Patterns of sea otter haul-out behavior of California tidal estuary in relation to environmental variables

This study provides the first in depth assessment of Sea Otter haul-out patterns in Elkhorn Slough, California and their relationship to environmental variables. Seasonal and daily water and air temperature fluctuations are a good predictor of Sea Otter haul-out patterns but are affected by the availability of haul-out sites at different tide levels. The cost effectiveness of this choice may be maximal at night because of lack of human disturbance. Southern Sea Otters (Enhydra lutris nereis) were observed during 50 bimonthly 24-h periods between August 2007 and July 2009 (n = 1187 h) from a shore-based observation site located above a non-territorial male resting area on the north side of Moss Landing Harbor. We counted the number of Sea Otters in the area (both in the water and on land) at 30-min intervals. We also recorded tide height, and air and water temperature. Thirty-minute counts averaged 42 Sea Otters using the area (land and water) during the day and 66 at night. The average number of Sea Otters hauled out in the study area during the same haul-out event was 22, and the maximum number was 93. Sea Otters were observed hauled out on 70% of the days surveyed, and the proportion of Sea Otters hauled out was significantly higher at night. Higher numbers of Sea Otters on land was significantly correlated with lower air and water temperature, and with mid-range tide-heights. We speculate that haul-out behavior could play an important role in energy conservation; however, human-related traffic patterns in the area may negatively affect this energy conservation strategy

Enhanced selectivity towards O2 and H2 dissociation on ultrathin Cu films on Ru(0001)

The following article appeared in Journal of Chemical Physics 137.7 (2012): 074706 and may be found at http://scitation.aip.org/content/aip/journal/jcp/137/7/10.1063/1.4746942The reactivity of Cu monolayer (ML) and bilayer films grown on Ru(0001) towards O2 and H2 has been investigated. O2 initial sticking coefficients were determined using the King and Wells method in the incident energy range 40-450 meV, and compared to the corresponding values measured on clean Ru(0001) and Cu(111) surfaces. A relative large O2 sticking coefficient (∼0.5-0.8) was measured for 1 ML Cu and even 2 ML Cu/Ru(0001). At low incident energies, this is one order of magnitude larger than the value observed on Cu(111). In contrast, the corresponding reactivity to H2 was near zero on both Cu monolayer and bilayer films, for incident energies up to 175 meV. Water adsorption on 2 ML Cu/Ru(0001) was found to behave quite differently than on the Ru(0001) and Cu(111) surfaces. Our study shows that Cu/Ru(0001) is a highly selective system, which presents a quite different chemical reactivity towards different species in the same range of collision energiesThe authors gratefully acknowledge the financial support by the Ministerio de Educación y Ciencia through projects CONSOLIDER-INGENIO 2010 on Molecular Nanoscience and FIS2007-61114 and Comunidad de Madrid through the program NANOMAGNET S-0505/MAT/0194. P.P. acknowledges support through the Marie Curie AMAROUT EU action and the Spanish MICINN “Juan de la Cierva” contrac

Velocity-selected molecular pulses produced by an electric guide

Electrostatic velocity filtering is a technique for the production of continuous guided beams of slow polar molecules from a thermal gas. We extended this technique to produce pulses of slow molecules with a narrow velocity distribution around a tunable velocity. The pulses are generated by sequentially switching the voltages on adjacent segments of an electric quadrupole guide synchronously with the molecules propagating at the desired velocity. This technique is demonstrated for deuterated ammonia (ND$_{3}$), delivering pulses with a velocity in the range of $20-100\,\rm{m/s}$ and a relative velocity spread of $(16\pm 2)\,$ at FWHM. At velocities around $60\,\rm{m/s}$, the pulses contain up to $10^6$ molecules each. The data are well reproduced by Monte-Carlo simulations, which provide useful insight into the mechanisms of velocity selection.Comment: 8 pages, 6 figure

Photoionization Broadening of the 1S-2S Transition in a Beam of Atomic Hydrogen

We consider the excitation dynamics of the two-photon \sts transition in a beam of atomic hydrogen by 243 nm laser radiation. Specifically, we study the impact of ionization damping on the transition line shape, caused by the possibility of ionization of the 2S level by the same laser field. Using a Monte-Carlo simulation, we calculate the line shape of the \sts transition for the experimental geometry used in the two latest absolute frequency measurements (M. Niering {\it et al.}, PRL 84, 5496 (2000) and M. Fischer {\it et al.}, PRL 92, 230802 (2004)). The calculated line shift and line width are in excellent agreement with the experimentally observed values. From this comparison we can verify the values of the dynamic Stark shift coefficient for the \sts transition for the first time on a level of 15%. We show that the ionization modifies the velocity distribution of the metastable atoms, the line shape of the \sts transition, and has an influence on the derivation of its absolute frequency.Comment: 10 pages, 5 figure

