Project acronym AMBH
Project Ancient Music Beyond Hellenisation
Researcher (PI) Stefan HAGEL
Host Institution (HI) OESTERREICHISCHE AKADEMIE DER WISSENSCHAFTEN
Call Details Advanced Grant (AdG), SH5, ERC-2017-ADG
Summary From medieval times, Arabic as well as European music was analysed in terms that were inherited from Classical Antiquity and had thus developed in a very different music culture. In spite of recent breakthroughs in the understanding of the latter, whose technicalities we access not only through texts and iconography, but also through instrument finds and surviving notated melodies, its relation to music traditions known from later periods and different places is almost uncharted territory.
The present project explores relations between Hellenic/Hellenistic music as pervaded the theatres and concert halls throughout and beyond the Roman empire, Near Eastern traditions – from the diatonic system emerging from cuneiform sources to the flourishing musical world of the caliphates – and, as far as possible, African musical life south of Egypt as well – a region that maintained close ties both with the Hellenised culture of its northern neighbours and with the Arabian Peninsula.
On the one hand, this demands collaboration between Classical Philology and Arabic Studies, extending methods recently developed within music archaeological research related to the Classical Mediterranean. Arabic writings need to be examined in close reading, using recent insights into the interplay between ancient music theory and practice, in order to segregate the influence of Greek thinking from ideas and facts that must relate to contemporaneous ‘Arabic’ music-making. In this way we hope better to define the relation of this tradition to the ‘Classical world’, potentially breaking free of Orientalising bias informing modern views. On the other hand, the study and reconstruction, virtual and material, of wind instruments of Hellenistic pedigree but found outside the confinements of the Hellenistic ‘heartlands’ may provide evidence of ‘foreign’ tonality employed in those regions – specifically the royal city of Meroë in modern Sudan and the Oxus Temple in modern Tajikistan.
Summary
From medieval times, Arabic as well as European music was analysed in terms that were inherited from Classical Antiquity and had thus developed in a very different music culture. In spite of recent breakthroughs in the understanding of the latter, whose technicalities we access not only through texts and iconography, but also through instrument finds and surviving notated melodies, its relation to music traditions known from later periods and different places is almost uncharted territory.
The present project explores relations between Hellenic/Hellenistic music as pervaded the theatres and concert halls throughout and beyond the Roman empire, Near Eastern traditions – from the diatonic system emerging from cuneiform sources to the flourishing musical world of the caliphates – and, as far as possible, African musical life south of Egypt as well – a region that maintained close ties both with the Hellenised culture of its northern neighbours and with the Arabian Peninsula.
On the one hand, this demands collaboration between Classical Philology and Arabic Studies, extending methods recently developed within music archaeological research related to the Classical Mediterranean. Arabic writings need to be examined in close reading, using recent insights into the interplay between ancient music theory and practice, in order to segregate the influence of Greek thinking from ideas and facts that must relate to contemporaneous ‘Arabic’ music-making. In this way we hope better to define the relation of this tradition to the ‘Classical world’, potentially breaking free of Orientalising bias informing modern views. On the other hand, the study and reconstruction, virtual and material, of wind instruments of Hellenistic pedigree but found outside the confinements of the Hellenistic ‘heartlands’ may provide evidence of ‘foreign’ tonality employed in those regions – specifically the royal city of Meroë in modern Sudan and the Oxus Temple in modern Tajikistan.
Max ERC Funding
775 959 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym ARCHADAPT
Project The architecture of adaptation to novel environments
Researcher (PI) Christian Werner Schlötterer
Host Institution (HI) VETERINAERMEDIZINISCHE UNIVERSITAET WIEN
Call Details Advanced Grant (AdG), LS8, ERC-2011-ADG_20110310
Summary One of the central goals in evolutionary biology is to understand adaptation. Experimental evolution represents a highly promising approach to study adaptation. In this proposal, a freshly collected D. simulans population will be allowed to adapt to laboratory conditions under two different temperature regimes: hot (27°C) and cold (18°C). The trajectories of adaptation to these novel environments will be monitored on three levels: 1) genomic, 2) transcriptomic, 3) phenotypic. Allele frequency changes during the experiment will be measured by next generation sequencing of DNA pools (Pool-Seq) to identify targets of selection. RNA-Seq will be used to trace adaptation on the transcriptomic level during three developmental stages. Eight different phenotypes will be scored to measure the phenotypic consequences of adaptation. Combining the adaptive trajectories on these three levels will provide a picture of adaptation for a multicellular, outcrossing organism that is far more detailed than any previous results.
