Project acronym BIGSEA
Project Biogeochemical and ecosystem interactions with socio-economic activity in the global ocean
Researcher (PI) Eric Douglas Galbraith
Host Institution (HI) UNIVERSIDAD AUTONOMA DE BARCELONA
Country Spain
Call Details Consolidator Grant (CoG), PE10, ERC-2015-CoG
Summary The global marine ecosystem is being deeply altered by human activity. On the one hand, rising concentrations of atmospheric greenhouse gases are changing the physical and chemical state of the ocean, exerting pressure from the bottom up. Meanwhile, the global fishery has provided large economic benefits, but in so doing has restructured ecosystems by removing most of the large animal biomass, a major top-down change. Although there has been a tremendous amount of research into isolated aspects of these impacts, the development of a holistic understanding of the full interactions between physics, chemistry, ecology and economic activity might appear impossible, given the myriad complexities. This proposal lays out a strategy to assemble a team of trans-disciplinary expertise, that will develop a unified, data-constrained, grid-based modeling framework to represent the most important interactions of the global human-ocean system. Building this framework requires solving a series of fundamental problems that currently hinder the development of the full model. If these problems can be solved, the resulting model will reveal novel emergent properties and open the doors to a range of previously unexplored questions of high impact across a range of disciplines. Key questions include the ways in which animals interact with oxygen minimum zones with implications for fisheries, the impacts fish harvesting may have on nutrient recycling, spatio-temporal interactions between managed and unmanaged fisheries, and fundamental questions about the relationships between fish price, fishing cost, and multiple markets in a changing world. Just as the first coupled ocean-atmosphere models revealed a wealth of new behaviours, the coupled human-ocean model proposed here has the potential to launch multiple new fields of enquiry. It is hoped that the novel approach will contribute to a paradigm shift that treats human activity as one component within the framework of the Earth System.
Summary
The global marine ecosystem is being deeply altered by human activity. On the one hand, rising concentrations of atmospheric greenhouse gases are changing the physical and chemical state of the ocean, exerting pressure from the bottom up. Meanwhile, the global fishery has provided large economic benefits, but in so doing has restructured ecosystems by removing most of the large animal biomass, a major top-down change. Although there has been a tremendous amount of research into isolated aspects of these impacts, the development of a holistic understanding of the full interactions between physics, chemistry, ecology and economic activity might appear impossible, given the myriad complexities. This proposal lays out a strategy to assemble a team of trans-disciplinary expertise, that will develop a unified, data-constrained, grid-based modeling framework to represent the most important interactions of the global human-ocean system. Building this framework requires solving a series of fundamental problems that currently hinder the development of the full model. If these problems can be solved, the resulting model will reveal novel emergent properties and open the doors to a range of previously unexplored questions of high impact across a range of disciplines. Key questions include the ways in which animals interact with oxygen minimum zones with implications for fisheries, the impacts fish harvesting may have on nutrient recycling, spatio-temporal interactions between managed and unmanaged fisheries, and fundamental questions about the relationships between fish price, fishing cost, and multiple markets in a changing world. Just as the first coupled ocean-atmosphere models revealed a wealth of new behaviours, the coupled human-ocean model proposed here has the potential to launch multiple new fields of enquiry. It is hoped that the novel approach will contribute to a paradigm shift that treats human activity as one component within the framework of the Earth System.
Max ERC Funding
1 600 000 €
Duration
Start date: 2016-07-01, End date: 2021-12-31
Project acronym BOPNIE
Project Boundary value problems for nonlinear integrable equations
Researcher (PI) Jonatan Carl Anders Lenells
Host Institution (HI) KUNGLIGA TEKNISKA HOEGSKOLAN
Country Sweden
Call Details Consolidator Grant (CoG), PE1, ERC-2015-CoG
Summary The purpose of this project is to develop new methods for solving boundary value problems (BVPs) for nonlinear integrable partial differential equations (PDEs). Integrable PDEs can be analyzed by means of the Inverse Scattering Transform, whose introduction was one of the most important developments in the theory of nonlinear PDEs in the 20th century. Until the 1990s the inverse scattering methodology was pursued almost entirely for pure initial-value problems. However, in many laboratory and field situations, the solution is generated by what corresponds to the imposition of boundary conditions rather than initial conditions. Thus, an understanding of BVPs is crucial.
