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Glauconitic laminated crusts from hydrothermal alteration of Jurassic pillow-lavas (Betic Cordillera, S Spain): a microbial influence case.

1. Introduction

Glauconitic micas related to volcanic and hydrothermal processes are scarcely documented in the literature (Buatier et al., 1989, 1993; Alt et al., 1992; Clayton and Pearce, 2000; Ionescu et al., 2006; Clauer et al., 2011) with respect to glauconitic facies from sedimentary environments (e.g. Porrenga, 1967; Odin and Letolle, 1980; Odin and Matter, 1981; Bornhold and Giresse, 1985; Odin and Fullagar, 1988; Amorosi, 1995; Jimenez-Millan et al., 1998; Eder et al., 2007; Sanchez-Navas et al., 2008; Baldermann et al., 2013). In both cases--volcanic-hydrothermal and sedimentary-diagenetic--glauconite, a Fe- and K-rich mica structure mineral (Odin and Matter, 1981), is mainly recorded as peloidal grains. This research provides a very different texture of glauconitic micas forming laminated crusts associated with spaces between pillow-lava bodies.

Jurassic pillow-lavas, intercalated between pelagic sediments, have been studied by numerous authors in the Median Subbetic domain of the External Zones of the Betic Cordillera (Southern Spain) (Comas et al., 1986; Puga et al., 1988, 1989; Portugal et al., 1995; Morata et al., 1996; Vera et al., 1997). These submarine volcanic rocks are held to be related to an extensional process of crustal thinning. The intrusion of volcanic and subvolcanic bodies in the Subbetic Zone during the Jurassic generated hydrothermal systems that produced intense alteration of the igneous and sedimentary host materials. The processes of fluid-rock interaction caused the formation of phyllosilicates filling the network of veins and fractures (Abad et al., 2003; Jimenez-Millan et al., 2008).

In this study we describe and analyse the morphology and composition of the vein minerals associated with spaces among the pillow-lava bodies, which are composed mainly by greenish phyllosilicates, quartz and calcite. Samples were characterised using a variety of techniques, including powder X-ray diffraction, petrographic microscopy, scanning and transmission electron microscopy, electron microprobe, and X-ray fluorescence. Results on the morphology and microstructure of the glauconitic crusts provide a basis for the discussion of a possible influence of microbial activity on the origin and growth of the crusts.

2. Geological setting

The Betic Cordillera (Southern Spain) is the westernmost European chain related to the Alpine orogeny. The External Zones of this cordillera (Prebetic and Subbetic) are constituted mainly by sedimentary marine deposits deposited in the Southern Iberian Palaeomargin from the Triassic to the Miocene. During the early-late Jurassic in the Southern Iberian Palaeomargin there was an intense submarine volcanic activity in wide sectors of the pelagic basin. The analysed pillow-lava outcrops come from the Jurassic submarine volcanic rocks of the Median Subbetic palaeogeographic unit. These volcanic rocks have a WSW-ENE orientation, and are 5-10 km wide and around 250 km long. Basaltic pillow-lava flows dominate, interbedded with pyroclastic rocks and pelagic sediments. The maximum thickness of these volcanic rocks, described in the literature, is over 300 m (Vera et al., 1997). The Lower Jurassic submarine volcanic rocks of the Median Subbetic are considered as transitional alkaline, originated in an extensional process of crustal thinning (Portugal et al., 1995; Vera et al., 1997).

The Campotejar outcrop (coordinates 37[degrees]30'12"N, 3[degrees]37'50"W) is located close to the motorway joining the cities of Jaen and Granada, at km 79 (Granada province) (Fig. 1a). Pillow-lava bodies are well exposed in the talus of the highway (Fig. 1b). In the case studied here, voids among the pillows are commonly filled with a variety of material, including broken-up fragments of glassy-lava, sediment materials (limestones, marls) and secondary vein minerals. The studied clay minerals were obtained from the veins (Fig. 1b).

Previous works investigated the petrology and geochemistry of these volcanic rocks (Comas et al., 1986; Puga et al., 1988, 1989; Portugal et al., 1995; Morata et al., 1996). The main minerals in the pillow-lava are olivine (varies between chrysolite to hyalosiderite), Ti-augite, plagioclase (variable from bytownite to oligoclase) and minoritary biotite, Ti-hornblende, apatite and Fe-Ti oxides (Puga et al., 1989; Morata et al., 1996).

3. Methods

Petrographic microscope, in addition to magnifying binocular glasses, were used to determine the morphology of the crusts on 15 thin sections and 13 polished slabs. Whole-rock samples were studied using a Philips PW 1710 powder diffractometer with CuK[alpha] radiation, a graphite monochromator and an automatic divergence slit at the Instituto Andaluz de Ciencias de la Tierra (IACT, Granada). Oriented aggregates were prepared by sedimentation on glass slides. Ethylene glycol (EG) treatment was carried out on the aggregates to corroborate the identification of smectites on the basis of the expandability of these phases.

