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  • 1
    Publication Date: 2022-05-25
    Description: © The Author(s), 2013. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 10 (2013): 6225-6245, doi:10.5194/bg-10-6225-2013.
    Description: Ocean ecosystems are increasingly stressed by human-induced changes of their physical, chemical and biological environment. Among these changes, warming, acidification, deoxygenation and changes in primary productivity by marine phytoplankton can be considered as four of the major stressors of open ocean ecosystems. Due to rising atmospheric CO2 in the coming decades, these changes will be amplified. Here, we use the most recent simulations performed in the framework of the Coupled Model Intercomparison Project 5 to assess how these stressors may evolve over the course of the 21st century. The 10 Earth system models used here project similar trends in ocean warming, acidification, deoxygenation and reduced primary productivity for each of the IPCC's representative concentration pathways (RCPs) over the 21st century. For the "business-as-usual" scenario RCP8.5, the model-mean changes in the 2090s (compared to the 1990s) for sea surface temperature, sea surface pH, global O2 content and integrated primary productivity amount to +2.73 (±0.72) °C, −0.33 (±0.003) pH unit, −3.45 (±0.44)% and −8.6 (±7.9)%, respectively. For the high mitigation scenario RCP2.6, corresponding changes are +0.71 (±0.45) °C, −0.07 (±0.001) pH unit, −1.81 (±0.31)% and −2.0 (±4.1)%, respectively, illustrating the effectiveness of extreme mitigation strategies. Although these stressors operate globally, they display distinct regional patterns and thus do not change coincidentally. Large decreases in O2 and in pH are simulated in global ocean intermediate and mode waters, whereas large reductions in primary production are simulated in the tropics and in the North Atlantic. Although temperature and pH projections are robust across models, the same does not hold for projections of subsurface O2 concentrations in the tropics and global and regional changes in net primary productivity. These high uncertainties in projections of primary productivity and subsurface oxygen prompt us to continue inter-model comparisons to understand these model differences, while calling for caution when using the CMIP5 models to force regional impact models.
    Description: This work was supported by EU FP7 project CARBOCHANGE (under grant agreement No. 264879), EU FP7 project MEECE (under grant agreement No. 212085), EU FP7 project SOCCLI (under grant agreement No. 317699), and ANR project MACROES. S. C. Doney acknowledges the US National Science Foundation (AGS-1048827). This work has been supported by the Research Council of Norway through the EarthClim (207711/E10) and NOTUR/NorStore projects. M. Vichi acknowledges the support of the Italian Ministry of Education, University and Research and the Ministry for Environment, Land and Sea through the project GEMINA.
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  • 2
    Publication Date: 2022-05-25
    Description: © The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 12 (2015): 653-679, doi:10.5194/bg-12-653-2015.
    Description: The land and ocean absorb on average just over half of the anthropogenic emissions of carbon dioxide (CO2) every year. These CO2 "sinks" are modulated by climate change and variability. Here we use a suite of nine dynamic global vegetation models (DGVMs) and four ocean biogeochemical general circulation models (OBGCMs) to estimate trends driven by global and regional climate and atmospheric CO2 in land and oceanic CO2 exchanges with the atmosphere over the period 1990–2009, to attribute these trends to underlying processes in the models, and to quantify the uncertainty and level of inter-model agreement. The models were forced with reconstructed climate fields and observed global atmospheric CO2; land use and land cover changes are not included for the DGVMs. Over the period 1990–2009, the DGVMs simulate a mean global land carbon sink of −2.4 ± 0.7 Pg C yr−1 with a small significant trend of −0.06 ± 0.03 Pg C yr−2 (increasing sink). Over the more limited period 1990–2004, the ocean models simulate a mean ocean sink of −2.2 ± 0.2 Pg C yr−1 with a trend in the net C uptake that is indistinguishable from zero (−0.01 ± 0.02 Pg C yr−2). The two ocean models that extended the simulations until 2009 suggest a slightly stronger, but still small, trend of −0.02 ± 0.01 Pg C yr−2. Trends from land and ocean models compare favourably to the land greenness trends from remote sensing, atmospheric inversion results, and the residual land sink required to close the global carbon budget. Trends in the land sink are driven by increasing net primary production (NPP), whose statistically significant trend of 0.22 ± 0.08 Pg C yr−2 exceeds a significant trend in heterotrophic respiration of 0.16 ± 0.05 Pg C yr−2 – primarily as a consequence of widespread CO2 fertilisation of plant production. Most of the land-based trend in simulated net carbon uptake originates from natural ecosystems in the tropics (−0.04 ± 0.01 Pg C yr−2), with almost no trend over the northern land region, where recent warming and reduced rainfall offsets the positive impact of elevated atmospheric CO2 and changes in growing season length on carbon storage. The small uptake trend in the ocean models emerges because climate variability and change, and in particular increasing sea surface temperatures, tend to counter\-act the trend in ocean uptake driven by the increase in atmospheric CO2. Large uncertainty remains in the magnitude and sign of modelled carbon trends in several regions, as well as regarding the influence of land use and land cover changes on regional trends.
