Quantum saturation and condensation of excitons in Cu2_2O: a theoretical study

Recent experiments on high density excitons in Cu$_2$O provide evidence for degenerate quantum statistics and Bose-Einstein condensation of this nearly ideal gas. We model the time dependence of this bosonic system including exciton decay mechanisms, energy exchange with phonons, and interconversion between ortho (triplet-state) and para (singlet-state) excitons, using parameters for the excitonic decay, the coupling to acoustic and low-lying optical phonons, Auger recombination, and ortho-para interconversion derived from experiment. The single adjustable parameter in our model is the optical-phonon cooling rate for Auger and laser-produced hot excitons. We show that the orthoexcitons move along the phase boundary without crossing it (i.e., exhibit a ``quantum saturation''), as a consequence of the balance of entropy changes due to cooling of excitons by phonons and heating by the non-radiative Auger two-exciton recombination process. The Auger annihilation rate for para-para collisions is much smaller than that for ortho-para and ortho-ortho collisions, explaining why, under the given experimental conditions, the paraexcitons condense while the orthoexcitons fail to do so.Comment: Revised to improve clarity and physical content 18 pages, revtex, figures available from G. Kavoulakis, Physics Department, University of Illinois, Urban

Relativistic superfluid models for rotating neutron stars

This article starts by providing an introductory overview of the theoretical mechanics of rotating neutron stars as developped to account for the frequency variations, and particularly the discontinuous glitches, observed in pulsars. The theory suggests, and the observations seem to confirm, that an essential role is played by the interaction between the solid crust and inner layers whose superfluid nature allows them to rotate independently. However many significant details remain to be clarified, even in much studied cases such as the Crab and Vela. The second part of this article is more technical, concentrating on just one of the many physical aspects that needs further development, namely the provision of a satisfactorily relativistic (local but not microscopic) treatment of the effects of the neutron superfluidity that is involved.Comment: 42 pages LateX. Contribution to Physics of Neutron Star Interiors, ed. D. Blasche, N.K. Glendenning, A. Sedrakian (ECT workshop, Trento, June 2000

Model-independent search for CP violation in D0→K−K+π−π+ and D0→π−π+π+π− decays

A search for CP violation in the phase-space structures of D0 and View the MathML source decays to the final states K−K+π−π+ and π−π+π+π− is presented. The search is carried out with a data set corresponding to an integrated luminosity of 1.0 fb−1 collected in 2011 by the LHCb experiment in pp collisions at a centre-of-mass energy of 7 TeV. For the K−K+π−π+ final state, the four-body phase space is divided into 32 bins, each bin with approximately 1800 decays. The p-value under the hypothesis of no CP violation is 9.1%, and in no bin is a CP asymmetry greater than 6.5% observed. The phase space of the π−π+π+π− final state is partitioned into 128 bins, each bin with approximately 2500 decays. The p-value under the hypothesis of no CP violation is 41%, and in no bin is a CP asymmetry greater than 5.5% observed. All results are consistent with the hypothesis of no CP violation at the current sensitivity

Balancing end-to-end budgets of the Georges Bank ecosystem

Author Posting. © Elsevier, 2007. This is the author's version of the work. It is posted here by permission of Elsevier for personal use, not for redistribution. The definitive version was published in Progress In Oceanography 74 (2007): 423-448, doi:10.1016/j.pocean.2007.05.003.Oceanographic regimes on the continental shelf display a great range in the time scales of physical exchange, biochemical processes and trophic transfers. The close surface-to-seabed physical coupling at intermediate scales of weeks to months means that the open ocean simplification to a purely pelagic food web is inadequate. Top-down trophic depictions, starting from the fish populations, are insufficient to constrain a system involving extensive nutrient recycling at lower trophic levels and subject to physical forcing as well as fishing. These pelagic-benthic interactions are found on all continental shelves but are particularly important on the relatively shallow Georges Bank in the northwest Atlantic. We have generated budgets for the lower food web for three physical regimes (well mixed, transitional and stratified) and for three seasons (spring, summer and fall/winter). The calculations show that vertical mixing and lateral exchange between the three regimes are important for zooplankton production as well as for nutrient input. Benthic suspension feeders are an additional critical pathway for transfers to higher trophic levels. Estimates of production by mesozooplankton, benthic suspension feeders and deposit feeders, derived primarily from data collected during the GLOBEC years of 1995-1999, provide input to an upper food web. Diets of commercial fish populations are used to calculate food requirements in three fish categories, planktivores, benthivores and piscivores, for four decades, 1963-2002, between which there were major changes in the fish communities. Comparisons of inputs from the lower web with fish energetic requirements for plankton and benthos indicate that we obtained reasonable agreement for the last three decades, 1973 to 2002. However, for the first decade, the fish food requirements were significantly less than the inputs. This decade, 1963-1972, corresponds to a period characterized by a strong Labrador Current and lower nitrate levels at the shelf edge, demonstrating how strong bottom-up physical forcing may determine overall fish yields.The research was done under the aegis of the U.S.-GLOBEC Northwest Atlantic Georges Bank Study, a program sponsored jointly by the U.S. National Science Foundation and the U.S. National Oceanic and Atmospheric Administration. We acknowledge NOAA-CICOR award NA17RJ1233 (J.H. Steele), NSF awards OCE0217399 (D.J. Gifford), OCE0217122 (J.J. Bisagni) and OCE0217257 (M.E. Sieracki). W.T. Stockhausen was supported by the NOAA Sponsored Coastal Ocean Research Program