In an exciting sequence of events taking place in the last two decades, new tools have become available to deal with BVPs for integrable PDEs. Although some important issues have already been resolved, several major problems remain open.
The aim of this project is to solve a number of these open problems and to find solutions of BVPs which were heretofore not solvable. More precisely, the proposal has eight objectives:
1. Develop methods for solving problems with time-periodic boundary conditions.
2. Answer some long-standing open questions raised by series of wave-tank experiments 35 years ago.
3. Develop a new approach for the study of space-periodic solutions.
4. Develop new approaches for the analysis of BVPs for equations with 3 x 3-matrix Lax pairs.
5. Derive new asymptotic formulas by using a nonlinear version of the steepest descent method.
6. Construct disk and disk/black-hole solutions of the stationary axisymmetric Einstein equations.
7. Solve a BVP in Einstein's theory of relativity describing two colliding gravitational waves.
8. Extend the above methods to BVPs in higher dimensions.
Summary
The purpose of this project is to develop new methods for solving boundary value problems (BVPs) for nonlinear integrable partial differential equations (PDEs). Integrable PDEs can be analyzed by means of the Inverse Scattering Transform, whose introduction was one of the most important developments in the theory of nonlinear PDEs in the 20th century. Until the 1990s the inverse scattering methodology was pursued almost entirely for pure initial-value problems. However, in many laboratory and field situations, the solution is generated by what corresponds to the imposition of boundary conditions rather than initial conditions. Thus, an understanding of BVPs is crucial.
In an exciting sequence of events taking place in the last two decades, new tools have become available to deal with BVPs for integrable PDEs. Although some important issues have already been resolved, several major problems remain open.
The aim of this project is to solve a number of these open problems and to find solutions of BVPs which were heretofore not solvable. More precisely, the proposal has eight objectives:
1. Develop methods for solving problems with time-periodic boundary conditions.
2. Answer some long-standing open questions raised by series of wave-tank experiments 35 years ago.
3. Develop a new approach for the study of space-periodic solutions.
4. Develop new approaches for the analysis of BVPs for equations with 3 x 3-matrix Lax pairs.
5. Derive new asymptotic formulas by using a nonlinear version of the steepest descent method.
6. Construct disk and disk/black-hole solutions of the stationary axisymmetric Einstein equations.
7. Solve a BVP in Einstein's theory of relativity describing two colliding gravitational waves.
8. Extend the above methods to BVPs in higher dimensions.
Max ERC Funding
2 000 000 €
Duration
Start date: 2016-05-01, End date: 2022-02-28
Project acronym BSD
Project Euler systems and the conjectures of Birch and Swinnerton-Dyer, Bloch and Kato
Researcher (PI) Victor Rotger cerda
Host Institution (HI) UNIVERSITAT POLITECNICA DE CATALUNYA
Country Spain
Call Details Consolidator Grant (CoG), PE1, ERC-2015-CoG
Summary In order to celebrate mathematics in the new millennium, the Clay Mathematics Institute established seven $1.000.000 Prize Problems. One of these is the conjecture of Birch and Swinnerton-Dyer (BSD), widely open since the 1960's. The main object of this proposal is developing innovative and unconventional strategies for proving groundbreaking results towards the resolution of this problem and their generalizations by Bloch and Kato (BK).
Breakthroughs on BSD were achieved by Coates-Wiles, Gross, Zagier and Kolyvagin, and Kato. Since then, there have been nearly no new ideas on how to tackle BSD. Only very recently, three independent revolutionary approaches have seen the light: the works of (1) the Fields medalist Bhargava, (2) Skinner and Urban, and (3) myself and my collaborators. In spite of that, our knowledge of BSD is rather poor. In my proposal I suggest innovating strategies for approaching new horizons in BSD and BK that I aim to develop with the team of PhD and postdoctoral researchers that the CoG may allow me to consolidate. The results I plan to prove represent a departure from the achievements obtained with my coauthors during the past years:
I. BSD over totally real number fields. I plan to prove new ground-breaking instances of BSD in rank 0 for elliptic curves over totally real number fields, generalizing the theorem of Kato (by providing a new proof) and covering many new scenarios that have never been considered before.
II. BSD in rank r=2. Most of the literature on BSD applies when r=0 or 1. I expect to prove p-adic versions of the theorems of Gross-Zagier and Kolyvagin in rank 2.
