Tectonic and magmatic evolution of the active volcanic front in El
Transcription
Tectonic and magmatic evolution of the active volcanic front in El
Geothermics 35 (2006) 368–408 Tectonic and magmatic evolution of the active volcanic front in El Salvador: insight into the Berlı́n and Ahuachapán geothermal areas Samuele Agostini a,∗ , Giacomo Corti a , Carlo Doglioni b , Eugenio Carminati b , Fabrizio Innocenti a,c , Sonia Tonarini a , Piero Manetti a , Gianfranco Di Vincenzo a , Domenico Montanari a a c Istituto di Geoscienze e Georisorse (CNR), Via G. Moruzzi 1, 56124 Pisa, Italy b Dipartimento di Scienze della Terra, Università di Roma, La Sapienza, Piazzale Aldo Moro 5, 00185 Roma, Italy Dipartimento di Scienze della Terra, Università di Pisa, Via S. Maria 53, 56126 Pisa, Italy Received 28 February 2006; accepted 30 May 2006 Available online 11 September 2006 Abstract In El Salvador, Central America, active deformation takes the form of a major dextral strike-slip fault system, the El Salvador Fault Zone, resulting from the oblique subduction of the Cocos Plate. The fault system is laterally discontinuous, being subdivided into different major en-echelon segments that partially overlap to form pull-apart structures. Volcanic activity is spatially confined to the fault segments and absent in the intervening pull-apart basins; no significant temporal gap exists in the erupted products, at least during the Plio-Quaternary. Detailed analyses within the geothermal fields of Berlı́n and Ahuachapán have revealed important volcano-structural and petrologic differences between the two areas. In the Berlı́n area active deformation is controlled by the regional transcurrent stress field, resulting in the development of systems of right-lateral E–W-trending strike-slip faults. Conversely, the structural setting of the Ahuachapán area is more complex, reflecting an interaction among different stress fields. Berlı́n products exhibit a marked geochemical and isotopic homogeneity indicating the presence of a single magmatic system. At Ahuachapán, on the other hand, the rocks display significant variations in both Sr isotopes and the LILE/HFSE ratios: this area is characterized by multiple volcanic centres, fed by different magma batches that reach the surface without reciprocal interactions in shallow reservoirs. Thus, the characteristics of the volcanic products at ∗ Corresponding author. Tel.: +39 050 3152266; fax: +39 050 3153280. E-mail address: [email protected] (S. Agostini). 0375-6505/$30.00 © 2006 Published by Elsevier Ltd on behalf of CNR. doi:10.1016/j.geothermics.2006.05.003 S. Agostini et al. / Geothermics 35 (2006) 368–408 369 Berlı́n and Ahuachapán reflect their different tectonic settings, with important implications for geothermal investigations. © 2006 Published by Elsevier Ltd on behalf of CNR. Keywords: Geothermal exploration; Structural geology; Petrology; Geochemistry; Berlı́n; Ahuachapán; El Salvador 1. Introduction El Salvador is located within the Central American Volcanic Front (CAVF), a volcanic chain extending for more than 1000 km from Guatemala to Costa Rica, and related to the subduction of the relatively young lithosphere (age <25 Ma) of the Cocos Plate beneath the Caribbean Plate (DeMets, 2001) (Fig. 1). The CAVF is divided into several distinct structural segments with different geological and geophysical features (Carr and Stoiber, 1990). The El Salvador segment is characterized by strong tectonic and volcanic activity. The latter has been continuous since at least the early Neogene; during the Holocene 21 volcanoes were active, 6 of which erupted in historical times (Siebert and Simkin, 2002). The widespread magmatic activity has resulted in a relatively high heat flow that has created areas of shallow thermal anomaly whose exploitation is economically feasible. In El Salvador, 22% of the electric energy produced annually is currently being generated by geothermal plants (Bertani, 2005). New geological, geochronological, geochemical and petrological data on the El Salvador volcanic front are presented here, with particular attention paid to the geothermal fields of Berlı́n and Ahuachapán (Fig. 2). A detailed description is given of the volcano-tectonic evolution of the front, which could lead to more reliable evaluations of the real potential of El Salvador’s geothermal resources. 