Preserving the Futures of Young Offenders: A Proposal for Federal Juvenile Expungement Legislation

Picture a sixteen-year-old named Sam. Perhaps this person reminds you of yourself as a teenager. Now imagine that Sam has made a terrible mistake and is arrested for cocaine possession. Perhaps they got the drugs from another kid at school or from a family member. But now Sam has a federal criminal record, which is likely to stick with them for life. [...] This Note argues that federal courts should have the power to expunge juvenile records in cases like Sam’s. It advocates for legislation granting federal courts the power to expunge the criminal records of offenders who were under eighteen at the time of their offenses. Part I describes the history of federal juvenile expungement law, which leaves most juvenile offenders with no possibility of record relief. Part II describes the collateral consequences of a juvenile record and advocates for expungement as a means of reducing recidivism amongst juvenile offenders. Part III proposes a federal statutory framework for expungement of juvenile records. Finally, Part IV addresses likely counterarguments to statutorily guaranteeing expungement for a broader set of juvenile offenses. This abstract has been taken from the author\u27s introduction

Nanoscale Processes in the Environment: Nanobiogeochemistry of Microbe/Mineral Interactions

This project involves the application of nanoscience to the fields of fundamental and applied environmental geochemistry and biogeochemistry [1] Probing ligand-mineral interactions at the nanoscale: We have developed a chemical force microscopy (CFM) technique that probes the forces of interaction in aqueous solution between complex organic molecules and mineral surfaces in both distance and force nanospace. Using this method, previously unknown interactions between microbially produced siderophores and iron oxide mineral surfaces have been revealed Iron is a required nutrient for all organisms including bacteria, fungi and plants. The insoluble nature of iron in oxidizing, circumneutral aqueous environments, however, limits concentrations to levels well below the 10 -7 -10 -8 M required for bacterial growth. A response to this limitation is the extracellular release of low molecular weight biomolecules known as siderophores. With formation constants (K f ) on the order of 10 20-10 5 0 , the siderophore-Fe(III) complex is highly stable and thermodynamically favorable under environmental conditions. Indeed, much is known about siderophore interaction with soluble sources of iron; however, the largest source of iron in soils are solid forms, specifically, oxide minerals. Siderophores are known to release ferric iron from minerals, but the nature of the interaction of siderophores with the surface and the associated dissolution mechanism has been unknown. The CFM techniques used in this study have allowed us to directly measure the forces of interaction between siderophores and mineral surfaces for the first time A protein coupling technique was employed to covalently attach the siderophore azotobactin to a hydrazide terminated AFM tip. The activated tip was probed against two minerals: goethite (aFeOOH) and its isostructural Al-equivalent diaspore (a-AlOOH). Upon contact with each mineral surface, the adhesion force between azotobactin and the iron containing goethite was two to three times the value observed for the isostructural Al-equivalent diaspore. The relative force affinity for the iron containing mineral (versus aluminum) correlates with the difference between the aqueous complex formation constants estimated for azotobactin and Fe(III) (aq) (K f =10 2 8 ) and Al(III) (aq) (K f~1 0 1 6 ). Further, the adhesion force between azotobactin and goethite significantly decreases (4 nN to 2 nN) when small amounts of soluble iron (0.1 mM FeCl 3 ·6H 2 O) are added to the system at pH 3.5 suggesting a significant specific interaction between azotobactin's chelating groups and the mineral surface. Specifically, plateau features in the force data generated upon tip retraction fro

Nanoscale Processes in the Environment: Nanobiogeochemistry of Microbe/Mineral Interactions

This project involves the application of nanoscience to the fields of fundamental and applied environmental geochemistry and biogeochemistry [1] Probing ligand-mineral interactions at the nanoscale: We have developed a chemical force microscopy (CFM) technique that probes the forces of interaction in aqueous solution between complex organic molecules and mineral surfaces in both distance and force nanospace. Using this method, previously unknown interactions between microbially produced siderophores and iron oxide mineral surfaces have been revealed Iron is a required nutrient for all organisms including bacteria, fungi and plants. The insoluble nature of iron in oxidizing, circumneutral aqueous environments, however, limits concentrations to levels well below the 10 -7 -10 -8 M required for bacterial growth. A response to this limitation is the extracellular release of low molecular weight biomolecules known as siderophores. With formation constants (K f ) on the order of 10 20-10 5 0 , the siderophore-Fe(III) complex is highly stable and thermodynamically favorable under environmental conditions. Indeed, much is known about siderophore interaction with soluble sources of iron; however, the largest source of iron in soils are solid forms, specifically, oxide minerals. Siderophores are known to release ferric iron from minerals, but the nature of the interaction of siderophores with the surface and the associated dissolution mechanism has been unknown. The CFM techniques used in this study have allowed us to directly measure the forces of interaction between siderophores and mineral surfaces for the first time A protein coupling technique was employed to covalently attach the siderophore azotobactin to a hydrazide terminated AFM tip. The activated tip was probed against two minerals: goethite (aFeOOH) and its isostructural Al-equivalent diaspore (a-AlOOH). Upon contact with each mineral surface, the adhesion force between azotobactin and the iron containing goethite was two to three times the value observed for the isostructural Al-equivalent diaspore. The relative force affinity for the iron containing mineral (versus aluminum) correlates with the difference between the aqueous complex formation constants estimated for azotobactin and Fe(III) (aq) (K f =10 2 8 ) and Al(III) (aq) (K f~1 0 1 6 ). Further, the adhesion force between azotobactin and goethite significantly decreases (4 nN to 2 nN) when small amounts of soluble iron (0.1 mM FeCl 3 ·6H 2 O) are added to the system at pH 3.5 suggesting a significant specific interaction between azotobactin's chelating groups and the mineral surface. Specifically, plateau features in the force data generated upon tip retraction fro