Chemical weathering gradients are defined by the changes in the measured elemental concentrations in solids and pore waters with depth in soils and regoliths. An increase in the mineral weathering rate increases the change in these concentrations with depth while increases in the weathering velocity decrease the change. The solid-state weathering velocity is the rate at which the weathering front propagates through the regolith and the solute weathering velocity is equivalent to the rate of pore water infiltration. These relationships provide a unifying approach to calculating both solid and solute weathering rates from the respective ratios of the weathering velocities and gradients. Contemporary weathering rates based on solute residence times can be directly compared to long-term past weathering based on changes in regolith composition. Both rates incorporate identical parameters describing mineral abundance, stoichiometry, and surface area.
Weathering gradients were used to calculate biotite weathering rates in saprolitic regoliths in the Piedmont of Northern Georgia, USA and in Luquillo Mountains of Puerto Rico. Solid-state weathering gradients for Mg and K at Panola produced reaction rates of 3 to 6×10−17 mol m−2 s−1 for biotite. Faster weathering rates of 1.8 to 3.6×10−16 mol m−2 s−1 are calculated based on Mg and K pore water gradients in the Rio Icacos regolith. The relative rates are in agreement with a warmer and wetter tropical climate in Puerto Rico. Both natural rates are three to six orders of magnitude slower than reported experimental rates of biotite weathering. 相似文献
Dissolution rates were calculated for a range of grain sizes of anorthite and biotite dissolved under far from equilibrium conditions at pH 3, T = 20 °C. Dissolution rates were normalized to initial and final BET surface area, geometric surface area, mass and (for biotite only) geometric edge surface area. Constant (within error) dissolution rates were only obtained by normalizing to initial BET surface area for biotite. The normalizing term that gave the smallest variation about the mean for anorthite was initial BET surface area. In field studies, only current (final) surface area is measurable. In this study, final geometric surface area gave the smallest variation for anorthite dissolution rates and final geometric edge surface area for biotite dissolution rates. 相似文献
The Middle-Lower Yangtze River Valley Metallogenic Belt (MLYB) is located on the northern margin of the Yangtze Plate (Eastern China). Ore deposits in the belt are mainly clustered in seven ore districts, and are closely associated with Mesozoic intermediate-felsic magmatic rock. Among the seven ore districts, the Luzong and Ningwu districts host large-scale iron resources in volcanic basins. The Makou magnetite-apatite deposit in the southern Luzong Basin was previously interpreted to be related to a quartz syenite porphyry. In this study, we conducted field geological studies and determined the age and geochemistry of the Makou intrusive rocks. Petrography and electron probe micro analysis (EPMA) indicated that the Makou ore-hosting rocks have intense albite alteration. The wallrock alteration is spatially restricted, and comprises albite alteration (Stage I), magnetite mineralization (Stage II), quartz-sulfide alteration (Stage III) and carbonate alteration (Stage IV) stages. Fluid inclusions in syn-mineralization apatite homogenized at 252.2–322.6 °C, which slightly lower than is typical for magnetite-apatite deposits in the region. Field study revealed that the quartz syenite porphyry at Makou disrupted the orebodies along clear-cut intrusive contacts, and that the quartz syenite porphyry does not contain iron mineralization, suggesting it has no direct genetic relationship with the iron mineralization. The ore-hosting albitite and ore-forming biotite diorite have LA-ICP-MS zircon U-Pb ages of 129.6 ± 1.2 Ma and 131.2 ± 3.3 Ma, respectively, and the iron mineralization was dated by mass spectrometer phlogopite 40Ar-39Ar at 130.76 ± 0.77 Ma. We propose that the Makou magnetite-apatite deposit is genetically related to the biotite diorite, rather than to the quartz syenite porphyry in the mine pit. The biotite diorite closely resembles intrusions related to magnetite-apatite deposits elsewhere in the region. 相似文献
Crystallization experiments have been conducted in the system Na2O–K2O–MgO–FeO–Al2O3–SiO2–H2O (with 4% normative corundum) in order to constrain the stability of biotite as a function of water activity and the Mg# of biotite [Mg/(Mg +Fetotal)] in equilibrium with peraluminous granitic melts. The temperature at which biotite breakdown starts is strongly dependent on the Mg# of biotite. At 500 MPa, the temperature of biotite breakdown to form orthopyroxene increases from 750 °C to 830 °C, as the Mg# of biotite increases from 0.4 to 0.5. Considering that the system investigated is relevant for Ca-poor peraluminous biotite-bearing rocks (metapelites), the biotite dehydration curves obtained are used to discuss the melting reactions and the temperatures that lead to the formation of two distinct types of two-mica granites found in the South Bohemian batholith (specifically the Eisgarn and Deštná granites). The phase relationships were determined experimentally for the composition of these two granites in order to constrain the composition of the biotite in equilibrium with the melt in the protoliths. We demonstrate that Eisgarn granitic melts may have been generated at temperatures in the range 830–850 °C from melting reactions involving biotite with a Mg# up to 0.5 as a reactant. In contrast, Deštná granitic melts cannot have been generated from dehydration melting reactions involving biotite. 相似文献