Byne's disease

Last updated
An affected gastropod shell (a juvenile Agathistoma) from a museum collection Effects of Bynesian decay on a gastropod shell.jpg
An affected gastropod shell (a juvenile Agathistoma ) from a museum collection

Byne's disease, more accurately known as Bynesian decay, is a peculiar and permanently damaging condition resulting from an ongoing chemical reaction which often attacks mollusk shells and other calcareous specimens that are in storage or on display for long periods of time. It is a form of efflorescence of salts formed by the reaction of acidic vapors with the basic calcareous surface. The efflorescence can sometimes superficially resemble a growth of mold. Although first described in the early 19th century, Bynesian decay was not well understood until almost a hundred years later. The condition is named after the man (Loftus Byne) who is best known for describing it in the late 19th century, even though he was not the first person to describe it in print. In addition, Byne mistakenly assumed that the condition was caused by bacteria, and thus the condition came to be referred to as a "disease".

Contents

In addition to mollusk shells, various other natural history specimens are susceptible to this form of decay, including eggshells [1] and some fossils and mineral samples that are composed of calcium carbonate. This condition is of concern for museum scientists, and also for anyone who has a private collection of specimens of these kinds. In order to avoid Bynesian decay, the use of metal, non-reactive polymers and acid-free materials of archival quality are preferred over common paper, wood-based materials, ordinary glues and varnishes in collection environments. Management of affected specimens includes washing and thorough drying, with a subsequent reallocation to an archival setting.

Appearance

Crystallized salt clusters (efflorescence) produced by Byne's disease on a gastropod shell's surface Bynesian decay efflorescence.tif
Crystallized salt clusters (efflorescence) produced by Byne's disease on a gastropod shell's surface
Some affected mollusk shells. The efflorescence is clearly visible in both specimens. This decay was deliberately produced under extreme conditions. Bynesian Decay 001.JPG
Some affected mollusk shells. The efflorescence is clearly visible in both specimens. This decay was deliberately produced under extreme conditions.

Byne's disease can appear as a powdery white coating on a shell or other calcareous specimen. It also often looks as if the specimen has been "infected" with mold; however, under magnification, the mold-like appearance is revealed to be a crystalline growth of salts. [2] [3]

History

In 1839, the British naturalist and malacologist Thomas Brown (1785–1862) briefly mentioned this form of deterioration in his book A Conchologist's Text-Book. [2] Agnes Kenyon also described the condition in 1896, suggesting that "saline particles in the atmosphere [were] evidently exerting a corrosive effect". [2]

Origin of the name

In 1899, the British amateur conchologist and naturalist Loftus St. George Byne (1872–1947) [4] described this condition, [5] in a presentation to the Conchological Society of Great Britain in Ireland, and did so again in another presentation in June of that same year. [2]

...a dullness first pervading the exterior of certain smooth species more markedly e.g. Conus , Cypraea , and especially Naticidae. Then grey acid efflorescence, both tasting and smelling strongly of vinegar covers the whole surface like a powder, rising doubtless from the interior, and the specimens are soon almost irretrievably ruined.

Byne was convinced that butyric acid was present together with calcium acetate in the affected shells, although he never really described the methods he used in the so-called "extensive chemical tests" he claimed to have applied to these specimens. Among other conclusions, he assumed that the butyric acid originated from bacterial activity. He also concluded that the decaying effect 'travelled from shell to shell and drawer to drawer', [6] and thus the condition came to be called a "disease". [2] [7]

Clarification and resolution

The true nature of the "disease" was partially clarified in 1934, when the British government chemist John Ralph Nicholls explained that oak cabinets at the Natural History Museum in London were giving off acetic acid fumes, which were attacking the shells stored in them. [2]

In 1985, almost 150 years after the Byne's disease was first mentioned in the literature, Norman H. Tennent and Thomas Baird published an extensive study on the subject. Their deep analysis, involving many complex and sophisticated techniques such as X-Ray diffraction, infrared spectroscopy, thermogravimetric analysis and nuclear magnetic resonance spectroscopy, finally revealed the true nature of the decaying process. They identified the substances involved (the calcium salts), as well as the chemical reactions that originated them. They concluded that Byne's disease is not actually a disease, and is in fact caused by simple chemical reactions which occur in the presence of acidic vapors originating from the immediate environment in which the specimens are stored. [3]

