolysis study. |
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Rate Constant |
Rate Constant value. |
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Rate Constant Units |
Units of measure describing the rate constant. |
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Rate Constant Value Description |
The mathematical symbol to describe the measured/estimated value. |
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Reliability |
Indication of the adequacy of data at the discretion of the person preparing the Robust Summary. |
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Reliability Remarks |
Comments about how the reliability of data was determined and other related remarks. If a numeric or other coded system, such as Klimisch Codes are used to denote reliability, identify and/or define the coding system. |
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Remarks |
Comments, discussions, or other related EPA remarks. |
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Result Type |
The type of kinetic expression represented by the test result or range, if applicable. |
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Results Remarks |
Sponsor provided additional descriptive text about the results of the study. |
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Route of Administration |
How the chemical was administered to the test animal. |
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Route of Challenge Exposure |
Indicate the route of challenge exposure. |
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Route of Induction |
Indicate the route of induction exposure. |
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Salinity |
The salt content in water, in parts per thousand, ranging from brackish (12 to 20 parts per thousand), to full strength sea water (33 to 38 parts per thousand). |
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Sensitization Score |
Numeric characterization of the Sensitization properties of the test substance at this dosage, ranging from 0 (no Sensitization potential) to 4. |
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Sensitizer |
The type of sensitizer/oxidant, if any, used in the study or assumed for the estimation. |
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Sensitizer Concentration |
The concentration of the sensitizer/oxidant (if any) used in an indirect photolysis study. |
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Sensitizer Concentration Units |
The units applicable to the sensitizer/oxidant concentration |
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Solvent Name |
The name of the solvent in which solubility is being tested. |
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Species |
Organism/cell culture used in the experiment. |
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Species or in Vitro System |
Organism/cell culture used in the experiment. |
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Sponsor Name |
The name of the individual company or consortium (i.e., two or more companies) making a commitment in the HPV Challenge Program to provide data for a chemical or category of chemicals
(e.g., Eastman Chemical Company). |
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Sponsored Chemical Result Type |
Indicator showing whether the test result represents a measured or an estimated value for the sponsored chemical. |
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Statistical Results |
Note statistical results, with appropriate p value and 95% Confidence Limit. |
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Strain |
Strain of the tested species for Genetic Toxicity in vitro. |
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Study Reference |
Identify reference(s) used to compile the summary by entering: author(s), year, title, laboratory name, laboratory report number, report date (if published, list journal name, volume, pages). |
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Study Type |
Type of experiment performed. |
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Submission Name |
The sponsor provided name associated with the submission. |
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Submitter's Name |
The name of the individual company or consortium formally providing test plan related information. |
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Surface Tension Concentration Units |
The unit of the concentration of the substance during the surface tension determination, preferably in mg/L. |
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Surface Tension Concentration Value |
The concentration of the substance during the determination. |
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Survival Rate Females |
Percentage of female animals that survived per dose/concentration. |
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Survival Rate Males |
Percentage of male animals that survived per dose/concentration. |
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Survival Rate Total |
Percentage of animals that survived per dose/concentration. |
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Systemic Toxicity |
The effect of a substance on body tissues after absortion into the bloodstream. |
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TCO2 |
The amount of carbon dioxide (CO2) that theoretically can be produced if the test substance is completely oxidized by microorganisms to CO2, water and the oxidation products of any other elements in the molecule. Calculated from the test substance's chemical structure; units mg CO2 per mg of test substance. |
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TCO2 Units |
The units of measure for CO2. |
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Temperature |
The temperature, preferably in ºC, used in the experimental determination of the Test Value or assumed in the model, if estimated. |
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Temperature Unit |
Unit of measure used for the given temperature. |
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Temperature Upper Range |
The upper concentration value. |
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Test Concentrations |
Is the concentration nominal or measured? |
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Test Conditions Remarks |
Additional comments describing the characteristics of the Test Conditions. |
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Test or Estimation Type |