III. Darmon's 2000 conjecture on Stark-Heegner points. I plan to prove Darmon’s striking conjecture announced at the ICM2000 by recasting it in terms of special values of p-adic L-functions.
Summary
In order to celebrate mathematics in the new millennium, the Clay Mathematics Institute established seven $1.000.000 Prize Problems. One of these is the conjecture of Birch and Swinnerton-Dyer (BSD), widely open since the 1960's. The main object of this proposal is developing innovative and unconventional strategies for proving groundbreaking results towards the resolution of this problem and their generalizations by Bloch and Kato (BK).
Breakthroughs on BSD were achieved by Coates-Wiles, Gross, Zagier and Kolyvagin, and Kato. Since then, there have been nearly no new ideas on how to tackle BSD. Only very recently, three independent revolutionary approaches have seen the light: the works of (1) the Fields medalist Bhargava, (2) Skinner and Urban, and (3) myself and my collaborators. In spite of that, our knowledge of BSD is rather poor. In my proposal I suggest innovating strategies for approaching new horizons in BSD and BK that I aim to develop with the team of PhD and postdoctoral researchers that the CoG may allow me to consolidate. The results I plan to prove represent a departure from the achievements obtained with my coauthors during the past years:
I. BSD over totally real number fields. I plan to prove new ground-breaking instances of BSD in rank 0 for elliptic curves over totally real number fields, generalizing the theorem of Kato (by providing a new proof) and covering many new scenarios that have never been considered before.
II. BSD in rank r=2. Most of the literature on BSD applies when r=0 or 1. I expect to prove p-adic versions of the theorems of Gross-Zagier and Kolyvagin in rank 2.
III. Darmon's 2000 conjecture on Stark-Heegner points. I plan to prove Darmon’s striking conjecture announced at the ICM2000 by recasting it in terms of special values of p-adic L-functions.
Max ERC Funding
1 428 588 €
Duration
Start date: 2016-09-01, End date: 2021-08-31
Project acronym CATA-LUX
Project Light-Driven Asymmetric Organocatalysis
Researcher (PI) Paolo Melchiorre
Host Institution (HI) FUNDACIO PRIVADA INSTITUT CATALA D'INVESTIGACIO QUIMICA
Country Spain
Call Details Consolidator Grant (CoG), PE5, ERC-2015-CoG
Summary Visible light photocatalysis and metal-free organocatalytic processes are powerful strategies of modern chemical research with extraordinary potential for the sustainable preparation of organic molecules. However, these environmentally respectful approaches have to date remained largely unrelated. The proposed research seeks to merge these fields of molecule activation to redefine their synthetic potential.
Light-driven processes considerably enrich the modern synthetic repertoire, offering a potent way to build complex organic frameworks. In contrast, it is extremely challenging to develop asymmetric catalytic photoreactions that can create chiral molecules with a well-defined three-dimensional arrangement. By developing innovative methodologies to effectively address this issue, I will provide a novel reactivity framework for conceiving light-driven enantioselective organocatalytic processes.
I will translate the effective tools governing the success of ground state asymmetric organocatalysis into the realm of photochemical reactivity, exploiting the potential of key organocatalytic intermediates to directly participate in the photoexcitation of substrates. At the same time, the chiral organocatalyst will ensure effective stereochemical control. This single catalyst system, where stereoinduction and photoactivation merge in a sole organocatalyst, will serve for developing novel enantioselective photoreactions. In a complementary dual catalytic approach, the synergistic activities of an organocatalyst and a metal-free photosensitiser will combine to realise asymmetric variants of venerable photochemical processes, which have never before succumbed to a stereocontrolled approach.
This proposal challenges the current perception that photochemistry is too unselective to parallel the impressive levels of efficiency reached by the asymmetric catalysis of thermal reactions, expanding the way chemists think about making chiral molecules
Summary
Visible light photocatalysis and metal-free organocatalytic processes are powerful strategies of modern chemical research with extraordinary potential for the sustainable preparation of organic molecules. However, these environmentally respectful approaches have to date remained largely unrelated. The proposed research seeks to merge these fields of molecule activation to redefine their synthetic potential.