2. Geodynamic setting El Salvador is located on the Caribbean Plate close to its western and northern margins (Fig. 1). To the north, this plate interacts with the North American Plate along the Cayman-Motagua sinistral transcurrent fault. In continental Central America, the contact between the two plates occurs along the complex Motagua fault system, which is located about 100 km from the northwestern Fig. 1. Geodynamic setting of Central America (after DeMets, 2001; Corti et al., 2005a). Dashed white line indicates the volcanic front. 370 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 2. Schematic tectonic map of El Salvador. Dashed columns show the main N–S grabens. Arrows indicate the active stress field (black arrows: the axes of maximum compression; white arrows: the axes of maximum extension); ESFZ, El Salvador Fault Zone. border of El Salvador (Fig. 2). The relative motion associated with this fault system is ∼20 mm/yr (Fig. 1). To the west, the oceanic Cocos Plate is being subducted beneath the Caribbean Plate along the Middle America Trench, at rates of 73–84 mm/yr (Fig. 1) (DeMets, 2001). Several studies suggest that the convergence between the two plates is oblique and partitioned between trenchorthogonal compression and strike-slip deformation parallel to the volcanic front, associated with the northwestward transport of a fore-arc sliver relative to the Caribbean Plate (Fig. 1) (Harlow and White, 1985; White, 1991; DeMets, 2001). The transcurrent component of the movement is estimated to be ∼14 mm/yr (Fig. 1). This complex kinematics is reflected in seismic activity, characterised by earthquakes of two distinct types, subduction-related and strike-slip-related (e.g. Dewey et al., 2004; Martı́nez-Dı́az et al., 2004). Fig. 3. Historical destructive earthquakes and focal mechanisms of crustal-depth earthquakes available for the El Salvador area (numbers: year and magnitude of the events). The thick black line indicates the inferred trace of the El Salvador Fault Zone (ESFZ) (modified after Bosse et al., 1978; Martı́nez-Dı́az et al., 2004; Corti et al., 2005a). RL, Rı́o Lempa; SM, San Miguel; SS, San Salvador. S. Agostini et al. / Geothermics 35 (2006) 368–408 371 The transcurrent component of the movement between the Cocos and the Caribbean plates is probably accommodated onland by slip along a major E–W trending dextral transcurrent fault system (El Salvador Fault Zone, ESFZ; Martı́nez-Dı́az et al., 2004) running along the volcanic front and representing the source of the strong strike-slip seismicity (Figs. 2 and 3; see Section 2.1). Between the dextral ESFZ and the sinistral Motagua fault system, a series of N–S trending grabens testify to the existence of a broad zone of nearly E–W extension (Fig. 2) (Guzmán-Speziale, 2001; see Section 3). Historical and recorded seismicity constrain the exten- Fig. 4. (a) Segmentation of the El Salvador Fault Zone (ESFZ) east of San Salvador. BS, Berlı́n segment; IA, intervening area; IL, Lake Ilopango; SMS, San Miguel segment; SVS, San Vicente segment. (b) Landsat image. (c) Line drawing of major structures in the area west of San Salvador, with the hypothesised pull-apart structure linking two major segments of the ESFZ. 372 S. Agostini et al. / Geothermics 35 (2006) 368–408 sional rates along the grabens of northern Central America to ∼8 mm/yr (Guzmán-Speziale, 2001). 2.1. Strike-slip deformation in El Salvador Geological field work carried out in continental El Salvador suggests that the main structures belonging to the ESFZ have an approximate E–W strike, and are characterized by right-lateral kinematics. These faults running sub-parallel to, and north of, the volcanic front affect Late Pleistocene and Holocene deposits and present a strong morpho-tectonic signature testifying to very recent activity (Fig. 2) (Corti et al., 2005a). The active tectonics of the ESFZ is further corroborated by the strong transcurrent crustal seismicity associated with this fault zone (Martı́nezDı́az et al., 2004). In particular, the major upper crustal seismic events that have taken place since 1912 in El Salvador occur parallel to, and north of, the volcanic front (e.g. Martı́nez-Dı́az et al., 2004). Reliable focal mechanisms indicate strike-slip events with one of the planes oriented E–W (Fig. 3). At least