The identification of western forest species by means of remote sensing
Identification of western forest species by means of aerial remote sensing
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Identification of western forest species by means of aerial remote sensing
Considering lack of development of endemic species in Iceland
Analytical model for molecular flow of reactive gaseous species through cylindrical reactors with apertures at either end, evaluating surviving flux magnitude
Crop species recognition and mensuration in Sacramento Valley from ERTS-1 data
Identification of coastal vegetation species in ERTS-1 imagery of Delaware Bay
A method is presented to observe surface species subject to electron-induced desorption by Auger electron spectroscopy. The surface to be examined is moved under the electron beam at constant velocity, establishing a time independent condition and eliminating the time response of the electron spectrometer as a limiting factor. The dependence of the Auger signal on the surface velocity, incident electron current, beam diameter, and desorption cross section are analyzed. The method is illustrated by the Auger analysis of PTFE, in which the fluorine is removed by electron induced desorption.
The goal of the second recognition map was to delineate various crop species in a portion of the Sacramento Valley, and at the same time to determine how accurately each could be classified and measured from ERTS-1 data. The new recognition map, a new and concise display of the old map, and classification and mensuration accuracy data are presented and discussed. The mensuration accuracy, in particular, is affected by the presence of an edge effect one resolution wide surrounding nearly all fields. Points on the edge are misclassified because they contain a mixture of, crop and bare soil. Using a processing technique to estimate the proportions of unresolved objects in this edge region, a much improved mensuration capability will be demonstrated.
The potential function parameters to fit the data obtained by Kell et al. (1968) are determined. The data of Kell et al. cover the temperature range from 150 to 450 C. Data for the temperature range from 500 to 1000 C are from Sugaware et al. (1964). These calculations have been extended to include OH-OH and OH-H2O pairwise interactions. For the latter interaction the formalism was extended to the case of unequal dipole quadrupole moments in the potential function for the interacting species.
A method is presented to observe surface species subject to electron-induced desorption by Auger electron spectroscopy. The surface to be examined is moved under the electron beam at constant velocity, establishing a time-independent condition and eliminating the time response of the electron spectrometer as a limiting factor. The dependence of the Auger signal on the sample velocity, incident electron current, beam diameter, and desorption cross section is analyzed. It is shown that it is advantageous to analyze the moving sample with a high beam current, in contrast to the usual practice of using a low beam current to minimize desorption from a stationary sample. The method is illustrated by the analysis of a friction transfer film of PTFE, in which the fluorine is removed by electron-induced desorption. The method is relevant to surface studies in the field of lubrication and catalysis.
The exhaust products of a solid rocket motor using as propellant 14% binder, 16% aluminum, and 70% (wt) ammonium perchlorate consist of hydrogen chloride, water, alumina, and other compounds. The equilibrium and some frozen compositions of the chemical species upon interaction with the atmosphere were computed. The conditions under which hydrogen chloride interacts with the water vapor in humid air to form an aerosol containing hydrochloric acid were computed for various weight ratios of air/exhaust products. These computations were also performed for the case of a combined SRM and hydrogen-oxygen rocket engine. Regimes of temperature and relative humidity where this aerosol is expected were identified. Within these regimes, the concentration of HCL in the aerosol and weight fraction of aerosol to gas phase were plotted. Hydrochloric acid aerosol formation was found to be particularly likely in cool humid weather.
A survey is presented of free radicals and electronically excited metastable species as high energy propellants for rocket engines. Nascent or atomic forms of diatomic gases are considered free radicals as well as the highly reactive diatomic triatomic molecules that posess unpaired electrons. Manufacturing and storage problems are described, and a review of current experimental work related to the manufacture of atomic hydrogen propellants is presented.
A correlation interferometer has been developed for the measurement of carbon monoxide and methane at 2.35 micrometers in the troposphere and in the stratosphere. This instrument has been tested in laboratory tests, solar-looking outdoor tests, and downward-looking airplane-based tests. The aircraft tests were flown on a Falcon fanjet provided by The Canada Centre for Remote Sensing over both polluted and unpolluted regions of North America. The results of these various tests are discussed. Based on the results obtained for carbon monoxide and methane, a study was undertaken to investigate the feasibility of measuring other atmospheric trace species by correlation interferometry. Results of the feasibility study for carbon dioxide, water vapor, ammonia, nitrous oxide, nitric oxide, nitrogen dioxide, sulfur dioxide, and several hydrocarbons are presented.
A tunable CW laser has been used to selectively remove either of the two metastable species, 3P 0,2, which are initially present in a neon metastable beam. The method is applicable to other rare gases and provides the opportunity for separate investigation of effects due to atoms in either the 3P 0 or 3P 2 state.
The intensity-time behavior for protons and helium, as well as for carbon, oxygen and iron ions was measured following the 1974 September 19 solar flare for energies between 0.5 and approximately 5 MeV per nucleon. The profiles displayed a time dispersion which is inversely proportional to velocity for each individual species. In addition, at a given velocity the time dispersion also depended on the charge to mass ratio of the ion. Based on this latter dependence, it was concluded that while carbon and oxygen are essentially fully stripped, iron nuclei are not, having an effective charge Q = 10 + or - 5. The observed dispersion cannot be explained by purely rigidity dependent diffusive propagation.
A hybrid chemical kinetic computer program was assembled which provides a rapid solution to problems involving flowing or static, chemically reacting, gas mixtures. The computer program uses existing subroutines for problem setup, initialization, and preliminary calculations and incorporates a stiff ordinary differential equation solution technique. A number of check cases were recomputed with the hybrid program and the results were almost identical to those previously obtained. The computational time saving was demonstrated with a propane-oxygen-argon shock tube combustion problem involving 31 chemical species and 64 reactions. Information is presented to enable potential users to prepare an input data deck for the calculation of a problem.
One of the principal factors in animal toxicity studies is the choice of animal species. A limited study of the relative toxicity of the pyrolysis products from cotton and wool indicated that values of concentrations and doses required to produce death in 50% of the test animals obtained with Swiss albino mice were approximately one-half the values obtained with Sprague-Dawley rats. The toxicity of cotton relative to that of wool was the same using Swiss albino mice or Sprague-Dawley rats. Rankings of relative toxicity appear to be more sensitive to differences in apparatus and procedure than to interspecies differences.
The intensity-time behavior for protons and alpha-particles, as well as for carbon, oxygen, and iron ions, has been measured following the solar flare of September 19, 1974, for energies between 0.5 and about 5 MeV per nucleon. The profiles display a time dispersion which is inversely proportional to velocity for each individual species. In addition, at a given velocity the time dispersion also depends on the charge-to-mass ratio of the ion. Based on this latter dependence, it is concluded that while carbon and oxygen are essentially fully stripped, iron nuclei are not, having an effective charge of 10 plus or minus 5. The observed dispersion cannot be explained by purely rigidity-dependent diffusive propagation.
The results of an investigation are presented evaluating the potential of atomic and molecular fluorescence as a stratospheric monitor of the concentrations of any one of 18 minor species: Cl, Cl2, ClO, ClO2, CO, H2, HCHO, HCl, HNO2, HNO3, H2S, NH3, NO, NO2, N2O, O, OH, and SO2. All spectral regions from the vacuum ultraviolet through the infrared were included. It was found that suitable systems can be constructed for the stratospheric monitoring of CO (5 ppb), NO2 (less than 1 ppb), OH (0.2 ppt), and O (50-200 ppt). The fluorescence sensitivities for Cl (0.5-1.0 ppt), H2 (0.2 ppm at 10 torr) and SO2 (1-10 ppb) are marginally insufficient with current technology.