4C measured in trace gases in clean air helps to determine the sources of such gases, their long-range transport in the atmosphere, and their exchange with other carbon cycle reservoirs. In order to separate sources, transport and exchange, it is necessary to interpret measurements using models of these processes. We present atmospheric ' 4C02 measurements made in New Zealand since 1954 and at various Pacific Ocean sites for shorter periods. We analyze these for latitudinal and seasonal variation, the latter being consistent with a seasonally varying exchange rate between the stratosphere and troposphere. The observed seasonal cycle does not agree with that predicted by a zonally averaged global circulation model. We discuss recent accelerator mass spectrometry measurements of atmospheric 14CH4 and the problems involved in determining the fossil fuel methane source. Current data imply a fossil carbon contribution of ca 25%, and the major sources of uncertainty in this number are the uncertainty in the nuclear power source of 14CH4, and in the measured value for S'4C in atmospheric methane.

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The radiocarbon dating of volcanic ash (tephra) deposits in New Zealand has been difficult on sites remote from the eruption, which contain either little carbon or degraded and contaminated charcoal. Although many studies of contamination removal from macroscopic charcoals from tephra sequences have been made, little attention has been paid to those containing no visible charcoal, because of the difficulty of obtaining sufficient carbon for radiometric dating. We report here experiments using accelerator mass spectrometry to establish a reliable method for dating a low-carbon aeolian and peat deposit containing a tephra horizon. Results so far demonstrate that improvements to existing chemical pretreatment methods are possible, and that dates obtained on oxidized fine-grained residues can approach the maximum age determined on good quality charred wood samples.

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