A new sodian-beryllian cordierite from Soto,Argentina, and the relationship between distortion index,Be content,and state of hydration     

W. Schreyer  C. E. Gordillo  G. Werding 《Contributions to Mineralogy and Petrology》1979,70(4):421-428

In a cordieritite marking the contact of a granite massif one of the large porphyroblasts of cordierite was found to contain relatively high amounts of BeO (0.93 wt.%) and Na₂O (1.25 wt.%), while others are very poor in these components. Na and Be were introduced following the substitution NaBeAl. Like in other sodian beryllian cordierites the distortion index is low (0.12), and a negative correlation between and Be contents is established using additional data from the literature.Dehydration of NaBe-cordierites through heating consistently leads to increasing , and subsequent hydrothermal rehydration of the Soto sample reestablished low . This behavior is consistent with that implied by the model of Stout (1975) which, however, does not apply to the pure system Mg-cordierite-water. Nevertheless it is not certain that the unusual behavior of NaBe-cordierites is due to hydrogen bonding of H₂O molecules within the structural channels of cordierite to oxygens of the framework, although the Type II water molecules occurring exclusively in alkali-bearing cordierites and having their H-H vectors parallel [010] (Goldman et al. 1977) would seem mechanically fitter to have this effect than the Type I water with H-H parallel [001] as proposed by Stout (1975). An alternative explanation of this dehydration/rehydration behavior implies positional shifts of sodium within the channels depending on whether or not water is available.  相似文献   

Synthetic dumortierite: its PTX-dependent compositional variations in the system Al2O3-B2O3-SiO2-H2O     

Günter Werding  Werner Schreyer 《Contributions to Mineralogy and Petrology》1990,105(1):11-24

Dumortierite, generally simplified as Al₇BSi₃O₁₈, was synthesized in the pure system Al₂O₃–B₂O₃–SiO₂–H₂O (ABSH) using gels with variable Al/Si ratios mixed with H₃BO₃ and H₂O in known proportions as starting materials. Synthesis conditions ranged from 3 to 5 and 15 to 20 kbar fluid pressure at 650° to 880°C. On the basis of analyses, synthetic dumortierite shows relatively narrow homogeneity ranges with regard to Al/Si which, however, vary as a function of pressure: at low pressures (3–5 kbar) Al/Si is 2.77–2.94 versus 2.33–2.55 at high pressures (15–20 kbar). Outside of these homogeneity limits, dumortierite was found to coexist with quartz or corundum, depending on the starting composition. Whereas synthetic dumortierite invaribly contains 1.0 boron atom per formula unit (p.f.u.) based on 18 oxygens, the water contents vary drastically as a function of pressure and temperature (1.32–2.30 wt.% H₂O or 0.85–1.47 H p.f.u.). H₂O is an essential component in dumortierite. Structural formulae based on complete chemical analyses of the dumortierites synthesized reveal that there is invariably an Si-deficiency against the ideal number of 3.0 p.f.u. In the calculation procedure used here, this deficiency is balanced by assuming tetrahedral Al. The remaining Al, taken to occupy the octahedral sites, is always below the ideal number of 7.0 p.f.u. Charge-balancing the structure with the hydrogen found analytically leads to two different mechanisms of H incorporation: (1) 3H⁺ + octahedral vacancy for Al^[6]; (2) H⁺ + tetrahedral Al for Si^[4]. Dumortierite synthesized at high fluid pressure contains little Al^[4] and, thus, little H⁺ of type 2; its hydrogen is predominantly present as type 1. Conversely, dumortierite formed at low fluid pressures is high in Al^[4] and hydrogen type 2. The amounts of hydrogen type 1 in low-pressure dumortierites decrease with rising temperatures of synthesis. Typical structural formulae are: (Al_6.670.33)[Al_0.49Si_2.51–O_13.53(OH)_1.47](BO₃) for a low-pressure product, and (Al_6.680.32)[Al_0.09Si_2.91O_13.94(OH)_1.06](BO₃) for a high-pressure product. Independently of the synthesis conditions, dumortierite was found always to be orthorhombic, with b₀/a₀ deviating slightly, but significantly from the valid for hexagonal lattice geometry. As a function of increasing Al/Si in the synthetic crystals, their a₀, c₀, and V₀ rise, whereas b₀ decreases. Thus b₀/a₀ decreases most sensitively with rising Al/Si and also with growing Al^[4]. More experimentation is required before the compositional variations of dumortierite found here can be applied successfully to geothermobarometry of natural rocks.  相似文献   

