Towards String Predictions

The aim of superstring phenomenology is to develop the tools and methodology needed to confront string theory with experimental data. The first mandatory task is to find string solutions which reproduce the observable data. The subsequent goal is to extract potential signatures beyond the observable data. Recently, by studying exact flat directions of non-Abelian singlet fields, we demonstrated the existence of free fermionic heterotic-string models in which the $SU(3)\times SU(2)\times U(1)_Y$-charged matter spectrum, just below the string scale, consists solely of the MSSM spectrum. In this paper we study the possibility that the exact flat directions leave a $U(1)_{Z^\prime}$ symmetry unbroken at the Planck scale. We demonstrate in a specific example that such unbroken $U(1)_{Z^\prime}$ is in general expected to be not of the GUT type but of intrinsic stringy origin. We study its phenomenological characteristics and the consequences in the case that $U(1)_{Z^\prime}$ remains unbroken down to low energies. We suggest that observation in forthcoming colliders of a $Z^\prime$, with universal couplings for the two light generations but different couplings for the heavy generation may provide evidence for the $Z_2\times Z_2$ orbifold which underlies the free fermionic models.Comment: 18 pages. Standard Latex. References adde

Structure of the Cytoplasmic Loop between Putative Helices II and III of the Mannitol Permease of Escherichia coli: A Tryptophan and 5-Fluorotryptophan Spectroscopy Study

In this work, four single tryptophan (Trp) mutants of the dimeric mannitol transporter of Escherichia coli, EIImtl, are characterized using Trp and 5-fluoroTrp (5-FTrp) fluorescence spectroscopy. The four positions, 97, 114, 126, and 133, are located in a region shown by recent studies to be involved in the mannitol translocation process. To spectroscopically distinguish between the Trp positions in each subunit of dimeric EIImtl, 5-FTrp was biosynthetically incorporated because of its much simpler photophysics compared to those of Trp. The steady-state and time-resolved fluorescence methodologies used point out that all four positions are in structured environments, both in the absence and in the presence of a saturating concentration of mannitol. The fluorescence decay of all 5-FTrp-containing mutants was highly homogeneous, suggesting similar microenvironments for both probes per dimer. However, Stern-Volmer quenching experiments using potassium iodide indicate different solvent accessibilities for the two probes at positions 97 and 133. A 5 Å two-dimensional (2D) projection map of the membrane-embedded IICmtl dimer showing 2-fold symmetry is available. The results of this work are in better agreement with a 7 Å projection map from a single 2D crystal on which no symmetry was imposed.

Weather radar for urban hydrological applications: lessons learnt and research needs identified from 4 pilot catchments in North-West Europe

International audienceThis study investigates the impact of rainfall estimates of different spatial resolutions on the hydraulic outputs of the models of four of the EU RainGain project’s pilot locations (the Cranbrook catchment (UK), the Herent catchment (Belgium), the Morée-Sausset catchment (France) and the Kralingen District (The Netherlands)). Two storm events, one convective and one stratiform, measured by a polarimetric X-band radar located in Cabauw (The Netherlands) were selected for analysis. The original radar estimates, at 100 m and 1 min resolutions, were aggregated to a spatial resolution of 1000 m. These estimates were then applied to the high-resolution semi-distributed hydraulic models of the four urban catchments, all of which have similar size (between 5 and 8 km2), but different morphological, hydrological and hydraulic characteristics. When doing so, methodologies for standardising rainfall inputs and making results comparable were implemented. The response of the different catchments to rainfall inputs of varying spatial resolution is analysed in the light of model configuration, catchment and storm characteristics. Rather surprisingly, the results show that for the two events under consideration the spatial resolution (i.e. 100 m vs 1000 m) of rainfall inputs does not have a significant influence on the outputs of urban drainage models. The present study will soon be extended to more storms as well as model structures and resolutions, with the final aim of identifying critical spatial-temporal resolutions for urban catchment modelling in relation to catchment and storm event characteristics

Paclitaxel, ifosfamide and cisplatin with granulocyte colony-stimulating factor or recombinant human interleukin 3 and granulocyte colony-stimulating factor in ovarian cancer: a feasibility study.