    Description: S. Sitch acknowledges financial support by RCUK through NERC (grant no. NE/J010154/). N. Gruber and C. Heinze acknowledge financial support by the European Commission through the EU FP7 projects CARBOCHANGE (grant no. 264879) and GEOCARBON (grant no. 283080). N. Gruber was additionally supported through ETH Zurich. S. C. Doney acknowledges support from the US National Science Foundation (NSF AGS-1048827). P. Friedlingstein, A. Arneth, and S. Zaehle acknowledge support by the European Commission through the EU FP7 project EMBRACE (grant no. 282672). A. Arneth and S. Sitch acknowledge the support of the European Commission-funded project LUC4C (grant no. 603542). The research leading to these results received funding from the European Community’s Seventh Framework Programme (FP7 2007–2013) under grant agreement no. 238366. A. Ahlström and B. Smith acknowledge funding through the Mistra Swedish Research Programme on Climate, Impacts and Adaptation (SWECIA). C. Heinze acknowledges support from NOTUR/NorStore projects NN2980K and NS2980K.
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  • 3
    Publication Date: 2022-05-25
    Description: © The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 12 (2015): 6955-6984, doi:10.5194/bg-12-6955-2015.
    Description: Past model studies have projected a global decrease in marine net primary production (NPP) over the 21st century, but these studies focused on the multi-model mean rather than on the large inter-model differences. Here, we analyze model-simulated changes in NPP for the 21st century under IPCC's high-emission scenario RCP8.5. We use a suite of nine coupled carbon–climate Earth system models with embedded marine ecosystem models and focus on the spread between the different models and the underlying reasons. Globally, NPP decreases in five out of the nine models over the course of the 21st century, while three show no significant trend and one even simulates an increase. The largest model spread occurs in the low latitudes (between 30° S and 30° N), with individual models simulating relative changes between −25 and +40 %. Of the seven models diagnosing a net decrease in NPP in the low latitudes, only three simulate this to be a consequence of the classical interpretation, i.e., a stronger nutrient limitation due to increased stratification leading to reduced phytoplankton growth. In the other four, warming-induced increases in phytoplankton growth outbalance the stronger nutrient limitation. However, temperature-driven increases in grazing and other loss processes cause a net decrease in phytoplankton biomass and reduce NPP despite higher growth rates. One model projects a strong increase in NPP in the low latitudes, caused by an intensification of the microbial loop, while NPP in the remaining model changes by less than 0.5 %. While models consistently project increases NPP in the Southern Ocean, the regional inter-model range is also very substantial. In most models, this increase in NPP is driven by temperature, but it is also modulated by changes in light, macronutrients and iron as well as grazing. Overall, current projections of future changes in global marine NPP are subject to large uncertainties and necessitate a dedicated and sustained effort to improve the models and the concepts and data that guide their development.