Chemistry

A shell of Corbicula fluminea, a freshwater bivalve, which has been exposed to damp and acidic air. This decay was deliberately produced under extreme conditions. The dark periostracum in this shell is a normal variant. Bynesian Decay 002.JPG
A shell of Corbicula fluminea , a freshwater bivalve, which has been exposed to damp and acidic air. This decay was deliberately produced under extreme conditions. The dark periostracum in this shell is a normal variant.
A lighter colored and undamaged shell of Corbicula fluminea Toegeknepen korfmossel.jpg
A lighter colored and undamaged shell of Corbicula fluminea

Bynesian decay usually starts when specimens are stored or displayed for considerable periods of time in an enclosed space. The storage method itself usually causes this problem, when containers, cabinets or display cases are entirely or partially made of wood, plywood or other wood products such as Masonite, or when the specimens are surrounded by, or in contact with, various other kinds of materials that are cellulose-based and can turn water vapor acidic. [7] [8]

Other potentially damaging materials include non-archival quality cardboard, card, paper, cotton and cork, all of which give off acidic vapors over time. PVC and polyurethane plastics are also a problem, as they also degrade and give off acidic vapors with time. [8] High humidity of the air is a significant contributing factor, as is lack of ventilation of the specimens. High ambient temperatures can increase the rapidity of the decay. [7]

Generally, in cabinets or display cases that are entirely or partially made of wood, the hydrolysis of acetyl groups in the wood hemicelluloses creates acetic acid. The rate at which the acetic acid is produced is proportional to the concentration of esters in the wood, the humidity, the temperature, and the overall acidity of the environment. [9] Acidic fumes can also be released from formaldehyde which can occur in wood as a degradation product of lignin. Acidic fumes can also be given off from ubiquitous formaldehyde resins (commonly urea-formaldehyde resins). [9]

In the first case, acetic acid reacts with the calcium carbonate (one of the main components of freshwater, marine and land shells, birds' eggs and other such specimens) producing calcium acetate, a salt. Formaldehyde can be oxidized by the oxygen in air to create formic acid, which then has basically the same effects as acetic acid, reacting with calcium carbonate to produce a salt. The salts (calcium acetate and calcium formate) crystallize through the specimen's outer surface, destroying its fine detail and exposing more areas for further reaction. As the condition progresses, the salt crystals build up over the specimen's surface, which becomes increasingly eroded. [7]

The calcium carbonate and acetic acid chemical reaction occurs as follows: [10]

CaCO3 + 2CH3COOHCa(CH3COO)2 + H2O + CO2

Calcium carbonate and formic acid chemical reaction occurs as follows: [11]

CaCO3 + 2CH2O2Ca(HCOO)2 + H2O + CO2

Calcium carbonate and sulfuric acid chemical reaction occurs as follows: [12]

CaCO3 + H2SO4CaSO4 + H2O + CO2

In this last reaction, calcium carbonate reacts with sulfuric acid and produces calcium sulfate, water and carbon dioxide.

Prevention and management

When specimens are to be placed in any size of container for long-term storage or display, the consistent use of only archival-quality materials prevents the development of Byne's disease. Thus, materials such as metal cabinets and display cases, archival quality paper labels and card trays are used in museum collections of specimens that might be vulnerable to this reaction. [7] [8] It is also worth mentioning that sea shells, after collecting, need to be washed thoroughly in freshwater to remove the salt that is on and in the shell, and then dried thoroughly before they are stored. Salt attracts moisture and makes shells more vulnerable to Bynesian decay. [2]

The following is a chart that shows non-archival materials and their archival equivalents: [8]

Traditional non-archival materialsArchival materials without acidic fumes
wood, plywood, masonitemetal
paper acid-free paper
card and cardboardacid-free card
corkpolyester fiberfill
colored plastic foam ethafoam: white polyethylene foam
ethylene vinyl acetate mylar
ballpoint pen ink, other everyday inks carbon ink (or pencil)
ordinary glue archival glue
ordinary cellulose tapearchival cellulose tape
ordinary (polyetheylene) zipper storage bagsarchival (polypropylene) zipper storage bags

If possible, the use of wood and wood products should be avoided entirely. Many varnishes and paints are well known emitters of volatile organic compounds (VOCs), [13] some of which may be acidic, and thus have the potential to damage calcium carbonate specimens. Because of this, these coatings should also be avoided; water-based varnishes and paints are considered less harmful, and should be preferred. [8]

