| QUERY NAME: Biodegradation Data, TABLE NAME: V_FATE_SIDS_4_EZ |
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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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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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Category Chemical 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 Name |
The ninth collective index name of the category chemical. |
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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 Units |
The unit of the concentration of the substance in water during the pH determination, preferably in mg/L. |
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Concentration Value |
Concentration that causes the indicated effect on the indicated percentage of the test subjects. |
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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 Substance Remarks |
Information on the control substance, if any, including name, initial concentration, and degradation results. |
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Deviations from Test Guideline Flag |
Indication that a study contains deviations from the standard test protocol. |
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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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Half-Life |
Degration half-life as described in the study. |
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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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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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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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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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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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Program Flag |
Program that the submission is associated with. |
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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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Results Remarks |
Sponsor provided additional descriptive text about the results of the study. |
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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 CAS Number |
A standardized number assigned by the Chemical Abstracts Service (CAS) to identify a chemical or category (e.g., 10595-60-5). |
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Sponsored Chemical Name |
The ninth collective index name of the sponsored chemical or category. |
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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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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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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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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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Test Conditions Remarks |
Additional comments describing the characteristics of the Test Conditions. |
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Test Substance 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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Test Substance Chemical Name |
The ninth collective index name of the test substance. |
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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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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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Year Study Performed |
If known, the sponsor provided year in which the test being described was conducted. |