The use of soil chemistry data to address post-mortem diagenesis in bone mineral

The soluble and exchangeable ions for a soil profile from the Roonka archaeological site. Lower Murray Basin, South Australia, are compared with the total elemental content of the soils. Since the chemical composition of post-mortem ionic substitution phases and secondary minerals in archaeological bone will depend on the availability of ions to the soil solution under field conditions, it is suggested that models addressing diagenesis in bone employ soluble and exchangeable ions rather than total elemental soil data.     

Book review

Oriental Carpet and Textile Studies

vol. III, no. 2., ed. Robert Pinner and Walter B. Denny. Published by the Islamic Department of Sotheby’ s and OCTS, Ltd., London (n.d., 1990?). 262 pages, with 12 colour plates and many black and white illus. and diagrams; soft‐bound with colour cover.

Textile Conservation and Research

by Mechtilde Fleury‐Lemburg. Bern, Switzerland: Abegg Stiftung. 1988, 532 pp.

An Introduction to Kurdish Rugs and Other Weavings

William Eagleton. New York, Interlink Books. 1988. 144 pp., 124 full‐page color plates.

Kordi: Lives, Rugs, Flatweaves of the Kurds in Khorasan

Wilfried Stanzer, Vienna, Adil Besim. 1988. 220 pp., 78 full‐page color plates, 48 color figures in text.

Carpets in the Baluch Tradition

by Siawosch Azadi. English trans. by Maria Schlatter and Robert Pinner. Klinkhardt and Biermann, Munich, 1986.

Armenian Rugs: Fabric of a Culture. An Exhibition at the Balch Institute for Ethnic Studies

August 17‐October 29, 1988. Co‐sponsored by the Armenian Rug Society. Ed. Pamela B. Nelson. 40 pp; colour and black and white photographs, maps and “selected bibliography”. Philadelphia: Balch Institute for Ethnic Studies, 1988.

Women's Costume of the Near and Middle East

by Jennifer Scarce, London and Sydney: Unwin Hyman Publishers, 1987. pp. 192     

Charcot-Marie-Tooth disease from first description to genetic localization of mutations

Charcot-Marie-Tooth disease is a hereditary motor and sensory neuropathy first described in 1886. Our increasing knowledge of this disease correlates well with the development of methods used in neurology over the past 100 years. Although its physiopathology and treatment is still not fully understood, current developments in techniques are opening the way to future discoveries. We have divided its history into three theoretical periods: the first from 1886 to 1956, which was devoted to clinical and pathological study of the disease; the second from 1956 to 1982, which saw the development of electromyography in the investigation of neuromuscular diseases; and the last and current period based upon genetic research, using the methods of molecular biology.