six of the major destructive earthquakes (M ≥ 6) along the volcanic front seem to be related to slip along the ESFZ segment located between Rı́o Lempa and Lago Ilopango (Fig. 4a) (Martı́nez-Dı́az et al., 2004). Geological and seismological analyses suggest that the ESFZ is laterally discontinuous, and divided into large segments that are particularly evident east of the city of San Salvador (Fig. 4a) (Martı́nez-Dı́az et al., 2004; Corti et al., 2005a). Between the city and San Miguel, two major segments have been identified, the first of which extends from the Ilopango Caldera to the San Vicente Volcano-Rı́o Lempa area (San Vicente segment), and the second from Rı́o Lempa eastwards (Berlı́n segment; Fig. 4a). The two segments overlap in a dextral en-echelon style with the formation of an intervening pull-apart basin. East of San Miguel, the strain may be transferred to a third segment (San Miguel segment) that is, however, poorly known as yet. West of San Salvador the existence of another major segment of the ESFZ can be hypothesized on the basis of strike-slip focal mechanisms (e.g. Martı́nez-Dı́az et al., 2004). The structural pattern obtained through analysis of satellite images and aerial photos suggests that this segment can be linked to the Ilopango-San Vicente sector of the ESFZ through another major pull-apart basin, extending between Santa Ana and San Salvador (Fig. 4b). 3. The volcanic front: structure and stratigraphy Subduction of the oceanic Cocos Plate under the Caribbean Plate resulted in the development of a volcanic front that, in El Salvador, comprises 21 active volcanoes, 3 of which (Santa Ana, San Salvador and San Miguel) erupted after 1900 (Siebert and Simkin, 2002). The CAVF runs from southern Mexico to Costa Rica, with gaps in which active volcanism is absent. Carr et al. (1982, 2004) recognized a number of breaks separating seven segments that are assumed to be tectonically controlled. The active volcanic front in El Salvador constitutes one of these segments, located between those of Guatemala and Nicaragua. In El Salvador, detailed structural investigations have, however, led to the identification of at least three E–W segments arranged en-echelon (Fig. 5); again, this architecture is assumed to be controlled by regional tectonics. The El Salvador area is almost entirely made up of Cenozoic to Recent volcanic rocks and reworked volcanic material. The sedimentary basement is exposed sporadically in the NW corner of the region, where the Metapán Formation (Jurassic-Cretaceous) outcrops. This formation consists of quartz-rich conglomerates, limestones and sandstones with rare intercalations of volcanic rocks (Bosse et al., 1978). S. Agostini et al. / Geothermics 35 (2006) 368–408 373 Fig. 5. Schematic representation of the main segments of the volcanic front (dotted ellipses) within El Salvador. AH, Ahuachapán; B, Berlı́n; SA, Santa Ana Volcano; SM, San Miguel Volcano; SS, San Salvador. Fig. 6. General stratigraphic section and nomenclature for Upper Cenozoic formations in El Salvador region (modified from Donnelly et al., 1990). 374 S. Agostini et al. / Geothermics 35 (2006) 368–408 The Cenozoic volcanic products are the result of the trenchward (i.e. southward) migration of the volcanic front (e.g. La Femina et al., 2002). Several volcanic formations, ranging from Paleocene to Recent, have been distinguished on the geological map of El Salvador (Bosse et al., 1978; Donnelly et al., 1990); a generalized stratigraphic section of the outcropping products is reported in Fig. 6. The oldest (Paleocene-Miocene) formations (Morazán and Chalatenango) are exposed in the northern inner part of the region, close to the border with Honduras. PleistoceneHolocene products, including the active volcanoes, are comprehensively grouped within the San Salvador Formation, which, for the most part, developed over the Miocene-Pliocene Bálsamo Formation, formed by an assemblage of volcanoclastics and volcanic breccias with intercalated lavas and scorias. Locally, a relatively thin layer of Plio-Quaternary volcanics known as the Cuscatlán Formation (e.g. Donnelly et al., 1990) may be present between the Bálsamo and the San Salvador Formations. 