    Description: C. Laufkötter and the research leading to these results have received funding from the European Community’s Seventh Framework Programme (FP7 2007–2013) under grant agreements no. 238366 (Greencycles II) and 264879 (CarboChange). M. Vogt and N. Gruber acknowledge funding by ETH Zürich. S. C. Doney and I. D. Lima acknowledge support from NSF (AGS-1048827).
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  • 4
    Publication Date: 2022-05-25
    Description: © The Author(s), 2016. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 13 (2016): 4023-4047, doi:10.5194/bg-13-4023-2016.
    Description: Accurate projections of marine particle export production (EP) are crucial for predicting the response of the marine carbon cycle to climate change, yet models show a wide range in both global EP and their responses to climate change. This is, in part, due to EP being the net result of a series of processes, starting with net primary production (NPP) in the sunlit upper ocean, followed by the formation of particulate organic matter and the subsequent sinking and remineralisation of these particles, with each of these processes responding differently to changes in environmental conditions. Here, we compare future projections in EP over the 21st century, generated by four marine ecosystem models under the high emission scenario Representative Concentration Pathways (RCP) 8.5 of the Intergovernmental Panel on Climate Change (IPCC), and determine the processes driving these changes. The models simulate small to modest decreases in global EP between −1 and −12 %. Models differ greatly with regard to the drivers causing these changes. Among them, the formation of particles is the most uncertain process with models not agreeing on either magnitude or the direction of change. The removal of the sinking particles by remineralisation is simulated to increase in the low and intermediate latitudes in three models, driven by either warming-induced increases in remineralisation or slower particle sinking, and show insignificant changes in the remaining model. Changes in ecosystem structure, particularly the relative role of diatoms matters as well, as diatoms produce larger and denser particles that sink faster and are partly protected from remineralisation. Also this controlling factor is afflicted with high uncertainties, particularly since the models differ already substantially with regard to both the initial (present-day) distribution of diatoms (between 11–94 % in the Southern Ocean) and the diatom contribution to particle formation (0.6–3.8 times higher than their contribution to biomass). As a consequence, changes in diatom concentration are a strong driver for EP changes in some models but of low significance in others. Observational and experimental constraints on ecosystem structure and how the fixed carbon is routed through the ecosystem to produce export production are urgently needed in order to improve current generation ecosystem models and their ability to project future changes.
    Description: The research leading to these results has received funding from the European Community’s Seventh Framework Programme (FP7 2007-2013) under grant agreement no. 238366. Meike Vogt and Nicolas Gruber acknowledge funding by ETH Zürich. Judith Hauck was funded by the Helmholtz Post- Doc Programme (Initiative and Networking Fund of the Helmholtz Association). Scott C. Doney and Ivan D. Lima acknowledge the support of the National Science Foundation through the Center for Microbial Oceanography Research and Education (C-MORE), an NSF Science and Technology Center (EF-0424599).
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  • 5
    Publication Date: 2022-05-25
    Description: © The Author(s), 2017. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Geoscientific Model Development 10 (2017): 2169-2199, doi:10.5194/gmd-10-2169-2017.
