Project acronym ADNABIOARC
Project From the earliest modern humans to the onset of farming (45,000-4,500 BP): the role of climate, life-style, health, migration and selection in shaping European population history
Researcher (PI) Ron Pinhasi
Host Institution (HI) UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN
Country Ireland
Call Details Starting Grant (StG), SH6, ERC-2010-StG_20091209
Summary The colonisation of Europe by anatomically modern humans (AMHs) ca. 45,000 years before present (BP) and the transition to farming ca. 8,000 BP are two major events in human prehistory. Both events involved certain cultural and biological adaptations, technological innovations, and behavioural plasticity which are unique to our species. The reconstruction of these processes and the causality between them has so far remained elusive due to technological, methodological and logistical complexities. Major developments in our understanding of the anthropology of the Upper Palaeolithic, Mesolithic and Neolithic, and advances in ancient DNA (aDNA) technology and chronometric methods now allow us to assess in sufficient resolution the interface between these evolutionary processes, and changes in human culture and behaviour.
The proposed research will investigate the complex interface between the morphological, genetic, behavioural, and cultural factors that shaped the population history of European AMHs. The PI s interdisciplinary expertise in these areas, his access to and experience of relevant skeletal collections, and his ongoing European collaborations will allow significant progress in addressing these fundamental questions. The approach taken will include (a) the collection of bioarchaeological, aDNA, stable isotope (for the analysis of ancient diet) and radiometric data on 500 skeletons from key sites/phases in Europe and western Anatolia, and (b) the application of existing and novel aDNA, bioarchaeological and simulation methodologies. This research will yield results that transform our current understanding of major demographic and evolutionary processes and will place Europe at the forefront of anthropological biological and genetic research.
Summary
The colonisation of Europe by anatomically modern humans (AMHs) ca. 45,000 years before present (BP) and the transition to farming ca. 8,000 BP are two major events in human prehistory. Both events involved certain cultural and biological adaptations, technological innovations, and behavioural plasticity which are unique to our species. The reconstruction of these processes and the causality between them has so far remained elusive due to technological, methodological and logistical complexities. Major developments in our understanding of the anthropology of the Upper Palaeolithic, Mesolithic and Neolithic, and advances in ancient DNA (aDNA) technology and chronometric methods now allow us to assess in sufficient resolution the interface between these evolutionary processes, and changes in human culture and behaviour.
The proposed research will investigate the complex interface between the morphological, genetic, behavioural, and cultural factors that shaped the population history of European AMHs. The PI s interdisciplinary expertise in these areas, his access to and experience of relevant skeletal collections, and his ongoing European collaborations will allow significant progress in addressing these fundamental questions. The approach taken will include (a) the collection of bioarchaeological, aDNA, stable isotope (for the analysis of ancient diet) and radiometric data on 500 skeletons from key sites/phases in Europe and western Anatolia, and (b) the application of existing and novel aDNA, bioarchaeological and simulation methodologies. This research will yield results that transform our current understanding of major demographic and evolutionary processes and will place Europe at the forefront of anthropological biological and genetic research.
Max ERC Funding
1 088 386 €
Duration
Start date: 2011-01-01, End date: 2015-12-31
Project acronym BLENDS
Project Between Direct and Indirect Discourse: Shifting Perspective in Blended Discourse
Researcher (PI) Emar Maier
Host Institution (HI) RIJKSUNIVERSITEIT GRONINGEN
Country Netherlands
Call Details Starting Grant (StG), SH4, ERC-2010-StG_20091209
Summary A fundamental feature of language is that it allows us to reproduce what others have said. It is traditionally assumed that there
are two ways of doing this: direct discourse, where you preserve the original speech act verbatim, and indirect discourse,
where you paraphrase it in your own words. In accordance with this dichotomy, linguists have posited a number of universal
characteristics to distinguish the two modes. At the same time, we are seeing more and more examples that seem to fall
somewhere in between. I reject the direct indirect distinction and replace it with a new paradigm of blended discourse.
Combining insights from philosophy and linguistics, my framework has only one kind of speech reporting, in which a speaker
always attempts to convey the content of the reported words from her own perspective, but can quote certain parts verbatim,
thereby effectively switching to the reported perspective.
To explain why some languages are shiftier than others, I hypothesize that a greater distance from face-to-face
communication, with the possibility of extra- and paralinguistic perspective marking, necessitated the introduction of
an artificial direct indirect separation. I test this hypothesis by investigating languages that are closely tied to direct
communication: Dutch child language, as recent studies hint at a very late acquisition of the direct indirect distinction; Dutch
Sign Language, which has a special role shift marker that bears a striking resemblance to the quotational shift of blended
discourse; and Ancient Greek, where philologists have long been observing perspective shifts.
In sum, my research combines a new philosophical insight on the nature of reported speech with formal semantic rigor and
linguistic data from child language experiments, native signers, and Greek philology.
Summary
A fundamental feature of language is that it allows us to reproduce what others have said. It is traditionally assumed that there
are two ways of doing this: direct discourse, where you preserve the original speech act verbatim, and indirect discourse,
where you paraphrase it in your own words. In accordance with this dichotomy, linguists have posited a number of universal
characteristics to distinguish the two modes. At the same time, we are seeing more and more examples that seem to fall
somewhere in between. I reject the direct indirect distinction and replace it with a new paradigm of blended discourse.
Combining insights from philosophy and linguistics, my framework has only one kind of speech reporting, in which a speaker
always attempts to convey the content of the reported words from her own perspective, but can quote certain parts verbatim,
thereby effectively switching to the reported perspective.
To explain why some languages are shiftier than others, I hypothesize that a greater distance from face-to-face
communication, with the possibility of extra- and paralinguistic perspective marking, necessitated the introduction of
an artificial direct indirect separation. I test this hypothesis by investigating languages that are closely tied to direct
communication: Dutch child language, as recent studies hint at a very late acquisition of the direct indirect distinction; Dutch
Sign Language, which has a special role shift marker that bears a striking resemblance to the quotational shift of blended
discourse; and Ancient Greek, where philologists have long been observing perspective shifts.
In sum, my research combines a new philosophical insight on the nature of reported speech with formal semantic rigor and
linguistic data from child language experiments, native signers, and Greek philology.
Max ERC Funding
677 254 €
Duration
Start date: 2011-03-01, End date: 2016-08-31
Project acronym BRAINBALANCE
Project Rebalancing the brain:
Guiding brain recovery after stroke
Researcher (PI) Alexander Thomas Sack
Host Institution (HI) UNIVERSITEIT MAASTRICHT
Country Netherlands
Call Details Starting Grant (StG), SH4, ERC-2010-StG_20091209
Summary Damage to parietal cortex after stroke causes patients to become unaware of large parts of their surroundings and body parts. This so-called spatial neglect is hypothesised to be brought about by a stroke-induced imbalance between the left and right hemisphere. Some patients experience a partial recovery of lost abilities, but the factors that drive this rebalancing are unknown. The research proposed here will overcome this bottleneck in our understanding of the brain recovery phenomenon, and develop therapeutic approaches that for the first time will control, steer and speed up brain rebalancing after stroke. To that goal, we introduce a revolutionary approach in which TMS, fMRI, and EEG are applied simultaneously in healthy human volunteers to artificially unbalance the brain, and then study and control processes of rebalancing. Because we are one of the few groups worldwide that has accomplished this methodology, and that has the expertise to fully analyse the data it will yield, we are in a unique position to deliver both fundamental insights into brain plasticity, and derived new therapies. In brief, we will use TMS to (i) mimic spatial neglect in healthy volunteers while simultaneously monitoring the underlying neural network effects using fMRI/EEG, and to (ii) determine which exact brain reorganisation leads to an optimal behavioral recovery after injury. Importantly, we will use cutting-edge fMRI pattern recognition and machine learning algorithms to predict which concrete TMS treatment will specifically support this optimal functional reorganisation in the unbalanced brain. Finally, we will directly translate these fundamental findings into clinical practise and apply novel TMS protocols to rebalance the brain in patients suffering from parietal stroke.
Summary
Damage to parietal cortex after stroke causes patients to become unaware of large parts of their surroundings and body parts. This so-called spatial neglect is hypothesised to be brought about by a stroke-induced imbalance between the left and right hemisphere. Some patients experience a partial recovery of lost abilities, but the factors that drive this rebalancing are unknown. The research proposed here will overcome this bottleneck in our understanding of the brain recovery phenomenon, and develop therapeutic approaches that for the first time will control, steer and speed up brain rebalancing after stroke. To that goal, we introduce a revolutionary approach in which TMS, fMRI, and EEG are applied simultaneously in healthy human volunteers to artificially unbalance the brain, and then study and control processes of rebalancing. Because we are one of the few groups worldwide that has accomplished this methodology, and that has the expertise to fully analyse the data it will yield, we are in a unique position to deliver both fundamental insights into brain plasticity, and derived new therapies. In brief, we will use TMS to (i) mimic spatial neglect in healthy volunteers while simultaneously monitoring the underlying neural network effects using fMRI/EEG, and to (ii) determine which exact brain reorganisation leads to an optimal behavioral recovery after injury. Importantly, we will use cutting-edge fMRI pattern recognition and machine learning algorithms to predict which concrete TMS treatment will specifically support this optimal functional reorganisation in the unbalanced brain. Finally, we will directly translate these fundamental findings into clinical practise and apply novel TMS protocols to rebalance the brain in patients suffering from parietal stroke.
Max ERC Funding
1 344 853 €
Duration
Start date: 2011-04-01, End date: 2016-03-31
Project acronym BRAINDEVELOPMENT
Project How brain development underlies advances in cognition and emotion in childhood and adolescence
Researcher (PI) Eveline Adriana Maria Crone
Host Institution (HI) UNIVERSITEIT LEIDEN
Country Netherlands
Call Details Starting Grant (StG), SH4, ERC-2010-StG_20091209
Summary Thanks to the recent advances in mapping brain activation during task performance using functional Magnetic Resonance Imaging (i.e., studying the brain in action), it is now possible to study one of the oldest questions in psychology: how the development of neural circuitry underlies the development of cognition and emotion. The ‘Storm and Stress’ of adolescence, a period during which adolescents develop cognitively with great speed but are also risk-takers and sensitive to opinions of their peer group, has puzzled scientists for centuries. New technologies of brain mapping have the potential to shed new light on the mystery of adolescence. The approach proposed here concerns the investigation of brain regions which underlie developmental changes in cognitive, emotional and social-emotional functions over the course of child and adolescent development.
For this purpose I will measure functional brain development longitudinally across the age range 8-20 years by using a combined cross-sectional longitudinal design including 240 participants. Participants will take part in two testing sessions over a four-year-period in order to track the within-subject time courses of functional brain development for cognitive, emotional and social-emotional functions and to understand how these functions develop relative to each other in the same individuals, using multilevel models for change. The cross-sectional longitudinal assessment of cognitive, emotional and social-emotional functional brain development in relation to brain structure and hormone levels is unique in the international field and has the potential to provide new explanations for old questions. The application of brain mapping combined with multilevel models for change is original, and allows for the examination of developmental trajectories rather than age comparisons. An integrative mapping (i.e., combined with task performance and with biological markers) of functional brain development is important not only for theory development, but also for understanding how children learn new tasks and participate in a complex social world, and eventually to tailor educational programs to the needs of children.
Summary
Thanks to the recent advances in mapping brain activation during task performance using functional Magnetic Resonance Imaging (i.e., studying the brain in action), it is now possible to study one of the oldest questions in psychology: how the development of neural circuitry underlies the development of cognition and emotion. The ‘Storm and Stress’ of adolescence, a period during which adolescents develop cognitively with great speed but are also risk-takers and sensitive to opinions of their peer group, has puzzled scientists for centuries. New technologies of brain mapping have the potential to shed new light on the mystery of adolescence. The approach proposed here concerns the investigation of brain regions which underlie developmental changes in cognitive, emotional and social-emotional functions over the course of child and adolescent development.
For this purpose I will measure functional brain development longitudinally across the age range 8-20 years by using a combined cross-sectional longitudinal design including 240 participants. Participants will take part in two testing sessions over a four-year-period in order to track the within-subject time courses of functional brain development for cognitive, emotional and social-emotional functions and to understand how these functions develop relative to each other in the same individuals, using multilevel models for change. The cross-sectional longitudinal assessment of cognitive, emotional and social-emotional functional brain development in relation to brain structure and hormone levels is unique in the international field and has the potential to provide new explanations for old questions. The application of brain mapping combined with multilevel models for change is original, and allows for the examination of developmental trajectories rather than age comparisons. An integrative mapping (i.e., combined with task performance and with biological markers) of functional brain development is important not only for theory development, but also for understanding how children learn new tasks and participate in a complex social world, and eventually to tailor educational programs to the needs of children.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-02-01, End date: 2016-01-31
Project acronym CELLTYPESANDCIRCUITS
Project Neural circuit function in the retina of mice and humans
Researcher (PI) Botond Roska
Host Institution (HI) FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION
Country Switzerland
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary The mammalian brain is assembled from thousands of neuronal cell types that are organized into distinct circuits to perform behaviourally relevant computations. To gain mechanistic insights about brain function and to treat specific diseases of the nervous system it is crucial to understand what these local circuits are computing and how they achieve these computations. By examining the structure and function of a few genetically identified and experimentally accessible neural circuits we plan to address fundamental questions about the functional architecture of neural circuits. First, are cell types assigned to a unique functional circuit with a well-defined function or do they participate in multiple circuits (multitasking cell types), adjusting their role depending on the state of these circuits? Second, does a neural circuit perform a single computation or depending on the information content of its inputs can it carry out radically different functions? Third, how, among the large number of other cell types, do the cells belonging to the same functional circuit connect together during development? We use the mouse retina as a model system to address these questions. Finally, we will study the structure and function of a specialised neural circuit in the human fovea that enables humans to read. We predict that our insights into the mechanism of multitasking, network switches and the development of selective connectivity will be instructive to study similar phenomena in other brain circuits. Knowledge of the structure and function of the human fovea will open up new opportunities to correlate human retinal function with human visual behaviour and our genetic technologies to study human foveal function will allow us and others to design better strategies for restoring vision for the blind.
Summary
The mammalian brain is assembled from thousands of neuronal cell types that are organized into distinct circuits to perform behaviourally relevant computations. To gain mechanistic insights about brain function and to treat specific diseases of the nervous system it is crucial to understand what these local circuits are computing and how they achieve these computations. By examining the structure and function of a few genetically identified and experimentally accessible neural circuits we plan to address fundamental questions about the functional architecture of neural circuits. First, are cell types assigned to a unique functional circuit with a well-defined function or do they participate in multiple circuits (multitasking cell types), adjusting their role depending on the state of these circuits? Second, does a neural circuit perform a single computation or depending on the information content of its inputs can it carry out radically different functions? Third, how, among the large number of other cell types, do the cells belonging to the same functional circuit connect together during development? We use the mouse retina as a model system to address these questions. Finally, we will study the structure and function of a specialised neural circuit in the human fovea that enables humans to read. We predict that our insights into the mechanism of multitasking, network switches and the development of selective connectivity will be instructive to study similar phenomena in other brain circuits. Knowledge of the structure and function of the human fovea will open up new opportunities to correlate human retinal function with human visual behaviour and our genetic technologies to study human foveal function will allow us and others to design better strategies for restoring vision for the blind.
Max ERC Funding
1 499 000 €
Duration
Start date: 2010-11-01, End date: 2015-10-31
Project acronym COMPLEXDATA
Project Statistics for Complex Data: Understanding Randomness, Geometry and Complexity with a view Towards Biophysics
Researcher (PI) Victor Michael Panaretos
Host Institution (HI) ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Country Switzerland
Call Details Starting Grant (StG), PE1, ERC-2010-StG_20091028
Summary The ComplexData project aims at advancing our understanding of the statistical treatment of varied types of complex data by generating new theory and methods, and to obtain progress in concrete current biophysical problems through the implementation of the new tools developed. Complex Data constitute data where the basic object of observation cannot be described in the standard Euclidean context of statistics, but rather needs to be thought of as an element of an abstract mathematical space with special properties. Scientific progress has, in recent years, begun to generate an increasing number of new and complex types of data that require statistical understanding and analysis. Four such types of data that are arising in the context of current scientific research and that the project will be focusing on are: random integral transforms, random unlabelled shapes, random flows of functions, and random tensor fields. In these unconventional contexts for statistics, the strategy of the project will be to carefully exploit the special aspects involved due to geometry, dimension and randomness in order to be able to either adapt and synthesize existing statistical methods, or to generate new statistical ideas altogether. However, the project will not restrict itself to merely studying the theoretical aspects of complex data, but will be truly interdisciplinary. The connecting thread among all the above data types is that their study is motivated by, and will be applied to concrete practical problems arising in the study of biological structure, dynamics, and function: biophysics. For this reason, the programme will be in interaction with local and international contacts from this field. In particular, the theoretical/methodological output of the four programme research foci will be applied to gain insights in the following corresponding four application areas: electron microscopy, protein homology, DNA molecular dynamics, brain imaging.
Summary
The ComplexData project aims at advancing our understanding of the statistical treatment of varied types of complex data by generating new theory and methods, and to obtain progress in concrete current biophysical problems through the implementation of the new tools developed. Complex Data constitute data where the basic object of observation cannot be described in the standard Euclidean context of statistics, but rather needs to be thought of as an element of an abstract mathematical space with special properties. Scientific progress has, in recent years, begun to generate an increasing number of new and complex types of data that require statistical understanding and analysis. Four such types of data that are arising in the context of current scientific research and that the project will be focusing on are: random integral transforms, random unlabelled shapes, random flows of functions, and random tensor fields. In these unconventional contexts for statistics, the strategy of the project will be to carefully exploit the special aspects involved due to geometry, dimension and randomness in order to be able to either adapt and synthesize existing statistical methods, or to generate new statistical ideas altogether. However, the project will not restrict itself to merely studying the theoretical aspects of complex data, but will be truly interdisciplinary. The connecting thread among all the above data types is that their study is motivated by, and will be applied to concrete practical problems arising in the study of biological structure, dynamics, and function: biophysics. For this reason, the programme will be in interaction with local and international contacts from this field. In particular, the theoretical/methodological output of the four programme research foci will be applied to gain insights in the following corresponding four application areas: electron microscopy, protein homology, DNA molecular dynamics, brain imaging.
Max ERC Funding
681 146 €
Duration
Start date: 2011-06-01, End date: 2016-05-31
Project acronym COMPUSLANG
Project Neural and computational determinants of left cerebral dominance in speech and language
Researcher (PI) Anne-Lise Mamessier
Host Institution (HI) UNIVERSITE DE GENEVE
Country Switzerland
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary More than a century after Wernicke and Broca established that speech perception and production rely on temporal and prefrontal cortices of the left brain hemisphere, the biological determinants for this organization are still unknown. While functional neuroanatomy has been described in great detail, the neuroscience of language still lacks a physiologically plausible model of the neuro-computational mechanisms for coding and decoding of speech acoustic signal. We propose to fill this gap by testing the biological validity and exploring the computational implications of one promising proposal, the Asymmetric Sampling in Time theory. AST assumes that speech signals are analysed in parallel at multiple timescales and that these timescales differ between left and right cerebral hemispheres. This theory is original and provocative as it implies that a single computational difference, distinct integration windows in right and left auditory cortices could be sufficient to explain why speech is preferentially processed by the left brain, and possible even why the human brain has evolved toward such an asymmetric functional organization. Our proposal has four goals: 1/ to validate, invalidate or amend AST on the basis of physiological experiments in healthy human subjects including functional magnetic resonance imaging (fMRI), combined electroencephalography (EEG) and fMRI, magnetoencephalography (MEG) and subdural electrocorticography (EcoG), 2/ to use computational modeling to probe those aspects of the theory that currently remain inaccessible to empirical testing (evaluation, assessment), 3/ to apply AST to binaural artificial hearing with cochlear implants, 4/ to test for disorders of auditory sampling in autism and dyslexia, two language neurodevelopmental pathologies in which a genetic basis implicates the physiological underpinnings of AST, and 5/ to assess potential generalisation of AST to linguistic action in the context of speech production.
Summary
More than a century after Wernicke and Broca established that speech perception and production rely on temporal and prefrontal cortices of the left brain hemisphere, the biological determinants for this organization are still unknown. While functional neuroanatomy has been described in great detail, the neuroscience of language still lacks a physiologically plausible model of the neuro-computational mechanisms for coding and decoding of speech acoustic signal. We propose to fill this gap by testing the biological validity and exploring the computational implications of one promising proposal, the Asymmetric Sampling in Time theory. AST assumes that speech signals are analysed in parallel at multiple timescales and that these timescales differ between left and right cerebral hemispheres. This theory is original and provocative as it implies that a single computational difference, distinct integration windows in right and left auditory cortices could be sufficient to explain why speech is preferentially processed by the left brain, and possible even why the human brain has evolved toward such an asymmetric functional organization. Our proposal has four goals: 1/ to validate, invalidate or amend AST on the basis of physiological experiments in healthy human subjects including functional magnetic resonance imaging (fMRI), combined electroencephalography (EEG) and fMRI, magnetoencephalography (MEG) and subdural electrocorticography (EcoG), 2/ to use computational modeling to probe those aspects of the theory that currently remain inaccessible to empirical testing (evaluation, assessment), 3/ to apply AST to binaural artificial hearing with cochlear implants, 4/ to test for disorders of auditory sampling in autism and dyslexia, two language neurodevelopmental pathologies in which a genetic basis implicates the physiological underpinnings of AST, and 5/ to assess potential generalisation of AST to linguistic action in the context of speech production.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-02-01, End date: 2016-01-31
Project acronym CONQUEST
Project Controlled quantum effects and spin technology
- from non-equilibrium physics to functional magnetics
Researcher (PI) Henrik Ronnow
Host Institution (HI) ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Country Switzerland
Call Details Starting Grant (StG), PE3, ERC-2010-StG_20091028
Summary The technology of the 20th century was dominated by a single material class: The semiconductors, whose properties can be tuned between those of metals and insulators all of which describable by single-electron effects. In contrast, quantum magnets and strongly correlated electron systems offer a full palette of quantum mechanical many-electron states. CONQUEST aim to discover, understand and demonstrate control over such quantum states. A new experimental approach, building on established powerful laboratory and neutron scattering techniques combined with dynamical control-perturbations, will be developed to study correlated quantum effects in magnetic materials. The immediate goal is to open a new field of non-equilibrium and time dependent studies in solid state physics. The long-term vision is that the approach might nurture the materials of the 21st century.
