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Conservation of Wet Faunal Remains: Bone, Antler, and Ivory

(PDF Version, 145 KB)

CCI Note 4/3 is part of CCI Notes Series 4 (Archaeological and Field Conservation)

Caution: This Note discusses actions that will physically affect the object, and/or procedures that involve the use of chemicals. Exercise caution, and seek qualified assistance if in doubt.

Introduction

Faunal remains are often damp or wet when first excavated, and must be dried before they can be studied or stored in a research collection. Undeteriorated specimens of bone, antler, and ivory can be treated by a non-specialist, but deteriorated specimens may require the advice of a conservator. This Note discusses ways to assess the condition of bone,Endnote1 and outlines procedures to preserve these materials.

Assessing the Specimens

First determine whether the material is bone, antler, or ivory (CCI Notes 6/1 Care of Ivory, Bone, Horn and Antler). Ivory, which has multiple layers, is more dense than bone or antler and is more likely to crack or delaminate while drying.

Next determine the condition of the material. One good indication of condition is the hardness of the surface. To test hardness, gently press the surface of the bone in several areas. If it compresses or feels spongy, the material has deteriorated. Deterioration can be roughly divided into three categories: a hard surface indicates little or no deterioration; a soft surface with hard bone beneath indicates slight to moderate deterioration; and an extremely soft surface indicates a high degree of deterioration. In the latter case, it may be necessary to consolidate the material prior to drying.

Bone that is hard or has only a slight softening of the surface can probably be air-dried safely, but bone that is soft is likely to be sensitive to water loss. However, hardness is only one indication of condition. Some burial conditions selectively damage one or more components of bone, leaving an object that is hard but still susceptible to damage (e.g. shrinkage, twisting, cracking, or delamination) when air-dried. Therefore, even if a bone is hard and apparently durable, test dry a few pieces. If any problems are noted, a decision can then be made about consolidating the other pieces.

Before drying, note areas of damage and measure any large cracks. Repeat these measurements occasionally throughout the drying process, as colour changes during drying may make the cracks appear larger.

Cleaning

Note: These water-based treatments are for damp or wet bone; dry bone, such as surface finds or pieces from hot-climate excavations, should never be re-wetted without the advice of a conservator.

Archaeological remains are generally covered with dirt, and are often penetrated by the roots of small plants. To remove dirt, briefly rinse the object in water. Bone in good condition can be immersed for a few minutes but should never be left to soak. Do not use detergents as they may contain colorants, perfumes, and other additives that might contaminate the bone, rendering it useless for chemical analysis or dating. Stubborn dirt deposits can be gently dislodged with a paintbrush or wooden probe, but do this cautiously as wet bone can be soft and easily abraded. Rootlets growing in the bone can sometimes be removed with tweezers. However, take care not to pull fragments of bone off with the rootlets, which are often branched beneath the surface. To prevent this, cut the rootlets off at the surface with fine scissors. Note that dirt and rootlets are not harmful if left in situ, so always consult an archaeologist about the degree of cleaning required.

Bones retrieved from middens may occasionally be coated with excessive amounts of animal fat. Permafrost on Arctic sites provides excellent conditions for the preservation of fats and oils from sea mammals, but once the artifact is excavated this fat may go rancid and pose a health hazard if it is not removed. To determine the appropriate treatment, consult a conservator.

Excavated bone is often stained with tannins and metal corrosion products. As these stains will generally not cause further damage to the structure of the bone, and most faunal material is used for research collections rather than for display, staining is not a major concern. However, if stain removal is necessary, consult a conservator before commencing. Many of the acids, bleaches, or chelating agents used to remove stains can damage bone.

Skeletal material from saltwater environments will have absorbed the chlorides, nitrates, and sulphates that are dissolved in the water. These soluble salts must be removed before the material is dried or they will form salt crystals that can physically destroy the structure of the bone. Even if this damage is not visible immediately after drying, changes in humidity levels over the years will cause the continual solubilization and re-crystallization of the salt until cracks form in the bone. A white effluorescence is evidence of contamination by soluble salts. To remove salts, soak the bone in successive baths of fresh tap water. Monitor each bath for traces of soluble salts with a conductivity meter to determine when the salts have been removed, i.e. continue monitoring until a reading smaller than the error rate of the instrument is achieved. Other test methods (chloride-ion electrodes, test papers, silver/nitrate or ion-specific titrations) are also available for determining the chloride content.