Because the reactions involved in Bynesian decay require a certain quantity of moisture in the air in order for them to take place, keeping the air somewhat dry, i.e. keeping the environmental relative humidity under control is beneficial. This is achieved by careful monitoring of the relative humidity (using instruments such as a hygrometer), and applying dehumidifiers when necessary; sometimes, simple air conditioning systems may suffice. Extremely low humidity can damage some specimens, so caution is recommended. Usually, a relative humidity maintained around 50% is considered to be adequate. [7] [8] Applying sorbents containing a strong base, such as potassium hydroxide, inside the storage environment to protect the specimens against degradation is also possible. Copy paper or KOH-impregnated filter paper are some low cost examples of sorbents which can be used. These strong bases have a preference to react with acid, thus they compete successfully with the calcium carbonate specimens for any acidic vapors that may be present. The bases also help reduce the overall acid concentration inside the enclosed space. [10]

The damage to specimens is unfortunately not reversible; however, the decay can be arrested by washing or soaking the specimens in water, followed by a very thorough drying. The specimens must then be placed in an environment that consists of only archival materials, in a completely archival setting. [2] [8]

Pyrite disease

In collections that contain fossils, high humidity can also affect pyrite (or its polymorph marcasite) (iron disulfide) fossils in a somewhat similar condition, which is known as pyrite disease. The iron disulfide can react with water and oxygen to form iron sulfates and sulfuric acid, in a process sometimes termed Bynesian decay. [8] [14]

Related Research Articles

<span class="mw-page-title-main">Calcium</span> Chemical element, symbol Ca and atomic number 20

Calcium is a chemical element with the symbol Ca and atomic number 20. As an alkaline earth metal, calcium is a reactive metal that forms a dark oxide-nitride layer when exposed to air. Its physical and chemical properties are most similar to its heavier homologues strontium and barium. It is the fifth most abundant element in Earth's crust, and the third most abundant metal, after iron and aluminium. The most common calcium compound on Earth is calcium carbonate, found in limestone and the fossilised remnants of early sea life; gypsum, anhydrite, fluorite, and apatite are also sources of calcium. The name derives from Latin calx "lime", which was obtained from heating limestone.

In chemistry, a salt is a chemical compound consisting of an ionic assembly of positively charged cations and negatively charged anions, which results in a compound with no net electric charge. A common example is table salt, with positively charged sodium ions and negatively charged chloride ions.

<span class="mw-page-title-main">Alkaline earth metal</span> Group of chemical elements

The alkaline earth metals are six chemical elements in group 2 of the periodic table. They are beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), barium (Ba), and radium (Ra). The elements have very similar properties: they are all shiny, silvery-white, somewhat reactive metals at standard temperature and pressure.

<span class="mw-page-title-main">Calcium carbonate</span> Chemical compound

Calcium carbonate is a chemical compound with the chemical formula CaCO3. It is a common substance found in rocks as the minerals calcite and aragonite, most notably in chalk and limestone, eggshells, gastropod shells, shellfish skeletons and pearls. Materials containing much calcium carbonate or resembling it are described as calcareous. Calcium carbonate is the active ingredient in agricultural lime and is created when calcium ions in hard water react with carbonate ions to create limescale. It has medical use as a calcium supplement or as an antacid, but excessive consumption can be hazardous and cause hypercalcemia and digestive issues.

Calcium silicate is the chemical compound Ca2SiO4, also known as calcium orthosilicate and is sometimes formulated as 2CaO·SiO2. It is also referred to by the shortened trade name Cal-Sil or Calsil. It occurs naturally as the mineral larnite.

<span class="mw-page-title-main">Petrifaction</span> Process of fossilisation

In geology, petrifaction or petrification is the process by which organic material becomes a fossil through the replacement of the original material and the filling of the original pore spaces with minerals. Petrified wood typifies this process, but all organisms, from bacteria to vertebrates, can become petrified. Petrifaction takes place through a combination of two similar processes: permineralization and replacement. These processes create replicas of the original specimen that are similar down to the microscopic level.

<span class="mw-page-title-main">Barium carbonate</span> Chemical compound

Barium carbonate is the inorganic compound with the formula BaCO3. Like most alkaline earth metal carbonates, it is a white salt that is poorly soluble in water. It occurs as the mineral known as witherite. In a commercial sense, it is one of the most important barium compounds.

<span class="mw-page-title-main">Efflorescence</span> Migration of a salt to the surface of a porous material

In chemistry, efflorescence is the migration of a salt to the surface of a porous material, where it forms a coating. The essential process involves the dissolving of an internally held salt in water, or occasionally in another solvent. The water, with the salt now held in solution, migrates to the surface, then evaporates, leaving a coating of the salt.

