The presence and metabolism of endogenous steroid hormones in meat-producing animals has been the subject of much research over the past 40 years. While significant data are available, no comprehensive review has yet been performed. Species considered in this review are bovine, porcine, ovine, equine, caprine and cervine, while steroid hormones include the androgenic-anabolic steroids testosterone, nandrolone and boldenone, as well as their precursors and metabolites. Information on endogenous steroid hormone concentrations is primarily useful in two ways: (1) in relation to pathological versus 'normal' physiology and (2) in relation to the detection of the illegal abuse of these hormones in residue surveillance programmes. Since the major focus of this review is on the detection of steroids abuse in animal production, the information gathered to date is used to guide future research. A major deficiency in much of the existing published literature is the lack of standardization and formal validation of experimental approach. Key articles are cited that highlight the huge variation in reported steroid concentrations that can result when samples are analysed by different laboratories under different conditions. These deficiencies are in most cases so fundamental that it is difficult to make reliable comparisons between data sets and hence it is currently impossible to recommend definitive detection strategies. Standardization of the experimental approach would need to involve common experimental protocols and collaboratively validated analytical methods. In particular, standardization would need to cover everything from the demographic of the animal population studied, the method of sample collection and storage (especially the need to sample live versus slaughter sampling since the two methods of surveillance have very different requirements, particularly temporally), sample preparation technique (including mode of extraction, hydrolysis and derivatization), the end-point analytical detection technique, validation protocols, and the statistical methods applied to the resulting data. Although efforts are already underway (at HFL and LABERCA) to produce more definitive data and promote communication among the scientific community on this issue, the convening of a formal European Union working party is recommended.
The Athabasca Oil Sands are one of four natural oil sands deposits in Northern Alberta, Canada. As a number of new mines are planned in the area, there is a need to establish background levels of natural hydrocarbon release prior to these developments. To this end, various environmental samples were taken from selected tributaries in the oil sands region of the Athabasca River Basin and analysed by gas chromatography/mass spectrometry (GC/MS) for polycyclic aromatic hydrocarbons (PAHs) and their alkylated analogues. Samples were collected over 3 years (1998±2000) to provide an increased understanding of the spatial distribution, nature and extent of natural hydrocarbon release to the environment. Results indicated that levels of total PAHs were elevated in the tributaries (up to 34.7 mg/g) compared to the main stem Athabasca River (52 mg/g). As expected, samples from the oil sands deposits contained the greatest amounts of PAHs and alkylated PAHs. Pro®les of the alkylated PAH distributions were very similar, indicating that all the samples tested were from a common petrogenic source.# 2001 AEHS
The Athabasca Oil Sands is one of the four natural oil sands deposits in Northern Alberta, Canada, and are by far the largest oil sand deposit in North America, covering an area of 46,000 km2. Sediment samples were collected from the bed and bank of several tributaries that have naturally occurring exposures of oil sand material. Oil sand deposited along the lower Athabasca River, more than 100 km downstream of naturally occurring oil sand exposures, were also sampled. The levels of alkylated polycyclic aromatic hydrocarbons (PAHs) in samples collected from these various locations ranged from not detected to almost 50 ppm. Using dibenzothiophene/chrysene (C2/D2 vs. C3/D3) double ratio plots, it is possible to approximate the relative degree of degradation or weathering of the PAHs from these various sediment deposits along the lower Athabasca River and its tributaries. Similarly a plot of dibenzothiophene/phenanthrene (D2/P2 vs. D3/P3) indicate the possible origins of the oil. A combination of these plots, D3/P3 vs. D3/C3, was particularly useful in identifying weathering characteristics of different sources of the oil. Comparison of alkylated PAH distributions between the lower Athabasca River and the tributaries show slight differences consistent with different petrogenic sources and/or different weathering patterns.
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