Insoluble salts are characterized by hard white concretions on the surface of the bone. Unlike soluble salts, these substances are inert and can generally be left on the bone. However, if they are obscuring details, they can be removed by a conservator. Note that removal should be done while the bone is still wet as drying hardens the concretions and makes their removal more difficult.

Consolidation

The decision to consolidate must be considered carefully, as consolidants can interfere with the chemical analysis or dating of the bone. It may be preferable to allow minor cracking to take place rather than to limit future analysis. If the material is to be consolidated, some samples should probably be left untreated to provide uncontaminated material for testing.

Consolidation should be undertaken only by a conservator or with the advice of a conservator. Any cleaning or salt or stain removal that is necessary must be conducted first. Consolidants may be water- or solvent-based. It is important decide which type to use before drying commences as water-based consolidants must be applied while the bone is still wet.

Drying

Material that is in good or only slightly deteriorated condition can usually be dried without problems. Air-drying is the simplest method although the evaporation of water can create enormous stresses in the structure. Because bone responds to changes in relative humidity by expanding and contracting to different degrees in three different dimensions — longitudinal, radial, and tangential — even undeteriorated bone can crack while drying. During the drying process, the outer surfaces tend to dry first and contract around the still damp, expanded interior. This can cause large areas to shrink, crack, or warp if the bone structure has been weakened through deterioration. Exposed areas of cancellous or less dense bone will also dry faster than thicker, compact bone, again leading to areas of stress. Ivory, because of its dense laminated structure, is more prone to splitting than bone or antler, and should be watched more closely during drying.

Air-drying should be slow and controlled. The simplest method is to lay the clean wet bone on a table or an open mesh rack, and allow it to dry slowly. Turn bones frequently to ensure even drying, and monitor all pieces for the appearance of cracks, delamination, or other physical changes. The development of new cracks or enlargement of existing cracks is an indication that the bone is drying too quickly. If this is the case, cover the bone with a polythethylene sheet to reduce the rate of evaporation.

Bone should be dried at moderate humidity and cool temperature, out of sunlight, and away from any heat sources. The rate at which the bone dries can be slowed by increasing the relative humidity. This can be accomplished by reducing the temperature (place the object in a refrigerator or a cool basement room) or by increasing the relative humidity in the vicinity of the bone (hang wet cloths over the drying racks or add room humidifiers).

Deteriorated bone may respond poorly to air-drying. If cracking occurs when test samples are dried, the bone may require consolidation or de-watering prior to drying. Water can be removed from bone by immersing it in several baths of increasing concentration of a polar solvent such as ethyl alcohol. The lower surface tension of the solvent relative to water decreases the drying stresses created by evaporation. However, most solvents are toxic, flammable, and pose severe risks if handled without proper ventilation, safety equipment, and hazardous waste disposal. Therefore, immersions in solvents should not be attempted by a non-specialist.

The drying process can be monitored by weighing the object on a regular basis, usually daily or twice per week. There should be a slow, steady decrease in weight that tapers off until there is no measurable change, at which point the bone can be considered dry.

Wet bone is very susceptible to mould growth, particularly in high relative humidity (over 65 %), warm temperatures, and stagnant air. It is therefore important to check the bone regularly throughout the drying process. Mould on bone is usually characterized by white fluffy strands on the surface or fine hairs bridging the cavities of the bone. If mould is found, carefully wipe the fungal growth off with a damp paintbrush. Try to lift the filaments off the surface and out of the cavities. Rinse the brush frequently to avoid re-contaminating the surface. After cleaning, spray the surface lightly with isopropyl alcohol (rubbing alcohol, at least 30 %v/v in water) to kill the remaining spores. Note that mould spores are difficult to kill, so watch the object carefully for new outbreaks. Also be sure to disinfect any materials that have been in contact with the object. Clean the brush with soap and water and dip it in isopropyl alcohol before using it again.

