Paul Dennis edited results2.tex  over 8 years ago

Commit id: 65a5f9b997efff7df63aad21068a64eaddb47099

deletions | additions      

       

Whilst the lowest temperature vein calcite does have the lowest $\delta$^{13}C value (32$^{\circ}$C and 1.6‰_{VPDB} there is no overall correlation between temperature and carbon isotopic composition, Figure 6(b). In contrast there is a clear inverse covariation between T($\Delta$_{47}) and $\delta$^{18}O. A change in precipitation temperature from 30$^{\circ}$-100$^{\circ}$C is accompanied by a near 3‰ decrease in the $\delta$^{18}O value of the vein calcite from -7 to -10‰_{VPDB}, Figure 6(c).  Using the measured T$\Delta$_{47}) T($\Delta$_{47})  and $\delta$^{18}O values we have calculated the composition of the fluid that is in isotopic equilibrium with the samples of vein calcite. For this we used the Kim and O'Neill (1996) calibration of the calcite-water fractionation factor. The data plotted in Figure 6(d) show a marked linear covariation with data covariationthat resembles a two end-member mixing line. Data  for the two sections DLR7 and DLR7(i) being are  the same within measurement error. At the high temperature end the calcite is in equilibrium with water at 100-110$^{\circ}$C and having with  an enriched $\delta$^{18}O value close to +6‰_{VSMOW}. The low temperature end (30-40$^{\circ}$C) is characterized by more negative values of $\delta$^{18}O between -2 and -4‰_{VSMOW}. It is important to note that T($\Delta$_{47}) and the fluid $\delta$^{18}O plotted in Figure 6(d) are not independent and thus the errors are not orthogonal. We have plotted the 90\% error envelope corresponding to a $\pm$0.014‰ (1$\sigma$) and $\pm$0.1‰ precison for $\Delta$_{47} and $\delta$^{18}O respectively. This was determined using a monte-carlo simulation of 1000 independent $\Delta$_{47} and $\delta$^{18}O pairs. The errors are dominated by the precision at which $\Delta$_{47} can be measured with the first eigen vector of the error ellipse oriented parallel to the isopleths of constant calcite $\delta$^{18}O value. This lends a false sense of precision to the observed trend. Not-with-standing this observation the trend is real with a gradient greater than the local gradient slope  of the calcite $\delta$^{18}O isolpleths. This is revealed in the inverse covariation of T($\Delta$_{47}) and calcite $\delta$^{18}O values plotted in figure 6(c).