1 Introduction
The current study addresses thermal effects generated by an intrusive magmatic activity onto embedding sedimentary deposits of the Tunisian Eastern margin (Fig. 1). This margin comprises the area between the Cap Bon in the North and the Gabes in the South. The study is based on subsurface data and samples recovered in the oil wells of this area. Samples were collected all along the drillings and in tighten steps near the magmatic intervals. The study aim is to appraise the impact of both heat and chemical elements income – relevant to the magmatic rocks setup – on the neoformation of new mineral phases and the improvement of their crystallinity degree.
2 Geological frame
2.1 Eastern margin structure
The geological structure of the eastern margin of Tunisia results from two main tectonic behaviours:
- • successive rifting, with north–south to NE–SW extensions along the Trias, Jurassic and Lower Cretaceous, which led to series of horsts, grabens and semi-graben structures;
- • the migration of the African plate towards Eurasia during the Upper Cretaceous and the Cenozoic initiated NW–SE compression and formation of the Atlasic mountain folding [8,12,26].
2.2 Magmatic manifestations during the Upper Cretaceous
Subsurface magmatic rocks have been recovered in almost all the drillings across the Upper Cretaceous series of the eastern margin of Tunisia (Fig. 1). There are three main types of magmatic rocks [16,17,23] (Fig. 2):
- • microdoleritic intrusions typical of fissural magmatic activity, forming dykes and sills;
- • lava flows interstratified within the Cretaceous deposits;
- • pyroclastic products (pumice, tufas) bearing witness to a synsedimentary explosive volcanic activity, which appeared during the Senonian. The pyroclastic fragments are composed of pumice debris, vitreous shards, or volcanic ashes amended by carbonate. The microscopic study shows that rocks are formed of pumice and scoria and pumice debris cemented by carbonate that may reach 40% of the rock. They correspond to a volcanism situated in carbonated sedimentation environment. Volcanoclastites are rare crystals and are affected by an intense post-magmatic transformation that made impossible their identification.
2.3 Upper Cretaceous sedimentary deposits
The sedimentary facies of the Upper Cretaceous are strictly related to palaeogeographic directions guided by the basin structure. The transgression started during the Aptian and went on during the Cenomanian. The transgressive episode carried on and the facies became increasingly carbonated during the Coniacian–Santonian. During the Campanian–Maastrichtian, the transpressive facies became mainly carbonated and most often chalky. This sedimentation was characterised [22] by two high zones separated by a NW–SE trending subsidence zone. This structure influenced sedimentary rates during the Upper Cretaceous.
2.4 The primary clay mineral suite
The clay mineral suite of the Upper Cretaceous formations outcropping in central Tunisia has been explored by numerous authors [1,14,24,26]. The authors point to the predominance of the smectite, together with little kaolinite and a very low amount of illite. It seems therefore that away from the occasional thermal influence of magmatic activity and the effect of burial diagenesis, the Upper Cretaceous reveals smectite dominance associated with illite and kaolinite. The authors interpret the predominance of smectite coming with small amount of kaolinite and illite as detrital heritage of the mineralogical suite, indicating tectonic stability during this period.
3 Methods
The clay minerals ( < 2 μm fraction) have been analysed by X-ray diffraction. Clay samples collected in the cuttings were carefully selected under binocular magnifier to avoid contamination with well mud and fallouts. They were rinsed several times with water and then dried in free air. Consolidated samples were crushed. Calcareous samples were treated with 0.1 N chlorhydric acid. Then samples were washed and centrifuged. We used a pipette to collect the suspension in the upper slice. We put the suspension on a glass slide and let it evaporate at ambient air. The oriented clay aggregates were analysed by a Philips Panalytical diffractometer (XPERT-PRO) with a cobalt anticathode, a step size [0.017° 2θ], with X-rayed angular domain [0–35° 2θ] and step time [20.0298 s]. The oriented aggregates were run at air-dried state (after drying in ambient temperature), after saturation with ethylene glycol, and heated at 500 °C during 2 hours. Minerals are defined following the position of reflections (001) on the three diffractograms. Semi-quantitative estimation of the clay minerals was done based on the relative surface of the main peak of each mineral (air-dried X ray diffractogramm). Error odds are of 5%. SEM microscopy was performed on some samples to investigate clay minerals’ morphologies.
