scholarly journals On temperature and pressure regulation in prismatic spectrographs

It is well known that displacements of spectrum lines during a photographic exposure can be caused by changes in the temperature of the dispersing apparatus and of the air in the spectrograph. In the case of grating instruments elaborate precautions are sometimes taken to keep the room in which the spectrograph is housed at a constant temperature. Birge* has described the precautions taken at the University of Wisconsin, where the grating spectrograph is mounted in a double-walled room, the space between the walls being kept constant by suitable electric heating. In the photography of faint spectra prismatic spectrographs are sometimes to be preferred to gratings on account of their superior light-gathering power, and it is of importance to consider the errors in measurement and loss of definition due to variations in temperature. The change in refractive index with temperature appears to vary rather considerably with different melts of glass. Giffordf has measured the temperature coefficients for a series of glasses in air, and his results show that these are positive for all the glasses investigated, with one exception, Fluor Crown, which would not be suitable for the construction of prisms for spectrographs. The change in refractive index per degree Centigrade for glasses of the type suitable for the construction of prisms is shown to be of the order of 5 X 10 -6 , and since for a typical glass at λ = 5875 A, the change per Ångstrom unit is 9 X 10 -6 , the shift in wavelength per degree Centigrade would be upwards of half an Ångström unit. The temperature coefficient of some glasses seems to be considerably greater than the above value. Displacements of spectrum lines are also effected by changes in the barometric pressure during long exposures. There are, of course, many days on which this effect may be neglected, but this source of error does not appear to have received the attention that it merits. The refractive index of air at 760 mm. pressure and 20° C. is about 1•000275, so that if we assume that n p = n 760 — [( n — 1) (760 — p)/760] the change in n per cm. pressure is about 3·6 X 10 -6 , and taking the change in n per Ångström unit at D 3 as 9 X 10 -6 , we expect a shift of about 0·4 A per cm. pressure. A change in pressure as great as 1 cm. during the course of an exposure would be unusual,but changes exceeding 1 mm. are not infrequent during long exposures, and it is evident that they cannot be ignored. It is usual to expose the comparison spectrum, comprising the lines of standard wavelength, either simultaneously with the spectrum under investigation, or in instalments at regular intervals, but it has been shown that errors due to displacements* can only be eliminated in this way in the case of lines which are symmetrical, and in any case there is a loss of definition and resolving power with a loss of accuracy of the settings in the course of measurement. The experiments described in this communication relate to a prism spectrograph recently constructed for the writer by Messrs. Adam Hilger, and although the methods adopted and the conclusions reached seem fairly obvious, they may be worthy of record in view of the fact that satisfactory results were obtained only after trials extending over many months, and the details of construction appear to be of vital importance.

Author(s):  
Hans Ris

The High Voltage Electron Microscope Laboratory at the University of Wisconsin has been in operation a little over one year. I would like to give a progress report about our experience with this new technique. The achievement of good resolution with thick specimens has been mainly exploited so far. A cold stage which will allow us to look at frozen specimens and a hydration stage are now being installed in our microscope. This will soon make it possible to study undehydrated specimens, a particularly exciting application of the high voltage microscope.Some of the problems studied at the Madison facility are: Structure of kinetoplast and flagella in trypanosomes (J. Paulin, U. of Georgia); growth cones of nerve fibers (R. Hannah, U. of Georgia Medical School); spiny dendrites in cerebellum of mouse (Scott and Guillery, Anatomy, U. of Wis.); spindle of baker's yeast (Joan Peterson, Madison) spindle of Haemanthus (A. Bajer, U. of Oregon, Eugene) chromosome structure (Hans Ris, U. of Wisconsin, Madison). Dr. Paulin and Dr. Hanna are reporting their work separately at this meeting and I shall therefore not discuss it here.


Author(s):  
Patricia N. Hackney

Ustilago hordei and Ustilago violacea are yeast-like basidiomycete pathogens ofHordeum vulgare and Silene alba respectively. The mating type system in both species of Ustilago is bipolar, with alleles, A,a, (U.hordei) and a1, a2 (U.violacea) at a single locus. Haploid sporidia maintain the asexual phase by budding, while the sexual phase is initiated by conjugation tube formation between the mating types during budding and conjugation.For observation of budding, sporidia were prepared by culturing the four types on YEG (yeast extract glucose) broth for 24 hours. After centrifugation at 5000g cells were either left unmated or mated in a1/a2,A/a combinations. The sporidia were then mixed 1:1 with 4% agar and the resulting 1mm cubes fixed in 8% gluteraldehyde and post fixed in osmium tetroxide. After dehydration and embedding cubes were thin sectioned with a LKB ultratome and photographed in a Zeiss 9s transmission electron microscope or in an AE1 electron microscope of MK11 1MEV at the High Voltage Electron Microscopy Center of the University of Wisconsin-Madison.


1923 ◽  
Vol 9 (1) ◽  
pp. 81-90
Author(s):  
W. L. Westermann ◽  
A. G. Laird

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