Following the XRD and optical study, carbon-coated polished thin sections were examined by Scanning Electron Microscopy (SEM) with an energy dispersive X-ray spectroscopy (EDX) microanalyser, and analysed with an Electron Microprobe (EMPA). Observations using back-scattered electron (BSE) imaging were carried out with a Merlin Carl Zeiss SEM in the Centro de Instrumentacion Cientifico-Tecnica of the Universidad de Jaen (Spain) and a Leo 1430-VPSEM at the Centro de Instrumentacion Cientifica (CIC) of the Universidad de Granada. An accelerating voltage of 20 kV, with a beam current of 1-2 nA, and counting time of 50 s, were used to analyse the silicates by SEM, using the following standards: albite (Na), periclase (Mg), wollastonite (Si and Ca), and orthoclase (K), and synthetic [Al.sub.2][O.sub.3] (Al), [Fe.sub.2][O.sub.3] (Fe) and MnTi[O.sub.3] (Ti and Mn). In addition, the green laminated crusts were split and pieces from the inner surfaces of the crusts were mounted, coated with gold, and examined under the SEM with secondary electrons to study the crystal morphology. The equipments used were a SCI Quanta 400 and a FEG Zeiss Auriga at the CIC. Microprobe analyses of phyllosilicates were performed using wavelength-dispersive spectroscopy (WDX) on a Cameca SX100 at the CIC. The instrument was set at an accelerating voltage of 15 kV, with a beam current of 15 nA and a electron beam diameter of <5 [micro]m. Data were reduced using the procedure of Pouchou and Pichoir (1985); the standards used were albite, sanidine, periclase, diopside, quartz, vanadinite, rutile, fluorite and synthetic oxides ([Al.sub.2][O.sub.3], [Fe.sub.2][O.sub.3], NiO and MnTi[O.sub.3]). Finally, powdered portions of the crusts were prepared using C-coated formvar Cu grids in a Philips CM20 (STEM) at the CIC equipped with a solidstate EDX detector, operating at 200 kV and with a La[B.sub.6] filament. Albite, biotite, spessartine, muscovite, olivine, titanite, MnS and CaS were used as standards to derive K-factors for the transformation of intensity ratios to concentration ratios following the procedures of Cliff and Lorimer (1975). The structural formulae of glauconitic micas and smectites were calculated on the basis of 22 negative charges [O.sub.10][(OH).sub.2].

Whole-rock analyses of the green crusts (2 samples) were carried out at the CIC (Universidad de Granada) for major element oxides using X-ray fluorescence (XRF) with a Phillips PW 1040/10 spectrometer, whereas trace element contents were determined using an inductively coupled plasma-mass spectrometer (ICP-MS) Perkin Elmer Sciex-Elan 5000.

4. Results

The studied materials, occurring in the inter-pillow spaces, are predominantly green and white crystal growths. The morphology of the infilling is conditioned by the shape, irregular but sometimes stratiform, of these voids. The largest mineralisation found measured 55 cm in length.

The internal structure of these mineralisations is graded from the walls of the pillow-lava body outwards (Figs. 2 and 3). Usually, the walls are covered by planar laminated green crusts (locally, very dark green). Inner parts of the mineralisations are composed by white crystals, predominantly calcite and secondarily quartz. Quartz usually occupies the most internal parts of the infilling. In some cases, when the infilling of the voids was not complete, they are preserved as geodes.

Two types of crusts can be differentiated according to mineralogy, colour and morphology: green laminated crusts, and black crusts and lentils.

4.1. Green laminated crusts

Morphology and microstructure

The green laminated crusts are usually developed from the walls of the pillow-lava showing a planar morphology with a thickness of 2-36 [micro]m (mean value of 12 mm) (Fig. 2). In some veins, bands of calcite crystals grow directly over pillow-lava walls or thin black films, and they are covered by the green laminated crusts (Fig. 2c). Commonly, the calcite and quartz mass occupying the most internal parts of the veins are crossed by green laminated columns stemming from the green laminated crusts commonly located directly on the walls of the pillow-lava (Fig. 3). The columns are < 130 [micro]m length and < 26 [micro]m in diameter, and parallel to each other. Other irregular growths of green minerals occurring inside the calcite growth, sometimes resembling oncoid-like morphologies, are really transversal sections of columns (Fig. 3a, d).

Detailed analyses under magnifying glass and petrographic microscope allowed us to characterise the laminated texture of planar crusts and columns. In both cases, laminae are irregular and not densely packed, embedded in a quartz or calcitic matrix (Figs. 4 and 5). Laminae are 20-60 [micro]m thick and made up of cylindrical filaments with a darker core (dark green or black) and a blue-green thin coat (Fig. 5). Some green filaments grow perpendicular to the lamination, measuring 100-450 pm in length (Fig. 4). Dichotomous branching is commonly observed in the perpendicular filaments (Fig. 4d-f). The filaments are locally composed of an arrangement of microspheres (Fig. 4f).

Study of these filaments through SEM-BSE imaging of the thin sections reveals two parts: an inner part corresponding to the darker green core (on magnifying glasses) without textural traits, and an outer part consisting of a ring of needle-like crystals disposed as a coating around the inner part, with druse arrangement corresponding to the blue-green external coat (Fig. 6). The inner part is 22-45 [micro]m in diameter and the outer coating is 8-12 [micro]m thick. The calcite crystals near these filaments are adapted to the surface of the needlelike outer coating. In addition, SEM-BSE images show the generalised presence of voids at the centre of the filaments (Fig. 6b, black arrow). The width of the voids ranges from 3.5 to 8.5 [micro]m. The wider the void, the less the material composing the darker green core in the inner part of the filaments. A very detailed examination of the inner and outer parts of the filaments under SEM-BSE images allowed us to identify very small lath-like crystals (< 1 [micro]m length) making up the inner part, and comparatively larger lath-like crystals (> 5 [micro]m length) composing the outer coating. The inner part is constituted by randomly arranged crystals, whereas in the outer part the crystals are oriented perpendicular to the filament. The transition between inner and outer parts is characterised by a progressive orientation of the crystals through palm-tree branches and progressively larger crystals (Fig. 7).

Secondary electron and TEM images show that the green material constituting the needle-like coating of the filaments actually consists of idiomorphic lath-like crystals < 10.5 [micro]m long and < 0.8 [micro]m wide (Fig. 8). Detailed examination of these lath-like crystals evidences that some samples present irregular margins and small filamentous to coccoid-shaped forms with < 0.5 [micro]m length and 0.1 [micro]m width (Fig. 9a, b). The morphologies of the crystals are similar to the clay flakes described by Geptner et al. (2008) in glauconites from Paleogene volcano-terrigenous rocks from Kamchatka.

A characteristic irregular film covers the green crystals in some parts of the analysed samples (Fig. 9c, d), locally showing filament-like structures (locally branched) around 15 mm in length and < 1 [micro]m in diameter (Fig. 9e, f).