    Description: The Ocean Model Intercomparison Project (OMIP) focuses on the physics and biogeochemistry of the ocean component of Earth system models participating in the sixth phase of the Coupled Model Intercomparison Project (CMIP6). OMIP aims to provide standard protocols and diagnostics for ocean models, while offering a forum to promote their common assessment and improvement. It also offers to compare solutions of the same ocean models when forced with reanalysis data (OMIP simulations) vs. when integrated within fully coupled Earth system models (CMIP6). Here we detail simulation protocols and diagnostics for OMIP's biogeochemical and inert chemical tracers. These passive-tracer simulations will be coupled to ocean circulation models, initialized with observational data or output from a model spin-up, and forced by repeating the 1948–2009 surface fluxes of heat, fresh water, and momentum. These so-called OMIP-BGC simulations include three inert chemical tracers (CFC-11, CFC-12, SF6) and biogeochemical tracers (e.g., dissolved inorganic carbon, carbon isotopes, alkalinity, nutrients, and oxygen). Modelers will use their preferred prognostic BGC model but should follow common guidelines for gas exchange and carbonate chemistry. Simulations include both natural and total carbon tracers. The required forced simulation (omip1) will be initialized with gridded observational climatologies. An optional forced simulation (omip1-spunup) will be initialized instead with BGC fields from a long model spin-up, preferably for 2000 years or more, and forced by repeating the same 62-year meteorological forcing. That optional run will also include abiotic tracers of total dissolved inorganic carbon and radiocarbon, CTabio and 14CTabio, to assess deep-ocean ventilation and distinguish the role of physics vs. biology. These simulations will be forced by observed atmospheric histories of the three inert gases and CO2 as well as carbon isotope ratios of CO2. OMIP-BGC simulation protocols are founded on those from previous phases of the Ocean Carbon-Cycle Model Intercomparison Project. They have been merged and updated to reflect improvements concerning gas exchange, carbonate chemistry, and new data for initial conditions and atmospheric gas histories. Code is provided to facilitate their implementation.
    Description: J. C. Orr and L. Bopp were supported by the EU H2020 CRESCENDO project (grant 641816). J. L. Bullister was supported by the NOAA Climate Program Office H. Graven was supported by an EU Marie Curie Career Integration Grant. A. Mouchet benefited from an EU H2020 Marie Curie project (grant 660893). R. G. Najjar was supported by NASA’s Ocean Biology and Biogeochemistry Program and NASA’s Interdisciplinary Science Program. F. Joos was supported by the Swiss National Science Foundation.
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  • 6
    Publication Date: 2022-05-25
    Description: © 2008 Author(s). This article is distributed under the terms of the Creative Commons Attribution 3.0 License. The definitive version was published in Biogeosciences 5 (2008): 597-614, doi:10.5194/bg-5-597-2008
    Description: Fully coupled climate carbon cycle models are sophisticated tools that are used to predict future climate change and its impact on the land and ocean carbon cycles. These models should be able to adequately represent natural variability, requiring model validation by observations. The present study focuses on the ocean carbon cycle component, in particular the spatial and temporal variability in net primary productivity (PP) and export production (EP) of particulate organic carbon (POC). Results from three coupled climate carbon cycle models (IPSL, MPIM, NCAR) are compared with observation-based estimates derived from satellite measurements of ocean colour and results from inverse modelling (data assimilation). Satellite observations of ocean colour have shown that temporal variability of PP on the global scale is largely dominated by the permanently stratified, low-latitude ocean (Behrenfeld et al., 2006) with stronger stratification (higher sea surface temperature; SST) being associated with negative PP anomalies. Results from all three coupled models confirm the role of the low-latitude, permanently stratified ocean for anomalies in globally integrated PP, but only one model (IPSL) also reproduces the inverse relationship between stratification (SST) and PP. An adequate representation of iron and macronutrient co-limitation of phytoplankton growth in the tropical ocean has shown to be the crucial mechanism determining the capability of the models to reproduce observed interactions between climate and PP.
    Description: This work was supported by the EU grants 511106-2 (FP6 RTD project EUR-OCEANS) and GOCE-511176 (FP6 RTP project CARBOOCEAN) by the European Commission. TLF and FJ also acknowledge support from the Swiss National Science Foundations. SCD and MJB received support from NASA NNG06G127G.
