Three-dimensional multipass SAR focusing: experiments with long-term spaceborne data

Synthetic aperture radar (SAR) interferometry is a modern efficient technique that allows reconstructing the height profile of the observed scene. However, apart for the presence of critical nonlinear inversion steps, particularly crucial in abrupt topography scenarios, it does not allow one to separate different scattering mechanisms in the elevation (height) direction within the ground pixel. Overlay of scattering at different elevations in the same azimuth-range resolution cell can be due either to the penetration of the radiation below the surface or to perspective ambiguities caused by the side-looking geometry. Multibaseline three-dimensional (3-D) SAR focusing allows overcoming such a limitation and has thus raised great interest in the recent research. First results with real data have been only obtained in the laboratory and with airborne systems, or with limited time-span and spatial-coverage spaceborne data. This work presents a novel approach for the tomographic processing of European Remote Sensing satellite (ERS) real data for extended scenes and long time span. Besides facing problems common to the airborne case, such as the nonuniformly spaced passes, this processing requires tackling additional difficulties specific to the spaceborne case, in particular a space-varying phase calibration of the data due to atmospheric variations and possible scene deformations occurring for years-long temporal spans. First results are presented that confirm the capability of ERS multipass tomography to resolve multiple targets within the same azimuth-range cell and to map the 3-D scattering properties of the illuminated scene.     

Linear and adaptive spaceborne threedimensional SAR tomography: a comparison on real data

Three-dimensional (3-D) synthetic aperture radar (SAR) imaging is a recent technique, based on coherent SAR data combination, and aims to obtain a full 3-D analysis in space. It is a multibaseline extension of the SAR interferometry concept and offers new options for the analysis and monitoring of ground scenes by means of the capability of separating the scattering phenomena along the height dimension. In this work, the authors summarise and extend the results obtained by processing real ERS satellite urban data characterised by a long time span of acquisition and non-uniformly spaced satellite passes, comparing the performance in height focusing obtained with a singular value decomposition (SVD)-based method and adaptive beamforming.     

Differential tomography: a new framework for SAR interferometry

A new interferometric mode crossing the differential synthetic aperture radar (SAR) interferometry and multibaseline SAR tomography concepts, that can be termed differential SAR tomography, is proposed. Its potentials, coming from the joint elevation-velocity resolution capability of multiple scatterers, are discussed. Processing is cast in a bidimensional baseline-time spectral analysis framework, with sparse sampling. The use of a modern data-dependent bidimensional spectral estimator is proposed for joint baseline-time processing. Simulated results are reported for different baseline-time acquisition patterns and two motion conditions of layover scatterers, showing that this new challenging interferometric technique is promising.     

Focusing of 915 MHz Electromagnetic Power on Deep Human Tissues: A Mathematical Model Study

The distribution of ohmic power in a CAT scan section of a human chest irradiated with 915 MHz peripheral sources is calculated using the moment method. In the simulation, the chest section (assumed to be uniformally developed along the cranio-caudal axis for a height equivalent to the field penetration) is subdivided in 235 subvolumes of known electric constants. The focusing of power on a selected region of the chest is obtained by properly exciting the sources. An optimization method allows selecting the amplitudes and phases in such a way that the power level in all subvolumes outside the focal region is kept below a given threshold.     

Pharmacokinetic study in rats after single intravenous and oral administrations of [14C]-ITF-296

Fifteen mycoplasma-free chickens were contact exposed to five chickens that had been experimentally infected with one of three different strains (two field strains and one laboratory strain) of Mycoplasma synoviae (MS). Culture and polymerase chain reaction (PCR) were positive by 3 days postinoculation (PI) in the experimentally infected birds. Lateral transmission was found by 7-14 days postexposure. Positive serum plate agglutination (SPA) results were detected 3-4 wk after positive culture and/or PCR in individual birds. By 42 days PI, all the birds in the groups exposed to field strain K1858 or K3344 had become infected as determined by culture and PCR, whereas only half of the birds in the group exposed to laboratory strain WUV1853 had become infected. Because of the unanticipated lack of seroconversion to hemagglutination inhibition (HI) and enzyme-linked immunosorbent assay (ELISA) in infected chickens, the study was extended. Each group was split into two groups of 10 birds each, one of which was vaccinated with a live B1/LaSota Newcastle disease (ND) vaccine virus to determine if a viral respiratory challenge might incite a stronger antibody response to the mycoplasma infection. All the birds were tested for seroconversion 14 and 21 days later. Of the birds vaccinated for ND, a slightly greater number were MS positive by SPA than the nonvaccinated birds. This effect was not present 21 days after vaccination, and there was no significant difference in the MS HI results from these groups, suggesting that the viral respiratory infection had little direct impact on seroconversion. The virulent field strain (K3344) elicited a stronger MS antibody response than the other strains. All results from the MS ELISA were negative in all groups through 9 wk. Positive results from PCR analysis correlated well with culture results, whereas serologic tests did not detect MS infection for several weeks. Monitoring programs solely dependent on seroconversion may be inadequate for diagnosis and control of mycoplasma infections.     

Zinc deficiency in field-grown pecan trees: changes in leaf nutrient concentrations and structure

BACKGROUND: Zinc (Zn) deficiency is a typical nutritional disorder in pecan trees [ Carya illinoinensis (Wangenh.) C. Koch] grown under field conditions in calcareous soils in North America, including northern Mexico and south‐western United States. The aim of this study was to assess the morphological and nutritional changes in pecan leaves affected by Zn deficiency as well as the Zn distribution within leaves. RESULTS: Zinc deficiency led to decreases in leaf chlorophyll concentrations, leaf area and trunk cross‐sectional area. Zinc deficiency increased significantly the leaf concentrations of K and Ca, and decreased the leaf concentrations of Zn, Fe, Mn and Cu. All nutrient values found in Zn‐deficient leaves were within the sufficiency ranges, with the only exception of Zn, which was approximately 44, 11 and 9 µg g^?1 dry weight in Zn‐sufficient, moderately and markedly Zn‐deficient leaves, respectively. Zinc deficiency led to decreases in leaf thickness, mainly due to a reduction in the thickness of the palisade parenchyma, as well as to increases in stomatal density and size. The localisation of Zn was determined using the fluorophore Zinpyr‐1 and ratio‐imaging technique. Zinc was mainly localised in the palisade mesophyll area in Zn‐sufficient leaves, whereas no signal could be obtained in Zn‐deficient leaves. CONCLUSION: The effects of Zn deficiency on the leaf characteristics of pecan trees include not only decreases in leaf chlorophyll and Zn concentrations, but also a reduction in the thickness of the palisade parenchyma, an increase in stomatal density and pore size and the practical disappearance of Zn leaf pools. These characteristics must be taken into account to design strategies to correct Zn deficiency in pecan tree in the field. Copyright © 2012 Society of Chemical Industry