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Phyllosilicates in hydrothermally altered basalts from DSDP Hole 504B, Leg 83 — a TEM and AEM study

dc.contributor.authorPeacor, Donald R.en_US
dc.contributor.authorShau, Yen-Hongen_US
dc.date.accessioned2006-09-11T18:49:07Z
dc.date.available2006-09-11T18:49:07Z
dc.date.issued1992-10en_US
dc.identifier.citationShau, Yen-Hong; Peacor, Donald R.; (1992). "Phyllosilicates in hydrothermally altered basalts from DSDP Hole 504B, Leg 83 — a TEM and AEM study." Contributions to Mineralogy and Petrology 112(1): 119-133. <http://hdl.handle.net/2027.42/47300>en_US
dc.identifier.issn1432-0967en_US
dc.identifier.issn0010-7999en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47300
dc.description.abstractPhyllosilicates occurring as replacements of olivine, clinopyroxene and interstitial materials and as veins or fracture-fillings in hydrothermally altered basalts from DSDP Hole 504B, Leg 83 have been studied using transmission and analytical electron microscopy. The parageneses of phyllosilicates generally change systematically with depth and with the degree of alteration, which in turn is related to permeability of basalts. Saponite and some mixed-layer chlorite/smectite are the dominant phyllosilicates at the top of the transition zone. Chlorite, corrensite, and mixed-layer chlorite/corrensite occur mainly in the lower transition zone and upper levels of the sheeted dike zone. Chlorite, talc, and mixed-layer talc/chlorite are the major phyllosilicates in the sheeted dike zone, although replacement of talc or ohvine by saponite is observed. The phyllosilicates consist of parallel or subparallel discrete packets of coherent layers with packet thicknesses generally ranging from< 100 Å to a few hundred Å. The packets of saponite layers are much smaller or less well defined than those of chlorite, corrensite and talc, indicating poorer crystal-linity of saponite. by contrast, chlorite and talc from the lower transition zone and the sheeted dike zone occur in packets up to thousands of Å thick. The Si/(Si+Al) ratio of these trioctahedral phyllosilicates increases and Fe/(Fe+Mg) decreases in the order chlorite, corrensite, saponite, and talc. These relations reflect optimal solid solution consistent with minimum misfit of articulated octahedral and tetrahedral sheets. Variations in composition of hydrothermal fluids and precursor minerals, especially in Si/(Si+Al) and Fe/(Fe+Mg) ratios, are thus important factors in controlling the parageneses of phyllosilicates. The phyllosilicates are generally well crystallized discrete phases, rather than mixed-layered phases, where they have been affected by relatively high fluid/rock ratios as in high-permeability basalts, in veins, or areas adjacent to veins. Intense alteration in basalts with high permeability (indicating high fluid/rock ratios) is characterized by pervasive albitization and zeolitization. Minimal alteration in the basalts without significant albitization and zeolitization is characterized by the occurrence of saponite±mixed-layer chlorite/smectite in the low-temperature alteration zone, and mixed-layer chlorite/corrensite or mixed-layer talc/chlorite in the high-temperature alteration zone. Textural non-equilibrium for phyllosilicates is represented by mixed layering and poorly defined packets of partially incoherent layers. The approach to textural equilibrium was controlled largely by the availability of fluid or permeability.en_US
dc.format.extent3740151 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherMineral Resourcesen_US
dc.subject.otherGeosciencesen_US
dc.subject.otherGeologyen_US
dc.subject.otherMineralogyen_US
dc.titlePhyllosilicates in hydrothermally altered basalts from DSDP Hole 504B, Leg 83 — a TEM and AEM studyen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelGeology and Earth Sciencesen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Geological Sciences, The University of Michigan, 48109, Ann Arbor, MI, USA; Department of Marine Resources, National Sun Yat-sen University, 804, Kaohsiung, Taiwain, Republic of Chinaen_US
dc.contributor.affiliationumDepartment of Geological Sciences, The University of Michigan, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47300/1/410_2004_Article_BF00310959.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00310959en_US
dc.identifier.sourceContributions to Mineralogy and Petrologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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