Project acronym AEROBIC
Project Assessing the Effects of Rising O2 on Biogeochemical Cycles: Integrated Laboratory Experiments and Numerical Simulations
Researcher (PI) Itay Halevy
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE
Call Details Starting Grant (StG), PE10, ERC-2013-StG
Summary The rise of atmospheric O2 ~2,500 million years ago is one of the most profound transitions in Earth's history. Yet, despite its central role in shaping Earth's surface environment, the cause for the rise of O2 remains poorly understood. Tight coupling between the O2 cycle and the biogeochemical cycles of redox-active elements, such as C, Fe and S, implies radical changes in these cycles before, during and after the rise of O2. These changes, too, are incompletely understood, but have left valuable information encoded in the geological record. This information has been qualitatively interpreted, leaving many aspects of the rise of O2, including its causes and constraints on ocean chemistry before and after it, topics of ongoing research and debate. Here, I outline a research program to address this fundamental question in geochemical Earth systems evolution. The inherently interdisciplinary program uniquely integrates laboratory experiments, numerical models, geological observations, and geochemical analyses. Laboratory experiments and geological observations will constrain unknown parameters of the early biogeochemical cycles, and, in combination with field studies, will validate and refine the use of paleoenvironmental proxies. The insight gained will be used to develop detailed models of the coupled biogeochemical cycles, which will themselves be used to quantitatively understand the events surrounding the rise of O2, and to illuminate the dynamics of elemental cycles in the early oceans.
This program is expected to yield novel, quantitative insight into these important events in Earth history and to have a major impact on our understanding of early ocean chemistry and the rise of O2. An ERC Starting Grant will enable me to use the excellent experimental and computational facilities at my disposal, to access the outstanding human resource at the Weizmann Institute of Science, and to address one of the major open questions in modern geochemistry.
Summary
The rise of atmospheric O2 ~2,500 million years ago is one of the most profound transitions in Earth's history. Yet, despite its central role in shaping Earth's surface environment, the cause for the rise of O2 remains poorly understood. Tight coupling between the O2 cycle and the biogeochemical cycles of redox-active elements, such as C, Fe and S, implies radical changes in these cycles before, during and after the rise of O2. These changes, too, are incompletely understood, but have left valuable information encoded in the geological record. This information has been qualitatively interpreted, leaving many aspects of the rise of O2, including its causes and constraints on ocean chemistry before and after it, topics of ongoing research and debate. Here, I outline a research program to address this fundamental question in geochemical Earth systems evolution. The inherently interdisciplinary program uniquely integrates laboratory experiments, numerical models, geological observations, and geochemical analyses. Laboratory experiments and geological observations will constrain unknown parameters of the early biogeochemical cycles, and, in combination with field studies, will validate and refine the use of paleoenvironmental proxies. The insight gained will be used to develop detailed models of the coupled biogeochemical cycles, which will themselves be used to quantitatively understand the events surrounding the rise of O2, and to illuminate the dynamics of elemental cycles in the early oceans.
This program is expected to yield novel, quantitative insight into these important events in Earth history and to have a major impact on our understanding of early ocean chemistry and the rise of O2. An ERC Starting Grant will enable me to use the excellent experimental and computational facilities at my disposal, to access the outstanding human resource at the Weizmann Institute of Science, and to address one of the major open questions in modern geochemistry.
Max ERC Funding
1 472 690 €
Duration
Start date: 2013-09-01, End date: 2018-08-31
Project acronym BIONICS
Project Bio-Inspired Routes for Controlling the Structure and Properties of Materials: Reusing proven tricks on new materials
Researcher (PI) Boaz Pokroy
Host Institution (HI) TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY
Call Details Starting Grant (StG), PE5, ERC-2013-StG
Summary "In the course of biomineralization, organisms produce a large variety of functional biogenic crystals that exhibit fascinating mechanical, optical, magnetic and other characteristics. More specifically, when living organisms grow crystals they can effectively control polymorph selection as well as the crystal morphology, shape, and even atomic structure. Materials existing in nature have extraordinary and specific functions, yet the materials employed in nature are quite different from those engineers would select.