Light-driven processes considerably enrich the modern synthetic repertoire, offering a potent way to build complex organic frameworks. In contrast, it is extremely challenging to develop asymmetric catalytic photoreactions that can create chiral molecules with a well-defined three-dimensional arrangement. By developing innovative methodologies to effectively address this issue, I will provide a novel reactivity framework for conceiving light-driven enantioselective organocatalytic processes.
I will translate the effective tools governing the success of ground state asymmetric organocatalysis into the realm of photochemical reactivity, exploiting the potential of key organocatalytic intermediates to directly participate in the photoexcitation of substrates. At the same time, the chiral organocatalyst will ensure effective stereochemical control. This single catalyst system, where stereoinduction and photoactivation merge in a sole organocatalyst, will serve for developing novel enantioselective photoreactions. In a complementary dual catalytic approach, the synergistic activities of an organocatalyst and a metal-free photosensitiser will combine to realise asymmetric variants of venerable photochemical processes, which have never before succumbed to a stereocontrolled approach.
This proposal challenges the current perception that photochemistry is too unselective to parallel the impressive levels of efficiency reached by the asymmetric catalysis of thermal reactions, expanding the way chemists think about making chiral molecules
Max ERC Funding
2 000 000 €
Duration
Start date: 2016-11-01, End date: 2021-10-31
Project acronym CHAMELEON
Project Intuitive editing of visual appearance from real-world datasets
Researcher (PI) Diego Gutierrez Perez
Host Institution (HI) UNIVERSIDAD DE ZARAGOZA
Country Spain
Call Details Consolidator Grant (CoG), PE6, ERC-2015-CoG
Summary Computer-generated imagery is now ubiquitous in our society, spanning fields such as games and movies, architecture, engineering, or virtual prototyping, while also helping create novel ones such as computational materials. With the increase in computational power and the improvement of acquisition techniques, there has been a paradigm shift in the field towards data-driven techniques, which has yielded an unprecedented level of realism in visual appearance. Unfortunately, this leads to a series of problems, identified in this proposal: First, there is a disconnect between the mathematical representation of the data and any meaningful parameters that humans understand; the captured data is machine-friendly, but not human friendly. Second, the many different acquisition systems lead to heterogeneous formats and very large datasets. And third, real-world appearance functions are usually nonlinear and high-dimensional. As a result, visual appearance datasets are increasingly unfit to editing operations, which limits the creative process for scientists, engineers, artists and practitioners in general. There is an immense gap between the complexity, realism and richness of the captured data, and the flexibility to edit such data.
We believe that the current research path leads to a fragmented space of isolated solutions, each tailored to a particular dataset and problem. We propose a research plan at the theoretical, algorithmic and application levels, putting the user at the core. We will learn key relevant appearance features in terms humans understand, from which intuitive, predictable editing spaces, algorithms, and workflows will be defined. In order to ensure usability and foster creativity, we will also extend our research to efficient simulation of visual appearance, exploiting the extra dimensionality of the captured datasets. Achieving our goals will finally enable us to reach the true potential of real-world captured datasets in many aspects of society.
Summary
Computer-generated imagery is now ubiquitous in our society, spanning fields such as games and movies, architecture, engineering, or virtual prototyping, while also helping create novel ones such as computational materials. With the increase in computational power and the improvement of acquisition techniques, there has been a paradigm shift in the field towards data-driven techniques, which has yielded an unprecedented level of realism in visual appearance. Unfortunately, this leads to a series of problems, identified in this proposal: First, there is a disconnect between the mathematical representation of the data and any meaningful parameters that humans understand; the captured data is machine-friendly, but not human friendly. Second, the many different acquisition systems lead to heterogeneous formats and very large datasets. And third, real-world appearance functions are usually nonlinear and high-dimensional. As a result, visual appearance datasets are increasingly unfit to editing operations, which limits the creative process for scientists, engineers, artists and practitioners in general. There is an immense gap between the complexity, realism and richness of the captured data, and the flexibility to edit such data.
We believe that the current research path leads to a fragmented space of isolated solutions, each tailored to a particular dataset and problem. We propose a research plan at the theoretical, algorithmic and application levels, putting the user at the core. We will learn key relevant appearance features in terms humans understand, from which intuitive, predictable editing spaces, algorithms, and workflows will be defined. In order to ensure usability and foster creativity, we will also extend our research to efficient simulation of visual appearance, exploiting the extra dimensionality of the captured datasets. Achieving our goals will finally enable us to reach the true potential of real-world captured datasets in many aspects of society.
