The survival of organic matter in bone:: A review

被引:417
作者
Collins, MJ [1 ]
Nielsen-Marsh, CM
Hiller, J
Smith, CI
Roberts, JP
Prigodich, RV
Weiss, TJ
Csapò, J
Millard, AR
Turner-Walker, G
机构
[1] Newcastle Univ, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Trinity Coll, Dept Chem, Hartford, CT 06106 USA
[3] Univ Stirling, Dept Sci Biol, Stirling FK9 4LA, Scotland
[4] Pannon Agr Univ, Kaposvar, Hungary
[5] Univ Durham, Dept Archaeol, Durham DH1 3HP, England
[6] Norwegian Univ Sci & Technol, N-7491 Trondheim, Norway
关键词
bone diagenesis; collagen; osteocalcin; DNA; racemization; porosity; cholesterol;
D O I
10.1111/1475-4754.t01-1-00071
中图分类号
K85 [文物考古];
学科分类号
0601 ;
摘要
If bone is considered as a composite of collagen (protein) and bioapatite (mineral), then three pathways of diagenesis are identified: (1) chemical deterioration of the organic phase; (2) chemical deterioration of the mineral phase; and (3) (micro)biological attack of the composite. The first of these three pathways is relatively unusual and will only occur in environments that are geochemically stable for bone mineral. However, because rates of biomolecular deterioration in the burial environment are slow, such bones would yield useful biomolecular information. In most environments, bones are not in thermodynamic equilibrium with the soil solution, and undergo chemical deterioration (path 2). Dissolution of the mineral exposes collagen to biodeterioration, and in most cases the initial phase of dissolution will be followed by microbial attack (path 3). Biological attack (3) also proceeds by initial demineralization; therefore paths 2 and 3 are functionally equivalent. However, in a bone that follows path 3 the damage is more localized than in path 2, and regions equivalent to path 1 may therefore exist outside these zones of destruction. Other biomolecules, such as blood proteins, cellular lipids and DNA, exist within the physiological spaces within bone. For these biomolecules, death history may be particularly important for their survival.
引用
收藏
页码:383 / 394
页数:12
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