Project acronym ANTILEAK
Project Development of antagonists of vascular leakage
Researcher (PI) Pipsa SAHARINEN
Host Institution (HI) HELSINGIN YLIOPISTO
Country Finland
Call Details Consolidator Grant (CoG), LS4, ERC-2017-COG
Summary Dysregulation of capillary permeability is a severe problem in critically ill patients, but the mechanisms involved are poorly understood. Further, there are no targeted therapies to stabilize leaky vessels in various common, potentially fatal diseases, such as systemic inflammation and sepsis, which affect millions of people annually. Although a multitude of signals that stimulate opening of endothelial cell-cell junctions leading to permeability have been characterized using cellular and in vivo models, approaches to reverse the harmful process of capillary leakage in disease conditions are yet to be identified. I propose to explore a novel autocrine endothelial permeability regulatory system as a potentially universal mechanism that antagonizes vascular stabilizing ques and sustains vascular leakage in inflammation. My group has identified inflammation-induced mechanisms that switch vascular stabilizing factors into molecules that destabilize vascular barriers, and identified tools to prevent the barrier disruption. Building on these discoveries, my group will use mouse genetics, structural biology and innovative, systematic antibody development coupled with gene editing and gene silencing technology, in order to elucidate mechanisms of vascular barrier breakdown and repair in systemic inflammation. The expected outcomes include insights into endothelial cell signaling and permeability regulation, and preclinical proof-of-concept antibodies to control endothelial activation and vascular leakage in systemic inflammation and sepsis models. Ultimately, the new knowledge and preclinical tools developed in this project may facilitate future development of targeted approaches against vascular leakage.
Summary
Dysregulation of capillary permeability is a severe problem in critically ill patients, but the mechanisms involved are poorly understood. Further, there are no targeted therapies to stabilize leaky vessels in various common, potentially fatal diseases, such as systemic inflammation and sepsis, which affect millions of people annually. Although a multitude of signals that stimulate opening of endothelial cell-cell junctions leading to permeability have been characterized using cellular and in vivo models, approaches to reverse the harmful process of capillary leakage in disease conditions are yet to be identified. I propose to explore a novel autocrine endothelial permeability regulatory system as a potentially universal mechanism that antagonizes vascular stabilizing ques and sustains vascular leakage in inflammation. My group has identified inflammation-induced mechanisms that switch vascular stabilizing factors into molecules that destabilize vascular barriers, and identified tools to prevent the barrier disruption. Building on these discoveries, my group will use mouse genetics, structural biology and innovative, systematic antibody development coupled with gene editing and gene silencing technology, in order to elucidate mechanisms of vascular barrier breakdown and repair in systemic inflammation. The expected outcomes include insights into endothelial cell signaling and permeability regulation, and preclinical proof-of-concept antibodies to control endothelial activation and vascular leakage in systemic inflammation and sepsis models. Ultimately, the new knowledge and preclinical tools developed in this project may facilitate future development of targeted approaches against vascular leakage.
Max ERC Funding
1 999 770 €
Duration
Start date: 2018-05-01, End date: 2023-04-30
Project acronym AROMA-CFD
Project Advanced Reduced Order Methods with Applications in Computational Fluid Dynamics
Researcher (PI) Gianluigi Rozza
Host Institution (HI) SCUOLA INTERNAZIONALE SUPERIORE DI STUDI AVANZATI DI TRIESTE
Country Italy
Call Details Consolidator Grant (CoG), PE1, ERC-2015-CoG
Summary The aim of AROMA-CFD is to create a team of scientists at SISSA for the development of Advanced Reduced Order Modelling techniques with a focus in Computational Fluid Dynamics (CFD), in order to face and overcome many current limitations of the state of the art and improve the capabilities of reduced order methodologies for more demanding applications in industrial, medical and applied sciences contexts. AROMA-CFD deals with strong methodological developments in numerical analysis, with a special emphasis on mathematical modelling and extensive exploitation of computational science and engineering. Several tasks have been identified to tackle important problems and open questions in reduced order modelling: study of bifurcations and instabilities in flows, increasing Reynolds number and guaranteeing stability, moving towards turbulent flows, considering complex geometrical parametrizations of shapes as computational domains into extended networks. A reduced computational and geometrical framework will be developed for nonlinear inverse problems, focusing on optimal flow control, shape optimization and uncertainty quantification. Further, all the advanced developments in reduced order modelling for CFD will be delivered for applications in multiphysics, such as fluid-structure interaction problems and general coupled phenomena involving inviscid, viscous and thermal flows, solids and porous media. The advanced developed framework within AROMA-CFD will provide attractive capabilities for several industrial and medical applications (e.g. aeronautical, mechanical, naval, off-shore, wind, sport, biomedical engineering, and cardiovascular surgery as well), combining high performance computing (in dedicated supercomputing centers) and advanced reduced order modelling (in common devices) to guarantee real time computing and visualization. A new open source software library for AROMA-CFD will be created: ITHACA, In real Time Highly Advanced Computational Applications.