Summary
The technology of the 20th century was dominated by a single material class: The semiconductors, whose properties can be tuned between those of metals and insulators all of which describable by single-electron effects. In contrast, quantum magnets and strongly correlated electron systems offer a full palette of quantum mechanical many-electron states. CONQUEST aim to discover, understand and demonstrate control over such quantum states. A new experimental approach, building on established powerful laboratory and neutron scattering techniques combined with dynamical control-perturbations, will be developed to study correlated quantum effects in magnetic materials. The immediate goal is to open a new field of non-equilibrium and time dependent studies in solid state physics. The long-term vision is that the approach might nurture the materials of the 21st century.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-04-01, End date: 2016-03-31
Project acronym CRITIQUEUE
Project Critical queues and reflected stochastic processes
Researcher (PI) Johannes S.H. Van Leeuwaarden
Host Institution (HI) TECHNISCHE UNIVERSITEIT EINDHOVEN
Country Netherlands
Call Details Starting Grant (StG), PE1, ERC-2010-StG_20091028
Summary Our primary motivation stems from queueing theory, the branch of applied probability that deals with congestion phenomena. Congestion levels are typically nonnegative, which is why reflected stochastic processes arise naturally in queueing theory. Other applications of reflected stochastic processes are in the fields of branching processes and random graphs.
We are particularly interested in critically-loaded queueing systems (close to 100% utilization), also referred to as queues in heavy traffic. Heavy-traffic analysis typically reduces complicated queueing processes to much simpler (reflected) limit processes or scaling limits. This makes the analysis of complex systems tractable, and from a mathematical point of view, these results are appealing since they can be made rigorous. Within the large
body of literature on heavy-traffic theory and critical stochastic processes, we launch two new research lines:
(i) Time-dependent analysis through scaling limits.
(ii) Dimensioning stochastic systems via refined scaling limits and optimization.
Both research lines involve mathematical techniques that combine stochastic theory with asymptotic theory, complex analysis, functional analysis, and modern probabilistic methods. It will provide a platform enabling collaborations between researchers in pure and applied probability and researchers in performance analysis of queueing systems. This will particularly be the case at TU/e, the host institution, and at
the affiliated institution EURANDOM.
Summary
Our primary motivation stems from queueing theory, the branch of applied probability that deals with congestion phenomena. Congestion levels are typically nonnegative, which is why reflected stochastic processes arise naturally in queueing theory. Other applications of reflected stochastic processes are in the fields of branching processes and random graphs.
We are particularly interested in critically-loaded queueing systems (close to 100% utilization), also referred to as queues in heavy traffic. Heavy-traffic analysis typically reduces complicated queueing processes to much simpler (reflected) limit processes or scaling limits. This makes the analysis of complex systems tractable, and from a mathematical point of view, these results are appealing since they can be made rigorous. Within the large
body of literature on heavy-traffic theory and critical stochastic processes, we launch two new research lines:
(i) Time-dependent analysis through scaling limits.
(ii) Dimensioning stochastic systems via refined scaling limits and optimization.
Both research lines involve mathematical techniques that combine stochastic theory with asymptotic theory, complex analysis, functional analysis, and modern probabilistic methods. It will provide a platform enabling collaborations between researchers in pure and applied probability and researchers in performance analysis of queueing systems. This will particularly be the case at TU/e, the host institution, and at
the affiliated institution EURANDOM.
Max ERC Funding
970 800 €
Duration
Start date: 2010-08-01, End date: 2016-07-31
Project acronym CTLANDROS
Project Reactive Oxygen Species in CTL-mediated Cell Death: from Mechanism to Applications
Researcher (PI) Denis Martinvalet
Host Institution (HI) UNIVERSITE DE GENEVE
Country Switzerland
Call Details Starting Grant (StG), LS6, ERC-2010-StG_20091118
Summary Cytotoxic T lymphocytes (CTL) and natural killer (NK) cells release granzyme and perforin from cytotoxic granules into the immune synapse to induce apoptosis of target cells that are either virus-infected or cancerous. Granzyme A activates a caspase-independent apoptotic pathway and induces mitochondrial damage characterized by superoxide anion production and loss of the mitochondrial transmembrane potential, without disrupting the integrity of the mitochondrial outer membrane; while causing single-stranded DNA damage. GzmB induces both caspase-dependent and caspase-independent cell death. In the caspase-dependent pathway, mitochondrial functions are altered as evidenced by the loss of mitochondrial transmembrane potential and the generation of reactive oxygen species (ROS). The mitochondrial outer membrane (MOM) is disrupted, resulting in the release of apoptogenic factors. To date, research on mitochondrial-dependent apoptosis has focused on mitochondrial outer membrane permeabilization (MOMP) however whether the generation of ROS is incidental or essential to the execution of apoptosis remains unclear. Like human GzmA, human GzmB promotes cell death in a ROS-dependent manner. Preliminary data suggest that human GzmB can induce ROS in a MOMP-independent manner as Bax and Bak double knockout MEF cells treated with human GzmB and perforin still display a robust ROS production and dye in an ROS-dependent manner. Since GzmA and GzmB induce cell death in a ROS-dependent manner, we hypothesize that oxygen free radicals are central to the execution of programmed cell death induced by the cytotoxic granules. Therefore, the goal of this proposal is to dissect the key molecular events triggered by ROS that lead to Citotoxic Tcell-induced target cell death. A combination of biochemical, genetic and proteomic approaches in association with Electron Spin Resonance (ESR) spectroscopy methodology will be used to unravel the essential role ROS play in CTL-mediated killing.
Summary
Cytotoxic T lymphocytes (CTL) and natural killer (NK) cells release granzyme and perforin from cytotoxic granules into the immune synapse to induce apoptosis of target cells that are either virus-infected or cancerous. Granzyme A activates a caspase-independent apoptotic pathway and induces mitochondrial damage characterized by superoxide anion production and loss of the mitochondrial transmembrane potential, without disrupting the integrity of the mitochondrial outer membrane; while causing single-stranded DNA damage. GzmB induces both caspase-dependent and caspase-independent cell death. In the caspase-dependent pathway, mitochondrial functions are altered as evidenced by the loss of mitochondrial transmembrane potential and the generation of reactive oxygen species (ROS). The mitochondrial outer membrane (MOM) is disrupted, resulting in the release of apoptogenic factors. To date, research on mitochondrial-dependent apoptosis has focused on mitochondrial outer membrane permeabilization (MOMP) however whether the generation of ROS is incidental or essential to the execution of apoptosis remains unclear. Like human GzmA, human GzmB promotes cell death in a ROS-dependent manner. Preliminary data suggest that human GzmB can induce ROS in a MOMP-independent manner as Bax and Bak double knockout MEF cells treated with human GzmB and perforin still display a robust ROS production and dye in an ROS-dependent manner. Since GzmA and GzmB induce cell death in a ROS-dependent manner, we hypothesize that oxygen free radicals are central to the execution of programmed cell death induced by the cytotoxic granules. Therefore, the goal of this proposal is to dissect the key molecular events triggered by ROS that lead to Citotoxic Tcell-induced target cell death. A combination of biochemical, genetic and proteomic approaches in association with Electron Spin Resonance (ESR) spectroscopy methodology will be used to unravel the essential role ROS play in CTL-mediated killing.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-05-01, End date: 2016-04-30
Project acronym DEPORT REGIMES
Project The Social Life of State Deportation Regimes:
A Comparative Study of the Implementation Interface
Researcher (PI) Barak Kalir
Host Institution (HI) UNIVERSITEIT VAN AMSTERDAM
Country Netherlands
Call Details Starting Grant (StG), SH2, ERC-2013-StG
Summary The deportation of irregular migrants is a burning issue in public debates all around the world. Most states invest heavily in effective deportation regimes, but when it comes to implementation, deportation regimes are notorious for not achieving their declared goals. Everywhere, marked discrepancies persist between deportation policies and actual practices of deportation.
This project compares the implementation of deportation regimes in four different states – Israel, Greece, Spain and Ecuador – in order to provide a closely researched assessment of implementation practices. It interrogates a core assumption in much of the scholarly literature on the “deportation turn”, namely, that there is a global convergence of state deportation regimes.
The project adds a crucial – yet, so far underexplored – perspective on irregular migration: the interface of street-level state agents and civil-society actors in shaping practices of deportation. Existing studies look either at the “top level” of the state (policies, laws, procedures, etc.), or at the “underground level” of its “victims” (irregular migrants’ survival strategies, trafficking networks, etc.). This project privileges the “meso level” of the deportation regime, bringing to light the agency of those who exercise discretion in interpreting laws and policies at the “implementation interface”. It makes an original contribution to the anthropology of the state, by demonstrating that the territorial sovereignty of states is constantly renegotiated at this level.
The project will produce knowledge on the dilemmas, tactics and occasional alliances of those who carry out and those who obstruct deportation regimes. It will provide new insights into actors’ motivations and worldviews, and explore the dynamics of both “implementation deficits” and “implementation surpluses”. The fine-grained comparative methodology is aimed at producing findings that will be of theoretical significance and of vital importance for policymakers, street-level agents and civil-society actors in dealing with the realities of irregular migration in the 21st century.
Summary
The deportation of irregular migrants is a burning issue in public debates all around the world. Most states invest heavily in effective deportation regimes, but when it comes to implementation, deportation regimes are notorious for not achieving their declared goals. Everywhere, marked discrepancies persist between deportation policies and actual practices of deportation.
This project compares the implementation of deportation regimes in four different states – Israel, Greece, Spain and Ecuador – in order to provide a closely researched assessment of implementation practices. It interrogates a core assumption in much of the scholarly literature on the “deportation turn”, namely, that there is a global convergence of state deportation regimes.
The project adds a crucial – yet, so far underexplored – perspective on irregular migration: the interface of street-level state agents and civil-society actors in shaping practices of deportation. Existing studies look either at the “top level” of the state (policies, laws, procedures, etc.), or at the “underground level” of its “victims” (irregular migrants’ survival strategies, trafficking networks, etc.). This project privileges the “meso level” of the deportation regime, bringing to light the agency of those who exercise discretion in interpreting laws and policies at the “implementation interface”. It makes an original contribution to the anthropology of the state, by demonstrating that the territorial sovereignty of states is constantly renegotiated at this level.
The project will produce knowledge on the dilemmas, tactics and occasional alliances of those who carry out and those who obstruct deportation regimes. It will provide new insights into actors’ motivations and worldviews, and explore the dynamics of both “implementation deficits” and “implementation surpluses”. The fine-grained comparative methodology is aimed at producing findings that will be of theoretical significance and of vital importance for policymakers, street-level agents and civil-society actors in dealing with the realities of irregular migration in the 21st century.
Max ERC Funding
1 488 410 €
Duration
Start date: 2014-03-01, End date: 2019-02-28
Project acronym DRAGNET
Project "DRAGNET: A high-speed, wide-angle camera for catching extreme astrophysical events"
Researcher (PI) Jason William Thomas Hessels
Host Institution (HI) STICHTING ASTRON, NETHERLANDS INSTITUTE FOR RADIO ASTRONOMY
Country Netherlands
Call Details Starting Grant (StG), PE9, ERC-2013-StG
Summary "Looking up on a starry night, it’s easy to imagine that the Universe is unchanging. In reality, however, the Universe is teeming with activity: there are massive explosions from accreting black holes, bright radio flashes from ultra-magnetic pulsars, and likely other spectacles that have so far escaped our prying eyes. These fleeting events can happen faster than the blink of an eye and, importantly, they trace the most extreme astrophysical phenomena. Catching these rare performances poses a major challenge for observational astronomers, but the scientific payoff is well worth the effort.
With this proposal, I will mould the Low-Frequency Array (LOFAR) telescope into DRAGNET, the world's premier high-speed, wide-angle camera for radio astronomy. Radio waves are a unique and powerful way of investigating the most extreme astrophysical processes. With DRAGNET I will characterize the rate of fast radio transients, i.e. astrophysical bursts lasting less than a second, and search for new astrophysical phenomena in this largely unexplored domain. This has the potential to give us transformative insight into the extremes of gravity and dense matter. Alongside this, I will simultaneously monitor hundreds of radio-emitting neutron stars (pulsars) on a regular basis. This will allow me to understand why some neutron stars pulse regularly, while others show rapid switches in their emission properties. This will address the physics behind the strongest magnetic fields in the Universe.
I have led the construction of LOFAR's high-time-resolution observing capabilities; in this project I will capitalize on that investment and do cutting-edge science that is beyond the reach of any other existing telescope. Simply put, this project will establish a world-leading research group in the emerging field of fast radio transients and will crystallize the wide-field radio telescope as an essential tool for unveiling the bustling activity that makes our Universe so interesting to study."
Summary
"Looking up on a starry night, it’s easy to imagine that the Universe is unchanging. In reality, however, the Universe is teeming with activity: there are massive explosions from accreting black holes, bright radio flashes from ultra-magnetic pulsars, and likely other spectacles that have so far escaped our prying eyes. These fleeting events can happen faster than the blink of an eye and, importantly, they trace the most extreme astrophysical phenomena. Catching these rare performances poses a major challenge for observational astronomers, but the scientific payoff is well worth the effort.
With this proposal, I will mould the Low-Frequency Array (LOFAR) telescope into DRAGNET, the world's premier high-speed, wide-angle camera for radio astronomy. Radio waves are a unique and powerful way of investigating the most extreme astrophysical processes. With DRAGNET I will characterize the rate of fast radio transients, i.e. astrophysical bursts lasting less than a second, and search for new astrophysical phenomena in this largely unexplored domain. This has the potential to give us transformative insight into the extremes of gravity and dense matter. Alongside this, I will simultaneously monitor hundreds of radio-emitting neutron stars (pulsars) on a regular basis. This will allow me to understand why some neutron stars pulse regularly, while others show rapid switches in their emission properties. This will address the physics behind the strongest magnetic fields in the Universe.
I have led the construction of LOFAR's high-time-resolution observing capabilities; in this project I will capitalize on that investment and do cutting-edge science that is beyond the reach of any other existing telescope. Simply put, this project will establish a world-leading research group in the emerging field of fast radio transients and will crystallize the wide-field radio telescope as an essential tool for unveiling the bustling activity that makes our Universe so interesting to study."
Max ERC Funding
1 964 587 €
Duration
Start date: 2014-01-01, End date: 2018-12-31
Project acronym ECOSPACE
Project EcoSpace: Spatial-Dynamic Modelling of Adaptation Options to Climate Change at the Ecosystem Scale
Researcher (PI) Lars Gerard Hein
Host Institution (HI) WAGENINGEN UNIVERSITY
Country Netherlands
Call Details Starting Grant (StG), SH3, ERC-2010-StG_20091209
Summary Climate change will necessitate adjustments in ecosystem management in order to maintain the functioning of ecosystems and the supply of ecosystem services. The aim of this project is to develop a spatially explicit, dynamic modelling approach for identifying and analysing adaptation strategies for ecosystem management.
In particular, the project will develop and apply a general, spatial model integrating climate change scenarios, ecosystem dynamics, response thresholds, ecosystem services supply and management options. The scientific innovation of the project lies in the application of an ecosystem services approach to analyse adaptation options, the integration of complex ecosystem dynamics and societal impacts, and the spatially explicit modelling of economic benefits supplied by ecosystems.
The general model will be tested and validated on the basis of three case studies, focussing on: (i) flood protection in the Netherlands; (ii) impacts of climate change in northern Norway; and (iii) optimising land use including production of biofuels stock in Kalimantan, Indonesia. The first two areas are particularly vulnerable to climate change, and the third area is relevant because of its importance as a source of biofuel (palmoil) with associated environmental and social impacts. Each case study will be implemented in collaboration with local and international partners, and will result in the identification of economic efficient, sustainable and equitable local adaptation options.
Summary
Climate change will necessitate adjustments in ecosystem management in order to maintain the functioning of ecosystems and the supply of ecosystem services. The aim of this project is to develop a spatially explicit, dynamic modelling approach for identifying and analysing adaptation strategies for ecosystem management.
In particular, the project will develop and apply a general, spatial model integrating climate change scenarios, ecosystem dynamics, response thresholds, ecosystem services supply and management options. The scientific innovation of the project lies in the application of an ecosystem services approach to analyse adaptation options, the integration of complex ecosystem dynamics and societal impacts, and the spatially explicit modelling of economic benefits supplied by ecosystems.
The general model will be tested and validated on the basis of three case studies, focussing on: (i) flood protection in the Netherlands; (ii) impacts of climate change in northern Norway; and (iii) optimising land use including production of biofuels stock in Kalimantan, Indonesia. The first two areas are particularly vulnerable to climate change, and the third area is relevant because of its importance as a source of biofuel (palmoil) with associated environmental and social impacts. Each case study will be implemented in collaboration with local and international partners, and will result in the identification of economic efficient, sustainable and equitable local adaptation options.
Max ERC Funding
759 600 €
Duration
Start date: 2010-11-01, End date: 2015-10-31
Project acronym ECOSTRESS
Project Physiological Reaction to Predation- A General Way to Link Individuals to Ecosystems
Researcher (PI) Dror Hawlena
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), LS8, ERC-2013-StG
Summary This proposal aims to advance a new general theory that links plasticity in prey responses to predation and biogeochemical processes to explain context-dependent variations in ecosystem functioning. The physiological reaction of prey to predation involves allocating resources from production to support emergency functions. An example of such a reaction is an increase in maintenance respiration concomitant with higher carbohydrate and lower N demand. Such changes in prey energy and elemental budget should alter the role prey play in regulating the quality of detrital inputs to soils. Nutrient content of detritus is an important determinant of the way soil communities regulate ecosystem processes. Thus, the physiological reaction of prey to predation can potentially explicate changes in ecosystem functioning. My first empirical examination of a few selected mechanisms of this theory has yielded very promising insights.
The main objectives of this proposal are: (1) To systematically test whether prey reactions to predation are consistent with the proposed theory’s predictions across species and ecosystems; (2) to examine the interface between stress physiology and anti-predatory behaviors in explaining predator induced diet shift, and (3) to evaluate how predator induced responses at the individual level regulate ecosystem processes. To address these objectives, I propose combining manipulative field experiments, highly controlled laboratory and garden experiments, and stable-isotopes pulse chase approaches. I will examine individual prey responses and the emerging patterns across five food-chains that represent phylogenetically distant taxa and disparate ecosystems. The proposed study is expected to revolutionize our understanding of the mechanisms by which aboveground predators regulate ecosystem processes. Promoting such a mechanistic understanding is crucial to predict how human-induced changes in biodiversity will affect life-supporting ecosystem services.
Summary
This proposal aims to advance a new general theory that links plasticity in prey responses to predation and biogeochemical processes to explain context-dependent variations in ecosystem functioning. The physiological reaction of prey to predation involves allocating resources from production to support emergency functions. An example of such a reaction is an increase in maintenance respiration concomitant with higher carbohydrate and lower N demand. Such changes in prey energy and elemental budget should alter the role prey play in regulating the quality of detrital inputs to soils. Nutrient content of detritus is an important determinant of the way soil communities regulate ecosystem processes. Thus, the physiological reaction of prey to predation can potentially explicate changes in ecosystem functioning. My first empirical examination of a few selected mechanisms of this theory has yielded very promising insights.
The main objectives of this proposal are: (1) To systematically test whether prey reactions to predation are consistent with the proposed theory’s predictions across species and ecosystems; (2) to examine the interface between stress physiology and anti-predatory behaviors in explaining predator induced diet shift, and (3) to evaluate how predator induced responses at the individual level regulate ecosystem processes. To address these objectives, I propose combining manipulative field experiments, highly controlled laboratory and garden experiments, and stable-isotopes pulse chase approaches. I will examine individual prey responses and the emerging patterns across five food-chains that represent phylogenetically distant taxa and disparate ecosystems. The proposed study is expected to revolutionize our understanding of the mechanisms by which aboveground predators regulate ecosystem processes. Promoting such a mechanistic understanding is crucial to predict how human-induced changes in biodiversity will affect life-supporting ecosystem services.