Documentation

Documentation of the treatment of faunal remains is often sparse or non-existent. However, new developments and the increasing importance of analysis for research of this material make the recording of specific treatments very important. Therefore, record any detergent, solvent, consolidant, or other chemical that is applied to faunal remains and add this information to the archaeological record. This will alert researchers to possible interference from these materials during future testing.

Conclusion

This Note provides broad guidelines for cleaning and drying bone, antler, and ivory. Most bone can be safely treated with minimal intervention provided the material is assessed and selected carefully, and the cleaning and drying process is monitored. For more complex treatments involving the use of detergents, consolidants, chemicals, or solvents, consult a conservator.

Bibliography

  1. Cronyn, J.M. The Elements of Archaeological Conservation. London: Routledge, 1990.
  2. Pearson, C., ed. Conservation of Marine Archaeological Objects. London: Butterworths & Co., 1987.
  3. Sease, C. A Conservation Manual for the Field Archaeologist. Archaeological Research Tools, vol. 4. Los Angeles: Institute of Archaeology, University of California, 1987.
  4. Starling, K., and D. Watkinson, eds. Archaeological Bone, Antler and Ivory. Occasional Papers, Nº 5. London: The United Kingdom Institute for Conservation, 1987.

LR-Physics collabore avec le CRM et l’Université de Liège

Dans le cadre du bicentenaire de l’Université de Liège, LR-Physics accompagne une innovation dans les matériaux impliquant des acteurs de la Province de Liège.

Le résultat du projet, encore confidentiel, sera diffusé lors de l’inauguration de la rentrée académique de l’Université de Liège 2017

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[ Authors ] Xiaoming Ma, Sheng Ran, Paul C. Canfield, Sergey L. Bud'ko [ Abstract ] 57Fe Mossbauer spectroscopy was used to perform a microscopic study on the extremely pressure and strain sensitive compound, CaFe2As2, with different degrees of strain introduced by grinding and annealing. At the base temperature, in the antiferromagnetic/orthorhombic phase, compared to a sharp sextet Mossbauer spectrum of single crystal CaFe2As2, which is taken as an un-strained sample, an obviously broadened sextet and an extra doublet were observed for ground CaFe2As2 powders with different degrees of strain. The Mossbauer results suggest that the magnetic phase transition of CaFe2As2 can be inhomogeneously suppressed by the grinding induced strain to such an extent that the antiferromagnetic order in parts of the grains forming the powdered sample remain absent all the way down to 4.6 K. However, strain has almost no effect on the temperature dependent hyperfine magnetic field in the grains with magnetic order. Additional electronic and asymmetry information was obtained from the isomer shift and quadrupole splitting. Similar isomer shift values in the magnetic phase for samples with different degrees of strain, indicate that the stain does not bring any significant variation of the electronic density at 57Fe nucleus position. The absolute values of quadrupole shift in the magnetic phase decrease and approach zero with increasing degrees of strain, indicating that the strain reduces the average lattice asymmetry at Fe atom position.

Augmentation de la TVA de l’électricité: comment l’éviter?

L’approvisionnement en électricité de nos pays occidentaux est en train de changer fondamentalement.

Les centrales classiques de type TGV ou nucléaire semblent être promises à un pâle avenir alors que la production distribuée, au moyen par exemple de petites co-génératrices  ou de panneaux photovoltaïques, est en pleine croissance. Le développement de cette production distribuée est en train de conduire à l’apparition de micro-réseaux, c’est-à-dire de petits réseaux électriques opérés en parallèle avec le réseau électrique principal. Ces petits réseaux peuvent posséder en plus de moyens de production d’électricité,  des moyens de stockage ou encore des charges électriques flexibilisées, c’est-à-dire des charges dont la consommation pourra être modulée sur demande. Les moyens de production, de stockage ou de modulation de la charge du micro-réseau pourront aussi bien être au service de ce dernier, qu’au service du réseau électrique global.

La micro-grid: késako?