Summary
The aim of AROMA-CFD is to create a team of scientists at SISSA for the development of Advanced Reduced Order Modelling techniques with a focus in Computational Fluid Dynamics (CFD), in order to face and overcome many current limitations of the state of the art and improve the capabilities of reduced order methodologies for more demanding applications in industrial, medical and applied sciences contexts. AROMA-CFD deals with strong methodological developments in numerical analysis, with a special emphasis on mathematical modelling and extensive exploitation of computational science and engineering. Several tasks have been identified to tackle important problems and open questions in reduced order modelling: study of bifurcations and instabilities in flows, increasing Reynolds number and guaranteeing stability, moving towards turbulent flows, considering complex geometrical parametrizations of shapes as computational domains into extended networks. A reduced computational and geometrical framework will be developed for nonlinear inverse problems, focusing on optimal flow control, shape optimization and uncertainty quantification. Further, all the advanced developments in reduced order modelling for CFD will be delivered for applications in multiphysics, such as fluid-structure interaction problems and general coupled phenomena involving inviscid, viscous and thermal flows, solids and porous media. The advanced developed framework within AROMA-CFD will provide attractive capabilities for several industrial and medical applications (e.g. aeronautical, mechanical, naval, off-shore, wind, sport, biomedical engineering, and cardiovascular surgery as well), combining high performance computing (in dedicated supercomputing centers) and advanced reduced order modelling (in common devices) to guarantee real time computing and visualization. A new open source software library for AROMA-CFD will be created: ITHACA, In real Time Highly Advanced Computational Applications.
Max ERC Funding
1 656 579 €
Duration
Start date: 2016-05-01, End date: 2021-04-30
Project acronym BHIVE
Project Bio-derived HIgh Value polymers through novel Enzyme function
Researcher (PI) Emma Rusi Master
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Country Finland
Call Details Consolidator Grant (CoG), LS9, ERC-2014-CoG
Summary Recent advances in systems-level study of cells and organisms have revealed the enormous potential to live more sustainably through better use of biological processes. Plants sustainably synthesize the most abundant and diverse materials on Earth. By applying recent advances in life science technology, we can better harness renewable plant resources and bioconversion processes, to develop environmentally and politically sustainable human enterprise and lifestyles. At the same time, the global market for high-value biochemicals and bioplastics from forest and agricultural sources is rapidly increasing, which presents new opportunities for forest and agricultural sectors.
The overall aim of BHIVE is to illuminate uncharted regions of genome and metagenome sequences to discover entirely new protein families that can be used to sustainably synthesize novel, high-value biomaterials from renewable plant resources. The approach will include three parallel research thrusts: 1) strategic analysis of transcriptome and metagenome sequences to identify proteins with entirely unknown function relevant to biomass (lignocellulose) transformation, 2) mapping of uncharted regions within phylogenetic trees of poorly characterized enzyme families with recognized potential to modify the chemistry and biophysical properties of plant polysaccharides, and 3) the design and development of novel enzyme screens to directly address the increasing limitations of existing assays to uncover entirely new protein functions. BHIVE will be unique in its undivided focus on characterizing lignocellulose-active proteins encoded by the 30-40% of un-annotated sequence, or genomic “dark matter”, typical of nearly all genome sequences. In this way, BHIVE tackles a key constraint to fully realizing the societal and environmental benefits of the genomics era.