I propose to emulate specific strategies used by organisms in forming structural biogenic crystals, and to apply these strategies biomimetically so as to form new structural materials with new properties and characteristics. This bio-inspired approach will involve the adoption of three specific biological strategies. We believe that this procedure will open up new ways to control the structure and properties of smart materials.
The three bio-inspired strategies that we will utilize are:
(i) to control the short-range order of amorphous materials, making it possible to predetermine the polymorph obtained when they transform from the amorphous to the succeeding crystalline phase;
(ii) to control the morphology of single crystals of various functional materials so that they can have intricate and curved surfaces and yet maintain their single-crystal nature;
(iii) to entrap organic molecules into single crystals of functional materials so as to tailor and manipulate their electronic structure.
The proposed research has significant potential for opening up new routes for the formation of novel functional materials. Specifically, it will make it possible for us
(1) to produce single, intricately shaped crystals without the need to etch, drill or polish;
(2) to control the short-range order of amorphous materials and hence the polymorph of the successive crystalline phase;
(3) to tune the band gap of semiconductors via incorporation of tailored bio-molecules."
Summary
"In the course of biomineralization, organisms produce a large variety of functional biogenic crystals that exhibit fascinating mechanical, optical, magnetic and other characteristics. More specifically, when living organisms grow crystals they can effectively control polymorph selection as well as the crystal morphology, shape, and even atomic structure. Materials existing in nature have extraordinary and specific functions, yet the materials employed in nature are quite different from those engineers would select.
I propose to emulate specific strategies used by organisms in forming structural biogenic crystals, and to apply these strategies biomimetically so as to form new structural materials with new properties and characteristics. This bio-inspired approach will involve the adoption of three specific biological strategies. We believe that this procedure will open up new ways to control the structure and properties of smart materials.
The three bio-inspired strategies that we will utilize are:
(i) to control the short-range order of amorphous materials, making it possible to predetermine the polymorph obtained when they transform from the amorphous to the succeeding crystalline phase;
(ii) to control the morphology of single crystals of various functional materials so that they can have intricate and curved surfaces and yet maintain their single-crystal nature;
(iii) to entrap organic molecules into single crystals of functional materials so as to tailor and manipulate their electronic structure.
The proposed research has significant potential for opening up new routes for the formation of novel functional materials. Specifically, it will make it possible for us
(1) to produce single, intricately shaped crystals without the need to etch, drill or polish;
(2) to control the short-range order of amorphous materials and hence the polymorph of the successive crystalline phase;
(3) to tune the band gap of semiconductors via incorporation of tailored bio-molecules."
Max ERC Funding
1 500 000 €
Duration
Start date: 2013-09-01, End date: 2018-08-31
Project acronym BOTTOM-UP_SYSCHEM
Project Systems Chemistry from Bottom Up: Switching, Gating and Oscillations in Non Enzymatic Peptide Networks
Researcher (PI) Gonen Ashkenasy
Host Institution (HI) BEN-GURION UNIVERSITY OF THE NEGEV
Call Details Starting Grant (StG), PE5, ERC-2010-StG_20091028
Summary The study of synthetic molecular networks is of fundamental importance for understanding the organizational principles of biological systems and may well be the key to unraveling the origins of life. In addition, such systems may be useful for parallel synthesis of molecules, implementation of catalysis via multi-step pathways, and as media for various applications in nano-medicine and nano-electronics. We have been involved recently in developing peptide-based replicating networks and revealed their dynamic characteristics. We argue here that the structural information embedded in the polypeptide chains is sufficiently rich to allow the construction of peptide 'Systems Chemistry', namely, to facilitate the use of replicating networks as cell-mimetics, featuring complex dynamic behavior. To bring this novel idea to reality, we plan to take a unique holistic approach by studying such networks both experimentally and via simulations, for elucidating basic-principles and towards applications in adjacent fields, such as molecular electronics. Towards realizing these aims, we will study three separate but inter-related objectives: (i) design and characterization of networks that react and rewire in response to external triggers, such as light, (ii) design of networks that operate via new dynamic rules of product formation that lead to oscillations, and (iii) exploitation of the molecular information gathered from the networks as means to control switching and gating in molecular electronic devices. We believe that achieving the project's objectives will be highly significant for the development of the arising field of Systems Chemistry, and in addition will provide valuable tools for studying related scientific fields, such as systems biology and molecular electronics.
