Remote sensing of canopy light use efficiency in temperate and boreal forests of North America using MODIS imagery

Light use efficiency (LUE) is an important variable characterizing plant eco-physiological functions and refers to the efficiency at which absorbed solar radiation is converted into photosynthates. The estimation of LUE at regional to global scales would be a significant advantage for global carbon cycle research. Traditional methods for canopy level LUE determination require meteorological inputs which cannot be easily obtained by remote sensing. Here we propose a new algorithm that incorporates the enhanced vegetation index (EVI) and a modified form of land surface temperature (T_m) for the estimation of monthly forest LUE based on Moderate Resolution Imaging Spectroradiometer (MODIS) imagery. Results demonstrate that a model based on EVI × T_m parameterized from ten forest sites can provide reasonable estimates of monthly LUE for temperate and boreal forest ecosystems in North America with an R² of 0.51 (p < 0.001) for the overall dataset. The regression coefficients (a, b) of the LUE–EVI × T_m correlation for these ten sites have been found to be closely correlated with the average EVI (EVI_ave, R² = 0.68, p = 0.003) and the minimum land surface temperature (LST_min, R² = 0.81, p = 0.009), providing a possible approach for model calibration. The calibrated model shows comparably good estimates of LUE for another ten independent forest ecosystems with an overall root mean square error (RMSE) of 0.055 g C per mol photosynthetically active radiation. These results are especially important for the evergreen species due to their limited variability in canopy greenness. The usefulness of this new LUE algorithm is further validated for the estimation of gross primary production (GPP) at these sites with an RMSE of 37.6 g C m^? 2 month^? 1 for all observations, which reflects a 28% improvement over the standard MODIS GPP products. These analyses should be helpful in the further development of ecosystem remote sensing methods and improving our understanding of the responses of various ecosystems to climate change.     

Catalytic effect of bis (cyclopentadienyl) nickel II on the improvement of the hydrogenation-dehydrogenation of Mg-MgH2 system

Bis(cyclopentadienyl) nickel II is one of the best precursors of nickel catalyst which remarkably improved the hydrogen absorption-desorption of Mg–MgH₂ system. The X-ray photoelectron spectroscopy (XPS) and Furrier Transformed Infrared Spectroscopy (FTIR) analyses revealed that bis (cyclopentadienyl) nickel II decomposed into metallic nickel during ball milling with MgH₂. The nickel thus formed has homogeneously doped over the Mg - MgH₂ surface. The Ni-doped Mg-MgH₂ have shown the excellent catalytic effect on hydrogen absorption-desorption. The catalyzed MgH₂ could desorb hydrogen below 225 °C (T_onset) under Ar flow, and absorb hydrogen at 50 °C under 1.5 MPa H₂ pressure. The hydrogen absorption-desorption temperatures are remarkably decreased as compared to the uncatalyzed Mg-MgH₂ system under the identical experimental conditions.     

Correlation between the milling time and hydrogen storage properties of ZrCrFe ternary alloy

Laves phases with AB₂ compositions are common type of topologically close packed structure. Furthermore, lave phases are capable of dissolving considerable amounts of ternary alloying additions. ZrCr₂ crystallized in the hexagonal C14 type of structure is one of interesting candidate among them, but it is not used as storage compound due to its excessive stability, at 323 K the equilibrium pressure is only 1.2 kPa. However the substitution of chromium by other elements can modify the crystal structure, the hydriding capacity and dissociation pressure of hydrogen. In this work Fe has been chosen as a substitute material for Cr and ZrCrFe ternary alloy is prepared using arc furnace. The mechanical alloying process has been introduced to produce nanocrystalline material. This paper presents comprehensive study on structural aspects of ball milled ZrCrFe alloy. On comparison of the XRD data, the broadening was found in the peak width with the increase of milling time which is clear indication of refinement of crystallite size. This refinement could also be confirmed from the SEM analysis also. PCT measurements were performed for a temperature range 303 K–373 K.     

