An unplanned release of tritiated water occurred at K reactor on SRS between 22-December and 25-December 1991. This water moved down through the effluent canal, Pen Branch, Steel Creek and finally to the Savannah River. Samples were collected in the Savannah River and associated waterways over a period of a month. The Environmental Technology Section (ETS) of the Savannah River Laboratory performed liquid scintillation analyses to monitor the passage of the tritiated water from SRS to the Atlantic Ocean.

This report gives a self-consistent conceptual design for the ``final focusing`` beam optics and analysis spectrometer optics for the Grating Acceleration Experiment, the Inverse Cerenkov Acceleration Experiment, and the Nonlinear Compton Scattering Experiment. The introductory section describes the basic principles and constraints involved in the overall design. The next two sections give second order TRANSPORT calculations for the final focus system and the spectrometer system for the three experiments. The fourth section presents Monte Carlo simulations of the expected x-y distributions for the spectrometer detector for the three experiments. Appendices A and B contains further details about the assumptions used in the Monte Carlo simulations. Appendix C contains the working drawings used for determining distances on the experimental floor.

This report gives a self-consistent conceptual design for the final focusing'' beam optics and analysis spectrometer optics for the Grating Acceleration Experiment, the Inverse Cerenkov Acceleration Experiment, and the Nonlinear Compton Scattering Experiment. The introductory section describes the basic principles and constraints involved in the overall design. The next two sections give second order TRANSPORT calculations for the final focus system and the spectrometer system for the three experiments. The fourth section presents Monte Carlo simulations of the expected x-y distributions for the spectrometer detector for the three experiments. Appendices A and B contains further details about the assumptions used in the Monte Carlo simulations. Appendix C contains the working drawings used for determining distances on the experimental floor.

This paper describes an implementation of hardware neural networks using highly linear thin-film resistor technology and an 8-bit binary weight circuit to produce customizable artificial neural network chips and systems. These neural networks are programmed using precision laser cutting and deposition. The fast turnaround of laser-based customization allows us to explore different neural network architectures and to rapidly program the synaptic weights. Our customizable chip allows us to expand an artificial network laterally and vertically. This flexibility permits us to build very large neural network systems.

Development of a computer system for access to distributed genome mapping data is continuing. This effort is to develop software which accesses multiple databases and retrieves data which contain information useful for accelerating mapping human chromosomes. For example, the molecular sequence databases (GenBank, EMBL Data Library, PIR, SwissProt) which contain data required for the development of oligonucleotides for probing DNA as well as for extracting data for primer pair development for PCR-based methods. It is also to develop software which qualitatively integrates the following mapping data: (1) markers regionally localized using cytogenetic methods, (2) polymorphic markers ordered by genetic linkage analysis, (3) clones ordered by various ``finger-printing`` methods, (4) fragments ordered by long-range restriction mapping, (5) single genomic fragments or clones that have STSs assigned to them, (6) nucleotide sequences, (7) the associated metadata such as the submitting investigator`s name, location, etc; the source organism; the chromosome the element is from; the chromosomal location is whatever detail is available.

Development of a computer system for access to distributed genome mapping data is continuing. This effort is to develop software which accesses multiple databases and retrieves data which contain information useful for accelerating mapping human chromosomes. For example, the molecular sequence databases (GenBank, EMBL Data Library, PIR, SwissProt) which contain data required for the development of oligonucleotides for probing DNA as well as for extracting data for primer pair development for PCR-based methods. It is also to develop software which qualitatively integrates the following mapping data: (1) markers regionally localized using cytogenetic methods, (2) polymorphic markers ordered by genetic linkage analysis, (3) clones ordered by various finger-printing'' methods, (4) fragments ordered by long-range restriction mapping, (5) single genomic fragments or clones that have STSs assigned to them, (6) nucleotide sequences, (7) the associated metadata such as the submitting investigator's name, location, etc; the source organism; the chromosome the element is from; the chromosomal location is whatever detail is available.