Summary
Recent advances in systems-level study of cells and organisms have revealed the enormous potential to live more sustainably through better use of biological processes. Plants sustainably synthesize the most abundant and diverse materials on Earth. By applying recent advances in life science technology, we can better harness renewable plant resources and bioconversion processes, to develop environmentally and politically sustainable human enterprise and lifestyles. At the same time, the global market for high-value biochemicals and bioplastics from forest and agricultural sources is rapidly increasing, which presents new opportunities for forest and agricultural sectors.
The overall aim of BHIVE is to illuminate uncharted regions of genome and metagenome sequences to discover entirely new protein families that can be used to sustainably synthesize novel, high-value biomaterials from renewable plant resources. The approach will include three parallel research thrusts: 1) strategic analysis of transcriptome and metagenome sequences to identify proteins with entirely unknown function relevant to biomass (lignocellulose) transformation, 2) mapping of uncharted regions within phylogenetic trees of poorly characterized enzyme families with recognized potential to modify the chemistry and biophysical properties of plant polysaccharides, and 3) the design and development of novel enzyme screens to directly address the increasing limitations of existing assays to uncover entirely new protein functions. BHIVE will be unique in its undivided focus on characterizing lignocellulose-active proteins encoded by the 30-40% of un-annotated sequence, or genomic “dark matter”, typical of nearly all genome sequences. In this way, BHIVE tackles a key constraint to fully realizing the societal and environmental benefits of the genomics era.
Max ERC Funding
1 977 781 €
Duration
Start date: 2015-09-01, End date: 2020-12-31
Project acronym BioDisOrder
Project Order and Disorder at the Surface of Biological Membranes.
Researcher (PI) Alfonso DE SIMONE
Host Institution (HI) UNIVERSITA DEGLI STUDI DI NAPOLI FEDERICO II
Country Italy
Call Details Consolidator Grant (CoG), PE4, ERC-2018-COG
Summary Heterogeneous biomolecular mechanisms at the surface of cellular membranes are often fundamental to generate function and dysfunction in living systems. These processes are governed by transient and dynamical macromolecular interactions that pose tremendous challenges to current analytical tools, as the majority of these methods perform best in the study of well-defined and poorly dynamical systems. This proposal aims at a radical innovation in the characterisation of complex processes that are dominated by structural order and disorder, including those occurring at the surface of biological membranes such as cellular signalling, the assembly of molecular machinery, or the regulation vesicular trafficking.
I outline a programme to realise a vision where the combination of experiments and theory can delineate a new analytical platform to study complex biochemical mechanisms at a multiscale level, and to elucidate their role in physiological and pathological contexts. To achieve this ambitious goal, my research team will develop tools based on the combination of nuclear magnetic resonance (NMR) spectroscopy and molecular simulations, which will enable probing the structure, dynamics, thermodynamics and kinetics of complex protein-protein and protein-membrane interactions occurring at the surface of cellular membranes. The ability to advance both the experimental and theoretical sides, and their combination, is fundamental to define the next generation of methods to achieve our transformative aims. We will provide evidence of the innovative nature of the proposed multiscale approach by addressing some of the great questions in neuroscience and elucidate the details of how functional and aberrant biological complexity is achieved via the fine tuning between structural order and disorder at the neuronal synapse.
Summary
Heterogeneous biomolecular mechanisms at the surface of cellular membranes are often fundamental to generate function and dysfunction in living systems. These processes are governed by transient and dynamical macromolecular interactions that pose tremendous challenges to current analytical tools, as the majority of these methods perform best in the study of well-defined and poorly dynamical systems. This proposal aims at a radical innovation in the characterisation of complex processes that are dominated by structural order and disorder, including those occurring at the surface of biological membranes such as cellular signalling, the assembly of molecular machinery, or the regulation vesicular trafficking.
I outline a programme to realise a vision where the combination of experiments and theory can delineate a new analytical platform to study complex biochemical mechanisms at a multiscale level, and to elucidate their role in physiological and pathological contexts. To achieve this ambitious goal, my research team will develop tools based on the combination of nuclear magnetic resonance (NMR) spectroscopy and molecular simulations, which will enable probing the structure, dynamics, thermodynamics and kinetics of complex protein-protein and protein-membrane interactions occurring at the surface of cellular membranes. The ability to advance both the experimental and theoretical sides, and their combination, is fundamental to define the next generation of methods to achieve our transformative aims. We will provide evidence of the innovative nature of the proposed multiscale approach by addressing some of the great questions in neuroscience and elucidate the details of how functional and aberrant biological complexity is achieved via the fine tuning between structural order and disorder at the neuronal synapse.
