A consistent spatial differencing scheme for the transonic full-potential equation in three dimensions

A full-potential steady transonic wing flow solver has been modified so that freestream density and residual are captured in regions of constant velocity. This numerically precise freestream consistency is obtained by slightly altering the differencing scheme without affecting the implicit solution algorithm. The changes chiefly affect the fifteen metrics per grid point, which are computed once and stored. With this new method, the outer boundary condition is captured accurately, and the smoothness of the solution is especially improved near regions of grid discontinuity

On 22-cycles of graphs

Let $G=(V,E)$ be a finite undirected graph. Orient the edges of $G$ in an arbitrary way. A $2$-cycle on $G$ is a function $d : E^2\to \mathbb{Z}$ such for each edge $e$, $d(e, \cdot)$ and $d(\cdot, e)$ are circulations on $G$, and $d(e, f) = 0$ whenever $e$ and $f$ have a common vertex. We show that each $2$-cycle is a sum of three special types of $2$-cycles: cycle-pair $2$-cycles, Kuratowski $2$-cycles, and quad $2$-cycles. In case that the graph is Kuratowski connected, we show that each $2$-cycle is a sum of cycle-pair $2$-cycles and at most one Kuratowski $2$-cycle. Furthermore, if $G$ is Kuratowski connected, we characterize when every Kuratowski $2$-cycle is a sum of cycle-pair $2$-cycles. A $2$-cycles $d$ on $G$ is skew-symmetric if $d(e,f) = -d(f,e)$ for all edges $e,f\in E$. We show that each $2$-cycle is a sum of two special types of skew-symmetric $2$-cycles: skew-symmetric cycle-pair $2$-cycles and skew-symmetric quad $2$-cycles. In case that the graph is Kuratowski connected, we show that each skew-symmetric $2$-cycle is a sum of skew-symmetric cycle-pair $2$-cycles. Similar results like this had previously been obtained by one of the authors for symmetric $2$-cycles. Symmetric $2$-cycles are $2$-cycles $d$ such that $d(e,f)=d(f,e)$ for all edges $e,f\in E$

The Liability Threshold Model for Censored Twin Data

Family studies provide an important tool for understanding etiology of diseases, with the key aim of discovering evidence of family aggregation and to determine if such aggregation can be attributed to genetic components. Heritability and concordance estimates are routinely calculated in twin studies of diseases, as a way of quantifying such genetic contribution. The endpoint in these studies are typically defined as occurrence of a disease versus death without the disease. However, a large fraction of the subjects may still be alive at the time of follow-up without having experienced the disease thus still being at risk. Ignoring this right-censoring can lead to severely biased estimates. We propose to extend the classical liability threshold model with inverse probability of censoring weighting of complete observations. This leads to a flexible way of modeling twin concordance and obtaining consistent estimates of heritability. We apply the method in simulations and to data from the population based Danish twin cohort where we describe the dependence in prostate cancer occurrence in twins

Recent applications of the transonic wing analysis computer code, TWING

An evaluation of the transonic-wing-analysis computer code TWING is given. TWING utilizes a fully implicit approximate factorization iteration scheme to solve the full potential equation in conservative form. A numerical elliptic-solver grid-generation scheme is used to generate the required finite-difference mesh. Several wing configurations were analyzed, and the limits of applicability of this code was evaluated. Comparisons of computed results were made with available experimental data. Results indicate that the code is robust, accurate (when significant viscous effects are not present), and efficient. TWING generally produces solutions an order of magnitude faster than other conservative full potential codes using successive-line overrelaxation. The present method is applicable to a wide range of isolated wing configurations including high-aspect-ratio transport wings and low-aspect-ratio, high-sweep, fighter configurations

Isoprene emission from Sphagnum species occupying different growth positions above the water table

Isoprene emission from Sphagnum species naturally growing at different positions above the water table were measured in a subarctic peatland and at monoliths from a temperate bog. Our objectives were to investigate (1) whether emission rates were species and/or moisture dependent, and (2) whether short-term temperature history had an influence on emission capacity. We expected greater emission capacities in moist than dry growing conditions, and from species adapted to wet habitats. We also expected that higher emission capacities would be found in response to elevated temperatures. Average peak growing season isoprene emission capacities (standardized to 20 degrees C and PAR 1000 mu mol m(-2) s(-1)) at the subarctic site were 106 and 74 mu g C m(-2) h(-1) from a S. balticum wet lawn and a S. balticum dry hummock/palsa, respectively. Emission capacities correlated strongly with gross primary productivity (GPP) and the average air temperature of the 48 hours prior to measurement (T-48), but the effect of T-48 seemed to be partly masked by the influence of GPP when moisture was not limiting. The laboratory experiments suggested that a typical hummock species, S. rubellum had higher capacity for isoprene emission than a typical lawn species S. magellanicum. Instantaneous emission rates increased with temperature, but no effect of temperature history was discernible. Sphagnum mosses are known to emit substantial amounts of isoprene, but in this study we also showed significant inter-species differences in emission capacity. The results imply that climate change induced alterations of peatland hydrology may change the total ecosystem isoprene source strength, as individual species adapt to new growth conditions or as a consequence of species succession