Mineralogy and geochemistry

The XRD patterns of oriented aggregates corresponding to the green material show glauconitic mica, calcite, and a small amount of smectite with a basal spacing of 14.92 [Angstrom], which expands to 16.63 [Angstrom] after EG solvation (Fig. 10). The 001 reflection of the dioctahedral mica is a narrow peak with a sharp appearance and high intensity, which does not change its position, shape, and intensity after EG solvation. Nevertheless, the 003 peak is slightly asymmetric, with a small shoulder towards lower 20[theta] angles and close to 35 [degrees]2[theta] showing two peaks, which is typical of celadonite (Odin and Matter, 1981). The sharp and symmetric peaks at 001 and 020, and the presence of the i 12 and 112 reflections, indicate a predominantly ordered structure.

The whole-rock analyses of the green crusts are characterised by a high loss on ignition (LOI) from 18.9% to 23.8%. The major elements (in oxides) range from 27.79-34.38% for Si[O.sub.2], 20.23-26.69% for CaO, 8.66-10.38% for [Fe.sub.2][O.sub.3], 4.61-5.55% for [Al.sub.2][O.sub.3], 4.39-5.44% for K2O, and 3.27-3.97% for MgO. The high values of CaO compared with literature data (Bornhold and Giresse, 1985) are related to the presence of calcite in the whole-rock sample of the green deposits. Regarding the trace elements, the most abundant are Rb (188 ppm), V (100 ppm), Cu (107 ppm), Li (70 ppm), and Ni (61 ppm), which are values close to the average composition of the upper continental crust (Taylor and McLennan, 1985) except for the Cu with a content twice the value of the Post Archean Average Shale (PAAS). The [SIGMA]REE ranges between 15 and 19 ppm, which corresponds to REE-poor group of glauconites of Jarrar et al. (2000).

Micro-chemical analyses of the studied growths made it possible to characterise the composition of glauconitic micas (glauconite and celadonite). The chemical compositions of dioctahedral micas are presented in Table 1. Si content is always > 3.70 atoms per formula unit (a.f.u.) and the amount of K is [greater than or equal to] 0.60 a.f.u. with a sum of interlayer cations ([SIGMA] inter.) varying in the range of 0.66-0.99 a.f.u. due to the presence of small quantities of Ca. The octahedral sheet is characterised by Fe contents of 0.54-1.08 a.f.u and Al and Mg contents in very similar quantities (0.40-0.80 a.f.u.). When these results are correlated with the BSE images of the filaments composing the laminated green crusts, clear differences can be seen among the chemical composition of lath-like crystals composing the outer coating of the filaments and the inner part (apparently homogeneous) also made up of lath-like crystals, yet smaller (Figs. 6, 7 and 11). The outer lath-like crystals show lower Fe contents and higher Al and Mg contents tan the inner crystals (Table 1, Fig. 11). In addition, there are clear differences in the K content of these two types of glauconitic micas. In the outer crystals, analyses reveal K contents ranging from 0.85-0.90 a.f.u., which are greater than in the inner glauconites, where EDX analyses show K contents of between 0.60-0.69 a.f.u. However, the Ca content, while low in both cases, is higher in the inner crystals. The result is a higher content of interlaminar cations in the outer micas. Finally, the tetrahedral Al is [greater than or equal to] 0.15 a.f.u. in the inner micas, whereas it is always [less than or equal to] 0.16 a.f.u. in the external crystals, as a consequence of a higher content of Si (Fig. 11b). These two sets of data point to two dioctahedral mica populations, glauconite and celadonite, as will be discussed later.

4.2. Black crusts and lens-shaped nappes

Morphology and microstructure

In addition to the green laminated crusts described above, irregular masses of dark green to black clay minerals have been recognised in the calcite infilling. They are lens-shaped discontinuous lentils or nappes < 20 mm long and < 3 mm thick (Fig. 12a). This material is also recorded in many samples as a thin black film or crust between the pillow-lava wall and the glauconitic micas of the green crust. In some cases calcitic growths may have formed earlier than the green laminated crust (Fig. 2c and 5a).

Under the petrographic microscope they appear to contain lath-like crystals < 450 [micro]m in length, randomly oriented (Fig. 12b, c). However, BSE images show convolute veil-like morphologies with a certain chaotic appearance, typical of poorly crystallized grains of smectite (Fig. 13a, b). The transition between these aggregates of flakes, that coalesce or open, and the glauconitic micas composing the green laminated crust can be viewed in Fig. 13c-e. At TEM scale, the aspect of these flakes is subidiomorphic, with curled edges and fractures, sized < 1 [micro]m (Fig. 13f).

Mineralogy and geochemistry

The less-abundant dark green (almost black) material is smectite-rich as was corroborated by the XRD patterns of oriented aggregates. This smectite is characterised by a basal spacing of 14.6 [Angstrom], which expands to 16.56 [Angstrom] after EG treatment. Not only can the 001 reflection be detected, but also the 002, 003 and 005 reflections (Fig.14).

Micro-chemical analyses of the studied growths indicate a saponitic composition normalized to 22 charges (Table 2). The Mg content (up to 2.45 a.f.u.) is always greater than the Fe (up to 0.84 a.f.u.). The main cation in the interlayer is Ca, ranging from 0.05 to 0.15 a.f.u.; Na is absent and K is always < 0.06 a.f.u.. The substitution of Si for Al in the tetrahedral position is scarce (< 0.4 a.f.u.).

