Part of my role for the project is
to select relevant material from the Biophysics collection for digitisation.
The Biophysics collection of paper, glass plate and acetate photographic
material produced by staff members and spans from the department's inception in
1947, to 1984. My brief was to select a subset of 4000 images from this
collection relating to DNA research carried out by Maurice Wilkins and others.
The bulk of the images came from the quarter plate glass
plate negative collection that comprises of 18300 individual items. While DNA
research accounts for a significant proportion, other departmental work notably
on muscle and the structure of collagen are also represented. The DNA related
slides had to be handpicked from this larger total. Fortunately, the entire
series had been indexed by the department. During the cataloguing project in
2011, these index books were digitised and transcribed into a spreadsheet, which
made the task of selection much easier.
The selection criteria used was based on my own
understanding of the collection and the brief of the project. Having worked on
the cataloguing project of the papers prior to this role, I felt confident in
my ability to determine which material should be included. For the most part
this was fairly academic as each slide indicated who created them and all
material from well known DNA researchers was selected (e.g. Wilkins, Franklin,
Gosling, Wilson etc.). When the creators’ relationship to DNA research was not
so obvious, such as visiting academics or PhD students, then I consulted the
catalogue to see whether they collaborated in DNA research. I decided to
include all work (not just DNA research) in the early years of the department
as often related project techniques and microscopy work helped shape the later
DNA research. Supplementary material relating to microscopy studies, chemical
analysis and model building and a smaller number of half plate glass plate
negatives and photographic prints were also included.
The jewel in the crown so to speak was the third main source
of material - the x-ray acetates. Remarkably, some of the original x-ray
exposures have survived and capture the various samples, salts and techniques
that the KCL Biophysics department used in their x-ray diffraction studies of
DNA and later RNA and nuceleoproteins. It was decided early on that all the
x-rays were to be digitised, due in part due to their intrinsic value but
secondly because of their unstable physical condition. Acetate film has a
tendency to deteriorate and undergo what is known as vinegar syndrome. This is
when the acetate degrades and begins to oxidise creating a vinegar smell. The
surface often begins to warp and crack and fades the original image. The
condition is autocatalytic which means that once it has begun it cannot
be stopped with the only stabilisation solution being to isolate and freeze the
material. Many of the x-rays show the early signs of this condition (small pock
marks) but the vast majority have retained clear x-ray patterns.
X-ray diffraction exposure showing clear warping and peeling of the emulsion layer but retaining the x-ray pattern of DNA. |
X-ray diffraction exposure of DNA with typical pock marks associated with acetate deterioration |
Digitisation is the best strategy for long term preservation of this material for several reasons. Firstly, by producing a digital copy we can retain valuable content before further deterioration ensues. Secondly, the digital copy will be more accessible than the original as a high quality scan can provide a greater degree of clarity than the physical copy and thirdly by producing a digital surrogate it reduces the risk of damage from physical handling and allows for the original material to be put into cold storage.
Overall, the images selected from the Biophysics Department
are representative of the biophysical approach to genetics taken between
1947-1969.The collection provides an unprecedented record of x-ray diffraction
studies in genetics as well as fully documenting the experimental work of
Maurice Wilkins and his colleagues carried out at King’s.
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