Pétrographie et altération de la matière organiquedu gisement de plomb–zinc–cuivre de tourist–Bou Beker,Maroc nord oriental

1996 ◽  
Vol 33 (10) ◽  
pp. 1363-1374 ◽  
Author(s):  
M. Bouadellah ◽  
A. C. Brown ◽  
Y. Héroux

Reflectance measurements and organic petrography were used to study altered organic matter in the dolomitic Middle Jurassic Beddiane sequence hosting the Beddiane lead–zinc deposit. Organic matter occurs in the lower dolostone units of the formation where zinc sulfide mineralization prevails. The upper units, where lead sulfide mineralization is dominant, contain lesser amounts of organic matter. The organic matter in the Beddiane sequence consists of macerals, amorphous kerogen, and solid bitumen, inertinite and vitrinite are ubiquitous. The amount of exinite increases toward mineralized areas but the ratio exinite/kerogen remains constant. Two types of vitrinite are considered on the basis of their reflectance: Vt1 with low reflectance values (0.3–0.5%) and Vt2 with higher values (0.7–1.25%). The ratio Vt1/Vt2 increases and the reflectance values for Vt1 decrease toward the zinc-prevailing units, Organic matter associated with the mineralization exhibits features such as oxidation halos and desiccation cracks, together with a low-fluorescent exinite. The association of the kerogen content, the trend in reflectance values, and the alteration features of the Mississippi Valley-type Beddiane deposit support the hypothesis that the regional flow of hot brines associated with the mineralization process was the cause of anomalous heating, that the occurrence of exinite maceral and its associated gas played a role in the ore deposition, and that the new chemical equilibrium reached by the zinc-dominant host rock after ore deposition is responsible for the suppressed reflectance values within and near the ore deposits.

1985 ◽  
Vol 22 (12) ◽  
pp. 1890-1892 ◽  
Author(s):  
R. W. Macqueen

The following seven papers were presented on May 16, 1984, at the Geological Association of Canada and Mineralogical Association of Canada joint annual meeting. The special session, organized by R. W. Macqueen and J. A. Coope, contained 10 papers and was sponsored by the Mineral Deposits Division of the Geological Association of Canada.Our objective in organizing the special session was to examine organically based processes and relationships that may be of major importance to the origin of ore deposits. As noted by Fyfe (1984), the concept of the geochemical cycle focuses attention on pathways of chemical elements and isotopes of the Earth's system during geologic history. It is clear from the chemistry of carbon-rich materials that a wide range of elements is concentrated directly or indirectly by biological processes operating as part of the geochemical cycle. Two of the papers of the special session examine some of these concentration processes, although definitive links to actual ore deposits cannot be made yet. Beveridge and Fyfe document the remarkable ability of the anionic cell walls of certain bacteria to concentrate metals and to provide sites for nucleation and growth of minerals. In a related paper, Mann and Fyfe show that several species of simple freshwater green algae readily concentrate large amounts of uranium under both experimental and natural conditions (Elliot Lake and Thames River, Ontario).Two papers deal with aspects of sulphate reduction. Birnbaum and Wireman describe controlled experiments that suggest that sulphate-reducing bacteria may be involved in the selective replacement of sulphate-evaporite minerals by silica and in the precipitation of silica in association with sulphide mineral phases in banded iron formations. Their work focuses directly on the effect that bacterial sulphate reduction has on silica solubility. Trudinger et al. examine the question of mechanisms of sulphate reduction at temperatures less than 200 °C and the bearing this has on origin of sulphide for low-temperature sulphide ore deposits. Although there is empirical evidence favouring abiological sulphate reduction at temperatures in the vicinity of 100 °C, Trudinger et al. have not been able to demonstrate abiological reduction of sulphate under controlled laboratory conditions and at temperatures under about 200 °C. Perhaps catalysts, as yet undiscovered, are involved in this process in nature.Impressive progress has been made in understanding the diagenetic evolution of organic matter in response to heat and pressure in geological environments: excellent reviews are found in Barnes et al. (1984) and Bustin et al. (1985). Simoneit's paper examines and reviews the genesis of petroleum in a most unusual setting, that of the active ocean ridge spreading centre of Guaymas Basin, Gulf of California. There, in the vicinity of black smokers and associated metallic sulphide deposits, petroleum originates instantaneously geologically as a result of hydrothermal activity. The question of genetic involvement of organic matter in the origin of the metallic sulphides (e.g., reduction of sulphate to H2S) cannot be answered yet for this setting with the available data.The final two special session papers included here are concerned with organic matter associated with mineralization in Canadian Shield Precambrian settings. Willingham et al. demonstrate that Elliot Lake – Blind River Early Proterozoic uranium deposits with minor amounts of associated gold also contain kerogen-like organic matter. Some of this organic matter has anomalously rich amounts of gold and uranium and appears to have originated as mats of cyanobacteria, possibly with the ability to concentrate these metals. For a number of settings in the Archean-aged Abitibi greenstone belt of Ontario and Quebec, Springer demonstrates that carbon, at least partly of organic origin, is closely associated with some gold deposits. Her interpretation is that carbon activated by shear-zone-associated hydrothermal fluids has provided sites for fixing some of the gold.Three of the papers given at the special session are not included here. H. T. Shacklette reviewed metal uptake by young conifer trees, demonstrating that nursery-grown seedlings of several species readily concentrated a variety of metals, including lead, zinc, tin, and gold, over a 7 year period. This work is of interest to those involved in geochemical prospecting and is now published elsewhere (King et al. 1984). R. W. Macqueen presented quantitative data on the genesis of sulphide by abiological bitumen–sulphate reactions at the Pine Point lead–zinc property, Northwest Territories, Canada (Macqueen and Powell 1983; Powell and Macqueen 1984). Although Trudinger et al. have not been able to demonstrate abiological reduction of sulphate at temperatures approximating those of Pine Point [Formula: see text], the data presented by Macqueen (Powell and Macqueen 1984) are consistent with the amounts, alteration, and composition of bitumens at Pine Point, as well as with the presence of native sulphur and the sulphur isotope compositions of the various Pine Point sulphur species. This work is continuing, and a more extensive account is in preparation. J. R. Watterson examined relationships between freezing climates and the local chemical behaviour of gold in the weathering cycle, concluding that ice-induced accumulation of organic acids, bacteria, and other organic matter at mineral surfaces may increase rates of chemical attack, leading to dissolution of normally insoluble metals such as gold (Watterson 1986).Interest in organic aspects of the geochemical cycle, including ore deposition, is growing dramatically (e.g., Fyfe 1984). Although the following papers address a limited range of topics within the field, they do indicate some of the diversity and variety of active processes and associations between metallic elements and organic components. Perhaps, in the not too distant future, we will be able to identify or even discover whole classes of ore deposits that owe their origin directly to organic influences operating within the geochemical cycle.