TAIR: A transonic airfoil analysis computer code

The operation of the TAIR (Transonic AIRfoil) computer code, which uses a fast, fully implicit algorithm to solve the conservative full-potential equation for transonic flow fields about arbitrary airfoils, is described on two levels of sophistication: simplified operation and detailed operation. The program organization and theory are elaborated to simplify modification of TAIR for new applications. Examples with input and output are given for a wide range of cases, including incompressible, subcritical compressible, and transonic calculations

Local starburst galaxies and their descendants

Despite strong interest in the starburst (hereafter SB) phenomenon, the concept remains ill-defined. We use a strict definition of SB to examine the statistical properties of local SB and post-starburst (hereafter PB) galaxies. We also seek relationships to active galaxies. Potential SB galaxies are selected from the SDSS DR7 and their stellar content is analysed. We apply an age dependent dust attenuation correction and derive star formation rates (SFR), ages and masses of the young and old populations. The photometric masses nicely agree with dynamical masses derived from the H-alpha emission line width. To select SB galaxies, we use the birthrate parameter b=SFR/, requiring b>=3. The PB sample is selected from the citerion EW(Hdelta_abs)>=6 A. Only 1% of star-forming galaxies are found to be SB galaxies. They contribute 3-6% to the stellar production and are therefore unimportant for the local star formation activity. The median SB age is 70 Myr, roughly independent of mass. The b-parameter strongly depends on burst age. Values close to b=60 are found at ages ~10 Myr, while almost no SBs are found at ages >1 Gyr. The median baryonic burst mass fraction of sub-L* galaxies is 5%, decreasing slowly with mass. The median mass fraction of the recent burst in the PB sample is 5-10%. The age-mass distribution of the progenitors of the PBs is bimodal with a break at log(M)~10.6 above which the ages are doubled. The SB and PB luminosity functions (hereafter LFs) follow each other closely until M_r~-21, when AGNs begin to dominate. The PB LF continues to follow the AGN LF while SB loose significance. This suggests that the number of luminous SBs is underestimated by about one dex at high luminosities, due to large amounts of dust and/or AGN blending. It also indicates that the SB phase preceded the AGN phase. We also discuss the conditions for global gas outflow caused by stellar feedback.Comment: Accepted for publication in Astronomy and Astrophysics. This is an extended, substantially revised and corrected version with partly modified conclusion

Variability of BVOC Emissions from Commercially Used willow (<i>Salix</i> spp.) Varieties

Willow (Salix spp.) trees are commonly used in short rotation coppices (SRC) to produce renewable energy. However, these plants are also known to emit high concentrations of biogenic volatile organic compounds (BVOCs), which have a large influence on air quality. Many different clones of commercially used Salix varieties exist today, but only a few studies have focused on BVOC emissions from these newer varieties. In this study, four varieties commercially propagated for biofuel production have been studied on a leaf-scale in the southern part of Sweden. The trees had either their first or second growing season, and measurements on BVOC emissions were done during the growing season in 2017 from the end of May to the beginning of September. Isoprene was the dominant emitted compound for all varieties but the average emission amongst varieties varied from 4.00 to 12.66 µg gdw−1 h−1. Average monoterpene (MT) (0.78–1.87 µg gdw−1 h−1) and sesquiterpene (SQT) emission rates (0.22–0.57 µg gdw−1 h−1) differed as well among the varieties. Besides isoprene, other compounds like ocimene, linalool and caryophyllene also showed a response to light but not for all varieties. Younger plants had several times higher emissions of non-isoprenoids (other VOCs) than the corresponding 1-year-old trees. The conclusions from this study show that the choice of variety can have a large impact on the regional BVOC emission budget. Genetics, together with stand age, should be taken into account when modelling BVOC emissions on a regional scale, for example, for air quality assessments