4. Geology of the Berlı́n and Ahuachapán geothermal areas 4.1. Berlı́n area The volcanic sequence in the Berlı́n area is characterized by a local basement corresponding to the Bálsamo Formation. Over the basement there are remnants of an old (Pleistocene) stratovolcano, covered by a sequence of ignimbrite layers and pumice fall deposits that are likely related to the formation of a caldera structure; the pyroclastics have an age around 0.1 Ma (D’Amore and Mejia, 1999). The youngest activity is represented by basaltic and basaltic-andesitic lava flows. The geothermal area lies within the ESFZ, close to the pull-apart structure linking the Berlı́n and San Vicente segments (Fig. 2). The structural analysis carried out in this area reveals that the E–W strike-slip faults of the ESFZ are associated with minor structures that can be assigned to three different sets according to their fault orientation (Fig. 7) (Corti et al., 2005a): (1) WNW–ESE (∼N110◦ E); (2) NW–SE (∼N130◦ E); (3) NNW–SSE to N–S (N170◦ E to N180◦ E). As observed in the classical strike-slip physical experiments (e.g. Tchalenko, 1970), these different fault sets can be related to an E–W dextral shear couple, with the E–W structures representing the main deformation zone (Y shears) and the subordinated fault trends representing Riedel (WNW–ESE), antithetic Riedel (NNW–SSE to N–S), shear and tension (NW–SE) fractures. Fault-slip analysis on different structural stations along the main structures indicates a dominant strike-slip stress field, with σ 1 and σ 3 oriented ∼NNW–SSE (∼N155◦ E) and ∼ENE–WSW (∼N65◦ E), respectively (Fig. 7) (Corti et al., 2005a). At volcanic edifices such as the Berlı́n one, tension fractures related to an extensional stress field may locally predominate and create complex interactions with the strike-slip structures, as suggested by small-scale analogue models of magma intrusion during transcurrence (Fig. 8; Corti et al., 2005b). 4.2. Ahuachapán-Cuyanasul area In the Ahuachapán region, four main volcanic stages were identified by geological mapping (González Partida et al., 1997). Several stratovolcanoes formed over the local Bálsamo basement (e.g. Cuyanausul, Cerro de Apaneca, Cerro Empalizada); they were dissected by a caldera event associated with abundant pyroclastic products; the structure is known as Concepción de Ataco Caldera (Fig. 9). The post-caldera activity took the form of small mixed volcanoes (Volcán de las Ninfas, Laguna Verde, Hoyo de Cuajuste) and domes (Cerro San Lázaro). The Ahuachapán- S. Agostini et al. / Geothermics 35 (2006) 368–408 375 Fig. 7. (A and B) Digital elevation model and map of active structures forming the El Salvador Fault Zone (ESFZ) between Ilopango Caldera and San Miguel. Inset in (A) shows the location of the study area. Digital Elevation Model data and Landsat Enhanced Thematic Mapper 7 satellite mosaic images courtesy of the University of Maryland, Global Land Cover Facility. IL, Ilopango; RL, Rı́o Lempa. Inset in (B) shows a schematic interpretation of the fault pattern. (C) Stereonets of fault-slip data collected along the ESFZ (Wulff net, lower hemisphere). The large black arrows indicate the direction of compression and extension (after Corti et al., 2005a). The localities of structural sites are reported in (B). Cuyanausul area is characterised by a complex tectonics since the region is located close to the western end of the Motagua and El Salvador fault systems and to the N–S grabens associated with the intraplate deformation of the Caribbean Plate (Fig. 9a). Detailed field work revealed the presence of faults of different strikes that can be assigned to four main groups (Fig. 9b): (a) N–S, (b) NW–SE, (c) NE–SW, and (d) E–W. The N–S and NW–SE trending structures predominate. Most of these faults are normal with a minor component of oblique motion (either sinistral or dextral). All the analyzed structural trends are very young, as they affect Late PleistoceneHolocene volcanic rocks. The structures with the most conspicuous morphological evidence are the NE–SW oriented faults that, in the area west of the geothermal power plant, seem to accommodate the active deformation. These structures cut both the N–S and the NW–SE faults. 