Summary
The study of synthetic molecular networks is of fundamental importance for understanding the organizational principles of biological systems and may well be the key to unraveling the origins of life. In addition, such systems may be useful for parallel synthesis of molecules, implementation of catalysis via multi-step pathways, and as media for various applications in nano-medicine and nano-electronics. We have been involved recently in developing peptide-based replicating networks and revealed their dynamic characteristics. We argue here that the structural information embedded in the polypeptide chains is sufficiently rich to allow the construction of peptide 'Systems Chemistry', namely, to facilitate the use of replicating networks as cell-mimetics, featuring complex dynamic behavior. To bring this novel idea to reality, we plan to take a unique holistic approach by studying such networks both experimentally and via simulations, for elucidating basic-principles and towards applications in adjacent fields, such as molecular electronics. Towards realizing these aims, we will study three separate but inter-related objectives: (i) design and characterization of networks that react and rewire in response to external triggers, such as light, (ii) design of networks that operate via new dynamic rules of product formation that lead to oscillations, and (iii) exploitation of the molecular information gathered from the networks as means to control switching and gating in molecular electronic devices. We believe that achieving the project's objectives will be highly significant for the development of the arising field of Systems Chemistry, and in addition will provide valuable tools for studying related scientific fields, such as systems biology and molecular electronics.
Max ERC Funding
1 500 000 €
Duration
Start date: 2010-10-01, End date: 2015-09-30
Project acronym C8
Project Consistent computation of the chemistry-cloud continuum and climate change in Cyprus
Researcher (PI) Johannes Lelieveld
Host Institution (HI) THE CYPRUS RESEARCH AND EDUCATIONAL FOUNDATION
Call Details Advanced Grant (AdG), PE10, ERC-2008-AdG
Summary We have developed a new numerical method to consistently compute atmospheric trace gas and aerosol chemistry and cloud processes. The method is computationally efficient so that it can be used in climate models. For the first time cloud droplet formation on multi-component particles can be represented based on first principles rather than parameterisations. This allows for a direct coupling in models between aerosol chemical composition and the continuum between hazes and clouds as a function of ambient relative humidity. We will apply the method in a new nested global-limited area model system to study atmospheric chemistry climate interactions and anthropogenic influences. We will focus on the Mediterranean region because it is a hot spot in climate change exposed to drying and air pollution. The limited area model will also be applied as cloud-resolving model to study aerosol influences on precipitation and storm development. By simulating realistic meteorological conditions at high spatial resolution our method can be straightforwardly tested against observations. Central questions are: - How does the simulated haze-cloud continuum compare with remote sensing measurements and what is the consequence of abandoning the traditional and artificial distinction between aerosols and clouds? - How are cloud and precipitation formation influenced by atmospheric chemical composition changes? - To what extent do haze and cloud formation in polluted air exert forcings of synoptic meteorological conditions and climate? - Can aerosol pollution in the Mediterranean region exacerbate the predicted and observed drying in a changing climate? The model system is user-friendly and will facilitate air quality and climate studies by regional scientists. The project will be part of the Energy, Environment and Water Centre of the newly founded Cyprus Institute, provide input to climate impact assessments and contribute to a regional outreach programme.
Summary
We have developed a new numerical method to consistently compute atmospheric trace gas and aerosol chemistry and cloud processes. The method is computationally efficient so that it can be used in climate models. For the first time cloud droplet formation on multi-component particles can be represented based on first principles rather than parameterisations. This allows for a direct coupling in models between aerosol chemical composition and the continuum between hazes and clouds as a function of ambient relative humidity. We will apply the method in a new nested global-limited area model system to study atmospheric chemistry climate interactions and anthropogenic influences. We will focus on the Mediterranean region because it is a hot spot in climate change exposed to drying and air pollution. The limited area model will also be applied as cloud-resolving model to study aerosol influences on precipitation and storm development. By simulating realistic meteorological conditions at high spatial resolution our method can be straightforwardly tested against observations. Central questions are: - How does the simulated haze-cloud continuum compare with remote sensing measurements and what is the consequence of abandoning the traditional and artificial distinction between aerosols and clouds? - How are cloud and precipitation formation influenced by atmospheric chemical composition changes? - To what extent do haze and cloud formation in polluted air exert forcings of synoptic meteorological conditions and climate? - Can aerosol pollution in the Mediterranean region exacerbate the predicted and observed drying in a changing climate? The model system is user-friendly and will facilitate air quality and climate studies by regional scientists. The project will be part of the Energy, Environment and Water Centre of the newly founded Cyprus Institute, provide input to climate impact assessments and contribute to a regional outreach programme.
