Project acronym AAATSI
Project Advanced Antenna Architecture for THZ Sensing Instruments
Researcher (PI) Andrea Neto
Host Institution (HI) TECHNISCHE UNIVERSITEIT DELFT
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary The Tera-Hertz portion of the spectrum presents unique potentials for advanced applications. Currently the THz spectrum is revealing the mechanisms at the origin of our universe and provides the means to monitor the health of our planet via satellite based sensing of critical gases. Potentially time domain sensing of the THz spectrum will be the ideal tool for a vast variety of medical and security applications.
Presently, systems in the THz regime are extremely expensive and consequently the THz spectrum is still the domain of only niche (expensive) scientific applications. The main problems are the lack of power and sensitivity. The wide unused THz spectral bandwidth is, herself, the only widely available resource that in the future can compensate for these problems. But, so far, when scientists try to really use the bandwidth, they run into an insurmountable physical limit: antenna dispersion. Antenna dispersion modifies the signal’s spectrum in a wavelength dependent manner in all types of radiation, but is particularly deleterious to THz signals because the spectrum is too wide and with foreseeable technology it cannot be digitized.
The goal of this proposal is to introduce break-through antenna technology that will eliminate the dispersion bottle neck and revolutionize Time Domain sensing and Spectroscopic Space Science. Achieving these goals the project will pole vault THz imaging technology into the 21-th century and develop critically important enabling technologies which will satisfy the electrical engineering needs of the next 30 years and in the long run will enable multi Tera-bit wireless communications.
In order to achieve these goals, I will first build upon two major breakthrough radiation mechanisms that I pioneered: Leaky Lenses and Connected Arrays. Eventually, ultra wide band imaging arrays constituted by thousands of components will be designed on the bases of the new theoretical findings and demonstrated.
Summary
The Tera-Hertz portion of the spectrum presents unique potentials for advanced applications. Currently the THz spectrum is revealing the mechanisms at the origin of our universe and provides the means to monitor the health of our planet via satellite based sensing of critical gases. Potentially time domain sensing of the THz spectrum will be the ideal tool for a vast variety of medical and security applications.
Presently, systems in the THz regime are extremely expensive and consequently the THz spectrum is still the domain of only niche (expensive) scientific applications. The main problems are the lack of power and sensitivity. The wide unused THz spectral bandwidth is, herself, the only widely available resource that in the future can compensate for these problems. But, so far, when scientists try to really use the bandwidth, they run into an insurmountable physical limit: antenna dispersion. Antenna dispersion modifies the signal’s spectrum in a wavelength dependent manner in all types of radiation, but is particularly deleterious to THz signals because the spectrum is too wide and with foreseeable technology it cannot be digitized.
The goal of this proposal is to introduce break-through antenna technology that will eliminate the dispersion bottle neck and revolutionize Time Domain sensing and Spectroscopic Space Science. Achieving these goals the project will pole vault THz imaging technology into the 21-th century and develop critically important enabling technologies which will satisfy the electrical engineering needs of the next 30 years and in the long run will enable multi Tera-bit wireless communications.
In order to achieve these goals, I will first build upon two major breakthrough radiation mechanisms that I pioneered: Leaky Lenses and Connected Arrays. Eventually, ultra wide band imaging arrays constituted by thousands of components will be designed on the bases of the new theoretical findings and demonstrated.
Max ERC Funding
1 499 487 €
Duration
Start date: 2011-11-01, End date: 2017-10-31
Project acronym ABATSYNAPSE
Project Evolution of Alzheimer’s Disease: From dynamics of single synapses to memory loss
Researcher (PI) Inna Slutsky
Host Institution (HI) TEL AVIV UNIVERSITY
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary A persistent challenge in unravelling mechanisms that regulate memory function is how to bridge the gap between inter-molecular dynamics of single proteins, activity of individual synapses and emerging properties of neuronal circuits. The prototype condition of disintegrating neuronal circuits is Alzheimer’s Disease (AD). Since the early time of Alois Alzheimer at the turn of the 20th century, scientists have been searching for a molecular entity that is in the roots of the cognitive deficits. Although diverse lines of evidence suggest that the amyloid-beta peptide (Abeta) plays a central role in synaptic dysfunctions of AD, several key questions remain unresolved. First, endogenous Abeta peptides are secreted by neurons throughout life, but their physiological functions are largely unknown. Second, experience-dependent physiological mechanisms that initiate the changes in Abeta composition in sporadic, the most frequent form of AD, are unidentified. And finally, molecular mechanisms that trigger Abeta-induced synaptic failure and memory decline remain elusive.
To target these questions, I propose to develop an integrative approach to correlate structure and function at the level of single synapses in hippocampal circuits. State-of-the-art techniques will enable the simultaneous real-time visualization of inter-molecular dynamics within signalling complexes and functional synaptic modifications. Utilizing FRET spectroscopy, high-resolution optical imaging, electrophysiology, molecular biology and biochemistry we will determine the casual relationship between ongoing neuronal activity, temporo-spatial dynamics and molecular composition of Abeta, structural rearrangements within the Abeta signalling complexes and plasticity of single synapses and whole networks. The proposed research will elucidate fundamental principles of neuronal circuits function and identify critical steps that initiate primary synaptic dysfunctions at the very early stages of sporadic AD.
Summary
A persistent challenge in unravelling mechanisms that regulate memory function is how to bridge the gap between inter-molecular dynamics of single proteins, activity of individual synapses and emerging properties of neuronal circuits. The prototype condition of disintegrating neuronal circuits is Alzheimer’s Disease (AD). Since the early time of Alois Alzheimer at the turn of the 20th century, scientists have been searching for a molecular entity that is in the roots of the cognitive deficits. Although diverse lines of evidence suggest that the amyloid-beta peptide (Abeta) plays a central role in synaptic dysfunctions of AD, several key questions remain unresolved. First, endogenous Abeta peptides are secreted by neurons throughout life, but their physiological functions are largely unknown. Second, experience-dependent physiological mechanisms that initiate the changes in Abeta composition in sporadic, the most frequent form of AD, are unidentified. And finally, molecular mechanisms that trigger Abeta-induced synaptic failure and memory decline remain elusive.
To target these questions, I propose to develop an integrative approach to correlate structure and function at the level of single synapses in hippocampal circuits. State-of-the-art techniques will enable the simultaneous real-time visualization of inter-molecular dynamics within signalling complexes and functional synaptic modifications. Utilizing FRET spectroscopy, high-resolution optical imaging, electrophysiology, molecular biology and biochemistry we will determine the casual relationship between ongoing neuronal activity, temporo-spatial dynamics and molecular composition of Abeta, structural rearrangements within the Abeta signalling complexes and plasticity of single synapses and whole networks. The proposed research will elucidate fundamental principles of neuronal circuits function and identify critical steps that initiate primary synaptic dysfunctions at the very early stages of sporadic AD.
Max ERC Funding
2 000 000 €
Duration
Start date: 2011-12-01, End date: 2017-09-30
Project acronym ADULT
Project Analysis of the Dark Universe through Lensing Tomography
Researcher (PI) Hendrik Hoekstra
Host Institution (HI) UNIVERSITEIT LEIDEN
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary The discoveries that the expansion of the universe is accelerating due to an unknown “dark energy”
and that most of the matter is invisible, highlight our lack of understanding of the major constituents
of the universe. These surprising findings set the stage for research in cosmology at the start of the
21st century. The objective of this proposal is to advance observational constraints to a level where we can distinguish between physical mechanisms that aim to explain the properties of dark energy and the observed distribution of dark matter throughout the universe. We use a relatively new technique called weak gravitational lensing: the accurate measurement of correlations in the orientations of distant galaxies enables us to map the dark matter distribution directly and to extract the cosmological information that is encoded by the large-scale structure.
To study the dark universe we will analyse data from a new state-of-the-art imaging survey: the Kilo-
Degree Survey (KiDS) will cover 1500 square degrees in 9 filters. The combination of its large survey
area and the availability of exquisite photometric redshifts for the sources makes KiDS the first
project that can place interesting constraints on the dark energy equation-of-state using lensing data
alone. Combined with complementary results from Planck, our measurements will provide one of the
best views of the dark side of the universe before much larger space-based projects commence.
To reach the desired accuracy we need to carefully measure the shapes of distant background galaxies. We also need to account for any intrinsic alignments that arise due to tidal interactions, rather than through lensing. Reducing these observational and physical biases to negligible levels is a necessarystep to ensure the success of KiDS and an important part of our preparation for more challenging projects such as the European-led space mission Euclid.
Summary
The discoveries that the expansion of the universe is accelerating due to an unknown “dark energy”
and that most of the matter is invisible, highlight our lack of understanding of the major constituents
of the universe. These surprising findings set the stage for research in cosmology at the start of the
21st century. The objective of this proposal is to advance observational constraints to a level where we can distinguish between physical mechanisms that aim to explain the properties of dark energy and the observed distribution of dark matter throughout the universe. We use a relatively new technique called weak gravitational lensing: the accurate measurement of correlations in the orientations of distant galaxies enables us to map the dark matter distribution directly and to extract the cosmological information that is encoded by the large-scale structure.
To study the dark universe we will analyse data from a new state-of-the-art imaging survey: the Kilo-
Degree Survey (KiDS) will cover 1500 square degrees in 9 filters. The combination of its large survey
area and the availability of exquisite photometric redshifts for the sources makes KiDS the first
project that can place interesting constraints on the dark energy equation-of-state using lensing data
alone. Combined with complementary results from Planck, our measurements will provide one of the
best views of the dark side of the universe before much larger space-based projects commence.
To reach the desired accuracy we need to carefully measure the shapes of distant background galaxies. We also need to account for any intrinsic alignments that arise due to tidal interactions, rather than through lensing. Reducing these observational and physical biases to negligible levels is a necessarystep to ensure the success of KiDS and an important part of our preparation for more challenging projects such as the European-led space mission Euclid.
Max ERC Funding
1 316 880 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym AstroFunc
Project Molecular Studies of Astrocyte Function in Health and Disease
Researcher (PI) Matthew Guy Holt
Host Institution (HI) VIB
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Brain consists of two basic cell types – neurons and glia. However, the study of glia in brain function has traditionally been neglected in favor of their more “illustrious” counter-parts – neurons that are classed as the computational units of the brain. Glia have usually been classed as “brain glue” - a supportive matrix on which neurons grow and function. However, recent evidence suggests that glia are more than passive “glue” and actually modulate neuronal function. This has lead to the proposal of a “tripartite synapse”, which recognizes pre- and postsynaptic neuronal elements and glia as a unit.
However, what is still lacking is rudimentary information on how these cells actually function in situ. Here we propose taking a “bottom-up” approach, by identifying the molecules (and interactions) that control glial function in situ. This is complicated by the fact that glia show profound changes when placed into culture. To circumvent this, we will use recently developed cell sorting techniques, to rapidly isolate genetically marked glial cells from brain – which can then be analyzed using advanced biochemical and physiological techniques. The long-term aim is to identify proteins that can be “tagged” using transgenic technologies to allow protein function to be studied in real-time in vivo, using sophisticated imaging techniques. Given the number of proteins that may be identified we envisage developing new methods of generating transgenic animals that provide an attractive alternative to current “state-of-the art” technology.
The importance of studying glial function is given by the fact that every major brain pathology shows reactive gliosis. In the time it takes to read this abstract, 5 people in the EU will have suffered a stroke – not to mention those who suffer other forms of neurotrauma. Thus, understanding glial function is not only critical to understanding normal brain function, but also for relieving the burden of severe neurological injury and disease
Summary
Brain consists of two basic cell types – neurons and glia. However, the study of glia in brain function has traditionally been neglected in favor of their more “illustrious” counter-parts – neurons that are classed as the computational units of the brain. Glia have usually been classed as “brain glue” - a supportive matrix on which neurons grow and function. However, recent evidence suggests that glia are more than passive “glue” and actually modulate neuronal function. This has lead to the proposal of a “tripartite synapse”, which recognizes pre- and postsynaptic neuronal elements and glia as a unit.
However, what is still lacking is rudimentary information on how these cells actually function in situ. Here we propose taking a “bottom-up” approach, by identifying the molecules (and interactions) that control glial function in situ. This is complicated by the fact that glia show profound changes when placed into culture. To circumvent this, we will use recently developed cell sorting techniques, to rapidly isolate genetically marked glial cells from brain – which can then be analyzed using advanced biochemical and physiological techniques. The long-term aim is to identify proteins that can be “tagged” using transgenic technologies to allow protein function to be studied in real-time in vivo, using sophisticated imaging techniques. Given the number of proteins that may be identified we envisage developing new methods of generating transgenic animals that provide an attractive alternative to current “state-of-the art” technology.
The importance of studying glial function is given by the fact that every major brain pathology shows reactive gliosis. In the time it takes to read this abstract, 5 people in the EU will have suffered a stroke – not to mention those who suffer other forms of neurotrauma. Thus, understanding glial function is not only critical to understanding normal brain function, but also for relieving the burden of severe neurological injury and disease
Max ERC Funding
1 490 168 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym Beacon
Project Beacons in the Dark
Researcher (PI) Paulo César Carvalho Freire
Host Institution (HI) MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary BEACON aims at performing an ambitious multi-disciplinary (optical, radio astronomy and theoretical physics) study to enable a fundamentally improved understanding of gravitation and space-time. For almost a century Einstein's general relativity has been the last word on gravity. However, superstring theory predicts new gravitational phenomena beyond relativity. In this proposal I will attempt to detect these new phenomena, with a sensitivity 20 times better than state-of-the-art attempts. A successful detection would take physics beyond its current understanding of the Universe.
These new gravitational phenomena are emission of dipolar gravitational waves and the violation of the strong equivalence principle (SEP). I plan to look for them by timing newly discovered binary pulsars. I will improve upon the best current limits on dipolar gravitational wave emission by a factor of 20 within the time of this proposal. I also plan to develop a test of the Strong Equivalence Principle using a new pulsar/main-sequence star binary. The precision of this test is likely to surpass the current best limits within the time frame of this proposal and then keep improving indefinitely with time. This happens because this is the cleanest gravitational experiment ever carried out.
In order to further these goals, I plan to build the ultimate pulsar observing system. By taking advantage of recent technological advances in microwave engineering (particularly sensitive ultra-wide band receivers) digital electronics (fast analogue-to-digital converters and digital spectrometers) and computing, my team and me will be able to greatly improve the sensitivity and precision for pulsar timing experiments and exploit the capabilities of modern radio telescopes to their limits.
Pulsars are the beacons that will guide me in these new, uncharted seas.
Summary
BEACON aims at performing an ambitious multi-disciplinary (optical, radio astronomy and theoretical physics) study to enable a fundamentally improved understanding of gravitation and space-time. For almost a century Einstein's general relativity has been the last word on gravity. However, superstring theory predicts new gravitational phenomena beyond relativity. In this proposal I will attempt to detect these new phenomena, with a sensitivity 20 times better than state-of-the-art attempts. A successful detection would take physics beyond its current understanding of the Universe.
These new gravitational phenomena are emission of dipolar gravitational waves and the violation of the strong equivalence principle (SEP). I plan to look for them by timing newly discovered binary pulsars. I will improve upon the best current limits on dipolar gravitational wave emission by a factor of 20 within the time of this proposal. I also plan to develop a test of the Strong Equivalence Principle using a new pulsar/main-sequence star binary. The precision of this test is likely to surpass the current best limits within the time frame of this proposal and then keep improving indefinitely with time. This happens because this is the cleanest gravitational experiment ever carried out.
In order to further these goals, I plan to build the ultimate pulsar observing system. By taking advantage of recent technological advances in microwave engineering (particularly sensitive ultra-wide band receivers) digital electronics (fast analogue-to-digital converters and digital spectrometers) and computing, my team and me will be able to greatly improve the sensitivity and precision for pulsar timing experiments and exploit the capabilities of modern radio telescopes to their limits.
Pulsars are the beacons that will guide me in these new, uncharted seas.
Max ERC Funding
1 892 376 €
Duration
Start date: 2011-09-01, End date: 2016-08-31
Project acronym BRAINSIGNALS
Project Optical dissection of circuits underlying fast cholinergic signalling during cognitive behaviour
Researcher (PI) Huibert Mansvelder
Host Institution (HI) STICHTING VU
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Our ability to think, to memorize and focus our thoughts depends on acetylcholine signaling in the brain. The loss of cholinergic signalling in for instance Alzheimer’s disease strongly compromises these cognitive abilities. The traditional view on the role of cholinergic input to the neocortex is that slowly changing levels of extracellular acetylcholine (ACh) mediate different arousal states. This view has been challenged by recent studies demonstrating that rapid phasic changes in ACh levels at the scale of seconds are correlated with focus of attention, suggesting that these signals may mediate defined cognitive operations. Despite a wealth of anatomical data on the organization of the cholinergic system, very little understanding exists on its functional organization. How the relatively sparse input of cholinergic transmission in the prefrontal cortex elicits such a profound and specific control over attention is unknown. The main objective of this proposal is to develop a causal understanding of how cellular mechanisms of fast acetylcholine signalling are orchestrated during cognitive behaviour.
In a series of studies, I have identified several synaptic and cellular mechanisms by which the cholinergic system can alter neuronal circuitry function, both in cortical and subcortical areas. I have used a combination of behavioral, physiological and genetic methods in which I manipulated cholinergic receptor functionality in prefrontal cortex in a subunit specific manner and found that ACh receptors in the prefrontal cortex control attention performance. Recent advances in optogenetic and electrochemical methods now allow to rapidly manipulate and measure acetylcholine levels in freely moving, behaving animals. Using these techniques, I aim to uncover which cholinergic neurons are involved in fast cholinergic signaling during cognition and uncover the underlying neuronal mechanisms that alter prefrontal cortical network function.
Summary
Our ability to think, to memorize and focus our thoughts depends on acetylcholine signaling in the brain. The loss of cholinergic signalling in for instance Alzheimer’s disease strongly compromises these cognitive abilities. The traditional view on the role of cholinergic input to the neocortex is that slowly changing levels of extracellular acetylcholine (ACh) mediate different arousal states. This view has been challenged by recent studies demonstrating that rapid phasic changes in ACh levels at the scale of seconds are correlated with focus of attention, suggesting that these signals may mediate defined cognitive operations. Despite a wealth of anatomical data on the organization of the cholinergic system, very little understanding exists on its functional organization. How the relatively sparse input of cholinergic transmission in the prefrontal cortex elicits such a profound and specific control over attention is unknown. The main objective of this proposal is to develop a causal understanding of how cellular mechanisms of fast acetylcholine signalling are orchestrated during cognitive behaviour.
In a series of studies, I have identified several synaptic and cellular mechanisms by which the cholinergic system can alter neuronal circuitry function, both in cortical and subcortical areas. I have used a combination of behavioral, physiological and genetic methods in which I manipulated cholinergic receptor functionality in prefrontal cortex in a subunit specific manner and found that ACh receptors in the prefrontal cortex control attention performance. Recent advances in optogenetic and electrochemical methods now allow to rapidly manipulate and measure acetylcholine levels in freely moving, behaving animals. Using these techniques, I aim to uncover which cholinergic neurons are involved in fast cholinergic signaling during cognition and uncover the underlying neuronal mechanisms that alter prefrontal cortical network function.
Max ERC Funding
1 499 242 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym CEIDNFSTTAIS
Project Controlling excitability in developing neurons: from synapses to the axon initial segment
Researcher (PI) Juan Burrone
Host Institution (HI) KING'S COLLEGE LONDON
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary A critical question in neuroscience is to understand how neurons wire up to form a functional network. During the wiring of the brain it is important to establish mechanisms that act as safeguards to control and stabilize neuronal excitability in the face of large, chronic changes in neuronal or network activity. This is especially true for developing systems that undergo rapid and large scale forms of plasticity, which could easily lead to large imbalances in activity. If left unchecked, they could lead the network to its extremes: a complete loss of signal or epileptic-like activity. For this reason neurons employ different strategies to maintain their excitability within reasonable bounds. This proposal will focus on two crucial sites for neuronal information processing and integration: the synapse and the axon initial segment (AIS). Both sites undergo important structural and functional rearrangements in response to chronic activity changes, thus controlling the input-output function of a neuron and allowing the network to function efficiently. This proposal will explore novel forms of plasticity that occur during development and which are key to establishing a functional network. They range from understanding the role of activity during synapse formation to how pre- and postsynaptic structure and function become matched during development. Finally, it tackles a novel form of plasticity that lies downstream of synaptic inputs and is responsible for setting the threshold of action potential firing: the axon initial segment. Here, chronic changes in network activity results in a physical relocation of the AIS along the axon, which in turn alters the excitability of the neuron. This proposal will focus on the central issue of how a neuron alters both its input (synapses) and output (AIS) during development to maintain its activity levels within a set range and allow a functional network to form.