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  • 7
    Publication Date: 2022-05-25
    Description: © The Authors, 2010. This article is distributed under the terms of the Creative Commons Attribution 3.0 License. The definitive version was published in Biogeosciences 7 (2010): 621-640, doi:10.5194/bg-7-621-2010
    Description: Global climate change is predicted to alter the ocean's biological productivity. But how will we recognise the impacts of climate change on ocean productivity? The most comprehensive information available on its global distribution comes from satellite ocean colour data. Now that over ten years of satellite-derived chlorophyll and productivity data have accumulated, can we begin to detect and attribute climate change-driven trends in productivity? Here we compare recent trends in satellite ocean colour data to longer-term time series from three biogeochemical models (GFDL, IPSL and NCAR). We find that detection of climate change-driven trends in the satellite data is confounded by the relatively short time series and large interannual and decadal variability in productivity. Thus, recent observed changes in chlorophyll, primary production and the size of the oligotrophic gyres cannot be unequivocally attributed to the impact of global climate change. Instead, our analyses suggest that a time series of ~40 years length is needed to distinguish a global warming trend from natural variability. In some regions, notably equatorial regions, detection times are predicted to be shorter (~20–30 years). Analysis of modelled chlorophyll and primary production from 2001–2100 suggests that, on average, the climate change-driven trend will not be unambiguously separable from decadal variability until ~2055. Because the magnitude of natural variability in chlorophyll and primary production is larger than, or similar to, the global warming trend, a consistent, decades-long data record must be established if the impact of climate change on ocean productivity is to be definitively detected.
    Description: S. A. H. was supported by NASA grants NNG06GE77G and NNX07AL81G. J. L. S. and C. B. acknowledge support from the Carbon Mitigation Initiative funded by BP Amoco. S. C. D. and I. L. were supported by NSF grant EF-0424599. L. B. acknowledges support from the ANR-GlobPhy and FP7-MEECE projects.
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  • 8
    Publication Date: 2022-05-25
    Description: © Authors, 2010. This work is distributed under the Creative Commons Attribution 3.0 License. The definitive version was published in Biogeosciences 7 (2010): 979-1005, doi: 10.5194/bg-7-979-2010
    Description: Changes in marine net primary productivity (PP) and export of particulate organic carbon (EP) are projected over the 21st century with four global coupled carbon cycle-climate models. These include representations of marine ecosystems and the carbon cycle of different structure and complexity. All four models show a decrease in global mean PP and EP between 2 and 20% by 2100 relative to preindustrial conditions, for the SRES A2 emission scenario. Two different regimes for productivity changes are consistently identified in all models. The first chain of mechanisms is dominant in the low- and mid-latitude ocean and in the North Atlantic: reduced input of macro-nutrients into the euphotic zone related to enhanced stratification, reduced mixed layer depth, and slowed circulation causes a decrease in macro-nutrient concentrations and in PP and EP. The second regime is projected for parts of the Southern Ocean: an alleviation of light and/or temperature limitation leads to an increase in PP and EP as productivity is fueled by a sustained nutrient input. A region of disagreement among the models is the Arctic, where three models project an increase in PP while one model projects a decrease. Projected changes in seasonal and interannual variability are modest in most regions. Regional model skill metrics are proposed to generate multi-model mean fields that show an improved skill in representing observation-based estimates compared to a simple multi-model average. Model results are compared to recent productivity projections with three different algorithms, usually applied to infer net primary production from satellite observations.
    Description: This work was funded by the European Union projects CARBOOCEAN (511176-2) and EUROCEANS (511106-2) and is a contribution to the “European Project on Ocean Acidification” (EPOCA) which received funding from the European Community’s Seventh Framework Programme (FP7/2007–2013) under grant agreement no. 211384. Additional support was received from the Swiss National Science Foundation. SCD acknowledges support from the NASA Ocean Biology and Biogeochemistry Program (NNX07AL80G). LB aknowledges support from the EU Project MEECE (Marine Ecosystem Evolution in a Changing Environnement, grant agreement 212085).
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  • 9
    Publication Date: 2022-05-25
    Description: © The Author(s), 2013. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 10 (2013): 2711-2724, doi:10.5194/bg-10-2711-2013.
