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931.
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936.
P. T. Leat R. N. Thompson M. A. Morrison G. L. Hendry A. P. Dickin 《Contributions to Mineralogy and Petrology》1991,107(3):310-327
The Yampa volcanic field (late Miocene) consists of about 70 outcrops of monogenetic cinder cones, lavas, dykes, volcanic necks and hydrovolcanic pyroclastic deposits and is situated in the most northerly part of the Rio Grande rift. Contemporaneous extension in this part of the rift was small, but there is geological and geophysical evidence that, by the late Miocene, the area was underlain by hot asthenosphere convected by the Yellowstone mantle plume. The Yampa rocks are mafic and chemically diverse, including basanites, alkali basalts, potassic trachybasalts, hawaiites and shoshonites. About half the rocks bear the xenocryst suite feldspar, pyroxene, Fe–Ti oxide, amphibole, biotite. There is a tendency for xenocryst-free rocks to be the most mafic, interpreted to indicate that the xenocrysts are cognate, and represent cumulate material from fractional crystallization of the magmas in deep crustal magma chambers. The elemental and isotopic (Nd and Sr) variations can be modelled by mixing variable proportions of partial melts of local lithospheric mantle with an OIB end-member formed by partial melting of asthenosphere. The OIB end-member appears to have the elemental and isotopic composition of typical Northern Hemisphere OIB, in particular the plume-derived basanites of Loihi seamount, Hawaii. The OIB end-member at Yampa is interpreted to have been derived from mantle convected in the Yellowstone mantle plume. 相似文献
937.
938.
Remineralization Ratios in the Subtropical North Pacific Gyre 总被引:2,自引:0,他引:2
Yuan-Hui Li David M. Karl Christopher D. Winn Fred T. Mackenzie Kathleen Gans 《Aquatic Geochemistry》2000,6(1):65-85
Based on a new mixing model of two end-members, the water column remineralization ratios of P/N/Corg - O2 = 1/13 ± 1/135 ± 18/170 ± 9 are obtained for the Hawaii Ocean Time-series (HOT) data set at station ALOHA. The traditional Redfield ratios of P/N/Corg/–O2 = 1/16/106/138 have standard deviations of more than 50%, when they are based on the average composition of phytoplankton. Apparently, the remineralization processes in the water column have smoothed out the observed large variability of plankton compositions. A new molar formula for the remineralized plankton may be written as 135H280O105N13P or C25(CH2O)101(CH4)9(NH3)13(H3PO4). Oxidation of this formula results inC25(CH2O)101(CH4)9(NH3)13(H3PO4) + 170O2 135CO2 + 132H2O + 13NO3
- + H2PO4
- + 14H+.For comparison, remineralization using Redfield's formula gives:(CH2O)106(NH3)16(H3PO4) + 138O2 106CO2 + 122H2O + 16NO3
-+ H2PO4
- + 17H+ 相似文献
939.
I. P.?SwainsonEmail author M. T.?Dove D. C.?Palmer 《Physics and Chemistry of Minerals》2003,30(6):353-365
Infrared and Raman spectra of cristobalite are presented as a function of temperature through the phase transition. The modes are assigned and the assignments compared to those of earlier workers. The compatibility of modes at the G-point of the a-phase with the X and G-points of the ß-phase is given. In the transition region of ca. 500–550 K, smooth changes in intensity, frequency and linewidths are seen in many modes, indicative of coexistence of a- and ß-forms. 相似文献
940.
E. M. Chamorro Pérez I. Daniel J.-C. Chervin P. Dumas J. D. Bass T. Inoue 《Physics and Chemistry of Minerals》2006,33(7):502-510
High-pressure synchrotron infrared (IR) absorption spectra were collected between 650 and 4,000 cm−1 at ambient temperature for hydrous Mg-ringwoodite (γ-Mg2SiO4) up to 30 GPa. The main feature in the OH− stretching region is an extremely broad band centred at 3,150 cm−1. The hydrogen bond is strong for most protons and the most probable site for protonation is the tetrahedral edge. With increasing pressure, this band shifts downward while decreasing its integrated intensity until disappearance at a pressure of 25 GPa. Only one band at 2,450 cm−1 and an absorption plateau persist with a maximum wavenumber of 3,800 cm−1. This behaviour is reversible upon pressure release. We interpret this as a second-order phase transition occurring in hydrated Mg-ringwoodite at high pressure (beyond ∼ 25 GPa). This result is compatible with the observation by Kleppe et al. (Phys Chem Miner 29:473–476, 2002a) who suggested the presence of Si–O–Si linkages and/or partial increase in the coordination of Si. Beyond the phase transition, the protons are delocalized and their environment on the ringwoodite structure is probably quite different from that at low pressure. Data obtained in situ at high pressures and temperatures are needed to better understand the effect of protonation on the structure and to better constrain this phase transition. 相似文献