The Composition and Origin of the Connemara Dolomitic Marbles and Ophicalcites, Ireland

The Connemara ophicalcites and associated marbles contain varyingproportions of calcite, dolomite, tremolitic amphibole, serpentinizedolivine, diopside, humite, phlogopite, clinochlore, and quartz.They formed from a chemically precipitated 'primary' dolomitewith a small amount of mica and clay minerals in which muchof the trace and minor element content of the rock, e.g. Al,Fe, Ti, Zn, Ni, Cr, Zr, K, Rb, and rare earths was concentrated.The rock was probably silicified after deposition, possiblyduring metamorphism, and was probably not deposited with majoradmixed detrital quartz or feldspar. The formation during metamorphismof complementary segregated layers rich in either olivine (Fo_98±2)or calcite resulted from important chemical changes controlledby the composition of the stable metamorphic minerals, i.e.those for which solution concentrations exceeded the solubilityproduct for the pore fluid. The mineralogy influenced the localconcentrations of both major and trace elements and emphasizesthe importance of solutions and the stable metamorphic mineralogyin manipulating the composition of some metamorphic rocks. Somecriteria for recognizing segregated layers in metamorphic rocksare given. Serpentinization was probably by addition of water and silicaand not by movement of Fe or Mg. Chemical analyses of forty-threesamples each for twenty-six oxides and elements are given andthe first occurrence of humite in Connemara is reported.     

The Composition and Origin of the Connemara Dolomitic Marbles and Ophicalcites, Ireland

The Connemara ophicalcites and associated marbles contain varyingproportions of calcite, dolomite, tremolitic amphibole, serpentinizedolivine, diopside, humite, phlogopite, clinochlore, and quartz.They formed from a chemically precipitated ‘primary’dolomite with a small amount of mica and clay minerals in whichmuch of the trace and minor element content of the rock, e.g.Al, Fe, Ti, Zn, Ni, Cr, Zr, K, Rb, and rare earths was concentrated.The rock was probably silicified after deposition, possiblyduring metamorphism, and was probably not deposited with majoradmixed detrital quartz or feldspar. The formation during metamorphismof complementary segregated layers rich in either olivine (Fo_98?2)or calcite resulted from important chemical changes controlledby the composition of the stable metamorphic minerals, i.e.those for which solution concentrations exceeded the solubilityproduct for the pore fluid. The mineralogy influenced the localconcentrations of both major and trace elements and emphasizesthe importance of solutions and the stable metamorphic mineralogyin manipulating the composition of some metamorphic rocks. Somecriteria for recognizing segregated layers in metamorphic rocksare given. Serpentinization was probably by addition of water and silicaand not by movement of Fe or Mg. Chemical analyses of forty-threesamples each for twenty-six oxides and elements are given andthe first occurrence of humite in Connemara is reported.     

Regional Metasomatism and the Geochemistry of the Dalradian Metasediments of Connemara, Western Ireland

Based on 225 analyses of quartzites, siliceous granoblastites,calc silicate rocks, calcite and dolomite marbles, including120 analyses of pelites and semipelites, sedimentary trendsof chemical variation are identified in staurolite and sillimanitegrade rocks. The correlation of original clay mineral contentwith Ti, Fe, K, Rb, Y, Nb, Ca, Ni, Ga, Zn and probably Ba andMn is shown. A similar clay mineral (whose composition is calculated)was added to all the sediments except the quartz-rich sandstones,now quartzites. This pattern appears to be general for mostsediments, based on crustal averages. The form of the originaladdition of Sr in the sediments might be identified as eithercarbonate or feldspar by a Ca vs. Sr plot. The southern pelites in a 2–4 km peripheral zone to theConnemara orthogneisses and migmatites have been metasomatized.The crude order of elemental enrichment from the elements increasedthe most to those increased the least relative to the same stratigraphicalhorizons in the north is: Mn, Ba, Th, Cu, Ca, Sr, Y, Pb, Zn,Pr, Ge, Nd, La, Mg, S, Ce, Rb, Sm, Ti, Na, K and Ga while Si,Al, Cr, Ni, Co, Fe and P are unchanged or removed. The sourceof the material added is postulated to be the water-rich residualfraction of the migmatitic quartz diorite gneiss, the transportbeing by movement of a water-rich fluid out of the migmatites,the fixation being mainly in biotite and new, more calcic, plagioclaseporphyroblasts, there being a positive correlation between elementenrichment and ionic radius.     

Aluminous reaction textures in orthoamphibole-bearing rocks: the pressure–temperature evolution of the high-grade Proterozoic of the Bamble sector, south Norway

Aluminous reaction textures in orthoamphibole-bearing rocks from the Froland area, Bamble, south Norway, record the prograde pressure–temperature path of the high-grade Kongsbergian Orogeny (c. 1600–1500 Ma) and the low–mid amphibolite facies overprint during the Sveconorwegian Orogeny (c. 1100–1000 Ma). The rocks contain anthophyllite/gedrite, garnet, cordierite, biotite, quartz, andalusite, kyanite, Cr-rich staurolite, tourmaline, ilmenite, rutile and corundum in a variety of parageneses. The P–T path is deduced from petrographic observations, mineral chemistry and zoning, geothermometry and (N)FMASH equilibria. The results indicate the sequence of metamorphic stages outlined below. (a) An M₁ phase characterized by the presence of strongly deformed andalusite, gedrite and tourmaline. (b) An M₂ phase with the development of kyanite after andalusite and the growth of staurolite associated with strong Na–Al–Mg zoning in orthoamphibole, indicating an increase in pressure (4 8 kbar) and temperature (500° 650°C). (c) Pressure decrease at high P (6–7 kbar) and high T (600–700 °C) during M_3a with the production of cordierite ° Corundum between kyanite, staurolite and orthoamphibole and cordierite growth between corundum and orthoamphibole. (d) Temperature increase to 740 ± 60 °C and 7 kbar; static growth of garnet (M_3b) at the metamorphic climax (peak T). The heat supply necessary to explain the temperature increase between the M_3a and M_3b phases is correlated with synkinematic enderbitic–charnockitic and basic intrusions in the Arendal granulite facies terrain. (e) M_3b metamorphic conditions were followed by an initial isobaric cooling path (early M₄) and late-stage pressure decrease (late M₄). Early M₄ conditions of 6–7 kbar and 550–600 °C, assuming P_H2O < P_total are indicated by a retrograde talc–kyanite–quartz assemblage in late quartz–cordierite veins. Late M₄ conditions of 3–4 kbar and 420–530 °C are inferred from a kyanite–andalusite–chlorite–quartz assemblage in vein-cordierite. The M₁–M₃ stages are interpreted as being the result of the same metamorphic P–T path, which was caused by both tectonic and magmatic thickening. A prolonged crustal residence time is proposed for the Bamble sector before uplift during the later stages of M₄ occurred.