    Description: Global climate change is expected to affect the ocean's biological productivity. The most comprehensive information available about the global distribution of contemporary ocean primary productivity is derived from satellite data. Large spatial patchiness and interannual to multidecadal variability in chlorophyll a concentration challenges efforts to distinguish a global, secular trend given satellite records which are limited in duration and continuity. The longest ocean color satellite record comes from the Sea-viewing Wide Field-of-view Sensor (SeaWiFS), which failed in December 2010. The Moderate Resolution Imaging Spectroradiometer (MODIS) ocean color sensors are beyond their originally planned operational lifetime. Successful retrieval of a quality signal from the current Visible Infrared Imager Radiometer Suite (VIIRS) instrument, or successful launch of the Ocean and Land Colour Instrument (OLCI) expected in 2014 will hopefully extend the ocean color time series and increase the potential for detecting trends in ocean productivity in the future. Alternatively, a potential discontinuity in the time series of ocean chlorophyll a, introduced by a change of instrument without overlap and opportunity for cross-calibration, would make trend detection even more challenging. In this paper, we demonstrate that there are a few regions with statistically significant trends over the ten years of SeaWiFS data, but at a global scale the trend is not large enough to be distinguished from noise. We quantify the degree to which red noise (autocorrelation) especially challenges trend detection in these observational time series. We further demonstrate how discontinuities in the time series at various points would affect our ability to detect trends in ocean chlorophyll a. We highlight the importance of maintaining continuous, climate-quality satellite data records for climate-change detection and attribution studies.
    Description: CB and JLS acknowledge financial support from the Carbon Mitigation Initiative with support from BP. JLS and RRR were partly supported by the NF-UBC Nereus Program. SAH was supported by NERC grant NE/G013055/1. SCD acknowledges support from NSF grant EF-0424599.
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  • 10
    Publication Date: 2022-05-25
    Description: © The Author(s), 2013. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 10 (2013); 6833-6850, doi:10.5194/bg-10-6833-2013.
    Description: We investigated the mechanisms of phytoplankton competition during the spring bloom, one of the most dramatic seasonal events in lower-trophic-level ecosystems, in four state-of-the-art plankton functional type (PFT) models: PISCES, NEMURO, PlankTOM5 and CCSM-BEC. In particular, we investigated the relative importance of different ecophysiological processes on the determination of the community structure, focusing both on the bottom-up and the top-down controls. The models reasonably reproduced the observed global distribution and seasonal variation of phytoplankton biomass. The fraction of diatoms with respect to the total phytoplankton biomass increases with the magnitude of the spring bloom in all models. However, the governing mechanisms differ between models, despite the fact that current PFT models represent ecophysiological processes using the same types of parameterizations. The increasing trend in the percentage of diatoms with increasing bloom magnitude is mainly caused by a stronger nutrient dependence of diatom growth compared to nanophytoplankton (bottom-up control). The difference in the maximum growth rate plays an important role in NEMURO and PlankTOM5 and determines the absolute values of the percentage of diatoms during the bloom. In CCSM-BEC, the light dependency of growth plays an important role in the North Atlantic and the Southern Ocean. The grazing pressure by zooplankton (top-down control), however, strongly contributes to the dominance of diatoms in PISCES and CCSM-BEC. The regional differences in the percentage of diatoms in PlankTOM5 are mainly determined by top-down control. These differences in the mechanisms suggest that the response of marine ecosystems to climate change could significantly differ among models, even if the present-day ecosystem is reproduced to a similar degree of confidence. For further understanding of plankton competition and for the prediction of future change in marine ecosystems, it is important to understand the relative differences in each physiological rate and life history rate in the bottom-up and the top-down controls between PFTs.
    Description: T. Hashioka, Y. Yamanaka and T. Hirata, were supported by the Grant-in-Aid for the Global COE Program from MEXT, by the Global Environment Research Fund (S-5) from the Ministry of the Environment and by the Strategic Young Researcher Overseas Visits Program for Accelerating Brain Circulation from JSPS. S. Doney, I. Lima and S. Sailley acknowledge support from C-MORE (NSF EF-0424599).
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