Max ERC Funding
1 999 945 €
Duration
Start date: 2019-06-01, End date: 2024-05-31
Project acronym CAPTUR3D
Project CAPTURING THE PHYSICS OF LIFE ON 3D-TRAFFICKING SUBCELLULAR NANOSYSTEMS
Researcher (PI) Francesco CARDARELLI
Host Institution (HI) SCUOLA NORMALE SUPERIORE
Country Italy
Call Details Consolidator Grant (CoG), PE3, ERC-2019-COG
Summary Which physical principles govern life regulation at the level of subcellular, membrane-enclosed nanosystems, such as transport vesicles and organelles? How do they achieve controlled movements across the crowded intracellular world? Which is the structural and functional organization of their surface and their lumen? This is only a small subset of key open questions that the biophysical approach envisaged here will allow to answer directly within living matter, for the first time.
Thus far, state-of-the-art optical microscopy tools for delivering quantitative information in living matter failed to subtract the natural 3D movement of subcellular nanosystems while preserving the spatial and temporal resolution required to probe their structure and function at the molecular level.
CAPTUR3D will tackle this bottleneck. An excitation light-beam will be focused in a periodic orbit around the nanosystem of interest and used to localize its position with unprecedented spatial (~10 nm) and temporal (~1000 Hz frequency response) resolution. Such privileged observation point will push biophysical investigations to a new level. For the first time, state-of-the-art imaging technologies and analytical tools (e.g. fluorescence correlation spectroscopy), will be used to perform molecular investigations on a moving, nanoscopic reference system.
The insulin secretory granule (ISG) is selected as a paradigmatic case study. Key open issues at the ISG level are selected, namely: (i) ISG-environment interactions and their role in directing ISG trafficking, (ii) ISG-membrane spatiotemporal organization, (iii) ISG-lumen structural and functional organization, (iv) ISG alterations in type-2 diabetes (T2D). These issues will be tackled directly within human-derived Langherans islets.
CAPTUR3D is envisioned not only to foster our knowledge on T2D physiopathology but also to concomitantly drive an unprecedented revolution in the way we address living matter at the subcellular scale.
Summary
Which physical principles govern life regulation at the level of subcellular, membrane-enclosed nanosystems, such as transport vesicles and organelles? How do they achieve controlled movements across the crowded intracellular world? Which is the structural and functional organization of their surface and their lumen? This is only a small subset of key open questions that the biophysical approach envisaged here will allow to answer directly within living matter, for the first time.
Thus far, state-of-the-art optical microscopy tools for delivering quantitative information in living matter failed to subtract the natural 3D movement of subcellular nanosystems while preserving the spatial and temporal resolution required to probe their structure and function at the molecular level.
CAPTUR3D will tackle this bottleneck. An excitation light-beam will be focused in a periodic orbit around the nanosystem of interest and used to localize its position with unprecedented spatial (~10 nm) and temporal (~1000 Hz frequency response) resolution. Such privileged observation point will push biophysical investigations to a new level. For the first time, state-of-the-art imaging technologies and analytical tools (e.g. fluorescence correlation spectroscopy), will be used to perform molecular investigations on a moving, nanoscopic reference system.
The insulin secretory granule (ISG) is selected as a paradigmatic case study. Key open issues at the ISG level are selected, namely: (i) ISG-environment interactions and their role in directing ISG trafficking, (ii) ISG-membrane spatiotemporal organization, (iii) ISG-lumen structural and functional organization, (iv) ISG alterations in type-2 diabetes (T2D). These issues will be tackled directly within human-derived Langherans islets.
CAPTUR3D is envisioned not only to foster our knowledge on T2D physiopathology but also to concomitantly drive an unprecedented revolution in the way we address living matter at the subcellular scale.