Genetically Determined Height and Risk of Non-hodgkin Lymphoma

Although the evidence is not consistent, epidemiologic studies have suggested that taller adult height may be associated with an increased risk of some non-Hodgkin lymphoma (NHL) subtypes. Height is largely determined by genetic factors, but how these genetic factors may contribute to NHL risk is unknown. We investigated the relationship between genetic determinants of height and NHL risk using data from eight genome-wide association studies (GWAS) comprising 10,629 NHL cases, including 3,857 diffuse large B-cell lymphoma (DLBCL), 2,847 follicular lymphoma (FL), 3,100 chronic lymphocytic leukemia (CLL), and 825 marginal zone lymphoma (MZL) cases, and 9,505 controls of European ancestry. We evaluated genetically predicted height by constructing polygenic risk scores using 833 height-associated SNPs. We used logistic regression to estimate odds ratios (OR) and 95% confidence intervals (CI) for association between genetically determined height and the risk of four NHL subtypes in each GWAS and then used fixed-effect meta-analysis to combine subtype results across studies. We found suggestive evidence between taller genetically determined height and increased CLL risk (OR = 1.08, 95% CI = 1.00\u20131.17, p = 0.049), which was slightly stronger among women (OR = 1.15, 95% CI: 1.01\u20131.31, p = 0.036). No significant associations were observed with DLBCL, FL, or MZL. Our findings suggest that there may be some shared genetic factors between CLL and height, but other endogenous or environmental factors may underlie reported epidemiologic height associations with other subtypes

Imperfect detection and its consequences for monitoring for conservation

Biodiversity monitoring is important to identify conservation needs and test the efficacy of management actions. Variants of “abundance” (N) are among the most widely monitored quantities, e.g., (true) abundance, number of occupied sites (distribution, occupancy) or species richness.We propose a sampling-based view of monitoring that clearly acknowledges two sampling processes involved when monitoring N. First, measurements from the surveyed sample area are generalized to a larger area, hence the importance of a probability sample. Second, even within sampled areas only a sample of units (individuals, occupied sites, species) is counted owing to imperfect detectability p. If p < 1, counts are random variables and their expectation E(n) is related to N via the relationship E(n) ÿ*p. Whenever p < 1, counts vary even under identical conditions and underestimate N, and patterns in counts confound patterns in N with those in p. In addition, part of the population N may be unavailable for detection, e.g., temporarily outside the sampled quadrat, underground or for another reason not exposed to sampling; hence a more general way of describing a count is E(n) ÿ*a*p, where a is availability probability and p detection, given availability. We give two examples of monitoring schemes that highlight the importance of explicitly accounting for availability and detectability. In the Swiss reptile Red List update, the widespread and abundant slow worm (Anguis fragilis) was recorded in only 22.1% of all sampled quadrats. Only an analysis that accounted for both availability and detectability gave realistic estimates of the species’ distribution. Among 128 bird species monitored in the Swiss breeding bird survey, de tection in occupied 1 km quadrats averaged only 64% and varied tremendously by species (3–99 %); hence observed distributions greatly underestimated range sizes and should not be compared among species.We believe that monitoring design and analyses should properly account for these two sampling processes to enable valid inferences about biodiversity. We argue for a more rigorous approach to both monitoring design and analysis to obtain the best possible information about the state of nature. An explicit recognition of, and proper accounting for, the two sampling processes involved in most monitoring programs will go a long way towards this goa