Low-Cloud Feedback in CAM5-CLUBB: Physical Mechanisms and Parameter Sensitivity Analysis
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Survival rates of large trees determine forest biomass dynamics. Survival rates of small trees are linked to mechanisms that maintain biodiversity across tropical forests. How species survival rates change with size offers insight into the links between biodiversity and ecosystem function across tropical forests. We tested patterns of size-dependent tree survival across the tropics using data from 1781 species and over two million individuals to assess whether tropical forests can be characterized by size-dependent life-history survival strategies. We found species were classifiable into four “survival modes” that explain life-history variation that shapes carbon-cycling and the relative abundances within forests. Frequently collected functional traits, such as wood density, leaf mass per area, and seed mass, were not generally predictive of species’ survival modes. Mean annual temperature and cumulative water deficit predicted the proportion of biomass of survival modes, indicating important links between evolutionary strategies, climate, and carbon cycling. The application of survival modes in demographic simulations predicted biomass change across forest sites. Our results reveal globally identifiable size-dependent survival strategies that differ across diverse systems in a consistent way. The abundance of survival modes and interaction with climate ultimately determine forest structure, carbon storage in biomass, and future forest trajectories.
Improving the kinetics of O 2 reduction on oxide surfaces is critical in many energy and fuel conversion technologies. Here we show that the acidity scale for binary oxides is a powerful descriptor for tuning and predicting oxygen surface exchange kinetics on mixed conducting oxides. By infiltrating a selection of binary oxides from strongly basic (Li 2 O) to strongly acidic (SiO 2 ) onto the surface of Pr 0.1 Ce 0.9 O 2-δ samples, it was possible to vary the chemical surface exchange coefficient k chem by 6 orders of magnitude, with basic oxides such as Li 2 O increasing k chem by nearly 1,000 times, with surface concentrations as low as 50 ppm impacting k chem . Strikingly, although the pre-exponential of k chem scales linearly with the acidity of the infiltrated binary oxide, there is nearly no change in the activation energy. Here, the origin of these dramatic changes is proposed to arise from the systematic increase in electron concentration at the Pr 0.1 Ce 0.9 O 2-δ surface with the decreasing acidity of the infiltrated binary oxide.
Exposing ZrO 2 to strong acid induces protonic defects that permit ultrafast electron transfer through at least 4 nm of ZrO 2 .
Multivalent counterions can be used to control both the conductivity and opening of a nanogate functionalized with weak polyelectrolytes.
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Significance The capture and conversion of sunlight into a useful chemical fuel (H 2 , CH 4 , CH 3 OH, etc.) is a central goal of the field of artificial photosynthesis. Water oxidation to generate O 2 and protons stands as the major bottleneck in these processes. Relatively few stable photosensitizers can generate sufficient oxidizing power to drive water oxidation, and those that do contain rare elements such as ruthenium. In this paper, we show that metal-free organic photosensitizers are capable of driving photoelectrochemical water oxidation. Significantly, these photosensitizers exhibit comparable activity to that of ruthenium-containing photosensitizers under broadband illumination. In addition, we report to our knowledge the first demonstration of a molecular photosensitizer, outside of natural photosynthesis, that can drive water oxidation utilizing only red light.
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Special nuclear material (SNM) monitoring often requires high resolution gamma-ray spectroscopy for material characterization. Portable systems and rapid deployment are also highly valued for some applications. Deployable gamma-ray imaging spectrometers using pixelated CdZnTe semiconductor detectors have become commercially available within the past three years to meet these requirements. CdZnTe systems have demonstrated room-temperature energy resolutions below 0.5% FWHM at 662 keV using single pixel events and below 0.7% FWHM at 662 keV using all events. The systems are able to go from storage to measurement in less than two minutes. Special nuclear materials were measured at the Y-12 National Security Complex and at the Device Assembly Facility at the Nevada National Security Site. The use of a CdZnTe system to measure uranium enrichment was demonstrated and uranium spectral features were compared to a commercially available high purity germanium (HPGe) spectrometer. The use of passive gamma ray spectroscopy techniques to estimate plutonium grade using CdZnTe detectors was demonstrated for the first time.