Tales of mystery and imagination in stable isotope geochemistry: celebrating the 75th birthday of Jochen Hoefs.

We celebrate the contribution of Jochen Hoefs to the development of stable isotope (bio)geochemistry on the occasion of his 75th birthday.

Lead in ancient Rome's city waters.

It is now universally accepted that utilization of lead for domestic purposes and water distribution presents a major health hazard. The ancient Roman world was unaware of these risks. How far the gigantic network of lead pipes used in ancient Rome compromised public health in the city is unknown. Lead isotopes in sediments from the harbor of Imperial Rome register the presence of a strong anthropogenic component during the beginning of the Common Era and the Early Middle Ages. They demonstrate that the lead pipes of the water distribution system increased Pb contents in drinking water of the capital city by up to two orders of magnitude over the natural background. The Pb isotope record shows that the discontinuities in the pollution of the Tiber by lead are intimately entwined with the major issues affecting Late Antique Rome and its water distribution system.

Isotopic identification of natural vs. anthropogenic lead sources in marine sediments from the inner Ría de Vigo (NW Spain).

San Simón Bay, the inner part of the Ría de Vigo (NW Spain), an area previously identified as highly polluted by Pb, was selected for the application of Pb stable isotope ratios as a fingerprinting tool in subtidal and intertidal sediment cores. Lead isotopic ratios were determined by inductively coupled plasma mass spectrometry on extracts from bulk samples after total acid digestion. Depth-wise profiles of (206)Pb/(207)Pb, (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)Pb and (208)Pb/(207)Pb ratios showed, in general, an upward decrease for both intertidal and subtidal sediments as a consequence of the anthropogenic activities over the last century, or centuries. Waste channel samples from a nearby ceramic factory showed characteristic Pb stable isotope ratios different from those typical of coal and petrol. Natural isotope ratios from non-polluted samples were established for the study area, differentiating sediments from granitic or schist-gneiss sources. A binary mixing model employed on the polluted samples allowed estimating the anthropogenic inputs to the bay. These inputs represented between 25 and 98% of Pb inputs in intertidal samples, and 9-84% in subtidal samples, their contributions varying with time. Anthropogenic sources were apportioned according to a three-source model. Coal combustion-related emissions were the main anthropogenic source Pb to the bay (60-70%) before the establishment of the ceramic factory in the area (in the 1970s) which has since constituted the main source (95-100%), followed by petrol-related emissions. The Pb inputs history for the intertidal area was determined for the 20th century, and, for the subtidal area, the 19th and 20th centuries.

Pb and 206Pb/207Pb isotopic analysis of a tree bark pocket near Sheffield, UK recording historical change in airborne pollution during the 20th century.

A section of tree trunk (beech, Fagus sylvatica) containing a bark pocket progressively enclosed at the junction of two branches was collected from a semi-rural location near Sheffield, UK. According to the annual growth rings, the bark pocket formed between ca. 1919 and 1998 (the date of felling). The bark pocket was divided into consecutive samples of differing radial depth (and thus age), that were analysed by ICP mass spectrometry. The Pb concentration varied from 7 to 78 mg kg (-1) and the 206Pb/207Pb isotope ratio from 1.11 to 1.15. In contrast, the current surface bark contained 46 mg kg(-1) Pb and recorded a 206Pb/207Pb ratio of 1.11. The changing elemental and isotopic composition of the bark pocket recorded historical change in the level and sources of airborne Pb pollution. An overall increase in Pb concentration with time was accompanied by a progressive reduction in 206Pb/207Pb from ca. 1935 to 1943. Mass balance calculations indicated that Pb additives in petrol contributed significantly to the rise in concentration, accounting for a maximum of 50% of the total Pb for ca. 1986-1998, but that other sources were generally dominant. The highest Pb concentrations were recorded from ca. 1951 to 1973, suggesting a high level of industrial pollution. A reduction in Pb concentration and reversal of the trend in 206Pb/207Pb was observed in the current bark.