Summary
A critical question in neuroscience is to understand how neurons wire up to form a functional network. During the wiring of the brain it is important to establish mechanisms that act as safeguards to control and stabilize neuronal excitability in the face of large, chronic changes in neuronal or network activity. This is especially true for developing systems that undergo rapid and large scale forms of plasticity, which could easily lead to large imbalances in activity. If left unchecked, they could lead the network to its extremes: a complete loss of signal or epileptic-like activity. For this reason neurons employ different strategies to maintain their excitability within reasonable bounds. This proposal will focus on two crucial sites for neuronal information processing and integration: the synapse and the axon initial segment (AIS). Both sites undergo important structural and functional rearrangements in response to chronic activity changes, thus controlling the input-output function of a neuron and allowing the network to function efficiently. This proposal will explore novel forms of plasticity that occur during development and which are key to establishing a functional network. They range from understanding the role of activity during synapse formation to how pre- and postsynaptic structure and function become matched during development. Finally, it tackles a novel form of plasticity that lies downstream of synaptic inputs and is responsible for setting the threshold of action potential firing: the axon initial segment. Here, chronic changes in network activity results in a physical relocation of the AIS along the axon, which in turn alters the excitability of the neuron. This proposal will focus on the central issue of how a neuron alters both its input (synapses) and output (AIS) during development to maintain its activity levels within a set range and allow a functional network to form.
Max ERC Funding
1 500 000 €
Duration
Start date: 2012-03-01, End date: 2017-02-28
Project acronym CHAOSNETS
Project "Building Scalable, Secure, and Reliable ""Chaotic"" Wireless Networks"
Researcher (PI) Kyle Andrew Stuart Jamieson
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary As a result of their unplanned, license-free nature, WiFi networks have grown quickly in recent years, giving users unprecedented improvements in wireless access to the Internet. But being “chaotic,” i.e. unplanned, they have grown to be victims of their own success: when eager users set up too many wireless access points in a densely-populated area, the resulting noise and interference hurt everyones throughput and connectivity. Cellular mobile telephone networks are planned carefully, but in order to expand coverage indoors, providers are turning to customer-deployed femtocells, thus incuring the drawbacks of chaotic WiFi networks. We propose a ground-up redesign of chaotic wireless networks, with new architectural contributions focusing on what information the physical layer should pass up to higher layers. We propose a new physical layer interface called SoftAoA that passes angle-of-arrival (AoA) information from the physical layer up to higher layers. Using this expanded physical layer interface, we will first investigate fountain coding and receiver-based rate adaptation methods to improve wireless capacity in the vagaries of the “grey zone” of marginal coverage. Second, we will investigate improvements to security and localization that can be made based on the profiling of incoming packets’ AoA at an access point. Finally, we will investigate how a chaotically-deployed network can mitigate the interference it experiences from networks not under the same administrative control, and manage the interference it causes to those networks. The result will be more scalable, secure, and reliable chaotic wireless networks that play an even more prominent role in our lives.
Summary
As a result of their unplanned, license-free nature, WiFi networks have grown quickly in recent years, giving users unprecedented improvements in wireless access to the Internet. But being “chaotic,” i.e. unplanned, they have grown to be victims of their own success: when eager users set up too many wireless access points in a densely-populated area, the resulting noise and interference hurt everyones throughput and connectivity. Cellular mobile telephone networks are planned carefully, but in order to expand coverage indoors, providers are turning to customer-deployed femtocells, thus incuring the drawbacks of chaotic WiFi networks. We propose a ground-up redesign of chaotic wireless networks, with new architectural contributions focusing on what information the physical layer should pass up to higher layers. We propose a new physical layer interface called SoftAoA that passes angle-of-arrival (AoA) information from the physical layer up to higher layers. Using this expanded physical layer interface, we will first investigate fountain coding and receiver-based rate adaptation methods to improve wireless capacity in the vagaries of the “grey zone” of marginal coverage. Second, we will investigate improvements to security and localization that can be made based on the profiling of incoming packets’ AoA at an access point. Finally, we will investigate how a chaotically-deployed network can mitigate the interference it experiences from networks not under the same administrative control, and manage the interference it causes to those networks. The result will be more scalable, secure, and reliable chaotic wireless networks that play an even more prominent role in our lives.
Max ERC Funding
1 457 675 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym COLDNANO
Project UltraCOLD ion and electron beams for NANOscience
Researcher (PI) Daniel Comparat
Host Institution (HI) CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary COLDNANO (UltraCOLD ion and electron beams for NANOscience), aspires to build novel ion and electron sources with superior performance in terms of brightness, energy spread and minimum achievable spot size. Such monochromatic, spatially focused and well controlled electron and ion beams are expected to open many research possibilities in material sciences, in surface investigations (imaging, lithography) and in semiconductor diagnostics. The proposed project intends to develop sources with the best beam quality ever produced and to assess them in some advanced surface science research domains. Laterally, I will develop expertise exchange with one Small and Medium Enterprise who will exploit industrial prototypes.
The novel concept is to create ion and electron sources using advanced laser cooling techniques combined with the particular ionization properties of cold atoms. It would then be first time that “laser cooling” would lead to a real industrial development.
A cesium magneto-optical trap will first be used. The atoms will then be excited by lasers and ionized in order to provide the electron source. The specific extraction optics for the electrons will be developed. This source will be compact and portable to be used for several applications such as Low Energy Electron Microscopy, functionalization of semi-conducting surfaces or high resolution Electron Energy Loss Spectrometry by coupling to a Scanning Transmission Electron Microscope.
Based on the knowledge developed with the first experiment, a second ambitious xenon dual ion and electron beam machine will then be realized and used to study the scattering of ion and electron at low energy.
Finally, I present a very innovative scheme to control the time, position and velocity of individual particles in the beams. Such a machine providing ions or electrons on demand would open the way for the “ultimate” resolution in time and space for surface analysis, lithography, microscopy or implantation.
Summary
COLDNANO (UltraCOLD ion and electron beams for NANOscience), aspires to build novel ion and electron sources with superior performance in terms of brightness, energy spread and minimum achievable spot size. Such monochromatic, spatially focused and well controlled electron and ion beams are expected to open many research possibilities in material sciences, in surface investigations (imaging, lithography) and in semiconductor diagnostics. The proposed project intends to develop sources with the best beam quality ever produced and to assess them in some advanced surface science research domains. Laterally, I will develop expertise exchange with one Small and Medium Enterprise who will exploit industrial prototypes.
The novel concept is to create ion and electron sources using advanced laser cooling techniques combined with the particular ionization properties of cold atoms. It would then be first time that “laser cooling” would lead to a real industrial development.
A cesium magneto-optical trap will first be used. The atoms will then be excited by lasers and ionized in order to provide the electron source. The specific extraction optics for the electrons will be developed. This source will be compact and portable to be used for several applications such as Low Energy Electron Microscopy, functionalization of semi-conducting surfaces or high resolution Electron Energy Loss Spectrometry by coupling to a Scanning Transmission Electron Microscope.
Based on the knowledge developed with the first experiment, a second ambitious xenon dual ion and electron beam machine will then be realized and used to study the scattering of ion and electron at low energy.
Finally, I present a very innovative scheme to control the time, position and velocity of individual particles in the beams. Such a machine providing ions or electrons on demand would open the way for the “ultimate” resolution in time and space for surface analysis, lithography, microscopy or implantation.
Max ERC Funding
1 944 000 €
Duration
Start date: 2012-02-01, End date: 2017-01-31
Project acronym CRISP
Project Towards compressive information processing systems
Researcher (PI) Enrico Magli
Host Institution (HI) POLITECNICO DI TORINO
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary This proposal targets the emerging frontier research field of compressive sampling (CS), and particularly its application in the framework of complex information processing systems, including several related innovative and unconventional aspects. Future systems will have to handle unprecedented amounts of information such as those generated in multiview video, medical and hyperspectral imaging applications, increasingly suffering from limited communication and computational resources. CS is a breakthrough technology that will have a profound impact on how these systems are conceived. It offers a viable and elegant solution, acquiring and representing an information signal through a small set of linear projections of it, allowing to dramatically reduce communication, storage and processing requirements, and is one of the topics that will dominate signal processing research in the next years. At the core of this research proposal is the concept of employing CS not only as a standalone tool, but inside an information processing system. The main challenge is to develop theory and algorithms that will allow to perform all signal manipulations typical of conventional systems directly on the linear measurements, as reconstructing the signal samples would be unfeasible due to excessive complexity. Such operations include compression, encryption, communication, reconstruction, signal analysis, information extraction and decision, and distributed signal processing, leading to a very multidisciplinary and technically challenging research agenda. Ultimately, our research aims at developing and demonstrating the fundamental tools that will fuel next-generation information processing systems with an order-of-magnitude better performance at a lower cost than today. Europe has several successful industries active in communications and signal processing. The future success of these sectors critically depends on the ability to innovate and integrate new technology.
Summary
This proposal targets the emerging frontier research field of compressive sampling (CS), and particularly its application in the framework of complex information processing systems, including several related innovative and unconventional aspects. Future systems will have to handle unprecedented amounts of information such as those generated in multiview video, medical and hyperspectral imaging applications, increasingly suffering from limited communication and computational resources. CS is a breakthrough technology that will have a profound impact on how these systems are conceived. It offers a viable and elegant solution, acquiring and representing an information signal through a small set of linear projections of it, allowing to dramatically reduce communication, storage and processing requirements, and is one of the topics that will dominate signal processing research in the next years. At the core of this research proposal is the concept of employing CS not only as a standalone tool, but inside an information processing system. The main challenge is to develop theory and algorithms that will allow to perform all signal manipulations typical of conventional systems directly on the linear measurements, as reconstructing the signal samples would be unfeasible due to excessive complexity. Such operations include compression, encryption, communication, reconstruction, signal analysis, information extraction and decision, and distributed signal processing, leading to a very multidisciplinary and technically challenging research agenda. Ultimately, our research aims at developing and demonstrating the fundamental tools that will fuel next-generation information processing systems with an order-of-magnitude better performance at a lower cost than today. Europe has several successful industries active in communications and signal processing. The future success of these sectors critically depends on the ability to innovate and integrate new technology.
Max ERC Funding
1 390 000 €
Duration
Start date: 2011-11-01, End date: 2017-06-30
Project acronym CU-ANGIO
Project Prostate cancer localization by contrast-ultrasound angiogenesis imaging
Researcher (PI) Massimo Mischi
Host Institution (HI) TECHNISCHE UNIVERSITEIT EINDHOVEN
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary Prostate cancer causes over 1/4 of new cancer cases and 1/10 of cancer deaths in western males. Efficient methods for early treatment are available. Many lives could therefore be saved by early cancer detection, but this is not viable due to the inadequacy of the available noninvasive diagnostics. Systematic biopsy is the only reliable detection technique, but it is hampered by high costs and causes serious discomfort and health risks because of its invasiveness. Moreover, precise cancer localization is not possible, impeding the use of available focal treatments.
This research will push the frontiers of prostate cancer diagnostics by a revolutionary method for localization of cancer angiogenesis (microvascular growth). Different from all methods for angiogenesis imaging, invariably based on the assessment of blood perfusion, I aim at quantifying the local dispersion dynamics of an intravascular tracer. Dispersion is the spreading process of the tracer within the vasculature, which I firmly believe to correlate much better than perfusion with microvascular architectures and, therefore, with cancer angiogenesis.
The assessment of local dispersion is challenging and will be pursued through an intravenous injection of an ultrasound contrast bolus and novel spatiotemporal analysis of the bolus passage through the prostate circulation, measured by three-dimensional ultrasound imaging.
If successful, the proposed method will represent a breakthrough for early noninvasive and accurate prostate cancer localization, precise focal treatment, and treatment follow-up, with strong potential for use for other types of cancers, such as breast cancer. Moreover, this method will facilitate further groundbreaking research in the therapeutic control of angiogenesis in several pathologies.
This exciting research builds on my multidisciplinary expertise in ultrasound contrast dilution methods and on consistent and successful collaborations with leading clinical and industrial partners.
Summary
Prostate cancer causes over 1/4 of new cancer cases and 1/10 of cancer deaths in western males. Efficient methods for early treatment are available. Many lives could therefore be saved by early cancer detection, but this is not viable due to the inadequacy of the available noninvasive diagnostics. Systematic biopsy is the only reliable detection technique, but it is hampered by high costs and causes serious discomfort and health risks because of its invasiveness. Moreover, precise cancer localization is not possible, impeding the use of available focal treatments.
This research will push the frontiers of prostate cancer diagnostics by a revolutionary method for localization of cancer angiogenesis (microvascular growth). Different from all methods for angiogenesis imaging, invariably based on the assessment of blood perfusion, I aim at quantifying the local dispersion dynamics of an intravascular tracer. Dispersion is the spreading process of the tracer within the vasculature, which I firmly believe to correlate much better than perfusion with microvascular architectures and, therefore, with cancer angiogenesis.
The assessment of local dispersion is challenging and will be pursued through an intravenous injection of an ultrasound contrast bolus and novel spatiotemporal analysis of the bolus passage through the prostate circulation, measured by three-dimensional ultrasound imaging.
If successful, the proposed method will represent a breakthrough for early noninvasive and accurate prostate cancer localization, precise focal treatment, and treatment follow-up, with strong potential for use for other types of cancers, such as breast cancer. Moreover, this method will facilitate further groundbreaking research in the therapeutic control of angiogenesis in several pathologies.
This exciting research builds on my multidisciplinary expertise in ultrasound contrast dilution methods and on consistent and successful collaborations with leading clinical and industrial partners.
Max ERC Funding
1 430 955 €
Duration
Start date: 2012-06-01, End date: 2018-05-31
Project acronym DEBRIS
Project Debris in extrasolar planetary systems
Researcher (PI) Mark Charles Wyatt
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary This proposal concerns the debris discs of nearby stars; ie, discs of asteroids, comets and dust. Such dust can be imaged, providing clues to the underlying planetary system. Debris images have already predicted planets later confirmed in direct imaging. Most debris lies in cold outer (~100AU) regions of planetary systems, but a growing number of stars have hot dust in regions where terrestrial planets are expected (few AU). This proposal aims learn about the planetary systems of nearby stars through study of their debris discs. Specific focus is on the frontier area of characterisation and modelling of dust within planetary systems, which is important for the design of missions to detect habitable planets, a high priority goal for the next decade. The PI has played a significant role in debris disc studies, and proposes to consolidate an independent research team in Cambridge. The proposal covers 3 studies supported by 3 PDRAs. Specific objectives are: 1) Debris disc observations: Carry out survey for cold debris around unbiased sample of nearest 500 stars with Herschel and SCUBA2. Follow-up bright discs with high resolution imaging using ALMA and JWST to characterise sub-structure from planets and search for dust at multiple radii. Pioneer survey for hot dust using polarisation and interferometry. 2) Debris disc modelling: Develop new model to follow the interplay between collisions, radiation pressure, P-R drag, sublimation, disintegration, and dynamical interactions with planets. Use model to consider nature of small particle halos, resonant ring structures formed by terrestrial planets, and level of cometary dust scattered into inner regions. 3) Debris disc origin: Demonstrate constraints placed on planet formation models through studies of dust from Earth-moon forming impacts, effect of planetesimals on late-stage planetary dynamics, population synthesis explaining planets and debris, constraints on primordial size and stirring of debris.
Summary
This proposal concerns the debris discs of nearby stars; ie, discs of asteroids, comets and dust. Such dust can be imaged, providing clues to the underlying planetary system. Debris images have already predicted planets later confirmed in direct imaging. Most debris lies in cold outer (~100AU) regions of planetary systems, but a growing number of stars have hot dust in regions where terrestrial planets are expected (few AU). This proposal aims learn about the planetary systems of nearby stars through study of their debris discs. Specific focus is on the frontier area of characterisation and modelling of dust within planetary systems, which is important for the design of missions to detect habitable planets, a high priority goal for the next decade. The PI has played a significant role in debris disc studies, and proposes to consolidate an independent research team in Cambridge. The proposal covers 3 studies supported by 3 PDRAs. Specific objectives are: 1) Debris disc observations: Carry out survey for cold debris around unbiased sample of nearest 500 stars with Herschel and SCUBA2. Follow-up bright discs with high resolution imaging using ALMA and JWST to characterise sub-structure from planets and search for dust at multiple radii. Pioneer survey for hot dust using polarisation and interferometry. 2) Debris disc modelling: Develop new model to follow the interplay between collisions, radiation pressure, P-R drag, sublimation, disintegration, and dynamical interactions with planets. Use model to consider nature of small particle halos, resonant ring structures formed by terrestrial planets, and level of cometary dust scattered into inner regions. 3) Debris disc origin: Demonstrate constraints placed on planet formation models through studies of dust from Earth-moon forming impacts, effect of planetesimals on late-stage planetary dynamics, population synthesis explaining planets and debris, constraints on primordial size and stirring of debris.
Max ERC Funding
1 497 920 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym DEVSPACE
Project The development of the hippocampal spatial representation system
Researcher (PI) Francesca Cacucci
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary This proposal will address how a multimodal cognitive system, the neural representation of space in the hippocampus, emerges during development. There is a long tradition in neuroscience of studying the development of primary sensory systems, but fewer studies have concentrated on the development of brain networks supporting higher-order cognitive representations.
Our recent findings (Wills, Cacucci et al. Science, 2010) provide a starting point to fill this gap, charting the emergence of spatial responses of hippocampal formation neurons, using in vivo recording in awake, behaving rats.
The hippocampal formation supports neural representations of the environment ('cognitive maps') by means of which an animal can locate itself and navigate to a goal location. It contains three classes of spatially-tuned cells: place cells, which code for location, head direction cells, which code for directional orientation and grid cells, which may code for distance travelled.
The key aim of this proposal is to delineate the developmental processes that create this neural representation of space, focusing on the representations of place and direction.
We will delineate which sensory information is capable of driving spatial firing, and whether early hippocampal coding is truly spatial in the sense of representing configurations of stimuli and not single cues. How are abstract spatial constructs (place and head direction) built from raw sensory information during development? We will test whether boundary sensitive neurons and angular velocity tuned neurons are the elemental 'building blocks' making up place and directional signals, as suggested by many theoretical models.
We will also investigate the role of experience in the construction of spatial representations. Do the network architectures underlying spatial firing emerge through experience-dependent learning mechanisms, or are they the result of self-organizing processes which take place independently of experience?
Summary
This proposal will address how a multimodal cognitive system, the neural representation of space in the hippocampus, emerges during development. There is a long tradition in neuroscience of studying the development of primary sensory systems, but fewer studies have concentrated on the development of brain networks supporting higher-order cognitive representations.
Our recent findings (Wills, Cacucci et al. Science, 2010) provide a starting point to fill this gap, charting the emergence of spatial responses of hippocampal formation neurons, using in vivo recording in awake, behaving rats.
The hippocampal formation supports neural representations of the environment ('cognitive maps') by means of which an animal can locate itself and navigate to a goal location. It contains three classes of spatially-tuned cells: place cells, which code for location, head direction cells, which code for directional orientation and grid cells, which may code for distance travelled.
The key aim of this proposal is to delineate the developmental processes that create this neural representation of space, focusing on the representations of place and direction.
We will delineate which sensory information is capable of driving spatial firing, and whether early hippocampal coding is truly spatial in the sense of representing configurations of stimuli and not single cues. How are abstract spatial constructs (place and head direction) built from raw sensory information during development? We will test whether boundary sensitive neurons and angular velocity tuned neurons are the elemental 'building blocks' making up place and directional signals, as suggested by many theoretical models.
We will also investigate the role of experience in the construction of spatial representations. Do the network architectures underlying spatial firing emerge through experience-dependent learning mechanisms, or are they the result of self-organizing processes which take place independently of experience?