Max ERC Funding
2 196 000 €
Duration
Start date: 2009-01-01, End date: 2014-12-31
Project acronym CMetC
Project Selective Carbon-Carbon Bond Activation: A Wellspring of Untapped Reactivity
Researcher (PI) Ilan Marek
Host Institution (HI) TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY
Call Details Advanced Grant (AdG), PE5, ERC-2013-ADG
Summary The creation of new molecular entities and subsequent exploitation of their properties is central to a broad spectrum of research disciplines from medicine to materials. Most –if not all- of the efforts of organic chemists were directed to the development of creative strategies to built carbon-carbon and carbon-heteroatom bonds in a predictable and efficient manner. But is the creation of new bonds the only approach that organic chemistry should follow? Could we design the synthesis of challenging molecular skeleton no more through the construction of carbon-carbon bonds but rather through selective cleavage of carbon-carbon bonds (C-C bond activation)? The goal of this work is to develop powerful synthetic approaches for the selective C-C bond activation and demonstrate that it has the potential to be a general principle in organic synthesis for the regio-, diastereo- and even enantiomerically enriched preparation of adducts despite that C-C single bonds belong among the least reactive functional groups in chemistry. The realization of this synthetic potential requires the ability to functionalize selectively one C-C bond in compounds containing many such bonds and an array of functional groups. This site selective C-C bond activation is one of the greatest challenges that must be met to be used widely in complex-molecular synthesis. To emphasize the practicality of C-C bond activation, we will prepare in a single-pot operation challenging molecular framework possessing various stereogenic centers from very simple starting materials through selective C-C bond activation. Ideally, alkenes will be in-situ transformed into alkanes that will subsequently undergo the C-C activation even in the presence of functional group. This work will lead to ground-breaking advances when non-strained cycloalkanes (cyclopentane, cyclohexane) will undergo this smooth C-C bond activation with friendly and non toxic organometallic species.
Summary
The creation of new molecular entities and subsequent exploitation of their properties is central to a broad spectrum of research disciplines from medicine to materials. Most –if not all- of the efforts of organic chemists were directed to the development of creative strategies to built carbon-carbon and carbon-heteroatom bonds in a predictable and efficient manner. But is the creation of new bonds the only approach that organic chemistry should follow? Could we design the synthesis of challenging molecular skeleton no more through the construction of carbon-carbon bonds but rather through selective cleavage of carbon-carbon bonds (C-C bond activation)? The goal of this work is to develop powerful synthetic approaches for the selective C-C bond activation and demonstrate that it has the potential to be a general principle in organic synthesis for the regio-, diastereo- and even enantiomerically enriched preparation of adducts despite that C-C single bonds belong among the least reactive functional groups in chemistry. The realization of this synthetic potential requires the ability to functionalize selectively one C-C bond in compounds containing many such bonds and an array of functional groups. This site selective C-C bond activation is one of the greatest challenges that must be met to be used widely in complex-molecular synthesis. To emphasize the practicality of C-C bond activation, we will prepare in a single-pot operation challenging molecular framework possessing various stereogenic centers from very simple starting materials through selective C-C bond activation. Ideally, alkenes will be in-situ transformed into alkanes that will subsequently undergo the C-C activation even in the presence of functional group. This work will lead to ground-breaking advances when non-strained cycloalkanes (cyclopentane, cyclohexane) will undergo this smooth C-C bond activation with friendly and non toxic organometallic species.