The tolerability and efficacy of four courses of paclitaxel and ifosfamide plus cisplatin every 3 weeks was evaluated in patients with residual or refractory ovarian cancer. Additionally, supportive haematological effects of recombinant human interleukin 3 (rhIL-3) and recombinant human granulocyte colony-stimulating factor (G-CSF) were studied. Paclitaxel starting dose was 135 mg m(-2) (day 1), with ifosfamide dose 1.2 g m(-2) day(-1) (days 2-4) and cisplatin dose 30 mg m(-2) day(-1) (days 2-4). All 16 patients received 5.0 microg kg(-1) day(-1) G-CSF (days 7-16) and, in addition, eight patients were randomized to receive 10 microg kg(-1) day(-1) rhIL-3 (days 5-9). Paclitaxel and ifosfamide doses were reduced when grade IV haematological toxicity occurred. In the absence of grade IV haematological toxicity and normal recovery of haematopoiesis, paclitaxel dose was escalated. Toxicity was evaluable in 56 courses, with haematological effects in 52. Despite antiemetic treatment, nausea and vomiting (> or = grade I) occurred in 50 courses. Five patients had persisting peripheral neuropathy. Renal and liver function were not affected. Grade IV neutropenia occurred in 12 out of 52 courses, with neutropenic fever in two patients, both of whom died from fatal septicaemia. Grade IV thrombocytopenia without bleeding was observed in 15 courses. Grade IV haematological toxicity was associated with hepatic metastases and concurrent increases in alkaline phosphatase (P <0.001) and gamma-glutamyltransferase (P=0.007). No relation was found between haematological toxicity and pharmacokinetic parameters of paclitaxel. Patients treated with rhIL-3 showed a tendency to a faster platelet recovery (not affecting platelet nadir), and the cisplatin dose intensity was higher (P=0.025). Six of the nine evaluable patients had a tumour response. The overall median progression-free survival was 7 months and the overall mean survival was 13 months. In conclusion, this potentially interesting combination as second-line treatment showed a low tolerability with unexpected mortality, while rhIL-3 administration tended to induce a more rapid platelet recovery

The Higgs Mass as the Discriminator of Electroweak Models

In the Minimal Supersymmetric Model (MSSM) and the Next to Minimal Supersymmetric Model [(M+1)SSM], an upper bound on the lightest higgs mass can be calculated. On the other hand, vacuum stability implies a lower limit on the mass of the higgs boson in the Standard Model (SM). We find that a gap exists for $m_t \stackrel{>}{\sim} 165$ GeV between the SM and both the MSSM and the (M+1)SSM bounds. Thus, if the new top quark mass measurement by CDF remains valid, a first measurement of the higgs mass will serve to exclude either the SM or the MSSM/(M+1)SSM higgs sectors. In addition, we discuss Supersymmetric Grand Unified Theories, other extentions of the SM, the discovery potential of the lightest higgs, and the assumptions on which our conclusions are based.Comment: 9 pages, 2 figures, VAND-TH-94-1

On the origins of the mitotic shift in proliferating cell layers

Background: During plant and animal development, monolayer cell sheets display a stereotyped distribution of polygonal cell shapes. In interphase cells these shapes range from quadrilaterals to decagons, with a robust average of six sides per cell. In contrast, the subset of cells in mitosis exhibits a distinct distribution with an average of seven sides. It remains unclear whether this ‘mitotic shift’ reflects a causal relationship between increased polygonal sidedness and increased division likelihood, or alternatively, a passive effect of local proliferation on cell shape. Methods: We use a combination of probabilistic analysis and mathematical modeling to predict the geometry of mitotic polygonal cells in a proliferating cell layer. To test these predictions experimentally, we use Flp-Out stochastic labeling in the Drosophila wing disc to induce single cell clones, and confocal imaging to quantify the polygonal topologies of these clones as a function of cellular age. For a more generic test in an idealized cell layer, we model epithelial sheet proliferation in a finite element framework, which yields a computationally robust, emergent prediction of the mitotic cell shape distribution. Results: Using both mathematical and experimental approaches, we show that the mitotic shift derives primarily from passive, non-autonomous effects of mitoses in neighboring cells on each cell’s geometry over the course of the cell cycle. Computationally, we predict that interphase cells should passively gain sides over time, such that cells at more advanced stages of the cell cycle will tend to have a larger number of neighbors than those at earlier stages. Validating this prediction, experimental analysis of randomly labeled epithelial cells in the Drosophila wing disc demonstrates that labeled cells exhibit an age-dependent increase in polygonal sidedness. Reinforcing these data, finite element simulations of epithelial sheet proliferation demonstrate in a generic framework that passive side-gaining is sufficient to generate a mitotic shift. Conclusions: Taken together, our results strongly suggest that the mitotic shift reflects a time-dependent accumulation of shared cellular interfaces over the course of the cell cycle. These results uncover fundamental constraints on the relationship between cell shape and cell division that should be general in adherent, polarized cell layers