Radio Planetary Nebulae in the Small Magellanic Cloud

We present ten new radio continuum (RC) detections at catalogued planetary nebula (PN) positions in the Small Magellanic Cloud (SMC): SMPS6, LIN 41, LIN 142, SMP S13, SMP S14, SMP S16, J18, SMP S18, SMP S19 and SMP S22. Additionally, six SMC radio PNe previously detected, LIN 45, SMP S11, SMPS17, LIN321, LIN339 and SMPS24 are also investigated (re-observed) here making up a population of 16 radio detections of catalogued PNe in the SMC. These 16 radio detections represent ~15 % of the total catalogued PN population in the SMC. We show that six of these objects have characteristics that suggest that they are PN mimics: LIN 41, LIN 45, SMP S11, LIN 142, LIN 321 and LIN 339. We also present our results for the surface brightness - PN radius relation ({\Sigma}-D) of the SMC radio PN population. These are consistent with previous SMC and LMC PN measurements of the ({\Sigma}-D) relation.Comment: Accepted for publication in Astrophysics and Space Scienc

Concentration of Solutions for a Singularly Perturbed Neumann Problem in non smooth domains

We consider the equation $-\epsilon^{2}\Delta u + u = u^ {p}$ in a bounded domain $\Omega\subset\R^{3}$ with edges. We impose Neumann boundary conditions, assuming $1<p<5$, and prove concentration of solutions at suitable points of $\partial\Omega$ on the edges.Comment: 24 pages. Second Version, minor changes. To appear in Annales de l'Institut Henri Poincar\'e - Analyse non lin\'eair

Resonance scattering at lyman-alpha by an atomic hydrogen cell

Hydrogen cell and ion chamber for obtaining photoelectric data on resonance scattering at lyman alpha lin

Influence of sow dietary polyunsaturated fatty acid source on the immunoglobulin profile of piglets

To examine the effect of different n-3 polyunsaturated fatty acid (PUFA) sources in sow diets on piglets’ immunoglobulin (Ig) profile, two groups of twelve sows each were fed different diets from day 45 of pregnancy and during lactation on two commercial farms. On farm I, a palm oil diet (25 g/kg; PALM) and a linseed oil containing diet (20 g/kg; LIN) were fed. On farm II, the same PALM diet and a fish oil containing diet (20 g/kg; FISH) were fed. All diets contained equal amounts of C18:2n-6 (13 g/kg). One day before parturition, blood (for serum) was taken and shortly after parturition, colostrum was taken from the sows (not from sows on farm I) for determination of Ig levels. On day 5 post partum and the day before weaning, blood (for serum) was taken from 4 piglets of six sows per group (24 piglets in total per group; for 5-d old piglets on farm II, only 6 piglets of the FISH group were sampled). In all samples total IgG, IgA, IgM concentration and specific F4-IgG, -IgA and -IgM titer (Log2 titer) against E. coli were determined. On farm I, the sows of the LIN group showed a trend towards lower IgG titers compared to the PALM group around farrowing (P<0.1). On farm II, the sows on the FISH diet showed a significantly (P<0.05) lower F4-IgG titer compared to the sows fed PALM. The colostrum samples on farm II showed no differences between both groups. On farm I, the 5-d old piglets from the LIN group had significantly higher IgA and IgM concentrations and higher F4-IgA and F4-IgM titers (P<0.05). F4-IgA and F4-IgG titers were also significantly higher at weaning in the LIN group compared to the PALM group. On farm II, the piglets of the FISH group had a significantly higher IgG concentration and F4-IgA titer (P<0.05) and a trend towards a higher IgM concentration (P<0.1) around weaning compared to the PALM group. It seems that fish oil in the maternal diet increases total IgG concentration, while linseed oil reduces total IgG and increases total IgA compared to a palm fat containing diet. Both fish and linseed oil seem to have a positive effect on total IgM concentration compared to the palm diet

The effectiveness of using variable speed limit on the performance of an interrupted flow

