Fusion of indigenous knowledge and gamma spectrometry for soil mapping to support knowledge-based extension in Tanzania

Food shortages often threaten central Tanzania. Sustainable action adapted to local environmental conditions is desperately needed. In the framework of the TransSEC project, two food value chains in the Dodoma region of Tanzania were inspected in order to make propositions for improvement , spanning from soil preparation to product consumption. Therefore, soil mapping approaches were required to obtain rapid and reliable information. This would enable local farmers to participate in the development of upgrading strategies and extensionists to develop recommendations that take local soil conditions into account. In this study, a combination of participatory soil mapping and gamma ray spectrometry-assisted transect mapping was applied to establish local soil maps of two villages in the Dodoma region. Participatory mapping included key informant interviews, group discussions and transect walks. Local farmers indicated reference profiles for local soil types. Their gamma radiation signatures delivered base information for further soil exploration and soil unit delineation in the field. Finally, high resolution satellite images were used to establish the village soil maps. This approach allows capture of the major soil differences within a village territory and reduction of the costs of chemical analyses. Challenges were soil unit separation with gamma ray spectrometry due to erosional redistribution processes at the surface, correct translation of specific terms from local tongues as well as variable individual soil knowledge of local participants. Ultimately, the combination of local soil knowledge with innovative scientific mapping yielded quick results with sufficient spatial resolution for extension work.     

Long-term tests of a Jülich planar short stack with reversible solid oxide cells in both fuel cell and electrolysis modes

A two-cell planar stack in the Jülich F-design with solid oxide cells has been built and the reversible operation between fuel cell and electrolysis modes has been demonstrated. The cells were anode supported cells (ASC) with yttria-stabilized zirconia (YSZ) electrolytes, Ni/YSZ hydrogen electrodes and perovskite oxygen electrodes with lanthanum strontium cobalt ferrite (LSCF). This paper summarizes and discusses the preliminary experimental results on the long-term aging tests of the reversible solid oxide planar short stack for fuel cell operation (4000 h) at a current density of 0.5 A cm⁻² which shows a degradation of 0.6% per 1000 h and for steam electrolysis operation (3450 h) and co-electrolysis operation of CO₂ and H₂O (640 h) under different current densities from −0.3 to −0.875 A cm⁻² which show different degradation rates depending on current density and on steam or co-electrolysis.     

Sequestration and metabolism of protoxic pyrrolizidine alkaloids by larvae of the leaf beetle Platyphora boucardi and their transfer via pupae into defensive secretions of adults

Several neotropical leaf-beetles of the genus Platyphora ingest and specifically metabolize plant acquired pyrrolizidine alkaloids (PAs) of the lycopsamine type (e.g., rinderine or intermedine) and enrich the processed alkaloids in their exocrine defensive secretions. In contrast to the related palaearctic leaf beetles of the genus Oreina, which absorb and store only the non-toxic alkaloid N-oxides, Platyphora sequesters PAs exclusively as protoxic tertiary amines. In this study, the ability of P. boucardi larvae to accumulate PAs was investigated. Tracer studies with [¹⁴C]rinderine and its N-oxide revealed that P. boucardi larvae, like adult beetles, utilize the two alkaloidal forms with the same efficiency, but accumulate the alkaloid as a tertiary amine exclusively. Ingested rinderine is rapidly epimerized to intermedine, which is localized in the hemolymph and all other tissues; it is also detected on the larval surface. Like adults, larvae are able to synthesize their own alkaloid esters (beetle PAs) from orally administered [¹⁴C]retronecine and endogenous aliphatic 2-hydroxy acids. These retronecine esters show the same tissue distribution as intermedine. A long-term feeding experiment lasting for almost four months revealed that retronecine esters synthesized from [¹⁴C]retronecine in the larvae are transferred from larvae via pupae into the exocrine glands of adult beetles. Pupae contain ca. 45% of the labeled retronecine originally ingested, metabolized, and stored by larvae; ca. 12% of larval radioactivity could be recovered from the defensive secretions of adults sampled successively over two and a half months. Almost all of this radioactivity is found in the insect-made retronecine esters that are highly enriched in the defensive secretions, i.e., more than 200-fold higher concentration compared to pupae.     