Max ERC Funding
1 491 930 €
Duration
Start date: 2012-01-01, End date: 2017-12-31
Project acronym DIAL
Project Diamond Lasers: Revolutionising Laser Engineering
Researcher (PI) Alan John Kemp
Host Institution (HI) UNIVERSITY OF STRATHCLYDE
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary Over the last three years, synthetic single crystal diamond with high optical quality has become available for the first time. The time is thus ripe to exploit this unique material for laser engineering. Building on their pioneering work characterising, modelling and experimentally proving this material, this team will explore novel means to harness its the extraordinary properties – a thermal conductivity that is one to two orders of magnitude greater than conventional solid-state laser materials, an extremely high rigidity, excellent resistance to mechanical stress, a wide transparency window, and very good Raman gain properties. The thermal conductivity of diamond, in particular, has the potential to revolutionise solid-state laser design. To date, the design of a solid-state laser has largely been driven by the need to manage heat – the use of diamond can remove this requirement leading to simpler and more compact designs for high performance lasers. This programme will focus on introducing laser gain to structures based on novel high optical quality diamond. Four principal approaches will be examined:
1. Developing high thermal conductivity hybrid structures by sandwiching thin slices of laser gain material between layers of diamond.
2. Using the high Raman gain in diamond to develop high performance diamond Raman lasers
3. Exploiting optically efficient, room-temperature colour centres in diamond to develop a revolutionary suite of broadly tuneable and ultrafast visible lasers.
4. Exploring the direct doping of diamond with laser ions, building on the rapid recent progress in diamond synthesis.
Encompassing laser physics, materials science and device engineering, this programme will balance risk and reward to help position Europe as the world-leader in laser engineering. The lasers developed will be important tools in vital sectors such as science (e.g. biological imaging), energy (e.g. wind speed sensing) and medicine (e.g. treating vascular lesions).
Summary
Over the last three years, synthetic single crystal diamond with high optical quality has become available for the first time. The time is thus ripe to exploit this unique material for laser engineering. Building on their pioneering work characterising, modelling and experimentally proving this material, this team will explore novel means to harness its the extraordinary properties – a thermal conductivity that is one to two orders of magnitude greater than conventional solid-state laser materials, an extremely high rigidity, excellent resistance to mechanical stress, a wide transparency window, and very good Raman gain properties. The thermal conductivity of diamond, in particular, has the potential to revolutionise solid-state laser design. To date, the design of a solid-state laser has largely been driven by the need to manage heat – the use of diamond can remove this requirement leading to simpler and more compact designs for high performance lasers. This programme will focus on introducing laser gain to structures based on novel high optical quality diamond. Four principal approaches will be examined:
1. Developing high thermal conductivity hybrid structures by sandwiching thin slices of laser gain material between layers of diamond.
2. Using the high Raman gain in diamond to develop high performance diamond Raman lasers
3. Exploiting optically efficient, room-temperature colour centres in diamond to develop a revolutionary suite of broadly tuneable and ultrafast visible lasers.
4. Exploring the direct doping of diamond with laser ions, building on the rapid recent progress in diamond synthesis.
Encompassing laser physics, materials science and device engineering, this programme will balance risk and reward to help position Europe as the world-leader in laser engineering. The lasers developed will be important tools in vital sectors such as science (e.g. biological imaging), energy (e.g. wind speed sensing) and medicine (e.g. treating vascular lesions).
Max ERC Funding
1 479 707 €
Duration
Start date: 2011-10-01, End date: 2016-09-30
Project acronym E-MARS
Project Evolution of Mars
Researcher (PI) Cathy Monique Quantin
Host Institution (HI) UNIVERSITE LYON 1 CLAUDE BERNARD
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary The primary questions that drive the Mars exploration program focus on life. Has the Martian climate ever been favorable for life development? Such scenario would imply a distinct planetary system from today with a magnetic flied able to retain the atmosphere. Where is the evidence of such past climate and intern conditions? The clues for answering these questions are locked up in the geologic record of the planet. The volume of data acquired in the past 15 years by the 4 Martian orbiters (ESA and NASA) reach the petaoctet, what is indecent as regard to the size of the Martian community. e-Mars propose to built a science team composed by the PI, Two post-doctorates, one PhD student and one engineer to exploit the data characterizing the surface of Mars. e-Mars proposes the unprecedented approach to combine topographic data, imagery data in diverse spectral domain and hyperspectral data from multiple orbiter captors to study the evolution of Mars and to propose pertinent landing sites for next missions. e-Mars will focus on three scientific themes: the composition of the Martian crust to constraint the early evolution of the planet, the research of possible habitable places based on evidence of past liquid water activity from both morphological record and hydrated mineral locations, and the study of current climatic and geological processes driven by the CO2 cycle. These scientific themes will be supported by three axis of methodological development: the geodatabase management via Geographic Information Systems (G.I.S.)., the automatic hyperspectral data analysis and the age estimates of planetary surface based on small size crater counts.
Summary
The primary questions that drive the Mars exploration program focus on life. Has the Martian climate ever been favorable for life development? Such scenario would imply a distinct planetary system from today with a magnetic flied able to retain the atmosphere. Where is the evidence of such past climate and intern conditions? The clues for answering these questions are locked up in the geologic record of the planet. The volume of data acquired in the past 15 years by the 4 Martian orbiters (ESA and NASA) reach the petaoctet, what is indecent as regard to the size of the Martian community. e-Mars propose to built a science team composed by the PI, Two post-doctorates, one PhD student and one engineer to exploit the data characterizing the surface of Mars. e-Mars proposes the unprecedented approach to combine topographic data, imagery data in diverse spectral domain and hyperspectral data from multiple orbiter captors to study the evolution of Mars and to propose pertinent landing sites for next missions. e-Mars will focus on three scientific themes: the composition of the Martian crust to constraint the early evolution of the planet, the research of possible habitable places based on evidence of past liquid water activity from both morphological record and hydrated mineral locations, and the study of current climatic and geological processes driven by the CO2 cycle. These scientific themes will be supported by three axis of methodological development: the geodatabase management via Geographic Information Systems (G.I.S.)., the automatic hyperspectral data analysis and the age estimates of planetary surface based on small size crater counts.
Max ERC Funding
1 392 000 €
Duration
Start date: 2011-11-01, End date: 2017-10-31
Project acronym EDECS
Project Exploring Dark Energy through Cosmic Structures: Observational Consequences of Dark Energy Clustering
Researcher (PI) Pier Stefano Corasaniti
Host Institution (HI) CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary Understanding the nature of Dark Energy (DE) in the Universe is the central challenge of modern cosmology. Einstein’s Cosmological Constant (Λ) provides the simplest explanation fitting the available cosmological data thus far. However, its unnaturally tuned value indicates that other hypothesis must be explored. Furthermore, current observations do not by any means rule out alternative models in favor of the simplest “concordance” ΛCDM. In the absence of theoretical prejudice, observational tests have mainly focused on the DE equation of state. However, the detection of the inhomogeneous nature of DE will provide smoking-gun evidence that DE is dynamical, ruling out Λ. This key aspect has been mostly overlooked so far, particularly in the optimization design of the next generation of surveys dedicated to DE searches which will map the distribution of matter in the Universe with unprecedented accuracy. The success of these observations relies upon the ability to model the non-linear gravitational processes which affect the collapse of Dark Matter (DM) at small and intermediate scales. Therefore, it is of the highest importance to investigate the role of DE inhomogeneities throughout the non-linear evolution of cosmic structure formation. To achieve this, we will use specifically designed high-resolution numerical simulations and analytical methods to study the non-linear regime in different DE models. The hypothesis to be tested is whether the intrinsic clustering of DE can alter the predictions of the standard ΛCDM model. We will investigate the observational consequences on the DM density field and the properties of DM halos. The results will have a profound impact in the quest for DE and reveal new observable imprints on the distribution of cosmic structures, whose detection may disclose the ultimate origin of the DE phenomenon.
Summary
Understanding the nature of Dark Energy (DE) in the Universe is the central challenge of modern cosmology. Einstein’s Cosmological Constant (Λ) provides the simplest explanation fitting the available cosmological data thus far. However, its unnaturally tuned value indicates that other hypothesis must be explored. Furthermore, current observations do not by any means rule out alternative models in favor of the simplest “concordance” ΛCDM. In the absence of theoretical prejudice, observational tests have mainly focused on the DE equation of state. However, the detection of the inhomogeneous nature of DE will provide smoking-gun evidence that DE is dynamical, ruling out Λ. This key aspect has been mostly overlooked so far, particularly in the optimization design of the next generation of surveys dedicated to DE searches which will map the distribution of matter in the Universe with unprecedented accuracy. The success of these observations relies upon the ability to model the non-linear gravitational processes which affect the collapse of Dark Matter (DM) at small and intermediate scales. Therefore, it is of the highest importance to investigate the role of DE inhomogeneities throughout the non-linear evolution of cosmic structure formation. To achieve this, we will use specifically designed high-resolution numerical simulations and analytical methods to study the non-linear regime in different DE models. The hypothesis to be tested is whether the intrinsic clustering of DE can alter the predictions of the standard ΛCDM model. We will investigate the observational consequences on the DM density field and the properties of DM halos. The results will have a profound impact in the quest for DE and reveal new observable imprints on the distribution of cosmic structures, whose detection may disclose the ultimate origin of the DE phenomenon.
Max ERC Funding
1 468 800 €
Duration
Start date: 2012-04-01, End date: 2017-08-31
Project acronym EGGS
Project The first Galaxies
Researcher (PI) Johan Peter Uldall Fynbo
Host Institution (HI) KOBENHAVNS UNIVERSITET
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary The goal of this project is to discover the first galaxies that formed after the Big Bang. The astrophysics of galaxy formation is deeply fascinating. From tiny density fluctuations of quantum mechanical nature believed to have formed during an inflationary period a tiny fraction of a second after the Big Bang during structure slowly formed through gravitational collapse. This process is strongly dependent on the nature of the dominant, but unknown form of matter - the dark matter. In the project proposed here I will study the epoch of first galaxy formation and the subsequent few billion years of cosmic evolution using gamma-ray bursts and Lyman-α (Lyα) emitting galaxies as probes. I am the principal investigator on two observational projects utilizing these probes. In the first project, I will over three years starting October 2009 be using the new X-shooter spectrograph on the European Southern Observatory Very Large Telescope to build a sample of ~100 gamma-ray bursts with UV/optical/near-IR spectroscopic follow-up. The objective of this project is to measure primarily metallicities, molecular content, and dust content of the gamma-ray burst host galaxies. I am primarily interested in the redshift range from 9 to 2 corresponding to about 500 million years to 3 billions years after the Big Bang. In the 2nd project we will use the new European Southern Observatory survey telescope VISTA. I am co-PI of the Ultra-VISTA project that over the next 5 years starting December 2009 will create an ultradeep image (about 2000 hr of total integration time) of a piece of sky known as the COSMOS field. I am responsible for the part of the project that will use a narrow-band filter to search for Lyα emitting galaxies at a redshift of 8.8 (corresponding to about 500 million years after the Big Bang) - believed to correspond to the epoch of formation of some of the very first galaxies.
Summary
The goal of this project is to discover the first galaxies that formed after the Big Bang. The astrophysics of galaxy formation is deeply fascinating. From tiny density fluctuations of quantum mechanical nature believed to have formed during an inflationary period a tiny fraction of a second after the Big Bang during structure slowly formed through gravitational collapse. This process is strongly dependent on the nature of the dominant, but unknown form of matter - the dark matter. In the project proposed here I will study the epoch of first galaxy formation and the subsequent few billion years of cosmic evolution using gamma-ray bursts and Lyman-α (Lyα) emitting galaxies as probes. I am the principal investigator on two observational projects utilizing these probes. In the first project, I will over three years starting October 2009 be using the new X-shooter spectrograph on the European Southern Observatory Very Large Telescope to build a sample of ~100 gamma-ray bursts with UV/optical/near-IR spectroscopic follow-up. The objective of this project is to measure primarily metallicities, molecular content, and dust content of the gamma-ray burst host galaxies. I am primarily interested in the redshift range from 9 to 2 corresponding to about 500 million years to 3 billions years after the Big Bang. In the 2nd project we will use the new European Southern Observatory survey telescope VISTA. I am co-PI of the Ultra-VISTA project that over the next 5 years starting December 2009 will create an ultradeep image (about 2000 hr of total integration time) of a piece of sky known as the COSMOS field. I am responsible for the part of the project that will use a narrow-band filter to search for Lyα emitting galaxies at a redshift of 8.8 (corresponding to about 500 million years after the Big Bang) - believed to correspond to the epoch of formation of some of the very first galaxies.
Max ERC Funding
1 002 000 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym ELEGANSNEUROCIRCUITS
Project Neuromodulation of Oxygen Chemosensory Circuits in Caenorhabditis elegans
Researcher (PI) Manuel Zimmer
Host Institution (HI) FORSCHUNGSINSTITUT FUR MOLEKULARE PATHOLOGIE GESELLSCHAFT MBH
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary An animal’s decision on how to respond to the environment is based not only on the sensory information available, but further depends on internal factors such as stress, sleep / wakefulness, hunger / satiety and experience. Neurotransmitters and neuropeptides in the brain modulate neural circuits accordingly so that appropriate behaviors are generated. Aberrant neuromodulation is implicated in diseases such as insomnia, obesity or anorexia. Given the complexity of most neural systems studied, we lack good models of how neuromodulators systemically affect the activities of neural networks.
To overcome this problem, I propose to study neural circuits in the nematode C. elegans, which is a genetically tractable model organism with a simple and anatomically defined nervous system. I will focus on the neural circuits involved in oxygen chemosensory behaviors. Worms can smell oxygen and they use this information to navigate through heterogeneous environments. This enables them to find food and to engage in social interactions. Oxygen chemosensory behaviors are highly modulated by experience and nutritional status, but the underlying mechanisms are not understood.
I established behavioral assays that allow studying the modulation of oxygen behaviors in a rigorously quantifiable manner. I also acquired expertise in micro-fabrication technologies and developed imaging devices to measure the activity of neurons in live animals. The first two aims of this proposal focus on the application of these technologies to study (A) how neuropeptides mediate experience dependent modulation of oxygen chemosensory circuits; and (B) how food availability and nutritional status modulate the same neural circuits. Aim (C) is an innovative engineering approach in which I will develop new microfluidic technologies that allow the simultaneous recording of oxygen evoked behaviors and neural activity. This will be beneficial for aims A and B and will pave way for new future research directions.
Summary
An animal’s decision on how to respond to the environment is based not only on the sensory information available, but further depends on internal factors such as stress, sleep / wakefulness, hunger / satiety and experience. Neurotransmitters and neuropeptides in the brain modulate neural circuits accordingly so that appropriate behaviors are generated. Aberrant neuromodulation is implicated in diseases such as insomnia, obesity or anorexia. Given the complexity of most neural systems studied, we lack good models of how neuromodulators systemically affect the activities of neural networks.
To overcome this problem, I propose to study neural circuits in the nematode C. elegans, which is a genetically tractable model organism with a simple and anatomically defined nervous system. I will focus on the neural circuits involved in oxygen chemosensory behaviors. Worms can smell oxygen and they use this information to navigate through heterogeneous environments. This enables them to find food and to engage in social interactions. Oxygen chemosensory behaviors are highly modulated by experience and nutritional status, but the underlying mechanisms are not understood.
I established behavioral assays that allow studying the modulation of oxygen behaviors in a rigorously quantifiable manner. I also acquired expertise in micro-fabrication technologies and developed imaging devices to measure the activity of neurons in live animals. The first two aims of this proposal focus on the application of these technologies to study (A) how neuropeptides mediate experience dependent modulation of oxygen chemosensory circuits; and (B) how food availability and nutritional status modulate the same neural circuits. Aim (C) is an innovative engineering approach in which I will develop new microfluidic technologies that allow the simultaneous recording of oxygen evoked behaviors and neural activity. This will be beneficial for aims A and B and will pave way for new future research directions.
Max ERC Funding
1 500 000 €
Duration
Start date: 2012-01-01, End date: 2017-06-30
Project acronym ENTERAPIC
Project Energy-Efficient Multi-Terabit/s Photonic Interconnects
Researcher (PI) Christian Gunter Koos
Host Institution (HI) KARLSRUHER INSTITUT FUER TECHNOLOGIE
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary The rapid growth of data traffic requires radically new approaches for high-speed data transmission to increase the bandwidth and power efficiency by orders of magnitude. The proposed research aims at novel system and device concepts for low-energy high-capacity optical interconnects in data centers. Data rates of 10 Tbit/s and beyond are envisaged by coherent multicarrier transmission. Parametric frequency conversion in high-Q Kerr-nonlinear resonators will be used to generate broadband combs of frequency-locked optical carriers. Integrated silicon photonic systems will allow for power-efficient multichannel modulation and detection. Novel reconfigurable optical signal processors will avoid excessive digital post-processing and hence reduce overall energy consumption.
Summary
The rapid growth of data traffic requires radically new approaches for high-speed data transmission to increase the bandwidth and power efficiency by orders of magnitude. The proposed research aims at novel system and device concepts for low-energy high-capacity optical interconnects in data centers. Data rates of 10 Tbit/s and beyond are envisaged by coherent multicarrier transmission. Parametric frequency conversion in high-Q Kerr-nonlinear resonators will be used to generate broadband combs of frequency-locked optical carriers. Integrated silicon photonic systems will allow for power-efficient multichannel modulation and detection. Novel reconfigurable optical signal processors will avoid excessive digital post-processing and hence reduce overall energy consumption.
Max ERC Funding
1 498 800 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym FADER
Project Flight Algorithms for Disaggregated Space Architectures
Researcher (PI) Pinchas Pini Gurfil
Host Institution (HI) TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary Standard spacecraft designs comprise modules assembled in a single monolithic structure. When unexpected situations occur, the spacecraft are unable to adequately respond, and significant functional and financial losses are unavoidable. For instance, if the payload of a spacecraft fails, the whole system becomes unserviceable and substitution of the entire spacecraft is required. It would be much easier to replace the payload module only than launch a completely new satellite. This idea gives rise to an emerging concept in space engineering termed disaggregated spacecraft. Disaggregated space architectures (DSA) consist of several physically-separated modules, interacting through wireless communication links to form a single virtual platform. Each module has one or more pre-determined functions: Navigation, attitude control, power generation and payload operation. The free-flying modules, capable of resource sharing, do not have to operate in a tightly-controlled formation, but are rather required to remain in bounded relative position and attitude, termed cluster flying. DSA enables novel space system architectures, which are expected to be much more efficient, adaptable, robust and responsive. The main goal of the proposed research is to develop beyond the state-of-the-art technologies in order to enable operational flight of DSA, by (i) developing algorithms for semi-autonomous long-duration maintenance of a cluster and cluster network, capable of adding and removing spacecraft modules to/from the cluster and cluster network; (ii) finding methods so as to autonomously reconfigure the cluster to retain safety- and mission-critical functionality in the face of network degradation or component failures; (iii) designing semi-autonomous cluster scatter and re-gather maneuvesr to rapidly evade a debris-like threat; and (iv) validating the said algorithms and methods in the Distributed Space Systems Laboratory in which the PI serves as a Principal Investigator.