Max ERC Funding
1 985 750 €
Duration
Start date: 2021-03-01, End date: 2026-02-28
Project acronym CAVE
Project Challenges and Advancements in Virtual Elements
Researcher (PI) Lourenco Beirao da veiga
Host Institution (HI) UNIVERSITA' DEGLI STUDI DI MILANO-BICOCCA
Country Italy
Call Details Consolidator Grant (CoG), PE1, ERC-2015-CoG
Summary The Virtual Element Method (VEM) is a novel technology for the discretization of partial differential equations (PDEs), that shares the same variational background as the Finite Element Method. First but not only, the VEM responds to the strongly increasing interest in using general polyhedral and polygonal meshes in the approximation of PDEs without the limit of using tetrahedral or hexahedral grids. By avoiding the explicit integration of the shape functions that span the discrete space and introducing an innovative construction of the stiffness matrixes, the VEM acquires very interesting properties and advantages with respect to more standard Galerkin methods, yet still keeping the same coding complexity. For instance, the VEM easily allows for polygonal/polyhedral meshes (even non-conforming) with non-convex elements and possibly with curved faces; it allows for discrete spaces of arbitrary C^k regularity on unstructured meshes.
The main scope of the project is to address the recent theoretical challenges posed by VEM and to assess whether this promising technology can achieve a breakthrough in applications. First, the theoretical and computational foundations of VEM will be made stronger. A deeper theoretical insight, supported by a wider numerical experience on benchmark problems, will be developed to gain a better understanding of the method's potentials and set the foundations for more applicative purposes. Second, we will focus our attention on two tough and up-to-date problems of practical interest: large deformation elasticity (where VEM can yield a dramatically more efficient handling of material inclusions, meshing of the domain and grid adaptivity, plus a much stronger robustness with respect to large grid distortions) and the cardiac bidomain model (where VEM can lead to a more accurate domain approximation through MRI data, a flexible refinement/de-refinement procedure along the propagation front, to an exact satisfaction of conservation laws).
Summary
The Virtual Element Method (VEM) is a novel technology for the discretization of partial differential equations (PDEs), that shares the same variational background as the Finite Element Method. First but not only, the VEM responds to the strongly increasing interest in using general polyhedral and polygonal meshes in the approximation of PDEs without the limit of using tetrahedral or hexahedral grids. By avoiding the explicit integration of the shape functions that span the discrete space and introducing an innovative construction of the stiffness matrixes, the VEM acquires very interesting properties and advantages with respect to more standard Galerkin methods, yet still keeping the same coding complexity. For instance, the VEM easily allows for polygonal/polyhedral meshes (even non-conforming) with non-convex elements and possibly with curved faces; it allows for discrete spaces of arbitrary C^k regularity on unstructured meshes.
The main scope of the project is to address the recent theoretical challenges posed by VEM and to assess whether this promising technology can achieve a breakthrough in applications. First, the theoretical and computational foundations of VEM will be made stronger. A deeper theoretical insight, supported by a wider numerical experience on benchmark problems, will be developed to gain a better understanding of the method's potentials and set the foundations for more applicative purposes. Second, we will focus our attention on two tough and up-to-date problems of practical interest: large deformation elasticity (where VEM can yield a dramatically more efficient handling of material inclusions, meshing of the domain and grid adaptivity, plus a much stronger robustness with respect to large grid distortions) and the cardiac bidomain model (where VEM can lead to a more accurate domain approximation through MRI data, a flexible refinement/de-refinement procedure along the propagation front, to an exact satisfaction of conservation laws).
Max ERC Funding
980 634 €
Duration
Start date: 2016-07-01, End date: 2021-06-30
Project acronym CAVITYQPD
Project Cavity quantum phonon dynamics
Researcher (PI) Mika Antero Sillanpaeae
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Country Finland
Call Details Consolidator Grant (CoG), PE3, ERC-2013-CoG
Summary "Large bodies usually follow the classical equations of motion. Deviations from this can be called
macroscopic quantum behavior. These phenomena have been experimentally verified with cavity Quantum
Electro Dynamics (QED), trapped ions, and superconducting Josephson junction systems. Recently, evidence
was obtained that also moving objects can display such behavior. These objects are micromechanical
resonators (MR), which can measure tens of microns in size and are hence quite macroscopic. The degree of
freedom is their vibrations: phonons.