Max ERC Funding
1 379 600 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym Emotions in Conflict
Project Direct and Indirect Emotion Regulation as a New Path of Conflict Resolution
Researcher (PI) Eran Halperin
Host Institution (HI) INTERDISCIPLINARY CENTER (IDC) HERZLIYA
Country Israel
Call Details Starting Grant (StG), SH4, ERC-2013-StG
Summary Intractable conflicts are one of the gravest challenges to both humanity and science. These conflicts are initiated and perpetuated by people; therefore changing people's hearts and minds constitutes a huge step towards resolution. Research on emotions in conflicts has led to the realization that intergroup emotions are critical to conflict dynamics. This project’s intrinsic question is whether and how intergroup emotions can be regulated to alter attitudes and behavior towards peace. I offer an innovative path, using two strategies of emotion regulation. The first is Direct Emotion Regulation, where traditional, effective emotion regulation strategies can be used to change intergroup emotional experiences and subsequently political positions in conflict situations. The second, Indirect Emotion Regulation, serves to implicitly alter concrete cognitive appraisals, thus changing attitudes by changing discrete emotions. This is the first attempt ever to integrate psychological aggregated knowledge on emotion regulation with conflict resolution. I propose 16 studies, conducted in the context of the intractable Israeli-Palestinian conflict. Seven studies will focus on direct emotion regulation, reducing intergroup anger and hatred, while 9 studies will focus on indirect regulation, aspiring to reduce fear and despair. In both paths, correlational and in-lab experimental studies will be used to refine adequate strategies of down regulating destructive emotions, the results of which will be used to develop innovative, theory-driven education and media interventions that will be tested utilizing wide scale experience sampling methodology. This project aspires to bridge the gap between basic and applied science, creating a pioneering, interdisciplinary framework which contributes to existing knowledge on emotion regulation in conflict and implements ways to apply it in real-world circumstances.
Summary
Intractable conflicts are one of the gravest challenges to both humanity and science. These conflicts are initiated and perpetuated by people; therefore changing people's hearts and minds constitutes a huge step towards resolution. Research on emotions in conflicts has led to the realization that intergroup emotions are critical to conflict dynamics. This project’s intrinsic question is whether and how intergroup emotions can be regulated to alter attitudes and behavior towards peace. I offer an innovative path, using two strategies of emotion regulation. The first is Direct Emotion Regulation, where traditional, effective emotion regulation strategies can be used to change intergroup emotional experiences and subsequently political positions in conflict situations. The second, Indirect Emotion Regulation, serves to implicitly alter concrete cognitive appraisals, thus changing attitudes by changing discrete emotions. This is the first attempt ever to integrate psychological aggregated knowledge on emotion regulation with conflict resolution. I propose 16 studies, conducted in the context of the intractable Israeli-Palestinian conflict. Seven studies will focus on direct emotion regulation, reducing intergroup anger and hatred, while 9 studies will focus on indirect regulation, aspiring to reduce fear and despair. In both paths, correlational and in-lab experimental studies will be used to refine adequate strategies of down regulating destructive emotions, the results of which will be used to develop innovative, theory-driven education and media interventions that will be tested utilizing wide scale experience sampling methodology. This project aspires to bridge the gap between basic and applied science, creating a pioneering, interdisciplinary framework which contributes to existing knowledge on emotion regulation in conflict and implements ways to apply it in real-world circumstances.
Max ERC Funding
1 499 344 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym ENCODING IN AXONS
Project Identifying mechanisms of information encoding in myelinated single axons
Researcher (PI) Maarten Kole
Host Institution (HI) KONINKLIJKE NEDERLANDSE AKADEMIE VAN WETENSCHAPPEN - KNAW
Country Netherlands
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary A major challenge in neuroscience is to understand how information is stored and coded within single nerve cells (neurons) and across neuron populations in the brain. Nerve cell fibres (axons) are thought to provide the wiring to connect neurons and conduct the electrical nerve impulse (action potential; AP). Recent discoveries, however, show that the initial part of axons actively participates in modulating APs and providing a means to enhance the computational repertoire of neurons in the central nervous system. To decrease the temporal delay in information transmission over long distances most axons are myelinated. Here, we will test the hypothesis that the degree of myelination of single axons directly and indirectly influences the mechanisms of AP generation and neural coding. We will use a novel approach of patch-clamp recording combined with immunohistochemical and ultrastructural identification to develop a detailed model of single myelinated neocortical axons. We also will investigate the neuron-glia interactions responsible for the myelination process and measure whether their development follows an activity-dependent process. Finally, we will elucidate the physiological and molecular similarities and discrepancies between myelinated and experimentally demyelinated single neocortical axons. These studies will provide a novel methodological framework to study central nervous system axons and yield basic insights into myelin physiology and pathophysiology.
Summary
A major challenge in neuroscience is to understand how information is stored and coded within single nerve cells (neurons) and across neuron populations in the brain. Nerve cell fibres (axons) are thought to provide the wiring to connect neurons and conduct the electrical nerve impulse (action potential; AP). Recent discoveries, however, show that the initial part of axons actively participates in modulating APs and providing a means to enhance the computational repertoire of neurons in the central nervous system. To decrease the temporal delay in information transmission over long distances most axons are myelinated. Here, we will test the hypothesis that the degree of myelination of single axons directly and indirectly influences the mechanisms of AP generation and neural coding. We will use a novel approach of patch-clamp recording combined with immunohistochemical and ultrastructural identification to develop a detailed model of single myelinated neocortical axons. We also will investigate the neuron-glia interactions responsible for the myelination process and measure whether their development follows an activity-dependent process. Finally, we will elucidate the physiological and molecular similarities and discrepancies between myelinated and experimentally demyelinated single neocortical axons. These studies will provide a novel methodological framework to study central nervous system axons and yield basic insights into myelin physiology and pathophysiology.
Max ERC Funding
1 994 640 €
Duration
Start date: 2011-04-01, End date: 2016-03-31
Project acronym EURO-NEUROSTRESS
Project Dissecting the Central Stress Response: Bridging the Genotype-Phenotype Gap
Researcher (PI) Alon Chen
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE
Country Israel
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary The biological response to stress is concerned with the maintenance of homeostasis in the presence of real or perceived challenges. This process requires numerous adaptive responses involving changes in the central nervous and neuroendocrine systems. When a situation is perceived as stressful, the brain activates many neuronal circuits linking centers involved in sensory, motor, autonomic, neuroendocrine, cognitive, and emotional functions in order to adapt to the demand. However, the details of the pathways by which the brain translates stressful stimuli into the final, integrated biological response are presently incompletely understood. Nevertheless, it is clear that dysregulation of these physiological responses to stress can have severe psychological and physiological consequences, and there is much evidence to suggest that inappropriate regulation, disproportional intensity, or chronic and/or irreversible activation of the stress response is linked to the etiology and pathophysiology of anxiety disorders and depression.
Understanding the neurobiology of stress by focusing on the brain circuits and genes, which are associated with, or altered by, the stress response will provide important insights into the brain mechanisms by which stress affects psychological and physiological disorders. This is an integrated multidisciplinary project from gene to behavior using state-of-the-art moue genetics and animal models. We will employ integrated molecular, biochemical, physiological and behavioral methods, focusing on the generation of mice genetic models as an in vivo tool, in order to study the central pathways and molecular mechanisms mediating the stress response. Defining the contributions of known and novel gene products to the maintenance of stress-linked homeostasis may improve our ability to design therapeutic interventions for, and thus manage, stress-related disorders.
Summary
The biological response to stress is concerned with the maintenance of homeostasis in the presence of real or perceived challenges. This process requires numerous adaptive responses involving changes in the central nervous and neuroendocrine systems. When a situation is perceived as stressful, the brain activates many neuronal circuits linking centers involved in sensory, motor, autonomic, neuroendocrine, cognitive, and emotional functions in order to adapt to the demand. However, the details of the pathways by which the brain translates stressful stimuli into the final, integrated biological response are presently incompletely understood. Nevertheless, it is clear that dysregulation of these physiological responses to stress can have severe psychological and physiological consequences, and there is much evidence to suggest that inappropriate regulation, disproportional intensity, or chronic and/or irreversible activation of the stress response is linked to the etiology and pathophysiology of anxiety disorders and depression.
Understanding the neurobiology of stress by focusing on the brain circuits and genes, which are associated with, or altered by, the stress response will provide important insights into the brain mechanisms by which stress affects psychological and physiological disorders. This is an integrated multidisciplinary project from gene to behavior using state-of-the-art moue genetics and animal models. We will employ integrated molecular, biochemical, physiological and behavioral methods, focusing on the generation of mice genetic models as an in vivo tool, in order to study the central pathways and molecular mechanisms mediating the stress response. Defining the contributions of known and novel gene products to the maintenance of stress-linked homeostasis may improve our ability to design therapeutic interventions for, and thus manage, stress-related disorders.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-04-01, End date: 2016-03-31
Project acronym EVOLOME
Project Genetic and phenotypic precursors of antibiotic resistance in evolving bacterial populations: from single cell to population level analyses
Researcher (PI) Nathalie Balaban
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), LS8, ERC-2010-StG_20091118
Summary Soon after new antibiotics are introduced, bacterial strains resistant to their action emerge. Recently, non-specific factors that promote the later appearance of specific mechanisms of resistance have been found. Some of these so-called global factors (as opposed to specific resistance mechanisms) emerge as major players in shaping the rate of evolution of resistance. For example, a mutation in the mismatch repair system is a global genetic factor that increases the mutation rate and therefore leads to an increased probability to evolve resistance.
In addition to global genetic factors, it is becoming clear that global phenotypic factors play a crucial role in resistance evolution. For example, activation of stress responses can also result in an elevated mutation rate and accelerated evolution of drug resistance. A natural question which arises in this context is how sub-populations of phenotypic variants differ in their evolutionary potential, and how that, in turn, affects the rate at which an entire population adapts to antibiotic stress.
I propose a multidisciplinary approach to the systematic and quantitative study of the non-specific factors that affect the mode and tempo of evolution towards antibiotic resistance. Our preliminary results indicate that the presence of dormant bacteria that survive antibiotic treatment affects the rate of resistance evolution in bacterial populations. I will exploit the established expertise of my lab using microfluidic devices for single cell analyses to track the emergence of resistance at the single-cell level, in real-time, and to study the correlation between the phenotype of single bacteria and the probability to evolve resistance. My second approach will take advantage of the recent developments in experimental evolution and high throughput sequencing and combine those with single cells observations for the systematic search of E.coli genes that affect the rate of resistance evolution. We will study replicate populations of E.coli, founded by either laboratory strains or clinical isolates, as they evolve in parallel, under antibiotic stress. Evolved populations will be compared with ancestral populations in order to identify genes and phenotypes that have changed during the evolution of antibiotic resistance. Finally, in silico evolution that simulates the experimental conditions will be developed to analyze the contribution of global factors on resistance evolution.
The evolution of antibiotic resistance is not only a fascinating demonstration of the power of evolution but also represents one of the major health threats today. I anticipate that this multidisciplinary study of the global factors that influence the evolution of resistance, from the single cell to the population level, will shed light on the mechanisms used by bacteria to accelerate evolution in general, as well as provide clues as to how to prevent the emergence of antibiotic resistance.
Summary
Soon after new antibiotics are introduced, bacterial strains resistant to their action emerge. Recently, non-specific factors that promote the later appearance of specific mechanisms of resistance have been found. Some of these so-called global factors (as opposed to specific resistance mechanisms) emerge as major players in shaping the rate of evolution of resistance. For example, a mutation in the mismatch repair system is a global genetic factor that increases the mutation rate and therefore leads to an increased probability to evolve resistance.
In addition to global genetic factors, it is becoming clear that global phenotypic factors play a crucial role in resistance evolution. For example, activation of stress responses can also result in an elevated mutation rate and accelerated evolution of drug resistance. A natural question which arises in this context is how sub-populations of phenotypic variants differ in their evolutionary potential, and how that, in turn, affects the rate at which an entire population adapts to antibiotic stress.
I propose a multidisciplinary approach to the systematic and quantitative study of the non-specific factors that affect the mode and tempo of evolution towards antibiotic resistance. Our preliminary results indicate that the presence of dormant bacteria that survive antibiotic treatment affects the rate of resistance evolution in bacterial populations. I will exploit the established expertise of my lab using microfluidic devices for single cell analyses to track the emergence of resistance at the single-cell level, in real-time, and to study the correlation between the phenotype of single bacteria and the probability to evolve resistance. My second approach will take advantage of the recent developments in experimental evolution and high throughput sequencing and combine those with single cells observations for the systematic search of E.coli genes that affect the rate of resistance evolution. We will study replicate populations of E.coli, founded by either laboratory strains or clinical isolates, as they evolve in parallel, under antibiotic stress. Evolved populations will be compared with ancestral populations in order to identify genes and phenotypes that have changed during the evolution of antibiotic resistance. Finally, in silico evolution that simulates the experimental conditions will be developed to analyze the contribution of global factors on resistance evolution.
The evolution of antibiotic resistance is not only a fascinating demonstration of the power of evolution but also represents one of the major health threats today. I anticipate that this multidisciplinary study of the global factors that influence the evolution of resistance, from the single cell to the population level, will shed light on the mechanisms used by bacteria to accelerate evolution in general, as well as provide clues as to how to prevent the emergence of antibiotic resistance.
Max ERC Funding
1 458 200 €
Duration
Start date: 2010-11-01, End date: 2015-10-31
Project acronym FAMILIFE
Project Families of migrant origin: a life course perspective
Researcher (PI) Helga Antoinette Gerda De Valk
Host Institution (HI) KONINKLIJKE NEDERLANDSE AKADEMIE VAN WETENSCHAPPEN - KNAW
Country Netherlands
Call Details Starting Grant (StG), SH3, ERC-2010-StG_20091209
Summary Over the last decades European societies have become more ethnically diverse. However, a more comprehensive understanding of the life course and population dynamics in migrant families is still lacking. Ignoring a large share of the population in studies on family and population dynamics is exclusive and does not reflect reality. My project is first of all innovative in providing a more comprehensive overview of individual life courses of migrants: events in different life domains are linked and full life trajectories are analysed and explained. I will focus not only on the causes but also study the consequences of life course decisions. The second project goal is to explain the effect of migration on intergenerational solidarity and family ties. The analyses will link different phases in the life course as well as different generations. Families of different migrant and native origin will be compared in these parts. Third, I will make unique comparisons between the life course trajectories in the countries of origin and settlement of migrants. Bringing in the perspective of the sending country is original and crucial for understanding to what extent life course choices are related to the integration process in the host society, or to a trend that also occurs in the country of origin. A final major novelty of this project is that different recent data sources are linked within each of the components of the project. The combination of data from the Gender and Generations Survey (GGS), The Integration of the Second Generation (TIES) survey, the PAIRFAM survey, the European Social Survey, the Demographic and Health Surveys and the census, allow for a more complete understanding of the life courses of migrants and population dynamics in migrant families.
Summary
Over the last decades European societies have become more ethnically diverse. However, a more comprehensive understanding of the life course and population dynamics in migrant families is still lacking. Ignoring a large share of the population in studies on family and population dynamics is exclusive and does not reflect reality. My project is first of all innovative in providing a more comprehensive overview of individual life courses of migrants: events in different life domains are linked and full life trajectories are analysed and explained. I will focus not only on the causes but also study the consequences of life course decisions. The second project goal is to explain the effect of migration on intergenerational solidarity and family ties. The analyses will link different phases in the life course as well as different generations. Families of different migrant and native origin will be compared in these parts. Third, I will make unique comparisons between the life course trajectories in the countries of origin and settlement of migrants. Bringing in the perspective of the sending country is original and crucial for understanding to what extent life course choices are related to the integration process in the host society, or to a trend that also occurs in the country of origin. A final major novelty of this project is that different recent data sources are linked within each of the components of the project. The combination of data from the Gender and Generations Survey (GGS), The Integration of the Second Generation (TIES) survey, the PAIRFAM survey, the European Social Survey, the Demographic and Health Surveys and the census, allow for a more complete understanding of the life courses of migrants and population dynamics in migrant families.
Max ERC Funding
1 012 800 €
Duration
Start date: 2011-02-01, End date: 2016-08-31
Project acronym FAMINE
Project Relocated Remembrance: the Great Famine in Irish (Diaspora) Fiction, 1847-1921
Researcher (PI) Marguerite Christina Maria Corporaal
Host Institution (HI) STICHTING KATHOLIEKE UNIVERSITEIT
Country Netherlands
Call Details Starting Grant (StG), SH5, ERC-2010-StG_20091209
Summary The Great Hunger (1845-49) radically transformed Ireland: it led to the wide-scale eviction of farmers, killed one million of the rural population, and caused massive emigration to other parts of the British Empire and the United States. Moreover, the Great Famine encouraged anti-English, nationalist sentiments and its trauma is pivotal to the development of an Irish postcolonial consciousness between 1847-1921. There is a vast unexplored transatlantic corpus of prose fiction, written between the aftermath of the Famine and the Anglo-Irish Treaty of 1921, which remembers the years of starvation and diaspora.
My project is the first to inventorise and bring together this under-researched body of literature, written in Ireland and by Irish immigrants in England, Canada and the United States. This fiction requires intensive examination for significant reasons, offering alternative perspectives on how the Famine was culturally experienced than previous studies have displayed, and representing subaltern voices and recollections. Moreover, the texts are written in the homeland as well as in diaspora, by migrated Irish or their descendants. An examination of the corpus will therefore move beyond the largely nation-oriented frontiers of cultural memory studies towards innovative, transnational approaches.
The project specifically investigates how remembrance is mediated through time, from one generation to another, and space, in diaspora. It aims to evolve a novel theoretical model about the interaction between temporal and spatial relocation in literary remembrance. This pioneering model will generate groundbreaking insights into the interaction between memory and ethnic identity in comparative contexts of cultural dislocation, a colonised homeland and migrant communities; and in processes of cultural relocation: de-colonisation and ethnic integration. At the same time, the project will analyse genre aspects which play a dynamic role in processes of cultural remembrance, contributing a new perspective to the interdisciplinary debate on media of recollection in cultural memory studies.
Summary
The Great Hunger (1845-49) radically transformed Ireland: it led to the wide-scale eviction of farmers, killed one million of the rural population, and caused massive emigration to other parts of the British Empire and the United States. Moreover, the Great Famine encouraged anti-English, nationalist sentiments and its trauma is pivotal to the development of an Irish postcolonial consciousness between 1847-1921. There is a vast unexplored transatlantic corpus of prose fiction, written between the aftermath of the Famine and the Anglo-Irish Treaty of 1921, which remembers the years of starvation and diaspora.
My project is the first to inventorise and bring together this under-researched body of literature, written in Ireland and by Irish immigrants in England, Canada and the United States. This fiction requires intensive examination for significant reasons, offering alternative perspectives on how the Famine was culturally experienced than previous studies have displayed, and representing subaltern voices and recollections. Moreover, the texts are written in the homeland as well as in diaspora, by migrated Irish or their descendants. An examination of the corpus will therefore move beyond the largely nation-oriented frontiers of cultural memory studies towards innovative, transnational approaches.
The project specifically investigates how remembrance is mediated through time, from one generation to another, and space, in diaspora. It aims to evolve a novel theoretical model about the interaction between temporal and spatial relocation in literary remembrance. This pioneering model will generate groundbreaking insights into the interaction between memory and ethnic identity in comparative contexts of cultural dislocation, a colonised homeland and migrant communities; and in processes of cultural relocation: de-colonisation and ethnic integration. At the same time, the project will analyse genre aspects which play a dynamic role in processes of cultural remembrance, contributing a new perspective to the interdisciplinary debate on media of recollection in cultural memory studies.
Max ERC Funding
741 000 €
Duration
Start date: 2010-10-01, End date: 2015-09-30
Project acronym FEMTOMAGNETISM
Project Femtosecond Laser Control of Spins in Magnetic Materials: from fundamentals to nanoscale dynamics
Researcher (PI) Alexey Voldemarovitsj Kimel
Host Institution (HI) STICHTING KATHOLIEKE UNIVERSITEIT
Country Netherlands
Call Details Starting Grant (StG), PE3, ERC-2010-StG_20091028
Summary The aim of the project is to develop femtosecond optical control of magnetism: a new area at the junction of coherent nonlinear optics, near-field optics and magnetism. In particular, I am aiming to investigate nonthermal effects of light on magnetic order and to apply this knowledge for highly efficient ultrafast (10-12 seconds and faster) optical control of magnetism at the nanoscale.
The ever increasing demand for faster information processing has triggered an intense search for ways to manipulate magnetically stored bits at the ultimately short time-scale. Although efficient, ultrafast and nonthermal laser control of magnetism may open new prospect of magnetic data storage and manipulation, many fundamental questions concerning the mechanisms that are responsible for the nonthermal effect of photons on spins and ultrafast laser induced changes of magnetic order are poorly understood. This is mainly because an ultrashort laser pulse brings a medium into a strongly non-equilibrium state where conventional description of magnetic phenomena in terms of thermodynamics is no longer valid. In this proposal I am planning to address these fundamental questions using novel experimental approaches for both the excitation and observation of magnetism on an ultrafast timescale. In particular, the proposal involves: a) development of polarization pulse shaping, where specially shaped laser pulses yield control over coherent optical excitations in a medium; b) exploring the ultrafast response of magnetic order with advanced optical and X-ray techniques.
The ultimate goal is to combine the fundamental knowledge of femtosecond opto-magnetism obtained in this project with the methods of near-field optics to achieve ultrafast control of spins in magnetic nanostructures.
Summary
The aim of the project is to develop femtosecond optical control of magnetism: a new area at the junction of coherent nonlinear optics, near-field optics and magnetism. In particular, I am aiming to investigate nonthermal effects of light on magnetic order and to apply this knowledge for highly efficient ultrafast (10-12 seconds and faster) optical control of magnetism at the nanoscale.
The ever increasing demand for faster information processing has triggered an intense search for ways to manipulate magnetically stored bits at the ultimately short time-scale. Although efficient, ultrafast and nonthermal laser control of magnetism may open new prospect of magnetic data storage and manipulation, many fundamental questions concerning the mechanisms that are responsible for the nonthermal effect of photons on spins and ultrafast laser induced changes of magnetic order are poorly understood. This is mainly because an ultrashort laser pulse brings a medium into a strongly non-equilibrium state where conventional description of magnetic phenomena in terms of thermodynamics is no longer valid. In this proposal I am planning to address these fundamental questions using novel experimental approaches for both the excitation and observation of magnetism on an ultrafast timescale. In particular, the proposal involves: a) development of polarization pulse shaping, where specially shaped laser pulses yield control over coherent optical excitations in a medium; b) exploring the ultrafast response of magnetic order with advanced optical and X-ray techniques.