Max ERC Funding
2 367 495 €
Duration
Start date: 2013-11-01, End date: 2018-10-31
Project acronym CNTM
Project Cryptography on Non-Trusted Machines
Researcher (PI) Stefan Dziembowski
Host Institution (HI) UNIWERSYTET WARSZAWSKI
Call Details Starting Grant (StG), PE5, ERC-2007-StG
Summary This project is about the design of cryptographic schemes that are secure even if implemented on not-secure devices. The motivation for this problem comes from an observation that most of the real-life attacks on cryptographic devices do not break their mathematical foundations, but exploit vulnerabilities of their implementations. This concerns both the cryptographic software executed on PCs (that can be attacked by viruses), and the implementations on hardware (that can be subject to the side-channel attacks). Traditionally fixing this problem was left to the practitioners, since it was a common belief that theory cannot be of any help here. However, new exciting results in cryptography suggest that this view was too pessimistic: there exist methods to design cryptographic protocols in such a way that they are secure even if the hardware on which they are executed cannot be fully trusted. The goal of this project is to investigate these methods further, unify them in a solid mathematical theory (many of them were developed independently), and propose new ideas in this area. The project will be mostly theoretical (although some practical experiments may be performed). Our main interest lies within the theory of private circuits, bounded-retrieval model, physically-observable cryptography, and human-assisted cryptography. We view these theories just as the departing points, since the area is very fresh and we expect to soon witness completely new ideas in this field.
Summary
This project is about the design of cryptographic schemes that are secure even if implemented on not-secure devices. The motivation for this problem comes from an observation that most of the real-life attacks on cryptographic devices do not break their mathematical foundations, but exploit vulnerabilities of their implementations. This concerns both the cryptographic software executed on PCs (that can be attacked by viruses), and the implementations on hardware (that can be subject to the side-channel attacks). Traditionally fixing this problem was left to the practitioners, since it was a common belief that theory cannot be of any help here. However, new exciting results in cryptography suggest that this view was too pessimistic: there exist methods to design cryptographic protocols in such a way that they are secure even if the hardware on which they are executed cannot be fully trusted. The goal of this project is to investigate these methods further, unify them in a solid mathematical theory (many of them were developed independently), and propose new ideas in this area. The project will be mostly theoretical (although some practical experiments may be performed). Our main interest lies within the theory of private circuits, bounded-retrieval model, physically-observable cryptography, and human-assisted cryptography. We view these theories just as the departing points, since the area is very fresh and we expect to soon witness completely new ideas in this field.
Max ERC Funding
872 550 €
Duration
Start date: 2008-11-01, End date: 2013-10-31
Project acronym CONFINEDCHEM
Project Synthetic Confined Environments as Tools for Manipulating Chemical Reactivities and Preparing New Nanostructures
Researcher (PI) Rafal Klajn
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE
Call Details Starting Grant (StG), PE5, ERC-2013-StG
Summary "Nature has long inspired chemists with its abilities to stabilize ephemeral chemical species, to perform chemical reactions with unprecedented rates and selectivities, and to synthesize complex molecules and fascinating inorganic nanostructures. What natural systems consistently exploit - which is yet fundamentally different from how chemists perform reactions - is their aspect of nanoscale confinement. The goal of the proposed research program is to integrate the worlds of organic and inorganic colloidal chemistry by means of manipulating chemical reactivities and synthesizing novel molecules and nanostructures inside synthetic confined environments created using novel, unconventional approaches based on inorganic, nanostructured building blocks. The three types of confined spaces we propose are as follows: 1) nanopores within reversibly self-assembling colloidal crystals (""dynamic nanoflasks""), 2) cavities of bowl-shaped metallic nanoparticles (NPs), and 3) surfaces of spherical NPs. By taking advantage of these unique tools, we will attempt to develop, respectively, 1) a conceptually new method for catalyzing chemical reactions using light, 2) nanoscale inclusion chemistry (a field based on host-guest ""complexes"" assembled form nanosized components) and 3) to use NPs as platforms for the development of new organic reactions. While these objectives are predominantly of a fundamental nature, they can easily evolve into a variety of practical applications. Specifically, we will pursue diverse goals such as the preparation of 1) a new family of inverse opals (with potentially fascinating optical and mechanical properties), 2) artificial chaperones (NPs assisting in protein folding), and 3) size- and shape-controlled polymeric vesicles. Overall, it is believed that this marriage of organic and colloidal chemistry has the potential to change the fundamental way we perform chemical reactions, paving the way to the discovery of new phenomena and unique structures."