Max ERC Funding
1 629 519 €
Duration
Start date: 2016-11-01, End date: 2023-04-30
Project acronym DELMIT
Project Maintaining the Human Mitochondrial Genome
Researcher (PI) Maria Falkenberg Gustafsson
Host Institution (HI) GOETEBORGS UNIVERSITET
Country Sweden
Call Details Consolidator Grant (CoG), LS1, ERC-2015-CoG
Summary Mitochondria are required to convert food into usable energy forms and every cell contains thousands of them. Unlike most other cellular compartments, mitochondria have their own genomes (mtDNA) that encode for 13 of the about 90 proteins present in the respiratory chain. All proteins necessary for mtDNA replication, as well as transcription and translation of mtDNA-encoded genes, are encoded in the nucleus. Mutations in nuclear-encoded proteins required for mtDNA maintenance is an important cause of neurodegeneration and muscle diseases. The common result of these defects is either mtDNA depletion or accumulation of multiple deletions of mtDNA in postmitotic tissues.
The long-term goal (or vision) of research in my laboratory is to understand in molecular detail how mtDNA is replicated and how this process is regulated in mammalian cells. To this end we use a protein biochemistry approach, which we combine with in vivo verification in cell lines. My group was in 2004 the first to reconstitute mtDNA replication in vitro and we have continued to develop even more elaborate system ever since. In the current application, the major focus is studies of the mitochondrial D-loop region, a triple-stranded structure in the mitochondrial genome. The D-loop functions as a regulatory hub and we will determine how initiation and termination of mtDNA replication is controlled from this region. We will also determine the physical organization of the mtDNA replication machinery at the replication fork and establish how mtDNA deletions, a classical hallmark of human ageing, are formed.
Summary
Mitochondria are required to convert food into usable energy forms and every cell contains thousands of them. Unlike most other cellular compartments, mitochondria have their own genomes (mtDNA) that encode for 13 of the about 90 proteins present in the respiratory chain. All proteins necessary for mtDNA replication, as well as transcription and translation of mtDNA-encoded genes, are encoded in the nucleus. Mutations in nuclear-encoded proteins required for mtDNA maintenance is an important cause of neurodegeneration and muscle diseases. The common result of these defects is either mtDNA depletion or accumulation of multiple deletions of mtDNA in postmitotic tissues.
The long-term goal (or vision) of research in my laboratory is to understand in molecular detail how mtDNA is replicated and how this process is regulated in mammalian cells. To this end we use a protein biochemistry approach, which we combine with in vivo verification in cell lines. My group was in 2004 the first to reconstitute mtDNA replication in vitro and we have continued to develop even more elaborate system ever since. In the current application, the major focus is studies of the mitochondrial D-loop region, a triple-stranded structure in the mitochondrial genome. The D-loop functions as a regulatory hub and we will determine how initiation and termination of mtDNA replication is controlled from this region. We will also determine the physical organization of the mtDNA replication machinery at the replication fork and establish how mtDNA deletions, a classical hallmark of human ageing, are formed.
Max ERC Funding
1 999 985 €
Duration
Start date: 2016-11-01, End date: 2021-10-31
Project acronym ECOHERB
Project Drivers and impacts of invertebrate herbivores across forest ecosystems globally.
Researcher (PI) Daniel Metcalfe
Host Institution (HI) UMEA UNIVERSITET
Country Sweden
Call Details Consolidator Grant (CoG), PE10, ERC-2015-CoG
Summary Forests slow global climate change by absorbing atmospheric carbon dioxide but this ecosystem service is limited by soil nutrients. Herbivores potentially alter soil nutrients in a range of ways, but these have mostly only been recorded for large mammals. By comparison, the impacts of the abundant invertebrates in forests have largely been ignored and are not included in current models used to generate the climate predictions so vital for designing governmental policies
The proposed project will use a pioneering new interdisciplinary approach to provide the most complete picture yet available of the rates, underlying drivers and ultimate impacts of key nutrient inputs from invertebrate herbivores across forest ecosystems worldwide. Specifically, we will:
(1) Establish a network of herbivory monitoring stations across all major forest types, and across key environmental gradients (temperature, rainfall, ecosystem development).