The ultimate goal is to combine the fundamental knowledge of femtosecond opto-magnetism obtained in this project with the methods of near-field optics to achieve ultrafast control of spins in magnetic nanostructures.
Max ERC Funding
1 500 000 €
Duration
Start date: 2010-12-01, End date: 2015-11-30
Project acronym FIELDGRADIENTS
Project Phase Transitions and Chemical Reactions in Electric Field Gradients
Researcher (PI) Yoav Tsori
Host Institution (HI) BEN-GURION UNIVERSITY OF THE NEGEV
Country Israel
Call Details Starting Grant (StG), PE3, ERC-2010-StG_20091028
Summary We will study phase transitions and chemical and biological reactions in liquid mixtures
in electric field gradients. These new phase transitions are essential in statistical
physics and thermodynamics. We will examine theoretically the complex and yet unexplored
phase ordering dynamics in which droplets nucleate and move under the external nonuniform
force. We will look in detail at the interfacial instabilities which develop when the
field is increased. We will investigate how time-varying potentials produce
electromagnetic waves and how their spatial decay in the bistable liquid leads to phase
changes.
These transitions open a new and general way to control the spatio-temporal behaviour of
chemical reactions by directly manipulating the solvents' concentrations. When two or more
reagents are preferentially soluble in one of the mixture's components, field-induced
phase separation leads to acceleration of the reaction. When the reagents are soluble in
different solvents, field-induced demixing will lead to the reaction taking place at a
slow rate and at a two-dimensional surface. Additionally, the electric field allows us to
turn the reaction on or off. The numerical study and simulations will be complemented by
experiments. We will study theoretically and experimentally biochemical reactions. We will
find how actin-related structures are affected by field gradients. Using an electric field
as a tool we will control the rate of actin polymerisation. We will investigate if an
external field can damage cancer cells by disrupting their actin-related activity. The above
phenomena will be studied in a microfluidics environment. We will elucidate the separation
hydrodynamics occurring when thermodynamically miscible liquids flow in a channel and how
electric fields can reversibly create and destroy optical interfaces, as is relevant in
optofluidics. Chemical and biological reactions will be examined in the context of
lab-on-a-chip.
Summary
We will study phase transitions and chemical and biological reactions in liquid mixtures
in electric field gradients. These new phase transitions are essential in statistical
physics and thermodynamics. We will examine theoretically the complex and yet unexplored
phase ordering dynamics in which droplets nucleate and move under the external nonuniform
force. We will look in detail at the interfacial instabilities which develop when the
field is increased. We will investigate how time-varying potentials produce
electromagnetic waves and how their spatial decay in the bistable liquid leads to phase
changes.
These transitions open a new and general way to control the spatio-temporal behaviour of
chemical reactions by directly manipulating the solvents' concentrations. When two or more
reagents are preferentially soluble in one of the mixture's components, field-induced
phase separation leads to acceleration of the reaction. When the reagents are soluble in
different solvents, field-induced demixing will lead to the reaction taking place at a
slow rate and at a two-dimensional surface. Additionally, the electric field allows us to
turn the reaction on or off. The numerical study and simulations will be complemented by
experiments. We will study theoretically and experimentally biochemical reactions. We will
find how actin-related structures are affected by field gradients. Using an electric field
as a tool we will control the rate of actin polymerisation. We will investigate if an
external field can damage cancer cells by disrupting their actin-related activity. The above
phenomena will be studied in a microfluidics environment. We will elucidate the separation
hydrodynamics occurring when thermodynamically miscible liquids flow in a channel and how
electric fields can reversibly create and destroy optical interfaces, as is relevant in
optofluidics. Chemical and biological reactions will be examined in the context of
lab-on-a-chip.
Max ERC Funding
1 482 200 €
Duration
Start date: 2010-08-01, End date: 2015-07-31
Project acronym FIRSTLIGHT
Project Unveiling first light from the infant Universe
Researcher (PI) Luitje Vincent Ewoud Koopmans
Host Institution (HI) RIJKSUNIVERSITEIT GRONINGEN
Country Netherlands
Call Details Starting Grant (StG), PE9, ERC-2010-StG_20091028
Summary I request ERC funding to set up a dedicated science team to detect, for the first time, the redshifted 21-cm radio line emission of neutral hydrogen (HI) with LOFAR coming from the first billion years of the age of the Universe (the Epoch of Reionization and the Dark Ages ).
The study of this pristine neutral hydrogen gas is a rapidly emerging field of astrophysics, both theoretically and observationally. A number of expert international groups in the US/Australia (MWA), China (21CMA), India (GMRT) and the Netherlands (LOFAR) are contending to be the first to detect this hydrogen gas. My proposed ERC project is high-risk and high-gain; however, all risks are controlled and the scientific rewards of detection of neutral hydrogen at these early times would have a tremendous impact and open a new frontier in astronomy. The study of neutral hydrogen, as in the nearby Universe, will revolutionize our knowledge of astrophysical processes in the first phases of the Universe, just after recombination.
The LOFAR Epoch-of-Reionization Key-Science Project (LOFAR EoR-KSP), of which I am a PI, aims to be the first, and if being the first fails, to provide the best detection of this neutral HI gas. Indeed, we are in a very good starting position to reach both goals. Our team has access to the most sensitive telescope available for these studies (LOFAR) and leads a Key Science Project with guaranteed observing time. Our KSP is rapidly ramping up to the observational phase of the project (2010), and now more than ever requires dedicated scientists that together in a small team maximize the scientific return of the project (i.e. detect and study HI). If successful, our research team would be in a position to start leading similar projects with the Square Kilometer Array (SKA). It is crucial that we gear up for the use of that future instrument and retain Europe s position at the forefront of astrophysics and radio astronomy.
Summary
I request ERC funding to set up a dedicated science team to detect, for the first time, the redshifted 21-cm radio line emission of neutral hydrogen (HI) with LOFAR coming from the first billion years of the age of the Universe (the Epoch of Reionization and the Dark Ages ).
The study of this pristine neutral hydrogen gas is a rapidly emerging field of astrophysics, both theoretically and observationally. A number of expert international groups in the US/Australia (MWA), China (21CMA), India (GMRT) and the Netherlands (LOFAR) are contending to be the first to detect this hydrogen gas. My proposed ERC project is high-risk and high-gain; however, all risks are controlled and the scientific rewards of detection of neutral hydrogen at these early times would have a tremendous impact and open a new frontier in astronomy. The study of neutral hydrogen, as in the nearby Universe, will revolutionize our knowledge of astrophysical processes in the first phases of the Universe, just after recombination.
The LOFAR Epoch-of-Reionization Key-Science Project (LOFAR EoR-KSP), of which I am a PI, aims to be the first, and if being the first fails, to provide the best detection of this neutral HI gas. Indeed, we are in a very good starting position to reach both goals. Our team has access to the most sensitive telescope available for these studies (LOFAR) and leads a Key Science Project with guaranteed observing time. Our KSP is rapidly ramping up to the observational phase of the project (2010), and now more than ever requires dedicated scientists that together in a small team maximize the scientific return of the project (i.e. detect and study HI). If successful, our research team would be in a position to start leading similar projects with the Square Kilometer Array (SKA). It is crucial that we gear up for the use of that future instrument and retain Europe s position at the forefront of astrophysics and radio astronomy.
Max ERC Funding
1 500 000 €
Duration
Start date: 2010-10-01, End date: 2016-09-30
Project acronym HHIT
Project The here and the hereafter in Islamic traditions
Researcher (PI) Christian Robert Lange
Host Institution (HI) UNIVERSITEIT UTRECHT
Country Netherlands
Call Details Starting Grant (StG), SH2, ERC-2010-StG_20091209
Summary The aim of this project is to write a history of the Muslim paradise and hell. Researchers (PI, RF and two doctoral researchers) will assess the extent to which Islamic traditions favour or reject a view of human existence as directed toward the otherworld. They will do so by examining a variety of intellectual traditions from the inception of Islam in the 7th century CE until today. The focus of investigation will not just be on the ‘high tradition’ of Islamic theology and jurisprudence, but also on mystical, philosophical, artistic and ‘popular’ traditions, thereby avoiding a monolithic, essentialising account of Islam’s attitude toward the hereafter.
As has been argued, the relationship between this world (dunya) and the otherworld (akhira) is as important to Islam as the mind/body dualism is to the intellectual history of the West. However, no sustained effort of analysis has been made in modern Islamic Studies to reflect on the dunya/akhira relationship, and on the boundary that separates the two. This project will be the first comprehensive and systematic attempt in this direction. Five axes of research will underlie this endeavor: (1) the eschatological imaginaire, (2) material culture and the arts, (3) theology and law, (4) mysticism and philosophy, and (5) modern and contemporary visions of the hereafter.
The project (proposed duration: 48 months), which is to begin on 1 March 2011, will be based at the Utrecht University and led by Dr Christian Lange (PhD Harvard, 2006, 70%), currently Lecturer in Islamic Studies at New College/School of Divinity. The research team will include one research assistant (100%, 45 months) and two doctoral researchers (100%, 36 months). Financial support is solicited to facilitate the survey of manuscripts and manuscript research in various collections in North America, Europe and Asia, and to help organise two scholarly symposia in Islamic eschatology and one comparative conference.
Summary
The aim of this project is to write a history of the Muslim paradise and hell. Researchers (PI, RF and two doctoral researchers) will assess the extent to which Islamic traditions favour or reject a view of human existence as directed toward the otherworld. They will do so by examining a variety of intellectual traditions from the inception of Islam in the 7th century CE until today. The focus of investigation will not just be on the ‘high tradition’ of Islamic theology and jurisprudence, but also on mystical, philosophical, artistic and ‘popular’ traditions, thereby avoiding a monolithic, essentialising account of Islam’s attitude toward the hereafter.
As has been argued, the relationship between this world (dunya) and the otherworld (akhira) is as important to Islam as the mind/body dualism is to the intellectual history of the West. However, no sustained effort of analysis has been made in modern Islamic Studies to reflect on the dunya/akhira relationship, and on the boundary that separates the two. This project will be the first comprehensive and systematic attempt in this direction. Five axes of research will underlie this endeavor: (1) the eschatological imaginaire, (2) material culture and the arts, (3) theology and law, (4) mysticism and philosophy, and (5) modern and contemporary visions of the hereafter.
The project (proposed duration: 48 months), which is to begin on 1 March 2011, will be based at the Utrecht University and led by Dr Christian Lange (PhD Harvard, 2006, 70%), currently Lecturer in Islamic Studies at New College/School of Divinity. The research team will include one research assistant (100%, 45 months) and two doctoral researchers (100%, 36 months). Financial support is solicited to facilitate the survey of manuscripts and manuscript research in various collections in North America, Europe and Asia, and to help organise two scholarly symposia in Islamic eschatology and one comparative conference.
Max ERC Funding
978 368 €
Duration
Start date: 2011-03-01, End date: 2015-04-30
Project acronym HigherVision
Project The function of higher-order cortical and thalamic pathways during vision
Researcher (PI) Sonja Birgit Hofer
Host Institution (HI) UNIVERSITAT BASEL
Country Switzerland
Call Details Starting Grant (StG), LS5, ERC-2013-StG
Summary When interacting with the environment we depend on our perception of the world around us. Visual perception relies on information flow from the eye to the visual cortex, where it is relayed and transformed via a series of cortical processing stages. Most research so far has focused on feedforward processing of visual information. However, it is increasingly obvious that perception crucially depends on how sensory input is interpreted in the context of an animal’s behavioural state, goals and actions. These non-sensory signals may be relayed by prominent long-range projections from higher-order cortical and thalamic areas, whose contribution to vision remains largely unexplored. Recent advances in imaging techniques and genetic tools for visualizing and manipulating neuronal activity enable us for the first time to study directly what information is conveyed through these major alternative visual pathways in the behaving animal and how they influence the processing of feedforward sensory information to allow us to actively perceive and interpret the environment.
Using state-of-the-art methodology combining in vivo imaging, electrophysiology, animal behaviour, virtual reality, genetic tools and targeted optogenetics using advanced optics, we will determine the functional role of (i) cortical feedback and (ii) higher-order thalamic signals during cortical processing of visual information in the behaving mouse. Specifically, we will investigate what information these projections convey to the visual cortex in anaesthetized and awake mice, whether they provide signals mediating the increased saliency of behaviourally relevant stimuli, and whether they enable the integration of sensory and motor information during locomotion and navigation. Together, the proposed work will answer fundamental questions about the role of these important but poorly understood visual pathways in active processing of visual input as animals interact with their environment.
Summary
When interacting with the environment we depend on our perception of the world around us. Visual perception relies on information flow from the eye to the visual cortex, where it is relayed and transformed via a series of cortical processing stages. Most research so far has focused on feedforward processing of visual information. However, it is increasingly obvious that perception crucially depends on how sensory input is interpreted in the context of an animal’s behavioural state, goals and actions. These non-sensory signals may be relayed by prominent long-range projections from higher-order cortical and thalamic areas, whose contribution to vision remains largely unexplored. Recent advances in imaging techniques and genetic tools for visualizing and manipulating neuronal activity enable us for the first time to study directly what information is conveyed through these major alternative visual pathways in the behaving animal and how they influence the processing of feedforward sensory information to allow us to actively perceive and interpret the environment.
Using state-of-the-art methodology combining in vivo imaging, electrophysiology, animal behaviour, virtual reality, genetic tools and targeted optogenetics using advanced optics, we will determine the functional role of (i) cortical feedback and (ii) higher-order thalamic signals during cortical processing of visual information in the behaving mouse. Specifically, we will investigate what information these projections convey to the visual cortex in anaesthetized and awake mice, whether they provide signals mediating the increased saliency of behaviourally relevant stimuli, and whether they enable the integration of sensory and motor information during locomotion and navigation. Together, the proposed work will answer fundamental questions about the role of these important but poorly understood visual pathways in active processing of visual input as animals interact with their environment.
Max ERC Funding
1 499 194 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym INCPAR
Project Incomplete Parenthesis: Determining how and why secondary propositions can be elliptical or fragmented from a cross-linguistic and multifaceted theoretical perspective
Researcher (PI) Mark De Vries
Host Institution (HI) RIJKSUNIVERSITEIT GRONINGEN
Country Netherlands
Call Details Starting Grant (StG), SH4, ERC-2010-StG_20091209
Summary This linguistic research aims to determine and theoretically explain the properties of incomplete parenthesis, in comparison to
regular ellipsis and fragments. Thereby, we will provide a systematic typology of (incomplete) parenthetical constructions and
amalgamated sentences based on grammatical features, taking into account the effects of syntax, information structure and
prosody. We also add a cross-linguistic perspective by comparing the inventory and behavior of parentheses in a number of
languages from different families, and we will collect the results in a specialized database that will be made publicly available
via an online application.
Summary
This linguistic research aims to determine and theoretically explain the properties of incomplete parenthesis, in comparison to
regular ellipsis and fragments. Thereby, we will provide a systematic typology of (incomplete) parenthetical constructions and
amalgamated sentences based on grammatical features, taking into account the effects of syntax, information structure and
prosody. We also add a cross-linguistic perspective by comparing the inventory and behavior of parentheses in a number of
languages from different families, and we will collect the results in a specialized database that will be made publicly available
via an online application.
Max ERC Funding
1 499 554 €
Duration
Start date: 2011-02-01, End date: 2016-01-31
Project acronym INFORMATIONFLOW
Project Information Flow and Its Impact on Financial Markets
Researcher (PI) Ilan Kremer
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), SH1, ERC-2010-StG_20091209
Summary The importance of information asymmetry in financial markets has long been recognized in financial economics. Most existing models focus on the role of privately informed investors who influence prices through their trades. But in many cases the agents who have the biggest information advantage are insiders or the firms themselves; they are precluded from trading but can affect the information flow to the market. This endogenous information flow and its effect on financial market is the focus of the proposed project.
By the term information flow we refer to a wide range of channels through which firms can communicate. The information can be part of a mandatory disclosure or a voluntary one. It can be verifiable or non-verifiable information. In addition there can be an implicit information transmission. A firm may choose certain actions to convey its private information (i.e. signaling) without any explicit announcements.
The way firms convey this information may provide key insights into the behavior of financial markets and in particular the development of financial crises. The project combines theoretical and empirical work. In the theory part I plan to examine the channels mentioned above and develop testable implications. In the empirical part I plan to test these implications.
Summary
The importance of information asymmetry in financial markets has long been recognized in financial economics. Most existing models focus on the role of privately informed investors who influence prices through their trades. But in many cases the agents who have the biggest information advantage are insiders or the firms themselves; they are precluded from trading but can affect the information flow to the market. This endogenous information flow and its effect on financial market is the focus of the proposed project.
By the term information flow we refer to a wide range of channels through which firms can communicate. The information can be part of a mandatory disclosure or a voluntary one. It can be verifiable or non-verifiable information. In addition there can be an implicit information transmission. A firm may choose certain actions to convey its private information (i.e. signaling) without any explicit announcements.
The way firms convey this information may provide key insights into the behavior of financial markets and in particular the development of financial crises. The project combines theoretical and empirical work. In the theory part I plan to examine the channels mentioned above and develop testable implications. In the empirical part I plan to test these implications.
Max ERC Funding
1 500 000 €
Duration
Start date: 2010-10-01, End date: 2016-09-30
Project acronym INTEGRATION
Project International Integration and Social Identity: Theory and Evidence
Researcher (PI) Moses Shayo
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), SH1, ERC-2013-StG
Summary Understanding economic and political integration has long been a central concern for economists. An important missing ingredient in the existing literature is the analysis of endogenously determined social identity. By “social identity” I refer to the fact that individuals often care deeply about the groups to which they belong. By “endogenously determined” I refer to the fact that individuals do not automatically identify with every group they belong to: whether or not an individual identifies with a given group depends on the characteristics of this group as well as on how close to this group the individual perceives herself. Empirical results obtained over the past decade allow us to integrate identity concerns into standard economic models. I propose to develop and test a theory of integration that does just that.
Consider two states that may either be independent countries or form a union. The stability and desirability of unification may sometimes depend on the extent to which citizens identify with the union or with their states. But the profile of identities itself depends on the political-economic outcome under unification. The first step in developing the theory is to translate the evidence concerning behavior in groups into a concise statement of what it means to “identify” with a particular group and what factors shape identification decisions. The theory will then study the equilibrium outcomes of a political economy model of integration, where actions and identities are endogenously determined.
The second part of the project will empirically examine the relation between social identities, individual characteristics, and European integration. To appropriately measure identification, I propose to employ experimental methods based on revealed preference conducted with a large and diverse sample of European citizens. This will be complemented by historical multi-country survey data on self-reported identity, political attitudes and behavior.
Summary
Understanding economic and political integration has long been a central concern for economists. An important missing ingredient in the existing literature is the analysis of endogenously determined social identity. By “social identity” I refer to the fact that individuals often care deeply about the groups to which they belong. By “endogenously determined” I refer to the fact that individuals do not automatically identify with every group they belong to: whether or not an individual identifies with a given group depends on the characteristics of this group as well as on how close to this group the individual perceives herself. Empirical results obtained over the past decade allow us to integrate identity concerns into standard economic models. I propose to develop and test a theory of integration that does just that.
Consider two states that may either be independent countries or form a union. The stability and desirability of unification may sometimes depend on the extent to which citizens identify with the union or with their states. But the profile of identities itself depends on the political-economic outcome under unification. The first step in developing the theory is to translate the evidence concerning behavior in groups into a concise statement of what it means to “identify” with a particular group and what factors shape identification decisions. The theory will then study the equilibrium outcomes of a political economy model of integration, where actions and identities are endogenously determined.
The second part of the project will empirically examine the relation between social identities, individual characteristics, and European integration. To appropriately measure identification, I propose to employ experimental methods based on revealed preference conducted with a large and diverse sample of European citizens. This will be complemented by historical multi-country survey data on self-reported identity, political attitudes and behavior.
Max ERC Funding
1 050 000 €
Duration
Start date: 2014-03-01, End date: 2019-02-28
Project acronym INTERCOM
Project Communication between immune cells via release of RNA-carrying vesicles: Lessons from viruses
Researcher (PI) Esther Neline Marielle Nolte
Host Institution (HI) UNIVERSITEIT UTRECHT
Country Netherlands
Call Details Starting Grant (StG), LS6, ERC-2013-StG
Summary "Communication between immune cells is crucial for regulating the magnitude and quality of immune responses. A newly uncovered means of intercellular communication involves transfer of small cell-derived vesicles. I recently discovered that vesicles released by immune cells are enriched for small noncoding RNAs, which may act as regulatory RNAs that can influence gene expression in vesicle-targeted cells. Furthermore, remarkable parallels emerged between RNAs abundantly present in cell-derived vesicles and a group of host RNAs specifically incorporated into retroviruses. These shared RNAs may underlie the formation or function of both cell-derived vesicles and retroviruses. Until now, mechanisms behind selective incorporation of small RNAs into cell-derived vesicles and their function in vesicle-targeted cells are poorly understood.
Aim of INTERCOM: To resolve how the exchange of small RNAs via cell-derived vesicles contributes to intercellular communication between immune cells. Key objectives: 1. To determine the diversity and plasticity of the RNA content of vesicle subpopulations released by immune cells. 2. To explain functional differences between immune cell vesicle populations based on their RNA contents. 3. To determine the function of structural RNAs shared by immune cell-derived vesicles and retroviruses.