5. Interpretation

The genesis of glauconitic minerals in sedimentary environments, widely studied in the literature, is commonly related to sea-bottom confined microenvironments under low sedimentation rate at water-depths ranging 60-350 m by crystallisation of glauconitic smectite (e.g., Odin and Matter, 1981; Odin and Fullagar, 1988; Amorosi, 1995). Maturation from nascent glauconite (glauconitic smectite) to highly evolved glauconite is related to a decrease in Al, Si, Mg, Ca and Na and an increase in K and Fe, producing a decreasingly expandable smectitic component (e.g., Odin and Matter, 1981; Amorosi, 1995; Eder et al., 2007; Sanchez-Navas et al., 2008). In such contexts, glauconite is an authigenic mineral developed as pelletal facies (mud coprolites, foraminiferal tests and mineral debris), and less frequently as films growing in holes, cracks and borings on hardgrounds and omission surfaces that may be associated with phosphates (e.g., Odin and Letolle, 1981; Odin and Matter, 1981; Fischer, 1990; Jimenez-Millan et al., 1998; Wigley and Compton, 2007). According to the chemical ranges for stages of glaucony evolution reported by Odin and Fullagar (1988), the K2O content of the glauconitic micas of this work indicates high maturity (Table 3, Fig. 15). In fact, the most mature glauconitic micas compositionally reach celadonite composition in view of the current nomenclature (Rieder et al., 1998; Toth et al., 2010). Celadonite is the most evolved stage of glauconitisation according to Toth et al. (2010), although in the geological literature the term glauconite is often applied to green grains at any stage of evolution (e.g. Odin and Fullagar, 1988). In this work, we report the textural transition between glauconite and celadonite (Fig. 7). The progressive orientation of the glauconite short lath-like crystals organized as palm-tree branches just in the transition, then through well-oriented large lath-like crystals of celadonite, is congruent with the most evolved stage interpreted as being celadonite with respect to earlier glauconite.

According to the AIPEA (Association Internationale pour l'Etude des Argiles) Nomenclature Committee, glauconite is defined as a Fe-rich dioctahedral mica with tetrahedral Al (or [Fe.sup.3+]) usually >0.2 a.f.u., and octahedral [R.sup.3+] >1.2 atoms (Bailey, 1980), which consist mainly of [Fe.sup.3+], distinguishing from muscovite and phengitic micas. In this work, geochemical and mineralogical analyses of the green crusts recorded among the pillow-lava bodies allowed us to identify glauconitic micas without a smectitic component. Nonetheless, the black to dark-green films between pillow-lava and green laminated crusts correspond almost exclusively to saponitic smectites (Fig. 16). Other mineral phases occupying more internal parts of the studied vein network are calcite and quartz.

The morphology and texture of the studied glauconitic micas is clearly different from the traditional classification of glaucony habits of Millot (1964) and other works (e.g., Odin and Fullagar, 1988), mainly focused on sedimentary environments. Given the type of deposits related to the infilling of voids and veins among pillow-lavas, the environmental context for the genesis of the studied glauconite must be related to hydrothermal rather than sedimentary processes. However, these glauconites are exceptional in the literature because previous (scarce) descriptions of glauconite in hydrothermal environments refer to granular/pelletal glauconites and not to laminated crusts and columns (Buatier et al., 1989, 1993; D'Antonio and Kristensen, 2005; Ionescu et al., 2006; Geptner et al., 2008; Clauer et al., 2011). In addition, celadonite is a typical hydrothermal alteration product of marine basalts in the field veinlets (Andrews, 1980; Delmont, 1985; Staudigel et al., 1986; Odin et al., 1988; Tazaki and Fyfe, 1992; Renac et al., 2010; Toth et al., 2010). It is likely that some studies reporting glauconite from hydrothermal environments are in fact describing celadonite.

5.1. Glauconitic micas and hydrothermal alteration

The composition of the veins filling inter-pillow spaces in the Median Subbetic is very important when interpreting the genetic conditions. Secondary clay minerals and their association with carbonates can reveal whether the alteration occurred under oxidizing or reducing conditions, as a direct consequence of the fluid/rock mass ratio (D'Antonio and Kristensen, 2005; Renac et al., 2010). If the main phase of hydrothermal alteration occurred under oxidizing conditions with a high sea-water/rock ratio, in an open-circulation regime, it would precipitate abundant glauconite and celadonite. Andrews (1980) observed that celadonite forms on fissures open to the top of the volcanic pile (with presence of nannofossils), which is significant in terms of the probable origin of the fluids from which celadonite forms. In addition, when fluids circulate quickly, the environment is sufficiently oxidized for celadonite crystal growth. According to D'Antonio and Kristensen (2005), a high LOI confirms a high sea-water/rock ratio; in the samples of the Median Subbetic, values from 18.9% to 23.8% were detected from XRF analyses.

The studied green crusts composed by clay minerals--mainly glauconite and celadonite, and to a lesser extent by saponitic smectites--appear surrounded by white crystal masses of calcite and quartz, where the black crust and lensshaped nappes of saponite are recorded (Figs. 2, 3 and 12). Nevertheless, glauconite and celadonite are ferric 2:1 phyllosilicates, which implies that the two minerals formed in a semi-confined environment with cation-rich fluids (Odin et al., 1988). The environment cannot be extremely confined (reducing), because the iron in these micas is mainly ferric. In addition, as it is well-documented that the oxidation of iron can be readily mediated by neutrophilic microbes under very low oxygen conditions (e.g. Benz et al., 1998), we cannot exclude the activity of iron-oxidizing microbes. Studies on the hydrothermal alteration of basalts by sea-water at low temperature show an early oxidative phase (Odin et al., 1988; Alt, 1999; Clayton and Pearce, 2000; D'Antonio and Kristensen, 2005). The early alteration mainly proceeds as circulation and diffusion of oxygenated sea-water along veins and inter-pillow spaces coupled with diffusion into the rock (Alt, 1999; Clayton and Pearce, 2000). Another example is shown by Clauer et al. (2011), with crystallisation of glauconite and nontronite generated from hydrothermal fluids mixed with seawater in hydrothermal mounds near the Galapagos Spreading Center. Fe was mobilised by a breakdown of volcanic glass or hydrothermal fluids (in that case [Fe.sub.2]+), while sea-water had to be an additional supplier of K (Clayton and Pearce, 2000; D'Antonio and Kristensen, 2005; Renac et al., 2010; Baker et al., 2012). The volcanic edifices of the Median Subbetic are composed of K-rich pillow-lavas (Vera et al., 1997) and they are potential sources of K. Thus, Fe and K had to be added to the oxidation zone and fixed in the precipitation of Fe-rich dioctahedral micas (glauconite and celadonite).

