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Basalts mass balance

The flow of hydrothermal solutions iato the oceans from hydrothermal vents, ie, springs coming from the sea floor ia areas of active volcanism, and the chemical reactions occurring there by high temperature alteration of basalts ate of significance ia the mass balance of and. Eurthermore,... [Pg.216]

Bulk rock chemistry of hydrothermally altered midoceanic ridge basalt has been well studied and used to estimate the geochemical mass balances of oceans today (Wolery and Sleep, 1976 Humphris and Thompson, 1978 Mottl, 1983). In contrast, very few analytical data on hydrothermally altered volcanic rocks that recently erupted at back-arc basins are available. However, a large number of analytical data have been accumulated on the hydrothermally altered Miocene volcanic rocks from the Green tuff region in the Japanese Islands which are inferred to have erupted in a back-arc tectonic setting (section 1.5.3). [Pg.407]

Elucidation of the origin of sulfur in volcanic systems is complicated by the fact that next to SO2, significant amounts of H2S, sulfate and elemental sulfur can also be present. The bulk sulfur isotope composition must be calculated using mass balance constraints. The principal sulfur gas in equilibrium with basaltic melts at low pressure and high temperature is SO2. With decreasing temperature and/or increasing... [Pg.122]

Figure 6 Effect of basalt storage on the isotopic composition of the upper mantle (representing 50% of total mantle, by mass) as a function of reservoir mass, age, and Os depletion of the upper mantle. The results are presented in terms of mass of stored mafic cmst, as a percentage of total mass of the mantle. Mass balance calculations assume that the missing Re, complementing depletion in the upper mantle, resides in subducted basaltic cmst existing as a stored reservoir within the mantle. (Basaltic cmst assumed to have 0.900 ng g Re and 0.005 ng Os upper mantle has 0.280 ng g Re and 3.1 ng g Os). Depletion of Os is with reference to primitive upper mantle composition of Meisel et al. (2001) of Os/ Os = 0.1296 0.0010. The upper curve assumes that the entire upper mantle is depleted to the extent of average abyssal peridotites, with Os/ Os = 0.1247 (Snow and Reisberg, 1995). The other curves are for more moderate amounts of mantle depletion. PUM indicates primitive upper mantle estimates, (after Walker et al., 2002 Bennett et al., 2002). Figure 6 Effect of basalt storage on the isotopic composition of the upper mantle (representing 50% of total mantle, by mass) as a function of reservoir mass, age, and Os depletion of the upper mantle. The results are presented in terms of mass of stored mafic cmst, as a percentage of total mass of the mantle. Mass balance calculations assume that the missing Re, complementing depletion in the upper mantle, resides in subducted basaltic cmst existing as a stored reservoir within the mantle. (Basaltic cmst assumed to have 0.900 ng g Re and 0.005 ng Os upper mantle has 0.280 ng g Re and 3.1 ng g Os). Depletion of Os is with reference to primitive upper mantle composition of Meisel et al. (2001) of Os/ Os = 0.1296 0.0010. The upper curve assumes that the entire upper mantle is depleted to the extent of average abyssal peridotites, with Os/ Os = 0.1247 (Snow and Reisberg, 1995). The other curves are for more moderate amounts of mantle depletion. PUM indicates primitive upper mantle estimates, (after Walker et al., 2002 Bennett et al., 2002).
Strontium isotope ratios and abundances in samples from the oceanic crust may be used to determine the complete chemical mass balance of strontium exchange between seawater and basalt, including the loss of basaltic strontium to hydrothermal solutions, and uptake of basaltic or seawater strontium from hydrothermal solutions. A mass balance of this exchange can be made in four steps, (i) The relative amount of basaltic and seawater strontium in altered basalt can be determined from the measured Sr/ Sr of an altered sample as a (linear) mixture of strontium from the two end members, the (contemporaneous) seawater and basalt, (ii) The inventory of the basaltic and seawater strontium in an altered sample (in mg/kg) may then be determined from the above ratio of seawater and basalt in the sample and the total strontium abundance measured for this sample, (iii) Seawater strontium addition to the basalt is given directly by the seawater strontium inventory calculated in Step (ii). (iv) The determination of flux of basaltic strontium in or out of an altered sample is more complicated because it has to be related to the original inventory of strontium. It is determined as the difference between the original basaltic inventory and the basaltic strontium present in the altered sample. [Pg.1785]