Tools in virology research will be used in combination with several high-end technologies, which were uniquely adapted in my lab for vesicle-related research. These include a high-resolution flow cytometric method suited to analyze individual nano-sized vesicles, RNA deep sequencing with previously developed data analysis methods, and super-resolution microscopic imaging.
The proposed work advances our understanding of communication processes in the immune system. This knowledge can be applied in defining vesicle RNA-based biomarkers for immune-related diseases and in designing genetically engineered cell-derived vesicles for therapeutic application."
Summary
"Communication between immune cells is crucial for regulating the magnitude and quality of immune responses. A newly uncovered means of intercellular communication involves transfer of small cell-derived vesicles. I recently discovered that vesicles released by immune cells are enriched for small noncoding RNAs, which may act as regulatory RNAs that can influence gene expression in vesicle-targeted cells. Furthermore, remarkable parallels emerged between RNAs abundantly present in cell-derived vesicles and a group of host RNAs specifically incorporated into retroviruses. These shared RNAs may underlie the formation or function of both cell-derived vesicles and retroviruses. Until now, mechanisms behind selective incorporation of small RNAs into cell-derived vesicles and their function in vesicle-targeted cells are poorly understood.
Aim of INTERCOM: To resolve how the exchange of small RNAs via cell-derived vesicles contributes to intercellular communication between immune cells. Key objectives: 1. To determine the diversity and plasticity of the RNA content of vesicle subpopulations released by immune cells. 2. To explain functional differences between immune cell vesicle populations based on their RNA contents. 3. To determine the function of structural RNAs shared by immune cell-derived vesicles and retroviruses.
Tools in virology research will be used in combination with several high-end technologies, which were uniquely adapted in my lab for vesicle-related research. These include a high-resolution flow cytometric method suited to analyze individual nano-sized vesicles, RNA deep sequencing with previously developed data analysis methods, and super-resolution microscopic imaging.
The proposed work advances our understanding of communication processes in the immune system. This knowledge can be applied in defining vesicle RNA-based biomarkers for immune-related diseases and in designing genetically engineered cell-derived vesicles for therapeutic application."
Max ERC Funding
1 499 806 €
Duration
Start date: 2013-11-01, End date: 2018-10-31
Project acronym JSMA
Project Jews and Slavs in the Middle Ages: Interaction and Cross-Fertilization
Researcher (PI) Alexander Kulik
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), SH6, ERC-2010-StG_20091209
Summary The central purpose of this project is to bring down interdisciplinary barriers by showing how the Slavic and the Jewish heritage can each be approached as a unique repository of the unknown texts, traditions, and sensibilities of the other. By focusing on previously unexplored or under-explored medieval texts, I aim to reconstruct the Jewish and Slavic legacies, some of whose materials have been considered lost, while others were misinterpreted or neglected.
This research project will resort to historical and philological techniques hitherto considered mutually incompatible in this field. The study intends to use methods of cultural archaeology to explore medieval Judeo-Slavic transparency. By cultural transparency we understand the mutual permeability of different cultures, which facilitates the exchange of ideas and genres of creativity between them. Cultural archeology involves methods of multi-disciplinary research based on the assumption that Eastern Europe constituted a melting pot characterized by an intensive cross-fertilization of cultural legacies. Cultural archaeology studies different historical, religious, and literary texts by looking at them as a palimpsest in which earlier texts and types of discourse come to the fore as shaped by their contemporary socio-cultural settings.
The proposed theme has far-reaching methodological implications beyond the Judeo-Slavic cultural realm. This project will build a model of cross-cultural interaction to achieve a better understanding of the situations in which different faith-based ethnic cultures cohabit.
Summary
The central purpose of this project is to bring down interdisciplinary barriers by showing how the Slavic and the Jewish heritage can each be approached as a unique repository of the unknown texts, traditions, and sensibilities of the other. By focusing on previously unexplored or under-explored medieval texts, I aim to reconstruct the Jewish and Slavic legacies, some of whose materials have been considered lost, while others were misinterpreted or neglected.
This research project will resort to historical and philological techniques hitherto considered mutually incompatible in this field. The study intends to use methods of cultural archaeology to explore medieval Judeo-Slavic transparency. By cultural transparency we understand the mutual permeability of different cultures, which facilitates the exchange of ideas and genres of creativity between them. Cultural archeology involves methods of multi-disciplinary research based on the assumption that Eastern Europe constituted a melting pot characterized by an intensive cross-fertilization of cultural legacies. Cultural archaeology studies different historical, religious, and literary texts by looking at them as a palimpsest in which earlier texts and types of discourse come to the fore as shaped by their contemporary socio-cultural settings.
The proposed theme has far-reaching methodological implications beyond the Judeo-Slavic cultural realm. This project will build a model of cross-cultural interaction to achieve a better understanding of the situations in which different faith-based ethnic cultures cohabit.
Max ERC Funding
1 044 000 €
Duration
Start date: 2010-11-01, End date: 2016-10-31
Project acronym LIE ANALYSIS
Project Lie Group Analysis for Medical Image Processing
Researcher (PI) Remco Duits
Host Institution (HI) TECHNISCHE UNIVERSITEIT EINDHOVEN
Country Netherlands
Call Details Starting Grant (StG), PE1, ERC-2013-StG
Summary The aim of this project is to substantially improve computer algorithms for image analysis in medical imaging. Currently available techniques often require significant application-specific tuning and have a limited application scope. This is mostly due to the use of non-generic feature spaces that involve many physical dimensions and lack mathematical foundation.
Instead, we derive inspiration from the superior generic pattern recognition capabilities of the human brain and propose a novel operator design aiming at better results and wider applicability.
This novel operator design combines (partial and ordinary) differential equations on non-compact Lie groups (induced by stochastic processes and sub-Riemannian geometric control) with wavelet transforms. Many mathematical challenges arise in the analysis and (numerical) solutions of these operators.
The research departs from previously developed insights of the PI on 'invertible orientation scores', which can be regarded as a specific instance in a general Lie group theoretical framework. Within this general framework one obtains a comprehensive invertible score defined on a higher dimensional Lie group beyond position space. The key challenge is to appropriately exploit these scores, their survey of multiple features per position, their underlying group structure, and their invertibility. We will tackle this via left-invariant evolutions and left-invariant sub-Riemannian optimal control within the score.
The orientation score approach will be systematically extended towards multi-scale-and-orientation, multi-velocity and multi-frequency encoding and processing, widening the application scope. Moreover, improvements in contextual enhancement via invertible scores and improvements in optimal curve extractions in the Lie group domain of the score will be pursued.
We will develop and apply the resulting algorithms to a wide range of medical imaging challenges in neurological, retinal and cardiac applications.
Summary
The aim of this project is to substantially improve computer algorithms for image analysis in medical imaging. Currently available techniques often require significant application-specific tuning and have a limited application scope. This is mostly due to the use of non-generic feature spaces that involve many physical dimensions and lack mathematical foundation.
Instead, we derive inspiration from the superior generic pattern recognition capabilities of the human brain and propose a novel operator design aiming at better results and wider applicability.
This novel operator design combines (partial and ordinary) differential equations on non-compact Lie groups (induced by stochastic processes and sub-Riemannian geometric control) with wavelet transforms. Many mathematical challenges arise in the analysis and (numerical) solutions of these operators.
The research departs from previously developed insights of the PI on 'invertible orientation scores', which can be regarded as a specific instance in a general Lie group theoretical framework. Within this general framework one obtains a comprehensive invertible score defined on a higher dimensional Lie group beyond position space. The key challenge is to appropriately exploit these scores, their survey of multiple features per position, their underlying group structure, and their invertibility. We will tackle this via left-invariant evolutions and left-invariant sub-Riemannian optimal control within the score.
The orientation score approach will be systematically extended towards multi-scale-and-orientation, multi-velocity and multi-frequency encoding and processing, widening the application scope. Moreover, improvements in contextual enhancement via invertible scores and improvements in optimal curve extractions in the Lie group domain of the score will be pursued.
We will develop and apply the resulting algorithms to a wide range of medical imaging challenges in neurological, retinal and cardiac applications.
Max ERC Funding
1 267 550 €
Duration
Start date: 2014-01-01, End date: 2018-12-31
Project acronym MARKETS
Project The evolution of plant-fungal markets
Researcher (PI) Erica Tobyn Kiers
Host Institution (HI) STICHTING VU
Country Netherlands
Call Details Starting Grant (StG), LS8, ERC-2013-StG
Summary Throughout the Earth’s history, the mutualism between plants and their fungal partners has mediated nutrient cycles and energy flow in ecosystems. Underground, mycorrhizal fungi and plant roots form vast networks of connected individuals, in which sugars from roots are exchanged for nutrients from fungi.
How is cooperation maintained in plant-fungal networks? Selfish individuals can potentially exploit the collaboration, reaping nutrient benefits while paying no costs. So, why cooperate at all?
I recently demonstrated that plant and fungal partners are able to detect variation in nutrient provisioning by the other, and adjust their own strategy accordingly (Kiers et al. Science 2011). We argued that the partnership functions like an economic market: partners compete by trading resources, and those offering the best rate of exchange are rewarded.
While this work suggests that plants and fungi can successfully negotiate conditions of trade, we have yet to conclusively demonstrate what drives ‘fair’ trade dynamics. In particular, we do not know how partner performance is evaluated, nor how trade strategies respond to changes in resource levels.
I present an interdisciplinary program of research to address this problem by investigating four aspects critical to market regulation in nature: (1) Responses to external resources, (2) Partner decisions, (3) Network formation, (4) Conflict resolution within networks.
Using a combination of gene-level characterization, microscale manipulation of nutrient landscapes, experimental evolution, and game theory, I will test: (1) how plant and fungal trading strategies respond to changing resource levels; (2) how hosts control fungal ‘behavior’, stimulating them to collect specific nutrients; (3) the role of fungal fusion in network formation; (4) how genetic conflicts within a fungal network are resolved.
This work opens up a new field of research into how markets evolve and are stabilized in non-animal systems.
Summary
Throughout the Earth’s history, the mutualism between plants and their fungal partners has mediated nutrient cycles and energy flow in ecosystems. Underground, mycorrhizal fungi and plant roots form vast networks of connected individuals, in which sugars from roots are exchanged for nutrients from fungi.
How is cooperation maintained in plant-fungal networks? Selfish individuals can potentially exploit the collaboration, reaping nutrient benefits while paying no costs. So, why cooperate at all?
I recently demonstrated that plant and fungal partners are able to detect variation in nutrient provisioning by the other, and adjust their own strategy accordingly (Kiers et al. Science 2011). We argued that the partnership functions like an economic market: partners compete by trading resources, and those offering the best rate of exchange are rewarded.
While this work suggests that plants and fungi can successfully negotiate conditions of trade, we have yet to conclusively demonstrate what drives ‘fair’ trade dynamics. In particular, we do not know how partner performance is evaluated, nor how trade strategies respond to changes in resource levels.
I present an interdisciplinary program of research to address this problem by investigating four aspects critical to market regulation in nature: (1) Responses to external resources, (2) Partner decisions, (3) Network formation, (4) Conflict resolution within networks.
Using a combination of gene-level characterization, microscale manipulation of nutrient landscapes, experimental evolution, and game theory, I will test: (1) how plant and fungal trading strategies respond to changing resource levels; (2) how hosts control fungal ‘behavior’, stimulating them to collect specific nutrients; (3) the role of fungal fusion in network formation; (4) how genetic conflicts within a fungal network are resolved.
This work opens up a new field of research into how markets evolve and are stabilized in non-animal systems.
Max ERC Funding
1 492 438 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym METAFERW
Project Modeling and controlling traffic congestion and propagation in large-scale urban multimodal networks
Researcher (PI) Nikolaos Geroliminis
Host Institution (HI) ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Country Switzerland
Call Details Starting Grant (StG), SH3, ERC-2013-StG
Summary "As cities grow rapidly and more people through different modes compete for limited urban road infrastructure to travel, it is important to manage traffic space to improve accessibility for travelers. This project tackles the problem of modeling and optimization in large-scale congested traffic networks with an aggregated realistic representation of dynamics and route choice and multiple modes of transport. This is a highly motivating problem both because of the socio-economic influence of congestion and the challenges embedded in the optimization framework and the modeling aspects. Currently most optimization methods for transport networks (i) are suited for toy networks with simplified dynamics that are far from real-sized networks, (ii) apply decentralized control, which is not appropriate for heterogeneously loaded networks, (iii) investigate engineering solutions through micro-simulation models and scenario analysis that make the problem intractable in real time, (iv) are not considering interactions and conflicts between transport modes (car, bus, delivery vehicle). This problem is even more challenging if one considers that transportation networks have a hierarchical structure with freeways and urban roads with mixed or separated traffic (e.g. bus-only lanes), that have dissimilar traffic flow dynamics. Lack of coordination among the jurisdictions during traffic operations or limited means of traffic data monitoring and communication can impede such mixed traffic network ideal goal. Traditionally, choices of people in transportation networks are based on equilibrium conditions with small variations.The huge amount of datasets (including thousands of GPS data from taxis, cars and buses and road detector data from heavily populated cities worldwide) can provide a unique way to understand how really people make choices, how these choices affect the development and spreading of congestion in networks and integrate them in the macroscopic dynamics and optimization"
Summary
"As cities grow rapidly and more people through different modes compete for limited urban road infrastructure to travel, it is important to manage traffic space to improve accessibility for travelers. This project tackles the problem of modeling and optimization in large-scale congested traffic networks with an aggregated realistic representation of dynamics and route choice and multiple modes of transport. This is a highly motivating problem both because of the socio-economic influence of congestion and the challenges embedded in the optimization framework and the modeling aspects. Currently most optimization methods for transport networks (i) are suited for toy networks with simplified dynamics that are far from real-sized networks, (ii) apply decentralized control, which is not appropriate for heterogeneously loaded networks, (iii) investigate engineering solutions through micro-simulation models and scenario analysis that make the problem intractable in real time, (iv) are not considering interactions and conflicts between transport modes (car, bus, delivery vehicle). This problem is even more challenging if one considers that transportation networks have a hierarchical structure with freeways and urban roads with mixed or separated traffic (e.g. bus-only lanes), that have dissimilar traffic flow dynamics. Lack of coordination among the jurisdictions during traffic operations or limited means of traffic data monitoring and communication can impede such mixed traffic network ideal goal. Traditionally, choices of people in transportation networks are based on equilibrium conditions with small variations.The huge amount of datasets (including thousands of GPS data from taxis, cars and buses and road detector data from heavily populated cities worldwide) can provide a unique way to understand how really people make choices, how these choices affect the development and spreading of congestion in networks and integrate them in the macroscopic dynamics and optimization"
Max ERC Funding
1 242 162 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym MINT
Project From micro-scale interaction networks to ecosystem-level processes in microbial communities
Researcher (PI) Otto Xavier Cordero Sanchez
Host Institution (HI) EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH
Country Switzerland
Call Details Starting Grant (StG), LS8, ERC-2013-StG
Summary What makes understanding the ecology and evolution of microbes such a unique challenge is the fact that, while the life of microbes unfold at scales of a few micrometers, their impact on ecosystems can be perceived at the scale of meters or kilometers. Our inability to map ecosystem-level processes to the micro-scale interactions that take place in microbial communities is one of the main obstacles hindering the development of mechanistic models that allow us to interpret microbial diversity and predict community dynamics. The overarching goal of this research project is to understand how the biotic interactions between microbes at the scale of micrometers impact microbial community structure and dynamics. By reconstructing the spatial structure and the interaction networks of microbial populations colonizing particles of a few tens of microns in diameter in aquatic environments, the proposed research will build mechanistic models that will serve to i) clarify the structure-function mapping of microbial ‘species’ in the environment, ii) understand microbial community assembly at the relevant physical scales iii) model how perturbations in the environment lead to micro-scale shifts in community structure and iv) elucidate how biotic interactions influence genome evolution in microbial communities. The results of this project will fill a fundamental gap in microbial sciences, allowing us to connect micro-scale population and community interactions to the global diversity and function of microbial communities.
Summary
What makes understanding the ecology and evolution of microbes such a unique challenge is the fact that, while the life of microbes unfold at scales of a few micrometers, their impact on ecosystems can be perceived at the scale of meters or kilometers. Our inability to map ecosystem-level processes to the micro-scale interactions that take place in microbial communities is one of the main obstacles hindering the development of mechanistic models that allow us to interpret microbial diversity and predict community dynamics. The overarching goal of this research project is to understand how the biotic interactions between microbes at the scale of micrometers impact microbial community structure and dynamics. By reconstructing the spatial structure and the interaction networks of microbial populations colonizing particles of a few tens of microns in diameter in aquatic environments, the proposed research will build mechanistic models that will serve to i) clarify the structure-function mapping of microbial ‘species’ in the environment, ii) understand microbial community assembly at the relevant physical scales iii) model how perturbations in the environment lead to micro-scale shifts in community structure and iv) elucidate how biotic interactions influence genome evolution in microbial communities. The results of this project will fill a fundamental gap in microbial sciences, allowing us to connect micro-scale population and community interactions to the global diversity and function of microbial communities.
Max ERC Funding
1 940 085 €
Duration
Start date: 2013-11-01, End date: 2018-10-31
Project acronym MIRNACLOCKNETWORKS
Project Towards a systemic view of the circadian clock: Integration of miRNAs into the molecular, cellular and neural circadian networks
Researcher (PI) Sebastian Kadener
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary Circadian (24hs) rhythms in locomotor activity are one of the best-characterized behaviors at the molecular, cellular and neural levels. Despite that, our understanding of how these rhythms are generated is still limited. A major shortcoming of the current approaches in the field is that they depict the circadian clock as a mere addition of steps (and/or combination of parts). By doing so, the circadian oscillator is portrayed as a static rather than a dynamic system. We have recently shown for the first time that miRNA-mediated regulation plays a role in circadian timekeeping in Drosophila. In the present project we will exploit complementary and cutting-edge approaches that will provide an integrative and comprehensive view of the circadian timekeeping system. As we believe that miRNAs are key mediators of this integration, we will dissect their role in the circadian clock at the molecular, cellular and neural levels in Drosophila. At the molecular level, we will determine the mechanisms, and proteins that mediate the circadian regulation of miRNAs function. Moreover, by the use of high-throughput methodology we will assess and characterize the impact of translational regulation on both the circadian transcriptome and proteome. At the cellular level, we plan to determine how this type of regulation integrates with other circadian pathways and which specific pathways and proteins mediate this process. As a final goal of the proposed project we plan to generate a complete genetic interaction map of the known circadian regulators, which will integrate the different molecular and cellular events involved in timekeeping. This will be a key step towards the understanding of the circadian clock as a dynamic adjustable process. Last, but not least, we will study the role of miRNAs in the circadian neural network. For doing so we will set up an ex vivo approach (fly brain's culture) that will assess circadian parameters through fluorescent continuous live imaging.
Summary
Circadian (24hs) rhythms in locomotor activity are one of the best-characterized behaviors at the molecular, cellular and neural levels. Despite that, our understanding of how these rhythms are generated is still limited. A major shortcoming of the current approaches in the field is that they depict the circadian clock as a mere addition of steps (and/or combination of parts). By doing so, the circadian oscillator is portrayed as a static rather than a dynamic system. We have recently shown for the first time that miRNA-mediated regulation plays a role in circadian timekeeping in Drosophila. In the present project we will exploit complementary and cutting-edge approaches that will provide an integrative and comprehensive view of the circadian timekeeping system. As we believe that miRNAs are key mediators of this integration, we will dissect their role in the circadian clock at the molecular, cellular and neural levels in Drosophila. At the molecular level, we will determine the mechanisms, and proteins that mediate the circadian regulation of miRNAs function. Moreover, by the use of high-throughput methodology we will assess and characterize the impact of translational regulation on both the circadian transcriptome and proteome. At the cellular level, we plan to determine how this type of regulation integrates with other circadian pathways and which specific pathways and proteins mediate this process. As a final goal of the proposed project we plan to generate a complete genetic interaction map of the known circadian regulators, which will integrate the different molecular and cellular events involved in timekeeping. This will be a key step towards the understanding of the circadian clock as a dynamic adjustable process. Last, but not least, we will study the role of miRNAs in the circadian neural network. For doing so we will set up an ex vivo approach (fly brain's culture) that will assess circadian parameters through fluorescent continuous live imaging.
Max ERC Funding
1 478 606 €
Duration
Start date: 2011-02-01, End date: 2016-01-31
Project acronym NWScan
Project Bottom-up Nanowires as Scanning Multifunctional Sensors
Researcher (PI) Martino Poggio
Host Institution (HI) UNIVERSITAT BASEL
Country Switzerland
Call Details Starting Grant (StG), PE3, ERC-2013-StG
Summary Advances in growth and fabrication of semiconductor nanostructures have led to both the production of exquisitely sensitive force transducers and the development of solid-state quantum devices. Force transducers, typically monolithic Si cantilevers, are central to techniques such as AFM, and MFM. On the other hand, quantum devices including quantum wells, quantum dots (QDs), and single electron transistors are essential to technologies like lasers, optical detectors, and in experiments on quantum information. These two types of devices have – until now – occupied distinct material systems and have, for the most part, not been combined.
