Investigation and Assessment of Resource Consumption of Process Chains

AbstractMany different technologies and processes have been established in production within the last decades. These technologies have to be integrated into sophisticated process chains to achieve today's requirements of high performance products. For most of these products the costs can be determined or at least estimated accurately. However, resource intensive and thus cost intensive processes and their potential within the process chains are often neither identified nor quantified. For identifying, measuring and subsequently assessing the need of resources, like energy or material and their monetary as well as environmental impact, four different process chains of high industrial relevance have been chosen and investigated with regards to their resource consumption. These process chains are used for manufacturing turbine blades made of Inconel and titanium aluminide as well as for comparisons of a conventional and an innovative process chain to manufacture an insert for an injection mold. By measuring and assessing their resource consumption the most resource intensive and thus influential processes have been identified and their potential for resource reduction has been evaluated. Due to the change of single processes to reduce resource consumption and thus the conditions for subsequent processes, the requirements might change and lead to adaptions within the entire process chain. For the assessment of the process chains and the changes within the processes themselves, a scenario based assessment has been modelled. This results in an economic and ecologic evaluation of these process chains and enables a comparison of these to choose the most meaningful process chain

Phase transitions in biological membranes

Native membranes of biological cells display melting transitions of their lipids at a temperature of 10-20 degrees below body temperature. Such transitions can be observed in various bacterial cells, in nerves, in cancer cells, but also in lung surfactant. It seems as if the presence of transitions slightly below physiological temperature is a generic property of most cells. They are important because they influence many physical properties of the membranes. At the transition temperature, membranes display a larger permeability that is accompanied by ion-channel-like phenomena even in the complete absence of proteins. Membranes are softer, which implies that phenomena such as endocytosis and exocytosis are facilitated. Mechanical signal propagation phenomena related to nerve pulses are strongly enhanced. The position of transitions can be affected by changes in temperature, pressure, pH and salt concentration or by the presence of anesthetics. Thus, even at physiological temperature, these transitions are of relevance. There position and thereby the physical properties of the membrane can be controlled by changes in the intensive thermodynamic variables. Here, we review some of the experimental findings and the thermodynamics that describes the control of the membrane function.Comment: 23 pages, 15 figure

The influence of anesthetics, neurotransmitters and antibiotics on the relaxation processes in lipid membranes

In the proximity of melting transitions of artificial and biological membranes fluctuations in enthalpy, area, volume and concentration are enhanced. This results in domain formation, changes of the elastic constants, changes in permeability and slowing down of relaxation processes. In this study we used pressure perturbation calorimetry to investigate the relaxation time scale after a jump into the melting transition regime of artificial lipid membranes. This time corresponds to the characteristic rate of domain growth. The studies were performed on single-component large unilamellar and multilamellar vesicle systems with and without the addition of small molecules such as general anesthetics, neurotransmitters and antibiotics. These drugs interact with membranes and affect melting points and profiles. In all systems we found that heat capacity and relaxation times are related to each other in a simple manner. The maximum relaxation time depends on the cooperativity of the heat capacity profile and decreases with a broadening of the transition. For this reason the influence of a drug on the time scale of domain formation processes can be understood on the basis of their influence on the heat capacity profile. This allows estimations of the time scale of domain formation processes in biological membranes.Comment: 12 pages, 6 figure

What is the structure of the Roper resonance?

We investigate the structure of the nucleon resonance N^*(1440) (Roper) within a coupled-channel meson exchange model for pion-nucleon scattering. The coupling to pipiN states is realized effectively by the coupling to the sigmaN, piDelta and rhoN channels. The interaction within and between these channels is derived from an effective Lagrangian based on a chirally symmetric Lagrangian, which is supplemented by well known terms for the coupling of the Delta isobar, the omega meson and the 'sigma', which is the name given here to the strong correlation of two pions in the scalar-isoscalar channel. In this model the Roper resonance can be described by meson-baryon dynamics alone; no genuine N^*(1440) (3 quark) resonance is needed in order to fit piN phase shifts and inelasticities.Comment: 55 pages, 14 figure

