In 1934 Fermi postulated a theory for weak interactions containing a dimensionful coupling with a size of roughly 250 GeV. Only now are we finally exploring this energy regime. What arises is an open question: supersymmetry and large extra dimensions are two possible scenarios. Meanwhile, other experiments will begin providing definitive information into the nature of neutrino masses and CP violation. In this paper, we explore features of possible theoretical scenarios, and study the phenomenological implications of various models addressing the open questions surrounding these issues.

The authors have presented the motivations in gathering doubly polarized data in the quasi-elastic, resonance and DIS domains. These data were used to calculate the extended GDH integral. The comparison of this quantity with the spin dependent forward Compton amplitude {bar S}{sub 1} is of particular importance for the unification of the two strong interaction descriptions (nucleonic/hadronic vs. partonic) because {bar S}{sub 1} is the first quantity theoretically calculable in the full Q{sup 2} domain of the strong interaction. Such a data taking was made possible because of three major technical achievements: (1) the beam of high duty cycle (100%), high current (up to 70 {micro}A) and high polarization (70%); (2) the {sup 3}He target of high density (above 10 atm) with a polarization of 35% and a length of 40 cm; and (3) the large acceptance (6 msr) and high resolution ({Delta}P/P {approx_equal} 10{sup {minus}4}) spectrometers. These features, available at Jefferson Lab, enabled them to achieve the highest luminosity in the world (about 10{sup 36} s{sup {minus}1} cm{sup {minus}2} with a current of 15 {micro}A) as far as polarized {sup 3}He targets are concerned. Consequently they were able to gather, in a rather short period of time (3 months), …

The study of the exocrine pancreatic acinar cell has been central to the development of models of many cellular processes, especially of protein transport and secretion. Traditional methods used to examine this system have provided a wealth of qualitative information from which mechanistic models have been inferred. However they have lacked the ability to make quantitative measurements, particularly of the distribution of protein in the cell, information critical for grounding of models in terms of magnitude and relative significance. This dissertation describes the development and application of new tools that were used to measure the protein content of the major intracellular compartments in the acinar cell, particularly the zymogen granule. Soft x-ray microscopy permits image formation with high resolution and contrast determined by the underlying protein content of tissue rather than staining avidity. A sample preparation method compatible with x-ray microscopy was developed and its properties evaluated. Automatic computerized methods were developed to acquire, calibrate, and analyze large volumes of x-ray microscopic images of exocrine pancreatic tissue sections. Statistics were compiled on the protein density of several organelles, and on the protein density, size, and spatial distribution of tens of thousands of zymogen granules. The results of these measurements, and …