BV formulation of higher form gauge theories in a superspace

We discuss the extended BRST and anti-BRST symmetry (including shift symmetry) in the Batalin-Vilkovisky (BV) formulation for two and three form gauge theories. Further we develop the superspace formulation for the BV actions for these theories. We show that the extended BRST invariant BV action for these theories can be written manifestly covariant manner in a superspace with one Grassmann coordinate. On the hand a superspace with two Grassmann coordinates are required for a manifestly covariant formulation of the extended BRST and extended anti-BRST invariant BV actions for higher form gauge theories.Comment: 30 pages, No figure, version to appear in EPJ

The future of pediatric pulmonology: A survey of division directors, assessment of current research funding, and discussion of workforce trends

Adequacy of the US workforce in pediatric pulmonology has been a source of serious concern within the field for some time, as it has been for several pediatric subspecialties. Contributing factors have been thought to include low fill rates of fellowship training programs, aging, and retirement rates of the subspecialist population, and the perception of insufficient numbers of specialists in some regions to meet clinical care needs. Several approaches to assessing workforce needs have already been described, and stakeholder groups are currently working on additional analyses. Although the recent report by Harris et al. captured a broad snapshot of workforce perceptions of 485 pediatric pulmonologists, this study (reporting data collected in 2014) did not address the future scope of practice

Algae in Selected Illinois Streams, 1971-1976

During the 5-year period, October 1971 through September 1976, samples of water from 21 Illinois streams at 26 locations were collected monthly and examined to determine the concentration and genera of algae. Data have been evaluated for algal composition, density, diversity indices, and seasonal succession for each stream location. At most sampling locations, algal densities ranged from 500 to 2000 cts/ml. The 5-year geometric means extended from 880 to 1500 cts/ml. From 24 to 30 different algal genera were recovered from each station and, in all, 56 genera were detected. The average diversity index for each station ranged from 1.11 to 1.36 bits per individual. The highest density of 60,000 cts/ml occurred on July 11, 1975, in the Fox River at Algonquin. The diatoms Navicula and Cyclotella were the most frequently observed algae. In addition to these, the green algae Scenedesmus and Crucigenia and the diatom Melosira were often dominant. From sample to sample, season to season, and year to year, the genera found at any sampling station varied considerably. Generally, the annual maximum population occurred in the spring. However, the experience gained from this study supports the conclusion that it is impossible to predict algal density, composition, or succession in the flowing streams of Illinois.publishedpeer reviewedOpe

Concentration and Genera of Algae in Selected Illinois Streams, 197I-1973

During the period October 1971 to September 1973, samples of water from 35 Illinois streams at 41 locations were collected monthly and examined to determine the type, genera, and concentration of algae. Data for the 2-year period have been evaluated for algal density, composition, diversity indices, and seasonal succession for each location. Most stations had algal densities of from 500 to 2000 cts/ml, had between 15 and 24 different algal genera (41 genera total), and had a diversity index equal to or greater than 1.10. Stations on the Fox, Des Plaines, and Kaskaskia Rivers had algal densities in excess of 5000 cts/ml. This report should be useful to persons responsible for developing, regulating, or managing water resources in Illinois.publishedpeer reviewedOpe

Convenient Versus Unique Effective Action Formalism in 2D Dilaton-Maxwell Quantum Gravity

The structure of one-loop divergences of two-dimensional dilaton-Maxwell quantum gravity is investigated in two formalisms: one using a convenient effective action and the other a unique effective action. The one-loop divergences (including surface divergences) of the convenient effective action are calculated in three different covariant gauges: (i) De Witt, (ii) $\Omega$-degenerate De Witt, and (iii) simplest covariant. The on-shell effective action is given by surface divergences only (finiteness of the $S$-matrix), which yet depend upon the gauge condition choice. Off-shell renormalizability is discussed and classes of renormalizable dilaton and Maxwell potentials are found which coincide in the cases of convenient and unique effective actions. A detailed comparison of both situations, i.e. convenient vs. unique effective action, is given. As an extension of the procedure, the one-loop effective action in two-dimensional dilaton-Yang-Mills gravity is calculated.Comment: 25 pages, LaTeX file, HUPD-93-0

CX3CR1 Polymorphisms are associated with atopy but not asthma in German children

Chemokines and their receptors are involved in many aspects of immunity. Chemokine CX3CL1, acting via its receptor CX3CR1, regulates monocyte migration and macrophage differentiation as well as T cell-dependent inflammation. Two common, nonsynonymous polymorphisms in CX3CR1 have previously been shown to alter the function of the CX3CL1/CX3CR1 pathway and were suggested to modify the risk for asthma. Using matrix-assisted laser desorption/ionization time-of-flight technology, we genotyped polymorphisms Val249Ile and Thr280Met in a cross-sectional population of German children from Munich (n = 1,159) and Dresden ( n = 1,940). For 249Ile an odds ratio of 0.77 (95% confidence interval 0.63-0.96; p = 0.017) and for 280Met an odds ratio of 0.71 ( 95% confidence interval 0.56-0.89; p = 0.004) were found with atopy in Dresden but not in Munich. Neither polymorphism was associated with asthma. Thus, amino acid changes in CX3CR1 may influence the development of atopy but not asthma in German children. Potentially, other factors such as environmental effects may modify the role of CX3CR1 polymorphisms. Copyright (c) 2007 S. Karger AG, Basel

A solution of the coincidence problem based on the recent galactic core black hole mass density increase

A mechanism capable to provide a natural solution to two major cosmological problems, i.e. the cosmic acceleration and the coincidence problem, is proposed. A specific brane-bulk energy exchange mechanism produces a total dark pressure, arising when adding all normal to the brane negative pressures in the interior of galactic core black holes. This astrophysically produced negative dark pressure explains cosmic acceleration and why the dark energy today is of the same order to the matter density for a wide range of the involved parameters. An exciting result of the analysis is that the recent rise of the galactic core black hole mass density causes the recent passage from cosmic deceleration to acceleration. Finally, it is worth mentioning that this work corrects a wide spread fallacy among brane cosmologists, i.e. that escaping gravitons result to positive dark pressure.Comment: 14 pages, 3 figure

Primary ciliary dyskinesia: Recent advances in diagnostics, genetics, and characterization of clinical disease

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia that leads to oto-sino-pulmonary diseases and organ laterality defects in approximately 50% of cases. The estimated incidence of PCD is approximately 1 per 15,000 births, but the prevalence of PCD is difficult to determine, primarily because of limitations in diagnostic methods that focus on testing ciliary ultrastructure and function. Diagnostic capabilities have recently benefitted from (1) documentation of low nasal nitric oxide production in PCD and (2) discovery of biallelic mutations in multiple PCD-causing genes. The use of these complementary diagnostic approaches shows that at least 30% of patients with PCD have normal ciliary ultrastructure. More accurate identification of patients with PCD has also allowed definition of a strong clinical phenotype, which includes neonatal respiratory distress in >80% of cases, daily nasal congestion and wet cough starting soon after birth, and early development of recurrent/chronic middle-ear and sinus disease. Recent studies, using advanced imaging and pulmonary physiologic assessments, clearly demonstrate early onset of lung disease in PCD, with abnormal air flow mechanics by age 6-8 years that is similar to cystic fibrosis, and age-dependent onset of bronchiectasis. The treatment ofPCDis not standardized, and there are no validated PCD-specific therapies. Most patients with PCD receive suboptimal management, which should include airway clearance, regular surveillance of pulmonary function and respiratory microbiology, and use of antibiotics targeted to pathogens. The PCD Foundation is developing a network of clinical centers, which should improve diagnosis and management of PCD