Furthermore, the proposal addresses the question of how adaptation on these three levels is reversible if the environment reverts to ancestral conditions. The third aspect of adaptation covered in the proposal is the question of repeatability of adaptation. Again, this question will be addressed on the three levels: genomic, transcriptomic and phenotypic. Using replicates with different degrees of genetic similarity, as well as closely related species, we will test how similar the adaptive response is.
This large-scale study will provide new insights into the importance of standing variation for the adaptation to novel environments. Hence, apart from providing significant evolutionary insights on the trajectories of adaptation, the results we will obtain will have important implications for conservation genetics and commercial breeding.
Summary
One of the central goals in evolutionary biology is to understand adaptation. Experimental evolution represents a highly promising approach to study adaptation. In this proposal, a freshly collected D. simulans population will be allowed to adapt to laboratory conditions under two different temperature regimes: hot (27°C) and cold (18°C). The trajectories of adaptation to these novel environments will be monitored on three levels: 1) genomic, 2) transcriptomic, 3) phenotypic. Allele frequency changes during the experiment will be measured by next generation sequencing of DNA pools (Pool-Seq) to identify targets of selection. RNA-Seq will be used to trace adaptation on the transcriptomic level during three developmental stages. Eight different phenotypes will be scored to measure the phenotypic consequences of adaptation. Combining the adaptive trajectories on these three levels will provide a picture of adaptation for a multicellular, outcrossing organism that is far more detailed than any previous results.
Furthermore, the proposal addresses the question of how adaptation on these three levels is reversible if the environment reverts to ancestral conditions. The third aspect of adaptation covered in the proposal is the question of repeatability of adaptation. Again, this question will be addressed on the three levels: genomic, transcriptomic and phenotypic. Using replicates with different degrees of genetic similarity, as well as closely related species, we will test how similar the adaptive response is.
This large-scale study will provide new insights into the importance of standing variation for the adaptation to novel environments. Hence, apart from providing significant evolutionary insights on the trajectories of adaptation, the results we will obtain will have important implications for conservation genetics and commercial breeding.
Max ERC Funding
2 452 084 €
Duration
Start date: 2012-07-01, End date: 2018-06-30
Project acronym EPIC
Project Enabling Precision Immuno-oncology in Colorectal cancer
Researcher (PI) Zlatko TRAJANOSKI
Host Institution (HI) MEDIZINISCHE UNIVERSITAT INNSBRUCK
Call Details Advanced Grant (AdG), LS7, ERC-2017-ADG
Summary Immunotherapy with checkpoints blockers is transforming the treatment of advanced cancers. Colorectal cancer (CRC), a cancer with 1.4 million new cases diagnosed annually worldwide, is refractory to immunotherapy (with the exception of a minority of tumors with microsatellite instability). This is somehow paradoxical as CRC is a cancer for which we have shown that it is under immunological control and that tumor infiltrating lymphocytes represent a strong independent predictor of survival. Thus, there is an urgent need to broaden the clinical benefits of immune checkpoint blockers to CRC by combining agents with synergistic mechanisms of action. An attractive approach to sensitize tumors to immunotherapy is to harness immunogenic effects induced by approved conventional or targeted agents.
Here I propose a new paradigm to identify molecular determinants of resistance to immunotherapy and develop personalized in silico and in vitro models for predicting response to combination therapy in CRC. The EPIC concept is based on three pillars: 1) emphasis on antitumor T cell activity; 2) systematic interrogation of tumor-immune cell interactions using data-driven modeling and knowledge-based mechanistic modeling, and 3) generation of key quantitative data to train and validate algorithms using perturbation experiments with patient-derived tumor organoids and cutting-edge technologies for multidimensional profiling. We will investigate three immunomodulatory processes: 1) immunostimulatory effects of chemotherapeutics, 2) rewiring of signaling networks induced by targeted drugs and their interference with immunity, and 3) metabolic reprogramming of T cells to enhance antitumor immunity.