Summary
Standard spacecraft designs comprise modules assembled in a single monolithic structure. When unexpected situations occur, the spacecraft are unable to adequately respond, and significant functional and financial losses are unavoidable. For instance, if the payload of a spacecraft fails, the whole system becomes unserviceable and substitution of the entire spacecraft is required. It would be much easier to replace the payload module only than launch a completely new satellite. This idea gives rise to an emerging concept in space engineering termed disaggregated spacecraft. Disaggregated space architectures (DSA) consist of several physically-separated modules, interacting through wireless communication links to form a single virtual platform. Each module has one or more pre-determined functions: Navigation, attitude control, power generation and payload operation. The free-flying modules, capable of resource sharing, do not have to operate in a tightly-controlled formation, but are rather required to remain in bounded relative position and attitude, termed cluster flying. DSA enables novel space system architectures, which are expected to be much more efficient, adaptable, robust and responsive. The main goal of the proposed research is to develop beyond the state-of-the-art technologies in order to enable operational flight of DSA, by (i) developing algorithms for semi-autonomous long-duration maintenance of a cluster and cluster network, capable of adding and removing spacecraft modules to/from the cluster and cluster network; (ii) finding methods so as to autonomously reconfigure the cluster to retain safety- and mission-critical functionality in the face of network degradation or component failures; (iii) designing semi-autonomous cluster scatter and re-gather maneuvesr to rapidly evade a debris-like threat; and (iv) validating the said algorithms and methods in the Distributed Space Systems Laboratory in which the PI serves as a Principal Investigator.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-10-01, End date: 2016-09-30
Project acronym FISNT
Project Frontiers of Integrated Silicon Nanophotonics in Telecommunications
Researcher (PI) Jeremy Witzens
Host Institution (HI) RHEINISCH-WESTFAELISCHE TECHNISCHE HOCHSCHULE AACHEN
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary In the last decade, Silicon Photonics has been a rapidly growing field fueled by the promise of highly scalable, ultra-low power, high bandwidth and low cost silicon based optical communication systems. The last few years have seen the emergence of several dedicated world-class research groups, a dedicated international conference, heavy investments by the semiconductor industry giants, multiple private equity funded start-ups, as well as dedicated multi-user foundry services. Nevertheless, several critical roadblocks remain that have so far prevented the field from displacing older optical technologies, the resolution of which presents extremely challenging scientific challenges, requiring highly innovative devices and system architectures as well as bleeding edge process development. In a nutshell, state-of-the-art Silicon Photonics remains marginally too expensive for ultra-short distance links, too low performance for long haul communications, and still has too high a power consumption to displace electrical interconnects at the circuit board level. It is the goal of this proposal to reach three key milestones that in the applicant’s opinion are critical enablers for the field on its path towards becoming a truly disruptive technology.
Summary
In the last decade, Silicon Photonics has been a rapidly growing field fueled by the promise of highly scalable, ultra-low power, high bandwidth and low cost silicon based optical communication systems. The last few years have seen the emergence of several dedicated world-class research groups, a dedicated international conference, heavy investments by the semiconductor industry giants, multiple private equity funded start-ups, as well as dedicated multi-user foundry services. Nevertheless, several critical roadblocks remain that have so far prevented the field from displacing older optical technologies, the resolution of which presents extremely challenging scientific challenges, requiring highly innovative devices and system architectures as well as bleeding edge process development. In a nutshell, state-of-the-art Silicon Photonics remains marginally too expensive for ultra-short distance links, too low performance for long haul communications, and still has too high a power consumption to displace electrical interconnects at the circuit board level. It is the goal of this proposal to reach three key milestones that in the applicant’s opinion are critical enablers for the field on its path towards becoming a truly disruptive technology.
Max ERC Funding
1 917 080 €
Duration
Start date: 2011-10-01, End date: 2017-09-30
Project acronym FLYVISUALCIRCUITS
Project Linking neural circuits to visual guidance in flying flies
Researcher (PI) Andrew Straw
Host Institution (HI) ALBERT-LUDWIGS-UNIVERSITAET FREIBURG
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary The brain of a fly is capable of steering the animal through a complex environment at high relative speeds, avoiding stationary obstacles and moving predators. Because it is relatively easy to study how flies do this at several levels, from the behavioral to the cellular, fly vision has long been recognized as an ideal system to address a fundamental question in neuroscience- how does the distributed activity of neurons orchestrate animal-environment interactions to result in successful coordinated behavior? This work addresses this basic question with two related studies. The first concerns higher levels of visual processing and behavior. Do flies build a neural representation of nearby objects or, alternatively, is flight governed by a direct coupling of visual input into motor commands? The second identifies specific neurons responsible for visual guidance behaviors.
This work involves the establishment of a new research activity in the EU by a Principal Investigator who is moving from a third country (the US) into the EU. It uses a unique high-throughput, virtual reality free flight arena in which flies are tracked in realtime by a computer vision system. With this technology, physically unmanipulated and unrestrained flies are automatically and repeatedly presented with arbitrary visual stimuli projected on the arena walls and floor. Thousands of digitized 3D flight trajectories are gathered, and behavioral experiments using this system will be combined with targeted genetic manipulation of the nervous system and analyzed to reveal the magnitude and reliability of effects. This will be accomplished by using molecular genetic techniques to selectively perturb individually identified neurons in the brain and measuring the effect on flight control in response to precisely specified visual stimuli. Thus, by utilizing controlled stimulus conditions and measuring behavioral responses in detail, the results will show the contribution of individual neurons to behavior.
Summary
The brain of a fly is capable of steering the animal through a complex environment at high relative speeds, avoiding stationary obstacles and moving predators. Because it is relatively easy to study how flies do this at several levels, from the behavioral to the cellular, fly vision has long been recognized as an ideal system to address a fundamental question in neuroscience- how does the distributed activity of neurons orchestrate animal-environment interactions to result in successful coordinated behavior? This work addresses this basic question with two related studies. The first concerns higher levels of visual processing and behavior. Do flies build a neural representation of nearby objects or, alternatively, is flight governed by a direct coupling of visual input into motor commands? The second identifies specific neurons responsible for visual guidance behaviors.
This work involves the establishment of a new research activity in the EU by a Principal Investigator who is moving from a third country (the US) into the EU. It uses a unique high-throughput, virtual reality free flight arena in which flies are tracked in realtime by a computer vision system. With this technology, physically unmanipulated and unrestrained flies are automatically and repeatedly presented with arbitrary visual stimuli projected on the arena walls and floor. Thousands of digitized 3D flight trajectories are gathered, and behavioral experiments using this system will be combined with targeted genetic manipulation of the nervous system and analyzed to reveal the magnitude and reliability of effects. This will be accomplished by using molecular genetic techniques to selectively perturb individually identified neurons in the brain and measuring the effect on flight control in response to precisely specified visual stimuli. Thus, by utilizing controlled stimulus conditions and measuring behavioral responses in detail, the results will show the contribution of individual neurons to behavior.
Max ERC Funding
1 500 000 €
Duration
Start date: 2012-01-01, End date: 2017-12-31
Project acronym FUELLINGSYNAPSES
Project Regulation of neuronal connectivity and plasticity by activity-dependent mitochondrial trafficking to synapses
Researcher (PI) Josef Kittler
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Regulated trafficking of mitochondria is essential for providing ATP at the correct spatial location to power neural computation, and for providing calcium buffering at sites of calcium entry or release. In neurons, the concentration of mitochondria in specific regions such as growth cones and synapses is important for correct neuronal function and development. Moreover mutations in proteins regulating mitochondrial trafficking compromise neuronal development and the formation, function and plasticity of synapses, and defective mitochondrial trafficking is increasingly implicated in neurological diseases. Understanding the molecular mechanisms that allow neurons to tailor the distribution of mitochondria to changes in neuronal activity therefore has important implications for our understanding of neuronal function and communication. This proposal will study the mechanisms that control the trafficking of the energy providing mitochondria within neurons, and how this relates to neuronal connectivity and plasticity. Using imaging, electrophysiological, molecular and cell biological techniques, combined with viral transduction and mouse transgenic approaches we will determine the molecular mechanisms underlying the activity-dependent subcellular positioning of mitochondria in neurons. We will examine how the mitochondrial Ca2+-sensing GTPases Miro1 and Miro2 act to regulate mitochondrial movement, distribution and function and how this contributes to neuronal development, synaptogenesis and synaptic plasticity. A key goal will be to determine if different roles exist for constitutive versus activity-dependent control of mitochondrial transport by Miro1 and Miro2 in these processes. These studies will significantly advance our understanding of the molecular mechanisms that control mitochondrial localisation in neurons and the role that activity-dependent mitochondrial trafficking plays in regulating neuronal development, morphogenesis, connectivity and function.
Summary
Regulated trafficking of mitochondria is essential for providing ATP at the correct spatial location to power neural computation, and for providing calcium buffering at sites of calcium entry or release. In neurons, the concentration of mitochondria in specific regions such as growth cones and synapses is important for correct neuronal function and development. Moreover mutations in proteins regulating mitochondrial trafficking compromise neuronal development and the formation, function and plasticity of synapses, and defective mitochondrial trafficking is increasingly implicated in neurological diseases. Understanding the molecular mechanisms that allow neurons to tailor the distribution of mitochondria to changes in neuronal activity therefore has important implications for our understanding of neuronal function and communication. This proposal will study the mechanisms that control the trafficking of the energy providing mitochondria within neurons, and how this relates to neuronal connectivity and plasticity. Using imaging, electrophysiological, molecular and cell biological techniques, combined with viral transduction and mouse transgenic approaches we will determine the molecular mechanisms underlying the activity-dependent subcellular positioning of mitochondria in neurons. We will examine how the mitochondrial Ca2+-sensing GTPases Miro1 and Miro2 act to regulate mitochondrial movement, distribution and function and how this contributes to neuronal development, synaptogenesis and synaptic plasticity. A key goal will be to determine if different roles exist for constitutive versus activity-dependent control of mitochondrial transport by Miro1 and Miro2 in these processes. These studies will significantly advance our understanding of the molecular mechanisms that control mitochondrial localisation in neurons and the role that activity-dependent mitochondrial trafficking plays in regulating neuronal development, morphogenesis, connectivity and function.
Max ERC Funding
1 997 567 €
Duration
Start date: 2012-02-01, End date: 2018-01-31
Project acronym Future Proof
Project Theoretical and Algorithmic Foundations for Future Proof Information and Inference Systems
Researcher (PI) Volkan Cevher
Host Institution (HI) ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary A critical technological challenge for emerging information systems is to acquire, analyze and learn from the ever-increasing high-dimensional data produced by natural and man-made phenomena. Sampling, streaming, and recoding of even the most basic applications now produce a data deluge that severely stresses the available analog-to-digital converter, digital communication and storage resources, and easily swamps the back-end processing and learning systems.
Surprisingly, while the ambient data dimension is large in many problems, the relevant information therein typically resides in a much lower dimensional space. Viewed combinatorially and geometrically, natural constraints often cause data to cluster along low-dimensional structures, such as unions-of-subspaces or manifolds, having a few degrees of freedom relative to their size. This powerful notion suggests the potential for developing highly efficient methods for processing and learning by capturing and exploiting the inherent model, or data’s “information level.”
To this end, we seek to revolutionize scientific and practical modi operandi of data acquisition and learning by developing a new optimization and analysis framework based on the nascent low-dimensional models with broad applications—from inverse problems to analog-to-information conversion, and from automated representation learning to statistical regression. We attack the curse of dimensionality in specific ways, not only by relying on the blessing of dimensionality via concentration-of-measures, but also by exploiting geometric topologies and the diminishing returns (i.e., submodularity) within learning objectives. We believe only an approach such as ours can provide the theoretical scaffold for a future proof processing and learning framework that scales its operation to the problem’s information level, promising substantial reductions in hardware complexity, communication, storage, and computational resources.
Summary
A critical technological challenge for emerging information systems is to acquire, analyze and learn from the ever-increasing high-dimensional data produced by natural and man-made phenomena. Sampling, streaming, and recoding of even the most basic applications now produce a data deluge that severely stresses the available analog-to-digital converter, digital communication and storage resources, and easily swamps the back-end processing and learning systems.
Surprisingly, while the ambient data dimension is large in many problems, the relevant information therein typically resides in a much lower dimensional space. Viewed combinatorially and geometrically, natural constraints often cause data to cluster along low-dimensional structures, such as unions-of-subspaces or manifolds, having a few degrees of freedom relative to their size. This powerful notion suggests the potential for developing highly efficient methods for processing and learning by capturing and exploiting the inherent model, or data’s “information level.”
To this end, we seek to revolutionize scientific and practical modi operandi of data acquisition and learning by developing a new optimization and analysis framework based on the nascent low-dimensional models with broad applications—from inverse problems to analog-to-information conversion, and from automated representation learning to statistical regression. We attack the curse of dimensionality in specific ways, not only by relying on the blessing of dimensionality via concentration-of-measures, but also by exploiting geometric topologies and the diminishing returns (i.e., submodularity) within learning objectives. We believe only an approach such as ours can provide the theoretical scaffold for a future proof processing and learning framework that scales its operation to the problem’s information level, promising substantial reductions in hardware complexity, communication, storage, and computational resources.
Max ERC Funding
1 824 220 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym GasAroundGalaxies
Project Studying the gas around galaxies with the Multi Unit Spectroscopic Explorer and hydrodynamical simulations
Researcher (PI) Joop Schaye
Host Institution (HI) UNIVERSITEIT LEIDEN
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary "Gas accretion and galactic winds are two of the most important and poorly understood ingredients of models for the formation and evolution of galaxies. We propose to take advantage of two unique opportunities to embark on a multi-disciplinary program to advance our understanding of the circumgalactic medium (CGM).
We will use MUSE, a massive optical integral field spectrograph that we helped to develop and that will be commissioned on the VLT in 2012, to study the CGM in both absorption and emission. We will use 200 hours of guaranteed time to carry out deep redshift surveys of fields centred on bright z≈3.5 and z≈5 QSOs. This will yield hundreds of faint galaxies (mainly Lyα emitters) within 250 kpc of the lines of sight to the background QSOs, an order of magnitude increase compared to the best existing sample (bright, z≈2.3 galaxies). This will allow us to map the CGM in absorption in 3-D using HI and metal lines and to identify, for the first time, the counterparts to most metal absorbers. MUSE will also enable us to detect Lyα emission from the denser CGM (also using another 300 hours of guaranteed time targeting deep HST fields) and thus to directly explore its connection with galaxies and QSO absorbers.
We will use the new supercomputer of the Virgo consortium to carry out cosmological hydro simulations that contain 1-2 orders of magnitude more resolution elements than the largest existing (spatially adaptive) runs. We will use the results of our previous work to guide our choice of parameters in order to obtain a better match to the observed mass function of galaxies. In parallel, we will carry out a complementary program of zoomed simulations of individual galaxies. These will have the physics and resolution to include a cold gas phase and hence to bypass much of the ""subgrid"" physics used in the cosmological runs. Both types of simulations will be used to study the physics of gas flows around galaxies and to guide the interpretation of our observations."
Summary
"Gas accretion and galactic winds are two of the most important and poorly understood ingredients of models for the formation and evolution of galaxies. We propose to take advantage of two unique opportunities to embark on a multi-disciplinary program to advance our understanding of the circumgalactic medium (CGM).
We will use MUSE, a massive optical integral field spectrograph that we helped to develop and that will be commissioned on the VLT in 2012, to study the CGM in both absorption and emission. We will use 200 hours of guaranteed time to carry out deep redshift surveys of fields centred on bright z≈3.5 and z≈5 QSOs. This will yield hundreds of faint galaxies (mainly Lyα emitters) within 250 kpc of the lines of sight to the background QSOs, an order of magnitude increase compared to the best existing sample (bright, z≈2.3 galaxies). This will allow us to map the CGM in absorption in 3-D using HI and metal lines and to identify, for the first time, the counterparts to most metal absorbers. MUSE will also enable us to detect Lyα emission from the denser CGM (also using another 300 hours of guaranteed time targeting deep HST fields) and thus to directly explore its connection with galaxies and QSO absorbers.
We will use the new supercomputer of the Virgo consortium to carry out cosmological hydro simulations that contain 1-2 orders of magnitude more resolution elements than the largest existing (spatially adaptive) runs. We will use the results of our previous work to guide our choice of parameters in order to obtain a better match to the observed mass function of galaxies. In parallel, we will carry out a complementary program of zoomed simulations of individual galaxies. These will have the physics and resolution to include a cold gas phase and hence to bypass much of the ""subgrid"" physics used in the cosmological runs. Both types of simulations will be used to study the physics of gas flows around galaxies and to guide the interpretation of our observations."
Max ERC Funding
1 496 400 €
Duration
Start date: 2012-09-01, End date: 2017-08-31
Project acronym GRB-SN
Project The Gamma Ray Burst – Supernova Connection
and Shock Breakout Physics
Researcher (PI) Ehud Nakar
Host Institution (HI) TEL AVIV UNIVERSITY
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary Long gamma ray bursts (long GRBs) and core-collapse supernovae (CCSNe) are two of the most spectacular explosions in the Universe. They are a focal point of research for many reasons. Nevertheless, despite considerable effort during the last several decades, there are still many fundamental open questions regarding their physics.
Long GRBs and CCSNe are related. We know that they are both an outcome of a massive star collapse, where in some cases, such collapse produces simultaneously a GRB and a SN. However, we do not know how a single stellar collapse can produce these two apparently very different explosions. The GRB-SN connection raises many questions, but it also offers new opportunities to learn on the two types of explosions.
The focus of the proposed research is on the connection between CCSNe and GRBs, and on the physics of shock breakout. As I explain in this proposal, shock breakouts play an important role in this connection and therefore, I will develop a comprehensive theory of relativistic and Newtonian shock breakout. In addition, I will study the propagation of relativistic jets inside stars, including the effects of jet propagation and GRB engine on the emerging SN. This will be done by a set of interrelated projects that carefully combine analytic calculations and numerical simulations. Together, these projects will be the first to model a GRB and a SN that are simultaneously produced in a single star. This in turn will be used to gain new insights into long GRBs and CCSNe in general.
This research will also make a direct contribution to cosmic explosions research in general. Any observable cosmic explosion must go through a shock breakout and a considerable effort is invested these days in large field of view surveys in search for these breakouts. This program will provide a new theoretical base for the interpretation of the upcoming observations.
Summary
Long gamma ray bursts (long GRBs) and core-collapse supernovae (CCSNe) are two of the most spectacular explosions in the Universe. They are a focal point of research for many reasons. Nevertheless, despite considerable effort during the last several decades, there are still many fundamental open questions regarding their physics.
Long GRBs and CCSNe are related. We know that they are both an outcome of a massive star collapse, where in some cases, such collapse produces simultaneously a GRB and a SN. However, we do not know how a single stellar collapse can produce these two apparently very different explosions. The GRB-SN connection raises many questions, but it also offers new opportunities to learn on the two types of explosions.
The focus of the proposed research is on the connection between CCSNe and GRBs, and on the physics of shock breakout. As I explain in this proposal, shock breakouts play an important role in this connection and therefore, I will develop a comprehensive theory of relativistic and Newtonian shock breakout. In addition, I will study the propagation of relativistic jets inside stars, including the effects of jet propagation and GRB engine on the emerging SN. This will be done by a set of interrelated projects that carefully combine analytic calculations and numerical simulations. Together, these projects will be the first to model a GRB and a SN that are simultaneously produced in a single star. This in turn will be used to gain new insights into long GRBs and CCSNe in general.
This research will also make a direct contribution to cosmic explosions research in general. Any observable cosmic explosion must go through a shock breakout and a considerable effort is invested these days in large field of view surveys in search for these breakouts. This program will provide a new theoretical base for the interpretation of the upcoming observations.
Max ERC Funding
1 468 180 €
Duration
Start date: 2012-01-01, End date: 2017-12-31
Project acronym GxE-molmech
Project Gene x environment interactions in affective disorders - elucidating molecular mechanisms
Researcher (PI) Elisabeth Binder
Host Institution (HI) MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Exposure to traumatic experiences as well as chronic stress has been shown to increase the risk for a number of psychiatric disorders including major depression and anxiety disorders by inducing longterm alterations in the reactivity of the stress hormone system. These effects can be moderated by genetic variants, one of them being functional polymorphisms in glucocorticoid receptor (GR) co-chaperone gene FKBP5. Preliminary studies in my laboratory suggest that this GxE interaction is mediated by allele-specific de-methylation of intronic glucocorticoid response elements (GREs) within FKBP5. The overarching aim of this grant is to identify the molecular mechanisms by which FKBP5 polymorphisms and early trauma interact to increase the risk for a number of depressive and anxiety disorders. In this application, I propose to extend these preliminary data by experiments in healthy controls and depressed patients, human lymphoblastiod cell lines as well as an animal model in outbred mice showing similar GxE interaction to address the molecular mechanism of these DNA-methylation changes as well as their cellular and system level consequences. Finally we will use expression quantitative trait locus analysis for GR stimulated gene expression to identify new loci relevant for GxE interactions in stress-related disorders.