2004 ◽  
Vol 25 (1) ◽  
pp. 36 ◽  
Author(s):  
Craig P Marshall ◽  
Karen L Mackenzie ◽  
Junhong Chen ◽  
Dorothy Z Oehler ◽  
Graham A Logan ◽  
...  

The 1640 Ma (million years old) Here?s Your Chance (HYC) deposit at McArthur River, Northern Territory, Australia is one of the largest and least metamorphosed lead-zinc-silver deposits in the world. The mineralised interval has been divided into several orebodies and is separated by relatively barren sediment.


Author(s):  
Craig M. Bethke

Hydrothermal fluids, hot groundwaters that circulate within the Earth’s crust, play central roles in many geological processes, including the genesis of a broad variety of ore deposits, the chemical alteration of rocks and sediments, and the origin of hot springs and geothermal fields. Many studies have been devoted to modeling how hydrothermal fluids react chemically as they encounter wall rocks, cool, boil, and mix with other fluids. Such modeling proliferated in part because hydrothermal fluids are highly reactive and because the reaction products are commonly well preserved, readily studied, and likely to be of economic interest. Further impetus was provided by the development of reliable modeling software in the 1970s, a period of concern over the availability of strategic and critical minerals and of heightened interest in economic geology and the exploitation of geothermal energy. As a result, many of the earliest and most imaginative applications of geochemical modeling, beginning with Helgeson’s (1970) simulation of ore deposition in hydrothermal veins and the alteration of nearby country rock, have addressed the reaction of hydrothermal fluids. For example, Reed (1977) considered the origin of a precious metal district; Garven and Freeze (1984), Sverjensky (1984, 1987), and Anderson and Garven (1987) studied the role of sedimentary brines in forming Mississippi Valley-type and other ore deposits; Wolery (1978), Janecky and Seyfried (1984), Bowers et al. (1985), and Janecky and Shanks (1988) simulated hydrothermal interactions along the midocean ridges; and Drummond and Ohmoto (1985) and Spycher and Reed (1988) modeled how fluid boiling is related to ore deposition. In this chapter, we develop geochemical models of two hydrothermal processes: the formation of fluorite veins in the Albigeois ore district and the origin of “black smokers, ” a name given to hydrothermal vents found along the ocean floor at midocean ridges. As a first case study, we borrow from the modeling work of Rowan (1991), who considered the origin of fluorite (CaF2) veins in the Albigeois district of the southwest Massif Central, France. Production and reserves for the district as a whole total about 7 million metric tons, making it comparable to the more famous deposits of southern Illinois and western Kentucky, USA.