The anticipated outcome of EPIC is a precision immuno-oncology platform that integrates tumor organoids with high-throughput and high-content data for testing drug combinations, and machine learning for making therapeutic recommendations for individual patients.
Summary
Immunotherapy with checkpoints blockers is transforming the treatment of advanced cancers. Colorectal cancer (CRC), a cancer with 1.4 million new cases diagnosed annually worldwide, is refractory to immunotherapy (with the exception of a minority of tumors with microsatellite instability). This is somehow paradoxical as CRC is a cancer for which we have shown that it is under immunological control and that tumor infiltrating lymphocytes represent a strong independent predictor of survival. Thus, there is an urgent need to broaden the clinical benefits of immune checkpoint blockers to CRC by combining agents with synergistic mechanisms of action. An attractive approach to sensitize tumors to immunotherapy is to harness immunogenic effects induced by approved conventional or targeted agents.
Here I propose a new paradigm to identify molecular determinants of resistance to immunotherapy and develop personalized in silico and in vitro models for predicting response to combination therapy in CRC. The EPIC concept is based on three pillars: 1) emphasis on antitumor T cell activity; 2) systematic interrogation of tumor-immune cell interactions using data-driven modeling and knowledge-based mechanistic modeling, and 3) generation of key quantitative data to train and validate algorithms using perturbation experiments with patient-derived tumor organoids and cutting-edge technologies for multidimensional profiling. We will investigate three immunomodulatory processes: 1) immunostimulatory effects of chemotherapeutics, 2) rewiring of signaling networks induced by targeted drugs and their interference with immunity, and 3) metabolic reprogramming of T cells to enhance antitumor immunity.
The anticipated outcome of EPIC is a precision immuno-oncology platform that integrates tumor organoids with high-throughput and high-content data for testing drug combinations, and machine learning for making therapeutic recommendations for individual patients.
Max ERC Funding
2 460 500 €
Duration
Start date: 2018-10-01, End date: 2023-09-30
Project acronym EPICLINES
Project Elucidating the causes and consequences of the global pattern of epigenetic variation in Arabidopsis thaliana
Researcher (PI) Lars Magnus Henrik NORDBORG
Host Institution (HI) GREGOR MENDEL INSTITUT FUR MOLEKULARE PFLANZENBIOLOGIE GMBH
Call Details Advanced Grant (AdG), LS8, ERC-2017-ADG
Summary Epigenetics continues to fascinate, especially the notion that it blurs the line between “nature and nurture” and could make Lamarckian adaptation via the inheritance of acquired characteristics possible. That this is in principle possible is clear: in the model plant Arabidopsis thaliana (Thale cress), experimentally induced DNA methylation variation can be inherited and affect important traits. The question is whether this is important in nature. Recent studies of A. thaliana have revealed a pattern of correlation between levels of methylation and climate variables that strongly suggests that methylation is important in adaptation. However, somewhat paradoxically, the experiments also showed that much of the variation for this epigenetic trait appears to have a genetic rather than an epigenetic basis. This suggest that epigenetics may indeed be important for adaptation, but as part of a genetic mechanism that is currently not understood. The goal of this project is to determine whether the global pattern of methylation has a genetic or an epigenetic basis, and to use this information to elucidate the ultimate basis for the global pattern of variation: natural selection.
Summary
Epigenetics continues to fascinate, especially the notion that it blurs the line between “nature and nurture” and could make Lamarckian adaptation via the inheritance of acquired characteristics possible. That this is in principle possible is clear: in the model plant Arabidopsis thaliana (Thale cress), experimentally induced DNA methylation variation can be inherited and affect important traits. The question is whether this is important in nature. Recent studies of A. thaliana have revealed a pattern of correlation between levels of methylation and climate variables that strongly suggests that methylation is important in adaptation. However, somewhat paradoxically, the experiments also showed that much of the variation for this epigenetic trait appears to have a genetic rather than an epigenetic basis. This suggest that epigenetics may indeed be important for adaptation, but as part of a genetic mechanism that is currently not understood. The goal of this project is to determine whether the global pattern of methylation has a genetic or an epigenetic basis, and to use this information to elucidate the ultimate basis for the global pattern of variation: natural selection.