376 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 8. Top: fault pattern at the Berlı́n Caldera. Bottom: small-scale model of magma intrusion along a strike-slip fault (after Corti et al., 2005b) showing a remarkable similarity with faulting at the Berlı́n geothermal field. However, the occurrence of very recent N–S faults and grabens in the NE part of the study area (e.g. Fig. 9a) and the analysis of local seismicity suggest an active stress field characterised by E–W extension (Guzmán-Speziale, 2001). At a regional scale, the N–S structures seem to be more or less contemporaneous with the NE–SW faults. At the outcrop scale, there appear to be no temporal relationships between the E–W striking fault structures and the above-mentioned trends. On the basis of regional (largescale) tectonics, the E–W trend could be related to the dextral strike-slip fault system of the ESFZ, hidden below the volcanic edifices. These different structures could therefore testify to the interaction among different stress fields at a regional scale. In particular, the NW–SE and the E–W trends could be associated with the transcurrent stress field responsible for the development of the ESFZ, whereas the N–S structures are likely generated by the E–W extensional stresses that cause intraplate deformation and the development of the N–S graben systems. The NE–SW trend could be related to the Motagua stress field or to reactivation of a pre-existing fabric generated by this major fault system. 4.3. Geochronology There is some uncertainty with regard to the geochronological constraints of the Salvadorean volcanic formations. In the Ahuachapán area, González Partida et al. (1997) claimed, on the basis of K–Ar datings, that the Bálsamo Formation could be as young as the Pleistocene. In the Berlı́n region, on the other hand, the local volcanic basement represented by the Bálsamo is considered to be at least 2 Ma old (Anderson et al., 1994). S. Agostini et al. / Geothermics 35 (2006) 368–408 377 Fig. 9. (a) Landsat Thematic Mapper satellite image of the Ahuachapán area with detail of N–S normal faults, indicating a roughly E–W extension. (b) Graphic representation (Stereonets) of the structures measured at outcrop scale superimposed on a digital elevation model, showing the main faults of the Ahuachapán area. Black dots evidence rim of Concepción de Ataco Caldera. In order to better constrain the stratigraphic sequence at Berlı́n and Ahuachapán, we selected six samples for 39 Ar–40 Ar isotopic age determinations (see Table 1 for their location). The three from Berlı́n constitute a sequence ranging from local basement (Bálsamo, ES 46) to the youngest products (ES 8-scoria, and ES 27-lava). Likewise, the Ahuachapán samples encompass the age Table 1 Location of the collected samples Sample Place Rock type Latitude (N) Longitude (W) Formation BE 1 BE 2 BER 1 BER 3 ES 1 ES 2 ES 3 ES 4 ES 5 ES 6 ES 7 ES 8 ES 9 Berlı́n Berlı́n Berlı́n Berlı́n Volcán San Salvador (El Boquerón) Volcán San Salvador (El Boquerón) Volcán San Salvador Coatepeque Ilopango Ilopango Cojutepeque Berlı́n Berlı́n Pumice Lava flow Lava flow Lava fragments Lava block Lava Lava Dyke Lava dome Lava dome Lava Scoria Pumice 13◦ 30 26 13◦ 31 00 – 13◦ 35 04 13◦ 44 07 13◦ 45 29 13◦ 48 26 13◦ 53 37 13◦ 42 23 13◦ 42 32 13◦ 43 44 13◦ 31 39 13◦ 31 39 88◦ 32 13 88◦ 31 42 – 88◦ 34 11 89◦ 16 48 89◦ 16 12 89◦ 19 35 89◦ 31 49 89◦ 03 50 89◦ 04 05 88◦ 55 59 88◦ 29 44 88◦ 29 44 San Salvador Bálsamo Bálsamo Bálsamo San Salvador San Salvador San Salvador San Salvador Cuscatlán Cuscatlán Bálsamo San Salvador San Salvador 378 S. Agostini et al. / Geothermics 35 (2006) 368–408 Table 1 (Continued ) Sample ES 10 ES 16 ES 23 ES 27 ES 28 ES 29 ES 30 ES 31 ES 32 ES 35 ES 39 ES 40 ES 41 ES 42 ES 43 ES 44 ES 45 ES 46 ES 47 ES 48 ES 50 ES 51 ES 52 ES 53 ES 54a ES 54b ES 55 ES 56 ES 57 ES 58 ES 59 ES 60 ES 61 ES 62 ES 63 ES 64 ES 65 ES 66 ES 67 ES 68 ES 69 ES 70 Place Berlı́n San Francisco Gotera Berlı́n (Alegria) Berlı́n (Agua Caliente) Berlı́n (TR 18) CA-4 Cerro Nejapa CA-4 Guazapa CA-4 Cerro Rico Nueva Concepción Ahuachapán (Cuyanausul) Ahuachapán (Hoyo de Cuajuste) Ahuachapán (Poza del Diablo) Ahuachapán (Juayua) Ahuachapán (Cerro de Apaneca) Ahuachapán (Concepción de Ataco) Izalco CA-1 Puente Rı́o Lempa CA-1 Puente Rı́o Lempa San Miguel Conchagua Ahuachapán (Las Chinamas) Ahuachapán (Cerro San Lázaro) Ahuachapán (Cerro San Lázaro) Ahuachapán (Cerro San Lázaro) Ahuachapán (Rı́o Frı́o) Ahuachapán (Rı́o Frı́o) Ahuachapán (Chalchuapa) Ahuachapán (La Magdalena) Ahuachapán (La Magdalena) Ahuachapán (San Isidro) Ahuachapán (Turı́n) Ahuachapán (Cerro San Lázaro) Ahuachapán (Cuyanausul) Concepción de Ataco Concepción de Ataco Concepción de Ataco Concepción de Ataco Ahuachapán (Atiquizaia) Ciudad del Triunfo Ciudad del Triunfo Rı́o Lempa Berlı́n (Lomo Los Capules) Rock type Latitude (N) Longitude (W) Formation Glass fragments Perlitic lava Lava Lava Lava Lava Lava Neck Lava Lava Lava Altered lava Lava block Lava Lava Lava Dyke Lava Lava Lava Lava Lava Lava Lava Ignimbrite Ignimbrite Lava Lava Lava Lava Lava Lava Lava Dyke Lava Lava Lava Pumice Lava Lava Lava Lava 13◦ 31 39 88◦ 29 44 San Salvador Chalatenango San Salvador San Salvador San Salvador Bálsamo Bálsamo Bálsamo Bálsamo San Salvador San Salvador San Salvador San Salvador San Salvador Bálsamo San Salvador Bálsamo Bálsamo San Salvador San Salvador Bálsamo San Salvador San Salvador San Salvador Bálsamo Bálsamo San Salvador San Salvador San Salvador Bálsamo San Salvador San Salvador San Salvador Bálsamo Bálsamo Bálsamo Bálsamo San Salvador Bálsamo Bálsamo Bálsamo Bálsamo 13◦ 40 07 13◦ 31 00 13◦ 31 31 13◦ 30 07 13◦ 48 42 13◦ 50 36 14◦ 06 16 14◦ 09 11 13◦ 54 18 13◦ 52 57 13◦ 56 03 13◦ 51 25 13◦ 50 27 13◦ 53 08 13◦ 44 42 13◦ 37 00 13◦ 39 25 13◦ 30 36 13◦ 17 58 14◦ 01 16.5 13◦ 56 25.6 13◦ 56 25.6 13◦ 56 15.7 13◦ 59 40.5 13◦ 59 40.5 14◦ 02 39.4 14◦ 02 56.1 14◦ 03 34.9 14◦ 05 57.9 13◦ 57 50.9 13◦ 57 14.8 13◦ 54 41.2 13◦ 51 39.9 13◦ 49 51.5 13◦ 49 33.3 13◦ 48 50.2 13◦ 57 51.9 13◦ 33 00.1 13◦ 32 46.4 13◦ 35 14.4 13◦ 34 05.1 88◦ 05 36 88◦ 30 29 88◦ 30 13 88◦ 31 13 89◦ 11 43 89◦ 09 29 89◦ 14 04 89◦ 18 19 89◦ 46 11 89◦ 47 49 89◦ 47 21 89◦ 44 20 89◦ 48 35 89◦ 51 20 89◦ 37 39 88◦ 33 56 88◦ 42 37 88◦ 14 50 87◦ 48 54 89◦ 54 12.5 89◦ 46 36.9 89◦ 46 36.9 89◦ 46 47.6 89◦ 49 32.8 89◦ 49 32.8 89◦ 41 59.1 89◦ 42 11.3 89◦ 42 21.1 89◦ 42 24.6 89◦ 45 33.4 89◦ 47 15.5 89◦ 45 42.9 89◦ 50 33.9 89◦ 50 33.9 89◦ 51 22.6 89◦ 51 18.6 89◦ 44 28.0 88◦ 21 57.4 88◦ 20 09.0 88◦ 35 42.4 88◦ 31 10.6 All samples labeled ES were collected in El Salvador by the authors. The samples labeled BE and BER were taken in the Berlı́n area by other researchers but analyzed in the IGG-CNR laboratories. interval from the local basement (ES 43) to the volcanic rocks preceding the formation of the Cuayanausul Caldera (ES 35), and the post-caldera activity (ES 39). The results are reported in Table 2. The analytical procedure and results are described in detail in Appendix A. The geochronological data obtained indicate that the exposed volcanic sequence in Berlı́n and Ahuachapán is of Quaternary age. Thus, in both areas the top of the Bálsamo Formation was formed during the Pleistocene, further supporting geological observations on a temporal Table 2 40 Ar–39 Ar isotope ages for Berlı́n and Ahuachapán rocks Locality Berlı́n area ES 8 Berlı́n-Mercedes Humana ES 27 Berlı́n-Agua Caliente ES 46 Puente Rı́o Lempa Ahuachapán area ES 39 Cuyanausul-Hoyo de Cuajuste (post-caldera) ES 35 Cuyanausul (pre-caldera) ES 43 Concepción de Ataco a b c d e f g Formation No. of stepsa Total gas age (ka) 40 Ar* SS SS Ba 11 8 8 62 ± 53 50 ± 35 414 ± 29 SS 8 SS Ba 8 8 %b Plateau age (ka)c No. of steps plateaud Isochron age (ka) MSWDe (40 Ar/36 Ar)i f Preferred age (ka)g 1.2 2.6 27.7 55 ± 36 57 ± 35 411 ± 17 11 8 8 65 ± 72 106 ± 68 414 ± 27 0.26 1.53 0.33 294.8 ± 9.9 288 ± 20 293.8 ± 8.3 ≤115 ≤85 415 ± 27 58 ± 27 1.4 55 ± 15 8 54 ± 21 0.85 295.6 ± 2.4 ≤75 129 ± 31 248 ± 67 4.6 5.9 125 ± 19 239 ± 43 8 8 127 ± 20 272 ± 169 0.49 0.36 295.1 ± 3.0 293 ± 17 127 ± 20 248 ± 67 See Appendix A for details of heating steps. Percent of radiogenic 40 Ar. Average age resulting from gas released in different heating steps showing similar apparent age. Number of heating steps used to calculate plateau age. Mean square weighted deviate. Initial 40 Ar/36 Ar ratio. See Appendix A for criteria used. Errors are given at 2σ. SS, San Salvador Formation; Ba, Bálsamo Formation. S. Agostini et al. / Geothermics 35 (2006) 368–408 Sample 379 380 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 10. Total alkali vs. silica classification diagram (Le Maitre, 2002) for El Salvador volcanic rocks. Literature samples from active volcanic front (gray dots) from Carr’s database (http://www-rci.rutgers.edu/∼carr/index.html). SS in parentheses indicates samples from Ahuachapán and Berlı́n geothermal areas belonging to the San Salvador Formation. continuity