In 2011 the local clinical commissioning group introduced a policy restricting funding for elective hernia repairs. Anecdotally, it was felt that this resulted in an increased number of emergency hernia repairs in our trust. Our primary objective was to assess whether this was actually the case. Our secondary objective was to quantify the risks of non-elective hernia repair.

Propagation of ultrashort broadband pulses through a multiply scattering media result in complex spatio-temporal speckle pattern. Using spectral pulse shaping, we demonstrate the spatially localized temporal recompression of the output speckle to the Fourier-limit duration.

Propagation of an ultrashort laser pulse through a scattering medium forms a speckle pattern in the spatio-spectral domain. This pattern arises from the contribution of the randomly phased electric fields associated with the different optical paths in the medium. Studying the speckle field provides information both about the diffusion properties of the medium and spatio-temporal control of the transmitted or scattered light. In this paper a spatio-temporal characterization of the near-IR 120 fs pulse transmitted through a thick strongly scattering medium is undertaken using spatially and spectrally resolved Fourier-transform interferometry (SSI). The advantages of SSI over conventional pulse measurement techniques are discussed. The diffusion properties of the scattering samples are measured. We find a good agreement between our measured diffusion properties and those obtained using another method. The implications of this measurement technique are discussed. (C) 2012 Optical Society of America

The complexity of ultrafast molecular photoionization presents an obstacle to the modeling of pump-probe experiments. Here, a simple optimized model of atomic rubidium is combined with a molecular dynamics model to predict quantitatively the results of a pump-probe experiment in which long-range rubidium dimers are first excited, then ionized after a variable delay. The method is illustrated by the outline of two proposed feasible experiments and the calculation of their outcomes. Both of these proposals use Feshbach {sup 87}Rb{sub 2} molecules. We show that long-range molecular pump-probe experiments should observe spin-orbit precession given a suitable pump pulse, and that the associated high-frequency beat signal in the ionization probability decays after a few tens of picoseconds. If the molecule was to be excited to only a single fine-structure state, then a low-frequency oscillation in the internuclear separation would be detectable through the time-dependent ionization cross section, giving a mechanism that would enable observation of coherent vibrational motion in this molecule.

A comprehensive experimental analysis of spatio-temporal coupling effects inherent to the acousto-optic programmable dispersive filter (AOPDF) is presented. Phase and amplitude measurements of the AOPDF transfer function are performed using spatially and spectrally resolved interferometry. Spatio-temporal and spatio-spectral coupling effects are presented for a range of shaped pulses that are commonly used in quantum control experiments. These effects are shown to be attributable to a single mechanism: a group-delay--dependent displacement of the shaped pulse. The physical mechanism is explained and excellent quantitative agreement between the measured and calculated coupling speed is obtained. The implications for quantum control experiments are discussed.

Pulses of light propagating through multiply scattering media undergo complex spatial and temporal distortions to form the familiar speckle pattern. There is much current interest in both the fundamental properties of speckles and the challenge of spatially and temporally refocusing behind scattering media. Here we report on the spatially and temporally resolved measurement of a speckle field produced by the propagation of an ultrafast optical pulse through a thick strongly scattering medium. By shaping the temporal profile of the pulse using a spectral phase filter, we demonstrate the spatially localized temporal recompression of the output speckle to the Fourier-limit duration, offering an optical analogue to time-reversal experiments in the acoustic regime. This approach shows that a multiply scattering medium can be put to profit for light manipulation at the femtosecond scale, and has a diverse range of potential applications that includes quantum control, biological imaging and photonics.

The dynamics of the excited state during the photoassociation of cold molecules from cold rubidium atoms is studied in a series of pump-probe experiments. Dipole transitions similar to those of the atoms are observed in the molecular signal. While such behaviour is characteristic of the long-range molecules, the photoassociation of bound molecules is confirmed in additional experiments. The pump-probe signal observed on a 250 ps time scale did not, however, reveal wavepacket oscillations predicted by theory. This result is discussed using numerical simulations of photoassociation and a modification to the current experiments that could lead to the detection of wavepacket dynamics is suggested.

The expansion of laser cooling capabilities from the atomic to the molecular regime has proven challenging due to the lack of availability of an equivalent closed-loop cooling cycle within the rich molecular internal energy level structure. An enticing solution is the application of ultrafast coherent control techniques to ultracold molecule generation. Unlike continuous-wave photoassociation techniques, the use of broadband 'pump' and 'dump' pulses offers the opportunity to access deeply bound vibrational states. Unlike alternative vibrational cooling strategies such as stimulated Raman adiabatic passage or incoherent optical cycling, this approach preserves coherence and does not require a detailed knowledge of the system spectroscopy. We report on pump-probe experiments investigating the dynamical evolution of bound excited-state Rb2 dimers after photoassociation. Learning about these dynamics is an important step towards efficient pump-dump formation of deeply bound ground-state molecules. Based on a spectroscopic measurement of the initial state occupied by the interacting atom pairs, we provide evidence that background triplet molecules preassociated by the trapping lasers, additionally to unbound scattering atom pairs, may play an important role in photoassociation dynamics.

Received 8 September 2009DOI:https://doi.org/10.1103/PhysRevA.80.039901©2009 American Physical Society

Calculations relating to two experiments that demonstrate coherent control of preformed rubidium-85 molecules in a magneto-optical trap using ultrafast laser pulses are presented. The two experiments are a step toward the stabilization of ultracold rubidium dimers using ultrafast lasers. In the first experiment, it is shown that preassociated molecules in an incoherent mixture of states can be made to oscillate coherently using a single ultrafast pulse. A mechanism that can transfer molecular population to more deeply bound vibrational levels is used in the second. Optimal parameters of the control pulse are presented for the application of the mechanism to molecules in a magneto-optical trap. The calculations make use of an experimental determination of the initial state of molecules photoassociated by the trapping lasers in the magneto-optical trap and use shaped pulses consistent with a standard ultrafast laser system. The experiment's purpose is to demonstrate and evaluate the use of ultrafast shaped pulses to manipulate ultracold rubidium dimers with a view to the eventual stabilization of the molecules.

The success in cooling and trapping atomic gases to the point of quantum degeneracy has prompted a quest to create ultracold molecular gases. Atomic techniques can not be applied to molecular gases due to their richer internal structure. Effort has been applied to converting ultracold atoms to ultracold molecules. This should be done without the use of spontaneous decay to attain the coldest possible temperatures. A scheme has been suggested, in the works of Koch et al. (2006) and Mur-Petit et al. (2007) that mandates the excitation of preformed loosely bound atom pairs which then oscillate coherently and may be deexcited back to less vibrationally excited states. For this to work, knowledge of the behaviour of the excited wavepacket in a realistic experimental setting is essential. In this paper, the authors report on the calculation of a time-dependent wavefunction starting from a measured initial state under the influence of a measured excitation pulse.