Trois éléments sont indispensables pour réaliser un réseau électrique autonome:

●  des sources d’énergie renouvelable;

●  un système de stockage d’énergie;

●  un dispositif intelligent de gestion de la demande en énergie et en électricité.

Si les sources d’énergie renouvelables ont bénéficié d’avancées technologiques ces dernières années, le système de stockage ne vient que récemment de faire l’objet d’avance technologique notable de grands groupes tels que Tesla.

La micro-grid: la mise en application des batteries innovantes

Ces batteries Tesla, ou bien des batteries commercialisées par des concurrents de Tesla, feront d’ici peu leur apparition en Belgique au sein de micro-réseaux. Bien exploiter ces batteries signifie savoir déterminer de manière automatique quand les charger ou les décharger de manière à diminuer le prix de l’électricité au sein du micro-réseau. Le même problème se pose également avec les charges flexibles ou les co-génératrices présentes dans le micro-réseau.

Cela requiert de mettre au point de nouveaux produits logiciels pour la gestion des micro-réseaux et d’adapter des dispositifs d’automation existants. Il faut souligner que ce type de produits est en forte demande de par le monde et ce dû au fait que dans de nombreux pays, le marché des micro-réseaux réalise une croissance à plus de deux chiffres.

La micro-grid : une innovation porteuse d’emploi

De plus, ce marché des micro-réseaux, autour duquel de nombreuses PME locales pourraient se développer, représente assurément un secteur d’avenir pour la Wallonie. Sans une attitude pro-active dans le secteur, la Wallonie deviendra une région importatrice des services/technologies micro-réseaux plutôt qu’une région ayant pu développer des entreprises compétitives, comme cela a été le cas pour la production de panneaux photovoltaïques.

La micro-grid: vers l’indépendance énergétique

Les intercommunales vont être soumises à l’impôt, ce qui aura comme répercussion une augmentation de la facture d’électricité de 3 à 6 %. Avec le relèvement de la TVA sur l’électricité de 6 à 21 %, nul besoin de faire des études poussées pour s’apercevoir que la part contributive aux taxes et frais divers sur la facture d’électricité est clairement prépondérante par rapport au coût de l’énergie.

Avec la baisse du coût des panneaux photovoltaïques et celle des batteries de stockage, la micro-grid constitue une innovation concurrentielle par rapport aux services proposés du réseau central et offre une alternative de production d’énergie renouvelable décentralisée, voire autonome.

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LR-Physics is helping SMEs and traditional companies to leverage on R&D by:

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Amongst its clients, LR-Physics currently assists universities in their innovative projects, consortium of industrials to build solutions in Energy and financial software companies to enrich their predictive algorithm.

In order to sustain its growing demand, LR-Physics is looking for intrapreneurs willing to value their mathematical academical background through industrial applied Research.

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  • You have a university degree in computer science, statistics, mathematics, physics or similar quantitative field.
  • You are experienced in the application of wide range of statistical methods including data mining techniques.
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  • You are pro-active, autonomous and oriented applied research.
  • You are active on Research Social Networks like ResearchGate, Quora, LinkedIn.
  • You are willing to travel.

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  • A competitive salary based on academical degree and experience.
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Productivity through R&D

Since 2013, LR-Physics is helping its clients to build their R&D capabilities in order to improve productivity and drive performance through innovation.

LR-Physics is helping SMEs and traditional companies to leverage on R&D by:

  • Building and assisting tenders for Research & Development funding
  • Manage Research projects from scoping to Scientific & Technological watch
  • Building data models based on Material and Financial analysis

Amongst its clients, LR-Physics currently assists universities in their innovative projects, consortium of industrials to build solutions in Energy and financial software companies to enrich their predictive algorithm.

LR-Physics offer

LR-Physics offers the following services:

* Promotion of Research & Development in manufacturing SME

* Providing assistance on Product Development (Technological & Marketing) 

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​Grids make sense. They really do. The notion, popular enough among techno-libertarian types, that every single power-consuming unit (house, factory, bunker) might be better off generating its own power off-the-grid is mostly absurd. Some things make sense (are more efficient) to do together, particularly when those things are more or less consumed in the same ways by basically everyone. Like electricity. But maybe there’s something in between. Enter microgrids. ​​As detailed on IEEE Spectrum’s grid blog, post-Fukushima Japan has seen a boom in the development of relatively small-scale localized grids. At first, the point was largely to boost grid efficiency, but the focus has grown more and more to include local power generation.