Regarding the temperature of these deposits, the absence of secondary minerals such as chlorite, epidote and albite constrains the temperature of the hydrothermal alteration under zeolite-facies conditions (<100-150[degrees]C). According to Clayton and Pearce (2000) and D'Antonio and Kristensen (2005), the glauconite precipitation occurred at temperatures ranging 30-60[degrees]C. Recently, Clauer et al. (2011) recorded a crystallisation temperature of 32-63[degrees]C from 818O values in the Galapagos Spreading Center. In turn, Stakes and O'Neil (1982) and Odin et al. (1988) interpret temperatures < 50[degrees]C to form celadonite from 818O values, in agreement with the context of our studied samples. However, Odin et al. (1988) and Desprairies et al. (1989) affirm that celadonite occasionally forms at temperatures between 50 and 90[degrees]C.

Andrews (1980), Desprairies et al. (1984) and Delmont (1985) emphasised the association of celadonite with a black ferriferous saponite from veins developed in marine volcanic rocks. According to our observations, a late phase of alteration is typified by the formation of saponite and must have taken place under confined conditions resulting from the deposition of marine sediments. When iron-bearing fluids circulate more slowly or are trapped, then the environment is dominated by the reducing property of the pillow-basalt. According to D'Antonio and Kristensen (2005), glauconite characterises hydrothermal alteration under oxidizing conditions, whereas saponite and calcite characterise alteration under reducing conditions. In this sense, Clayton and Pearce (2000) established a clay-mineral transition from interestratified glauconite-nontronite, interstratified smectite-glauconite and saponite/beidellite mixture depending on the distance from fluid conduits. Moreover, we must bear in mind the local record of thin films of saponite directly on pillow-lava surfaces, before the development of the thick green laminated crusts. At any rate, there are significant similarities between the products of low temperature hydrothermal alteration in the pillow-lavas of this study as compared with those from ocean-ridge basalts and oceanic crusts (Alt, 1999; Clayton and Pearce, 2000; D'Antonio and Kristensen, 2005), with the presence of early Fe-rich dioctahedral micas followed by a later formation of saponite and carbonates.

The saponite composition of the studied crusts is characterised by a predominance of Ca in the interlayer (Table 2). Part of the Ca composing the hydrothermal fluids and favouring the precipitation of calcite and Ca-saponite was supplied by the surrounding limestones that were simultaneously altered. That is, after the burial of volcanic rocks by marine sediments, with the limitation of the sea-water circulation, the hydrothermal process favoured the precipitation of saponite and calcite under higher temperatures than the glauconitic ones. The restricted cold sea-water circulation led to increasing temperature and reducing conditions. The proposals of estimated saponite formation temperatures from 818O values reportedly range 130-170[degrees]C (Stakes and O'Neil, 1982) or 70[degrees]-130[degrees]C (Desprairies et al., 1989); that is, always higher temperatures than for glauconite and celadonite.

The thicker mineralisations of saponite form lens-shaped nappes inside calcitic veins (Fig. 12) with scarce glauconiteceladonite crystals, observed only under microscopy and BSE imaging (Figs. 13c-e). The transition from glauconitic micas to saponite is compositionally sharp, although texturally saponite presents the same lath-like appearance as glauconitic micas and progressively changes to a convoluted veil-like appearance away from the mineral boundary (Fig. 13c-e). This textural transition allows us to envisage saponite growing on and consuming previous glauconitic micas.

Low temperature hydrothermal alteration occurring in marine environment has been described in the Upper Jurassic basic volcanics of Transylvania with the presence of glauconite and Fe-saponite (Ionescu et al., 2006). D'Antonio and Kristensen (2005) analysed the secondary minerals generated by hydrothermal alteration affecting the basalts of oceanic crust in the West Philippine Sea Basin and recorded clay minerals, mostly glauconite, minor Al-saponite and Fe-beidellite, together with iddingsite, Ca-Na zeolites and calcite. Abad et al. (2003), in the Median Subbetic (Betic Cordillera), recorded and analysed saponite at the contact of marl-limestone rhythmites with a laccolith of dolerites as a consequence of hydrothermal alteration facilitated by an intense fracturation and the circulation of lower-temperature fluids; in the slightly altered rocks Ca-zeolites were also found (Jimenez-Millan et al., 2007). Saponite has also been described in relation to alteration process of marls by basaltic dykes (Henry et al., 2007) and in mudstones and limestones locally metasomatised by the emplacement of a basic sill (Kemp et al., 2005).

Four phases are proposed for the infilling of the veins and inter-pillow spaces of the studied outcrop (Fig. 17):

Very early alteration of the pillow-lava surface, with the influence of reducing fluids and under moderate temperatures (< 200 [degrees]C) during the last episode of volcanic activity recorded by the local black films of saponite and calcite;

Glauconitic micas (glauconite and celadonite) forming later at lower temperature (< 100 [degrees]C) under oxic conditions due to the circulation and diffusion of oxygenated sea-water along veins and inter-pillow spaces (oxidation of [Fe.sub.2]+ would be promoted by environmental conditions or microbial activity);

A second stage of saponite formation with calcite taking place under more confined/reducing conditions and comparatively higher temperature resulting from the deposition of marine sediments, probably affecting previous glauconitic micas;

Calcite and quartz became the latest product to close the remaining space (or producing geodes) among the pillow-lava bodies.

5.2. Presence of microbes during glauconite formation

The record of filaments and coccoid-shaped forms at different scales indicates the potential implication of microbes in the growth of the green laminated crusts (see Figs. 4-7 and 9). The presence of voids occupying the centre of the filaments composing the green laminated crust points to this possibility (Fig. 6). Moreover, the film showing filament-like structures covering the glauconitic crystals in some samples analysed would correspond to biofilm (Figs. 9e, f).