Overall, this proposal will follow up on one of the first putative molecular and systemic mechanisms identified for gene x environment interactions in affective disorders and will establish an animal model mimicking these specific interactions. The findings related to this proposal could be of major importance for understanding the biology of these disorders and to explore novel treatment options, including manipulations of epigenetic modifications.
Summary
Exposure to traumatic experiences as well as chronic stress has been shown to increase the risk for a number of psychiatric disorders including major depression and anxiety disorders by inducing longterm alterations in the reactivity of the stress hormone system. These effects can be moderated by genetic variants, one of them being functional polymorphisms in glucocorticoid receptor (GR) co-chaperone gene FKBP5. Preliminary studies in my laboratory suggest that this GxE interaction is mediated by allele-specific de-methylation of intronic glucocorticoid response elements (GREs) within FKBP5. The overarching aim of this grant is to identify the molecular mechanisms by which FKBP5 polymorphisms and early trauma interact to increase the risk for a number of depressive and anxiety disorders. In this application, I propose to extend these preliminary data by experiments in healthy controls and depressed patients, human lymphoblastiod cell lines as well as an animal model in outbred mice showing similar GxE interaction to address the molecular mechanism of these DNA-methylation changes as well as their cellular and system level consequences. Finally we will use expression quantitative trait locus analysis for GR stimulated gene expression to identify new loci relevant for GxE interactions in stress-related disorders.
Overall, this proposal will follow up on one of the first putative molecular and systemic mechanisms identified for gene x environment interactions in affective disorders and will establish an animal model mimicking these specific interactions. The findings related to this proposal could be of major importance for understanding the biology of these disorders and to explore novel treatment options, including manipulations of epigenetic modifications.
Max ERC Funding
1 254 120 €
Duration
Start date: 2012-03-01, End date: 2017-02-28
Project acronym HIPECMEM
Project Memory-Related Information Processing in Neuronal Circuits of the Hippocampus and Entorhinal Cortex
Researcher (PI) Jozsef Csicsvari
Host Institution (HI) INSTITUTE OF SCIENCE AND TECHNOLOGYAUSTRIA
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary This proposal will elucidate the circuit mechanism that underlies the spatial memory-related information processing in the interconnected brain areas of the hippocampus and entorhinal cortex (EC). Both of these areas are implicated in spatial memory and encode spatial information in neuronal activity patterns. The mechanisms underlying the emergence and coordination of spatial memory-related activity in these regions are needed to understand how these circuits process mnemonic information. Accordingly, here we aim at elucidating the representation of spatial memory by investigating these mechanisms at the circuit and synaptic levels of organisation. The first objective of this proposal is to characterise oscillatory synchronisation in hippocampo-EC circuits at different stages of memory processing. We hypothesise that network oscillations facilitate circuit interactions during memory processing. Therefore, using optogenetic techniques to disrupt oscillations, we aim at identifying critical periods during mnemonic processing when synchronisation is needed. Secondly, we intend to reveal how mnemonic information is encoded and exchanged between different areas of the hippocampo-EC system. We will test whether spatial memory-associated firing of dorsal hippocampal cells could be triggered by EC and/or ventral hippocampal cells that encode similar mnemonic features. In addition, this project will explore the role of temporal coding in the representation and consolidation of spatial memory traces. The third objective will investigate synaptic changes between connected CA3-CA3 and CA3-CA1 cell pairs during spatial learning. We will use cross-correlation analysis and electrical microstimulation to examine the rules that govern changes in synaptic efficacy by observing the probability of spike transmission.
Overall, the proposal provides a comprehensive approach to understanding how hippocampo-EC circuits organise and store information during mnemonic processes.
Summary
This proposal will elucidate the circuit mechanism that underlies the spatial memory-related information processing in the interconnected brain areas of the hippocampus and entorhinal cortex (EC). Both of these areas are implicated in spatial memory and encode spatial information in neuronal activity patterns. The mechanisms underlying the emergence and coordination of spatial memory-related activity in these regions are needed to understand how these circuits process mnemonic information. Accordingly, here we aim at elucidating the representation of spatial memory by investigating these mechanisms at the circuit and synaptic levels of organisation. The first objective of this proposal is to characterise oscillatory synchronisation in hippocampo-EC circuits at different stages of memory processing. We hypothesise that network oscillations facilitate circuit interactions during memory processing. Therefore, using optogenetic techniques to disrupt oscillations, we aim at identifying critical periods during mnemonic processing when synchronisation is needed. Secondly, we intend to reveal how mnemonic information is encoded and exchanged between different areas of the hippocampo-EC system. We will test whether spatial memory-associated firing of dorsal hippocampal cells could be triggered by EC and/or ventral hippocampal cells that encode similar mnemonic features. In addition, this project will explore the role of temporal coding in the representation and consolidation of spatial memory traces. The third objective will investigate synaptic changes between connected CA3-CA3 and CA3-CA1 cell pairs during spatial learning. We will use cross-correlation analysis and electrical microstimulation to examine the rules that govern changes in synaptic efficacy by observing the probability of spike transmission.
Overall, the proposal provides a comprehensive approach to understanding how hippocampo-EC circuits organise and store information during mnemonic processes.
Max ERC Funding
1 441 119 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym LATELIFEHEALTH
Project Mapping the late-life health promoting mechanisms in worms and mammals
Researcher (PI) Ehud Cohen
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Aberrant protein aggregation (proteotoxicity) is an underlying mechanistic event common to numerous late-onset human neurodegenerative maladies including Alzheimer’s (AD) disease. Recent studies indicated that the ageing process plays key roles in enabling protein aggregation to become toxic late in life. The insulin/IGF signaling pathway (IIS) is a major ageing, stress resistance and lifespan regulator in worms and mice. We found that IIS reduction protects worms and mice from toxicity associated with the AD linked peptide, Aβ. These findings point to the alteration of ageing by IIS reduction as a promising research avenue towards the development of neurodegeneration therapies. In the nematode C. elegans, both effects of IIS reduction; longevity and protection from proteotoxicity are dependent on the activity of the FOXO transcription factor DAF-16. However, these functions of DAF-16/FOXO differ temporally; in worms the mediation of longevity by DAF-16 is restricted to reproductive adulthood while protection from proteotoxicity extends also to late adulthood. This differential temporal activity pattern suggests that different DAF-16 co-factors and target genes play roles in the mediation of longevity and in protection from proteotoxicity. Thus, a careful characterization of the late life DAF-16 regulated protective mechanism is required to evaluate the therapeutic potential of IIS reduction as a future treatment for neurodegenerative disorders. Here I propose to use nematodes and mice to explore the DAF-16/FOXO co-factors and target genes that mediate stress resistance and protection from proteotoxicity in the aged organism. Dual experimental approach will be utilized to achieve this goal; a directed genetic screen for the identification of co-factors and temporally differential set of DNA microarrays for the recognition of late life DAF-16/FOX target genes. This project is expected to yield new insight and to serve as a platform for future studies.
Summary
Aberrant protein aggregation (proteotoxicity) is an underlying mechanistic event common to numerous late-onset human neurodegenerative maladies including Alzheimer’s (AD) disease. Recent studies indicated that the ageing process plays key roles in enabling protein aggregation to become toxic late in life. The insulin/IGF signaling pathway (IIS) is a major ageing, stress resistance and lifespan regulator in worms and mice. We found that IIS reduction protects worms and mice from toxicity associated with the AD linked peptide, Aβ. These findings point to the alteration of ageing by IIS reduction as a promising research avenue towards the development of neurodegeneration therapies. In the nematode C. elegans, both effects of IIS reduction; longevity and protection from proteotoxicity are dependent on the activity of the FOXO transcription factor DAF-16. However, these functions of DAF-16/FOXO differ temporally; in worms the mediation of longevity by DAF-16 is restricted to reproductive adulthood while protection from proteotoxicity extends also to late adulthood. This differential temporal activity pattern suggests that different DAF-16 co-factors and target genes play roles in the mediation of longevity and in protection from proteotoxicity. Thus, a careful characterization of the late life DAF-16 regulated protective mechanism is required to evaluate the therapeutic potential of IIS reduction as a future treatment for neurodegenerative disorders. Here I propose to use nematodes and mice to explore the DAF-16/FOXO co-factors and target genes that mediate stress resistance and protection from proteotoxicity in the aged organism. Dual experimental approach will be utilized to achieve this goal; a directed genetic screen for the identification of co-factors and temporally differential set of DNA microarrays for the recognition of late life DAF-16/FOX target genes. This project is expected to yield new insight and to serve as a platform for future studies.
Max ERC Funding
1 438 899 €
Duration
Start date: 2011-10-01, End date: 2017-09-30
Project acronym LOCALSTAR
Project Modelling star formation in the local universe
Researcher (PI) Clare Dobbs
Host Institution (HI) THE UNIVERSITY OF EXETER
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary The goal of this proposal is to revolutionize our understanding of star formation in nearby galaxies, using numerical simulations. Traditionally, research in star formation has considered the contraction of a giant molecular cloud (GMC), or more commonly a star forming core, under gravity. However there has been relatively little research on molecular clouds themselves, even though they provide the initial conditions for star formation, and thus determine the main assumptions for theories of star formation. The proposed research will focus on the scales of giant molecular clouds, the clouds of molecular hydrogen (H2) where most star formation takes place in nearby galaxies. These objects link galactic scale physics with the small scale physics of star formation. Only now are the computational resources becoming available to study the interstellar medium (ISM) numerically on galactic scales, and model the complex processes involved in GMC and star formation. Simultaneously observational programs (e.g. ALMA, Herschel, CARMA) are starting to resolve GMCs in nearby galaxies. Our research will involve performing calculations on scales from individual GMCs to interacting galaxies, and comparing to forthcoming observations to answer some of the most fundamental questions in star formation, such as why star formation is inefficient, how do GMCs form and what are their lifetimes.
Summary
The goal of this proposal is to revolutionize our understanding of star formation in nearby galaxies, using numerical simulations. Traditionally, research in star formation has considered the contraction of a giant molecular cloud (GMC), or more commonly a star forming core, under gravity. However there has been relatively little research on molecular clouds themselves, even though they provide the initial conditions for star formation, and thus determine the main assumptions for theories of star formation. The proposed research will focus on the scales of giant molecular clouds, the clouds of molecular hydrogen (H2) where most star formation takes place in nearby galaxies. These objects link galactic scale physics with the small scale physics of star formation. Only now are the computational resources becoming available to study the interstellar medium (ISM) numerically on galactic scales, and model the complex processes involved in GMC and star formation. Simultaneously observational programs (e.g. ALMA, Herschel, CARMA) are starting to resolve GMCs in nearby galaxies. Our research will involve performing calculations on scales from individual GMCs to interacting galaxies, and comparing to forthcoming observations to answer some of the most fundamental questions in star formation, such as why star formation is inefficient, how do GMCs form and what are their lifetimes.
Max ERC Funding
1 169 586 €
Duration
Start date: 2011-11-01, End date: 2017-05-31
Project acronym M&M´S
Project New Paradigms for MEMS & NEMS Integration
Researcher (PI) Frank Niklaus
Host Institution (HI) KUNGLIGA TEKNISKA HOEGSKOLAN
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary Micro- and nanoelectromechanical system (MEMS and NEMS) components are vital for many industrial and consumer products such as airbag systems in cars and motion controls in mobile phones, and many of these MEMS and NEMS enabled applications have a large impact on European industry and society. However, the potential of MEMS and NEMS is being critically hampered by their dependence on integrated circuit (IC) manufacturing technologies. Most micro- and nano-manufacturing methods have been developed by the IC industry and are characterized by highly standardized manufacturing processes that are adapted for extremely large production volumes of more than 10.000 wafers per month. In contrast, the vast majority of MEMS and NEMS applications only demands production volumes of less than 100 wafers per month in combination with different non-standardized manufacturing and integration processes for each product. If a much wider variety of diverse and even low-volume MEMS and NEMS products shall be exploited, the semiconductor manufacturing paradigm has to be broken. In this project, we therefore will focus on frontier research on new paradigms for flexible and cost-efficient manufacturing and integration of MEMS and NEMS within three related research areas:
(1) Wafer-Level Heterogeneous Integration for MEMS and NEMS, where we explore new and improved wafer-level heterogeneous integration technologies for MEMS and NEMS devices;
(2) Integration of Materials into MEMS Using High-Speed Wire Bonding Tools, where we explore new ways of integrating various types of wire materials into MEMS devices;
(3) Free-Form 3D Printing of Mono-Crystalline Silicon Micro- and Nanostructures, where we explore entirely novel ways of implementing mono-crystalline silicon MEMS and NEMS structures that can be arbitrarily shaped.
Summary
Micro- and nanoelectromechanical system (MEMS and NEMS) components are vital for many industrial and consumer products such as airbag systems in cars and motion controls in mobile phones, and many of these MEMS and NEMS enabled applications have a large impact on European industry and society. However, the potential of MEMS and NEMS is being critically hampered by their dependence on integrated circuit (IC) manufacturing technologies. Most micro- and nano-manufacturing methods have been developed by the IC industry and are characterized by highly standardized manufacturing processes that are adapted for extremely large production volumes of more than 10.000 wafers per month. In contrast, the vast majority of MEMS and NEMS applications only demands production volumes of less than 100 wafers per month in combination with different non-standardized manufacturing and integration processes for each product. If a much wider variety of diverse and even low-volume MEMS and NEMS products shall be exploited, the semiconductor manufacturing paradigm has to be broken. In this project, we therefore will focus on frontier research on new paradigms for flexible and cost-efficient manufacturing and integration of MEMS and NEMS within three related research areas:
(1) Wafer-Level Heterogeneous Integration for MEMS and NEMS, where we explore new and improved wafer-level heterogeneous integration technologies for MEMS and NEMS devices;
(2) Integration of Materials into MEMS Using High-Speed Wire Bonding Tools, where we explore new ways of integrating various types of wire materials into MEMS devices;
(3) Free-Form 3D Printing of Mono-Crystalline Silicon Micro- and Nanostructures, where we explore entirely novel ways of implementing mono-crystalline silicon MEMS and NEMS structures that can be arbitrarily shaped.
Max ERC Funding
1 495 982 €
Duration
Start date: 2011-11-01, End date: 2017-10-31
Project acronym NEURALCODES_EMO
Project Deciphering neural codes of valence-based emotional memories
Researcher (PI) Ron Paz
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Pioneering studies from the last decades have shown that we can use animal models to study the neural correlates of learning and emotional memories. These studies have identified a network of brain regions that co-orchestrate the dynamic processes that occur during acquisition, retrieval and update of memories with valence. In primates, these areas and their connectivity have evolved to allow a complex interaction between cognitive abilities and emotions. Although we know that emotional memories differ from neutral memories, the actual neural codes that underlie them are largely unknown. Understanding emotional memories at a detailed level in a primate model is a crucial step in our goal to understand ourselves, and would allow specific therapeutic interventions for a spectrum of psychiatric disorders.
Our primary objectives are: a. to develop a comprehensive battery of behavioral paradigms that targets emotional learning and memory in non-human primates; b. to understand the neural mechanisms that underlie long-term evolvement of these memories; c. to develop a computational and experimental framework to understand coding in these high-dimensionality networks. We combine large-scale inter- and intra-regional simultaneous electrophysiological recordings in the primate amygdala and prefrontal-cortices, with a set of focused paradigms that use behavioral generalization as a tool to probe the underlying neural building blocks. Generalization is a highly-evolved cognitive ability of primates and a desired feature of any learning algorithm. Importantly, it is a tool to modify the brain and unveil the structure of its internal representations i.e. the neural code. Together, it will form a unified framework to understand neural codes of learning and memory formation in valence-based situations. Our research will help establishing an emerging field of computational affective neuroscience, and our vision holds that Emotion is finally within the reach of neurophysiology.
Summary
Pioneering studies from the last decades have shown that we can use animal models to study the neural correlates of learning and emotional memories. These studies have identified a network of brain regions that co-orchestrate the dynamic processes that occur during acquisition, retrieval and update of memories with valence. In primates, these areas and their connectivity have evolved to allow a complex interaction between cognitive abilities and emotions. Although we know that emotional memories differ from neutral memories, the actual neural codes that underlie them are largely unknown. Understanding emotional memories at a detailed level in a primate model is a crucial step in our goal to understand ourselves, and would allow specific therapeutic interventions for a spectrum of psychiatric disorders.
Our primary objectives are: a. to develop a comprehensive battery of behavioral paradigms that targets emotional learning and memory in non-human primates; b. to understand the neural mechanisms that underlie long-term evolvement of these memories; c. to develop a computational and experimental framework to understand coding in these high-dimensionality networks. We combine large-scale inter- and intra-regional simultaneous electrophysiological recordings in the primate amygdala and prefrontal-cortices, with a set of focused paradigms that use behavioral generalization as a tool to probe the underlying neural building blocks. Generalization is a highly-evolved cognitive ability of primates and a desired feature of any learning algorithm. Importantly, it is a tool to modify the brain and unveil the structure of its internal representations i.e. the neural code. Together, it will form a unified framework to understand neural codes of learning and memory formation in valence-based situations. Our research will help establishing an emerging field of computational affective neuroscience, and our vision holds that Emotion is finally within the reach of neurophysiology.
Max ERC Funding
1 671 620 €
Duration
Start date: 2012-01-01, End date: 2017-08-31
Project acronym NEUROBAT
Project Neural codes for space in complex multi-scale environments: Insights from the bat
Researcher (PI) Nachum Ulanovsky
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Studies of spatial navigation and neural codes for space have followed two parallel tracks over the last 100 years: One research approach was to study animal navigation in the wild over large spatial scales (kilometers); this approach focused on non-mammalian species and on behavioral studies, with hardly any research on the underlying brain mechanisms. The other approach was to study the navigation of mammals (mostly rats) in mazes and small arenas; this approach revealed 'place cells' in the hippocampus, neurons that become active at specific locations; and 'grid cells' in entorhinal cortex – neurons that respond when the animal passes through the vertices of a hexagonal grid spanning the entire environment. However, it is unknown whether place- and grid-cells are relevant at all to large-scale navigation over kilometers. Thus, there is a large gap between the two parallel approaches to studying spatial memory and navigation – both a conceptual gap, and a gap in spatial scale. Here, we propose to bridge this gap, by recording from place cells and grid cells in a flying mammal – the bat – while it moves in 4 different environments of varying sizes, from centimeters to kilometers. We will conduct both standard (tethered) and wireless neural recordings, and will also pioneer the development of a novel sonar-based virtual reality system for studying large-scale navigation. The same neurons will be recorded across different spatial scales, which will allow comparing various neural-coding schemes. These new setups will allow the first testing for the existence of kilometer-sized hippocampal place-fields and entorhinal grids, in bats navigating through naturalistic virtual landscapes; they will also provide rich information on neural codes for 2-D and 3-D space in the mammalian brain. Our innovative project is expected to provide – for the first time – a true understanding of the brain mechanisms of large-scale, realistic navigation in complex 3-D environments.
Summary
Studies of spatial navigation and neural codes for space have followed two parallel tracks over the last 100 years: One research approach was to study animal navigation in the wild over large spatial scales (kilometers); this approach focused on non-mammalian species and on behavioral studies, with hardly any research on the underlying brain mechanisms. The other approach was to study the navigation of mammals (mostly rats) in mazes and small arenas; this approach revealed 'place cells' in the hippocampus, neurons that become active at specific locations; and 'grid cells' in entorhinal cortex – neurons that respond when the animal passes through the vertices of a hexagonal grid spanning the entire environment. However, it is unknown whether place- and grid-cells are relevant at all to large-scale navigation over kilometers. Thus, there is a large gap between the two parallel approaches to studying spatial memory and navigation – both a conceptual gap, and a gap in spatial scale. Here, we propose to bridge this gap, by recording from place cells and grid cells in a flying mammal – the bat – while it moves in 4 different environments of varying sizes, from centimeters to kilometers. We will conduct both standard (tethered) and wireless neural recordings, and will also pioneer the development of a novel sonar-based virtual reality system for studying large-scale navigation. The same neurons will be recorded across different spatial scales, which will allow comparing various neural-coding schemes. These new setups will allow the first testing for the existence of kilometer-sized hippocampal place-fields and entorhinal grids, in bats navigating through naturalistic virtual landscapes; they will also provide rich information on neural codes for 2-D and 3-D space in the mammalian brain. Our innovative project is expected to provide – for the first time – a true understanding of the brain mechanisms of large-scale, realistic navigation in complex 3-D environments.
