scholarly journals VII. The influence of water in the atmosphere on the solar spectrum and solar temperature

1883 ◽  
Vol 35 (224-226) ◽  
pp. 328-341 ◽  

In our paper on “Atmospheric Absorption in the Infra-red of the* Solar Spectrum” (“Proc. Roy. Soc.,” vol. 35, p. 80), we stated that the absorption by water coincided with the absorption bands to be found in the solar spectrum, and our proof rested in photographs which had been taken for some time back. In the diagram which we published (and in which are slight errors in shading at some parts, and which we here correct) we showed the coincidences as far as λ10,000, that being the limit to which we could accurately fix the wave-lengths.

1883 ◽  
Vol 35 (224-226) ◽  
pp. 80-83 ◽  

Any investigations on the subject of atmospheric absorption are of such importance in the study of meteorology, that we have deemed it advisable to present a preliminary notice of certain results obtained by us, without waiting to present a more detailed account which will be communicated at a future date. From 1874, when one of us commenced photographing the spectrum in the above region, till more than a year ago, the extremely various manners in which the absorptions took place caused considerable perplexity as to their origin, and it was only after we had completed our paper on the absorption of certain liquids, that a clue to the phenomena was apparently found. Since that time we have carefully watched the spectrum in relation to atmospheric moisture, and we think that more than a year’s observations in London, when taken in connexion with a month’s work, at an altitude of 8,500 feet on the Riffel, justify the conclusions we now lay before the Society. A study of the map of the infra-red region of the solar spectrum, and more especially a new and much more complete one, which is being prepared for presentation to the Royal Society by one of us, shows that the spectrum in this part is traversed by absorption lines of varying intensity. Besides these linear absorptions, photographs taken on days of different atmospheric conditions, show banded absorptions superposed over them. These latter are step by step absorptions increasing in intensity as they approach the limit of the spectrum at the least refrangible end. In the annexed diagram, fig. 4 shows the general appearance of this region up to λ 10,000 on a fairly dry day : the banded absorption is small, taking, place principally between λ 9420 and λ 9800 : a trace of absorption is also visible between λ 8330 and λ 9420. On a cold day, with a north-easterly wind blowing, and also at a high altitude on a dry day, these absorptions nearly if not quite disappear. If we examine photographs taken when the air is nearly saturated with moisture (in some form or another) we have a spectrum like fig. 1. Except with very prolonged exposure no trace of a spectrum below λ 8330 can be photographed. Fig. 2 shows the absorption bands, where there is a difference of about 3° between the wet and dry bulb, the latter standing at about 50°. It will be noticed that the spectrum extends to the limit of about λ 9420, when total absorption steps in and blocks out the rest of the spectrum. Fig. 3 shows the spectrum where the difference between the wet and the dry bulb is about 6°. Figs. 5 and 6 show the absorption of thicknesses of 1 foot and 3 inches of water respectively, where the source of light gives a continuous spectrum ; ⅛ inch water merely shows the absorption bands below 9420. It will be seen that there is an accurate coincidence between these “ water bands” and the absorption bands seen in the solar spectrum, and hence we cannot but assume that there is a connexion one with the other. In fact, on a dry day it is only necessary to place varying thicknesses of water before the slit of the spectroscope and to photograph the solar spectrum through them, in order to reproduce the phenomena observed on days in which there is more or less moisture present in the atmosphere. It is quite easy to deduce the moisture present in atmosphere at certain temperatures by a study of the photographs. There does appear a difference, however, in the intensity of the banded absorptions in hot weather and in cold about up to 50°. In the former they are less marked when the degree of saturation and the length of atmosphere traversed are the same as in the latter.


The infra-red solar spectrum has been the subject of a fairly continuous study since the first elementary observations of Sir John Herschel in 1832. Figure 12 reproduces the solar spectrum recorded by Langley & Abbott in 1900, and this early record serves as an example to show that much of the sun’s incident energy fails to reach the earth. The main absorbing constituents of the atmosphere are water vapour and CO 2 , and these are the cause of the deep bands in the infra-red spectrum. In recent years other rearr gases, such as O 3 , HDO, CO, CH 4 and N 2 O, have been identified through their characteristic absorption bands. It is interesting to note that the HDO absorption band at 3·67 μ , first reported by Gebbie, Harding, Hilsum & Roberts in 1949, is clearly recorded in the Langley & Abbott spectrum, although with deuterium unknown it was impossible for them to identify it. The rarer constituents of the atmosphere have interested a number of experi­menters in more recent years and, for example, Shaw, Chapman, Howard & Oxholm (1951) have identified some 800 lines of atmphoseric origin in the small region between 3·0 and 5·2 μ . However, at ground level measurements are only possible where some solar energy reaches the earth. In order to make observations in the regions normally obscured it is necessary to reduce the amount of water vapour and carbon dioxide in the path by going to high altitude. The percentage CO 2 content of the atmosphere is approximately constant, and hence the amount of CO 2 between the sun and an observer will be reduced to one-half in going to 18000 ft. and to about one-tenth in going to 50000 ft. The water-vapour content falls off much more rapidly and measurements can be made in the 2·5 to 3·5 μ band by going to only 30000 ft. Migeotte & Neven (1952 a, b ) have made an attempt to overcome the effects of the denser lower atmosphere by making observations from the summit of the Jungfraujoch at a height of almost 12000 ft. By carrying a spectrometer in a modern aircraft it is possible to make detailed observations from heights greater than 50000 ft. A program of high-altitude spectroscopy is being undertaken jointly by the Gassiot Committee of the Royal Society and the Royal Aircraft Establishment, Farnborough. The purpose of the program is to record the solar spectrum out into the far infra-red from a Canberra aircraft flying at these heights.