Benthic microbial communities are ubiquitously found on pillow-lavas in recent ocean crust (e.g. Edwards et al., 2005; Santelli et al., 2008; Santelli, 2009). According to Bach and Edwards (2003) and Santelli et al. (2008), basalt alteration reactions are capable of supplying sufficient energy for chemoorganotrophic growth of microbes.

In the context of this research, the record of microbial communities is compatible with the interpreted hydrothermal origin of the green laminated crusts. Modern microbialites occur abundantly in the vicinity of submarine hydrothermal vents, which are the source of nutrients for microbes. Microbes that precipitate iron compounds and other minerals have been described in such environments as hydrothermal chimneys, hydrothermal vents and deep-sea volcanoes (e.g., Juniper and Fouquet, 1988; Vanko et al., 1991; Ghiorse and Ehrlich, 1992; Mandernack and Tebo, 1993; Connell et al., 2009; Templeton et al., 2009; Reolid et al., 2011).

The low-temperature hydrothermal environment inferred for the origin of veins infilling the inter-pillow spaces is compatible with the presence of microbes. Precipitation of iron could be related to increasing pH and Eh created in the microenvironment around microbial clumps: oxidizing and alkaline conditions would have favoured the precipitation of [Fe.sup.3+], whereas C[O.sub.2] is reduced to form carbon organic compounds (carbohydrates). Microbial activity may promote glauconite formation working as a catalyzer, as well as the extracellular polymeric substances (EPS) serving as a specific trap for Fe and K. In the studied green laminated crusts, the existence of mucilaginous biofilms around the filaments and their role as a chelating compound secreted by microorganisms in the precipitation of glauconitic micas may be inferred by the occurrence of voids surrounded by glauconite reproducing the branching filamentous microstructures. Authigenesis occurred through the glauconite precursor precipitated on the EPS. The mineralisation of the microbial biofilms could have occurred simply as a result of passive attracting of [Fe.sub.2]+ ions from hydrothermal fluids to the negatively charged microbial EPS (e.g. Beveridge et al., 1997). At modern hydrothermal vents, the passive mineralisation is believed to constitute the most important process of microbe encrustation with iron (Konhauser, 1998). Whatever the source of [Fe.sub.2]+ (pillow-lava alteration or hydrothermal fluids), a rapid oxidation to [Fe.sup.3+] during its nucleation on microbial surfaces is possible.

Celadonite (the most advanced step in the glauconitisation process of Odin and Matter, 1981) can be interpreted as (1) a later abiotic precipitation on filament surface, the inner glauconite being the nucleation site for subsequent growth of more complex authigenic celadonite, or (2) more external glauconite composing the coating of the filament after successive reactions of recrystallisation trapping more and more potassium (Fig. 15). The distribution of glauconite and celadonite, representing a Fe decreasing trend to the outer part of the filaments, agrees with Fe-chemoorganotrophic processes for the precipitation of glauconite in the EPS, but passive mineralisation of EPS is also a potential mechanism.

The role of microbes in the genesis of glauconite has been pointed out previously in sedimentary environments (Geptner and Ivanovskaya, 2000; Zanin et al., 2004, 2006; Eder et al., 2007; Baldermann et al., 2013) and hydrothermal environments (Tazaki and Fyfe, 1992; Geptner et al., 2008). Tazaki and Fyfe (1992) reported celadonite and glauconite related to filamentous bacteria in the hydrothermal alteration of volcanic sandstones in deep-sea sediments from IzuBonin fore-arc (west Pacific Ocean). However, the cases described in the literature commonly concern green pellets, not laminated crusts. The laminated texture of these glauconitic crusts is congruent with the participation of microbes in the glauconite formation. Other examples from the Subbetic of laminated crusts and macro-oncoids composed by Fe-Mn oxyhydroxides and phosphates have been previously interpreted as related to chemosynthetic microbial communities in marine environments (e.g. Martin-Algarra and Sanchez-Navas, 2000; Reolid and Nieto, 2010). Therefore, the laminated texture is congruent with the inferred microbial origin, and also comparable with calcareous stromatolites widely known in the geological record.

Another clay mineral commonly recorded in the low temperature hydrothermal alteration of basalts is nontronite, which has been described in the literature as genetically related to bacteria in marine white smoker chimneys from the Galapagos Spreading Center and Mariana Trough by Kohler et al. (1994).

Microendolithic microbes from Devonian basalts corresponding to filaments with a branching pattern, preserved as clay minerals chamosite/glauconite and illite/glauconite, were reported by Eickmann et al. (2009). These authors further observed an inner part of the filaments consisting of chamosite/glauconite surrounded by illite-glauconite. The main difference with respect to the examples from pillow-lavas from the Median Subbetic would be the epilithic behaviour of the inferred microbes.

6. Conclusions

The aim of this research was to analyse the secondary minerals composing veins and infilling spaces among pillow-lava bodies from the Jurassic of the Median Subbetic, mainly focused on the characterisation of green laminated crusts and clay minerals.

The mineralogy, geochemistry, and geometric relationships of the minerals infilling the spaces among pillow-lavas allowed us to recognise different stages in the growth of these mineralisations. Saponite and calcite are deposited in a very preliminary phase of the alteration process over the pillowlava surface, under moderate temperature. Glauconite and celadonite form later under oxydizing and cooler conditions due to the circulation of sea-water, and promoted by the activity of chemoorganotrophic microbes, or as passive mineralisation of the extracellular polymeric substances. Microbes benefited both the oxidizing conditions related to the input of sea-water as well as input of reduced hydrothermal fluids rich in metals (they proliferated in the boundary between both conditions).

Subsequently, the temperature increases progressively towards higher values as a consequence of burial promoted by marine sedimentation, which also contributes to reducing conditions. Microbial activity stopped. A new episode of saponite and calcite formation, in some veins with evidence of glauconitic mica consumption, takes place. Finally, calcite and quartz precipitate as the latest products on the voids among pillow-lava bodies, sometimes with incomplete infilling resulting in geodes.


