The Bayesian approach to calibration of radiocarbon dates was used to wiggle-match the “floating” tree-ring chronology from a Pazyryk culture (Scythian-type complex from Sayan-Altai Mountain system, southern Siberia) burial ground in order to estimate the calendar age of its construction. Seventeen bidecadal tree-ring samples were 14C dated with high precision (±20–30 yr). The results of wiggle-matching show that the Pazyryk-type burial mounds in the southern Altai Mountains were created in the first part of 3rd century BC.

Seasonal variations of δ13C were analyzed for two Japanese cypress trees (Chamaecyparis obtusa), one buried and one living. Both trees were different in age but sampled in areas geographically close to each other in central Japan. A buried cypress with 394 annual rings was excavated from Old Fuji mudflow, the last glacial strata of the dormant Mt. Fuji volcano. The accelerator mass spectrometry (AMS) radiocarbon date of this glacial sample was 18,600 ± 120 BP (NUTA–4884). A living tree stem, which has 192 rings, was cut from the Izu Peninsula in 1986. In order to measure the seasonal δ13C fluctuation, the tree rings were divided equally into three earlywood and one or two latewood consecutive sections. The δ13C value within an annual ring generally increased from the first to the third or fourth sections then decreased in the last section. This pattern of the variation was similar in the glacial and modern samples. The δ13C value within an annual ring seems to be controlled by environmental factors (not plant physiological ones), since there was no isotopic shift in the seasonal δ13C variation at the earlywood-latewood boundary, which was controlled by plant physiology. The result suggests the potential to reconstruct the paleoenvironment within a year using the seasonal δ13C variation, though site-specific conditions such as soil characteristics would also affect to its fluctuation.

We performed a statistical analysis of the data on summer temperature anomalies in northern Fennoscandia (8–1995 AD) and found that a 70–130-yr cycle is present in this series during most of the time period. A comparison of the reconstructed northern Fennoscandia temperature with different indicators of solar activity (Wolf numbers, the length of solar Schwabe cycle, extended bi-decadal radiocarbon series, and data on sunspots observed by naked eye) shows that the more probable cause of the periodicity is the modulation of regional northern Fennoscandia climate by the long-term solar cycle of Gleissberg. The effect of this century-scale solar modulation of the global Northern Hemisphere temperature is weaker.

We have measured the radiocarbon content of tree rings from a section of Huon pine retrieved from Tasmania. The sample was divided into 39 five-ring sub-samples covering a period of 194 years. Radiocarbon ages of each of these sub-samples was determined by making four measurements of each sub-sample at the Arizona AMS laboratory (Table 1). The resulting 1σ precisions are about 0.5%. A comparison of our data with the appropriate curve in INTCAL98 indicates that the calendar age of our sample is close to 14,000 cal BP. Using this age calibration, we have constructed a plot of Δ14C versus assumed calendar age. This plot shows an essentially constant value over the youngest 125 rings of our sample. Over the oldest 75 yr of the sample, the Δ14C curve exhibits three fluctuations, the largest of which is about 65‰. The time of the peaks in the Huon-pine 14C curve corresponds approximately with the European Bølling/Allerød climatic event. Work is in progress to extend the data 100 yr more toward older ages.

Human bones from single inhumation burials and artifacts made from terrestrial mammal (ungulate) bone found in direct association with the skeletons were obtained from the Stone Age site of Schela Cladovei situated just below the Iron Gates Gorge of the River Danube. The results of stable isotope analyses of the human bone collagen are consistent with a heavy dependence on aquatic protein while radiocarbon dating of the samples reveals an offset of 300–500 years between the two sample types, indicating a freshwater reservoir effect in the human bone samples. Since protein consumption is by far the major source of nitrogen in the human diet we have assumed a linear relationship between δ15N and the level of aquatic protein in each individual's diet and derived a calibration for 14C age offset versus δ15N which has been applied to a series of results from the site at Lepenski Vir within the gorge. The corrected 14C ages (7310-6720 BP) are now consistent with the previous 14C age measurements made on charcoal from related contexts (7360–6560 BP). In addition, the data indicate a change from a primarily aquatic to a mixed terrestrial/aquatic diet around 7100 BP and this may be argued as supporting a shift from Mesolithic to Neolithic. This study also has wider implications for the accurate dating of human bone samples when the possibility exists of an aquatic component in the dietary protein and strongly implies that δ15N analysis should be undertaken routinely when dating human bones.