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A biocompatible, reliable, and particularly versatile synthesis of magnetic iron oxide nanoparticles (IONPs) is presented that uses iron(III) acetylacetonate Fe(acac)3 as an iron precursor and sodium borohydride as a reducing agent. Both the reaction temperature and the concentration of the reducing agent have considerable effects on the IONP size. These dependencies can be used to prepare IONPs ranging in size from 5 to 8 nm, as determined by transmission electron microscopy (TEM). Synthesis at room temperature or with higher sodium borohydride concentrations always resulted in smaller particle sizes. Powder X-ray diffraction patterns show the presence of an iron oxide phase with a cubic unit cell and allow for the determination of the lattice parameters and average crystallite sizes for all synthesized IONPs. Transmission Mössbauer spectroscopy shows that the as-synthesized IONPs are pure magnetite (Fe3O4) and is further used to elucidate the reaction pathway by analyzing iron intermediates formed prior to nanoparticle formation and precipitation. TEM and high-resolution TEM reveal quasi-spherical shapes and lattice fringes for most IONPs. With only minor modifications of the synthesis procedure, this versatile, one-pot synthesis is proven to be suitable for the production of bare (uncoated) IONPs, IONPs with hydrophilic poly(ethylene glycol), l-arginine, and l-glutamic acid coatings, as well as IONPs with hydrophobic coatings such as oleic acid. All coated IONPs were characterized by FT-IR spectroscopy. In addition, the bare IONPs could easily be modified post-synthesis with a suitable capping agent using ultrasonication. To verify the biocompatibility of the IONPs, in vitro cytotoxicity studies were carried out on bare IONPs with intestinal (Caco2) and liver epithelial (HepG2) cell cultures using an 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Phase contrast microscopy after hematoxylin-eosin staining showed the intact morphology of the Caco2 and HepG2 cells treated with IONPs.

Fe/SiO2 catalysts have been prepared by two different sol–gel methods, cogelation and dissolution. The cogelation and dissolution preparative methods lead to xerogels with fundamentally different pore width distributions. The nature of the iron species obtained has been examined in detail by UV–visible and Mössbauer spectroscopy, and magnetic, transmission electron microscopy, and X-ray diffraction studies. There is no evidence for the presence of any ordered iron(III) oxides in the samples but all three contain two types of iron species, specifically paramagnetic high-spin iron(III) ions isolated in silica and iron(III) containing nanoparticles with a broad width distribution centered on 1.5 nm, nanoparticles that contain antiferromagnetically coupled clusters of a few ligated bridged iron(III) ions.

Iron(III) species dispersed in silica have been synthesized with a sol-gel process. The iron(III) was introduced as the acetylacetonate complex into a solution of tetraethoxysilane to yield, after evaporative drying, pellets or monoliths.

Two gels were dried very slowly over a period of five months in order to prepare a defect free monolith useful for nonlinear optical studies. Z-scan experimental studies on the resulting, transparent, monolithic, doped solid revealed an optical Kerr effect, a third order nonlinear optical phenomenon showing a linear dependence of the refractive index on the irradiance with a nonlinear refractive index, n2, of −1.95 × 10−11 cm2/W.

Magnetic susceptibility studies between 4.2 and 295 K revealed paramagnetic behavior with a Curie constant of 4.433 (emu/mol)K and a Weiss temperature of −7.1 K. Magnetization studies at 5 K and at applied fields of up to 4 T and Mössbauer spectral studies between 4.2 and 295 K revealed a 50:50 mixture of paramagnetic species and nanoparticles with an average particle radius of 1.3 ± 0.2 nm. A blocking temperature of 70 K and a magnetic anisotropy energy of 2.4 × 105 J/m3 are derived from the Mössbauer spectra

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