Advances in macro-scale laser processing

Laser material processing is a technology with an increasing number of industrial applications, especially for aviation and automotive. The present keynote paper focusses on the advances in macro-scale laser processing, meaning that the laser generated structures are large enough to be visible with the naked eye. Next to that, also the reasons for the advances, especially the improvements regarding the power and the beam quality of the laser sources, the higher capabilities of the systems technologies and an increasing process understanding are shown. Nevertheless, challenges like a holistic understanding of the physical phenomena and the evolution of defects in some processing methods remain to be solved in future.     

采用计量型扫描力显微镜校准微纳米标准样板

为了建立质量保证体系,微米和纳米样板至今仍被广泛地应用于校准微纳米尺度的测量仪器中．介绍了应用由德国联邦物理研究所开发研究的、测量范围为25 mm×25 mm×5 mm的计量型扫描力显微镜(M-LRSFM)的校准方法．上述计量型扫描力显微镜配置有三个零拍的激光干涉仪,可分别测量沿x、y、z三条轴线方向的位移,因而其测量值可直接溯源于“米”定义．此种M-LRSFM能够校准横向的微纳尺度的结构尺寸,诸如阶梯高度、一维和二维光栅、镀层厚度、线宽、微纳尺度的表面粗糙度等．作为实例,介绍了一种横向样板的校准程序及获得的校准结果．研究表明这种方法适合于校验扫描电子显微镜(SEM)的放大倍率．     

SWOF - an open framework for shared workspaces to support different cooperation tasks

Computer supported collaborative work (CSCW) allows people to cooperate by computers from different places and at different times. To enable an easier integration of such collaborative components into web-based communities and portals, a Shared Workspace Open Framework (SWOF) was developed. This framework provides the basic features of shared workspaces and can be customized to different cooperation cases. High usability is an important aspect of the implementation. To achieve these aims SWOF focuses on an information space with more task-suited item-types that can help to pre-structure the information. Thus, on the one hand the system can help the users to write down the needed information in a consistent way and, on the other, could reduce the arguments between the group members on how to structure their workspace. As a use case for SWOF the development of a Web-based portal for the community of man-machine interaction was chosen. In the project MMI-Interaktiv, a portal is built with a SWOF-based shared workspace component. An evaluation for this use case is presented.     

Sendai viruses with altered P, V, and W protein expression

Wild-type Sendai virus expresses three proteins containing the N-terminal half of the P protein open reading frame due to mRNA editing; a full-length P protein (ca. 70% of the total), a V protein with the N-terminal half fused to a Cys-rich Zn(2+)-binding domain (ca. 25% of the total), and a W protein representing the N-terminal half alone (ca. 5% of the total). To examine the role of these proteins in the virus life cycle, we have prepared recombinant viruses in which the normal V mRNA expresses a W protein (V-stop; 70% P, 30% W), one which cannot edit its P gene mRNA (delta 6A; 100% P), and one which overedits its mRNA like parainfluenza virus type 3 (swap/8;20-40% P, 30% V, 30% W). All these viruses were readily recovered and grew to similar titers in eggs, and except for the P gene products, cell lines individually infected with these viruses accumulated similar amounts of viral macromolecules. The relative competitive advantage of each virus was determined by multiple cycle coinfections of eggs and found to be rSeV-Vstop = rSeV-wt > rSeV-delta 6A > rSeV-swap/8. On the other hand, rSeV-swap/8 underwent multiple cycles of replication in C57BI/6 mouse lungs and was highly virulent for these animals, whereas rSeV-delta 6A was avirulent in mice and this infection was quickly cleared. Remarkably, rSeV-Vstop appeared to be more virulent for inbred C57BI/6 mice than rSeV-wt, but was partially attenuated in infections of outbred ICR mice. Thus, the expression of either the V or the W proteins is sufficient for multiple cycles of infection and pathogenesis in C57BI/6 mice, whereas W can only partially substitute for V for pathogenesis in ICR mice.