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P.M. Okita

Publications and source records attributed to P.M. Okita.

4 recordsLinked to original sources
USGS1992

Manganese carbonate mineralization in the Molango district, Mexico

The Molango manganese deposit in Mexico is by far the largest known Mn deposit in North America. Mn carbonate mineralization is hosted by a finely laminated Upper Jurassic marine sedimentary sequence that forms the base of the Chipoco facies of the Taman Formation (Kimmeridgian). Manganese enrichment occurs over a total stratigraphic thickness of approximately 50 m, and a length of over 50 km along strike and serves as the protore for supergene Mn oxide ore. The carbonate ore zone comprises the basal 1 to 10 m of the Chipoco facies.The carbonate ore bed consists of fine-grained rhodochrosite and dispersed organic matter, magnetite, and maghemite but generally only trace quantities of pyrite. Fine laminations and clotted textures suggest deposition in a restricted marine environment. Manganese content is highest at the base of the mineralized interval, drops abruptly to subore grade, Mn-rich carbonates, and then gradually decreases upward to background levels (i.e., trace Mn in calcite). Chemical and mineralogical studies indicate that the predominant mineralogy changes upward from rhodochrosite in the ore zone, to mixed carbonates (Mn calcite, kutnohorite, + or - rhodochrosite), to Mn calcite.Several geologic and geochemical processes resulted in the formation of Mn carbonate by the early diagenetic reduction of Mn oxides through the oxidation of organic matter and iron sulfide. Mn oxides were concentrated at the margins of a dysaerobic to mildly anoxic stratified basin and became an important oxidizing agent of organic matter in the sediment pile. Effects of organic matter oxidation reactions included production of manganous ion (Mn (super +2) ), MnCO 3 precipitation, oxidation of iron monosulfide (precursor to pyrite), and formation of Fe oxide. The latter two processes explain the anomalously low pyrite and abundant magnetite content in the ore zone. The observed vertical variation of Mn carbonate mineralogy and the mineral compositions reflect variations in the concentrations of reduced manganese in the pore waters. Thus, Mn carbonate precipitated from pore water and did not form as a chemical sediment in the water column. The ultimate source of the manganese is uncertain but may have been fluvial-sediment loads or hydrothermal activity associated with the rifting of the Gulf of Mexico.

Economic Geology↗
USGS1992

Hydrothermal and metamorphic berthierine from the Kidd Creek volcanogenic massive sulfide deposit, Timmins, Ontario

Berthierine, a 7 A?? Fe-Al member of the serpentine group, occurs in the footwall stringer zone of the Archean Kidd Creek massive sulfide deposit, associated with quartz, muscovite, chlorite, pyrite, sphalerite, chalcopyrite, and local tourmaline, cassiterite, and halloysite. Petrographic and scanning electron microscopic (SEM) studies reveal different types of berthierine occurrences, including interlayers within the rims on deformed chlorite, intergrowths with muscovite and halloysite, and discrete coarse grains. This is the first reported occurrence of berthierine from volcanogenic massive sulfide deposits. Textural relations suggest that most of the berthierine formed as a primary hydrothermal mineral at relatively high temperatures (~350??C) in the footwall stringer zone, probably by the replacement of a pre-existing aluminous phase such as muscovite or chlorite. However, the intergrowth textures observed by SEM and TEM suggest that some of the berthierine originated by syn- or post-metamorphic replacement of chlorite. -from Authors

Canadian Mineralogist↗
USGS1988

Isotopic evidence for organic matter oxidation by manganese reduction in the formation of stratiform manganese carbonate ore

Unlike other marine-sedimentary manganese ore deposits, which are largely composed of manganese oxides, the primary ore at Molango (Hidalgo State, Mexico) is exclusively manganese carbonate (rhodochrosite, Mn-calcite, kutnahorite). Stable isotope studies of the carbonates from Molango provide critical new information relevant to the controversy over syngenetic and diagenetic models of stratiform manganese deposit formation. Negative δ 13 C values for carbonates from mineralized zones at Molango are strongly correlated with manganese content both on a whole rock scale and by mineral species. Whole rock δ 13 C data fall into three groups: high-grade ore = −16.4 to −11.5%.; manganese-rich, sub-ore-grade = −5.2 to 0%.; and unmineralized carbonates = 0 to +2.5%. (PDB). δ 18 O data show considerable overlap in values among the three groups: +4.8 to −2.8, −5.4 to −0.3%., and −7.4 to +6.2 (PDB), respectively. Isotopic data for individual co-existing minerals suggest a similar separation of δ 13 C values: δ 13 C values from calcite range from −1.1 to +0.7%. (PDB), whereas values from rhodochrosite are very negative, −12.9 to −5.5%., and values from kutnahorite or Mn-calcite are intermediate between calcite and rhodochrosite. 13 C data are interpreted to indicate that calcite ( i.e . unmineralized carbonate) formed from a normal marine carbon reservoir. However, 13 C data for the manganese-bearing carbonates suggest a mixed seawater and organic source of carbon. The presence of only trace amounts of pyrite suggests sulfate reduction may have played a minor part in oxidizing organic matter. It is possible that manganese reduction was the predominant reaction that oxidized organic matter and that it released organic-derived CO 2 to produce negative δ 13 C values and manganese carbonate mineralization.

Geochimica et Cosmochimica Acta↗