Max ERC Funding
2 498 468 €
Duration
Start date: 2018-06-01, End date: 2023-05-31
Project acronym EPIDEMICSonCHIP
Project EPIDEMICS in ant societies ON a CHIP
Researcher (PI) Sylvia Maria Cremer-Sixt
Host Institution (HI) INSTITUTE OF SCIENCE AND TECHNOLOGYAUSTRIA
Call Details Consolidator Grant (CoG), LS8, ERC-2017-COG
Summary Living in societies amplifies the risk of getting sick, as pathogens can easily spread along the dense social interaction networks of the hosts. Sanitary care and the organisational structure of societies are expected to limit the risk of epidemics. Yet, how the defences of the individual group members scale-up, combine and synergise towards society-level protection, is poorly understood, as the majority of societies can only be studied via correlational and modeling approaches. Insect societies provide a powerful system for experimental studies, as whole societies are accessible for surveillance and manipulative approaches. We can monitor every behavioural interaction between all members, determine their effects on colony-wide disease spread and replicate experiments arbitrarily. The fitness effects of collective disease defences can be quantified, as they result in a single fitness measure of colony productivity. This is because all members of a social insect colony form a reproductive entity composed of the reproductive queens and males and their sterile workers. I will use an ant host–fungal pathogen system to find out how initial infection develops into an epidemic, and, in turn, how colony-level defence emerges from the interactions between its members. To infer effect from cause, I will not only observe the colony after initial infection of a subset of colony members, but also manipulate the sanitary behaviours and spatiotemporal interaction of host individuals. To this end, I will engineer an automatised platform, following the principles of lab-on-a-chip techniques, to individually target and manipulate colony members, and to quantify their behaviours. Fitness effects will be read out by the quantity and quality of reproductive offspring in the next generation. Such a long-term whole-colony approach is required for understanding the evolution of social immunity, that is, how disease shapes society and how society shapes disease.
Summary
Living in societies amplifies the risk of getting sick, as pathogens can easily spread along the dense social interaction networks of the hosts. Sanitary care and the organisational structure of societies are expected to limit the risk of epidemics. Yet, how the defences of the individual group members scale-up, combine and synergise towards society-level protection, is poorly understood, as the majority of societies can only be studied via correlational and modeling approaches. Insect societies provide a powerful system for experimental studies, as whole societies are accessible for surveillance and manipulative approaches. We can monitor every behavioural interaction between all members, determine their effects on colony-wide disease spread and replicate experiments arbitrarily. The fitness effects of collective disease defences can be quantified, as they result in a single fitness measure of colony productivity. This is because all members of a social insect colony form a reproductive entity composed of the reproductive queens and males and their sterile workers. I will use an ant host–fungal pathogen system to find out how initial infection develops into an epidemic, and, in turn, how colony-level defence emerges from the interactions between its members. To infer effect from cause, I will not only observe the colony after initial infection of a subset of colony members, but also manipulate the sanitary behaviours and spatiotemporal interaction of host individuals. To this end, I will engineer an automatised platform, following the principles of lab-on-a-chip techniques, to individually target and manipulate colony members, and to quantify their behaviours. Fitness effects will be read out by the quantity and quality of reproductive offspring in the next generation. Such a long-term whole-colony approach is required for understanding the evolution of social immunity, that is, how disease shapes society and how society shapes disease.
Max ERC Funding
1 991 564 €
Duration
Start date: 2018-04-01, End date: 2023-03-31
Project acronym EVOCHLAMY
Project The Evolution of the Chlamydiae - an Experimental Approach
Researcher (PI) Matthias Horn
Host Institution (HI) UNIVERSITAT WIEN
Call Details Starting Grant (StG), LS8, ERC-2011-StG_20101109
Summary Chlamydiae are a unique group of obligate intracellular bacteria that comprises symbionts of protozoa as well as important pathogens of humans and a wide range of animals. The intracellular life style and the obligate association with a eukaryotic host was established early in chlamydial evolution and possibly also contributed to the origin of the primary phototrophic eukaryote. While much has been learned during the past decade with respect to chlamydial diversity, their evolutionary history, pathogenesis and mechanisms for host cell interaction, very little is known about genome dynamics, genome evolution, and adaptation in this important group of microorganisms. This project aims to fill this gap by three complementary work packages using experimental evolution approaches and state-of-the-art genome sequencing techniques.