I propose experimental research in order to push quantum mechanics closer to the classical world than ever
before. I will try find quantum behavior in the most classical objects, that is, slowly moving bodies. I will use
MR's, accessed via electrical resonators. Part of it will be in analogy to the previously studied macroscopic
systems, but with photons replaced by phonons. The experiments are done in a cryogenic temperature mostly
in dilution refrigerator. The work will open up new perspectives on how nature works, and can have
technological implications.
The first basic setup is the coupling of MR to microwave cavity resonators. This is a direct analogy to
optomechanics, and can be called circuit optomechanics. The goals will be phonon state transfer via a cavity
bus, construction of squeezed states and of phonon-cavity entanglement. The second setup is to boost the
optomechanical coupling with a Josephson junction system, and reach the single-phonon strong-coupling for
the first time. The third setup is the coupling of MR to a Josephson junction artificial atom. Here we will
access the MR same way as the motion of a trapped ions is coupled to their internal transitions. In this setup,
I am proposing to construct exotic quantum states of motion, and finally entangle and transfer phonons over
mm-distance via cavity-coupled qubits. I believe within the project it is possible to perform rudimentary Bell
measurement with phonons."
Summary
"Large bodies usually follow the classical equations of motion. Deviations from this can be called
macroscopic quantum behavior. These phenomena have been experimentally verified with cavity Quantum
Electro Dynamics (QED), trapped ions, and superconducting Josephson junction systems. Recently, evidence
was obtained that also moving objects can display such behavior. These objects are micromechanical
resonators (MR), which can measure tens of microns in size and are hence quite macroscopic. The degree of
freedom is their vibrations: phonons.
I propose experimental research in order to push quantum mechanics closer to the classical world than ever
before. I will try find quantum behavior in the most classical objects, that is, slowly moving bodies. I will use
MR's, accessed via electrical resonators. Part of it will be in analogy to the previously studied macroscopic
systems, but with photons replaced by phonons. The experiments are done in a cryogenic temperature mostly
in dilution refrigerator. The work will open up new perspectives on how nature works, and can have
technological implications.
The first basic setup is the coupling of MR to microwave cavity resonators. This is a direct analogy to
optomechanics, and can be called circuit optomechanics. The goals will be phonon state transfer via a cavity
bus, construction of squeezed states and of phonon-cavity entanglement. The second setup is to boost the
optomechanical coupling with a Josephson junction system, and reach the single-phonon strong-coupling for
the first time. The third setup is the coupling of MR to a Josephson junction artificial atom. Here we will
access the MR same way as the motion of a trapped ions is coupled to their internal transitions. In this setup,
I am proposing to construct exotic quantum states of motion, and finally entangle and transfer phonons over
mm-distance via cavity-coupled qubits. I believe within the project it is possible to perform rudimentary Bell
measurement with phonons."
Max ERC Funding
2 004 283 €
Duration
Start date: 2015-01-01, End date: 2019-12-31
Project acronym COMANCHE
Project Coherent manipulation and control of heat in solid-state nanostructures: the era of coherent caloritronics
Researcher (PI) Francesco Giazotto
Host Institution (HI) CONSIGLIO NAZIONALE DELLE RICERCHE
Country Italy
Call Details Consolidator Grant (CoG), PE3, ERC-2013-CoG
Summary "Electronic nanodevices have demonstrated to be versatile and effective tools for the investigation of exotic quantum phenomena under controlled and adjustable conditions. Yet, these have enabled to give access to the manipulation of charge flow with unprecedented precision. On the other hand, the wisdom dealing with control, measurements, storage, and conversion of heat in nanoscale devices, the so-called “caloritronics” (from the Latin word “calor”, i.e., heat), despite a number of recent advances is still at its infancy. Although coherence often plays a crucial role in determining the functionalities of nanoelectronic devices very little is known of its role in caloritronics. In such a context, coherent control of heat seems at present still very far from reach, and devising methods to phase-coherently manipulate the thermal current would represent a crucial breakthrough which could open the door to unprecedented possibilities in several fields of science.
