The early stages of adipocere formation in both pig and human adipose tissue in aqueous environments have been investigated. The aims were to determine the short-term changes occurring to fat deposits during decomposition and to ascertain the suitability of pigs as models for human decomposition. Subcutaneous adipose tissue from both species after immersion in distilled water for up to six months was compared using Fourier transform infrared spectroscopy, gas chromatography-mass spectrometry and inductively coupled plasma-mass spectrometry. Changes associated with decomposition were observed, but no adipocere was formed during the initial month of decomposition for either tissue type. Early-stage adipocere formation in pig samples during later months was detected. The variable time courses for adipose tissue decomposition were attributed to differences in the distribution of total fatty acids between species. Variations in the amount of sodium, potassium, calcium, and magnesium were also detected between species. The study shows that differences in total fatty acid composition between species need to be considered when interpreting results from experimental decomposition studies using pigs as human body analogs.

Current research investigating the effect of specific aquatic microenvironments on the formation of adipocere using domesticated pigs (Sus scrofa) has demonstrated the need for a fast and reliable method to separate and identify fatty acids present in adipocere. Adipocere is defined as a late-stage post-mortem decomposition product consisting of a mixture of free fatty acids (FFA), which have formed under favorable conditions due to the hydrolysis of triglycerides in adipose tissue. Whilst good separations of adipocere lipids have been achieved using TLC, this method is time consuming when processing large numbers of samples. This paper describes a rapid and simple method for the extraction, identification and quantification of FFA commonly found in adipocere, by solid-phase extraction (SPE) using aminopropyl disposable columns in combination with GC/MS. The recoveries of FFA associated with adipocere were all above 90%, with coefficients of variation below 10%, indicating that the technique was reproducible. The limits of quantification were registered at levels of parts per million. Standard curves were linear over the range of 50-1000 mg/mL, with all correlation coefficient values greater than 0.998. A marked increase in concentration of saturated fatty acids was observed during adipocere formation, ranging from 20 to 55% for palmitic acid, 13 to 23% for stearic acid and 2.8 to 4.1% for myristic acid. These results demonstrate the suitability of aminopropyl disposable SPE columns to efficiently and rapidly isolate FFA from adipocere prior to quantitative GC/MS analysis.

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An examination of the chemistry of adipocere formation in aquatic systems provides insight into how environmental factors affect the decomposition processes of human remains. Gas chromatography–mass spectrometry (GC-MS) and inductively coupled plasma–mass spectrometry (ICPMS) have been employed to monitor the changes to the chemistry of adipocere formed in aquatic environments used to model seawater, river and chlorinated water systems. Seawater was shown to inhibit adipocere formation, and a distinctively different elemental composition was produced in this environment due to the high concentrations of salts. By comparison, river water has been shown to accelerate the formation of adipocere. Chlorinated water appears to significantly enhance adipocere formation, based on a comparison with established fatty acid concentration values. However, a competing reaction to form chlorohydrins in chlorinated water is believed to be responsible for the unusual findings in this environment. The application of the chemical characterization of adipocere to an understanding of how this particular decomposition product forms in different water environments has been demonstrated, and there is potential to utilise this approach to identify the environment in which a body has been immersed.

Adipocere is a postmortem decomposition product that consists of a mixture of fatty acids. The rate of formation of adipocere from pig adipose tissue in an aqueous environment has been monitored. The effect of various clothing and carpet material types on the process was investigated. The fatty acid composition of the adipocere was determined at regular intervals using gas chromatography-mass spectrometry. Examination of the changes to fatty acid concentrations allowed the degree of adipocere formation in the different environments to be estimated. The study demonstrated that the rate at which adipocere forms is particularly accelerated by the presence of coverings produced from natural materials. Elemental analysis by inductively coupled plasma-mass spectrometry revealed, for the most part, little change to the cations present in the adipocere formed. However, an increase in Ca concentration was observed for tissue wrapped in acrylic carpet, which was associated with a CaCO(3) additive used in the carpet manufacture.