423 research outputs found

    A Comparison of Three Low Temperature Techniques of Specimen Preparation for X-Ray Microanalysis

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    A quantitative x-ray microanalytical comparison of intracellular ion concentrations in two tissues (chicken kidney and duck nasal salt gland), prepared as bulk frozen-hydrated, embedded freeze-dried and freeze-substituted samples, shows that there are similar losses of K+ and Pin freeze-dried and freeze-substituted samples in both types of tissue. It is suggested that this may be due to extraction by chloride-free Spurr\u27s resin during infiltration. There was also an indication of an increase in Na+ concentration in freeze-dried samples. In chicken kidney cells there was a reduction in Mg++ and Ca++ concentrations in freeze-dried and freeze-substituted samples and an increase in Cl- concentration in freeze-dried samples (which may have been partially due to contamination) and a decrease in freeze-substituted samples. In spite of these differences between kidney preparations, consistent differences in Na+ and Cl-concentrations between kidneys from normal chickens and chickens infected with IBV (infectious bronchitis virus) which causes perturbations in kidney physiology were observed in frozen-hydrated, freeze-dried and freeze-substituted preparations

    A neutron scattering study of the interplay between structure and magnetism in Ba(Fe1−x_{1-x}Cox_{x})2_2As2_2

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    Single crystal neutron diffraction is used to investigate the magnetic and structural phase diagram of the electron doped superconductor Ba(Fe1−x_{1-x}Cox_x)2_2As2_2. Heat capacity and resistivity measurements have demonstrated that Co doping this system splits the combined antiferromagnetic and structural transition present in BaFe2_2As2_2 into two distinct transitions. For xx=0.025, we find that the upper transition is between the high-temperature tetragonal and low-temperature orthorhombic structures with (TTO=99±0.5T_{\mathrm{TO}}=99 \pm 0.5 K) and the antiferromagnetic transition occurs at TAF=93±0.5T_{\mathrm{AF}}=93 \pm 0.5 K. We find that doping rapidly suppresses the antiferromagnetism, with antiferromagnetic order disappearing at x≈0.055x \approx 0.055. However, there is a region of co-existence of antiferromagnetism and superconductivity. The effect of the antiferromagnetic transition can be seen in the temperature dependence of the structural Bragg peaks from both neutron scattering and x-ray diffraction. We infer from this that there is strong coupling between the antiferromagnetism and the crystal lattice

    Utilization of soil organic phosphorus as a strategic approach for sustainable agriculture

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    Soil organic phosphorus (P org ) can significantly assist in minimizing the adverse effects of chemi- cal phosphorus fertilizers on aquatic and marine resources. Success to achieve the desired last- ing transformation is primarily reliant on the drastic reduction of wasteful applications of chemical phosphorus fertilizers, thereby paving the way for proper investment of soil P org reserves. To this end, organically-bound phosphorus can be viewed as a cornerstone for the future development of agriculture. Thus, we consider it very timely to emphasize the suitability of soil P org to lead the way

    A parameterization of Greenland's tip jets suitable for ocean or coupled climate models

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    Greenland's tip jets are low-level, high wind speed jets forced by an interaction of the synoptic-scale atmospheric flow and the steep, high orography of Greenland. These jets are thought to play an important role in both preconditioning for, and triggering of, open-ocean convection in the Irminger Sea. However, the relatively small spatial scale of the jets prevents their accurate representation in the relatively low resolution (~1 degree) atmospheric (re-)analyses which are typically used to force ocean general circulation models (e.g. ECMWF ERA-40 and NCEP reanalyses, or products based on these). Here we present a method of ‘bogussing’ Greenland's tip jets into such surface wind fields and thus, via bulk flux formulae, into the air-sea turbulent flux fields. In this way the full impact of these mesoscale tip jets can be incorporated in any ocean general circulation model of sufficient resolution. The tip jet parameterization is relatively simple, making use of observed linear gradients in wind speed along and across the jet, but is shown to be accurate to a few m s-1 on average. The inclusion of tip jets results in a large local increase in both the heat and momentum fluxes. When applied to a 1-dimensional mixed-layer model this results in a deepening of the winter mixed-layer of over 300 m. The parameterization scheme only requires 10 meter wind speed and mean sea level pressure as input fields; thus it is also suitable for incorporation into a coupled atmosphere-ocean climate model at the coupling stage

    Polar mesoscale cyclones in the northeast Atlantic: Comparing climatologies from ERA-40 and satellite imagery

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    Polar mesoscale cyclones over the subarctic are thought to be an important component of the coupled atmosphere–ocean climate system. However, the relatively small scale of these features presents some concern as to their representation in the meteorological reanalysis datasets that are commonly used to drive ocean models. Here polar mesocyclones are detected in the 40-Year European Centre for Medium-Range Weather Forecasts (ECMWF) Re-Analysis dataset (ERA-40) in mean sea level pressure and 500-hPa geopotential height, using an automated cyclone detection algorithm. The results are compared to polar mesocyclones detected in satellite imagery over the northeast Atlantic, for the period October 1993–September 1995. Similar trends in monthly cyclone numbers and a similar spatial distribution are found. However, there is a bias in the size of cyclones detected in the reanalysis. Up to 80% of cyclones larger than 500 km are detected in MSL pressure, but this hit rate decreases, approximately linearly, to ∼40% for 250-km-scale cyclones and to ∼20% for 100-km-scale cyclones. Consequently a substantial component of the associated air–sea fluxes may be missing from the reanalysis, presenting a serious shortcoming when using such reanalysis data for ocean modeling simulations. Eight maxima in cyclone density are apparent in the mean sea level pressure, clustered around synoptic observing stations in the northeast Atlantic. They are likely spurious, and a result of unidentified shortcomings in the ERA-40 data assimilation procedure