An ellipsoidal mirror for focusing neutral atomic and molecular beams

Manipulation of atomic and molecular beams is essential to atom optics applications including atom lasers, atom lithography, atom interferometry and neutral atom microscopy. The manipulation of charge-neutral beams of limited polarizability, spin or excitation states remains problematic, but may be overcome by the development of novel diffractive or reflective optical elements. In this paper, we present the first experimental demonstration of atom focusing using an ellipsoidal mirror. The ellipsoidal mirror enables stigmatic off-axis focusing for the first time and we demonstrate focusing of a beam of neutral, ground-state helium atoms down to an approximately circular spot, (26.8±0.5) μm×(31.4±0.8) μm in size. The spot area is two orders of magnitude smaller than previous reflective focusing of atomic beams and is a critical milestone towards the construction of a high-intensity scanning helium microscope

An ellipsoidal mirror for focusing neutral atomic and molecular beams

Manipulation of atomic and molecular beams is essential to atom optics applications including atom lasers, atom lithography, atom interferometry and neutral atom microscopy. The manipulation of charge-neutral beams of limited polarizability, spin or excitation states remains problematic, but may be overcome by the development of novel diffractive or reflective optical elements. In this paper, we present the first experimental demonstration of atom focusing using an ellipsoidal mirror. The ellipsoidal mirror enables stigmatic off-axis focusing for the first time and we demonstrate focusing of a beam of neutral, ground-state helium atoms down to an approximately circular spot, (26.8±0.5) μm×(31.4±0.8) μm in size. The spot area is two orders of magnitude smaller than previous reflective focusing of atomic beams and is a critical milestone towards the construction of a high-intensity scanning helium microscope

Collision Dynamics and Solvation of Water Molecules in a Liquid Methanol Film

Environmental molecular beam experiments are used to examine water interactions with liquid methanol films at temperatures from 170 K to 190 K. We find that water molecules with 0.32 eV incident kinetic energy are efficiently trapped by the liquid methanol. The scattering process is characterized by an efficient loss of energy to surface modes with a minor component of the incident beam that is inelastically scattered. Thermal desorption of water molecules has a well characterized Arrhenius form with an activation energy of 0.47{\pm}0.11 eV and pre-exponential factor of 4.6 {\times} 10^(15{\pm}3) s^(-1). We also observe a temperature dependent incorporation of incident water into the methanol layer. The implication for fundamental studies and environmental applications is that even an alcohol as simple as methanol can exhibit complex and temperature dependent surfactant behavior.Comment: 8 pages, 5 figure

Is it possible to detect gravitational waves with atom interferometers?

We investigate the possibility to use atom interferometers to detect gravitational waves. We discuss the interaction of gravitational waves with an atom interferometer and analyze possible schemes

Atom Interferometers

Interference with atomic and molecular matter waves is a rich branch of atomic physics and quantum optics. It started with atom diffraction from crystal surfaces and the separated oscillatory fields technique used in atomic clocks. Atom interferometry is now reaching maturity as a powerful art with many applications in modern science. In this review we first describe the basic tools for coherent atom optics including diffraction by nanostructures and laser light, three-grating interferometers, and double wells on AtomChips. Then we review scientific advances in a broad range of fields that have resulted from the application of atom interferometers. These are grouped in three categories: (1) fundamental quantum science, (2) precision metrology and (3) atomic and molecular physics. Although some experiments with Bose Einstein condensates are included, the focus of the review is on linear matter wave optics, i.e. phenomena where each single atom interferes with itself.Comment: submitted to Reviews of Modern Physic

Lattice model of gas condensation within nanopores

We explore the thermodynamic behavior of gases adsorbed within a nanopore. The theoretical description employs a simple lattice gas model, with two species of site, expected to describe various regimes of adsorption and condensation behavior. The model includes four hypothetical phases: a cylindrical shell phase (S), in which the sites close to the cylindrical wall are occupied, an axial phase (A), in which sites along the cylinder's axis are occupied, a full phase (F), in which all sites are occupied, and an empty phase (E). We obtain exact results at T=0 for the phase behavior, which is a function of the interactions present in any specific problem. We obtain the corresponding results at finite T from mean field theory. Finally, we examine the model's predicted phase behavior of some real gases adsorbed in nanopores