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Recommended nomenclature for the sapphirine and surinamite groups (sapphirine supergroup)

机译:蓝宝石和苏里南组的推荐命名法(蓝宝石超组)

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Minerals isostructural with sapphirine-1A, sapphirine-2M, and surinamite are closely related chain silicates that pose nomenclature problems because of the large number of sites and potential constituents, including several (Be, B, As, Sb) that are rare or absent in other chain silicates. Our recommended nomenclature for the sapphirine group (formerly aenigmatite group) makes extensive use of precedent, but applies the rales to all known natural compositions, with flexibility to allow for yet undiscovered compositions such as those reported in synthetic materials. These minerals are part of a polysomatic series composed of pyroxene or pyroxene-like and spinel modules, and thus we recommend that the sapphirine supergroup should encompass the polysomatic series. The first level in the classification is based on polysome, i.e. each group within the supergroup corresponds to a single polysome. At the second level, the sapphirine group is divided into subgroups according to the occupancy of the two largest M sites, namely, sapphirine (Mg), aenigmatite (Na), and rhonite (Ca). Classification at the third level is based on the occupancy of the smallest M site with most shared edges, Ml, at which the dominant cation is most often Ti (aenigmatite, rhonite, makarochkinite), Fe~(3+) (wilkinsonite, dorrite, hogtuvaite) or Al (sapphirine, khmaralite); much less common is Cr (krinovite) and Sb (welshite). At the fourth level, the two most polymerized T sites are considered together, e.g. ordering of Be at these sites distinguishes hogtuvaite, makarochkinite and khmaralite. Classification at the fifth level is based on X_(Mg) = Mg/(Mg + Fe2+) at the M sites (excluding the two largest and M7). In principle, this criterion could be expanded to include other divalent cations at these sites, e.g. Mn. To date, most minerals have been found to be either Mg-dominant (X_(Mg) > 0.5), or Fe~(2+)-dominant (X_(Mg) < 0.5), at these M sites. However, X_(Mg) ranges from 1.00 to 0.03 in material described as rhonite, i.e. there are two species present, one Mg-dominant, the other Fe~(2+)-dominant. Three other potentially new species are a Mg-dominant analogue of wilkinsonite, rhonite in the Allende meteorite, which is distinguished from rhonite and dorrite in that Mg rather than Ti or Fe~(3+) is dominant at M7, and an Al-dominant analogue of sapphirine, in which Al > Si at the two most polymerized T sites vs. Al < Si in sapphirine. Further splitting of the supergroup based on occupancies other than those specified above is not recommended.
机译:蓝宝石1A,蓝宝石2M和苏里南石等结构的矿物是密切相关的链状硅酸盐,由于其大量的位点和潜在的成分,其中包括几种稀有或不存在的元素(Be,B,As,Sb),它们引起了命名学上的问题。其他链状硅酸盐。我们推荐的蓝宝石族(以前为钠铅矿族)的命名法广泛使用了先例,但将罗尔斯应用于所有已知的天然成分,并具有灵活性,可以允许尚未发现的成分,例如合成材料中报道的那些。这些矿物是由辉石或类似辉石的模块和尖晶石模块组成的多体系列的一部分,因此,我们建议蓝宝石超族应包含多体系列。分类中的第一级基于多核糖体,即超组内的每个基团对应于单个多核糖体。在第二级,根据两个最大的M位置(蓝宝石(Mg),铜钠锰矿(Na)和菱锰矿(Ca))的占有率,将蓝宝石族划分为亚组。第三层的分类基于具有最多共享边缘的最小M位置的占有率M1,在该位置上,主要的阳离子最常见的是Ti(锂镁矾石,rhonite,锰铁钾锰矿),Fe〜(3 +)(wilkinsonite,软锰矿,钙铝榴石)或铝(蓝宝石,khmaralite);铬(钾锰铁矿)和锑(钨铁矿)要少得多。在第四级,将两个聚合度最高的T位点一起考虑,例如在这些位置上的Be的顺序区分了白铁矿,马卡奇石和khmaralite。第五级的分类基于M个位置(不包括两个最大的M7)的X_(Mg)= Mg /(Mg + Fe2 +)。原则上,该标准可以扩展到在这些位点上包括其他二价阳离子,例如。锰迄今为止,已发现在这M个位置上大多数矿物以Mg为主(X_(Mg)> 0.5)或Fe〜(2+)为主(X_(Mg)<0.5)。然而,在描述为菱锰矿的材料中,X_(Mg)的范围为1.00至0.03,即存在两种物质,一种为Mg-为主,另一种为Fe〜(2 +)-为主。其他三个潜在的新物种是威金森铁矿的镁占主导地位的类似物,阿连德陨石中的菱铁矿,其与菱锰矿和滑铁矿的区别在于,镁在M7而不是Ti或Fe〜(3+)占主导地位,而Al占优势蓝宝石的类似物,其中两个聚合度最高的T位点处的Al> Si相对于蓝宝石中的Al

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