(2) Perform laboratory experiments to examine the effects of herbivore excreta on soil processes under different temperature and moisture conditions.
(3) Integrate this information into a cutting-edge ecosystem model, to generate more accurate predictions of forest carbon sequestration under future climate change.
The network established will form the foundation for a unique long-term global monitoring effort which we intend to continue long after the current funding time scale. This work represents a powerful blend of several disciplines harnessing an array of cutting edge tools to provide fundamentally novel insights into an area of direct and urgent importance for the society.
Summary
Forests slow global climate change by absorbing atmospheric carbon dioxide but this ecosystem service is limited by soil nutrients. Herbivores potentially alter soil nutrients in a range of ways, but these have mostly only been recorded for large mammals. By comparison, the impacts of the abundant invertebrates in forests have largely been ignored and are not included in current models used to generate the climate predictions so vital for designing governmental policies
The proposed project will use a pioneering new interdisciplinary approach to provide the most complete picture yet available of the rates, underlying drivers and ultimate impacts of key nutrient inputs from invertebrate herbivores across forest ecosystems worldwide. Specifically, we will:
(1) Establish a network of herbivory monitoring stations across all major forest types, and across key environmental gradients (temperature, rainfall, ecosystem development).
(2) Perform laboratory experiments to examine the effects of herbivore excreta on soil processes under different temperature and moisture conditions.
(3) Integrate this information into a cutting-edge ecosystem model, to generate more accurate predictions of forest carbon sequestration under future climate change.
The network established will form the foundation for a unique long-term global monitoring effort which we intend to continue long after the current funding time scale. This work represents a powerful blend of several disciplines harnessing an array of cutting edge tools to provide fundamentally novel insights into an area of direct and urgent importance for the society.
Max ERC Funding
1 750 000 €
Duration
Start date: 2016-03-01, End date: 2022-02-28
Project acronym eLightning
Project Lightning propagation and high-energy emissions within coupled multi-model simulations
Researcher (PI) Alejandro Luque Estepa
Host Institution (HI) AGENCIA ESTATAL CONSEJO SUPERIOR DEINVESTIGACIONES CIENTIFICAS
Country Spain
Call Details Consolidator Grant (CoG), PE10, ERC-2015-CoG
Summary More than 250 years after establishing the electrical nature of the lightning flash, we still do not understand how a lightning channel advances. Most of these channels progress not continuously but in a series of sudden jumps and, as they jump, they emit bursts of energetic radiation. Despite increasingly accurate observations, there is no accepted explanation for this stepped progression.
This proposal addresses this open question. First, we propose a methodological breakthrough that will allow us to tackle the main bottleneck in the theoretical understanding of lightning: the wide disparity between length-scales within a lightning flash. We plan to apply techniques that have succeeded in other fields, such as multi-model coupled simulations and moving-mesh finite elements methods. Acting as a computational microscope, these techniques will reveal the small-scale electrodynamics around a lightning channel.
We will then apply these techniques to elucidate the intertwined problems of lightning channel stepping and thunderstorm-related high-energy emissions. The main hypothesis that we will test is that stepping is due to the formation of low-conductivity spots within the filamentary-discharge region that surrounds a lightning channel. This idea is motivated by observations from high-altitude atmospheric discharges. By resolving the small-scale dynamics, with our numerical method, we will also test hypothesis for high-energy emissions from the lighting channel, which crucially depend on the microscopic distribution of electric fields.
This interdisciplinary proposal, straddling between geophysics and gas discharge physics, seeks a double breakthrough: the methodological one of building multi-scale lightning simulations and the hypothesis-driven one of finding out the reason for stepping. If it succeeds, it will achieve a leap forward in our knowledge of lightning, undoubtedly one of the greatest spectacles in our planet's repertoire.
Summary
More than 250 years after establishing the electrical nature of the lightning flash, we still do not understand how a lightning channel advances. Most of these channels progress not continuously but in a series of sudden jumps and, as they jump, they emit bursts of energetic radiation. Despite increasingly accurate observations, there is no accepted explanation for this stepped progression.
This proposal addresses this open question. First, we propose a methodological breakthrough that will allow us to tackle the main bottleneck in the theoretical understanding of lightning: the wide disparity between length-scales within a lightning flash. We plan to apply techniques that have succeeded in other fields, such as multi-model coupled simulations and moving-mesh finite elements methods. Acting as a computational microscope, these techniques will reveal the small-scale electrodynamics around a lightning channel.