4 Sampling
More than 200 samples were analyzed. Two sampling series were accomplished:
- • packed samples in the vicinity of the magmatic material contact;
- • more spaced samples away from the magmatic occurrences to determine the influence of magmatic bodies on embedding argillaceous sediments.
The analyzed cuttings are of average size (a few centimetres). Herein we examine three wells considered the most representative:
- • a reference well, Ksar-1 (XSR1), without magmatic intrusion or emission;
- • Rhemoura-3 (RHE3) well goes through a basalt flow layer in the upper part and a microdolerite sill at depth;
- • Miskar-3 (MKR3) displays magmatic emission in the upper part, but several basaltic layer and pyroclastic layers in depth.
5 Results
5.1 Clay mineral series
Two main clay mineral suites have been identified:
5.1.1 Reference well XSR1, without magmatic rocks
Analysed samples (collected between 1370 and 1540 m) belong to an alternation of claystone and limestone of Turonian, Coniacian, Santonian, and Cenomanian age. The clay mineral suite is composed of kaolinite, illite, and smectite. Smectite (70 to 80%) is always prevalent, whereas kaolinite (5 to 15%) and illite (7 to 18%) are less important (Fig. 5). The lack of chlorite and mixed-layered illite–chlorite has to be noticed.
5.1.2 Well RHE3, with two magmatic intervals
The first interval is a basaltic lava flow (crosscut between 2531 and 2593 m) occupying a large part of the Abiod formation of Campanian–Maastrichtian age (Fig. 6). The basalt flow rests on whitish microcrystalline limestone and is covered by dark grey claystone that is mainly composed of smectite (70 to 80%), kaolinite (6 to 20%) and illite (6 to 10%). The absence of the chlorite and the mixed-layered illite–chlorite has to be noticed in this interval. The second magmatic interval (crosscut between 2671 m and 2691 m) is a microdoleritic-textured intrusion. This intrusion is embedded in Coniacian–Santonian clays and limestones. The analysed samples are located at both sides of the intrusion. Their clay fractions show mixed-layered illite–chlorite (37% to 60%) associated with chlorite (13% to 30%) and with illite (2% to 24%). The presence of kaolinite with proportions ranging from 5 to 25% and the absence of smectite has to be noticed. Chlorite is slightly swelling with reflection (001) shifting from 14 to 14.95 Å by ethylene glycol solvation. The clay mineral suite shows an increase in chlorite content when coming closer to the intrusion. In fact, the samples in immediate contact with the intrusion (2672 m and 2694.5 m) reveal the highest chlorite content.
5.1.3 Well MKR 3, with various magmatic activities
There are pyroclastic layers alternating with argillaceous limestones, as well as basaltic lava flows embedded in biomicrites and argillaceous limestones. There are two distinct clay mineral suites (Fig. 7). On either sides of the pyroclastic layer, the clay mineral suite is dominated by kaolinite (55% to 67%) associated with illite (9% to 35%) and smectite (9% to 28%). The lack of chloritic minerals has to be quoted. The clay minerals below the basaltic lava are composed of mixed-layered illite–chlorite (49% to 21%), chlorite (25% to 4%) and kaolinite, which increases away from the lava flow (from 7% to 38%). Illite contents range from 15% to 36%. Smectite is almost lacking; it has been detected only in two samples (3% and 2% at depths of 3920 and 3936 m, respectively). We notice that chlorite and mixed-layered illite–chlorite contents decrease when moving away from the basaltic lava flow, whereas kaolinite and illite contents increase in the meantime.
Chlorite and mixed-layered illite–chlorite minerals are bound to the magmatic intrusions (well RHE3) and the sole of the basaltic flow (well MKR3). There is no noteworthy change in the clay mineral series above the basalt flows (well RHE3) and near the pyroclastic deposits; in this latter configuration, clay mineral assemblages remain similar to those of the common detrital clay mineral series known elsewhere in the Upper Cretaceous of Tunisia, consisting of kaolinite, illite, and smectite, without chloritic minerals. The latter are directly bound to the emplacement of magmatic lavas.