Here we propose an original approach to set the experimental ground for the investigation and implementation of a new branch of science, the “coherent caloritronics”, which will take advantage of quantum circuits to phase-coherently manipulate and control the heat current in solid-state nanostructures. To tackle this challenging task our approach will follow three main separate approaches, i.e., the coherent control of heat transported by electrons in Josephson nanocircuits, the coherent manipulation of heat carried by electrons and exchanged between electrons and lattice phonons in superconducting proximity systems,
and finally, the control of the heat exchanged between electrons and photons by coherently tuning the coupling with the electromagnetic environment. We will integrate superconductors with normal-metal or semiconductor electrodes thus exploring new device concepts such as heat transistors, heat diodes, heat splitters, where thermal flux control is achieved thanks to the use of the quantum phase."
Summary
"Electronic nanodevices have demonstrated to be versatile and effective tools for the investigation of exotic quantum phenomena under controlled and adjustable conditions. Yet, these have enabled to give access to the manipulation of charge flow with unprecedented precision. On the other hand, the wisdom dealing with control, measurements, storage, and conversion of heat in nanoscale devices, the so-called “caloritronics” (from the Latin word “calor”, i.e., heat), despite a number of recent advances is still at its infancy. Although coherence often plays a crucial role in determining the functionalities of nanoelectronic devices very little is known of its role in caloritronics. In such a context, coherent control of heat seems at present still very far from reach, and devising methods to phase-coherently manipulate the thermal current would represent a crucial breakthrough which could open the door to unprecedented possibilities in several fields of science.
Here we propose an original approach to set the experimental ground for the investigation and implementation of a new branch of science, the “coherent caloritronics”, which will take advantage of quantum circuits to phase-coherently manipulate and control the heat current in solid-state nanostructures. To tackle this challenging task our approach will follow three main separate approaches, i.e., the coherent control of heat transported by electrons in Josephson nanocircuits, the coherent manipulation of heat carried by electrons and exchanged between electrons and lattice phonons in superconducting proximity systems,
and finally, the control of the heat exchanged between electrons and photons by coherently tuning the coupling with the electromagnetic environment. We will integrate superconductors with normal-metal or semiconductor electrodes thus exploring new device concepts such as heat transistors, heat diodes, heat splitters, where thermal flux control is achieved thanks to the use of the quantum phase."
Max ERC Funding
1 754 897 €
Duration
Start date: 2014-05-01, End date: 2019-04-30
Project acronym CrowdLand
Project Harnessing the power of crowdsourcing to improve land cover and land-use information
Researcher (PI) Steffen Martin Fritz
Host Institution (HI) INTERNATIONALES INSTITUT FUER ANGEWANDTE SYSTEMANALYSE
Country Austria
Call Details Consolidator Grant (CoG), SH3, ERC-2013-CoG
Summary Information about land cover, land use and the change over time is used for a wide range of applications such as nature protection and biodiversity, forest and water management, urban and transport planning, natural hazard prevention and mitigation, agricultural policies and monitoring climate change. Furthermore, high quality spatially explicit information on land cover change is an essential input variable to land use change modelling, which is increasingly being used to better understand the potential impact of certain policies. The amount of observed land cover change also serves as an important indicator of how well different regional, national and European policies have been implemented.
However, outside Europe and outside the developed world in particular, information on land cover and land cover change in poorer countries is hardly available and no national or regional dense sample based monitoring approaches such as LUCAS exists which deliver sufficiently accurate land cover and land cover change information. Moreover in particular in developing countries, there is no or very little information on land-use and crop management. Only very limited data available from FAO and an incomplete coverage of sub-national statistics (e.g. IFPRI) are available.
This research project will assess the potential of using crowdsourcing to close these big data gaps in developing and developed countries with a number of case studies and different data collection methods. The CrowdLand project will be carried out in two very different environments, i.e. Austria and Kenya.The overall research objectives of this project are to 1) test the potential of using social gaming to collect land use information 2) test the potential of using mobile money to collect data in developing countries 3) understand the data quality collected via crowdsourcing 4) apply advanced methods to filter crowdsourced data in order to attain improved accuracy.
Summary
Information about land cover, land use and the change over time is used for a wide range of applications such as nature protection and biodiversity, forest and water management, urban and transport planning, natural hazard prevention and mitigation, agricultural policies and monitoring climate change. Furthermore, high quality spatially explicit information on land cover change is an essential input variable to land use change modelling, which is increasingly being used to better understand the potential impact of certain policies. The amount of observed land cover change also serves as an important indicator of how well different regional, national and European policies have been implemented.