    Role of Nanoclays in Carbon stabilization in Andisols and Cambisols

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    Greenhouse gas (GHG) emissions and their consequent effect on global warming are an issue of global environmental concern. Increased carbon (C) stabilization and sequestration in soil organic matter (SOM) is one of the ways to mitigate these emissions. Here we evaluated the role of nanoclays isolated from soil on C stabilization in both a C rich Andisols and C depleted Cambisols. Nanoclays were analyzed for size and morphology by transmission electron microscopy, for elemental composition and molecular composition using pyrolysis-GC/MS. Moreover, nanoclays were treated with H2O2 to isolate stable SOM associated with them. Our result showed better nanoclay extraction efficiency and higher nanoclay yield for Cambisol compared to Andisols, probably related to their low organic matter content. Nanoclay fractions from both soils were different in size, morphology, surface reactivity and SOM content. Nanoclays in Andisols sequester around 5-times more C than Cambisols, and stabilized 6 to 8-times more C than Cambisols nanoclay after SOM chemical oxidation. Isoelectric points and surface charge of nanoclays extracted from the two soils was very different. However, the chemical reactivity of the nanoclay SOM was similar, illustrating their importance for C sequestration. Generally, the precise C stabilization mechanisms of both soils may be different, with nanoscale aggregation being more important in Andisols. We can conclude that independent of the soil type and mineralogy the nanoclay fraction may play an important role in C sequestration and stabilization in soil-plant systems

    Assessing soil P fractions changes with long-term phosphorus fertilization related to crop yield of soybean and maize

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    Long-term P Fertiliser application increases soil phosphorus (P) labile fractions, which can be associated with crop P uptake and grain yield and are useful to improve fertilizer recommendations. Research aims were to evaluate in long-term experiments with different P Fertiliser application in a Mollisol and a Vertisol: (a) the changes of soil P fractions and (b) the relationship between soil P fractions with long-term P Fertiliser application, with accumulated apparent P budget, grain P, total P uptake, soybean (Glycine max L.Merr.) and maize (Zea mays L.) grain yield. Soil P fractions were measured after 1 and 9 year since the beginning of the long-term experiments. Experiments included an initial Fertiliser application rate of 200 kg P ha−1 and annual P Fertiliser application rate of 36 kg P ha−1. Bray1-P, total, organic, and inorganic P in fine (53 μm) (CF) soil fractions, and in NaHCO3 extract were measured. Initial P Fertiliser application increased inorganic and total P fractions. However, Bray1-P, total P in NaHCO3 extract and in the CF were the fractions that most increased with continuous long-term P Fertiliser application in both sites. In the Mollisol, maize grain yield was unrelated to long-term P Fertiliser application. In the Vertisol, total P in NaHCO3 extract, and total and organic P in the CF were more closely related to soybean grain yield than Bray1-P. We proposed soil P indices of labile inorganic and organic P that showed close relationships with soybean grain yield and may be useful to improve the diagnosis of P soil fertility.Fil: Appelhans, Stefania Carolina. Universidad Nacional de Entre Ríos. Facultad de Ciencias Agropecuarias. Departamento de Producción Vegetal; Argentina. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Entre Ríos. Estación Experimental Agropecuaria Paraná; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Barbagelata, Pedro Aníbal. Universidad Nacional de Entre Ríos. Facultad de Ciencias Agropecuarias. Departamento de Producción Vegetal; Argentina. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Entre Ríos. Estación Experimental Agropecuaria Paraná; ArgentinaFil: Melchiori, Ricardo José Miguel. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Entre Ríos. Estación Experimental Agropecuaria Paraná; ArgentinaFil: Gutiérrez Boem, Flavio Hernán. Universidad de Buenos Aires. Facultad de Agronomía. Departamento de Ingeniería Agrícola y Uso de la Tierra. Cátedra de Fertilidad y Fertilizantes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Biociencias Agrícolas y Ambientales. Universidad de Buenos Aires. Facultad de Agronomía. Instituto de Investigaciones en Biociencias Agrícolas y Ambientales; Argentin

    Using organic phosphorus to sustain pasture productivity: A perspective

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    Organic phosphorus (P) in grazed pastures/grasslands could sustain production systems that historically relied on inorganic P fertiliser. Interactions between inorganic P, plants and soils have been studied extensively. However, less is known about the transformation of organic P to inorganic orthophosphate. This paper investigates what is known about organic P in pasture/grassland soils used for agriculture, as well as the research needed to utilise organic P for sustainable plant production. Organic P comprises > 50% of total soil P in agricultural systems depending on location, soil type and land use. Organic P hydrolysis and release of orthophosphate by phosphatase enzymatic activity is affected by a range of factors including: (a) the chemical nature of the organic P and its ability to interact with the soil matrix; (b) microorganisms that facilitate mineralisation; (c) soil mineralogy; (d) soil water electrolytes; and (e) soil physicochemical properties. Current biogeochemical knowledge of organic P processing in soil limits our ability to develop management strategies that promote the use of organic P in plant production. Information is particularly needed on the types and sources of organic P in grassland systems and the factors affecting the activity of enzymes that mineralise organic P. Integrated approaches analysing the soil matrix, soil water and soil biology are suggested to address this knowledge gap
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