Abstract. It is control that turns scientific knowledge into useful technology: in physics and engineering it provides a systematic way for driving a dynamical system from a given initial state into a desired target state with minimized expenditure of energy and resources. As one of the cornerstones for enabling quantum technologies, optimal quantum control keeps evolving and expanding into areas as diverse as quantumenhanced sensing, manipulation of single spins, photons, or atoms, optical spectroscopy, photochemistry, magnetic resonance (spectroscopy as well as medical imaging), quantum information processing and quantum simulation. In this communication, state-of-the-art quantum control techniques are reviewed and put into perspective by a consortium of experts in optimal control theory and applications to spectroscopy, imaging, as well as quantum dynamics of closed and open systems. We address key challenges and sketch a roadmap for future developments. ForewordThe authors of this paper represent the QUAINT consortium, a European Coordination Action on Optimal Control of Quantum Systems, funded by the European Commission Framework Programme 7, Future Emerging Technologies FET-OPEN programme and the Virtual Facility for Quantum Control (VF-QC). This consortium has considerable expertise in optimal control theory and its applications to quantum systems, both in existing areas, such as spectroscopy and imaging, and in emerging quantum technologies, such as quantum information processing, quantum communication, quantum simulation a e-mail: fwm@lusi.uni-sb.de and quantum sensing. The list of challenges for quantum control has been gathered by a broad poll of leading researchers across the communities of general and mathematical control theory, atomic, molecular-, and chemical physics, electron and nuclear magnetic resonance spectroscopy, as well as medical imaging, quantum information, communication and simulation. 144 experts in these fields have provided feedback and specific input on the state of the art, mid-term and long-term goals. Those have been summarized in this document, which can be viewed as a perspectives paper, providing a roadmap for the future development of quantum control. Because such an endeavour can hardly ever be complete (there are many additional areas of quantum control applications, such as spintronics, nano-optomechanical technologies etc.), this roadmap

To gain insight into the regulatory mechanisms of sugar signaling in plants, the effect of derivatives of the transport sugar sucrose (Suc), the Suc isomers palatinose and turanose, and the Suc analog fluoro-Suc were tested. Photo-autotrophic suspension culture cells of tomato (Lycopersicon peruvianum) were used to study their effect on the regulation of marker genes of source and sink metabolism, photosynthesis, and the activation of mitogen-activated protein kinases (MAPKs). Suc and glucose (Glc) resulted in reverse regulation of source and sink metabolism. Whereas the mRNA level of extracellular invertase (Lin6) was induced, the transcript level of small subunit of ribulose bisphosphate carboxylase (RbcS) was repressed. In contrast, turanose, palatinose, and fluoro-Suc only rapidly induced Lin6 mRNA level, whereas the transcript level of RbcS was not affected. The differential effect of the metabolizable and non-metabolizable sugars on RbcS mRNA regulation was reflected by the fact that only Suc and Glc inhibited photosynthesis and chlorophyll fluorescence. The activation of different signal transduction pathways by sugars was further supported by the analysis of the activation of MAPKs. MAPK activity was found to be strongly activated by turanose, palatinose, and fluoro-Suc, but not by Suc and Glc. To analyze the role of sugars in relation to pathogen perception, an elicitor preparation of Fusarium oxysporum lycopersici was used. The strong activation of MAPKs and the fast and transient induction of Lin6 expresssion by the fungal elicitor resembles the effect of turanose, palatinose, and fluoro-Suc and indicates that non-metabolizable sugars are sensed as stress-related stimuli.In recent years, sugars have been recognized as important signal molecules that affect a variety of physiological responses and in particular regulate genes involved in photosynthesis, sink metabolism, and defense response (Koch, 1996;Smeekens, 1998;Roitsch, 1999;Sheen et al., 1999). Whereas the effect of sugars on gene regulation is well established, the nature of the sugar signal, and the molecular mechanisms involved in sugar perception and intracellular signal transmission, are largely unknown. Suc is the major form of translocated carbon in higher plants and was shown to regulate a number of carbohydrate-responsive genes. Whereas in many cases the effects of Suc could be mimicked by hexoses, such as Glc and Fru, a few studies demonstrated the existence of Suc-specific regulatory pathways (Chiou and Bush, 1998;Rook et al., 1998). In principle, a sugar signal could be generated by extracellular recognition via a soluble or membranebound receptor molecule or by intracellular sensing at different stages of sugar metabolism. For hexoses, a dual role of hexokinase in sugar sensing and glycolysis has been proposed (Jang and Sheen, 1997; Jang et al., 1997) that is a matter of a controversial debate (Halford et al., 1999). Additional membranebased sensing systems have been implied both for hexoses and Suc. Primary lines of evidence are ...

Abstract. A flow-sensitive nuclear magnetic resonance (NMR) microimaging technique was applied to measure directly the in-vivo water flow in 6-d-old castor bean seedlings. The achieved in-plane resolution of the technique allowed discrimination between xylem and phloem water flow. Both the xylem-and the phloem-average flow velocities in the intact seedling could be quantified. Furthermore, the total conductive cross-sectional area of the xylem vessels and the phloem sieve elements could be determined using the non-invasive and non-destructive NMR microimaging technique. Hence, it was possible to calculate the in-vivo volume flow rates for both xylem and phloem water flow. Our non-destructive technique showed that previously used methods to measure phloem water flow affected the flow rate itself. In the intact seedlings we found values of 16.6 pl-h-1, two fold lower than those previously estimated from phloem exudation rates. Finally, our results demonstrate for the first time that water is internally circulated between phloem and xylem, and that water flow within the xylem is maintained by this internally circulated water, even in the absence of any significant transpiration or evaporation.

The fate of sucrose (Suc) supplied via the phloem to developing oilseed rape (Brassica napus) seeds has been investigated by supplying [14 C]Suc to pedicels of detached, developing siliques. The method gives high, sustained rates of lipid synthesis in developing embryos within the silique comparable with those on the intact plant. At very early developmental stages (3 d after anthesis), the liquid fraction that occupies most of the interior of the seed has a very high hexose-to-Suc ratio and [14 C]Suc entering the seeds is rapidly converted to hexoses. Between 3 and 12 d after anthesis, the hexose-to-Suc ratio of the liquid fraction of the seed remains high, but the fraction of [ 14 C]Suc converted to hexose falls dramatically. Instead, most of the [ 14 C]Suc entering the seed is rapidly converted to products in the growing embryo. These data, together with light and nuclear magnetic resonance microscopy, reveal complex compartmentation of sugar metabolism and transport within the seed during development. The bulk of the sugar in the liquid fraction of the seed is probably contained within the central vacuole of the endosperm. This sugar is not in contact with the embryo and is not on the path taken by carbon from the phloem to the embryo. These findings have important implications for the sugar switch model of embryo development and for understanding the relationship between the embryo and the surrounding endosperm.