Chlamydiae that naturally infect free-living amoebae, namely Protochlamydia amoebophila and Simkania negevensis, will be established as model systems for studying genome evolution of obligate intracellular bacteria (living in protozoa). Due to their larger, less reduced genomes compared to chlamydial pathogens, amoeba-associated Chlamydiae are ideally suited for these investigations. Experimental evolution approaches – among the prokaryotes so far almost exclusively used for studying free-living bacteria – will be applied to understand the genomic and molecular basis of the intracellular life style of Chlamydiae with respect to host adaptation, host interaction, and the character of the symbioses (mutualism versus parasitism). In addition, the role of amoebae for horizontal gene transfer among intracellular bacteria will be investigated experimentally. Taken together, this project will break new ground with respect to evolution experiments with intracellular bacteria, and it will provide unprecedented insights into the evolution and adaptive processes of intracellular bacteria in general, and the Chlamydiae in particular.
Summary
Chlamydiae are a unique group of obligate intracellular bacteria that comprises symbionts of protozoa as well as important pathogens of humans and a wide range of animals. The intracellular life style and the obligate association with a eukaryotic host was established early in chlamydial evolution and possibly also contributed to the origin of the primary phototrophic eukaryote. While much has been learned during the past decade with respect to chlamydial diversity, their evolutionary history, pathogenesis and mechanisms for host cell interaction, very little is known about genome dynamics, genome evolution, and adaptation in this important group of microorganisms. This project aims to fill this gap by three complementary work packages using experimental evolution approaches and state-of-the-art genome sequencing techniques.
Chlamydiae that naturally infect free-living amoebae, namely Protochlamydia amoebophila and Simkania negevensis, will be established as model systems for studying genome evolution of obligate intracellular bacteria (living in protozoa). Due to their larger, less reduced genomes compared to chlamydial pathogens, amoeba-associated Chlamydiae are ideally suited for these investigations. Experimental evolution approaches – among the prokaryotes so far almost exclusively used for studying free-living bacteria – will be applied to understand the genomic and molecular basis of the intracellular life style of Chlamydiae with respect to host adaptation, host interaction, and the character of the symbioses (mutualism versus parasitism). In addition, the role of amoebae for horizontal gene transfer among intracellular bacteria will be investigated experimentally. Taken together, this project will break new ground with respect to evolution experiments with intracellular bacteria, and it will provide unprecedented insights into the evolution and adaptive processes of intracellular bacteria in general, and the Chlamydiae in particular.
Max ERC Funding
1 499 621 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym HOPE
Project Host Protective Engineering of Cancer Immunity by Targeting the Intracellular Immune Checkpoint NR2F6
Researcher (PI) Gottfried BAIER
Host Institution (HI) MEDIZINISCHE UNIVERSITAT INNSBRUCK
Call Details Advanced Grant (AdG), LS7, ERC-2017-ADG
Summary "Because of its biological complexity, cancer is still poorly understood. Chronic inflammation has been shown, both experimentally and epidemiologically, to be a predisposition to, and also an inseparable aspect of clinically prevalent cancer entities. Therefore, a detailed understanding of both tumour and immune cell functions in cancer progression is a prerequisite for more successful therapeutic startegies. My team was the first to reveal the lymphocyte-intrinsic PKC/NR2F6 axis as an essential signalling node at the crossroads between inflammation and cancer. It is the mission of this project to identify molecular signatures that influence the risk of developing tumours employing established research tools and state-of-the-art genetic, biochemical, proteomic and transcriptomic as well as large scale CRISPR/Cas9 perturbation screening-based functional genomic technologies. Defining this as yet poorly elucidated effector pathway with its profoundly relevant role would enable development of preventive and immune-therapeutic strategies against NSCLC lung cancer and potentially also against other entities. Our three-pronged approach to achieve this goal is to: (i) delineate biological and clinical properties of the immunological PKC/NR2F6 network, (ii) validate NR2F6 as an immune-oncology combination target needed to overcome limitations to ""first generation anti-PD-1 checkpoint inhibitors"" rendering T cells capable of rejecting tumours and their metastases at distal organs and (iii) exploit human combinatorial T cell therapy concepts for prevention of immune-related adverse events as well as of tumour recurrence by reducing opportunities for the tumour to develop resistance in the clinic. Insight into the functions of NR2F6 pathway and involved mechanisms is a prerequisite for understanding how the microenvironment at the tumour site either supports tumour growth and spread or prevents tumour initiation and progression, the latter by host-protective cancer immunity."