5.2 Illite crystallinity
Special attention has been paid to the evolution of the illite crystallinity along the wells, by measurement of the width at half-height of the (001) reflexion of illite (EG solvated preparation) [5,10,15].
In the reference well XSR1, the (001) illite peak shows a width at half-height between 3.5 mm at 1540-m depth and 4.8 mm at 1440-m depth.
In well RHE3, illite crystallinity is rather low in the samples below the basaltic lava flow (around 2500-m depth) with a width at half-height of the (001) illite peak of about 4.5 mm (Fig. 8). Coming closer to the microdoleritic intrusion, illite crystallinity is improved, as shown by the decrease of its width at half-height (2.0 mm for samples between 2670 and 2695 m).
In well MKR3 (Fig. 9), samples at 3710 m and 3775 m have been collected at both top and bottom sides of the pyroclastic products. The measures of the crystallinity index are respectively 3.7 and 3.6 mm in this interval. The sample directly below the basaltic lava flow, at 3896-m depth, shows a higher illite crystallinity, with a half-height width of 2.5 mm. Moving away from the basalt layer, towards 3960-m depth, the width at half-height of the (001) illite reflexion reaches again 3.5 mm, like in the upper interval.
6 Discussion
Coming close to the intrusions, smectite disappears, mixed-layered illite–chlorite appears, and finally, near to the intrusion, the mixed-layered illite–chlorite diminishes on behalf of chlorite, which rises. The mineralogical sequence may possibly reflect ascending thermal gradient toward the intrusion and subjacent to the basaltic flow. Thus, the microdoleritic intrusion has a thermal effect on sub- and suprajacent sediments, whereas basaltic flows affect only the bedrock deposits and does not have any effect on cover sediments, deposited after its cooling. A similar example has been described in the Argana basin, Morocco [7].
Magmatic occurrences come with heat and chemical elements income, particularly magnesium. These two factors created changes in the equilibrium conditions of the different mineralogical phases. Detrital argillaceous minerals become metastable under these conditions. New mineral phases, such as chlorite and interstratified illite–chlorite, precipitate from hot fluids. Many authors [4,9,11,20,21] pointed out chlorite presence in hydrothermal environments and attributed it to contact metamorphism. Closer to the intrusion and beneath the basaltic lava flow, illite proportions slightly raise together with an improvement of its crystallinity. Detrital smectite initially present in argillaceous sediments becomes unstable under the new thermal conditions and turns into mixed-layered illite–chlorite. The latter results from the contact between smectite and the magmatic intrusion, as stated by many authors [2,18,21]. Experimental conditions [27] showed the transformation of smectite into mixed-layered illite–chlorite in hydrothermal conditions. During the intrusion and below the basaltic lava flows, new physicochemical conditions prevail. These will enable smectite transformation into mixed-layered illite–chlorite, which itself, in the course of time, turns into more stable chlorite and/or illite. Hydrothermal fluids related to the magmatic activity and the contemporary magmatic rocks alteration by interstitial water strongly heated are presumably enriched with magnesium. The latter is necessary for chlorite formation at the expense of other metastable minerals. In hydrothermal deposits in general, tri-octahedral clays, mainly chlorite and corrensite, may possibly result either from the progressive transformation of a tri-octahedral primary smectite or from direct precipitation from hydrothermal fluids [13]. In RHE3 and MKR3 wells, chlorite (Fig. 9A and B) seems to result from the second mechanism, because the smectites present in the basin are dioctahedral [3,6,12,19,25] and cannot possibly turn into chlorite.
7 Conclusion
The magmatic manifestations of the Upper Cretaceous on the localization and the repartition of the Tunisian eastern margin are directly linked to those of deep fault lanes that enabled basaltic magmas ascension. The emplacement of this magmatism comes along with circulation of hydrothermal fluids; it generated a local geothermal gradient. The sedimentary series of the Upper Cretaceous was locally affected by temperature rise. Income of heat and chemical elements, particularly magnesium, in relation with the placement of magmatic episodes, engendered new clay mineral equilibrium. Dissolution and precipitation by metasomatic mechanisms were induced by the hydrothermal fluids. Detrital argillaceous minerals, such as smectite, became metastable and new hydrothermal phases formed, such as chlorite, which does not exist in the outcrop or in the reference well. Illite crystallinity was improved too.