However, outside Europe and outside the developed world in particular, information on land cover and land cover change in poorer countries is hardly available and no national or regional dense sample based monitoring approaches such as LUCAS exists which deliver sufficiently accurate land cover and land cover change information. Moreover in particular in developing countries, there is no or very little information on land-use and crop management. Only very limited data available from FAO and an incomplete coverage of sub-national statistics (e.g. IFPRI) are available.
This research project will assess the potential of using crowdsourcing to close these big data gaps in developing and developed countries with a number of case studies and different data collection methods. The CrowdLand project will be carried out in two very different environments, i.e. Austria and Kenya.The overall research objectives of this project are to 1) test the potential of using social gaming to collect land use information 2) test the potential of using mobile money to collect data in developing countries 3) understand the data quality collected via crowdsourcing 4) apply advanced methods to filter crowdsourced data in order to attain improved accuracy.
Max ERC Funding
1 397 200 €
Duration
Start date: 2014-04-01, End date: 2020-03-31
Project acronym CWASI
Project Coping with water scarcity in a globalized world
Researcher (PI) Francesco Laio
Host Institution (HI) POLITECNICO DI TORINO
Country Italy
Call Details Consolidator Grant (CoG), SH3, ERC-2014-CoG
Summary We intend to set up a new globalized perspective to tackle water and food security in the 21st century. This issue is intrinsically global as the international trade of massive amounts of food makes societies less reliant on locally available water, and entails large-scale transfers of virtual water (defined as the water needed to produce a given amount of a food commodity). The network of virtual water trade connects a large portion of the global population, with 2800 km3 of virtual water moved around the globe in a year. We provide here definitive indications on the effects of the globalization of (virtual) water on the vulnerability to a water crisis of the global water system. More specifically, we formulate the following research hypotheses:
1) The globalization of (virtual) water resources is a short-term solution to malnourishment, famine, and conflicts, but it also has relevant negative implications for human societies.
2) The virtual water dynamics provide the suitable framework in order to quantitatively relate water-crises occurrence to environmental and socio-economic factors.
3) The risk of catastrophic, global-scale, water crises will increase in the next decades.
To test these hypotheses, we will capitalize on the tremendous amount of information embedded in nearly 50 years of available food and virtual water trade data. We will adopt an innovative research approach based on the use of: advanced statistical tools for data verification and uncertainty modeling; methods borrowed from the complex network theory, aimed at analyzing the propagation of failures through the network; multivariate nonlinear analyses, to reproduce the dependence of virtual water on time and on external drivers; multi-state stochastic modeling, to study the effect on the global water system of random fluctuations of the external drivers; and scenario analysis, to predict the future probability of occurrence of water crises.
Summary
We intend to set up a new globalized perspective to tackle water and food security in the 21st century. This issue is intrinsically global as the international trade of massive amounts of food makes societies less reliant on locally available water, and entails large-scale transfers of virtual water (defined as the water needed to produce a given amount of a food commodity). The network of virtual water trade connects a large portion of the global population, with 2800 km3 of virtual water moved around the globe in a year. We provide here definitive indications on the effects of the globalization of (virtual) water on the vulnerability to a water crisis of the global water system. More specifically, we formulate the following research hypotheses:
1) The globalization of (virtual) water resources is a short-term solution to malnourishment, famine, and conflicts, but it also has relevant negative implications for human societies.
2) The virtual water dynamics provide the suitable framework in order to quantitatively relate water-crises occurrence to environmental and socio-economic factors.
3) The risk of catastrophic, global-scale, water crises will increase in the next decades.
To test these hypotheses, we will capitalize on the tremendous amount of information embedded in nearly 50 years of available food and virtual water trade data. We will adopt an innovative research approach based on the use of: advanced statistical tools for data verification and uncertainty modeling; methods borrowed from the complex network theory, aimed at analyzing the propagation of failures through the network; multivariate nonlinear analyses, to reproduce the dependence of virtual water on time and on external drivers; multi-state stochastic modeling, to study the effect on the global water system of random fluctuations of the external drivers; and scenario analysis, to predict the future probability of occurrence of water crises.
Max ERC Funding
1 222 500 €
Duration
Start date: 2015-07-01, End date: 2020-12-31
