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Cummingtonites

Cummingtonite (Mg,Mn,Fe)7Si8022(OH,E,Cl)2 CALCIC AMPHIBOLES P2Jm C2lm... [Pg.300]

Table 5.44 Compositions (in weight %) of some natural amphiboles (from Deer et al., 1983) (1) = anthophyllite from a serpentinite (2) gedrite from a gedrite-kyanite-garnet paragenesis (3) cummingtonite from a oligoclase-biotite schist (4) common hornblende from a tonalite (5) pargasite from a metamorphic limestone (6) basaltic hornblende from a lathe (7) glaucophane from a glaucophane schist. ... Table 5.44 Compositions (in weight %) of some natural amphiboles (from Deer et al., 1983) (1) = anthophyllite from a serpentinite (2) gedrite from a gedrite-kyanite-garnet paragenesis (3) cummingtonite from a oligoclase-biotite schist (4) common hornblende from a tonalite (5) pargasite from a metamorphic limestone (6) basaltic hornblende from a lathe (7) glaucophane from a glaucophane schist. ...
Heating experiments on P2ilm amphiboles (cummingtonite) show transition to the C2lm polymorph at low T (50 to 100 °C Prewitt et ah, 1970 Sueno et ah, 1972) in analogy to the behavior of pigeonitic pyroxenes (P2jlc), which show transition to the form C2/c (cf. section 5.4.3). Phase stability limits are markedly conditioned by the chemistry of the system and, particularly, by the partial pres-... [Pg.308]

Site M4 is occupied in one of the two components by a cation with a large ionic radius (e.g., Ca ) and by cations of much shorter radii (e.g., Mg and Fe ) in the other component (hornblende-cummingtonite or actinolite-cummingtonite). [Pg.313]

Site A is partially or fully occupied in one component and completely empty in the other (hornblende-actinolite, hornblende-cummingtonite, gedrite-anthophyllite, richterite-riebeckite). [Pg.314]

To our knowledge, direct experimental data on amphibole mixtures have been obtained only for the (pseudo)binary system actinolite-cummingtonite (Cameron, 1975) at Ptotai = -Phjo = 2 kbar and for the (pseudo)binary system tremolite-pargasite at Ptotai = PhjO = 1 kbar (Oba, 1980). In both cases, an extended miscibility gap (or solvus field in the second case), is evident at low T(i.e., 600 to 800 °C), which is indicative of strong positive interactions in the solid mixtures. Unmixing of other compositional terms is also evident in microprobe investigations (see Ghose, 1982 for an appropriate discussion). [Pg.315]

Information on amphibole mixing properties comes from intracrystalline and intercrystalline Fe +-Mg distribution studies. Mueller (1960, 1961) described the coexistence of actinolite and cummingtonite in ferriferous metamorphosed bands of Bloom Lake (Quebec, Canada) based on the exchange equilibrium... [Pg.315]

Figure 539 Intracrystalline distribution of Fe +-Mg + between Y(Ml, M2, M3) and M4 sites in natural cummingtonites. (A) Regular site-mixing model. (B) Ideal site-mixing model. (C) Arrhenius plot of equilibrium constant. Figure 539 Intracrystalline distribution of Fe +-Mg + between Y(Ml, M2, M3) and M4 sites in natural cummingtonites. (A) Regular site-mixing model. (B) Ideal site-mixing model. (C) Arrhenius plot of equilibrium constant.
We recall to this purpose that ideal site mixing does not necessarily mean that the mixture as a whole is ideal, but that the intracrystalline site distribution may be described by a constant (without the necessity of introducing site-interaction parameters cf equation 5.109, for example). Generally speaking, if the adopted constant differs from 1 (as in the case of sodic amphiboles in figure 5.40 and of cummingtonites in figure 5.39), the mixture as a whole is obviously nonideal because site permutability does not reach the maximum value attained by the ideal condition (cf section 3.8.1). [Pg.318]

Cameron K. L. (1975). An experimental study of actinolite-cummingtonite phase relations with notes on the synthesis of Fe-rich anthophyllite. Amer. Mineral, 60 375-390. [Pg.823]

Hafner S. S. and Ghose S. (1971). Iron and magnesium distribution in cummingtonites. Zeit. Kristallog., 133 301-326. [Pg.833]

Klein C. Jr. (1964). Cummingtonite-grunerite series A chemical optical and X-ray study. Amer. Mineral, 49 963-982. [Pg.839]

Presnall D. C. (1969). The geometrical analysis of partial fusion. Amer. Jour. Scl, 267 1178-1194 Prewitt C. T, Papike J. J. and Ross M. (1970). Cummingtonite. A reversible, non-quenchable transition from P2i/m to C2/m symmetry. Earth. Planet. Scl Letters, 8 448-450. [Pg.849]

Viswanathan K., and Ghose S. (1965). The effect of Mg -Fe substitution on the cell dimension of cummingtonite. Amer. Mineral, 30 1106-1112. [Pg.858]

Intermediate members of the series that contain both Mg and Fe, may be identified as iron-rich cummingtonite, for example. Alternatively, a fibrous species whose composition and structure resembles grunerite occurs in South Africa. It is mined as asbestos and known commercially as amosite. Amosite is a varietal mineral name that has been used in the trade to describe mineral materials within the cummingtonite-grunerite series. The name is an acronym for asbestos mines of South Africa. Because it is not a proper mineral name, it may not be found in lists of minerals in standard miner-alogical texts. [Pg.25]

Amosite A commercial term for a type of amphibole-asbestos from South Africa consisting chiefly of fibrous members of the cummingtonite-grunerite series. Variable amounts of several fibrous members of the amphibole group and other minerals may be included in a particular sample. The name is an acronym derived from asbestos mines of 5outh Africa. [Pg.191]

Cummingtonite-asbestos The type of amphibole-asbestos composed of the mineral cummingtonite. [Pg.194]


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See also in sourсe #XX -- [ Pg.33 , Pg.34 , Pg.202 , Pg.233 , Pg.234 , Pg.237 ]




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Cummingtonite

Cummingtonite-asbestos

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