This research was carried out with the financial support of Projects UJA/2011/12/17 (Universidad de Jaen), P11RNM-7408 (Junta de Andalucia), RYC-2009-04316 (Ramon y Cajal Program, Ministerio de Ciencia e Innovacion + FSE) and CGL2011-30153-C02-01 (Spanish Ministry of Science and Innovation) as well as research groups RNM-200 and RNM-325. We are also grateful to A. Piedra, technician at the Laboratorio de Geologia of the Universidad de Jaen, for preparation of thin sections. Prof. J.M. Molina (Univ. Jaen) helped with the literature concerning petrology and mineralogy of the Jurassic volcanic rocks of the Median Subbetic. The constructive remarks of Prof. Massimo D'Antonio (Universita degli Studi di Napoli Federico II) improved the quality of this work. We are grateful to a native English speaker (Jean Louise Sanders) for reviewing the grammar.


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M. Reolid *, I. Abad

Departamento de Geologia and Centro de Estudios Avanzados en Ciencias de la Tierra, Universidad de Jaen, Campus Las Lagunillas sn, 23071 Jaen, Spain

e-mail addresses: (M.R., * corresponding author); (I.A.)

Received: 28 August 2013 / Accepted: 24 April 2014 / Available online: 30 October 2014

Table 1.- Structural formulae for glauconitic micas
of green material normalised to [O.sub.10][(OH).sub.2].

               Si    [sup.IV]   [sup.VI]    Fe     Mg
                        Al         Al

inner micas (glauconite)

Crt 1 03 2    3.79     0.21       0.50     0.98   0.49
Crt 1 03 5    3.82     0.18       0.56     0.91   0.50
Crt 1 03 8    3.74     0.26       0.44     1.05   0.51
Crt 1 04 3    3.75     0.25       0.43     1.08   0.47
Crt 1 04 5    3.76     0.24       0.44     1.05   0.49
Crt 1 05 2    3.80     0.20       0.41     1.03   0.53
Car1 4 1      3.85     0.15       0.57     0.83   0.61
Car1 4 2      3.81     0.19       0.46     0.96   0.59
Car1 4 4      3.80     0.20       0.49     0.93   0.60
Car1 5 3      3.76     0.24       0.43     1.01   0.56
Car1 5 4      3.79     0.21       0.56     0.84   0.61
Car1 5 5      3.77     0.23       0.40     1.05   0.55
Car1 6 1      3.80     0.20       0.48     1.02   0.52
Car1 6 2      3.74     0.26       0.48     0.97   0.56
Car1 7 4      3.81     0.19       0.44     1.02   0.53

outer micas (celadonite)

Crt 1 03 1    3.88     0.12       0.69     0.61   0.67
Crt 1 03 4    3.85     0.15       0.65     0.66   0.63
Crt 1 03 7    3.89     0.11       0.71     0.59   0.65
Crt 1 04 2    3.84     0.16       0.67     0.66   0.62
Crt 1 04 6    3.85     0.15       0.73     0.59   0.64
Crt 1 05 1    3.84     0.16       0.65     0.64   0.66
Car1 4 6      3.91     0.09       0.74     0.57   0.79
Car1 4 7      3.94     0.06       0.75     0.55   0.77
Car1 4 8      3.88     0.12       0.65     0.76   0.71
Car1 7 2      3.97     0.03       0.71     0.54   0.79

              [SIGMA]    K      Ca    [SIGMA]
                oct                   inter.

inner micas (glauconite)

Crt 1 03 2     1.97     0.66   0.13    0.79
Crt 1 03 5     1.97     0.65   0.14    0.78
Crt 1 03 8     2.00     0.66   0.11    0.77
Crt 1 04 3     1.97     0.69   0.11    0.80
Crt 1 04 5     1.98     0.68   0.11    0.79
Crt 1 05 2     1.97     0.69   0.12    0.81
Car1 4 1       2.01     0.63   0.10    0.73
Car1 4 2       2.00     0.66   0.12    0.78
Car1 4 4       2.01     0.67   0.09    0.76
Car1 5 3       2.00     0.64   0.17    0.81
Car1 5 4       2.02     0.61   0.15    0.77
Car1 5 5       2.00     0.67   0.09    0.77
Car1 6 1       2.02     0.60   0.06    0.66
Car1 6 2       2.01     0.65   0.13    0.78
Car1 7 4       1.99     0.64   0.11    0.74

outer micas (celadonite)

Crt 1 03 1     1.98     0.87   0.00    0.87
Crt 1 03 4     1.94     0.87   0.08    0.95
Crt 1 03 7     1.96     0.90   0.00    0.90
Crt 1 04 2     1.95     0.89   0.05    0.94
Crt 1 04 6     1.95     0.88   0.05    0.93
Crt 1 05 1     1.95     0.89   0.08    0.97
Car1 4 6       2.10     0.86   0.00    0.86
Car1 4 7       2.08     0.88   0.00    0.88
Car1 4 8       2.12     0.85   0.00    0.85
Car1 7 2       2.03     0.86   0.13    0.99

EDX analyses. Total Fe considered as [Fe.sup.3+]

Table 2.- Structural formulae for smectites of the black
crusts normalised to [O.sub.10][(OH).sub.2].