Metal-carbonate formation from ammonia solution by addition of metal salts—An effective method for CO2 capture from landfill gas (LFG)

The absorption of CO₂ from LFG in different weight concentration ammonia solution and metal salts (Zinc and Barium) is investigated in this study. Addition of metal salts results in useful metal carbonates when LFG is passed through the solution. Barium salts show a better potential of removing CO₂ as compared to Zinc salts. Addition of Barium salts to ammonia solution results in a new absorbent as no study has been focused on it till date. Also metal salts are added to alkaline wastewater which not only decreases the pH of the wastewater but also useful metal carbonates are obtained from wastewater when LFG is passed through it. Different parameters like CO₂ loading, reaction rate and change in pH are investigated. Formation of carbonates is proved by using SEM and XRD analysis. Raman spectroscopy was performed on the discarded liquid after removal of carbonates to understand the formation of bicarbonates, carbonates and carbamates.     

Hydrogen storage properties of Mg2Ni affected by Cr catalyst

The effect of Cr as a catalyst in different proportions was investigated to monitor the hydrogen storage properties of Mg₂Ni including their thermodynamic aspects. The P–C–T isotherms for absorption/desorption were measured at 225 °C, 250 °C, 275 °C and 300 °C temperatures. A significant increment in the plateau pressures at different temperature was observed, which shows the positive impact of Cr content in the formation of less stable hydrides. The active sites produced by the ball milling may be the reason for the formation of less stable hydrides. Decrements in the storage capacity with the Cr content were attributed to the formation of MgNi₂ phase which does not absorb hydrogen at the employed temperature-pressure conditions. XRD and SEM technique were used to identify the structural and morphological changes induced by the hydrogenation cycles.     

Active mode leakage reduction using fine-grained forward body biasing strategy

Leakage power minimization has become an important issue with technology scaling. Variable threshold voltage schemes have become popular for standby power reduction. In this work we look at another emerging aspect of this potent problem which is leakage power reduction in active mode of operation. In gate level circuits, a large number of gates are not switching in active mode at any given point in time but nevertheless are consuming leakage power. We propose a fine-grained forward body biasing (FBB) scheme for active mode leakage power reduction in gate level circuits without any delay penalty. Our results show that our optimal polynomial time FBB allocation algorithm results in 70.2% reduction in leakage currents. We also present an exact standard-cell placement driven FBB allocation algorithm that effectively reduces the area penalty using the post-placement area slack and results in 56.5%, 62.8% and 66.1% reduction in leakage currents for 0%, 4% and 8% area slack, respectively. Furthermore, we present a heuristic to solve the standard-cell placement driven FBB allocation problem that is computationally efficient and results in leakage within 2% of that from the exact formulation.     

Ascorbic acid-mediated synthesis and characterisation of iron oxide/gold core–shell nanoparticles.

The current article reports on providing surface modification of magnetic nanoparticles with gold to provide stability against aggregation. Gold-coated magnetite nanoparticles were synthesised to combine both magnetic as well as surface plasma resonance (SPR) properties in a single moiety. The nanocomposites were produced by reduction (using ascorbic acid) of gold chloride on to the surface of iron oxide nanoparticles. Ascorbic acid not only acts as a reducing agent, but also the oxidised form of ascorbic acid i.e. Dehydro-ascorbic acid acts as a capping agent to impart stability to as synthesised gold-coated iron oxide nanocomposites. The synthesised nanocomposite was monodispersed with a mean particle size of around 16 nm and polydispersity index of 0.190. X-ray diffraction analysis confirms presence of gold on the surface of magnetite nanoparticles. The synthesised nanocomposites had a total organic content of around 3.2% w/w and also showed a shifted SPR peak at 546 nm as compared to gold nanoparticles (528 nm). Both uncoated and gold-coated magnetite exhibited superparamagnetic behaviour at room temperature. Upon coating with gold shell, saturation magnetisation of iron oxide nanoparticles decreases from 42.806 to 3.54 emu/gram.     

Degradation kinetics of poly(HDDA‐co‐MMA)

1,6‐hexanediol diacrylate (HDDA) and methyl methacrylate (MMA) were copolymerized in different weight ratios using UV light induced photo‐polymerization to give poly(HDDA‐co‐MMA). Differential scanning calorimetry shows that copolymer was formed. The thermogravimetric and differential scanning calorimetric studies with different heating rates were carried out on these copolymers to understand the nature of degradation and to determine its kinetics. Different kinetic models were adopted to evaluate various parameters like the activation energy, the order, and the frequency factor. These analyses are important to study the binder removal from 3D‐shaped ceramic objects made by techniques like Solid free form fabrication. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

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