<span class="mw-page-title-main">Sodium acetate</span> Chemical compound

Sodium acetate, CH3COONa, also abbreviated NaOAc, is the sodium salt of acetic acid. This colorless deliquescent salt has a wide range of uses.

Scrubber systems are a diverse group of air pollution control devices that can be used to remove some particulates and/or gases from industrial exhaust streams. An early application of a carbon dioxide scrubber was in the submarine the Ictíneo I, in 1859; a role for which they continue to be used today. Traditionally, the term "scrubber" has referred to pollution control devices that use liquid to wash unwanted pollutants from a gas stream. Recently, the term has also been used to describe systems that inject a dry reagent or slurry into a dirty exhaust stream to "wash out" acid gases. Scrubbers are one of the primary devices that control gaseous emissions, especially acid gases. Scrubbers can also be used for heat recovery from hot gases by flue-gas condensation. They are also used for the high flows in solar, PV, or LED processes.

<span class="mw-page-title-main">Hexafluorosilicic acid</span> Octahedric silicon compound

Hexafluorosilicic acid is an inorganic compound with the chemical formula H
2
SiF
6
. Aqueous solutions of hexafluorosilicic acid consist of salts of the cation and hexafluorosilicate anion. These salts and their aqueous solutions are colorless.

Stone sealing is the application of a surface treatment to products constructed of natural stone to retard staining and corrosion. All bulk natural stone is riddled with interconnected capillary channels that permit penetration by liquids and gases. This is true for igneous rock types such as granite and basalt, metamorphic rocks such as marble and slate, and sedimentary rocks such as limestone, travertine, and sandstone. These porous channels act like a sponge, and capillary action draws in liquids over time, along with any dissolved salts and other solutes. Very porous stone, such as sandstone absorb liquids relatively quickly, while denser igneous stones such as granite are significantly less porous; they absorb smaller volumes, and more slowly, especially when absorbing viscous liquids.

<span class="mw-page-title-main">Alkali soil</span> Soil type with pH > 8.5

Alkali, or Alkaline, soils are clay soils with high pH, a poor soil structure and a low infiltration capacity. Often they have a hard calcareous layer at 0.5 to 1 metre depth. Alkali soils owe their unfavorable physico-chemical properties mainly to the dominating presence of sodium carbonate, which causes the soil to swell and difficult to clarify/settle. They derive their name from the alkali metal group of elements, to which sodium belongs, and which can induce basicity. Sometimes these soils are also referred to as alkaline sodic soils.
Alkaline soils are basic, but not all basic soils are alkaline.

<span class="mw-page-title-main">Bronze disease</span> Effect of chlorides on copper alloys

Bronze disease is an irreversible and nearly inexorable corrosion process that occurs when chlorides come into contact with bronze or other copper-bearing alloys. It can occur as both a dark green coating, or as a much lighter whitish fuzzy or furry green coating. It is not a bacterial infection, but the result of a chemical reaction with the chlorides that usually occurs due to contamination of the bronze object by saltwater or from burial in specific types of soil where chloride salts are present. If not treated, complete destruction of the affected artifact is possible. Treatment is very difficult, costly and not always effective. Transfer of chlorides from the contaminated artefact to other artefacts can spread the condition.

<span class="mw-page-title-main">Acetic acid</span> Colorless and faint organic acid found in vinegar

Acetic acid, systematically named ethanoic acid, is an acidic, colourless liquid and organic compound with the chemical formula CH3COOH. Vinegar is at least 4% acetic acid by volume, making acetic acid the main component of vinegar apart from water and other trace elements.

<span class="mw-page-title-main">Descaling agent</span>

A descaling agent or chemical descaler is a liquid chemical substance used to remove limescale from metal surfaces in contact with hot water, such as in boilers, water heaters, and kettles. Limescale is either white or brown in colour due to the presence of iron compounds. Glass surfaces may also exhibit scaling stains, as can many ceramic surfaces present in bathrooms and kitchen, and descaling agents can be used safely to remove those stains without affecting the substrate since both ceramics and glass are unreactive to most acids.

<span class="mw-page-title-main">Conservation and restoration of frescos</span> Art preservation techniques

The conservation and restoration of frescoes is the process of caring for and maintaining frescos, and includes documentation, examination, research, and treatment to insure their long-term viability, when desired.

