Portable snapshot spectral imaging for agriculture

High-resolution proximal and remote sensing applications can consolidate sustainable, prevention- and precision-oriented crop management strategies to decrease production risks. This paper shows significant perspectives, own developments and technical aspects of high resolution remote sensing in the context of field applications. Moreover, we provide an overview of snapshot hyperspectral imaging and potential field video sensors to identify areas of interest for their future development. One of the main conclusions of our paper is that non-scanning snapshot hyperspectral imaging technology may enable researchers to overcome the gap in the “point to image” transition of field sensing, while providing a flexible solution for regular variable-rate applications

Portable snapshot spectral imaging for agriculture

High-resolution proximal and remote sensing applications can consolidate sustainable, prevention- and precision-oriented crop management strategies to decrease production risks. This paper shows significant perspectives, own developments and technical aspects of high resolution remote sensing in the context of field applications. Moreover, we provide an overview of snapshot hyperspectral imaging and potential field video sensors to identify areas of interest for their future development. One of the main conclusions of our paper is that non-scanning snapshot hyperspectral imaging technology may enable researchers to overcome the gap in the “point to image” transition of field sensing, while providing a flexible solution for regular variable-rate applications

State-to-state methane-surface scattering as a probe of catalytic activity

Quantum state-resolved scattering experiments for methane molecules colliding with a catalytically active nickel surface are compared to scattering from a nickel surface passivated by a single layer of graphene. The vibrational state distribution of the scattered methane is observed to differ dramatically for the two surfaces. Quantum-mechanical inelastic scattering calculations show that these differences are related to the catalytic activity of the surface impact site. Our results demonstrate how inelastic scattering can be used to probe the reactive potential-energy surfaces of molecule-metal systems important to heterogeneous catalysis

Left Atrial Chamber and Appendage Function After Internal Atrial Defibrillation: A Prospective and Serial Transesophageal Echocardiographic Study

AbstractObjectives. The purpose of this prospective study was to assess left atrial chamber and appendage function after internal atrial defibrillation of atrial fibrillation and to evaluate the time course of recovery.Background. External cardioversion of atrial fibrillation may result in left atrial appendage dysfunction (“stunning”) and may promote thrombus formation. In contrast to external cardioversion, internal atrial defibrillation utilizes lower energies; however, it is unknown whether the use of lower energies may avoid stunning of the left atrial appendage.Methods. Transesophageal and transthoracic echocardiography were performed in 20 patients 24 h before and 1 and 7 days after internal atrial defibrillation to assess both left atrial chamber and appendage function. Transthoracic echocardiography was again performed 28 days after internal atrial defibrillation to assess left atrial function. The incidence and degree of spontaneous echo contrast accumulation (range 1+ to 4+) was noted, and peak emptying velocities of the left atrial appendage were measured before and after internal atrial defibrillation. To determine left atrial mechanical function, peak A wave velocities were obtained from transmitral flow velocity profiles.Results. Sinus rhythm was restored in all patients. The mean ± SD peak A wave velocities increased gradually after cardioversion, from 0.47 ± 0.16 m/s at 24 h to 0.61 ± 0.13 m/s after 7 days (p < 0.05) and 0.63 ± 0.13 m/s after 4 weeks. Peak emptying velocities of the left atrial appendage were 0.37 ± 0.16 m/s before internal atrial defibrillation, decreased significantly after internal atrial defibrillation to 0.23 ± 0.1 m/s at 24 h (p < 0.01) and then recovered to 0.49 ± 0.23 m/s (p < 0.01) after 7 days. The corresponding values for the degree of spontaneous echo contrast were 1.2 ± 1.2 before internal atrial defibrillation versus 2.0 ± 1.0 (p < 0.01) and 1.1 ± 1.3 (p < 0.01) 1 and 7 days after cardioversion, respectively. One patient developed a new thrombus in the left atrial appendage, and another had a thromboembolic event after internal atrial defibrillation.Conclusions. Internal atrial defibrillation causes depressed left atrial chamber and appendage function and may result in the subacute accumulation of spontaneous echo contrast and development of new thrombi after cardioversion. These findings have important clinical implications for anticoagulation therapy before and after low energy internal atrial defibrillation in patients with atrial fibrillation.(J Am Coll Cardiol 1997;29:131–8)

A scoring system for the follow up study of nuclear receptor coactivator complexes

We have systematically isolated a variety of coactivator complexes from HeLa S3 cells using proteomic approaches. In the present report, we have evaluated twelve coactivator complexes involved in nuclear receptor-dependent gene transcription that have been purified by using an immunoprecipitation method. The twelve purified coactivator complexes are SRC-1, SRC-2, SRC-3, CBP, p300, CAPER, E6-AP, ASC-1, CoREST, CRSP3, CRSP2, and CDK7 containing complexes. We have identified 153 protein components associated with these coactivator complexes using mass spectrometry. In order to systematically characterize the functional roles for these components in nuclear receptor-dependent gene transcription and their investigative potential, we have developed a scoring system. This scoring system is comprised of biological and experimental parameters. The biological evaluation considers aspects such as intrinsic enzymatic activity of a protein component, cellular signaling processes in which protein components may be involved, associations with human disease, specific protein motifs, and the known biological roles of other interacting partners of the identified protein. In the experimental evaluation, we include parameters, such as the availability of research materials for the functional study of the identified protein component; such as full-length cDNA clones, antibodies, and commercially available knock-out embryonic stem (ES) cells. Each scoring parameter has been assigned an arbitrary number of points according to perceived relative importance. On the basis of this scoring system, we prioritized each of the protein components in terms of the likelihood of their importance for coactivator complex networking in nuclear receptor-dependent gene transcription

The Sodium/Proline Transporter PutP of Helicobacter pylori

Helicobacter pylori is cause of chronic gastritis, duodenal ulcer and gastric carcinoma in humans. L-proline is a preferred energy source of the microaerophilic bacterium. Previous analyses revealed that HpputP and HpputA, the genes that are predicted to play a central role in proline metabolism as they encode for the proline transporter and proline dehydrogenase, respectively, are essential for stomach colonization. Here, the molecular basis of proline transport in H. pylori by HpPutP was investigated experimentally for the first time. Measuring radiolabeled substrate transport in H. pylori and E. coli heterologously expressing HpputP as well as in proteoliposomes reconstituted with HpPutP, we demonstrate that the observed proline transport in H. pylori is mediated by HpPutP. HpPutP is specific and exhibits a high affinity for L-proline. Notably, L-proline transport is exclusively dependent on Na+ as coupling ion, i.e., Na+/L-proline symport, reminiscent to the properties of PutP of E. coli even though H. pylori lives in a more acidic environment. Homology model-based structural comparisons and substitution analyses identified amino acids crucial for function. HpPutP-catalyzed proline uptake was efficiently inhibited by the known proline analogs 3,4-dehydro-D,L-proline and L-azetidine-2-carboxylic acid