between the Bálsamo products and the youngest volcanism. It is also worth noting that the current volcanic edifices in the Berlı́n and Ahuachapán-Concepción de Ataco areas were formed essentially during the last 100 ka. 5. Petrography and chemistry 5.1. Classification Whole-rock major and trace-element analyses of 54 representative samples from Berlı́n, Ahuachapán and the El Salvador volcanic front are given in Table 3 (see Table 1 for sample location; rock samples are labeled ES, BE and BER). Analyses of 28 borehole samples from geothermal wells drilled in the Berlı́n and Ahuachapán areas are also reported (Table 4; borehole samples from Berlı́n are labeled TR, and those from Ahuachapán are labeled AH and TO). The data are plotted in TAS (total alkali silica) and K2 O versus SiO2 classification diagrams together with data on volcanic rocks taken from the literature (Figs. 10 and 11). Overall, the studied rocks form a subalkaline association, ranging in composition from basalts to rhyolites with a predominance of relatively less evolved rocks, although the association displays different degrees of alkali enrichment. In the K2 O versus silica diagram most of the samples fall in the field of a typical calc-alkaline series; the few rocks exhibiting higher K2 O content lie astride the boundary line between calc-alkaline and high-K calc-alkaline associations (Fig. 11). A wide dispersion of K2 O values is observed in the basaltic rocks where, at comparable silica abundance, K2 O ranges from 0.60% (ES 67, SiO2 = 51.6%) to 1.55% (BER 3, SiO2 = 51.4%) (Table 3). It is noteworthy that the two samples with lowest and highest K2 O content belong to the Bálsamo Formation. The most evolved rocks exhibit similar potassium dispersions, and two distinct groups of rhyolites with high (≈5%) and low (≈2.2%) potassium abundance can be distinguished (Fig. 11). S. Agostini et al. / Geothermics 35 (2006) 368–408 381 Table 3 Major and trace elements of El Salvador volcanic rocks Bálsamo Formation ES 45 (Berlı́n) ES 69 (Berlı́n) BE 2 (Berlı́n) SiO2 (wt.%) TiO2 Al2 O3 Fe2 O3 FeO MnO MgO CaO Na2 O K2 O P2 O5 L.O.I. 47.63 1.07 18.58 5.84 6.05 0.19 4.31 10.60 2.63 0.67 0.24 0.82 50.03 1.12 17.48 3.39 7.50 0.19 3.91 9.54 2.87 1.14 0.34 1.28 50.68 1.22 17.92 12.10 51.19 1.14 17.55 11.70 0.20 4.27 9.51 2.73 1.39 0.32 −0.21 Total 98.63 98.79 100.13 Be (ppm) Sc V Cr Co Ni Cu Ga Rb Sr Y Zr Nb Cs Ba La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Hf Ta Tl Pb Th U 0.55 35 320 8 32 10 156 18.2 12.6 688 19.6 48.0 1.21 0.49 397 7.5 17.1 2.70 13.1 3.44 1.28 3.67 0.58 3.39 0.71 1.85 0.28 1.71 0.24 1.44 0.07 0.03 3.3 0.67 0.37 BER 3 (Berlı́n) ES 70 (Berlı́n) BER 1 (Berlı́n) ES 46 (Berlı́n) 60.49 1.03 15.61 8.84 0.20 3.99 9.24 2.78 1.54 0.34 0.07 58.14 0.99 16.70 8.25 0.60 0.20 2.08 5.23 4.29 2.21 0.41 0.31 99.74 99.41 281 11 32 5 84 0 20 0 24 466 32 129 4 39 427 42 210 5 698 16 33 1278 24 39 ES 43 (Ahuac.) ES 58 (Ahuac.) ES 50 (Ahuac.) 0.19 1.23 4.14 3.93 2.79 0.44 0.83 60.82 0.70 17.46 3.81 2.72 0.13 1.61 5.15 4.24 1.71 0.20 1.03 50.03 0.91 18.53 3.25 6.70 0.18 4.56 9.59 2.84 1.20 0.21 1.01 52.43 1.09 17.58 1.87 6.66 0.16 4.96 7.96 3.64 1.28 0.42 0.88 57.42 0.59 18.04 3.20 3.40 0.14 3.01 6.91 3.45 1.43 0.18 1.31 99.52 99.58 99.01 98.93 99.08 1.11 16 103 1 10 3 7 16.8 29.4 483 25.1 114.9 2.65 0.53 893 13.3 23.8 4.18 18.8 4.56 1.28 4.47 0.71 4.17 0.86 2.39 0.38 2.46 0.38 3.08 0.20 0.09 4.9 1.95 0.98 0.82 31 253 51 31 30 121 17.9 27.3 592 23.4 75.2 1.50 1.18 477 10.4 23.0 3.49 15.6 3.92 1.29 4.05 0.66 3.89 0.83 2.19 0.33 2.10 0.31 2.11 0.10 0.12 3.5 1.64 0.75 181 83 27 40 123 7 20 8 19 558 28 166 6 21 494 16 102 2 628 21 43 604 8 22 382 S. Agostini et al. / Geothermics 35 (2006) 368–408 Table 3 (Continued) San Salvador Formation ES 64 (Ahuac.) ES 65 (Ahuac.) ES 63 (Ahuac.) ES 54B (Ahuac.) ES 62 (Ahuac.) ES 54 (Ahuac.) ES 30 (Cerro Guazapa) ES 31 (Cerro Rico) ES 29 (Cerro Nejapa) ES 67 (Ciudad del Triunfo) SiO2 (wt.