<span class="mw-page-title-main">Conservation and restoration of bone, horn, and antler objects</span>

Conservation-restoration of bone, horn, and antler objects involves the processes by which the deterioration of objects either containing or made from bone, horn, and antler is contained and prevented. Their use has been documented throughout history in many societal groups as these materials are durable, plentiful, versatile, and naturally occurring/replenishing.

Workplace exposure monitoring is the monitoring of substances in a workplace that are chemical or biological hazards. It is performed in the context of workplace exposure assessment and risk assessment. Exposure monitoring analyzes hazardous substances in the air or on surfaces of a workplace, and is complementary to biomonitoring, which instead analyzes toxicants or their effects within workers.

<span class="mw-page-title-main">Agents of deterioration</span>

The 'ten agents of deterioration' are a conceptual framework developed by the Canadian Conservation Institute (CCI) used to categorise the major causes of change, loss or damage to cultural heritage objects. Also referred to as the 'agents of change', the framework was first developed in the late 1980s and early 1990s. The defined agents reflect and systematise the main chemical and physical deterioration pathways to which most physical material is subject. They are a major influence on the applied practice of conservation, restoration, and collection management, finding particular use in risk management for cultural heritage collections.

References

  1. Ryhl-Svendsen, M. (2001). "Bynes efflorescence on an egg shell". (IAQ): Museums and Archives.
  2. 1 2 3 4 5 6 7 8 Shelton, S. (1996). "The Shell Game: Mollusks Shell Deterioration in Collections and its Prevention" (PDF). The Festivus. 28 (7): 74–80. Archived from the original (PDF) on 2009-01-24.
  3. 1 2 Tennent, N. H.; Baird, T. (1985). "The Deterioration of Mollusca Collections: Identification of Shell Efflorescence". Studies in Conservation. International Institute For Conservation Of Historic And Artistic Works (IIC). 30 (2): 73–85. doi:10.2307/1506091. ISSN   0039-3630. JSTOR   1506091.
  4. Salisbury A. E. (1951). "Obituaries: Ronald Winckworth, 1884–1950". Proceedings of the malacological Society of London29 (1951-1953, Part I): 5-6.
  5. Callomon, P. "Byne’s Disease – Questions and Answers" Archived 2017-10-26 at the Wayback Machine . Accessed 25 April 2010.
  6. Byne, L. St G. (1899). "The corrosion of shells in cabinets". Journal of Conchology. 9 (6): 172–178.
  7. 1 2 3 4 5 6 Shelton, S. Y. (2008). "Byne's "Disease:" How To Recognize, Handle And Store Affected Shells and Related Collections" (PDF). Conserve O Gram. USA: National Park Service, U.S. Department of the Interior (11/15): 1–4.
  8. 1 2 3 4 5 6 7 8 Sturm, C. F.; Pearce, T.A.; Valdés, A. (2006). "Archival and Curatorial Methods". The Mollusks: A Guide to their Study, Collection, and Preservation. Universal Publishers. pp. 45–57. ISBN   1-58112-930-0.
  9. 1 2 Berndt, H. (1987). "Assessing the Detrimental Effects of Wood and Wood Products on the Environment Inside Display Cases". AIC, Vancouver, BC.
  10. 1 2 Brokerhof, A. (1999). "Application of Sorbents To Protect Calcareous Materials Against Acetic Acid Vapours". Indoor Air Pollution: Detection and Mitigation of Carbonyls, Presentation Abstracts and Additional Notes. The University of Strathclyde, Glasgow, Scotland 17–18 June 1998.
  11. Baltrusaitis, J., Usher, C. and Grassian, V. (2006). "Reactivity of Formic Acid on Calcium Carbonate Single Particle and Single Crystal Surfaces: Effect of Adsorbed Water". Microscopy and Microanalysis (Cambridge University Press) 12(Suppl 2): 796-797.
  12. Casiday, R. and Frey, R. Acid Rain Inorganic Reactions Experiment. Department of Chemistry, Washington University.
  13. Tétreault, J.; Stamatopoulou, E. (1997). "Determination of Concentrations of Acetic Acid Emitted from Wood Coatings in Enclosures". Studies in Conservation. 42 (3): 141–156. doi:10.2307/1506710. JSTOR   1506710.
  14. Cavallari, D.C.; Salvador, R.B.; Cunha, B.R. (2014). "Dangers to malacological collections: Bynesian decay and Pyrite decay". Collection Forum. 28 (1–2): 35–46. doi: 10.14351/0831-4985-28.1.35 .