Using average MORE or the range of compositions of oceanic basalts (e.g., Hofmann, 1988 Chapter 3.13 and http //petdb.ldeo.columbia.edu Lehnert et al., 2000), the fluxes derived here can be applied to determine the average compositions of oceanic crust that is subducted and recycled into the mantle. These compositions thus influence the composition of subduction zone magmas (see Chapter 3.18) and bear on the chemical mass balance of the mantle. [Pg.1790]

Input is balanced by output in a steady-state system. The concentration of an element in seawater remains constant if it is added to the sea at the same rate that it is removed from the ocean water by sedimentation. Input into the oceans consists primarily of (1) dissolved and particulate matter carried by streams, (2) volcanic hot spring and basalt material introduced directly, and (3) atmospheric inputs. Often the latter two processes can be neglected in the mass balance. Output is primarily by sedimentation occasionally, emission into the atmosphere may have to be considered. Note that the system considered is a single box model of the sea, that is, an ocean of constant volume, constant temperature and pressure, and uniform composition. [Pg.897]

In practice, W is directly inferred from heat flow and chemical mass balances. Warm hydro-thermal flow is a major sink for dissolved oceanic The Mg + in the warm hydrothermal fluid is removed quantitatively by reaction with basalt. Because the flux of Mg + into the ocean in river waters and the competing sinks (e.g. clays) can be estimated, the known Mg + concentration in sea water can be used to determine W. This argument is independent of CO2. [Pg.238]

Many of these reactions are in the direction needed to close the marine mass balances for major ions (Fig. 2.4). The exceptions are that they supply an unnecessary additional siiik for SO4 (CaSO precipitation) and a vast additional source of K+. The additional sink for SO4 does little damage to the marine SO4 mass balance in Fig. 2.4 because its removal affects ordy Ca + and only at the level of about 15% of the Ca + riverine inflow. The hydrothermal source for K+ cannot be rationalized as easily, because there is no adequate sink in the marine environment. Research into the sources and sinks of alkali metals reveals that K+ (and other alkali metals) that are released from basalts at high temperature are reincorporated back into basaltic rock on the sea floor at low temperature. Thus, is recycled in the vicinity of hydrothermal vents. The rates of release and incorporation are uncertain enough to obscure whether the net K+ flux is into or from the ocean in these regions. It is possible that the low-temperature removal of K+ to basalt represents a net sink large enough to accommodate the river inflow. [Pg.50]

Beyond the broad major-element constraints afforded by seismic imaging, the abundance of many trace elements in the mantle clearly records the extraction of core (Chapters 2.01 and 2.15) and continental crust (Chapter 2.03). Estimates of the bulk composition of continental cmst (Volume 3) show it to be tremendously enriched compared to any estimate of the bulk Earth in certain elements that are incompatible in the minerals that make up the mantle. Because the crust contains more than its share of these elements, there must be complementary regions in the mantle depleted of these elements—and there are. The most voluminous magmatic system on Earth, the mid-ocean ridges, almost invariably erupt basalts that are depleted in the elements that are enriched in the continental crust (Chapter 2.03). Many attempts have been made to calculate the amount of mantle depleted by continent formation, but the result depends on which group of elements is used and the assumed composition of both the crust and the depleted mantle. If one uses the more enriched estimates of bulk-continent composition, the less depleted estimates for average depleted mantle, and the most incompatible elements, then the mass-balance calculations allow the whole mantle to have been depleted by continent formation. If one uses elements that are not so severely enriched in the continental cmst, for example, samarium and neodymium, then smaller volumes of depleted mantle are required in order to satisfy simultaneously the abundance of these elements in the continental cmst and the quite significant fractionation of these elements in the depleted mantle as indicated by neodymium isotope systematics. [Pg.604]

Plank and Langmuir (1998) have pointed out that the sum of the two sedimentary subduction components is almost the same as the magmatic growth rate for the continents, indicating that at the present time the continents are in a steady state. However, the mass balance is not simple, for it has already been noted that the flux from the mantle to the continents is basaltic, whereas the flux from the continents into the mantle is closer to the composition of average continental crust and... [Pg.142]


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