Max ERC Funding
1 499 999 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym NEUROFEAR
Project Neuronal circuits controlling fear behavior
Researcher (PI) Cyril Herry
Host Institution (HI) INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Accurate adaptation to stimuli predicting threatening outcome is critical to survival. An insufficient fear reaction may lead the animal to overlook future signs of danger, whereas overreacting may lead the animal to failure to explore and miss opportunities for feeding or mating. Numerous data indicate that the medial prefrontal cortex (mPFC) plays a key role in the control of fear behavior and that distinct prefrontal areas differentially regulate the expression/inhibition of fear responses. Whereas lesions/inactivations of the mPFC infralimbic (IL) area promote fear expression, lesions/inactivations of the mPFC prelimbic area (PL) promote fear inhibition. Moreover, PL and IL receive segregated inputs from functionally distinct amygdala circuits activated during high and low fear states. These data suggest that a key function of mPFC circuits might be to integrate inputs from the amygdala to ultimately gate fear expression via projections to specific neuronal circuits. However, little is known about the underlying neuronal circuits. Is the rapid switch between expression/suppression of fear behaviors mediated by the same circuits or does the mPFC contain distinct circuits dedicated to the control of opposite behaviors? Is there an organization in terms of afferents and efferent at the level of mPFC neuronal circuits? To address these questions we will use a cross-level approach combining in vivo electrophysiological optogenetic and behavioral approaches to elucidate the anatomical/physiological properties of mPFC circuits and to address their functional role in the control of fear behavior. We will first examine the activation and connectivity of mPFC circuits using in vivo extracellular recordings and extracellular stimulations. We will next selectively manipulate these circuits during behavior using light-activated proteins to establish causal relationships. Finally we will study their plasticity and anatomical properties using in vivo intracellular recordings.
Summary
Accurate adaptation to stimuli predicting threatening outcome is critical to survival. An insufficient fear reaction may lead the animal to overlook future signs of danger, whereas overreacting may lead the animal to failure to explore and miss opportunities for feeding or mating. Numerous data indicate that the medial prefrontal cortex (mPFC) plays a key role in the control of fear behavior and that distinct prefrontal areas differentially regulate the expression/inhibition of fear responses. Whereas lesions/inactivations of the mPFC infralimbic (IL) area promote fear expression, lesions/inactivations of the mPFC prelimbic area (PL) promote fear inhibition. Moreover, PL and IL receive segregated inputs from functionally distinct amygdala circuits activated during high and low fear states. These data suggest that a key function of mPFC circuits might be to integrate inputs from the amygdala to ultimately gate fear expression via projections to specific neuronal circuits. However, little is known about the underlying neuronal circuits. Is the rapid switch between expression/suppression of fear behaviors mediated by the same circuits or does the mPFC contain distinct circuits dedicated to the control of opposite behaviors? Is there an organization in terms of afferents and efferent at the level of mPFC neuronal circuits? To address these questions we will use a cross-level approach combining in vivo electrophysiological optogenetic and behavioral approaches to elucidate the anatomical/physiological properties of mPFC circuits and to address their functional role in the control of fear behavior. We will first examine the activation and connectivity of mPFC circuits using in vivo extracellular recordings and extracellular stimulations. We will next selectively manipulate these circuits during behavior using light-activated proteins to establish causal relationships. Finally we will study their plasticity and anatomical properties using in vivo intracellular recordings.
Max ERC Funding
1 496 300 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym NeuroOptoGen
Project Optogenetic examination of the role of feedback on visual processing and perception
Researcher (PI) Hendrikje Nienborg
Host Institution (HI) EBERHARD KARLS UNIVERSITAET TUEBINGEN
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary We need to understand the brain mechanisms of perception and cognition in order to develop treatments for disorders in which these abilities fail, such as schizophrenia, attention-deficit-hyperactivity disorder or autism. Over the past half-century neurophysiologists have enormously advanced our knowledge of how the feed-forward connections give rise to the response properties in the visual cortex. However, although we know from anatomy that most afferents in cortex constitute feedback projections, their function is still largely unknown.
Visual perception in humans and monkeys depends on context. These perceptual phenomena are thought to be mediated by feedback, and many are altered in schizophrenic patients. Understanding the role of feedback is therefore important not only for unraveling fundamental mechanisms of cognition, but also for addressing their dysfunction in cognitive disorders. Until now technical limitations have made it nearly impossible to test the role of feedback.
Novel approaches allow us to examine the role of cortico-cortical feedback in visual perception in the behaving monkey. We will use optogenetic techniques and retrograde viral vectors (lentivirus pseudotyped with rabies glycoprotein) to target specific monosynaptic cortico-cortical projections in vivo. By expressing the light-sensitive proteins channelrhodopsin2 (ChrR2) or archaerhodopsin (Arch) in these projection neurons, we can activate (ChR2) or inactivate (Arch) them with light. We will combine this approach with multi-channel electrophysiology, behavior and computational analyses. We will first quantify the effect of (in)activating cortico-cortical feedback from visual cortex V2 on the neuronal responses in the primary visual, and then on the monkey’s visual perception during tasks manipulating attention. If successful, this work will help advance our functional understanding of feedback, and may open the possibility to examine the function of any connection in the primate brain.
Summary
We need to understand the brain mechanisms of perception and cognition in order to develop treatments for disorders in which these abilities fail, such as schizophrenia, attention-deficit-hyperactivity disorder or autism. Over the past half-century neurophysiologists have enormously advanced our knowledge of how the feed-forward connections give rise to the response properties in the visual cortex. However, although we know from anatomy that most afferents in cortex constitute feedback projections, their function is still largely unknown.
Visual perception in humans and monkeys depends on context. These perceptual phenomena are thought to be mediated by feedback, and many are altered in schizophrenic patients. Understanding the role of feedback is therefore important not only for unraveling fundamental mechanisms of cognition, but also for addressing their dysfunction in cognitive disorders. Until now technical limitations have made it nearly impossible to test the role of feedback.
Novel approaches allow us to examine the role of cortico-cortical feedback in visual perception in the behaving monkey. We will use optogenetic techniques and retrograde viral vectors (lentivirus pseudotyped with rabies glycoprotein) to target specific monosynaptic cortico-cortical projections in vivo. By expressing the light-sensitive proteins channelrhodopsin2 (ChrR2) or archaerhodopsin (Arch) in these projection neurons, we can activate (ChR2) or inactivate (Arch) them with light. We will combine this approach with multi-channel electrophysiology, behavior and computational analyses. We will first quantify the effect of (in)activating cortico-cortical feedback from visual cortex V2 on the neuronal responses in the primary visual, and then on the monkey’s visual perception during tasks manipulating attention. If successful, this work will help advance our functional understanding of feedback, and may open the possibility to examine the function of any connection in the primate brain.
Max ERC Funding
1 903 114 €
Duration
Start date: 2012-07-01, End date: 2017-06-30
Project acronym NEXTPHASE
Project NEXT generation of microwave PHotonic systems for AeroSpace Engineering
Researcher (PI) Yanne Chembo Kouomou
Host Institution (HI) CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary Aerospace and communication engineering technologies are in constant need of microwaves with extremely high spectral purity and stability. Unfortunately, the generation of such ultra-pure microwaves with compact, versatile and transportable sources is still a very complex challenge. In aerospace engineering, ultra-stable quartz oscillators are overwhelmingly dominant as key components for both navigation and detection systems. However, it is unanimously recognized today that their frequency stability performance is reaching its floor, and will not improve significantly anymore. In the search for an alternative standard for the next generation of ultra-pure microwave sources in aerospace technology, we propose the exploration of an elegant and promising solution relying on optical resonators with ultra-high Q factors (Q ~ 1E10). In these quasi-perfectly shaped cavities, nonlinear effects are significantly enhanced and microwave generation is performed through the extraction of the intermodal frequency. This approach has several advantages over existing or other prospective methods: conceptual simplicity, higher robustness, smaller power consumption, longer lifetime, immunity to interferences, very compact volume, frequency versatility, easy chip integration, as well as a strong potential for integrating the mainstream of standard photonic components for both microwave and lightwave technologies. Our ambition in the NextPhase project is to significantly outperform quartz oscillators and demonstrate performances comparable to cryogenic sapphire oscillators, with a compact (< 100 cm3), versatile (up to at least 200 GHz) and ultra-stable (Allan variance ~ 1E-15 at 1 s; phase noise floor < -160 dBc/Hz) microwave photonic generator. We also expect our work to open new opportunities of research in optical communications (photonic components for full-optical processing, carrier synthesis), as well as in fundamental aspects of condensed matter and quantum physics.
Summary
Aerospace and communication engineering technologies are in constant need of microwaves with extremely high spectral purity and stability. Unfortunately, the generation of such ultra-pure microwaves with compact, versatile and transportable sources is still a very complex challenge. In aerospace engineering, ultra-stable quartz oscillators are overwhelmingly dominant as key components for both navigation and detection systems. However, it is unanimously recognized today that their frequency stability performance is reaching its floor, and will not improve significantly anymore. In the search for an alternative standard for the next generation of ultra-pure microwave sources in aerospace technology, we propose the exploration of an elegant and promising solution relying on optical resonators with ultra-high Q factors (Q ~ 1E10). In these quasi-perfectly shaped cavities, nonlinear effects are significantly enhanced and microwave generation is performed through the extraction of the intermodal frequency. This approach has several advantages over existing or other prospective methods: conceptual simplicity, higher robustness, smaller power consumption, longer lifetime, immunity to interferences, very compact volume, frequency versatility, easy chip integration, as well as a strong potential for integrating the mainstream of standard photonic components for both microwave and lightwave technologies. Our ambition in the NextPhase project is to significantly outperform quartz oscillators and demonstrate performances comparable to cryogenic sapphire oscillators, with a compact (< 100 cm3), versatile (up to at least 200 GHz) and ultra-stable (Allan variance ~ 1E-15 at 1 s; phase noise floor < -160 dBc/Hz) microwave photonic generator. We also expect our work to open new opportunities of research in optical communications (photonic components for full-optical processing, carrier synthesis), as well as in fundamental aspects of condensed matter and quantum physics.
Max ERC Funding
1 384 628 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym PEBBLE2PLANET
Project From pebbles to planets: towards new horizons in the formation of planets
Researcher (PI) Anders Johansen
Host Institution (HI) LUNDS UNIVERSITET
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary "The goal of this ERC Starting Grant proposal is to make significant advances in our understanding of how planetesimals and gas giant planets form. I propose an ambitious research programme dedicated to answering three key questions at the frontier of planet formation theory: - How do mm-sized particles grow past the bouncing barrier? - What is the Initial Mass Function of planetesimals? - How do the cores of gas giants form and evolve?} I will address these questions using a combination of novel ideas and computer simulations to model three critical stages of planet formation: 1) the growth of pebbles into rocks and boulders by coagulation and vapour condensation, 2) the gravitational collapse of clumps of rocks and boulders into planetesimals with an array of sizes, and 3) the long term growth of planetesimals as they grow to become cores of gas giants by accreting pebbles embedded in the gas. These investigations will form an important theoretical foundation for understanding the next generation of observations of protoplanetary disc pebbles, planetesimal belts, and planetary systems. The self-consistent models for the formation of planets resulting from this proposal will shed light on the spatial distribution of pebbles in gas discs around young stars (observable with the ALMA telescopes), on the initial state of planetesimal belts (crucial for understanding the evolution of debris discs observable with JWST and the asteroid and Kuiper belts), and on the formation and evolution of the wealth of exoplanetary systems detected in the near future (by astrometry with the Gaia satellite, by ground-based radial velocity surveys, and by direct imaging with E-ELT)."
Summary
"The goal of this ERC Starting Grant proposal is to make significant advances in our understanding of how planetesimals and gas giant planets form. I propose an ambitious research programme dedicated to answering three key questions at the frontier of planet formation theory: - How do mm-sized particles grow past the bouncing barrier? - What is the Initial Mass Function of planetesimals? - How do the cores of gas giants form and evolve?} I will address these questions using a combination of novel ideas and computer simulations to model three critical stages of planet formation: 1) the growth of pebbles into rocks and boulders by coagulation and vapour condensation, 2) the gravitational collapse of clumps of rocks and boulders into planetesimals with an array of sizes, and 3) the long term growth of planetesimals as they grow to become cores of gas giants by accreting pebbles embedded in the gas. These investigations will form an important theoretical foundation for understanding the next generation of observations of protoplanetary disc pebbles, planetesimal belts, and planetary systems. The self-consistent models for the formation of planets resulting from this proposal will shed light on the spatial distribution of pebbles in gas discs around young stars (observable with the ALMA telescopes), on the initial state of planetesimal belts (crucial for understanding the evolution of debris discs observable with JWST and the asteroid and Kuiper belts), and on the formation and evolution of the wealth of exoplanetary systems detected in the near future (by astrometry with the Gaia satellite, by ground-based radial velocity surveys, and by direct imaging with E-ELT)."
Max ERC Funding
1 332 467 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym PERCEPT
Project Cortical circuits of visual perception
Researcher (PI) Steffen Dieter Katzner
Host Institution (HI) EBERHARD KARLS UNIVERSITAET TUEBINGEN
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Active perception relies on the concerted activity of populations of neurons in the cerebral cortex. These neuronal populations communicate via dense local and long-range connections, forming complex cortical circuits. While we are beginning to understand the elementary building blocks of such circuits during sensory processing, the circuit-level mechanisms by which top-down signals modulate sensory activity are largely unknown.
The core of my proposal is to dissect the cortical circuits underlying top-down guided visual perception during active behaviour. The primary innovation of this proposal is to seek large-scale recordings from single neurons of identified type across all cortical layers in an actively behaving animal performing a well- controlled perceptual task.
In Aim 1 we will develop novel paradigms to perform in the mouse visual perception experiments that achieve the ‘gold-standard’ in experimental control set by the behaving monkey. We will train mice in psychophysical tasks that offer exquisite control over the visual stimulus and the behavioural response, yield hundreds of trials per session, can be easily combined with recordings of neuronal activity and allow the manipulation of top-down factors.
In Aim 2 we will conduct, for the first time, a detailed, circuit-level analysis of top-down modulations of sensory processing in visual cortex. Specifically, we will identify inhibitory interneurons in the neuronal population with optogenetic techniques and ask how behavioural relevance modulates activity for different cell types.
This work will bring us closer to a functional explanation of active perception and will bridge the gap between two hitherto disconnected fields: it will open up questions of Cognitive Neuroscience for the field of Cellular Neuroscience.
Summary
Active perception relies on the concerted activity of populations of neurons in the cerebral cortex. These neuronal populations communicate via dense local and long-range connections, forming complex cortical circuits. While we are beginning to understand the elementary building blocks of such circuits during sensory processing, the circuit-level mechanisms by which top-down signals modulate sensory activity are largely unknown.
The core of my proposal is to dissect the cortical circuits underlying top-down guided visual perception during active behaviour. The primary innovation of this proposal is to seek large-scale recordings from single neurons of identified type across all cortical layers in an actively behaving animal performing a well- controlled perceptual task.
In Aim 1 we will develop novel paradigms to perform in the mouse visual perception experiments that achieve the ‘gold-standard’ in experimental control set by the behaving monkey. We will train mice in psychophysical tasks that offer exquisite control over the visual stimulus and the behavioural response, yield hundreds of trials per session, can be easily combined with recordings of neuronal activity and allow the manipulation of top-down factors.
In Aim 2 we will conduct, for the first time, a detailed, circuit-level analysis of top-down modulations of sensory processing in visual cortex. Specifically, we will identify inhibitory interneurons in the neuronal population with optogenetic techniques and ask how behavioural relevance modulates activity for different cell types.
This work will bring us closer to a functional explanation of active perception and will bridge the gap between two hitherto disconnected fields: it will open up questions of Cognitive Neuroscience for the field of Cellular Neuroscience.
Max ERC Funding
1 299 992 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym PFPMWC
Project Probing fundamental physics with multi-wavelength cosmology
Researcher (PI) Michael Brown
Host Institution (HI) THE UNIVERSITY OF MANCHESTER
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary "Recent measurements of the Cosmic Microwave Background (CMB) combined with the large-scale distribution of galaxies have defined a standard cosmological model. This model is a remarkable fit to the observations but also raises profound questions - we do not know how the initial conditions were imprinted in the early Universe, nor do we know the nature of the dark energy. In this proposal, I request funds to set up a new cosmology data analysis team at the University of Manchester to tackle these issues. Over the next five years, my team will pursue a program of work intended to have a large impact on two hugely important fields of observational cosmology which are uniquely suited to answering these questions --- the polarisation of the microwave background and weak gravitational lensing. The former is the most powerful way to probe the early Universe while the latter is potentially the most sensitive probe of dark energy. Building on the innovative methods I developed for the QUaD experiment, I will apply new analysis techniques to mitigate systematics and maximise the science return from current and future CMB polarisation experiments including the Planck satellite, the ground-based QUIJOTE experiment and phase 2 of the ground-based QUIET experiment. In the field of weak lensing, I will perform pioneering radio lensing analyses with forthcoming instruments including the Square Kilometre Array pathfinders, e-MERLIN and MeerKAT. One particularly novel idea which I will develop is the use of polarisation information to reduce noise and to minimise contamination from the intrinsic alignment of galaxies in radio lensing analyses. The research described in this proposal will allow my team to establish an international leadership position in both CMB polarisation and radio weak lensing research in advance of a possible CMB polarisation satellite mission and the commissioning of the Square Kilometre Array radio telescope towards the latter part of this decade."
Summary
"Recent measurements of the Cosmic Microwave Background (CMB) combined with the large-scale distribution of galaxies have defined a standard cosmological model. This model is a remarkable fit to the observations but also raises profound questions - we do not know how the initial conditions were imprinted in the early Universe, nor do we know the nature of the dark energy. In this proposal, I request funds to set up a new cosmology data analysis team at the University of Manchester to tackle these issues. Over the next five years, my team will pursue a program of work intended to have a large impact on two hugely important fields of observational cosmology which are uniquely suited to answering these questions --- the polarisation of the microwave background and weak gravitational lensing. The former is the most powerful way to probe the early Universe while the latter is potentially the most sensitive probe of dark energy. Building on the innovative methods I developed for the QUaD experiment, I will apply new analysis techniques to mitigate systematics and maximise the science return from current and future CMB polarisation experiments including the Planck satellite, the ground-based QUIJOTE experiment and phase 2 of the ground-based QUIET experiment. In the field of weak lensing, I will perform pioneering radio lensing analyses with forthcoming instruments including the Square Kilometre Array pathfinders, e-MERLIN and MeerKAT. One particularly novel idea which I will develop is the use of polarisation information to reduce noise and to minimise contamination from the intrinsic alignment of galaxies in radio lensing analyses. The research described in this proposal will allow my team to establish an international leadership position in both CMB polarisation and radio weak lensing research in advance of a possible CMB polarisation satellite mission and the commissioning of the Square Kilometre Array radio telescope towards the latter part of this decade."
Max ERC Funding
1 424 269 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym RECOSAMP
Project Sampling and Reconstruction driven by Sparsity Models with Applications in Sensor Networks and Neuroscience
Researcher (PI) Pier Luigi Dragotti
Host Institution (HI) IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary The problem of reconstructing or estimating partially observed or
sampled signals is animportant one that finds application
in many areas of signal processing and communications. Traditional
acquisition and reconstruction approaches are heavily influences by
classical Shannon sampling theory which gives an exact sampling
and interpolation formula for bandlimited signals. Recently, the
emerging theory of sparse sampling has challenged the way
we think about signal acquisition and has demonstrated that, by
using more sophisticated signal models, it is possible to break away
from the need to sample signals at the Nyquist rate.
The insight that
sub-Nyquist sampling can, under some circumstances, allow perfect
reconstruction is revolutionizing signal processing, communications
and inverse problems.
Given the
ubiquity of the sampling process, the implications of these new
research developments are far reaching.
This project is based on the applicant's recent work on the sampling
of sparse continuous-time signals and aims to extend the existing theory to include more
general signal models that are closer to the physical
characteristics of real data, to explore new domains where sparsity
and sampling can be effectively used and to provide a set
of new fast algorithms with clear and predictable performance.