The Boreholes of the Sea Urchin Genus Echinometra (Echinodermata: Echinoidea: Echinometridae) as a Microhabitat in Tropical South America*     

Sabine Schoppe  Bernd Werding 《Marine Ecology》1996,17(1-3):181-186

Abstract. Members of the genus Echinometru (Echinoideu: Echinometridue) inhabit hard substrata in shallow waters where they live in self-excavated dwellings. Boring by Echinometru spp. causes a secondary structure of the surface, thus forming additional microhabitats. In this study the effects of boring activities of Echinometru lucunter (L.) along the Caribbean coast of Colombia and of Echinometra vunbrunri A. Agassu in the Colombian Pacific is examined. Several species inhabit the boreholes occupied by these urchins. The associates live underneath the echinoid on the bottom of the borehole, where they find shelter from exposure and predators. The co-inhabitants of E. lucunter include the porcellanid Clusroroechus vunderhorsri (Schmitt ), the recently described brit-tlestar Ophiorhrix synoecim (Schoppe ), and the clingfish Acyrrus rubiginosus (Poey ). The species co-occumng with E. vunbrunti include the porcellanid crab Clusroroechus gorgonensis Werding amp; Haig and the clingfish Arcos decoris Briggs . With the exception of A. decoris, all of these species are obligatorily associated with the Echinomerra host.  相似文献   

Alkali-free tourmaline in the system MgO-Al₂O₃-B₂O₃-SiO₂-H₂O     

Günter Werding  Werner Schreyer 《Geochimica et cosmochimica acta》1984,48(6):1331-1344

An end member of the tourmaline series with a structural formula □(Mg₂Al)Al₆(BO₃)₃[Si₆O₁₈](OH)₄ has been synthesized in the system MgO-Al₂O₃-B₂O₃-SiO₂-H₂O where it represents the only phase with a tourmaline structure. Our experiments provide no evidence for the substitutions Al → Mg + H, Mg → 2H, B + H → Si, and AlAl → MgSi and we were not able to synthesize a phase “Mg-aluminobuergerite” characterized by Mg in the (3a)-site and a strong (OH)-deficiency reported by Rosenberg and Foit (1975). The alkali-free tourmaline has a vacant (3a)-site and is related to dravite by the □ + Al for Na + Mg substitution. It is stable from at least 300°C to about 800°C at low fluid pressures and 100% excess B₂O₃, and can be synthesized up to a pressure of 20 kbars. At higher temperatures the tourmaline decomposes into grandidierite or a boron-bearing phase possibly related to mullite (“B-mullite”), quartz, and unidentified solid phases, or the tourmaline melts incongruently into corundum + liquid, depending on pressure. In the absence of excess B₂O₃ tourmaline stability is lowered by about 60°C. Tourmaline may coexist with the other MgO-Al₂O₃-B₂O₃-SiO₂-H₂O phases forsterite, enstatite, chlorite, talc, quartz, grandidierite, corundum, spinel, “B-mullite,” cordierite, and sinhalite depending on the prevailing PTX-conditions.The (3a)-vacant tourmaline has the space group R3m with $\text{a =15.90}\text{A}\text{?}$, $\text{c = 7.115}\text{A}\text{?}$, and $\text{V = 1557.0}\text{A}\text{?}{}^3$. However, these values vary at room temperature with the pressure-temperature conditions of synthesis by $\text{±0.015}\text{A}\text{?}\text{in a}$, $\text{±0.010}\text{A}\text{?}\text{in c}$, and $\text{±4.0}\text{A}\text{?}{}^3\text{in V}$, probably as a result of MgAl order/disorder relations in the octahedral positions. Despite these variations intensity calculations support the assumed structural formula. Refractive indices are n_o = 1.631(2), n_E = 1.610(2), Δn = 0.021. The infrared spectrum is intermediate between those of dravite and elbaite. The common alkali and calcium deficiencies of natural tourmalines may at least partly be explained by miscibilities towards (3a)-vacant end members. The apparent absence of (3a)-vacant tourmaline in nature is probably due to the lack of fluids that carry boron but no Na or Ca.  相似文献   