Central radio galaxies in galaxy clusters: Joint surveys by eROSITA and ASKAP

The extended ROentgen Survey with an Imaging Telescope Array (eROSITA) telescope onboard the Spectrum-Roentgen-Gamma (SRG) mission has finished the first eROSITA All-Sky Survey (eRASS:1), and detected 10$^4$ galaxy clusters in the western Galactic hemisphere. In the radio band, the Australian Square Kilometre Array Pathfinder (ASKAP) telescope finished its pilot 1 phase of the project 'Evolutionary Map of the Universe' (EMU) with 220.000 sources in a 270 deg$^2$ field overlapping with eRASS:1. These two surveys are used to study radio-mode Active Galactic Nuclei (AGN) in clusters. In order to understand the efficiency of radio-mode feedback at the centers of galaxy clusters, we relate the radio properties of brightest cluster galaxies (BCG) to the X-ray properties of the host clusters. We identify the central radio sources in eRASS:1 clusters or calculate corresponding upper limits on the radio luminosity. Then, we derive relations between the X-ray properties of the clusters and the radio properties of the corresponding central radio source. We also apply a mid-infrared color criterion using WISE colors to identify AGN. In total we investigate a sample of 75 clusters. We find a statistically significant correlation between the X-ray luminosity of the cluster and the 944 MHz radio luminosity of the corresponding central radio galaxy. There is also a positive trend between the radio power and the largest linear size (LLS) of the radio source. The density and the LLS do not show any correlation. We find that in high luminosity clusters with L_X > $10^{43}$ erg s$^{-1}$ the kinetic luminosity of the radio jets is not longer correlated with the X-ray luminosity and discuss various reasons. We find an anti-correlation between the central cooling time t_cool and the radio luminosity L_R indicating a need for more powerful AGN in clusters with short central cooling times.Comment: 16 pages, 12 figures, accepted for publication in A&

Tonsillar metastasis of gastric cancer

Metastasis from a malignant tumor to the palatine tonsils is rare, with only 100 cases reported in the English-language literature. Tonsillar metastasis from a gastric cancer is very rare. We report here a case of palatine tonsillar metastasis after gastric cancer surgery. The patient was an 88-year-old woman who had gastric cancer with abdominal wall invasion. She had undergone a distal gastrectomy with abdominal wall resection and D2 lymph node dissection. Histologically, the tumor was primarily a moderately differentiated adenocarcinoma. It was stage IV (T4, N1, M0) using TNM clinical classification. The patient developed pharyngeal discomfort and abdominal pain and was hospitalized during the follow-up period, 1 year 9 months post-operatively. Multiple lung metastases, Virchow’s lymph node metastasis, and adrenal metastasis were observed. A mass of 2.5 cm was also observed in the right palatine tonsil. It was diagnosed as a moderately differentiated adenocarcinoma, a metastasis from gastric cancer. There was a concern of asphyxiation due to hemorrhage of the tumor; however, the tumor dislodged approximately 10 days after biopsy and tonsillar recurrence was not observed. The patient died 1 year 10 months post-operatively. In the literature there are cases with tonsillar metastases where surgical treatment, radiotherapy, and chemotherapy were performed and extension of survival was seen. Tonsillar metastasis is a form of systemic metastasis of a malignant tumor, and there is a high risk for asphyxiation from tumor dislodgement or hemorrhage. Thus, it is important to recognize tonsillar metastasis as an oncologic emergency

Oxidative Stress-Induced STIM2 Cysteine Modifications Suppress Store-Operated Calcium Entry

Store-operated calcium entry (SOCE) through STIM-gated ORAI channels governs vital cellular functions. In this context, SOCE controls cellular redox signaling and is itself regulated by redox modifications. However, the molecular mechanisms underlying this calcium-redox interplay and the functional outcomes are not fully understood. Here, we examine the role of STIM2 in SOCE redox regulation. Redox proteomics identify cysteine 313 as the main redox sensor of STIM2 in vitro and in vivo. Oxidative stress suppresses SOCE and calcium currents in cells overexpressing STIM2 and ORAI1, an effect that is abolished by mutation of cysteine 313. FLIM and FRET microscopy, together with MD simulations, indicate that oxidative modifications of cysteine 313 alter STIM2 activation dynamics and thereby hinder STIM2-mediated gating of ORAI1. In summary, this study establishes STIM2-controlled redox regulation of SOCE as a mechanism that affects several calcium-regulated physiological processes, as well as stress-induced pathologies