Source recording

Observe and compare the color changes that take place in the drops of indicator of different sizes and distances from the pollution source. Record your observations every 15 seconds. 

No matter what topic you choose or what subject matter you ultimately investigate, the process is the same. You need to take your time, gather good and reliable sources, record your information carefully, and write it in a lively, informative way. It is also important to enjoy what you are writing about and to have passion for your subject matter. As you begin to choose a subject, you can use some of the very broad topic areas suggested here or you can research others. Be persistent as you conduct your research and try to get as many different opinions from as many different sources as you can in order to come to your own conclusions. Just remember to let your writing and evidence speak for itself. If you do, your passion and dedication to your subject matter will be evident. 

For hardware components, documentation detailing the performance capability, compatibility, and assembly must also be available, along with manufacturer model and version numbers and the serial numbers where available. Preassembled hardware that is sealed does not have to be disassembled if this breaks the warranty. In such cases the details may be taken from the hardware specifi-cation/data sheet and the source recorded. 

Verify Sample Data and System Parameters, i.e., Check against Source Records to Ensure Accuracy of Data within the RDB Involves Checking of Data Loaded Manually or via Automated Upload from Legacy Systems Software Backups and Restoration of Data Training Records of Users Routine Maintenance/Calibration Routines Provision of Service Level Agreements (SLAs)... 

Weyhenmeyer C. E., Burns S. J., Waber H. N., Aesbach-Hertig W., Kipfer R., Loosli H. H., and Matter A. (2000) Cool glacial temperatures and changes in moisture source recorded in Oman groundwaters. Science 287, 842- 845. 

One reference is given, if known, for each type of source recorded. Where many references are available, a reference has been selected which either gives the full details of the sugar or reviews all of the earlier literature. References not given in the preceding text are listed at the end of the Tables. 

It is very likely that incomplete or missing records would prevent the verification of data integrity. Source records should be complete to facilitate an understanding of actual study conduct for critical phases of method development, method validation, and subject sample analysis. The records should confirm whether the testing was conducted in an appropriate manner, with well-designed and optimally controlled experiments. The documentation of actual laboratory events should demonstrate that the quantitative measures are suitable to achieve the objectives of the clinical or nonclinical protocol. The records should confirm that the reported results accurately reflect the actual concentration of the analyte in the biological matrix. It should be noted that the failure to adequately document critical details of study conduct has resulted in rejection of bioanalytical data for regulatory purposes. 

Data reported from accepted runs must include the results of all validation samples. Exclusion of individual data points from accepted runs because the results exceed the predefined acceptance limit is not acceptable. Along these lines, complete reporting of validation experiments includes a discussion of failed experiments, in conjunction with an explanation for rej ecting the data. When experiments are rejected, the basis for the rejection should be documented in the source record (e.g., spilled tubes, preparation error, and instrument failure) and disclosed in the validation report. The rejection or exclusion of failing validation results without justification is not acceptable and does not provide a forthright description of the true assay performance. 

Regardless of the format of the source record (e.g., worksheet or notebook, paper or electronic), essential documentation must include all information critical to study reconstruction. All details must be recorded contemporaneously with the actual study... 

Sample Accountability Source records should identify the source and number of subject samples2 received by the bioanalytical laboratory, the date of sample receipt, the condition of the samples upon receipt, and the storage location (e.g., equipment identifiers) and temperature conditions for the duration of storage. Courier receipts of the sample shipment should be maintained in the study file. 

Reference Standard and Critical Reagents Source records should document lot numbers, date of receipt or preparation (as appropriate), the identity, purity, and stability at the time of use, expiration date (as applicable), storage location (e.g., equipment identifiers), and temperature conditions. 

Continuity with the later history of tvaidan is also shown by the use of gold for casting vessels. Both Taiqing and other tvaidan sources record this use of alchemical gold. The received version of the Scripture of the Golden Liquor says ... 

Verify sample data and system parameters against source records to ensure the accuracy of data within the RDB (involves checking of data loaded manually or via automated upload from legacy systems) ... 

All the currently available information for the 100-N Area sources is discussed below. No data concerning unplanned releases are available from before 1973, but releases probably did occur. All historical records are being reviewed as part of the source record compilation task, as discussed in Chapter 5 of the RCRA Facility Investigation/Corrective Measures Study Uork Plan for the lOO-HR-l Operable Unit, Hanford Site, Richland, Washington (DOE-RL 1990). If additional information becomes available for any of the sources or unplanned releases, it will be incorporated in the RFI/CNS as appropriate. At present, no cleanup Invels have been negotiated for the unplanned releases. 

With respect to the source, record the location of the operator at various times in the shift. 

Carlyle, in a survey of nineteenth century British documentary sources, records that various preparations of lead(ll,lV) oxide... 

The source records of most immediate value are those which are already available routinely in machine-readable form. In Canada, these include (a) the vital records of marriages, births, and deaths, (b) certain specialized disease registers such as those of handicapping conditions and cancer, (c) the discharge summaries from a universal scheme of hospital insurance, and potentially (d) the records from the recently introduced universal medical care insurance. Experience has been gained with linking into individual and family histories all but the last of these four categories of records. 

In addition to regular maintenance and updating, source records should be updated whenever a change (e.g. of location) occurs and, in particular, when sources are transferred. The records for radioactive sources should include the following particulars ... 

Following decommissioning and termination of a hcence to use sources, records of sources that have been transferred should be retained for a suitable period as agreed by the regulatory body. 

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