Summary
"Nature has long inspired chemists with its abilities to stabilize ephemeral chemical species, to perform chemical reactions with unprecedented rates and selectivities, and to synthesize complex molecules and fascinating inorganic nanostructures. What natural systems consistently exploit - which is yet fundamentally different from how chemists perform reactions - is their aspect of nanoscale confinement. The goal of the proposed research program is to integrate the worlds of organic and inorganic colloidal chemistry by means of manipulating chemical reactivities and synthesizing novel molecules and nanostructures inside synthetic confined environments created using novel, unconventional approaches based on inorganic, nanostructured building blocks. The three types of confined spaces we propose are as follows: 1) nanopores within reversibly self-assembling colloidal crystals (""dynamic nanoflasks""), 2) cavities of bowl-shaped metallic nanoparticles (NPs), and 3) surfaces of spherical NPs. By taking advantage of these unique tools, we will attempt to develop, respectively, 1) a conceptually new method for catalyzing chemical reactions using light, 2) nanoscale inclusion chemistry (a field based on host-guest ""complexes"" assembled form nanosized components) and 3) to use NPs as platforms for the development of new organic reactions. While these objectives are predominantly of a fundamental nature, they can easily evolve into a variety of practical applications. Specifically, we will pursue diverse goals such as the preparation of 1) a new family of inverse opals (with potentially fascinating optical and mechanical properties), 2) artificial chaperones (NPs assisting in protein folding), and 3) size- and shape-controlled polymeric vesicles. Overall, it is believed that this marriage of organic and colloidal chemistry has the potential to change the fundamental way we perform chemical reactions, paving the way to the discovery of new phenomena and unique structures."
Max ERC Funding
1 499 992 €
Duration
Start date: 2013-10-01, End date: 2018-09-30
Project acronym FORECASToneMONTH
Project Forecasting Surface Weather and Climate at One-Month Leads through Stratosphere-Troposphere Coupling
Researcher (PI) Chaim Israel Garfinkel
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Call Details Starting Grant (StG), PE10, ERC-2015-STG
Summary Anomalies in surface temperatures, winds, and precipitation can significantly alter energy supply and demand, cause flooding, and cripple transportation networks. Better management of these impacts can be achieved by extending the duration of reliable predictions of the atmospheric circulation.
Polar stratospheric variability can impact surface weather for well over a month, and this proposed research presents a novel approach towards understanding the fundamentals of how this coupling occurs. Specifically, we are interested in: 1) how predictable are anomalies in the stratospheric circulation? 2) why do only some stratospheric events modify surface weather? and 3) what is the mechanism whereby stratospheric anomalies reach the surface? While this last question may appear academic, several studies indicate that stratosphere-troposphere coupling drives the midlatitude tropospheric response to climate change; therefore, a clearer understanding of the mechanisms will aid in the interpretation of the upcoming changes in the surface climate.
I propose a multi-pronged effort aimed at addressing these questions and improving monthly forecasting. First, carefully designed modelling experiments using a novel modelling framework will be used to clarify how, and under what conditions, stratospheric variability couples to tropospheric variability. Second, novel linkages between variability external to the stratospheric polar vortex and the stratospheric polar vortex will be pursued, thus improving our ability to forecast polar vortex variability itself. To these ends, my group will develop 1) an analytic model for Rossby wave propagation on the sphere, and 2) a simplified general circulation model, which captures the essential processes underlying stratosphere-troposphere coupling. By combining output from the new models, observational data, and output from comprehensive climate models, the connections between the stratosphere and surface climate will be elucidated.
Summary
Anomalies in surface temperatures, winds, and precipitation can significantly alter energy supply and demand, cause flooding, and cripple transportation networks. Better management of these impacts can be achieved by extending the duration of reliable predictions of the atmospheric circulation.
Polar stratospheric variability can impact surface weather for well over a month, and this proposed research presents a novel approach towards understanding the fundamentals of how this coupling occurs. Specifically, we are interested in: 1) how predictable are anomalies in the stratospheric circulation? 2) why do only some stratospheric events modify surface weather? and 3) what is the mechanism whereby stratospheric anomalies reach the surface? While this last question may appear academic, several studies indicate that stratosphere-troposphere coupling drives the midlatitude tropospheric response to climate change; therefore, a clearer understanding of the mechanisms will aid in the interpretation of the upcoming changes in the surface climate.