Calibration is essential for interpretation of radiocarbon dates, especially when the 14C dates are compared to historical or climatic records with a different chronological basis. 14C ages of samples from the marine environment, such as shells or fish bones, or samples with a marine component, such as human bone in coastal regions, require an additional consideration because of the reservoir age of the ocean. While the pre-industrial global mean reservoir correction, R(t), is about 400 years, local variations (ΔR) can be several hundred years or more. ΔR compilations on a global scale have been undertaken previously (Stuiver et al. 1986; Stuiver and Braziunas 1993), but have not been updated recently. Here we describe an on-line reservoir correction database accessed via mapping software. Rather than publishing a static ΔR compilation, new data will be incorporated when it becomes available. The on-line marine reservoir correction database can be accessed at the website http://www.calib.org/.

Faunal remains originating from terrestrial and marine mammals, and belonging to the same archaeological deposits were compared to evaluate the marine radiocarbon reservoir ages around the Hokkaido island, Japan. From five shell middens of different ages from the Jomon period (4900 BP) to the Ainu cultural period (800 BP), 107 animal bone samples were selected for radiocarbon measurements. The apparent age differences between Japanese deer and northern fur seal showed the clear effect of deep-water upwelling in this region. Our data showed relatively stable age differences from 4500 BP to 800 BP, with an estimated ΔR values around 380 14C yr. Results are consistent with previous estimation based on simulation models and oceanographic properties.

We assessed marine reservoir age R(t) for the costal area of the northwest Pacific using radiocarbon measurements of the annually banded coral core (Porites sp) collected on Ishigaki Island in southern Japan. Reservoir age R(t) during the early 1900s at the Pacific coast of Ishigaki Island ranged between 290 and 455 14C yr, with a weighted mean of 355 ± 25 14C yr (n=5, ±1 σ). The regional-specific ΔR, defined as 14C age difference of regional and world ocean surface layer, was 35 ± 25 14C yr (n=5, ±1σ) on average and increased between 1900 and 1950.

The radiocarbon reservoir age correction values (R) for the Russian Far East are estimated as 370 ± 26 yr for the northwestern Sea of Japan, and 711 ± 46 yr for the southern Kurile Islands.

Apparent marine radiocarbon ages are reported for the northern Indian Ocean region for the pre-nuclear period, based on measurements made in seven mollusk shells collected between 1930 and 1954. The conventional 14C ages of these shells range from 693 ± 44 to 434 ± 51 BP in the Arabian Sea and 511 ± 34 to 408 ± 51 BP in the Bay of Bengal. These ages correspond to mean ΔR correction values of 163 ± 30 yr for the northern Arabian Sea, 11 ± 35 yr for the eastern Bay of Bengal (Andaman Sea) and 32 ± 20 yr for the southern Bay of Bengal. Contrasting reservoir ages for these two basins are most likely due to differences in their thermocline ventilation rates.

The Lagoon of Venice was formed about 6000 years ago due to the marine transgression associated with the late Pleistocene sea level rise. Already by the time of the Republic of Venice (727–1797 AD) it was recognized that the future of the city and its many historical buildings was strongly correlated with the future of the lagoon itself. During the centuries many engineering projects such as modification of the fluvial systems, construction of coastal barriers, and dredging of navigation channels were carried out to preserve the lagoonal environment. The present-day lagoon is the result of all these processes and covers an area of 540 km2 with an average depth of 0.6 m. A series of radiocarbon age determinations carried out on material obtained from cores collected in the Lagoon of Venice indicate within the sedimentary units the existence of a number of discontinuities and slumping events due to the highly active lagoonal environment. The evaluation of data obtained from a variety of different materials—both terrestrial and marine—allowed us to determine for the first time the marine reservoir effect in the lagoon of Venice. The discussion includes a comparison with other relevant measurements and a possible explanation to the relatively high reservoir age (1200–1300 yr).