Summary
"Because of its biological complexity, cancer is still poorly understood. Chronic inflammation has been shown, both experimentally and epidemiologically, to be a predisposition to, and also an inseparable aspect of clinically prevalent cancer entities. Therefore, a detailed understanding of both tumour and immune cell functions in cancer progression is a prerequisite for more successful therapeutic startegies. My team was the first to reveal the lymphocyte-intrinsic PKC/NR2F6 axis as an essential signalling node at the crossroads between inflammation and cancer. It is the mission of this project to identify molecular signatures that influence the risk of developing tumours employing established research tools and state-of-the-art genetic, biochemical, proteomic and transcriptomic as well as large scale CRISPR/Cas9 perturbation screening-based functional genomic technologies. Defining this as yet poorly elucidated effector pathway with its profoundly relevant role would enable development of preventive and immune-therapeutic strategies against NSCLC lung cancer and potentially also against other entities. Our three-pronged approach to achieve this goal is to: (i) delineate biological and clinical properties of the immunological PKC/NR2F6 network, (ii) validate NR2F6 as an immune-oncology combination target needed to overcome limitations to ""first generation anti-PD-1 checkpoint inhibitors"" rendering T cells capable of rejecting tumours and their metastases at distal organs and (iii) exploit human combinatorial T cell therapy concepts for prevention of immune-related adverse events as well as of tumour recurrence by reducing opportunities for the tumour to develop resistance in the clinic. Insight into the functions of NR2F6 pathway and involved mechanisms is a prerequisite for understanding how the microenvironment at the tumour site either supports tumour growth and spread or prevents tumour initiation and progression, the latter by host-protective cancer immunity."
Max ERC Funding
2 484 325 €
Duration
Start date: 2018-10-01, End date: 2023-09-30
Project acronym MicroQuant
Project Microscopy of Tunable Many-Body Quantum Systems
Researcher (PI) Hanns-Christoph Nägerl
Host Institution (HI) UNIVERSITAET INNSBRUCK
Call Details Starting Grant (StG), PE3, ERC-2011-StG_20101014
Summary We propose to take the experimental investigation of strongly-correlated quantum matter in the context of ultracold gases to the next scientific level by applying “quantum gas microscopy” to quantum many-body systems with tunable interactions. Tunability, as provided near Feshbach resonances, has recently proven to be a key ingredient for a broad variety of strongly-correlated quantum gas phases with strong repulsive or attractive interactions and for investigating quantum phase transitions beyond the Mott-Hubbard type. Quantum gas microscopy, as recently demonstrated in two pioneering experiments, will be combined with tunability as given by bosonic Cs atoms to give direct access to spatial correlation functions in the strongly interacting regimes of e.g. the Tonks gases, to open up the atom-by-atom investigation of transport properties, and to allow the detection of entanglement. It will provide local control at the quantum level in a many-body system for entropy engineering and defect manipulation. It will allow the generation of random potentials that add to a periodic lattice potential for the study of glass phases and localization phenomena. In a second step, we will add bosonic and fermionic potassium (39-K and 40-K) to the apparatus to greatly enhance the capabilities of the tunable quantum gas microscope, opening up microscopy to fermionic and, in a third step, to fermionic dipolar systems of KCs polar ground-state molecules. In the case of atomic 40-K fermions with tunable contact interactions, the central goal will be to investigate magnetic systems, in particular to create anti-ferromagnetic many-body states. The Cs sample, for which we routinely achieve ultralow temperatures and extremely pure Bose-Einstein condensates, would serve as a perfect coolant and probe. With KCs, which is non-reactive and hence stable, we will enter a qualitatively new regime of fermionic systems with long-range dipolar interactions.