As
part of this work, he will also consider timely important problems
such as the localization of diffusive sources in sensor networks and
the analysis of neuronal signals of the brain. He will, for the
first time, pose these as sparse sampling problems and in this way
he expects to develop technologies with a step change in
performance.
Summary
The problem of reconstructing or estimating partially observed or
sampled signals is animportant one that finds application
in many areas of signal processing and communications. Traditional
acquisition and reconstruction approaches are heavily influences by
classical Shannon sampling theory which gives an exact sampling
and interpolation formula for bandlimited signals. Recently, the
emerging theory of sparse sampling has challenged the way
we think about signal acquisition and has demonstrated that, by
using more sophisticated signal models, it is possible to break away
from the need to sample signals at the Nyquist rate.
The insight that
sub-Nyquist sampling can, under some circumstances, allow perfect
reconstruction is revolutionizing signal processing, communications
and inverse problems.
Given the
ubiquity of the sampling process, the implications of these new
research developments are far reaching.
This project is based on the applicant's recent work on the sampling
of sparse continuous-time signals and aims to extend the existing theory to include more
general signal models that are closer to the physical
characteristics of real data, to explore new domains where sparsity
and sampling can be effectively used and to provide a set
of new fast algorithms with clear and predictable performance.
As
part of this work, he will also consider timely important problems
such as the localization of diffusive sources in sensor networks and
the analysis of neuronal signals of the brain. He will, for the
first time, pose these as sparse sampling problems and in this way
he expects to develop technologies with a step change in
performance.
Max ERC Funding
1 451 162 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym RSSCEMSR
Project Role of Secondary Sensory Cortices in Emotional Memory Storage/Retrieval
Researcher (PI) Benedetto Sacchetti
Host Institution (HI) UNIVERSITA DEGLI STUDI DI TORINO
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary "Sensory stimuli, like odors, sound and colors, acquire positive or negative value through their association with rewards or punishments, a process called “emotional learning”. Although we know a great deal about how the brain analyses sensory information, we know relatively little about how sensory representations become linked with values and where such emotional memory is stored. Recently, we have demonstrated that higher order sensory cortices are necessary for the long-term storage of aversive memories. We hypothesized that such cortices represent the link between the neural sites that elaborate the physical features of sensory stimuli and the areas elaborating affective information. The present study is aimed at elucidating this issue.
First, we will investigate if sensory cortices are mainly involved in the storage of aversive memories or alternatively if they participate also to the encoding of hedonic memories, i.e. if the brain normally uses higher order sensory cortices in order to allocate emotional positive as well negative memories. Then, we will address the crucial issue of whether and how these areas encode the emotional meaning that sensory stimuli acquire with the experience. Finally, we will study the functional dialogue that may occur during emotional memory storage/retrieval between sensory cortices and subcortical nuclei.
To tackle these topics, we will employ a multidisciplinary approach made of the combination of behavioural, electrophysiological, immunohistochemical and confocal analyses. In our aim, the results obtained will provide new and important information about the brain circuitry that stores affective memories. In particular, they could led to the idea that higher-level sensory cortices encode the emotional value acquired by sensory stimuli and thus through their connections with other cortical and subcortical centres they enable identical sensory stimuli to trigger different emotional responses depending on past emotional experience"
Summary
"Sensory stimuli, like odors, sound and colors, acquire positive or negative value through their association with rewards or punishments, a process called “emotional learning”. Although we know a great deal about how the brain analyses sensory information, we know relatively little about how sensory representations become linked with values and where such emotional memory is stored. Recently, we have demonstrated that higher order sensory cortices are necessary for the long-term storage of aversive memories. We hypothesized that such cortices represent the link between the neural sites that elaborate the physical features of sensory stimuli and the areas elaborating affective information. The present study is aimed at elucidating this issue.
First, we will investigate if sensory cortices are mainly involved in the storage of aversive memories or alternatively if they participate also to the encoding of hedonic memories, i.e. if the brain normally uses higher order sensory cortices in order to allocate emotional positive as well negative memories. Then, we will address the crucial issue of whether and how these areas encode the emotional meaning that sensory stimuli acquire with the experience. Finally, we will study the functional dialogue that may occur during emotional memory storage/retrieval between sensory cortices and subcortical nuclei.
To tackle these topics, we will employ a multidisciplinary approach made of the combination of behavioural, electrophysiological, immunohistochemical and confocal analyses. In our aim, the results obtained will provide new and important information about the brain circuitry that stores affective memories. In particular, they could led to the idea that higher-level sensory cortices encode the emotional value acquired by sensory stimuli and thus through their connections with other cortical and subcortical centres they enable identical sensory stimuli to trigger different emotional responses depending on past emotional experience"
Max ERC Funding
1 116 000 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym SENSTRIATUM
Project Sensory Integration in the Striatal Microcircuit
Researcher (PI) Gilad Daniel Silberberg
Host Institution (HI) KAROLINSKA INSTITUTET
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Motor behaviour requires the meaningful integration of a multitude of sensory information. The basal ganglia are essential for such sensory-motor processing and underlie motor planning, performance, and learning. The striatum is the input layer of the basal ganglia, acting as a “hub” that receives synaptic inputs from different brain regions, interacting primarily with the GABAergic striatal microcircuit. Sensory excitatory inputs to striatum arise from the thalamus and neocortex, targeting striatal projection neurons and interneurons.
Previous work in basal ganglia focused mainly on their role in motor and reward related functions, but the functional role of striatum in sensory processing is largely unknown. In this study I will elucidate the principles of sensory processing performed at the striatal microcircuit. In particular, I aim to answer these fundamental questions:
- How do striatal neurons integrate sensory input? How is sensory input from different sensory modalities integrated in the striatum? How are ipsi- and contralateral inputs integrated?
- What are the respective roles of cortical and thalamic sensory inputs in striatal function?
- How is the intra-striatal microcircuitry organized to support sensory integration?
To address these questions I will use a combination of electrophysiological, optical, and anatomical methods, including:
- In vivo whole-cell recordings from striatal neurons during visual and tactile stimulation.
- Multi-neuron whole-cell recordings in corticostriatal and thalamostriatal slices.
- Optical manipulation of identified neuronal subpopulations in slice and in vivo.
The proposed study will provide a new understanding of sensory processing at the level of basal ganglia and may provide insights regarding basal ganglia dysfunction.
Summary
Motor behaviour requires the meaningful integration of a multitude of sensory information. The basal ganglia are essential for such sensory-motor processing and underlie motor planning, performance, and learning. The striatum is the input layer of the basal ganglia, acting as a “hub” that receives synaptic inputs from different brain regions, interacting primarily with the GABAergic striatal microcircuit. Sensory excitatory inputs to striatum arise from the thalamus and neocortex, targeting striatal projection neurons and interneurons.
Previous work in basal ganglia focused mainly on their role in motor and reward related functions, but the functional role of striatum in sensory processing is largely unknown. In this study I will elucidate the principles of sensory processing performed at the striatal microcircuit. In particular, I aim to answer these fundamental questions:
- How do striatal neurons integrate sensory input? How is sensory input from different sensory modalities integrated in the striatum? How are ipsi- and contralateral inputs integrated?
- What are the respective roles of cortical and thalamic sensory inputs in striatal function?
- How is the intra-striatal microcircuitry organized to support sensory integration?
To address these questions I will use a combination of electrophysiological, optical, and anatomical methods, including:
- In vivo whole-cell recordings from striatal neurons during visual and tactile stimulation.
- Multi-neuron whole-cell recordings in corticostriatal and thalamostriatal slices.
- Optical manipulation of identified neuronal subpopulations in slice and in vivo.
The proposed study will provide a new understanding of sensory processing at the level of basal ganglia and may provide insights regarding basal ganglia dysfunction.
Max ERC Funding
1 494 445 €
Duration
Start date: 2012-02-01, End date: 2017-01-31
Project acronym SEROTONINANDDISEASE
Project Dissecting the gene regulatory mechanisms that generate serotonergic neurons and their link to mental disorders
Researcher (PI) Nuria Flames Bonilla
Host Institution (HI) AGENCIA ESTATAL CONSEJO SUPERIOR DEINVESTIGACIONES CIENTIFICAS
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Mental disorders constitute a human an economic burden for developed countries. Many mental disorders are linked to serotonin dysfunction, but the exact mechanism underlying these disorders is not well understood. Serotonin Related Mental Disorders (SRMD) are multigenic, making the identification of these mechanisms a difficult task. Understanding the molecular mechanisms that generate serotonergic neurons will provide us with the tools to identify mutations that could predispose to SRMD. In this grant we will use a multidisciplinary approach to dissect the transcriptional mechanisms that generate serotonergic neurons and use this knowledge to identify genetic links to SRMD. Serotonergic neurons are very ancient in evolution and enzymes and transporters responsible for the production of serotonin (serotonin pathway genes) are very well conserved in all metazoans. We would take advantage of this evolutionary conservation and use the genetic amenability of C. elegans to dissect the genetic mechanisms responsible for the generation of the serotonergic neurons. We will apply the lessons learned from C. elegans to unravel analogous mechanisms regulating mouse serotonergic differentiation. Our preliminary results show that the serotonergic pathway genes are co-regulated by the same factors and that this mechanism is evolutionary conserved. We will identify the cis-acting sequences (serotonergic motif) and trans-acting factors responsible for the activation of the serotonergic features, both in worms and mice. Finally, we will apply our knowledge on serotonergic differentiation to identify genetic association to SRMDs. Mutations in the serotonergic motif could lead to defects on the expression of the serotonergic genes, resulting in a dysfunctional serotonergic neuron. We will build a database of all human serotonergic motifs and look for mutations in these sites in SRMD patients. In summary, this grant will give us the tools to better understand and treat SRMD.
Summary
Mental disorders constitute a human an economic burden for developed countries. Many mental disorders are linked to serotonin dysfunction, but the exact mechanism underlying these disorders is not well understood. Serotonin Related Mental Disorders (SRMD) are multigenic, making the identification of these mechanisms a difficult task. Understanding the molecular mechanisms that generate serotonergic neurons will provide us with the tools to identify mutations that could predispose to SRMD. In this grant we will use a multidisciplinary approach to dissect the transcriptional mechanisms that generate serotonergic neurons and use this knowledge to identify genetic links to SRMD. Serotonergic neurons are very ancient in evolution and enzymes and transporters responsible for the production of serotonin (serotonin pathway genes) are very well conserved in all metazoans. We would take advantage of this evolutionary conservation and use the genetic amenability of C. elegans to dissect the genetic mechanisms responsible for the generation of the serotonergic neurons. We will apply the lessons learned from C. elegans to unravel analogous mechanisms regulating mouse serotonergic differentiation. Our preliminary results show that the serotonergic pathway genes are co-regulated by the same factors and that this mechanism is evolutionary conserved. We will identify the cis-acting sequences (serotonergic motif) and trans-acting factors responsible for the activation of the serotonergic features, both in worms and mice. Finally, we will apply our knowledge on serotonergic differentiation to identify genetic association to SRMDs. Mutations in the serotonergic motif could lead to defects on the expression of the serotonergic genes, resulting in a dysfunctional serotonergic neuron. We will build a database of all human serotonergic motifs and look for mutations in these sites in SRMD patients. In summary, this grant will give us the tools to better understand and treat SRMD.
Max ERC Funding
1 931 621 €
Duration
Start date: 2012-12-01, End date: 2018-11-30
Project acronym SPIA
Project Magnetic connectivity through the Solar Partially Ionized Atmosphere
Researcher (PI) Olena Khomenko
Host Institution (HI) INSTITUTO DE ASTROFISICA DE CANARIAS
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary The broad scientific objective of the SPIA proposal is to understand the magnetism of the Sun and stars and to establish connections between the magnetic activity in sub-surface layers and its manifestation in the outer atmosphere. The complex interactions in magnetized stellar plasmas are best studied via numerical simulations, a new powerful method of research that appeared in astrophysics with the development of large supercomputer facilities. With a coming era of large aperture solar telescopes, ATST and EST, spectropolarimetric observations of the Sun will become available at extraordinary high spatial and temporal resolutions. New modelling tools are required to understand the plasma behaviour at these scales. I propose to consolidate a research group of bright scientists around the PI to explore a novel promising approach for the description solar atmospheric plasma under multi-fluid approximation. The degree of plasma ionization in the photosphere and chromosphere of the Sun is extremely low and significant deviations from the classical magneto-hydrodynamic description are expected. A major development of the SPIA proposal will be the implementation of a multi-fluid plasma description, appropriate for a partially ionized medium, relaxing approximations of classical magneto-hydrodynamics. With the inclusion of standard radiative transfer into the three-dimensional multi-fluid code to be developed by the project team, it will be possible to perform simulations of solar sub-photospheric and photospheric regions, up to the low chromosphere, with a realism not achieved before. The importance of the non-ideal plasma effect for the energy balance of the solar chromosphere will be evaluated, and three-dimensional time-dependent models of multi-fluid magneto-convection will be created. This effort will produce a significant step toward the solution of the long-standing question of the origin of solar chromosphere, one of the most poorly understood regions of the Sun.
Summary
The broad scientific objective of the SPIA proposal is to understand the magnetism of the Sun and stars and to establish connections between the magnetic activity in sub-surface layers and its manifestation in the outer atmosphere. The complex interactions in magnetized stellar plasmas are best studied via numerical simulations, a new powerful method of research that appeared in astrophysics with the development of large supercomputer facilities. With a coming era of large aperture solar telescopes, ATST and EST, spectropolarimetric observations of the Sun will become available at extraordinary high spatial and temporal resolutions. New modelling tools are required to understand the plasma behaviour at these scales. I propose to consolidate a research group of bright scientists around the PI to explore a novel promising approach for the description solar atmospheric plasma under multi-fluid approximation. The degree of plasma ionization in the photosphere and chromosphere of the Sun is extremely low and significant deviations from the classical magneto-hydrodynamic description are expected. A major development of the SPIA proposal will be the implementation of a multi-fluid plasma description, appropriate for a partially ionized medium, relaxing approximations of classical magneto-hydrodynamics. With the inclusion of standard radiative transfer into the three-dimensional multi-fluid code to be developed by the project team, it will be possible to perform simulations of solar sub-photospheric and photospheric regions, up to the low chromosphere, with a realism not achieved before. The importance of the non-ideal plasma effect for the energy balance of the solar chromosphere will be evaluated, and three-dimensional time-dependent models of multi-fluid magneto-convection will be created. This effort will produce a significant step toward the solution of the long-standing question of the origin of solar chromosphere, one of the most poorly understood regions of the Sun.
Max ERC Funding
969 600 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym TeraGaN
Project GaN Quantum Devices for T-Ray Sources
Researcher (PI) Eva Maria Monroy Fernandez
Host Institution (HI) COMMISSARIAT A L ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES
Call Details Starting Grant (StG), PE7, ERC-2011-StG_20101014
Summary T-rays, often called terahertz radiation or submillimeter waves, are loosely defined as the wavelengths from 30 µm to 1,000 µm, or the frequencies from 10 THz to 300 GHz. This non-ionizing radiation appears as a harmless alternative to x-rays in medical, biological and security screening. Current solutions in terms of coherent sources of T-rays either require cryogenic temperatures or are relatively bulky equipments based on optically-pumped materials. The solid-state recourse consisting of GaAs-based quantum cascade lasers presents an intrinsic limitation in operation temperature: The low energy of the longitudinal-optical (LO) phonon in arsenide compounds hinders laser emission beyond 180 K at 4 THz, and forces operation below the liquid nitrogen temperature (< 70 K) for frequencies below 1 THz. Overcoming this limitation requires a technology revolution through introduction of a new material system. This project aims at exploring a novel semiconductor technology for high-performance photonic devices operating in the T-ray spectral region. The advanced materials that we will investigate consist of nitride-based [GaN/Al(Ga,In)N] superlattices and nanowires, where we can profit from unique properties of III-nitride semiconductors, namely the large LO-phonon energy and the strong electron-phonon interaction. Our target is to adapt the quantum cascade design and fabrication technology to these new materials, characterized by intense internal polarization fields. Our project aims at pushing intersubband transitions in this material family to unprecendently long wavelengths, in other to cover the whole T-ray spectral gap with coherent solid-state sources operating at room temperature and above.
Summary
T-rays, often called terahertz radiation or submillimeter waves, are loosely defined as the wavelengths from 30 µm to 1,000 µm, or the frequencies from 10 THz to 300 GHz. This non-ionizing radiation appears as a harmless alternative to x-rays in medical, biological and security screening. Current solutions in terms of coherent sources of T-rays either require cryogenic temperatures or are relatively bulky equipments based on optically-pumped materials. The solid-state recourse consisting of GaAs-based quantum cascade lasers presents an intrinsic limitation in operation temperature: The low energy of the longitudinal-optical (LO) phonon in arsenide compounds hinders laser emission beyond 180 K at 4 THz, and forces operation below the liquid nitrogen temperature (< 70 K) for frequencies below 1 THz. Overcoming this limitation requires a technology revolution through introduction of a new material system. This project aims at exploring a novel semiconductor technology for high-performance photonic devices operating in the T-ray spectral region. The advanced materials that we will investigate consist of nitride-based [GaN/Al(Ga,In)N] superlattices and nanowires, where we can profit from unique properties of III-nitride semiconductors, namely the large LO-phonon energy and the strong electron-phonon interaction. Our target is to adapt the quantum cascade design and fabrication technology to these new materials, characterized by intense internal polarization fields. Our project aims at pushing intersubband transitions in this material family to unprecendently long wavelengths, in other to cover the whole T-ray spectral gap with coherent solid-state sources operating at room temperature and above.
Max ERC Funding
1 627 236 €
Duration
Start date: 2012-01-01, End date: 2017-06-30
Project acronym ThermoReg
Project Peripheral and Central Mechanisms of Temperature Detection and Core Body Thermoregulation
Researcher (PI) Jan-Erik Siemens
Host Institution (HI) UNIVERSITATSKLINIKUM HEIDELBERG
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Internal temperature homeostasis is of critical importance to our health as deviation from a normal, tightly controlled level (37 °Celsius) can cause fatal organ failures. Temperature-sensitive cells in the hypothalamus detect deep brain temperature, which is directly relevant to core body temperature (CBT) regulation. However molecules and mechanisms underlying central temperature detection by hypothalamic neurons are unknown. I propose to use a multi-disciplinary approach to elucidate mechanisms of temperature detection by these cells. I have started to employ a genetic tagging approach that allows me to label temperature-activated hypothalamic neurons in vivo.
Hypothalamic neurons not only detect local brain temperature but also receive peripheral temperature signals from the somatosensory system. However, the impact of peripheral temperature information on central temperature regulation is largely unknown. Transient Receptor Potential (TRP) ion channels have been found to constitute important components in a variety of different sensory systems. In vertebrates, TRP family members TRPV1, TRPM8, and TRPA1, play prominent roles in the detection of thermal stimuli ranging from cold to hot ambient temperatures. How these receptors mediate their temperature sensitivity on the molecular level is largely unknown. I hypothesize that TRPs are components of supramolecular membrane-bound protein complexes that enable the receptors to function in a context-dependent manner, similar to the founding member of the TRP receptor family in the Drosophila eye. I will use a genetic biochemical strategy to identify components of somatosensory TRP channel protein complexes from native sensory ganglia of transgenic mice. Subsequently, characterization of the TRP Proteome will not only provide novel insights into TRP channel function as temperature sensors but may additionally yield novel targets for the treatment of inflammatory conditions and pain.
Summary
Internal temperature homeostasis is of critical importance to our health as deviation from a normal, tightly controlled level (37 °Celsius) can cause fatal organ failures. Temperature-sensitive cells in the hypothalamus detect deep brain temperature, which is directly relevant to core body temperature (CBT) regulation. However molecules and mechanisms underlying central temperature detection by hypothalamic neurons are unknown. I propose to use a multi-disciplinary approach to elucidate mechanisms of temperature detection by these cells. I have started to employ a genetic tagging approach that allows me to label temperature-activated hypothalamic neurons in vivo.