2007 ◽  
Vol 42 (8) ◽  
pp. 913-935 ◽  
Author(s):  
Veerle Vandeginste ◽  
Rudy Swennen ◽  
Sarah A. Gleeson ◽  
Rob M. Ellam ◽  
Kirk Osadetz ◽  
...  

Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 401
Author(s):  
Mohammed Bouabdellah ◽  
Wissale Boukirou ◽  
Adriana Potra ◽  
Erik Melchiorre ◽  
Hassan Bouzahzah ◽  
...  

Through integration of Pb-Zn ± Cu non-sulfide mineralogy, texture, and stable isotope (C, O, S) geochemistry, the world-class Touissit- Bou Beker and Jbel Bou Dahar Mississippi Valley-type districts of the Moroccan Atlasic system have been investigated in order to gain insights into the origin and processes that contributed to the formation of the base metal non-sulfide mineralization. In both districts, direct replacement (“red calamine”) and wallrock replacement (“white calamine”) ores are observed. Based on the mineral assemblages, ore textures, and crosscutting relations, three distinct mineralizing stages are recognized. The earliest, pre-non-sulfide gossanous stage was a prerequisite for the following supergene stages and constituted the driving force that ultimately promoted the leaching of most base metals such as Zn and Cu and alkalis from their rock sources. The following two stages, referred to as the main supergene “red calamine” and late “white calamine” ore stages, generated the bulk of mineable “calamine” ores in the Touissit-Bou Beker and Jbel Bou Dahar districts. Stable isotope compositions (d13CV-PDB, d18OV-SMOW, d34SCDT) support a three-stage model whereby metals were released by supergene acidic fluids and then precipitated by bacteria and archaea-mediated metal-rich meteoric fluids due to a decrease in temperature and/or increase of fO2. Oxygen isotope thermometry indicates decreasing precipitation temperatures with advancing paragenetic sequence from 33° to 18 °C, with wet to semi-arid to arid climatic conditions. The close spatial relationships between coexisting sulfide and non-sulfide mineralization along with stable isotope constraints suggest that the oxidation of sulfides occurred concurrently after the main stage of the Alpine orogeny between 15 Ma and the present. More importantly, the current data show for the first time the involvement of biologically controlled activity as the major driving process that triggered both oxidation and deposition of supergene mineralization at Jbel Bou Dahar and Touissit-Bou Beker districts. Conclusions drawn from this study therefore have implications for supergene Mississippi Valley-type (MVT) -derived non-sulfide deposits worldwide and account for the prominent role of biological processes in the genesis of this category of ore deposits.


1959 ◽  
Author(s):  
A.V. Heyl ◽  
A.F. Agnew ◽  
E.J. Lyons ◽  
C.H. Behre

Geosciences ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 172
Author(s):  
Jonathan Chick ◽  
Sydney E. McKim ◽  
Adriana Potra ◽  
Walter L. Manger ◽  
John R. Samuelsen

Southern Ozark Mississippi Valley-type ores are enriched in radiogenic Pb, with isotopic signatures suggesting that metals were supplied by two end-member components. While the less radiogenic component appears to be derived from various shale and sandstone units, the source of the more radiogenic component has not yet been identified. Analyses of cherts from the Early Ordovician Cotter Dolomite and tripolitic chert from the Early Mississippian Boone Formation contain highly radiogenic Pb, with isotopic ratios comparable to those of ores. However, most samples have lower 208Pb/204Pb and 207Pb/204Pb for a given 206Pb/204Pb compared to ores. These relationships demonstrate that the enriched Pb isotopic values of the ore array cannot be related to the host and regional lithologies sampled, suggesting that the source of high ratios may lay further afield. The slope of the linear trend defined by the Pb isotope ratios of ores corresponds to an age of about 1.19 Ga. Therefore, an alternative for the linear array is the involvement of Precambrian basement in supplying ore Pb. Rare earth element patterns show that diagenetic processes involving the action of groundwater and hydrothermal fluids affected the sampled lithologies to various degrees, with Cotter Dolomite having experienced the highest degree of alteration.


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