Type of test or estimation performed. |
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Test Organism |
The test species or organism in an experimental bioaccumulation study. |
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Test Results |
A text description of the results of a test which are not captured as fielded data. |
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Test Substance ID |
The system generatedl ID of the chemical substance actually used to perform the test (sponsored or supporting). |
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Test Substance Purity |
The purity of the chemical used in the study or estimation. Not applicable to mixtures. Note if not available. |
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Test Substance Result Type |
Indicator showing whether the test result represents a measured or an estimated value for the test substance. |
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Test Type |
Type of test performed. |
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Test Value |
The numeric results as described in the Robust Summary. |
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Test Value Lower Range |
The measured or estimated lower numeric value of the range for the endpoint property or effect. |
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Test Value Units |
Unit of measure used for the given Test Value or range for the endpoint. |
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Test Value Upper Range |
The measured or estimated upper numeric value of the range for the endpoint property or effect. |
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Test Vessel |
An indicator specifying whether or not the vessel used to conduct the test was open or closed. |
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ThOD |
The amount of oxygen that theoretically can be consumed (ThOD = theoretical oxygen demand) if the test substance is completely oxidized by microorganisms. Calculated from the test substance's chemical structure; units mg O2 per mg of test substance. |
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ThOD Units |
The units of measure for ThOD. |
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Time in Days |
The elapsed test measurement time, expressed in days, when the result is obtained. |
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Tissue |
Indicator of the type of tissue pertaining to the experimental BCF data. |
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Tissues Sampled |
All bodily tissue types monitored by the study. |
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TOC |
Total Organic Carbon: The sum of dissolved organic carbon and particulate organic carbon or suspended organic carbon. |
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TOC Units |
Units of measure. |
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Tool |
Tool used to asses the irritation scores. |
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Total Volume Applied |
The total volume of active/test substance applied/instilled. |
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Total Volume Applied Units |
The unit of measure applied to the total value of active/test substance. |
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Type of Concentration |
An indicator signifying whether the value reported is a lethal concentration of an effective concentration. |
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Type of Coverage |
Indicator whether the test material was covered on the site applied to. |
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Type of Exposure |
Further definition of dose administration. |
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Type of Study |
Indicate the type of study regardless of whether it is already specified in the guideline, as this field can be used for query purposes. |
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Type of Test |
Names a specific genetic toxicity test type, which is a refinement of the genotoxicity study type. |
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Unable to Measure or Estimate Justification |
A short description of why neither a measured test result nor estimated value will be provided for this endpoint. |
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Upper Range |
Upper concentration that establishes the No Observed Effect Concentration (NOEC). |
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Uptake Rate |
A description of the rate constant for the uptake phase in an experimental bioaccumulation study. |
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Uptake/Depuration Rate Units |
Units of the uptake and depuration rate constants in an experimental bioaccumulation study. |
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UV/VIS Absorption Spectrum |
The ability of the test substance to absorb light as a function of wavelength. |
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Value Description |
A mathematical symbol to further describe the measured or estimated endpoint test value. |
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Vehicle Amount |
The amount of carrier/solvent used to deliver the test substance to the experimental system. |
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Vehicle Name |
Chemical identity of the vehicle |
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Vehicle Units |
Units of measure describing the Vehicle Amount. |
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Vehicle Used |
Indicator that a chemical was used to emulsify or mix the experimental chemical to enhance its solubility. |
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Water Hardness |
The concentration of calcium and magnesium ions in water. |
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Water Hardness Units |
The unit of measure for the concentration of calcium and magnesium ions in water. |
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Water Hardness Upper Range |
The upper concentration value. |
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Water Media Type |
Indicate whether Saltwater or Freshwater organisms are being studied. |
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Water Solubility Category |
A solubility description based on the water solubility results. |
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Year Study Performed |
If known, the sponsor provided year in which the test being described was conducted. |
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