Summary
We propose to take the experimental investigation of strongly-correlated quantum matter in the context of ultracold gases to the next scientific level by applying “quantum gas microscopy” to quantum many-body systems with tunable interactions. Tunability, as provided near Feshbach resonances, has recently proven to be a key ingredient for a broad variety of strongly-correlated quantum gas phases with strong repulsive or attractive interactions and for investigating quantum phase transitions beyond the Mott-Hubbard type. Quantum gas microscopy, as recently demonstrated in two pioneering experiments, will be combined with tunability as given by bosonic Cs atoms to give direct access to spatial correlation functions in the strongly interacting regimes of e.g. the Tonks gases, to open up the atom-by-atom investigation of transport properties, and to allow the detection of entanglement. It will provide local control at the quantum level in a many-body system for entropy engineering and defect manipulation. It will allow the generation of random potentials that add to a periodic lattice potential for the study of glass phases and localization phenomena. In a second step, we will add bosonic and fermionic potassium (39-K and 40-K) to the apparatus to greatly enhance the capabilities of the tunable quantum gas microscope, opening up microscopy to fermionic and, in a third step, to fermionic dipolar systems of KCs polar ground-state molecules. In the case of atomic 40-K fermions with tunable contact interactions, the central goal will be to investigate magnetic systems, in particular to create anti-ferromagnetic many-body states. The Cs sample, for which we routinely achieve ultralow temperatures and extremely pure Bose-Einstein condensates, would serve as a perfect coolant and probe. With KCs, which is non-reactive and hence stable, we will enter a qualitatively new regime of fermionic systems with long-range dipolar interactions.
Max ERC Funding
1 477 500 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym NITRICARE
Project Nitrification Reloaded - a Single Cell Approach
Researcher (PI) Michael Wagner
Host Institution (HI) UNIVERSITAT WIEN
Call Details Advanced Grant (AdG), LS8, ERC-2011-ADG_20110310
Summary "Nitrification is a central component of the Earth’s biogeochemical nitrogen cycle. This process is driven by two groups of microorganisms, which oxidize ammonia via nitrite to nitrate. Their activities are of major ecological and economic importance and affect global warming, agriculture, wastewater treatment, and eutrophication. Despite the importance of nitrification for the health of our planet, there are surprisingly large gaps in our fundamental understanding of the microbiology of this process. Nitrifiers are difficult to isolate and thus most of our current knowledge stems from a few cultured model organisms that are hardly representative of the microbes driving nitrification in the environment. The overarching objective of NITRICARE is to close some of these knowledge gaps and obtain a comprehensive basic understanding of the identity, evolution, metabolism and ecological importance of those bacteria and archaea that actually catalyze nitrification in nature. For this purpose innovative single cell technologies like Raman-microspectroscopy, NanoSIMS and single cell genomics will be combined in novel ways and a Raman microfluidic device for high-throughput cell sorting will be developed. Application of these approaches will reveal the evolutionary history and metabolic versatility of uncultured ammonia oxidizing archaea and will provide important insights into their population structure. Furthermore, the proposed experiments will allow us to efficiently search for unknown nitrifiers, evaluate their ecological importance and test the hypothesis that organisms catalyzing both steps of nitrification may exist. For non-model nitrifiers we will develop a unique genetic approach to reveal the genetic basis of key metabolic features. Together, the genomic, metabolic, ecophysiological and genetic data will provide unprecedented insights into the biology of nitrifying microbes and open new conceptual horizons for the study of microbes in their natural environments."
Summary
"Nitrification is a central component of the Earth’s biogeochemical nitrogen cycle. This process is driven by two groups of microorganisms, which oxidize ammonia via nitrite to nitrate. Their activities are of major ecological and economic importance and affect global warming, agriculture, wastewater treatment, and eutrophication. Despite the importance of nitrification for the health of our planet, there are surprisingly large gaps in our fundamental understanding of the microbiology of this process. Nitrifiers are difficult to isolate and thus most of our current knowledge stems from a few cultured model organisms that are hardly representative of the microbes driving nitrification in the environment. The overarching objective of NITRICARE is to close some of these knowledge gaps and obtain a comprehensive basic understanding of the identity, evolution, metabolism and ecological importance of those bacteria and archaea that actually catalyze nitrification in nature. For this purpose innovative single cell technologies like Raman-microspectroscopy, NanoSIMS and single cell genomics will be combined in novel ways and a Raman microfluidic device for high-throughput cell sorting will be developed. Application of these approaches will reveal the evolutionary history and metabolic versatility of uncultured ammonia oxidizing archaea and will provide important insights into their population structure. Furthermore, the proposed experiments will allow us to efficiently search for unknown nitrifiers, evaluate their ecological importance and test the hypothesis that organisms catalyzing both steps of nitrification may exist. For non-model nitrifiers we will develop a unique genetic approach to reveal the genetic basis of key metabolic features. Together, the genomic, metabolic, ecophysiological and genetic data will provide unprecedented insights into the biology of nitrifying microbes and open new conceptual horizons for the study of microbes in their natural environments."