I propose a multi-pronged effort aimed at addressing these questions and improving monthly forecasting. First, carefully designed modelling experiments using a novel modelling framework will be used to clarify how, and under what conditions, stratospheric variability couples to tropospheric variability. Second, novel linkages between variability external to the stratospheric polar vortex and the stratospheric polar vortex will be pursued, thus improving our ability to forecast polar vortex variability itself. To these ends, my group will develop 1) an analytic model for Rossby wave propagation on the sphere, and 2) a simplified general circulation model, which captures the essential processes underlying stratosphere-troposphere coupling. By combining output from the new models, observational data, and output from comprehensive climate models, the connections between the stratosphere and surface climate will be elucidated.
Max ERC Funding
1 808 000 €
Duration
Start date: 2016-05-01, End date: 2021-04-30
Project acronym GeneREFORM
Project Genetically Encoded Multicolor Reporter Systems For Multiplexed MRI
Researcher (PI) Amnon Bar-Shir
Host Institution (HI) WEIZMANN INSTITUTE OF SCIENCE LTD
Call Details Starting Grant (StG), PE5, ERC-2015-STG
Summary In order to fully understand the complexity of biological processes that are reflected by simultaneous occurrences of intra and inter-cellular events, multiplexed imaging platforms are needed. Fluorescent reporter genes, with their “multicolor” imaging capabilities, have revolutionized science and their founders have been awarded the Nobel Prize. Nevertheless, the light signal source of these reporters, which restricts their use in deep tissues and in large animals (and potentially in humans), calls for alternatives.
Reporter genes for MRI, although in their infancy, showed several exceptionalities, including the ability to longitudinal study the same subject with unlimited tissue penetration and to coregister information from reporter gene expression with high-resolution anatomical images. Inspired by the multicolor capabilities of optical reporter genes, this proposal aims to develop, optimize, and implement genetically engineered reporter systems for MRI with artificial “multicolor” characteristics. Capitalizing on (i) the Chemical Exchange Saturation Transfer (CEST)-MRI contrast mechanism that allows the use of small bioorganic molecules as MRI sensors, (ii) the frequency encoding, color-like features of CEST, and on (iii) enzyme engineering procedures that allow the optimization of enzymatic activity for a desired substrate, a “multicolor” genetically encoded MRI reporter system is proposed.
By (a) synthesizing libraries of non-natural nucleosides (“reporter probes”) to generate artificially “colored” CEST contrast, and (b) performing directed evolution of deoxyribonucleoside kinase (dNK) enzymes (“reporter genes”) to phosphorylate those nucleosides, the “multicolor” genetically encoded MRI “reporter system” will be created. The orthogonally of the obtained pairs of substrate (CEST sensor)/ enzyme (mutant dNK) will allow their simultaneous use as a genetically encoded reporter system for in vivo “multicolor” monitoring of reporter gene expression with MRI.
Summary
In order to fully understand the complexity of biological processes that are reflected by simultaneous occurrences of intra and inter-cellular events, multiplexed imaging platforms are needed. Fluorescent reporter genes, with their “multicolor” imaging capabilities, have revolutionized science and their founders have been awarded the Nobel Prize. Nevertheless, the light signal source of these reporters, which restricts their use in deep tissues and in large animals (and potentially in humans), calls for alternatives.
Reporter genes for MRI, although in their infancy, showed several exceptionalities, including the ability to longitudinal study the same subject with unlimited tissue penetration and to coregister information from reporter gene expression with high-resolution anatomical images. Inspired by the multicolor capabilities of optical reporter genes, this proposal aims to develop, optimize, and implement genetically engineered reporter systems for MRI with artificial “multicolor” characteristics. Capitalizing on (i) the Chemical Exchange Saturation Transfer (CEST)-MRI contrast mechanism that allows the use of small bioorganic molecules as MRI sensors, (ii) the frequency encoding, color-like features of CEST, and on (iii) enzyme engineering procedures that allow the optimization of enzymatic activity for a desired substrate, a “multicolor” genetically encoded MRI reporter system is proposed.
By (a) synthesizing libraries of non-natural nucleosides (“reporter probes”) to generate artificially “colored” CEST contrast, and (b) performing directed evolution of deoxyribonucleoside kinase (dNK) enzymes (“reporter genes”) to phosphorylate those nucleosides, the “multicolor” genetically encoded MRI “reporter system” will be created. The orthogonally of the obtained pairs of substrate (CEST sensor)/ enzyme (mutant dNK) will allow their simultaneous use as a genetically encoded reporter system for in vivo “multicolor” monitoring of reporter gene expression with MRI.