Many years ago it was suggested by Hartley* that the limit of the solar spectrum towards the ultra-violet was attributable to absorption by atmospheric ozone, which, as he showed, would give rise to a general absorption beginning at about the place where the solar spectrum ends. In a recent paper by Prof. A. Fowler and myself,† the evidence for this view was very much strengthened. For it was shown that just on the limits of extinction the solar spectrum shows a series of narrow absorption bands which are eventually merged in the general absorption, and these narrow bands are precisely reproduced in the absorption spectrum of ozone. For my own part, I do not feel any doubt that ozone in the atmosphere is the effective cause limiting the solar spectrum.


The infra-red spectra of oriented films of sodium deoxyribonucleate have been investigated between 700 and 4000 cm -1 using polarized radiation and under varying degrees of relative humidity. Similar spectra have been obtained when the films have been deuterated by vapour-phase exchange with heavy water. It is found that the infra-red dichroism of nearly every band increases with the relative humidity. Many of the principal absorption bands can be assigned to separable modes of vibration in the bases, the phosphate groups or the absorbed water. Measurement of the dichroic ratios of certain of these bands indicates that at high relative humidity the bases must be nearly perpendicular to the orientation direction. The configuration deduced for the phosphate groups is unlike that proposed in the Crick-Watson model, but is in essential agreement with that recently proposed by Wilkins and his co-workers. Some observations are also reported on the corresponding spectra of sodium ribonucleate. Since no dichroism was observed, no conclusions can be drawn regarding the molecular configuration of this polymer.


1998 ◽  
Vol 536 ◽  
Author(s):  
S. B. Aldabergenova ◽  
M. Albrecht ◽  
A. A. Andreev ◽  
C. Inglefield ◽  
J. Viner ◽  
...  

AbstractWe report on strong Er3+ luminescence in the visible and infra-red regions at room temperature in amorphous GaN:Er thin films prepared by DC magnetron co-sputtering. The intensity of the Er3+ luminescence at 1.535 μm corresponding to 4I13/2 → 4I15/2 transitions is greatly enhanced after annealing at 750°C. In this material GaN crystallites have formed and embedded in the continuous amorphous matrix. The crystallites are 4 to 7 nm in diameter as analyzed by high resolution transmission electron microscopy. The absorption edge, extending three orders of magnitude in absorption coefficient in the spectral range from 0.5 to 3.5 eV, is superimposed on resonant absorption bands of Er3+ ions.The total photoluminescence spectrum consists of welldefined Er3+ luminescence peaks imposed on a broad band edge luminescence from the amorphous GaN host matrix.


1951 ◽  
Vol 4 (2) ◽  
pp. 172
Author(s):  
JB Willis

Making certain assumptions as to the shape of infra-red absorption bands and the shape of the slit function of the monochromator, expressions are obtained for the dependence on spectrometer slit-width of the intensity and half-width of absorption bands. Experimental data to confirm the accuracy of these deductions are presented.


1883 ◽  
Vol 36 (228-231) ◽  
pp. 137-138

M. Fievez has recently sent me a map of the solar spectrum from C to A* inclusive, and as part of this region is one which I have been measuring, I have examined the new publication with great interest. Photography and eye measurements do not exactly coincide in the detail of the grouping of the little a group as far as A, and A itself is shown by M. Fievez’s map as wanting some details which appear in the photographs. Thus in the photographs there are some seventeen lines, whilst in M. Fievez’s map there are but thirteen. Between A and a there are several lines of marked intensity in the photograph which are not shown in the new map. The wave-lengths of the different lines from above “ a ” to A are not the same as those given by Fievez, when they are taken from comparison photo-graphs of the 1st order of the red and 2nd of the ultra-violet on the same plate, or when checked by photographs of the 2nd order of the red with the 3rd order of the green taken in a similar manner. In my paper, “Phil. Trans.,” Part II, 1880, I gave a method of using mirrors by which this could be effected, but since Professor Rowland introduced his concave gratings this is much more readily carried out. He has kindly furnished me with gratings for the purpose, having about 14,400 lines to the inch, with focal distances of 7 feet 6 inches and 12 feet 6 inches respectively. These have been employed in determining the wave-lengths of this part of the spectrum. Cornu’s map was used as a reference for the ultra-violet wave-lengths, and Ångström’s map for those in the blue and green. The two maps may be taken as equally exact. The determination of A has been made by Maseart, Smyth, and others, besides Ångström and Langley, with discordant results. I think the above may be taken as accurate as are Cornu’s and Ångström maps.


Sign in / Sign up

Export Citation Format

Share Document