In Re R.R.N.: Redefining Caretaker for North Carolina Child Protective Services

In 2015, the North Carolina Supreme Court interpreted for the first time the definition of caretaker as provided in the State\u27s Juvenile Code. The court narrowed the definition, providing that the statutory language an adult relative entrusted with the juvenile\u27s care means an adult relative who has a significant degree of parental-type responsibility for the child. The court\u27s interpretation has made caretaker equivalent to in loco parentis, which results in a heightened standard that likely was not intended by the legislature. This Comment discusses the far-reaching effects of the court\u27s decision on North Carolina\u27s child welfare services, law enforcement, and practitioners who represent or interact with these agencies. This Comment also explores solutions to bridge the widening gap in service provision to the families and children of North Carolina

High Resolution Spectrometry of Leaf and Canopy Chemistry for Biochemical Cycling

High-resolution laboratory spectrophotometer and Airborne Imaging Spectrometer (AIS) data were used to analyze forest leaf and canopy chemistry. Fundamental stretching frequencies of organic bonds in the visible, near infrared and short-wave infrared are indicative of concentrations and total content of nitrogen, phosphorous, starch and sugar. Laboratory spectrophotometer measurements showed very strong negative correlations with nitrogen (measured using wet chemistry) in the visible wavelengths. Strong correlations with green wet canopy weight in the atmospheric water absorption windows were observed in the AIS data. A fairly strong negative correlation between the AIS data at 1500 nm and total nitrogen and nitrogen concentration was evident. This relationship corresponds very closely to protein absorption features near 1500 nm

Switched wave packets: A route to nonperturbative quantum control

The dynamic Stark effect due to a strong nonresonant but nonionizing laser field provides a route to quantum control via the creation of novel superposition states. We consider the creation of a field-free "switched" wave packet through adiabatic turn-on and sudden turn-off of a strong dynamic Stark interaction. There are two limiting cases for such wave packets. The first is a Raman-type coupling, illustrated by the creation of field-free molecular axis alignment. An experimental demonstration is given. The second case is that of dipole-type coupling, illustrated by the creation of charge localization in an array of quantum wells

Observation of high-order quantum resonances in the kicked rotor

Quantum resonances in the kicked rotor are characterized by a dramatically increased energy absorption rate, in stark contrast to the momentum localization generally observed. These resonances occur when the scaled Planck's constant hbar=(r/s)*4pi, for any integers r and s. However only the hbar=r*2pi resonances are easily observable. We have observed high-order quantum resonances (s>2) utilizing a sample of low temperature, non-condensed atoms and a pulsed optical standing wave. Resonances are observed for hbar=(r/16)*4pi r=2-6. Quantum numerical simulations suggest that our observation of high-order resonances indicates a larger coherence length than expected from an initially thermal atomic sample

Controlled supercontinuum generation for optimal pulse compression:a time-warp analysis of nonlinear propagation of ultra-broad-band pulses

We describe the virtues of the pump-probe approach for controlled supercontinuum generation in nonlinear media, using the example of pulse compression by cross-phase modulation in dielectrics. Optimization of a strong (pump) pulse and a weak (probe) pulse at the input into the medium opens the route to effective control of the supercontinuum phases at the output. We present an approximate semi-analytical approach which describes nonlinear transformation of the input pulse into the output pulse. It shows how the input and the output chirps are connected via a time-warp transformation which is almost independent of the shape of the probe pulse. We then show how this transformation can be used to optimize the supercontinuum generation to produce nearly single-cycle pulses tunable from mid-infrared to ultraviolet

Coherent Control and Entanglement in the Attosecond Electron Recollision Dissociation of D2+

We examine the attosecond electron recollision dissociation of D2+ recently demonstrated experimentally [H. Niikura et al., Nature (London) 421, 826 (2003)] from a coherent control perspective. In this process, a strong laser field incident on D2 ionizes an electron, accelerates the electron in the laser field to eV energies, and then drives the electron to recollide with the parent ion, causing D2+ dissociation. A number of results are demonstrated. First, a full dimensional Strong Field Approximation (SFA) model is constructed and shown to be in agreement with the original experiment. This is then used to rigorously demonstrate that the experiment is an example of coherent pump-dump control. Second, extensions to bichromatic coherent control are proposed by considering dissociative recollision of molecules prepared in a coherent superposition of vibrational states. Third, by comparing the results to similar scenarios involving field-free attosecond scattering of independently prepared D2+ and electron wave packets, recollision dissociation is shown to provide an example of wave-packet coherent control of reactive scattering. Fourth, this analysis makes clear that it is the temporal correlations between the continuum electron and D2+ wave packet, and not entanglement, that are crucial for the sub-femtosecond probing resolution demonstrated in the experiment. This result clarifies some misconceptions regarding the importance of entanglement in the recollision probing of D2+. Finally, signatures of entanglement between the recollision electron and the atomic fragments, detectable via coincidence measurements, are identified

Alignment dependent enhancement of the photo-electron cutoff for multi-photon ionization of molecules

The multiphoton ionization rate of molecules depends on the alignment of the molecular axis with respect to the ionizing laser polarization. By studying molecular frame photo-electron angular distributions from N$_2$, O$_2$ and benzene, we illustrate how the angle-dependent ionization rate affects the photo-electron cutoff energy. We find alignment can enhance the high energy cutoff of the photo-electron spectrum when probing along a nodal plane or when ionization is otherwise suppressed. This is supported by calculations using a tunneling model with a single ion state.Comment: 4 pages, 4 figure

Influence of asymmetry and nodal planes on high-harmonic generation in heteronuclear molecules

The relation between high-harmonic spectra and the geometry of the molecular orbitals in position and momentum space is investigated. In particular we choose two isoelectronic pairs of homonuclear and heteronuclear molecules, such that the highest occupied molecular orbital of the former exhibit at least one nodal plane. The imprint of such planes is a strong suppression in the harmonic spectra, for particular alignment angles. We are able to identify two distinct types of nodal planes. If the nodal planes are determined by the atomic wavefunctions only, the angle for which the yield is suppressed will remain the same for both types of molecules. In contrast, if they are determined by the linear combination of atomic orbitals at different centers in the molecule, there will be a shift in the angle at which the suppression occurs for the heteronuclear molecules, with regard to their homonuclear counterpart. This shows that, in principle, molecular imaging, which uses the homonuclear molecule as a reference and enables one to observe the wavefunction distortions in its heteronuclear counterpart, is possible.Comment: 14 pages, 7 figures. Figs. 3, 5 and 6 have been simplified in order to comply with the arXiv size requirement

Remote Sensing of Coniferous Forest Leaf Area

Many important ecological questions concern ecosystem processes occurring over large areas. However, our understanding o f ecosystem functions is derived primarily from research executed on small, intensively studied sites, and extrapolation to large areas is difficult