The urban traffic congestion is getting worse with ever increasing urban population and vehicle ownership. The long queues at intersections and blockage of traffic on urban arterial roads become routine during the peak hours. Interrupted traffic flow through signalised intersections and arterial roads have badly been affected by these occurrences. Thus this paper examines the possibility of employing variable speed limit (VSL) for upstream traffic during the peak period to improve the traffic performance through signalised intersections as well as in urban arterials. The micro simulation software VISSIM was used to examine a hypothetical road network under VSL application. An expected traffic flow near capacity condition was simulated several times to see the effectiveness. Results show that for a reasonable period of time, the VSL application to the upstream traffic improve the traffic performance at immediate downstream intersections in terms of vehicle delay (16%), average queue length (18%) and average number of stops per vehicles (16%), while intersections located far from the VSL application has no or little effect. Similarly, the arterial performances have also been improved for a short period of time on the immediate downstream link in terms of density (13%), space mean speed (10%) and traffic flow (2%), the effective is negligible on the links located far. In addition a slight improvement was noticed to the total journey time on the immediate lin

C. elegans LRP-2 functions in vulval precursor cell polarity

The C. elegans vulva is formed from divisions of three vulval precursor cells (VPCs) – P5.p, P6.p, and P7.p – arranged along the anteroposterior axis in the ventral epithelium (Sulston and Horvitz, 1977). Previous analyses show the orientation of P5.p and P7.p descendants is determined by the interaction of multiple Wnt signals. Specifically, in the absence of all Wnts, the VPCs display a randomized orientation, which is likely the default (Green et al., 2008; Minor et al. 2013). Two separate Wnts from the anchor cell, LIN-44 and MOM-2 acting through receptors LIN-17/Frizzled and LIN-18/Ryk, respectively, regulate P7.p orientation (Ferguson et al., 1987; Sternberg and Horvitz, 1988; Sawa et al., 1996; Inoue et al., 2004; Gleason et al., 2006). In the absence of these signals the orientation of the progeny of P7.p mimic those of P5.p and face toward the posterior of the worm, a phenotype referred to as posterior-reversed vulval lineage (P-Rvl). This posterior orientation is dependent on the instructive signal EGL-20, a Wnt expressed in the tail acting through CAM-1/ROR and VANG-1/Van Gogh, and is referred to as “ground polarity” (Green et al., 2008). Here we examine the role of a low-density lipoprotein receptor, lrp-2, and its role in controlling the orientation of P7.p daughter cells. To investigate this interaction double mutants were constructed with both alleles of lrp-2 and lin-17(n671) (Table 1). Much like cam-1(gm122) and vang-1(ok1142), both alleles of lrp-2 suppress the lin-17(n671) phenotype from 74 to approximately 50% P-Rvl leading us to hypothesize that lrp-2 functions in the same pathway as cam-1 and vang-1. Furthering this hypothesis we have shown that, like cam-1 and vang-1, lrp-2 controls the localization of SYS-1/b-catenin (Minor and Sternberg, 2019). To ensure that this phenotype was a result of loss of lrp-2 function as opposed to background effects we injected a fosmid (WRM0617cA02) containing the full-length sequence of lrp-2 and found that it does rescue the double mutant phenotype of lin-17(n671); lrp-2(gk272) from 55 to 73%. In order to better test this hypothesis a triple mutant was constructed between lin-17(n671), lrp-2(gk272), and cam-1(gm122) (Table 1). This triple mutant displays the same P-Rvl penetrance as both the lin-17(n671); lrp-2(gk272) and lin-17(n671); cam-1(gm122) double mutants confirming that lrp-2 functions in the same pathway as cam-1

Note on W3 Realizations of the Bosonic String

In order to investigate to what extent string theories are different vacua of a general string theory (the ``universal string"), we discuss realizations of the bosonic string as particular background of certain types of $W$-strings. Our discussions include linearized $W_3^{lin}$, non-critical $W_3$, linearized $W_3^{(2)lin}$ and critical $W_3^{(2)}$ realizations of the bosonic string.Comment: 9 pages, Late