             Si    [sup.IV]   [sup.VI]    Fe     Mg
                      Al         Al

CRNE A 1    3.65     0.35       0.14     0.72   2.18
CRNE A 2    3.64     0.36       0.15     0.84   2.00
CRNE A 4    3.65     0.35       0.15     0.76   2.14
CRNE A 6    3.64     0.36       0.16     0.77   2.13
CRNE A 10   3.70     0.30       0.17     0.65   2.20
CRNE A 13   3.65     0.30       0.13     0.73   2.20
CRNE A 15   3.67     0.33       0.13     0.54   2.34
CRNE A 16   3.67     0.33       0.14     0.55   2.34
CRNE A 17   3.70     0.30       0.15     0.54   2.32
CRNE A 21   3.68     0.32       0.18     0.59   2.21
CRNE A 22   3.68     0.33       0.11     0.52   2.44
CRNE A 24   3.70     0.30       0.11     0.51   2.45
CRNE A 26   3.71     0.29       0.13     0.50   2.39
CRNE A 27   3.73     0.27       0.14     0.49   2.41
CRNE A 29   3.66     0.34       0.14     0.56   2.33
CRNE A 31   3.67     0.33       0.17     0.57   2.26
CRNE B 7    3.72     0.28       0.12     0.56   2.36
CRNE B 8    3.81     0.19       0.20     0.52   2.21
CRNE B 10   3.76     0.24       0.14     0.49   2.37

            [SIGMA]oct    K      Ca    [SIGMA]

CRNE A 1       3.05      0.00   0.11    0.11
CRNE A 2       2.99      0.06   0.15    0.22
CRNE A 4       3.05      0.01   0.08    0.09
CRNE A 6       3.06      0.01   0.07    0.07
CRNE A 10      3.02      0.01   0.08    0.09
CRNE A 13      3.05      0.01   0.11    0.12
CRNE A 15      3.02      0.01   0.15    0.15
CRNE A 16      3.03      0.01   0.13    0.14
CRNE A 17      3.01      0.01   0.11    0.13
CRNE A 21      2.98      0.01   0.16    0.18
CRNE A 22      3.06      0.01   0.07    0.08
CRNE A 24      3.07      0.01   0.05    0.06
CRNE A 26      3.04      0.00   0.07    0.08
CRNE A 27      3.04      0.01   0.05    0.06
CRNE A 29      3.03      0.00   0.13    0.14
CRNE A 31      3.00      0.01   0.14    0.15
CRNE B 7       3.04      0.01   0.07    0.08
CRNE B 8       2.94      0.02   0.08    0.10
CRNE B 10      3.01      0.00   0.07    0.07

EMPA analyses. Total Fe considered as [Fe.sup.2+]

Table 3.- Chemical composition of glauconitic micas (wt. %)
of green crusts (EMPA analyses).

                      CRTE 1   CRTE 1   CRTE 1   CRTE 1   CRTE 1
                        1        2        4        5        7

Si[O.sub.2]           51.93    52.46    46.16    48.02    49.09
[A1.sub.2][O.sub.3]    8.33     9.08     8.04     8.13     6.81
MgO                    6.19     6.68     5.77     5.91     4.80
[Fe.sub2][O.sub.3]    13.92    10.95     9.13    10.66    18.18
MnO                    0.00     0.02     0.00     0.01     0.04
Ti[O.sub.2]            0.00     0.00     0.00     0.00     0.00
[Cr.sub.2[O.sub.3]     0.00     0.00     0.02     0.02     0.01
NiO                    0.05     0.00     0.00     0.00     0.00
[K.sub.2]O             8.57     9.01     7.96     8.25     6.82
CaO                    0.25     0.23     0.18     0.25     0.68
[Na.sub.2]O            0.02     0.02     0.00     0.01     0.01
F                      0.16     0.18     0.16     0.14     0.20
Cl                     0.10     0.10     0.17     0.18     0.12
Total                 89.01    88.45    77.26    81.26    86.45

                      CRTE 1   CRTE 1   CRTE 1   CRTE 1   CRTE 1
                        8        10       11       12       13

Si[O.sub.2]           51.08    48.13    50.69    47.56    47.40
[A1.sub.2][O.sub.3]    7.76     6.82     7.13     7.89     7.88
MgO                    4.80     4.88     4.71     5.87     5.91
[Fe.sub2][O.sub.3]    18.76    16.39    18.90    10.80    10.28
MnO                    0.04     0.01     0.03     0.04     0.00
Ti[O.sub.2]            0.00     0.01     0.00     0.00     0.00
[Cr.sub.2[O.sub.3]     0.00     0.02     0.02     0.05     0.00
NiO                    0.00     0.01     0.00     0.00     0.00
[K.sub.2]O             6.83     7.08     6.70     8.01     7.99
CaO                    0.66     0.65     0.64     1.00     0.43
[Na.sub.2]O            0.02     0.00     0.01     0.01     0.00
F                      0.19     0.20     0.16     0.14     0.16
Cl                     0.08     0.09     0.12     0.18     0.15
Total                 89.96    83.99    88.83    81.23    79.89

                      CRTE 1   CRTE 1   CRTE 1
                        15       16       17

Si[O.sub.2]           51.34    44.61    48.05
[A1.sub.2][O.sub.3]    7.04     6.95     6.74
MgO                    5.36     5.65     5.12
[Fe.sub2][O.sub.3]    17.83     8.63    15.97
MnO                    0.03     0.04     0.03
Ti[O.sub.2]            0.00     0.00     0.00
[Cr.sub.2[O.sub.3]     0.00     0.01     0.05
NiO                    0.01     0.01     0.00
[K.sub.2]O             7.21     7.87     7.17
CaO                    0.61     0.20     0.52
[Na.sub.2]O            0.02     0.00     0.05
F                      0.15     0.16     0.22
Cl                     0.10     0.21     0.20
Total                 89.45    73.97    83.70

                      CRTE 1   CRTE 1   CRTE 1
                        18       19       20

Si[O.sub.2]           47.92    47.63    47.72
[A1.sub.2][O.sub.3]    7.89     8.08     7.84
MgO                    6.01     6.03     6.19
[Fe.sub2][O.sub.3]     9.76     8.75     9.32
MnO                    0.01     0.02     0.01
Ti[O.sub.2]            0.00     0.00     0.00
[Cr.sub.2[O.sub.3]     0.02     0.04     0.00
NiO                    0.00     0.00     0.00
[K.sub.2]O             8.38     8.14     8.58
CaO                    0.26     0.26     0.55
[Na.sub.2]O            0.02     0.00     0.00
F                      0.17     0.15     0.12
Cl                     0.19     0.17     0.22
Total                 80.26    78.95    80.23
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Title Annotation:texto en ingles
Author:Reolid, M.; Abad, I.
Publication:Journal of Iberian Geology
Date:Dec 1, 2014
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