Lithium in NaBe-cordierites from El Peñón,Sierra de Córdoba,Argentina     

Gordillo  C. E.  Schreyer  W.  Werding  G.  Abraham  K. 《Contributions to Mineralogy and Petrology》1985,90(1):93-100

NaBe-cordierites (Fe/(Fe+Mn+Mg)=0.49–0.57) with BeO contents up to 1.16 weight % and additional Li₂O contents up to 0.21 wt.% occur in cordierite-apatite-uraninite-muscovite-biotite-chlorite-feldspar-quartz nodules within pegmatites penetrating gneissic roof pendants of a lower Palaeozoic granite batholith. Occasional small crystals of beryl are interpreted to coexist stably with unaltered cordierite. Be and Li are incorporated in cordieriteaccording to the substitutions Na^[Channel] + Be^[4] Al^[4] and Na^[Ch]+Li_[6]R^2+[6], respectively. The coexisting phyllosilicates do apparently not contain appreciable amounts of Li. According to powder IR-data, the analyzed water contents of the cordierites are dominantly of type II, and there is also little CO₂. Their distortion indices are rather low (0.121–0.145) and so are their optic angles (2V=50-51_°). Considering all eleven NaBeLi-cordierites known thus far there is a strong positive correlation between Na and (Be+Li) with a slope close to 1.0. However, there is virtually no correlation between Be and Li, their incorporation into cordierite depending on the local geochemical environment. A strong negative correlation exists between the distortion indices of the NaBeLi-cordierites and their Be contents. Li has a disturbing influence on this relationship, and the versus Na correlation is also statistically worse than versus Be.Deceased December 20, 1984  相似文献   

“Pseudosinhalite”, a new hydrous MgAl-borate: synthesis, phase characterization, crystal structure, and PT-stability     

Peter Daniels  Sigrid Krosse  Günter Werding  Werner Schreyer 《Contributions to Mineralogy and Petrology》1997,128(2-3):261-271

The new synthetic phase Mg₂Al₃O[BO₄]₂(OH) provisionally named “pseudosinhalite” is optically, chemically, and structurally similar to the mineral sinhalite, MgAl[BO₄], isostructural with forsterite. It grows hydrothermally from appropriate bulk compositions in the range 4–40?kbar at temperatures that increase with pressure (～650?→?900?°C), and it breaks down at higher temperatures to sinhalite?+?corundum?+?H₂O. At P?≥?20?kbar single-phase products of euhedral twinned crystals could often be obtained. Pseudosinhalite is monoclinic with a?=?7.455 (1) Å, b?=?4.330 (1) Å, c?=?9.825 (2) Å, β?=?110.68 (1)°, and space group P2₁/c. Crystal structure analysis reveals that pseudosinhalite is also based on hexagonal close packing (hcp) of oxygen atoms with Mg and Al in octahedral and B in tetrahedral coordination. In pseudosinhalite the winged octahedral chains in the plane of hcp are not straight as in sinhalite but have a zigzag, 3-repeat period (Dreierkette), and only 1/10 instead of 1/8 of all tetrahedral sites are filled by boron. Hydrogen is located at a split position between two oxygen atoms O5—O5, which are only 2.550 Å apart and thus generate strong hydrogen bonding. This may be responsible for the absence of an hydroxyl absorption band between 2800?cm^?1 and 3500?cm^?1 in the powder IR spectrum. The equilibrium breakdown curve of pseudosinhalite to form sinhalite, corundum, and water was determined by bracketing experiments to pass through 10?kbar, 745?°C and 35?kbar, 950?°C, giving a slope of about 8?°C/kbar, similar to dehydration curves of some silicates at high pressure. In nature pseudosinhalite could have been misidentified as sinhalite. A possible appearance, like sinhalite in boron-rich skarns, would require more aluminous bulk compositions than for sinhalite at relatively low temperatures. However, pseudosinhalite might also form as a hydrous alteration product of sinhalite at low temperatures, perhaps in association with szaibelyite, MgBO₂(OH).  相似文献