New developments in the growth of inorganic nanowires (NWs), however, are set to change the status quo. Researchers can now grow nanoscale structures from the bottom-up with unprecedented mechanical properties. Unlike traditional top-down cantilevers, which are etched or milled out of a larger block of material, bottom-up structures are assembled unit-by-unit to be almost defect-free on the atomic-scale. This near perfection gives NWs a much smaller mechanical dissipation than their top-down counterparts, while their higher resonance frequencies allow them to couple less strongly to common sources of noise. Meanwhile, layer-by-layer growth of NWs is rapidly developing such that both axial and radial heterostructures have now been realized. Such fine control allows for band-structure engineering and the production of devices including FETs, single photon sources, and QDs. NWs are also attractive hosts for optical emitters as their geometry favors the efficient extraction of photons.
These properties and the fact that a NW can be integrated as the tip of an SPM make NWs extremely promising devices. We propose to develop the use of NWs as scanning multifunctional sensors. We intend to 1) use NW cantilevers as force transducers in high-resolution scanning force microscopy, and 2) use NW quantum devices as scanning sensors.
Summary
Advances in growth and fabrication of semiconductor nanostructures have led to both the production of exquisitely sensitive force transducers and the development of solid-state quantum devices. Force transducers, typically monolithic Si cantilevers, are central to techniques such as AFM, and MFM. On the other hand, quantum devices including quantum wells, quantum dots (QDs), and single electron transistors are essential to technologies like lasers, optical detectors, and in experiments on quantum information. These two types of devices have – until now – occupied distinct material systems and have, for the most part, not been combined.
New developments in the growth of inorganic nanowires (NWs), however, are set to change the status quo. Researchers can now grow nanoscale structures from the bottom-up with unprecedented mechanical properties. Unlike traditional top-down cantilevers, which are etched or milled out of a larger block of material, bottom-up structures are assembled unit-by-unit to be almost defect-free on the atomic-scale. This near perfection gives NWs a much smaller mechanical dissipation than their top-down counterparts, while their higher resonance frequencies allow them to couple less strongly to common sources of noise. Meanwhile, layer-by-layer growth of NWs is rapidly developing such that both axial and radial heterostructures have now been realized. Such fine control allows for band-structure engineering and the production of devices including FETs, single photon sources, and QDs. NWs are also attractive hosts for optical emitters as their geometry favors the efficient extraction of photons.
These properties and the fact that a NW can be integrated as the tip of an SPM make NWs extremely promising devices. We propose to develop the use of NWs as scanning multifunctional sensors. We intend to 1) use NW cantilevers as force transducers in high-resolution scanning force microscopy, and 2) use NW quantum devices as scanning sensors.
Max ERC Funding
1 480 680 €
Duration
Start date: 2013-11-01, End date: 2018-10-31
Project acronym OPENGWTRIANGLE
Project Three ideas in open Gromov-Witten theory
Researcher (PI) Jake P. Solomon
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), PE1, ERC-2013-StG
Summary The questions motivating symplectic geometry, from classical mechanics to enumerative algebraic geometry, have been studied for centuries. Many recent advances in the field have stemmed from the theory of J-holomorphic curves, and in particular Gromov-Witten theory. The past 25 years of research have produced a fairly detailed picture of what can be expected from classical, closed Gromov-Witten theory. However, closed Gromov-Witten theory by itself lacks an interface with Lagrangian submanifolds, one of the fundamental structures of symplectic geometry. The nascent open Gromov-Witten theory, in which Lagrangian submanifolds enter as boundary conditions for J-holomorphic curves, provides such an interface.
The goal of the proposed research is to broaden and systematize our understanding of open Gromov-Witten theory. My strategy leverages three connections with more established fields of research to uncover new aspects of open Gromov-Witten theory. In return, open Gromov-Witten theory advances the connected fields and reveals links between them. First, the closed and open Gromov-Witten theories are intertwined. Representation theoretic structures in closed Gromov-Witten theory admit mixed open closed extensions. Further, real algebraic geometry gives rise to a large variety of Lagrangian submanifolds providing an important source of intuition for open Gromov Witten theory. In return, open Gromov-Witten theory techniques advance Welschinger's real enumerative geometry. Finally, open Gromov-Witten theory plays a key role in mirror symmetry, a conjectural correspondence between symplectic and complex geometry originating from string theory. In particular, open Gromov-Witten invariants appear in the construction of mirror geometries. Moreover, under mirror symmetry, Lagrangian submanifolds correspond roughly to holomorphic vector bundles. Well understood functionals associated to holomorphic vector bundles go over to open Gromov-Witten invariants.
Summary
The questions motivating symplectic geometry, from classical mechanics to enumerative algebraic geometry, have been studied for centuries. Many recent advances in the field have stemmed from the theory of J-holomorphic curves, and in particular Gromov-Witten theory. The past 25 years of research have produced a fairly detailed picture of what can be expected from classical, closed Gromov-Witten theory. However, closed Gromov-Witten theory by itself lacks an interface with Lagrangian submanifolds, one of the fundamental structures of symplectic geometry. The nascent open Gromov-Witten theory, in which Lagrangian submanifolds enter as boundary conditions for J-holomorphic curves, provides such an interface.
The goal of the proposed research is to broaden and systematize our understanding of open Gromov-Witten theory. My strategy leverages three connections with more established fields of research to uncover new aspects of open Gromov-Witten theory. In return, open Gromov-Witten theory advances the connected fields and reveals links between them. First, the closed and open Gromov-Witten theories are intertwined. Representation theoretic structures in closed Gromov-Witten theory admit mixed open closed extensions. Further, real algebraic geometry gives rise to a large variety of Lagrangian submanifolds providing an important source of intuition for open Gromov Witten theory. In return, open Gromov-Witten theory techniques advance Welschinger's real enumerative geometry. Finally, open Gromov-Witten theory plays a key role in mirror symmetry, a conjectural correspondence between symplectic and complex geometry originating from string theory. In particular, open Gromov-Witten invariants appear in the construction of mirror geometries. Moreover, under mirror symmetry, Lagrangian submanifolds correspond roughly to holomorphic vector bundles. Well understood functionals associated to holomorphic vector bundles go over to open Gromov-Witten invariants.
Max ERC Funding
1 249 000 €
Duration
Start date: 2013-10-01, End date: 2018-09-30
Project acronym OPTONEUROMOD
Project Optical dissection of prefrontal neuromodulation: from synapses through networks to behavior
Researcher (PI) Ofer Yizhar
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE
Country Israel
Call Details Starting Grant (StG), LS5, ERC-2013-StG
Summary The neocortex is organized into neural circuits that perform distinct computations, from sensory processing and motor control to memory, learning and language. Neuromodulatory systems projecting to the neocortex exert a powerful influence on cortical computations through neurotransmitters such as acetylcholine, monoamines and neuropeptides. The prefrontal cortex (PFC), a cortical region required for working memory, attention and goal-directed behavior, receives dense projections from multiple neuromodulatory systems that dramatically impact its function. Pioneering work has shown that pharmacological manipulation of these systems can potently modulate attention and cognitive function and that impaired neuromodulation can lead to psychiatric disease. Yet, much of the view of high level cortical function is focused on models that either ignore neuromodulation altogether or treat it as a reward or arousal signal.
We propose to elucidate the dynamics and mechanisms of prefrontal neuromodulatory tuning, from the level of synapses and cells to circuits and animal behavior. To achieve this goal, we will map the circuit-level impact of synaptic neuromodulatory inputs on the prefrontal cortex circuit dynamics, develop and apply two novel optogenetic approaches for light-based synaptic silencing and optical recording of cortical neuromodulatory activity in vivo, and establish the causal roles of PFC neuromodulation in attention and working memory. These experiments will enable us for the first time to delineate the specific contribution of distinct neuromodulatory systems to prefrontal function, integrating comprehensive cell- and circuit-level analysis with unique opto-physiological readouts in behaving animals. The project will yield an integrative view of prefrontal neuromodulation, revealing its impact on cortical function and dissecting its roles in cognitive function.
Summary
The neocortex is organized into neural circuits that perform distinct computations, from sensory processing and motor control to memory, learning and language. Neuromodulatory systems projecting to the neocortex exert a powerful influence on cortical computations through neurotransmitters such as acetylcholine, monoamines and neuropeptides. The prefrontal cortex (PFC), a cortical region required for working memory, attention and goal-directed behavior, receives dense projections from multiple neuromodulatory systems that dramatically impact its function. Pioneering work has shown that pharmacological manipulation of these systems can potently modulate attention and cognitive function and that impaired neuromodulation can lead to psychiatric disease. Yet, much of the view of high level cortical function is focused on models that either ignore neuromodulation altogether or treat it as a reward or arousal signal.
We propose to elucidate the dynamics and mechanisms of prefrontal neuromodulatory tuning, from the level of synapses and cells to circuits and animal behavior. To achieve this goal, we will map the circuit-level impact of synaptic neuromodulatory inputs on the prefrontal cortex circuit dynamics, develop and apply two novel optogenetic approaches for light-based synaptic silencing and optical recording of cortical neuromodulatory activity in vivo, and establish the causal roles of PFC neuromodulation in attention and working memory. These experiments will enable us for the first time to delineate the specific contribution of distinct neuromodulatory systems to prefrontal function, integrating comprehensive cell- and circuit-level analysis with unique opto-physiological readouts in behaving animals. The project will yield an integrative view of prefrontal neuromodulation, revealing its impact on cortical function and dissecting its roles in cognitive function.
Max ERC Funding
1 429 460 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym PathoPhageHost
Project Studying Pathogen Phage Host Interactions
Researcher (PI) Anat Herskovits
Host Institution (HI) TEL AVIV UNIVERSITY
Country Israel
Call Details Starting Grant (StG), LS6, ERC-2013-StG
Summary The DNA uptake competence system of the intracellular bacterial pathogen Listeria monocytogenes was considered non-functional. There are no known conditions for DNA transformation and the competence master activator gene, comK, is interrupted by a temperate (lysogenic) prophage. We have shown recently that the L. monocytogenes competence system is required during infection to promote bacterial escape from macrophage phagosomes, in a manner that is independent of DNA uptake. Remarkably, we found that regulation of the competence system relies on the formation of a functional comK gene via a controlled process of prophage excision. Prophage excision was specifically induced during intracellular growth, primarily within phagosomes, yet, unlike classic prophage induction, progeny virions were not produced and bacterial lysis did not occur. This study revealed a unique adaptation of a prophage to the intracellular life style of its host, whereby the prophage serves as a genetic switch to modulate the virulence of its host. In the proposed project we aim to investigate this phenomenon and study the give-and-take interactions between the L. monocytogenes 10403S strain and its ϕ10403S-prophage during mammalian infection. We will study the prophage determinants and mechanisms that control intracellular excision and maintenance as well as the mechanisms that prevent its virions production and bacterial lysis. We will explore the crosstalk between phage and bacterial regulatory factors and characterize the mammalian host signals/conditions that trigger this unique prophage response. Lastly, we will investigate the unexpected function of the competence system in phagosomal escape. In particular, we will explore the possibility that the competence system serves as an auxiliary secretion system, which secretes proteins that promote phagosomal escape.
Summary
The DNA uptake competence system of the intracellular bacterial pathogen Listeria monocytogenes was considered non-functional. There are no known conditions for DNA transformation and the competence master activator gene, comK, is interrupted by a temperate (lysogenic) prophage. We have shown recently that the L. monocytogenes competence system is required during infection to promote bacterial escape from macrophage phagosomes, in a manner that is independent of DNA uptake. Remarkably, we found that regulation of the competence system relies on the formation of a functional comK gene via a controlled process of prophage excision. Prophage excision was specifically induced during intracellular growth, primarily within phagosomes, yet, unlike classic prophage induction, progeny virions were not produced and bacterial lysis did not occur. This study revealed a unique adaptation of a prophage to the intracellular life style of its host, whereby the prophage serves as a genetic switch to modulate the virulence of its host. In the proposed project we aim to investigate this phenomenon and study the give-and-take interactions between the L. monocytogenes 10403S strain and its ϕ10403S-prophage during mammalian infection. We will study the prophage determinants and mechanisms that control intracellular excision and maintenance as well as the mechanisms that prevent its virions production and bacterial lysis. We will explore the crosstalk between phage and bacterial regulatory factors and characterize the mammalian host signals/conditions that trigger this unique prophage response. Lastly, we will investigate the unexpected function of the competence system in phagosomal escape. In particular, we will explore the possibility that the competence system serves as an auxiliary secretion system, which secretes proteins that promote phagosomal escape.
Max ERC Funding
1 490 400 €
Duration
Start date: 2013-10-01, End date: 2018-09-30
Project acronym PERSPECTIVE
Project Unraveling the Language of Perspective
Researcher (PI) Corien Liesbeth Anke Bary
Host Institution (HI) STICHTING KATHOLIEKE UNIVERSITEIT
Country Netherlands
Call Details Starting Grant (StG), SH4, ERC-2013-StG
Summary We always take in a certain perspective when we speak. Languages have a wide variety of linguistic means to express perspective. While perspectival elements are most of the time used from the perspective of the speaker, they can also be used from the perspective of someone else, a possibility that is fully exploited in narratives. The central aim of this project is to deepen our understanding of perspective shifts. It will not only elucidate the semantic and pragmatic mechanisms underlying interpretation shifts of specific expressions, but also unite them in a general formal model of perspective shift. Moreover, these insights will be used to unravel the linguistic grounding of narrative perspective. The project will focus on Ancient Greek, a language with a particularly rich perspective system. Not only do many classes of expressions involve perspective in some way (e.g. attitudinal particles, optative mood, tense and aspect, evaluatives, participles), but authors like Thucydides are also known for their subtle manipulation of narrative perspective. It is far from clear, however, how these shifts in narrative perspective are effected by the linguistic expressions used.
This project will study (i) the relation between attitudinal particles and perspective shifts, (ii) the role of evaluative expressions, and (iii) the relation between temporal perspective and narrative perspective. State-of-the-art computational methods will be used to extract data from existing corpora, revealing patterns that have eluded traditional methods; this methodology will be a major innovation in the field of classical philology.
The present project goes beyond previous semantic studies (i) by investigating more subtle and pervasive ways of perspective creation than the free indirect discourse technique and (ii) through the development of a general formal model of perspective shift, integrating the contribution of several perspective involving expressions.
Summary
We always take in a certain perspective when we speak. Languages have a wide variety of linguistic means to express perspective. While perspectival elements are most of the time used from the perspective of the speaker, they can also be used from the perspective of someone else, a possibility that is fully exploited in narratives. The central aim of this project is to deepen our understanding of perspective shifts. It will not only elucidate the semantic and pragmatic mechanisms underlying interpretation shifts of specific expressions, but also unite them in a general formal model of perspective shift. Moreover, these insights will be used to unravel the linguistic grounding of narrative perspective. The project will focus on Ancient Greek, a language with a particularly rich perspective system. Not only do many classes of expressions involve perspective in some way (e.g. attitudinal particles, optative mood, tense and aspect, evaluatives, participles), but authors like Thucydides are also known for their subtle manipulation of narrative perspective. It is far from clear, however, how these shifts in narrative perspective are effected by the linguistic expressions used.
This project will study (i) the relation between attitudinal particles and perspective shifts, (ii) the role of evaluative expressions, and (iii) the relation between temporal perspective and narrative perspective. State-of-the-art computational methods will be used to extract data from existing corpora, revealing patterns that have eluded traditional methods; this methodology will be a major innovation in the field of classical philology.
The present project goes beyond previous semantic studies (i) by investigating more subtle and pervasive ways of perspective creation than the free indirect discourse technique and (ii) through the development of a general formal model of perspective shift, integrating the contribution of several perspective involving expressions.
Max ERC Funding
1 044 798 €
Duration
Start date: 2013-12-01, End date: 2018-11-30
Project acronym PhyPD
Project New phylogenetic methods for inferring complex population dynamics
Researcher (PI) Tanja Stadler
Host Institution (HI) EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH
Country Switzerland
Call Details Starting Grant (StG), LS8, ERC-2013-StG
Summary The field of phylogenetics is undergoing an important change over recent time. For a long time phylogenetics focussed on describing the species tree as accurate as possible. More recently there is a shift towards a functional inference of the evolutionary process itself, i.e. researchers attempt to infer what processes are most likely responsible for the particular pattern of branching observed in a given phylogeny.
Phylogenetics has traditionally been developed for macroevolution. Recently, it has been recognized that the phylogenetic concept is also crucial for improving our understanding of epidemiological processes. In an epidemiological phylogeny, tips of the tree are corresponding to infected hosts (instead of extant species), and branching events correspond to transmission events (instead of speciation events).
In the first part of the project, I propose to develop novel phylogenetic methodology that will allow us to characterize fundamental evolutionary processes based on species phylogenies. I will aim at identifying key factors (such as environment, competition between species, or microevolutionary processes) determining macroevolutionary dynamics. Insight into these dynamics will allow us to address fundamental evolutionary questions such as the advantages of recombination as well as to revisit current debates about the impact of climate change on diversity.
In the second part of the proposed project, I will develop tools identifying the main drivers responsible for the spread of an epidemic, which may help informing public health intervention strategies. Furthermore, I aim at characterizing bottlenecks at transmission, which may become important for early treatment strategies or vaccine design.
Completion of the projects will deepen our understanding of macroevolutionary and epidemiological dynamics, as well as lead to novel phylogenetic tools allowing us to analyse the growing amount of available data, such as next-generation sequence data.
Summary
The field of phylogenetics is undergoing an important change over recent time. For a long time phylogenetics focussed on describing the species tree as accurate as possible. More recently there is a shift towards a functional inference of the evolutionary process itself, i.e. researchers attempt to infer what processes are most likely responsible for the particular pattern of branching observed in a given phylogeny.
Phylogenetics has traditionally been developed for macroevolution. Recently, it has been recognized that the phylogenetic concept is also crucial for improving our understanding of epidemiological processes. In an epidemiological phylogeny, tips of the tree are corresponding to infected hosts (instead of extant species), and branching events correspond to transmission events (instead of speciation events).
In the first part of the project, I propose to develop novel phylogenetic methodology that will allow us to characterize fundamental evolutionary processes based on species phylogenies. I will aim at identifying key factors (such as environment, competition between species, or microevolutionary processes) determining macroevolutionary dynamics. Insight into these dynamics will allow us to address fundamental evolutionary questions such as the advantages of recombination as well as to revisit current debates about the impact of climate change on diversity.
In the second part of the proposed project, I will develop tools identifying the main drivers responsible for the spread of an epidemic, which may help informing public health intervention strategies. Furthermore, I aim at characterizing bottlenecks at transmission, which may become important for early treatment strategies or vaccine design.
Completion of the projects will deepen our understanding of macroevolutionary and epidemiological dynamics, as well as lead to novel phylogenetic tools allowing us to analyse the growing amount of available data, such as next-generation sequence data.
Max ERC Funding
1 471 582 €
Duration
Start date: 2014-01-01, End date: 2018-12-31
Project acronym PneumoCell
Project Noise in gene expression as a determinant of virulence of the human pathogen Streptococcus pneumoniae
Researcher (PI) Jan-Willem Veening
Host Institution (HI) RIJKSUNIVERSITEIT GRONINGEN
Country Netherlands
Call Details Starting Grant (StG), LS6, ERC-2013-StG
Summary Not all cells in bacterial populations exhibit exactly the same phenotype, even though they grow in the same environment and are genetically identical. One of the main driving forces of phenotypic variation is stochasticity, or noise, in gene expression. Possible molecular origins contributing to noise in protein synthesis are stochastic fluctuations in the biochemical reactions of gene expression itself, namely transcription and translation.
The driving hypothesis of this application is that the human pathogen Streptococcus pneumoniae utilizes noisy gene expression to successfully colonize and invade its host. To test this supposition, the total amount of noise in key regulatory networks for virulence factor production will be quantified. Using natural and synthetic bistable switches as highly sensitive probes for noise, in combination with state-of-the-art single-cell imaging, microfluidics and direct transcriptome sequencing, the molecular mechanisms underlying noise generation in S. pneumoniae will be determined. By constructing strains with altered levels of phenotypic variation, the importance of noisy gene expression in S. pneumoniae pathogenesis will be tested.
S. pneumoniae is a leading cause of bacterial pneumoniae, meningitis, and sepsis worldwide. The molecular mechanisms that cause switching of S. pneumoniae to its virulent states are barely understood, although it becomes increasingly clear that noise-driven phenotypic variation plays an important role in pneumococcal pathogenesis. Therefore, understanding the molecular origins of phenotypic variation in S. pneumoniae might not only provide novel fundamental insights in gene expression, but also result in the identification of new anti-pneumococcal targets.
Summary
Not all cells in bacterial populations exhibit exactly the same phenotype, even though they grow in the same environment and are genetically identical. One of the main driving forces of phenotypic variation is stochasticity, or noise, in gene expression. Possible molecular origins contributing to noise in protein synthesis are stochastic fluctuations in the biochemical reactions of gene expression itself, namely transcription and translation.
The driving hypothesis of this application is that the human pathogen Streptococcus pneumoniae utilizes noisy gene expression to successfully colonize and invade its host. To test this supposition, the total amount of noise in key regulatory networks for virulence factor production will be quantified. Using natural and synthetic bistable switches as highly sensitive probes for noise, in combination with state-of-the-art single-cell imaging, microfluidics and direct transcriptome sequencing, the molecular mechanisms underlying noise generation in S. pneumoniae will be determined. By constructing strains with altered levels of phenotypic variation, the importance of noisy gene expression in S. pneumoniae pathogenesis will be tested.
S. pneumoniae is a leading cause of bacterial pneumoniae, meningitis, and sepsis worldwide. The molecular mechanisms that cause switching of S. pneumoniae to its virulent states are barely understood, although it becomes increasingly clear that noise-driven phenotypic variation plays an important role in pneumococcal pathogenesis. Therefore, understanding the molecular origins of phenotypic variation in S. pneumoniae might not only provide novel fundamental insights in gene expression, but also result in the identification of new anti-pneumococcal targets.