Max ERC Funding
2 499 107 €
Duration
Start date: 2012-05-01, End date: 2017-04-30
Project acronym QUNNECT
Project A Fiber Optic Transceiver for Superconducting Qubits
Researcher (PI) Johannes FINK
Host Institution (HI) INSTITUTE OF SCIENCE AND TECHNOLOGYAUSTRIA
Call Details Starting Grant (StG), PE3, ERC-2017-STG
Summary Many researchers in basic science and large IT companies are convinced that superconducting quantum processors will soon help solve complex problems faster, improve optimization and simulation, and boost the progress in artificial intelligence. A worldwide quantum web is the next logical step. It would not only improve communication security, it represents the key to unlock the full potential of the new quantum-computing paradigm.
Unfortunately, research in optical quantum networks and superconducting devices has progressed largely independently so far. While superconducting qubits are ideally suited for on-chip integration and fast processing, they are problematic for quantum communication. In fact, no solution exists to connect remote qubits via a room temperature link. The small energy scales in the electrical circuit make the fragile information carriers (single microwave photons) susceptible to interference, thermal noise and losses, which has hindered any significant progress in this direction.
Only just now we have gained sufficient insight into low loss materials, the required fabrication technology, and the precision measurement techniques necessary to bridge the two worlds, by controlling individual photons and phonons quantum coherently. We propose to integrate silicon photonics for low-loss fiber optic communication with superconducting circuits for quantum processing on a single microchip. As intermediary transducer we will focus on two approaches: (1) quantum ground state cooled nanoscale mechanical and (2) low-loss electro-optic nonlinear circuit elements. The novelty of our approach is the tight on-chip integration facilitated by the PIs interdisciplinary background in both, superconducting circuits and silicon nanophotonics. Integration will be the key for realizing a low-loss and high-bandwidth transceiver, for preparing remote entanglement of superconducting qubits, and for extending the range of current fiber optic quantum networks.
Summary
Many researchers in basic science and large IT companies are convinced that superconducting quantum processors will soon help solve complex problems faster, improve optimization and simulation, and boost the progress in artificial intelligence. A worldwide quantum web is the next logical step. It would not only improve communication security, it represents the key to unlock the full potential of the new quantum-computing paradigm.
Unfortunately, research in optical quantum networks and superconducting devices has progressed largely independently so far. While superconducting qubits are ideally suited for on-chip integration and fast processing, they are problematic for quantum communication. In fact, no solution exists to connect remote qubits via a room temperature link. The small energy scales in the electrical circuit make the fragile information carriers (single microwave photons) susceptible to interference, thermal noise and losses, which has hindered any significant progress in this direction.
Only just now we have gained sufficient insight into low loss materials, the required fabrication technology, and the precision measurement techniques necessary to bridge the two worlds, by controlling individual photons and phonons quantum coherently. We propose to integrate silicon photonics for low-loss fiber optic communication with superconducting circuits for quantum processing on a single microchip. As intermediary transducer we will focus on two approaches: (1) quantum ground state cooled nanoscale mechanical and (2) low-loss electro-optic nonlinear circuit elements. The novelty of our approach is the tight on-chip integration facilitated by the PIs interdisciplinary background in both, superconducting circuits and silicon nanophotonics. Integration will be the key for realizing a low-loss and high-bandwidth transceiver, for preparing remote entanglement of superconducting qubits, and for extending the range of current fiber optic quantum networks.
Max ERC Funding
1 500 000 €
Duration
Start date: 2018-02-01, End date: 2023-01-31