We will then apply these techniques to elucidate the intertwined problems of lightning channel stepping and thunderstorm-related high-energy emissions. The main hypothesis that we will test is that stepping is due to the formation of low-conductivity spots within the filamentary-discharge region that surrounds a lightning channel. This idea is motivated by observations from high-altitude atmospheric discharges. By resolving the small-scale dynamics, with our numerical method, we will also test hypothesis for high-energy emissions from the lighting channel, which crucially depend on the microscopic distribution of electric fields.
This interdisciplinary proposal, straddling between geophysics and gas discharge physics, seeks a double breakthrough: the methodological one of building multi-scale lightning simulations and the hypothesis-driven one of finding out the reason for stepping. If it succeeds, it will achieve a leap forward in our knowledge of lightning, undoubtedly one of the greatest spectacles in our planet's repertoire.
Max ERC Funding
1 960 826 €
Duration
Start date: 2016-06-01, End date: 2021-05-31
Project acronym EpiMech
Project Epithelial cell sheets as engineering materials: mechanics, resilience and malleability
Researcher (PI) Marino Arroyo Balaguer
Host Institution (HI) UNIVERSITAT POLITECNICA DE CATALUNYA
Country Spain
Call Details Consolidator Grant (CoG), PE8, ERC-2015-CoG
Summary The epithelium is a cohesive two-dimensional layer of cells attached to a fluid-filled fibrous matrix, which lines most free surfaces and cavities of the body. It serves as a protective barrier with tunable permeability, which must retain integrity in a mechanically active environment. Paradoxically, it must also be malleable enough to self-heal and remodel into functional 3D structures such as villi in our guts or tubular networks. Intrigued by these conflicting material properties, the main idea of this proposal is to view epithelial monolayers as living engineering materials. Unlike lipid bilayers or hydrogels, widely used in biotechnology, cultured epithelia are only starting to be integrated in organ-on-chip microdevices. As for any complex inert material, this program requires a fundamental understanding of the structure-property relationships. (1) Regarding their effective in-plane rheology, at short time-scales epithelia exhibit solid-like behavior while at longer times they flow as a consequence of the only qualitatively understood dynamics of the cell-cell junctional network. (2) As for material failure, excessive tension can lead to epithelial fracture, but as we have recently shown, matrix poroelasticity can also cause hydraulic fracture under stretch. However, it is largely unknown how adhesion molecules, membrane, cytoskeleton and matrix interact to give epithelia their robust and flaw-tolerant resilience. (3) Regarding shaping 3D epithelial structures, besides the classical view of chemical patterning, mechanical buckling is emerging as a major morphogenetic driving force, suggesting that it may be possible design 3D epithelial structures in vitro by mechanical self-assembly. Towards understanding (1,2,3), we will combine a broad range of theoretical, computational and experimental methods. Besides providing fundamental mechanobiological understanding, this project will provide a framework to manipulate epithelia in bioinspired technologies.
Summary
The epithelium is a cohesive two-dimensional layer of cells attached to a fluid-filled fibrous matrix, which lines most free surfaces and cavities of the body. It serves as a protective barrier with tunable permeability, which must retain integrity in a mechanically active environment. Paradoxically, it must also be malleable enough to self-heal and remodel into functional 3D structures such as villi in our guts or tubular networks. Intrigued by these conflicting material properties, the main idea of this proposal is to view epithelial monolayers as living engineering materials. Unlike lipid bilayers or hydrogels, widely used in biotechnology, cultured epithelia are only starting to be integrated in organ-on-chip microdevices. As for any complex inert material, this program requires a fundamental understanding of the structure-property relationships. (1) Regarding their effective in-plane rheology, at short time-scales epithelia exhibit solid-like behavior while at longer times they flow as a consequence of the only qualitatively understood dynamics of the cell-cell junctional network. (2) As for material failure, excessive tension can lead to epithelial fracture, but as we have recently shown, matrix poroelasticity can also cause hydraulic fracture under stretch. However, it is largely unknown how adhesion molecules, membrane, cytoskeleton and matrix interact to give epithelia their robust and flaw-tolerant resilience. (3) Regarding shaping 3D epithelial structures, besides the classical view of chemical patterning, mechanical buckling is emerging as a major morphogenetic driving force, suggesting that it may be possible design 3D epithelial structures in vitro by mechanical self-assembly. Towards understanding (1,2,3), we will combine a broad range of theoretical, computational and experimental methods. Besides providing fundamental mechanobiological understanding, this project will provide a framework to manipulate epithelia in bioinspired technologies.