Max ERC Funding
1 498 846 €
Duration
Start date: 2013-11-01, End date: 2018-10-31
Project acronym PORABEL
Project Nanopore integrated nanoelectrodes for biomolecular manipulation and sensing
Researcher (PI) Aleksandra Radenovic
Host Institution (HI) ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Country Switzerland
Call Details Starting Grant (StG), PE3, ERC-2010-StG_20091028
Summary In this proposal we aim to address several complex biophysical problems at single molecule level that remained elusive due to the lack of appropriate experimental approach where one could manipulate independently both interacting biomolecules and in the same time measure the strength of their interaction and correlate it with their electronic signature. In particular we are interested in finding out how biopolymer finds, enters and translocates nanopore. Equally intriguing is still unresolved mechanism of phage DNA ejection. We will also investigate how exactly proteins recognize the target binding places on DNA and if the protein DNA recognition is based on the complementarity of their charge patterns.
To allow addressing those biophysical problems we will develop novel experimental framework by integrating electrodes to the nanopore based force spectroscopy. The proposed strategy will enable two directions of the research: single molecule manipulation and single molecule detection /sensing equally suitable for investigating complex biophysical problems and molecular recognition assays.
By exploiting superior sensing and detection capabilities of our devices, we will investigate following practical applications improved nucleotide detection, selective protein detection and protein charge profiling via nanopore unfolding.
Unique combination of optical manipulation and nanofluidics could lead to new methods of bioanalysis, mechanical characterization and discrimination between specific and non-specific DNA protein interactions. This research proposal combines nanofabrication, optics, nano/microfluidics, electronics, computer programming, and biochemistry
Summary
In this proposal we aim to address several complex biophysical problems at single molecule level that remained elusive due to the lack of appropriate experimental approach where one could manipulate independently both interacting biomolecules and in the same time measure the strength of their interaction and correlate it with their electronic signature. In particular we are interested in finding out how biopolymer finds, enters and translocates nanopore. Equally intriguing is still unresolved mechanism of phage DNA ejection. We will also investigate how exactly proteins recognize the target binding places on DNA and if the protein DNA recognition is based on the complementarity of their charge patterns.
To allow addressing those biophysical problems we will develop novel experimental framework by integrating electrodes to the nanopore based force spectroscopy. The proposed strategy will enable two directions of the research: single molecule manipulation and single molecule detection /sensing equally suitable for investigating complex biophysical problems and molecular recognition assays.
By exploiting superior sensing and detection capabilities of our devices, we will investigate following practical applications improved nucleotide detection, selective protein detection and protein charge profiling via nanopore unfolding.
Unique combination of optical manipulation and nanofluidics could lead to new methods of bioanalysis, mechanical characterization and discrimination between specific and non-specific DNA protein interactions. This research proposal combines nanofabrication, optics, nano/microfluidics, electronics, computer programming, and biochemistry
Max ERC Funding
1 439 840 €
Duration
Start date: 2010-10-01, End date: 2015-09-30
Project acronym QUANT-DES-CNT
Project Quantum Design in Carbon Nanotubes
Researcher (PI) Shahal Ilani
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE
Country Israel
Call Details Starting Grant (StG), PE3, ERC-2010-StG_20091028
Summary Quantum design, the ability to control the microscopic properties of a quantum system, has proven to be an invaluable tool in experimental physics. Carbon nanotubes are an ideal system to implement quantum design in the solid-state; their strongly interacting electrons, unusual spin properties, and unique mechanical qualities make them an excellent platform for studying quantum phenomena in low dimensions. However, for many years this potential has been hindered by the dominance of strong electronic disorder in this
system. Fortunately, a series of recent breakthroughs in making nanotubes free of disorder has dramatically changed this situation, opening up a wide range of opportunities for high-precision experiments in these systems.
In this work I propose to develop a new technology that will enable quantum design experiments in
carbon nanotubes. This technology, which builds on my recent development of ultra-clean electronic devices in nanotubes, will allow us to create nanotube device-architectures that go far beyond those currently available. Specifically, we will be able to control the properties of individual electrons with microscopic precision (~100nm), manipulate their quantum states, and image their individual wavefunctions. This new toolset will be used to study previously unexplored realms in condensed matter physics, ranging from the correlated states-of-matter formed by electrons in one-dimension, to quantum information experiments with multiple electronic spins, and finally to mechanical studies of nanotube resonators in the quantum limit.
These studies will address some of the most fundamental aspects pertaining to the physics of electrons, spins and phonons in low dimensions.
Summary
Quantum design, the ability to control the microscopic properties of a quantum system, has proven to be an invaluable tool in experimental physics. Carbon nanotubes are an ideal system to implement quantum design in the solid-state; their strongly interacting electrons, unusual spin properties, and unique mechanical qualities make them an excellent platform for studying quantum phenomena in low dimensions. However, for many years this potential has been hindered by the dominance of strong electronic disorder in this
system. Fortunately, a series of recent breakthroughs in making nanotubes free of disorder has dramatically changed this situation, opening up a wide range of opportunities for high-precision experiments in these systems.
In this work I propose to develop a new technology that will enable quantum design experiments in
carbon nanotubes. This technology, which builds on my recent development of ultra-clean electronic devices in nanotubes, will allow us to create nanotube device-architectures that go far beyond those currently available. Specifically, we will be able to control the properties of individual electrons with microscopic precision (~100nm), manipulate their quantum states, and image their individual wavefunctions. This new toolset will be used to study previously unexplored realms in condensed matter physics, ranging from the correlated states-of-matter formed by electrons in one-dimension, to quantum information experiments with multiple electronic spins, and finally to mechanical studies of nanotube resonators in the quantum limit.
These studies will address some of the most fundamental aspects pertaining to the physics of electrons, spins and phonons in low dimensions.
Max ERC Funding
1 499 940 €
Duration
Start date: 2011-01-01, End date: 2015-12-31
Project acronym RECONTEXT
Project From neurons to behaviour: Context representation and memory reconsolidation in the entorhinal hippocampal system
Researcher (PI) Christian Doeller
Host Institution (HI) STICHTING KATHOLIEKE UNIVERSITEIT
Country Netherlands
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary One of the most intriguing topics in neuroscience and memory research today is ‘reconsolidation’: the phenomenon that a brief reminder renders an already consolidated memory labile again and that this fragile memory requires de novo protein synthesis to be reconsolidated. However, the functional role and the neural mechanisms of reconsolidation in humans are unclear. Another exciting line of research in neuroscience, based on the discovery of spatially tuned hippocampal place and entorhinal grid cells in rodents, suggests that during first exposure to an environment a spatial map-like representation is formed in the entorhinalhippocampal system and it has been proposed that events are then encoded onto this map in their spatial context. By combining the understanding of these two fields of animal research, translating it to systems neuroscience in humans and building on my recent discovery that place-cell and grid-cell like representations exist in humans, I will test the novel idea that these hippocampal and entorhinal representations of spatial context are a clue to understand the mechanisms of memory reconsolidation in humans. To examine this, I will use virtual-reality technologies combined with functional neuroimaging in humans. I will test the prediction that context reexposure leads to a reactivation of consolidated memories in neocortex and investigate the role of entorhinal-hippocampal context representations during memory reconsolidation. I will also examine the functional role and the mechanisms of a dynamic memory representation: How is new information integrated into reactivated memories? Finally, I will investigate conjunctive representations of cortical memories in the hippocampal formation. My eventual aim is to produce a coherent understanding of brain function from neural representations to systems-level involvement in behaviour which might help to understand the neural mechanisms underlying memory impairments in neuro-degenerative diseases.
Summary
One of the most intriguing topics in neuroscience and memory research today is ‘reconsolidation’: the phenomenon that a brief reminder renders an already consolidated memory labile again and that this fragile memory requires de novo protein synthesis to be reconsolidated. However, the functional role and the neural mechanisms of reconsolidation in humans are unclear. Another exciting line of research in neuroscience, based on the discovery of spatially tuned hippocampal place and entorhinal grid cells in rodents, suggests that during first exposure to an environment a spatial map-like representation is formed in the entorhinalhippocampal system and it has been proposed that events are then encoded onto this map in their spatial context. By combining the understanding of these two fields of animal research, translating it to systems neuroscience in humans and building on my recent discovery that place-cell and grid-cell like representations exist in humans, I will test the novel idea that these hippocampal and entorhinal representations of spatial context are a clue to understand the mechanisms of memory reconsolidation in humans. To examine this, I will use virtual-reality technologies combined with functional neuroimaging in humans. I will test the prediction that context reexposure leads to a reactivation of consolidated memories in neocortex and investigate the role of entorhinal-hippocampal context representations during memory reconsolidation. I will also examine the functional role and the mechanisms of a dynamic memory representation: How is new information integrated into reactivated memories? Finally, I will investigate conjunctive representations of cortical memories in the hippocampal formation. My eventual aim is to produce a coherent understanding of brain function from neural representations to systems-level involvement in behaviour which might help to understand the neural mechanisms underlying memory impairments in neuro-degenerative diseases.
Max ERC Funding
1 474 872 €
Duration
Start date: 2011-03-01, End date: 2016-02-29
Project acronym RRHEDSPS
Project Reconsidering Representation: How Electoral Districts Shape Party Systems
Researcher (PI) Orit Kedar
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), SH2, ERC-2010-StG_20091209
Summary An electoral system is an essential component of representative democracy. It translates preferences
of citizens to a legislative body and inevitably distorts preferences, voicing some more loudly than others.
Theorizing and empirically analyzing how the electoral system tilts the playing ground is the aim of this
study.
The number of seats allotted to an electoral district—the district magnitude (DM)—is perhaps the
most important component defining an electoral system. It is long established that DM affects key features
of the political landscape in a country, such as representation, the number of parties, the type of government
(single- or multi-party coalition), parties’ strategy, voters’ consideration, and even redistribution policy.
Most democracies, however, have districts of many different magnitudes, and the range often reaches thirty
seats gap between the smallest and largest districts in a country. Districts in Portugal, for instance, vary
between two and forty-eight seats, and in Switzerland between one and thirty-five. The voluminous
literature on electoral districts uniformly sidesteps this heterogeneity, focusing instead on a single middle
district per country.
The proposed study is the first large-scale study that theorizes about and empirically analyzes the
effects of within-country district structure. I address questions such as: how does district heterogeneity
shape representation at the national level? How does it affect the party system? And how does it affect party
coordination?
In the first part of the study I will theorize about various aspects of district heterogeneity in a country
(e.g., skewness, effective number of magnitudes). I will gain deep understanding for district distributions
and develop politically-relevant measures of heterogeneity. Drawing on insights from the theoretical part,
the second part will empirically examine how district heterogeneity affects the political landscape, and in
particular representation, party system, and party coordination. This part relies on extensive district- and
national-level data collection and data analysis in OECD countries as well as in-depth case analysis.
Analyzing the effect of district heterogeneity on representation, party systems, and party
coordination will open new avenues of research about design of electoral systems.
Summary
An electoral system is an essential component of representative democracy. It translates preferences
of citizens to a legislative body and inevitably distorts preferences, voicing some more loudly than others.
Theorizing and empirically analyzing how the electoral system tilts the playing ground is the aim of this
study.
The number of seats allotted to an electoral district—the district magnitude (DM)—is perhaps the
most important component defining an electoral system. It is long established that DM affects key features
of the political landscape in a country, such as representation, the number of parties, the type of government
(single- or multi-party coalition), parties’ strategy, voters’ consideration, and even redistribution policy.
Most democracies, however, have districts of many different magnitudes, and the range often reaches thirty
seats gap between the smallest and largest districts in a country. Districts in Portugal, for instance, vary
between two and forty-eight seats, and in Switzerland between one and thirty-five. The voluminous
literature on electoral districts uniformly sidesteps this heterogeneity, focusing instead on a single middle
district per country.
The proposed study is the first large-scale study that theorizes about and empirically analyzes the
effects of within-country district structure. I address questions such as: how does district heterogeneity
shape representation at the national level? How does it affect the party system? And how does it affect party
coordination?
In the first part of the study I will theorize about various aspects of district heterogeneity in a country
(e.g., skewness, effective number of magnitudes). I will gain deep understanding for district distributions
and develop politically-relevant measures of heterogeneity. Drawing on insights from the theoretical part,
the second part will empirically examine how district heterogeneity affects the political landscape, and in
particular representation, party system, and party coordination. This part relies on extensive district- and
national-level data collection and data analysis in OECD countries as well as in-depth case analysis.
Analyzing the effect of district heterogeneity on representation, party systems, and party
coordination will open new avenues of research about design of electoral systems.
Max ERC Funding
1 038 686 €
Duration
Start date: 2010-11-01, End date: 2016-10-31
Project acronym SALIENSY
Project Mapping the synaptic circuits for salience
Researcher (PI) Manuel Mameli
Host Institution (HI) UNIVERSITE DE LAUSANNE
Country Switzerland
Call Details Starting Grant (StG), LS5, ERC-2013-StG
Summary An unpredicted salient event – rewarding or aversive – triggers a rapid emotional reaction that has profound impact in making a future choice. The early neurobiological processes behind it are matter of intense study. However, the hierarchical anatomical and functional organization as well as the cellular mechanisms underlying acute perception of reward and aversive events remains unknown. Intriguingly, salience experience alters the activity in the medial globus pallidus of the basal ganglia and the lateral habenula (LHb) as well as in dopamine and serotonin neurons. Here, I hypothesize that rewarding and aversive experiences require the medial globus pallidus-LHb pathway, and rapid cellular adaptations in LHb to orchestrate dopamine and serotonin systems. To test this my specific aims are: 1 - Anatomical-functional circuit dissection to map LHb inputs from the medial globus pallidus, and LHb outputs to the midbrain using viral-based mapping 2 – Assess the effect of salience (reward, aversion) on the LHb using synaptic physiology and optogenetics and 3 - Causally link LHb activity with behaviours modelling reward/aversion to probe LHb function at the network level using in vivo electrophysiology and optogenetics. I propose to unravel early cellular processes fundamental to “pursue a reward, escape a danger”, which is relevant for encoding rewarding and aversive stimuli in health and neuropsychiatry (i.e. addiction, depression, post-traumatic stress disorders).
Summary
An unpredicted salient event – rewarding or aversive – triggers a rapid emotional reaction that has profound impact in making a future choice. The early neurobiological processes behind it are matter of intense study. However, the hierarchical anatomical and functional organization as well as the cellular mechanisms underlying acute perception of reward and aversive events remains unknown. Intriguingly, salience experience alters the activity in the medial globus pallidus of the basal ganglia and the lateral habenula (LHb) as well as in dopamine and serotonin neurons. Here, I hypothesize that rewarding and aversive experiences require the medial globus pallidus-LHb pathway, and rapid cellular adaptations in LHb to orchestrate dopamine and serotonin systems. To test this my specific aims are: 1 - Anatomical-functional circuit dissection to map LHb inputs from the medial globus pallidus, and LHb outputs to the midbrain using viral-based mapping 2 – Assess the effect of salience (reward, aversion) on the LHb using synaptic physiology and optogenetics and 3 - Causally link LHb activity with behaviours modelling reward/aversion to probe LHb function at the network level using in vivo electrophysiology and optogenetics. I propose to unravel early cellular processes fundamental to “pursue a reward, escape a danger”, which is relevant for encoding rewarding and aversive stimuli in health and neuropsychiatry (i.e. addiction, depression, post-traumatic stress disorders).
Max ERC Funding
1 500 000 €
Duration
Start date: 2014-03-01, End date: 2020-02-29
Project acronym SECURCIT
Project Transforming Citizenship through Hybrid Governance: The Impacts of Public-Private Security Assemblages
Researcher (PI) Rivke Jaffe
Host Institution (HI) UNIVERSITEIT VAN AMSTERDAM
Country Netherlands
Call Details Starting Grant (StG), SH2, ERC-2013-StG
Summary "This project is an anthropological study of how citizenship is being reconfigured through hybrid forms of governance. It will research these transformations by focusing on public-private ‘security assemblages’, with particular emphasis on the role of the private security industry. Much recent scholarly debate has focused on shifting modes of governance in a context of neoliberal globalization. Specific attention has focused on how governance is increasingly achieved through networks or assemblages of state, corporate and voluntary actors. Such assemblages of state and non-state actors blur the lines between public and private, and between local, national and transnational. This research will extend this debate by investigating the implications this form of governance has for how different groups enact and experience citizenship, concentrating on public-private security assemblages as hybrid, multi-scalar governance structures. It will examine how forms of ‘differentiated citizenship’ are produced, and how political subjectivities shift, as a result of these forms of security governance.
These transformations in citizenship will be analyzed through a multi-sited, comparative analysis of security assemblages in Jerusalem (Israel), Kingston (Jamaica) and Nairobi (Kenya). The project will research the composition, operation and regulation of public-private security assemblages, with special attention to the global mobilities of security experts and expertise. In each setting, the project will study the practices and discourses that structure relations between state and non-state security providers, clients and those seen as threats. It will focus on the ‘security encounter’ between these different actors, in which new social relationships and subjectivities are produced. The project is expected to lead to the development of an anthropological theory of security governance with both theoretical and applied relevance."
Summary
"This project is an anthropological study of how citizenship is being reconfigured through hybrid forms of governance. It will research these transformations by focusing on public-private ‘security assemblages’, with particular emphasis on the role of the private security industry. Much recent scholarly debate has focused on shifting modes of governance in a context of neoliberal globalization. Specific attention has focused on how governance is increasingly achieved through networks or assemblages of state, corporate and voluntary actors. Such assemblages of state and non-state actors blur the lines between public and private, and between local, national and transnational. This research will extend this debate by investigating the implications this form of governance has for how different groups enact and experience citizenship, concentrating on public-private security assemblages as hybrid, multi-scalar governance structures. It will examine how forms of ‘differentiated citizenship’ are produced, and how political subjectivities shift, as a result of these forms of security governance.
These transformations in citizenship will be analyzed through a multi-sited, comparative analysis of security assemblages in Jerusalem (Israel), Kingston (Jamaica) and Nairobi (Kenya). The project will research the composition, operation and regulation of public-private security assemblages, with special attention to the global mobilities of security experts and expertise. In each setting, the project will study the practices and discourses that structure relations between state and non-state security providers, clients and those seen as threats. It will focus on the ‘security encounter’ between these different actors, in which new social relationships and subjectivities are produced. The project is expected to lead to the development of an anthropological theory of security governance with both theoretical and applied relevance."
Max ERC Funding
1 484 656 €
Duration
Start date: 2014-04-01, End date: 2019-03-31
Project acronym SIAMCP
Project Follow the PAIN: Novel Somatotopically-Based Integrative Approach to Study Mechanisms of Detection, Transmission and Perpetuation of Nociceptive, Inflammatory and Neuropathic Pain
Researcher (PI) Alexander Binshtok
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary The worst of evils - pain is one of the main reasons for seeking medical help. Chronic pain affects almost one fifth of the population of Europe and leads to exorbitant medical expenses as well as extreme suffering. Despite extensive efforts, effective pain treatment has remained elusive. Inadequate understanding of the mechanisms of pain prevents the development of effective therapies. In order to better understand pain mechanisms, a novel integrative approach is needed. This approach should: to investigate the fundamental site of signal detection; the nociceptive terminals and to establish an understanding of the progression from peripheral nociception to central pain perception. Our project aims to integrate analysis at different levels of pain perception in normal and pathological conditions in order to elucidate mechanisms underlying chronic pain. Our approach propose to study pain related mechanisms along somatotopically define neuroaxis of vibrissae-barrel system. Using this unique system where peripheral receptor directly corresponds to its central analyzer, we will first characterize noxious signal detection by single channels in individual nociceptive terminal. We will follow propagation of nociceptive signal and monitor activity-dependent changes in corresponding circuits at trigeminal nuclei, thalamus and cortex. We will study modulation in of synaptic connectivity in the spino-thalamo-cortical pathway in models of chronic pain. This multi-disciplinary project will incorporate ground-breaking imaging techniques and state-of-the-art electrophysiological, histological and behavioural experiments to study pain-related mechanisms at the molecular and cellular levels as well as at the level of neuronal networks and behaviour.