Max ERC Funding
1 478 284 €
Duration
Start date: 2016-05-01, End date: 2021-04-30
Project acronym GeoArchMag
Project Beyond the Holocene Geomagnetic field resolution
Researcher (PI) Ron Shaar
Host Institution (HI) THE HEBREW UNIVERSITY OF JERUSALEM
Call Details Starting Grant (StG), PE10, ERC-2018-STG
Summary For decades the Holocene has been considered a flat and “boring” epoch from the standpoint of
paleomagnetism, mainly due to insufficient resolution of the available paleomagnetic data. However, recent
archaeomagnetic data have revealed that the Holocene geomagnetic field is anything but stable – presenting
puzzling intervals of extreme decadal-scale fluctuations and unexpected departures from a simple dipolar field
structure. This new information introduced an entirely new paradigm to the study of the geomagnetic field and
to a wide range of research areas relying on paleomagnetic data, such as geochronology, climate research, and
geodynamo exploration.
This proposal aims at breaking the resolution limits in paleomagnetism, and providing a continuous
time series of the geomagnetic field vector throughout the Holocene at decadal resolution and
unprecedented accuracy. To this end I will use an innovative assemblage of data sources, jointly unique to
the Levant, including rare archaeological finds, annual laminated stalagmites, varved sediments, and arid
playa deposits. Together, these sources can provide unprecedented yearly resolution, whereby the “absolute”
archaeomagnetic data can calibrate “relative” terrestrial data.
The geomagnetic data will define an innovative absolute geomagnetic chronology that will be used to
synchronize cosmogenic 10Be data and an extensive body of paleo-climatic indicators. With these in hand, I
will address four ground-breaking problems:
I) Chronology: Developing dating technique for resolving critical controversies in Levantine archaeology and
Quaternary geology.
II) Geophysics: Exploring fine-scale geodynamo features in Earth’s core from new generations of global
geomagnetic models.
III) Cosmogenics: Correlating fast geomagnetic variations with cosmogenic isotope production rate.
IV) Climate: Testing one of the most challenging controversial questions in geomagnetism: “Does the Earth's
magnetic field play a role in climate changes?”
Summary
For decades the Holocene has been considered a flat and “boring” epoch from the standpoint of
paleomagnetism, mainly due to insufficient resolution of the available paleomagnetic data. However, recent
archaeomagnetic data have revealed that the Holocene geomagnetic field is anything but stable – presenting
puzzling intervals of extreme decadal-scale fluctuations and unexpected departures from a simple dipolar field
structure. This new information introduced an entirely new paradigm to the study of the geomagnetic field and
to a wide range of research areas relying on paleomagnetic data, such as geochronology, climate research, and
geodynamo exploration.
This proposal aims at breaking the resolution limits in paleomagnetism, and providing a continuous
time series of the geomagnetic field vector throughout the Holocene at decadal resolution and
unprecedented accuracy. To this end I will use an innovative assemblage of data sources, jointly unique to
the Levant, including rare archaeological finds, annual laminated stalagmites, varved sediments, and arid
playa deposits. Together, these sources can provide unprecedented yearly resolution, whereby the “absolute”
archaeomagnetic data can calibrate “relative” terrestrial data.
The geomagnetic data will define an innovative absolute geomagnetic chronology that will be used to
synchronize cosmogenic 10Be data and an extensive body of paleo-climatic indicators. With these in hand, I
will address four ground-breaking problems:
I) Chronology: Developing dating technique for resolving critical controversies in Levantine archaeology and
Quaternary geology.
II) Geophysics: Exploring fine-scale geodynamo features in Earth’s core from new generations of global
geomagnetic models.
III) Cosmogenics: Correlating fast geomagnetic variations with cosmogenic isotope production rate.
IV) Climate: Testing one of the most challenging controversial questions in geomagnetism: “Does the Earth's
magnetic field play a role in climate changes?”
Max ERC Funding
1 786 381 €
Duration
Start date: 2018-11-01, End date: 2023-10-31