Max ERC Funding
1 989 875 €
Duration
Start date: 2016-09-01, End date: 2022-08-31
Project acronym EPIScOPE
Project Reversing the epigenetic state of oligodendrocyte precursors cells in multiple sclerosis
Researcher (PI) Goncalo DE Sa E SOUSA DE CASTELO BRANCO
Host Institution (HI) KAROLINSKA INSTITUTET
Country Sweden
Call Details Consolidator Grant (CoG), LS7, ERC-2015-CoG
Summary Oligodendrocytes (OL) are glial cells that mediate myelination of neurons, a process that is defective in multiple sclerosis (MS). Although OL precursor cells (OPCs) can initially promote remyelination in MS, this regenerative mechanism eventually fails in progressive MS. OPCs go through several epigenetic states that ultimately define their potential to differentiate and myelinate. OPCs in progressive MS stall in a distinct epigenetic state, incompatible with differentiation and remyelination. We hypothesize that these OPCs regress to an epigenetic state reminiscent of the state of embryonic OPCs, which remain undifferentiated.
In this proposal, we aim to uncover the causes behind the remyelination failure upon disease progression in MS. We will determine the epigenetic/transcriptional states of OPCs during development and in MS, using single cell and bulk RNA sequencing and quantitative proteomics. We will further investigate how the interplay between transcription factors (TFs), chromatin modifiers (ChMs) and non-coding RNAs (ncRNAs) contributes to the transition between epigenetic states of OPCs. The results will allow the identification of ChMs and ncRNAs that can modulate these states and thereby control OPC differentiation and myelination. We will use this knowledge to investigate whether we can reverse the epigenetic state of OPCs in MS, in order to promote their differentiation and remyelination. The unique combination of leading-edge techniques such as SILAC coupled with immunoprecipitation and mass-spectrometry, single-cell RNA sequencing, ChIP-Sequencing, among others, will allow us to provide insights into novel epigenetic mechanisms that might be underlying the effects of environmental and lifestyle risk factors for MS. Moreover, this project has the potential to lead to the discovery of new targets for epigenetic-based therapies for MS, which could provide major opportunities for improved clinical outcome of MS patients in the near future.
Summary
Oligodendrocytes (OL) are glial cells that mediate myelination of neurons, a process that is defective in multiple sclerosis (MS). Although OL precursor cells (OPCs) can initially promote remyelination in MS, this regenerative mechanism eventually fails in progressive MS. OPCs go through several epigenetic states that ultimately define their potential to differentiate and myelinate. OPCs in progressive MS stall in a distinct epigenetic state, incompatible with differentiation and remyelination. We hypothesize that these OPCs regress to an epigenetic state reminiscent of the state of embryonic OPCs, which remain undifferentiated.
In this proposal, we aim to uncover the causes behind the remyelination failure upon disease progression in MS. We will determine the epigenetic/transcriptional states of OPCs during development and in MS, using single cell and bulk RNA sequencing and quantitative proteomics. We will further investigate how the interplay between transcription factors (TFs), chromatin modifiers (ChMs) and non-coding RNAs (ncRNAs) contributes to the transition between epigenetic states of OPCs. The results will allow the identification of ChMs and ncRNAs that can modulate these states and thereby control OPC differentiation and myelination. We will use this knowledge to investigate whether we can reverse the epigenetic state of OPCs in MS, in order to promote their differentiation and remyelination. The unique combination of leading-edge techniques such as SILAC coupled with immunoprecipitation and mass-spectrometry, single-cell RNA sequencing, ChIP-Sequencing, among others, will allow us to provide insights into novel epigenetic mechanisms that might be underlying the effects of environmental and lifestyle risk factors for MS. Moreover, this project has the potential to lead to the discovery of new targets for epigenetic-based therapies for MS, which could provide major opportunities for improved clinical outcome of MS patients in the near future.
Max ERC Funding
1 895 155 €
Duration
Start date: 2016-09-01, End date: 2021-08-31