Summary
The worst of evils - pain is one of the main reasons for seeking medical help. Chronic pain affects almost one fifth of the population of Europe and leads to exorbitant medical expenses as well as extreme suffering. Despite extensive efforts, effective pain treatment has remained elusive. Inadequate understanding of the mechanisms of pain prevents the development of effective therapies. In order to better understand pain mechanisms, a novel integrative approach is needed. This approach should: to investigate the fundamental site of signal detection; the nociceptive terminals and to establish an understanding of the progression from peripheral nociception to central pain perception. Our project aims to integrate analysis at different levels of pain perception in normal and pathological conditions in order to elucidate mechanisms underlying chronic pain. Our approach propose to study pain related mechanisms along somatotopically define neuroaxis of vibrissae-barrel system. Using this unique system where peripheral receptor directly corresponds to its central analyzer, we will first characterize noxious signal detection by single channels in individual nociceptive terminal. We will follow propagation of nociceptive signal and monitor activity-dependent changes in corresponding circuits at trigeminal nuclei, thalamus and cortex. We will study modulation in of synaptic connectivity in the spino-thalamo-cortical pathway in models of chronic pain. This multi-disciplinary project will incorporate ground-breaking imaging techniques and state-of-the-art electrophysiological, histological and behavioural experiments to study pain-related mechanisms at the molecular and cellular levels as well as at the level of neuronal networks and behaviour.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-03-01, End date: 2016-02-29
Project acronym SPREC
Project Demographic and Phenotypic Signals of Population Responses to Environmental Change
Researcher (PI) Seyfi Arpat oezguel
Host Institution (HI) University of Zurich
Country Switzerland
Call Details Starting Grant (StG), LS8, ERC-2013-StG
Summary "A major goal in biodiversity conservation is to predict responses of biological populations to environmental change. To achieve this, we must identify early warning signals of the demographic changes that underlie population declines. Some studies have achieved phenomenological prediction of sudden changes, but recent advances that link trait-based information with demography hint that a mechanistic understanding is within reach. I propose to develop a predictive framework by identifying the demographic and phenotypic statistics that can be used as early warning signals of demographic regime shifts. I have investigated links between ecological and evolutionary processes in changing environments for many years, and I will now build on this experience to develop a predictive theory. First, we will analyse unique long-term individual-based datasets from nine mammal species. The species represent a continuum of life histories and environmental conditions, and some of them show population dynamic regime shifts. Second, we will construct trait-based demographic models of each system and perturb key parameters to simulate population and trait dynamics under multiple environmental scenarios. The simulations will yield time-series data from which we will estimate demographic and phenotypic statistics. We will test the ability of these statistics to predict demographic changes using a novel decision algorithm framework. Finally, using two laboratory microcosms, we will experimentally test the ability of these statistics to predict population responses to environmental change. This project will exploit nine unique natural systems to identify early warning signals of population change and test these on two experimental systems. Results will provide much-needed predictive insight into how wildlife populations respond to environmental change, and will be of highest importance to management of wildlife populations whether they are of conservation concern, invasive, or exploitable."
Summary
"A major goal in biodiversity conservation is to predict responses of biological populations to environmental change. To achieve this, we must identify early warning signals of the demographic changes that underlie population declines. Some studies have achieved phenomenological prediction of sudden changes, but recent advances that link trait-based information with demography hint that a mechanistic understanding is within reach. I propose to develop a predictive framework by identifying the demographic and phenotypic statistics that can be used as early warning signals of demographic regime shifts. I have investigated links between ecological and evolutionary processes in changing environments for many years, and I will now build on this experience to develop a predictive theory. First, we will analyse unique long-term individual-based datasets from nine mammal species. The species represent a continuum of life histories and environmental conditions, and some of them show population dynamic regime shifts. Second, we will construct trait-based demographic models of each system and perturb key parameters to simulate population and trait dynamics under multiple environmental scenarios. The simulations will yield time-series data from which we will estimate demographic and phenotypic statistics. We will test the ability of these statistics to predict demographic changes using a novel decision algorithm framework. Finally, using two laboratory microcosms, we will experimentally test the ability of these statistics to predict population responses to environmental change. This project will exploit nine unique natural systems to identify early warning signals of population change and test these on two experimental systems. Results will provide much-needed predictive insight into how wildlife populations respond to environmental change, and will be of highest importance to management of wildlife populations whether they are of conservation concern, invasive, or exploitable."
Max ERC Funding
1 499 136 €
Duration
Start date: 2013-12-01, End date: 2018-11-30
Project acronym SUMOFLU
Project Interplay between influenza viruses and host SUMO pathways
Researcher (PI) Benjamin Hale
Host Institution (HI) University of Zurich
Country Switzerland
Call Details Starting Grant (StG), LS6, ERC-2013-StG
Summary Influenza viruses cause a significant seasonal disease burden and continually threaten to initiate human pandemics. Antivirals are available for treatment of influenza, however drug-resistant viruses often emerge. Thus, there is urgent need to develop new antivirals with lower chances of selecting resistance. As viruses rely extensively on cellular functions, one way to minimise resistance is to target new antivirals against host factors. This concept requires a fundamental understanding of mechanisms underpinning the interplay between influenza viruses and their hosts.
In this project, we will investigate the role that host SUMO pathways play during influenza virus replication. SUMO proteins are important regulators of cell signalling, and are covalently linked to other proteins in order to alter structure, localization or function. As such, SUMO conjugation regulates many diverse aspects of biology. Our own work shows that global cellular SUMOylation increases during influenza virus infection, and that virus replication is severely impaired when cells are depleted of key enzymes and components required for general SUMO conjugation. Here, we will determine what viral components trigger SUMOylation, and which specific cellular enzymes are involved. We will characterize where in the cell SUMO conjugates accumulate, and for the first time apply large-scale affinity-based quantitative proteomics to the identification of proteins that become SUMO modified during infection. A key aim will be to correlate changes to the SUMO sub-proteome with the function of specific host SUMO-modifying enzymes, thereby establishing the mechanistic role of these modifications during virus replication.
Understanding basic mechanisms underlying SUMOylation during influenza virus infection will provide new insights into the fundamental biology of these important pathogens. The work could also lead to identification of key cellular pathways that can be exploited as novel therapeutic targets
Summary
Influenza viruses cause a significant seasonal disease burden and continually threaten to initiate human pandemics. Antivirals are available for treatment of influenza, however drug-resistant viruses often emerge. Thus, there is urgent need to develop new antivirals with lower chances of selecting resistance. As viruses rely extensively on cellular functions, one way to minimise resistance is to target new antivirals against host factors. This concept requires a fundamental understanding of mechanisms underpinning the interplay between influenza viruses and their hosts.
In this project, we will investigate the role that host SUMO pathways play during influenza virus replication. SUMO proteins are important regulators of cell signalling, and are covalently linked to other proteins in order to alter structure, localization or function. As such, SUMO conjugation regulates many diverse aspects of biology. Our own work shows that global cellular SUMOylation increases during influenza virus infection, and that virus replication is severely impaired when cells are depleted of key enzymes and components required for general SUMO conjugation. Here, we will determine what viral components trigger SUMOylation, and which specific cellular enzymes are involved. We will characterize where in the cell SUMO conjugates accumulate, and for the first time apply large-scale affinity-based quantitative proteomics to the identification of proteins that become SUMO modified during infection. A key aim will be to correlate changes to the SUMO sub-proteome with the function of specific host SUMO-modifying enzymes, thereby establishing the mechanistic role of these modifications during virus replication.
Understanding basic mechanisms underlying SUMOylation during influenza virus infection will provide new insights into the fundamental biology of these important pathogens. The work could also lead to identification of key cellular pathways that can be exploited as novel therapeutic targets
Max ERC Funding
1 482 452 €
Duration
Start date: 2014-02-01, End date: 2020-01-31
Project acronym TCCECJ
Project Theologies of conversion to Christianity in early modern east-central Europan Judaism
Researcher (PI) Pawel Tadeusz Maciejko
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Country Israel
Call Details Starting Grant (StG), SH6, ERC-2010-StG_20091209
Summary This project endeavors to recalibrate the accepted understanding of the Jewish-Christian interchange in the early modern East-Central Europe in light of an analysis of Jewish theological elaborations of conversion to Christianity. From the mid-seventeenth century onwards conversion to Christianity became one of the central intellectual (and not merely practical) concerns of Judaism. By attempting to reconstruct the theological conceptualizations of conversions (and not – as did other scholars – biographies of the converts), I shall challenge the prevailing scholarly paradigm of the existence of clear and impenetrable boundaries between Judaism and Christianity. My project seeks to systematically discuss this issue on the basis of an analysis of a large amount of previously unknown primary sources, thereby shedding significant new light on the Jewish Christian relations in Central Europe in the early modern period.
Summary
This project endeavors to recalibrate the accepted understanding of the Jewish-Christian interchange in the early modern East-Central Europe in light of an analysis of Jewish theological elaborations of conversion to Christianity. From the mid-seventeenth century onwards conversion to Christianity became one of the central intellectual (and not merely practical) concerns of Judaism. By attempting to reconstruct the theological conceptualizations of conversions (and not – as did other scholars – biographies of the converts), I shall challenge the prevailing scholarly paradigm of the existence of clear and impenetrable boundaries between Judaism and Christianity. My project seeks to systematically discuss this issue on the basis of an analysis of a large amount of previously unknown primary sources, thereby shedding significant new light on the Jewish Christian relations in Central Europe in the early modern period.
Max ERC Funding
1 045 200 €
Duration
Start date: 2011-02-01, End date: 2016-01-31
Project acronym THZ-PLASMON
Project Ultra-fast control of THz plasmon polariton resonances
Researcher (PI) Jaime Gomez Rivas
Host Institution (HI) STICHTING NEDERLANDSE WETENSCHAPPELIJK ONDERZOEK INSTITUTEN
Country Netherlands
Call Details Starting Grant (StG), PE3, ERC-2010-StG_20091028
Summary Active control of the optical properties of materials represents one of the most fundamental aspects of photonics. It is crucial to deepen our understanding on light-matter interactions, and for the development of novel technologies. Of special importance is the interaction of light with metal surfaces, leading to surface plasmon polaritons (SPPs). SPPs can give rise to giant local field enhancements in subwavelength volumes. Thanks to recent developments in plasmonics, electromagnetic fields can nowadays be controlled in subwavelength volumes and on ultra-fast time scales. However, research has been limited to optical and near-IR frequencies. The lack of studies at lower frequencies originates from the weak confinement of SPPs at these frequencies. Our objective is to overcome these limitations, demonstrating for the first time ultra-fast control in subwavelength dimensions of plasmonic resonances at THz frequencies. In particular, we plan to control localized surface plasmon polaritons (LSPPs), arising from the coherent oscillation of charges in particles. For this purpose, we will fabricate semiconductor particles supporting LSPPs, which will be controlled optically at very low fluences. We will show that the spatial distribution of giant field enhancements can be tuned with unprecedented accuracy by demonstrating its optical switching by several orders of magnitude. Moreover, we will study for the first time the active coupling of plasmonic resonances in periodic arrays of semiconductor particles. These arrays will constitute the plasmonic analogue to phased array antennas. The project will open new horizons in fundamental research, as well as in applications such as THz modulators and sensors.
Summary
Active control of the optical properties of materials represents one of the most fundamental aspects of photonics. It is crucial to deepen our understanding on light-matter interactions, and for the development of novel technologies. Of special importance is the interaction of light with metal surfaces, leading to surface plasmon polaritons (SPPs). SPPs can give rise to giant local field enhancements in subwavelength volumes. Thanks to recent developments in plasmonics, electromagnetic fields can nowadays be controlled in subwavelength volumes and on ultra-fast time scales. However, research has been limited to optical and near-IR frequencies. The lack of studies at lower frequencies originates from the weak confinement of SPPs at these frequencies. Our objective is to overcome these limitations, demonstrating for the first time ultra-fast control in subwavelength dimensions of plasmonic resonances at THz frequencies. In particular, we plan to control localized surface plasmon polaritons (LSPPs), arising from the coherent oscillation of charges in particles. For this purpose, we will fabricate semiconductor particles supporting LSPPs, which will be controlled optically at very low fluences. We will show that the spatial distribution of giant field enhancements can be tuned with unprecedented accuracy by demonstrating its optical switching by several orders of magnitude. Moreover, we will study for the first time the active coupling of plasmonic resonances in periodic arrays of semiconductor particles. These arrays will constitute the plasmonic analogue to phased array antennas. The project will open new horizons in fundamental research, as well as in applications such as THz modulators and sensors.
Max ERC Funding
1 492 800 €
Duration
Start date: 2011-06-01, End date: 2016-05-31
Project acronym UNIJURIS
Project Unilateralism and the protection of global interests: opportunities and limits of the exercise of state jurisdiction
Researcher (PI) Cedric Marie Joseph Ryngaert
Host Institution (HI) UNIVERSITEIT UTRECHT
Country Netherlands
Call Details Starting Grant (StG), SH2, ERC-2013-StG
Summary "In the 20th century, states have increasingly sought to apply their laws to situations and persons beyond their borders. They typically did so to protect their own interests from harm spilling over their borders. Recently, however, states appear to be giving their laws ‘extraterritorial’ application to protect global interests, not only when prosecuting international criminals, but also by enacting emissions trading schemes to tackle global warming, by taking sanctions against foreign vessels involved in illegal fishing on the high seas docking in their port, and by fighting foreign corrupt practices with a view to furthering good governance in developing countries. Thus, it appears that a novel principle of jurisdiction is crystallizing that protects global interests through unilateral application of domestic (or regional) law. It is the aim of this research to study this development in-depth, and to examine in particular whether, and under what circumstances, international law countenances such an exercise of unilateral jurisdiction that is aimed at the protection of global interests.
The project consists of two pillars. Pillar 1 studies three cases of states or regional organizations unilaterally applying their own laws to (partly) foreign situations considered as threatening global interests: (a) the exercise of unilateral jurisdiction aimed at mitigating climate change; (b) the exercise of port state jurisdiction aimed at protecting sustainable fishing and biological diversity on the high seas; (c) the exercise of unilateral jurisdiction to tackle foreign corruption practices. Pillar 2 is synthetic in nature, and assesses whether, and to what extent, general rules of jurisdiction and jurisdictional restraint concerning the protection of global interests are developing across various fields, including but not limited to the fields studied in Pillar 1."
Summary
"In the 20th century, states have increasingly sought to apply their laws to situations and persons beyond their borders. They typically did so to protect their own interests from harm spilling over their borders. Recently, however, states appear to be giving their laws ‘extraterritorial’ application to protect global interests, not only when prosecuting international criminals, but also by enacting emissions trading schemes to tackle global warming, by taking sanctions against foreign vessels involved in illegal fishing on the high seas docking in their port, and by fighting foreign corrupt practices with a view to furthering good governance in developing countries. Thus, it appears that a novel principle of jurisdiction is crystallizing that protects global interests through unilateral application of domestic (or regional) law. It is the aim of this research to study this development in-depth, and to examine in particular whether, and under what circumstances, international law countenances such an exercise of unilateral jurisdiction that is aimed at the protection of global interests.
The project consists of two pillars. Pillar 1 studies three cases of states or regional organizations unilaterally applying their own laws to (partly) foreign situations considered as threatening global interests: (a) the exercise of unilateral jurisdiction aimed at mitigating climate change; (b) the exercise of port state jurisdiction aimed at protecting sustainable fishing and biological diversity on the high seas; (c) the exercise of unilateral jurisdiction to tackle foreign corruption practices. Pillar 2 is synthetic in nature, and assesses whether, and to what extent, general rules of jurisdiction and jurisdictional restraint concerning the protection of global interests are developing across various fields, including but not limited to the fields studied in Pillar 1."
Max ERC Funding
1 341 529 €
Duration
Start date: 2013-11-01, End date: 2018-10-31
Project acronym USED
Project Ultrafast Spectroscopic Electron Diffraction (USED) of quantum solids and thin films
Researcher (PI) Fabrizio Carbone
Host Institution (HI) ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Country Switzerland
Call Details Starting Grant (StG), PE3, ERC-2010-StG_20091028
Summary Ultrafast Spectroscopic Electron Diffraction (USED) of quantum solids and thin films
Summary
Ultrafast Spectroscopic Electron Diffraction (USED) of quantum solids and thin films
Max ERC Funding
1 464 000 €
Duration
Start date: 2010-11-01, End date: 2015-10-31
Project acronym WALK AGAIN
Project Multi-pronged Strategies to Regain Voluntary Motor Functions after Spinal Cord Injury
Researcher (PI) Gregoire Richard Courtine
Host Institution (HI) ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Country Switzerland
Call Details Starting Grant (StG), LS5, ERC-2010-StG_20091118
Summary Severe spinal cord injury (SCI) permanently abolishes motor functions caudal to the lesion. Various strategies have been
pursued to promote functional recovery after such injuries. However, none of these attempts were able to return voluntary
movements in paralyzed subjects. Here, we propose an innovative transdisciplinary research program including parallel
approaches that will converge into an integrated multi-pronged therapy able to restore voluntary movements after paralyzing
SCI. To achieve this goal, we will capitalize on our recent breakthroughs that demonstrate the impressive capacity of
pharmacological and electrical spinal cord stimulations to promote full weight bearing walking in paralyzed rats when
combined with rehabilitation. In Walk Again, we will improve high level control of spinal circuits with synergistic combinations
of pharmacological agents, and with the design of multisite stimulation strategies using electrode arrays. Functional electrical
stimulation of muscles will provide complementary low level tuning capacities to adjust limb motion. To allow voluntary control,
we will establish a new line of research and pioneer brain-spinal interfaces by which cortical modulations will directly adjust
stimulations of spinal circuits and muscles. In the final stages, we will enable neurorehabilitation with this cortico-spinal
neuroprosthesis in the presence of anti-NogoA regenerative therapy. The underlying objective is to devise a fully-operative
neuroprosthetic system that will enable self-driven rehabilitation in a permissive plastic environment. Walk Again will fertilize
frontier research with pioneer ideas that will increase European competitiveness while paving the way toward viable clinical
applications to restore function in paralyzed individuals.
Summary
Severe spinal cord injury (SCI) permanently abolishes motor functions caudal to the lesion. Various strategies have been
pursued to promote functional recovery after such injuries. However, none of these attempts were able to return voluntary
movements in paralyzed subjects. Here, we propose an innovative transdisciplinary research program including parallel
approaches that will converge into an integrated multi-pronged therapy able to restore voluntary movements after paralyzing
SCI. To achieve this goal, we will capitalize on our recent breakthroughs that demonstrate the impressive capacity of
pharmacological and electrical spinal cord stimulations to promote full weight bearing walking in paralyzed rats when
combined with rehabilitation. In Walk Again, we will improve high level control of spinal circuits with synergistic combinations
of pharmacological agents, and with the design of multisite stimulation strategies using electrode arrays. Functional electrical
stimulation of muscles will provide complementary low level tuning capacities to adjust limb motion. To allow voluntary control,
we will establish a new line of research and pioneer brain-spinal interfaces by which cortical modulations will directly adjust
stimulations of spinal circuits and muscles. In the final stages, we will enable neurorehabilitation with this cortico-spinal
neuroprosthesis in the presence of anti-NogoA regenerative therapy. The underlying objective is to devise a fully-operative
neuroprosthetic system that will enable self-driven rehabilitation in a permissive plastic environment. Walk Again will fertilize
frontier research with pioneer ideas that will increase European competitiveness while paving the way toward viable clinical
applications to restore function in paralyzed individuals.
Max ERC Funding
1 395 540 €
Duration
Start date: 2010-12-01, End date: 2015-11-30
Project acronym WAROFWORDS
Project A War of Words: What Ancient Manchurian History Does to Korea and China Today
Researcher (PI) Remco Breuker
Host Institution (HI) UNIVERSITEIT LEIDEN
Country Netherlands
Call Details Starting Grant (StG), SH6, ERC-2013-StG
Summary The past is not past. Ancient history can influence the present day, affecting diplomatic and economic ties between states, and galvanizing public discourse and cultural expression. Since 2003, South Korea and China have been embroiled in a territorial dispute - over ancient states that ceased to exist as such over a millennium ago, in then Manchuria. Both sides have invested hundreds of millions of dollars in establishing the legitimacy of their claims, subsidizing academic research and publicity campaigns. Strategically positioned in the middle lies North Korea, its roots extending deeply into Manchurian history, and the object of Chinese strategic interests. The confrontation has appealed to the popular imagination in both countries. Amateur historians, artists, and film makers have voiced their opinions in writing, art, movies, and TV, in traditional and new (online) media. Why does the past elicit this intense activity in the present? What does the past mean for the present, and what does it do to it?
A WAR OF WORDS will engage this complex of Chinese claims to Manchu-Korean ancient history, South Korean reactions, public discourse and cultural expression in both states, and the role of North Korea. It will approach these issues from an interdisciplinary angle, as an interconnected whole of contemporary national interests, strategic visions for the future of Northeast Asia, revisionist ancient history, and notions of national identity. It will critically review historiography of Manchuria through the ages; chart policy-driven uses and abuses of history in academia and the public domain in the Koreas and China; and complement and challenge habitual IR and security studies perspectives on Northeast Asia, particularly North Korea, by foregrounding ancient Manchurian history and its politico-socio-cultural manifestations in the present. As such, it will radically alter our understanding of a region of tremendous geopolitical, economic, and cultural importance.
Summary
The past is not past. Ancient history can influence the present day, affecting diplomatic and economic ties between states, and galvanizing public discourse and cultural expression. Since 2003, South Korea and China have been embroiled in a territorial dispute - over ancient states that ceased to exist as such over a millennium ago, in then Manchuria. Both sides have invested hundreds of millions of dollars in establishing the legitimacy of their claims, subsidizing academic research and publicity campaigns. Strategically positioned in the middle lies North Korea, its roots extending deeply into Manchurian history, and the object of Chinese strategic interests. The confrontation has appealed to the popular imagination in both countries. Amateur historians, artists, and film makers have voiced their opinions in writing, art, movies, and TV, in traditional and new (online) media. Why does the past elicit this intense activity in the present? What does the past mean for the present, and what does it do to it?
A WAR OF WORDS will engage this complex of Chinese claims to Manchu-Korean ancient history, South Korean reactions, public discourse and cultural expression in both states, and the role of North Korea. It will approach these issues from an interdisciplinary angle, as an interconnected whole of contemporary national interests, strategic visions for the future of Northeast Asia, revisionist ancient history, and notions of national identity. It will critically review historiography of Manchuria through the ages; chart policy-driven uses and abuses of history in academia and the public domain in the Koreas and China; and complement and challenge habitual IR and security studies perspectives on Northeast Asia, particularly North Korea, by foregrounding ancient Manchurian history and its politico-socio-cultural manifestations in the present. As such, it will radically alter our understanding of a region of tremendous geopolitical, economic, and cultural importance.
Max ERC Funding
1 499 955 €
Duration
Start date: 2013-10-01, End date: 2018-09-30