Hypothalamic neurons not only detect local brain temperature but also receive peripheral temperature signals from the somatosensory system. However, the impact of peripheral temperature information on central temperature regulation is largely unknown. Transient Receptor Potential (TRP) ion channels have been found to constitute important components in a variety of different sensory systems. In vertebrates, TRP family members TRPV1, TRPM8, and TRPA1, play prominent roles in the detection of thermal stimuli ranging from cold to hot ambient temperatures. How these receptors mediate their temperature sensitivity on the molecular level is largely unknown. I hypothesize that TRPs are components of supramolecular membrane-bound protein complexes that enable the receptors to function in a context-dependent manner, similar to the founding member of the TRP receptor family in the Drosophila eye. I will use a genetic biochemical strategy to identify components of somatosensory TRP channel protein complexes from native sensory ganglia of transgenic mice. Subsequently, characterization of the TRP Proteome will not only provide novel insights into TRP channel function as temperature sensors but may additionally yield novel targets for the treatment of inflammatory conditions and pain.
Max ERC Funding
1 400 725 €
Duration
Start date: 2012-02-01, End date: 2018-01-31
Project acronym TOI
Project Theoretical Foundations and Observational Tests of Inflationary Cosmology
Researcher (PI) Daniel Baumann
Host Institution (HI) UNIVERSITEIT VAN AMSTERDAM
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary Observations of the temperature fluctuations in the cosmic microwave background (CMB) have transformed cosmology into a quantitative science. This revolution has led to a detailed understanding of the geometry and composition of the universe. However, the microphysical origin of the CMB fluctuations remains a mystery. Although quantum-mechanical fluctuations during a early period of inflationary expansion provide a remarkably successful description of the data, a concrete realization of inflation in a fundamental theory of particle physics remains elusive. Moreover, it seems almost certain that the inflationary era involved physics beyond the Standard Model. This is both a challenge and a fantastic opportunity to learn about physics at the highest energy scales from cosmological observations.
With the ERC grant I plan to form a group at Cambridge University that will explore both the theoretical foundations and the observational consequences of inflation. A key question that a satisfactory microscopic theory of inflation should answer is why the mass of the inflaton field is much smaller than its natural value. We will search for answers to this question both from the bottom up in effective field theory (EFT) and from the top down in string theory. We will furthermore initiate the first systematic study of large-field inflation, thereby providing the theoretical foundation for inflationary models with observable gravitational waves. To make contact with observations we will then develop an EFT for the inflationary fluctuations as Goldstone bosons of spontaneously broken time-translations. We will compare the predictions of that theory to the latest CMB observations. Finally, we will use the data to pursue two of the central signatures of the physics of inflation: gravitational waves and non-Gaussianity.
Summary
Observations of the temperature fluctuations in the cosmic microwave background (CMB) have transformed cosmology into a quantitative science. This revolution has led to a detailed understanding of the geometry and composition of the universe. However, the microphysical origin of the CMB fluctuations remains a mystery. Although quantum-mechanical fluctuations during a early period of inflationary expansion provide a remarkably successful description of the data, a concrete realization of inflation in a fundamental theory of particle physics remains elusive. Moreover, it seems almost certain that the inflationary era involved physics beyond the Standard Model. This is both a challenge and a fantastic opportunity to learn about physics at the highest energy scales from cosmological observations.
With the ERC grant I plan to form a group at Cambridge University that will explore both the theoretical foundations and the observational consequences of inflation. A key question that a satisfactory microscopic theory of inflation should answer is why the mass of the inflaton field is much smaller than its natural value. We will search for answers to this question both from the bottom up in effective field theory (EFT) and from the top down in string theory. We will furthermore initiate the first systematic study of large-field inflation, thereby providing the theoretical foundation for inflationary models with observable gravitational waves. To make contact with observations we will then develop an EFT for the inflationary fluctuations as Goldstone bosons of spontaneously broken time-translations. We will compare the predictions of that theory to the latest CMB observations. Finally, we will use the data to pursue two of the central signatures of the physics of inflation: gravitational waves and non-Gaussianity.
Max ERC Funding
1 493 535 €
Duration
Start date: 2011-10-01, End date: 2016-09-30
Project acronym URGENCY
Project Neurocomputational determinants of decision urgency in humans
Researcher (PI) Christopher Summerfield
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary A central question in the behavioural, cognitive and neural sciences is how humans choose between available alternatives (Does this patient have flu, or meningitis? Should I go on holiday to Spain, or Scotland?). However, much less attention has been devoted to the question of when an agent should decide. Longer deliberation is more likely to lead to better decisions (because it allows greater accumulation of decision-relevant evidence) but it also incurs a cost (because it delays reinforcement, and increases the chance that deadlines will be missed). Humans adjust their decision strategy to match the urgency with which a decision should be made, but how they do so is unknown. In the proposed research, we ask how humans compute the urgency associated with simple perceptual categorisation judgments, and use functional brain imaging to identify neural circuits involved in these computations. Our approach to this question is grounded in formal mathematical models of the decision process, allowing us to compare human performance to that of an ideal observer that computes decision urgency in order to maximise economic outcome. Using tools from experimental psychology, we measure the sensitivity of healthy individuals to quantities that are relevant for computing decision urgency. We will then use functional magnetic resonance imaging (fMRI) and magnetoencephalography (MEG) to ask where they are encoded in the human brain. Subsequently, we turn our attention to individuals who are prone to make impulsive decisions, using individual difference and pharmacological manipulations. We ask which decision-relevant information is computed inappropriately in impulsivity, and use fMRI and MEG to ask which brain regions may be responsible for atypical computations. This new ‘computational neuropsychiatry’ approach will allow us to move towards a neural and computational account decision-making deficits in disorders such as addiction and ADHD.
Summary
A central question in the behavioural, cognitive and neural sciences is how humans choose between available alternatives (Does this patient have flu, or meningitis? Should I go on holiday to Spain, or Scotland?). However, much less attention has been devoted to the question of when an agent should decide. Longer deliberation is more likely to lead to better decisions (because it allows greater accumulation of decision-relevant evidence) but it also incurs a cost (because it delays reinforcement, and increases the chance that deadlines will be missed). Humans adjust their decision strategy to match the urgency with which a decision should be made, but how they do so is unknown. In the proposed research, we ask how humans compute the urgency associated with simple perceptual categorisation judgments, and use functional brain imaging to identify neural circuits involved in these computations. Our approach to this question is grounded in formal mathematical models of the decision process, allowing us to compare human performance to that of an ideal observer that computes decision urgency in order to maximise economic outcome. Using tools from experimental psychology, we measure the sensitivity of healthy individuals to quantities that are relevant for computing decision urgency. We will then use functional magnetic resonance imaging (fMRI) and magnetoencephalography (MEG) to ask where they are encoded in the human brain. Subsequently, we turn our attention to individuals who are prone to make impulsive decisions, using individual difference and pharmacological manipulations. We ask which decision-relevant information is computed inappropriately in impulsivity, and use fMRI and MEG to ask which brain regions may be responsible for atypical computations. This new ‘computational neuropsychiatry’ approach will allow us to move towards a neural and computational account decision-making deficits in disorders such as addiction and ADHD.
Max ERC Funding
1 182 176 €
Duration
Start date: 2012-01-01, End date: 2017-06-30
Project acronym WAVELENGTH STANDARDS
Project Development of new wavelength standards for the search
for habitable planets
Researcher (PI) Ansgar Reiners
Host Institution (HI) GEORG-AUGUST-UNIVERSITAT GOTTINGENSTIFTUNG OFFENTLICHEN RECHTS
Call Details Starting Grant (StG), PE9, ERC-2011-StG_20101014
Summary "The search for extrasolar planets is moving into the domain of Earth-like, habitable planets with more precise measurement techniques and a focus on low-mass, very cool stars. New spectrographs are being developed with the goal to find Earth-like planets in the habitable zones of stars other than the Sun. Extensive photometric programs, both ground- and space-based are running and being planned to discover transiting planets particularly useful for detailed investigation of exo-planetary atmospheres. For the characterization of exo-planets, and to confirm the planetary status of transit candidates, high-precision radial velocity measurements (m/s) are required, in particular at near-infrared (NIR) wavelengths to discover Earth-like planets around low-mass stars. The largest obstacle for NIR programs is currently the lack of reliable wavelength standards. Potential calibration sources include absorption cells, gas emission lamps, and Fabry-Perot (FP) etalons. In most cases, detailed NIR characterization is still lacking. A very promising source is the Laser frequency comb (LFC), but the LFC signal paradoxically needs to be degenerated to be useful for astronomical spectrographs because spectral line density is usually too high. It is currently not clear whether the LFC can become a viable calibration scheme, in particular for programs carried out at 4m-class telescopes. I propose to systematically investigate wavelength calibration sources with a focus on NIR wavelengths and to develop wavelength calibration sources for NIR wavelengths. The development is of fundamental nature providing new strategies for the upcoming generation of NIR high-precision spectrographs. I suggest a new mechanism in which a FP should be coupled to a double-laser PDH mechanism providing reliable wavelength reference. Calibration lamps filled with UNe or CN are promising alternative sources of calibration lines and should be studied in detail."
Summary
"The search for extrasolar planets is moving into the domain of Earth-like, habitable planets with more precise measurement techniques and a focus on low-mass, very cool stars. New spectrographs are being developed with the goal to find Earth-like planets in the habitable zones of stars other than the Sun. Extensive photometric programs, both ground- and space-based are running and being planned to discover transiting planets particularly useful for detailed investigation of exo-planetary atmospheres. For the characterization of exo-planets, and to confirm the planetary status of transit candidates, high-precision radial velocity measurements (m/s) are required, in particular at near-infrared (NIR) wavelengths to discover Earth-like planets around low-mass stars. The largest obstacle for NIR programs is currently the lack of reliable wavelength standards. Potential calibration sources include absorption cells, gas emission lamps, and Fabry-Perot (FP) etalons. In most cases, detailed NIR characterization is still lacking. A very promising source is the Laser frequency comb (LFC), but the LFC signal paradoxically needs to be degenerated to be useful for astronomical spectrographs because spectral line density is usually too high. It is currently not clear whether the LFC can become a viable calibration scheme, in particular for programs carried out at 4m-class telescopes. I propose to systematically investigate wavelength calibration sources with a focus on NIR wavelengths and to develop wavelength calibration sources for NIR wavelengths. The development is of fundamental nature providing new strategies for the upcoming generation of NIR high-precision spectrographs. I suggest a new mechanism in which a FP should be coupled to a double-laser PDH mechanism providing reliable wavelength reference. Calibration lamps filled with UNe or CN are promising alternative sources of calibration lines and should be studied in detail."
Max ERC Funding
1 437 200 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym WIRINGVISION
Project Wiring up visual circuits: Interplay between gene expression and spontaneous and experience-dependent activity
Researcher (PI) Eloisa Herrera
Host Institution (HI) AGENCIA ESTATAL CONSEJO SUPERIOR DEINVESTIGACIONES CIENTIFICAS
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary A fundamental feature of the developing neural circuits is their ability to change in response to sensorial experience. This phenomenon has been particularly observed during the generation of cortical maps, where altering the pattern of sensory experience changes the spatial organization of sensory representations. The mechanisms underlying this form of plasticity include synaptic modification such as long-term potentiation and long-term depression, classically referred to as Hebbian-based rules. Today, there is growing evidence that prior to sensory experience, neural electrical activity plays a role in early brain development. In several developing circuits including retina, spinal cord, hippocampus and cortex, there are transient events that cause these circuits to spontaneously generate waves of correlated activity. However, the cellular and molecular mechanisms that translate these spontaneous activity patterns into mature neural circuits that will eventually be ruled by Hebbian-type plasticity remain largely unknown. The first part of this proposal deals with early events in development in which sensory-independent factors outline a first draft of neuronal connections: How spontaneous activity and molecular factors integrate to shape initial neuronal connectivity? Based in our own findings and using the mammalian visual system as a model, we will genetically silence spontaneous activity in a specific population of neurons and will screen for molecules induced by spontaneous waves. We will also dissect the relative contribution of the different stages of spontaneous waves and will try to understand the relationship of spontaneous activity with different families of axon guidance molecules during the assembly of neural circuits. In the second part of the project we will determine to what extent cortical maps wiring depends on the formation of early thalamic properties and how this wiring may be modified by experience to optimally support information processing.
Summary
A fundamental feature of the developing neural circuits is their ability to change in response to sensorial experience. This phenomenon has been particularly observed during the generation of cortical maps, where altering the pattern of sensory experience changes the spatial organization of sensory representations. The mechanisms underlying this form of plasticity include synaptic modification such as long-term potentiation and long-term depression, classically referred to as Hebbian-based rules. Today, there is growing evidence that prior to sensory experience, neural electrical activity plays a role in early brain development. In several developing circuits including retina, spinal cord, hippocampus and cortex, there are transient events that cause these circuits to spontaneously generate waves of correlated activity. However, the cellular and molecular mechanisms that translate these spontaneous activity patterns into mature neural circuits that will eventually be ruled by Hebbian-type plasticity remain largely unknown. The first part of this proposal deals with early events in development in which sensory-independent factors outline a first draft of neuronal connections: How spontaneous activity and molecular factors integrate to shape initial neuronal connectivity? Based in our own findings and using the mammalian visual system as a model, we will genetically silence spontaneous activity in a specific population of neurons and will screen for molecules induced by spontaneous waves. We will also dissect the relative contribution of the different stages of spontaneous waves and will try to understand the relationship of spontaneous activity with different families of axon guidance molecules during the assembly of neural circuits. In the second part of the project we will determine to what extent cortical maps wiring depends on the formation of early thalamic properties and how this wiring may be modified by experience to optimally support information processing.
Max ERC Funding
1 500 000 €
Duration
Start date: 2012-01-01, End date: 2017-06-30
Project acronym YODA
Project Topographic signaling and spatial landmarks of key polarized neuro-developmental processes
Researcher (PI) Valérie Lucienne Corinne Castellani
Host Institution (HI) CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Polarization, which confers asymmetry at molecular, cellular and tissue scales, is a fascinating process establishing fundamental features of biological systems. In multicellular organisms, symmetry breaking triggers the specification of embryonic body axes, governing the positioning of subsequent morphogenetic processes. Cells and tissues acquire complex polarity features, which remarkably, are highly precisely positioned within the body axes. How are polarization processes spatially oriented remlains fully enigmatic. During the formation of the nervous system, some crucial processes are polarized. Likewise, the navigation of neuronal projections in the body is a typical polarized process, axons selecting specific pathways to reach their targets. Studies in this field established crucial roles for topographic cues in controlling the polarized growth of neuronal projections. Up to now, my lab has focused on axon guidance mechanisms and while investigating the links between spatial position and neural circuit formation, I became convinced that topographic signalling must be equally required to set other key polarized processes of the developing nervous system. For example in the neuroepithelium, progenitor division is polarized along the apico-basal axis of the neural tube. Likewise in the young post-mitotic neuron, precise coordinates along the body axes define the site where the axon emerges. First, we postulate the existence of a topographic signaling giving to neuronal cells (but this might be a more general case) landmarks of the different embryonic axes so that polarization takes place with appropriate spatial orientation. Second, we make the assumption that this topographic signalling is ensured by cues initially identified for their role during axon navigation. Our goals are to explore these issues, using as a model the sensorimotor circuits, where several processes can be investigated for questioning the interplay between polarity and topography.
Summary
Polarization, which confers asymmetry at molecular, cellular and tissue scales, is a fascinating process establishing fundamental features of biological systems. In multicellular organisms, symmetry breaking triggers the specification of embryonic body axes, governing the positioning of subsequent morphogenetic processes. Cells and tissues acquire complex polarity features, which remarkably, are highly precisely positioned within the body axes. How are polarization processes spatially oriented remlains fully enigmatic. During the formation of the nervous system, some crucial processes are polarized. Likewise, the navigation of neuronal projections in the body is a typical polarized process, axons selecting specific pathways to reach their targets. Studies in this field established crucial roles for topographic cues in controlling the polarized growth of neuronal projections. Up to now, my lab has focused on axon guidance mechanisms and while investigating the links between spatial position and neural circuit formation, I became convinced that topographic signalling must be equally required to set other key polarized processes of the developing nervous system. For example in the neuroepithelium, progenitor division is polarized along the apico-basal axis of the neural tube. Likewise in the young post-mitotic neuron, precise coordinates along the body axes define the site where the axon emerges. First, we postulate the existence of a topographic signaling giving to neuronal cells (but this might be a more general case) landmarks of the different embryonic axes so that polarization takes place with appropriate spatial orientation. Second, we make the assumption that this topographic signalling is ensured by cues initially identified for their role during axon navigation. Our goals are to explore these issues, using as a model the sensorimotor circuits, where several processes can be investigated for questioning the interplay between polarity and topography.
Max ERC Funding
1 498 971 €
Duration
Start date: 2012-04-01, End date: 2017-03-31
Project acronym ZFISHSLEEP
Project Resolving the Neuropharmacology and Genetics of Zebrafish Sleep
Researcher (PI) Jason Rihel
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), LS5, ERC-2011-StG_20101109
Summary Sleep is a fundamental process, yet the genetic and neural mechanisms that regulate sleep are largely unknown. We have developed the zebrafish as a model system to study the regulation of sleep because it combines the genetics of invertebrates with the basic brain structures that regulate sleep in humans. We previously designed high throughput behavioural assays to measure sleep behaviours in the fish and used genetic tools to demonstrate that the wake-regulating hypocretin/orexin (Hcrt) system is functionally conserved in the zebrafish. We have also used our assays to perform a small molecule screen and identified both conserved and novel candidate regulators of sleep in zebrafish.
In Aim 1, we will observe the behaviour of wild type and Hcrt receptor mutants to a panel of small molecules known to alter zebrafish sleep. This aim tests the hypothesis that these compounds exert their effects on sleep and wake through the Hcrt system. In Aim 2, we will follow-up on the compounds that had differential effects in the mutants. We will monitor the activity of Hcrt neurons in response to drugs using a new neuroluminescent technique to observe the activity of neurons in freely behaving zebrafish larvae. This Aim will extend the behavioural data to the level of neural circuits. In Aim 3, we will use new methods to globally observe neuronal activity in the zebrafish brain to extend our analysis to neurons thought to interact with the Hcrt system. By observing activity across the sleep/wake cycle, we may also uncover novel sleep regulating neurons.
Overall, this project takes a multidisciplinary approach to the study of sleep and the Hcrt system, leveraging new methods from chemical biology, molecular genetics, and behavioural neuroscience in the zebrafish. As little is known about the mechanisms and sites of action for most sleep-altering compounds, any progress would advance the sleep field and could have clinical relevance to the treatment of sleep disorders.
Summary
Sleep is a fundamental process, yet the genetic and neural mechanisms that regulate sleep are largely unknown. We have developed the zebrafish as a model system to study the regulation of sleep because it combines the genetics of invertebrates with the basic brain structures that regulate sleep in humans. We previously designed high throughput behavioural assays to measure sleep behaviours in the fish and used genetic tools to demonstrate that the wake-regulating hypocretin/orexin (Hcrt) system is functionally conserved in the zebrafish. We have also used our assays to perform a small molecule screen and identified both conserved and novel candidate regulators of sleep in zebrafish.
In Aim 1, we will observe the behaviour of wild type and Hcrt receptor mutants to a panel of small molecules known to alter zebrafish sleep. This aim tests the hypothesis that these compounds exert their effects on sleep and wake through the Hcrt system. In Aim 2, we will follow-up on the compounds that had differential effects in the mutants. We will monitor the activity of Hcrt neurons in response to drugs using a new neuroluminescent technique to observe the activity of neurons in freely behaving zebrafish larvae. This Aim will extend the behavioural data to the level of neural circuits. In Aim 3, we will use new methods to globally observe neuronal activity in the zebrafish brain to extend our analysis to neurons thought to interact with the Hcrt system. By observing activity across the sleep/wake cycle, we may also uncover novel sleep regulating neurons.
Overall, this project takes a multidisciplinary approach to the study of sleep and the Hcrt system, leveraging new methods from chemical biology, molecular genetics, and behavioural neuroscience in the zebrafish. As little is known about the mechanisms and sites of action for most sleep-altering compounds, any progress would advance the sleep field and could have clinical relevance to the treatment of sleep disorders.
Max ERC Funding
1 902 750 €
Duration
Start date: 2012-02-01, End date: 2017-01-31