%) TiO2 Al2 O3 Fe2 O3 FeO MnO MgO CaO Na2 O K2 O P2 O5 L.O.I. 57.45 0.73 17.61 4.00 3.64 0.14 2.59 6.72 3.71 1.41 0.14 0.74 58.05 0.79 17.50 4.11 3.97 0.11 2.71 6.07 3.75 1.38 0.13 1.26 58.74 0.82 17.54 3.49 3.66 0.12 1.98 5.62 4.35 1.41 0.20 0.84 59.71 0.72 17.29 3.04 3.42 0.15 1.86 5.17 4.67 1.80 0.19 0.62 63.78 0.69 16.25 0.99 3.93 0.15 1.32 3.57 5.17 2.42 0.25 0.48 64.19 0.59 16.37 2.96 2.08 0.11 0.92 3.06 5.25 2.52 0.15 0.65 49.78 1.07 19.35 2.01 8.25 0.20 3.49 9.59 2.82 1.16 0.23 1.03 50.16 1.07 17.28 2.63 6.58 0.15 6.48 8.77 2.91 1.12 0.29 1.66 50.40 1.06 18.66 2.51 6.96 0.16 5.19 8.77 3.02 1.04 0.26 0.63 50.96 0.94 21.04 4.20 4.79 0.16 2.84 9.90 3.20 0.59 0.18 0.43 Total 98.88 99.83 98.77 98.64 99.00 98.85 98.98 99.10 98.66 99.23 Be (ppm) Sc V Cr Co Ni Cu Ga Rb Sr Y Zr Nb Cs Ba La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Hf Ta Tl Pb Th U 154 7 21 4 174 4 22 5 130 1 17 3 100 4 16 4 42 0 10 4 48 0 8 4 267 7 22 3 34 347 31 124 3 29 360 24 111 3 31 349 38 141 4 39 348 30 147 3 54 285 37 213 3 58 293 32 213 6 9 621 19 59 3 624 7 22 602 10 18 707 12 18 880 12 32 978 18 31 1067 18 31 399 5 15 S. Agostini et al. / Geothermics 35 (2006) 368–408 383 Table 3 (Continued) San Salvador Formation ES 7 (Cojutepeque) ES 68 (Ciudad del Triunfo) ES 32 (Nueva Concepción) ES 16 (San Francisco Gotera) ES 28 (Berlı́n) ES 23 (Berlı́n) ES 27 (Berlı́n) ES 8 (Berlı́n) ES 9 (Berlı́n) ES 10 (Berlı́n) SiO2 (wt.%) TiO2 Al2 O3 Fe2 O3 FeO MnO MgO CaO Na2 O K2 O P2 O5 L.O.I. 51.35 0.85 17.78 9.93 0.15 4.26 9.47 2.50 1.42 0.19 0.70 52.51 0.99 17.87 3.37 6.92 0.18 3.91 8.30 3.27 0.83 0.22 0.90 52.80 1.06 17.23 2.76 5.67 0.15 4.14 8.19 3.06 1.57 0.45 1.74 70.45 0.16 14.04 0.92 0.78 0.10 0.35 1.05 2.72 5.18 0.04 4.14 54.15 0.76 17.77 3.60 5.32 0.17 3.91 8.00 2.96 1.56 0.19 0.45 55.99 0.75 17.46 3.08 5.14 0.16 3.49 7.43 3.15 1.87 0.17 0.62 56.58 0.71 17.29 2.62 4.93 0.16 3.04 6.85 3.20 2.05 0.19 1.13 57.97 0.90 17.28 2.43 5.07 0.22 2.43 5.75 4.49 1.56 0.34 0.85 61.89 0.59 16.25 1.19 3.66 0.15 1.46 3.84 4.04 2.31 0.17 3.51 63.90 0.66 16.57 1.19 3.50 0.19 1.32 3.48 5.11 2.32 0.22 0.75 Total 98.60 99.27 98.82 99.93 98.84 99.31 98.75 99.29 99.06 99.21 Be (ppm) Sc V Cr Co Ni Cu Ga Rb Sr Y Zr Nb Cs Ba La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Hf Ta Tl Pb Th U 0.71 30 236 10 30 17 82 17.5 30.3 468 22.5 103.7 2.23 0.55 580 10.0 21.8 3.27 14.6 3.74 0.94 3.88 0.62 3.73 0.78 2.16 0.32 2.01 0.30 2.88 0.17 0.10 4.8 2.29 1.12 260 6 30 4 17 507 37 82 3 596 10 18 0.82 25 209 4 27 11 221 16.8 30.2 467 23.5 109.3 2.53 0.73 712 10.4 23.2 3.44 15.4 3.74 0.91 3.95 0.64 3.78 0.80 2.27 0.35 2.28 0.34 3.04 0.17 0.16 31.4 2.06 1.08 0.98 24 106 2 42 3 18 18.0 28.5 513 33.9 108.1 2.48 1.54 870 12.2 27.5 4.43 20.8 5.51 1.57 5.99 0.95 5.62 1.20 3.28 0.48 3.03 0.46 3.32 0.18 0.08 4.6 1.98 1.04 1.32 17 35 1 5 2 9 17.2 44.3 363 37.4 153.6 3.38 2.35 1135 14.4 32.8 4.97 22.4 5.73 1.38 6.07 1.00 6.04 1.31 3.68 0.56 3.63 0.56 4.54 0.23 0.26 7.8 2.91 1.56 384 S. Agostini et al. / Geothermics 35 (2006) 368–408 Table 3 (Continued) San Salvador Formation BE 1 (Berlı́n) SiO2 (wt.%) TiO2 Al2 O3 Fe2 O3 FeO MnO MgO CaO Na2 O K2 O P2 O5 L.O.I. Total Be (ppm) Sc V Cr Co Ni Cu Ga Rb Sr Y Zr Nb Cs Ba La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Hf Ta Tl Pb Th U ES 42 (Ahuac.) ES 57 (Ahuac.) ES 41 (Ahuac.) ES 55 (Ahuac.) ES 51 (Ahuac.) ES 59 (Ahuac.) ES 35 (Ahuac.) ES 56 (Ahuac.) ES 39 (Ahuac.) 0.11 1.22 2.34 4.11 2.36 0.16 2.62 47.72 1.08 17.29 4.35 7.74 0.19 6.91 10.10 2.62 0.60 0.15 0.65 48.41 1.31 16.64 6.38 3.05 0.15 8.27 9.42 3.09 1.08 0.32 0.65 49.62 0.92 18.28 3.18 6.76 0.18 4.61 9.57 2.84 1.17 0.21 0.75 49.64 1.25 17.30 1.27 7.56 0.15 7.32 8.95 3.36 1.20 0.33 0.59 55.39 0.84 18.10 2.19 6.09 0.16 3.22 6.95 3.83 1.48 0.21 0.42 55.74 0.84 17.94 2.05 5.98 0.15 3.29 7.00 3.69 1.61 0.19 0.90 57.31 0.85 17.47 3.56 3.81 0.14 3.03 5.73 3.97 1.92 0.22 1.07 58.31 0.74 17.72 7.00 0.33 0.07 1.74 5.61 3.71 1.57 0.15 1.92 58.92 0.77 18.18 3.21 3.29 0.14 2.15 5.83 4.30 2.01 0.26 0.48 59.13 0.70 17.89 1.65 4.97 0.14 2.41 5.57 3.85 2.13 0.17 1.40 59.95 0.62 16.88 1.55 4.65 0.14 2.16 5.62 3.75 2.25 0.19 1.45 100.42 99.40 98.77 98.09 98.92 98.88 99.38 99.08 98.87 99.54 100.01 99.21 65.36 0.70 16.50 4.94 0.48 45 343 26 46 23 109 18.0 6.0 393 21.6 56.1 1.30 0.17 309 5.6 12.4 2.03 9.8 2.89 1.08 3.38 0.57 3.53 0.76 2.12 0.31 2.01 0.27 1.66 0.10 0.03 2.1 0.98 0.37 ES 60 (Ahuac.) ES 52 (Ahuac.) 215 292 38 134 213 227 35 111 173 2 24 6 176 2 24 6 140 7 24 10 121 1 18 5 97 1 17 5 20 541 22 142 9 19 577 23 150 8 34 400 25 130 3 37 391 25 132 2 35 401 116 98 4 50 329 29 166 3 52 348 25 160 4 278 11 29 380 13 29 650 13 32 629 15 29 824 89 53 802 12 32 711 12 36 S. Agostini et al. / Geothermics 35 (2006) 368–408 385 Table 3 (Continued) San Salvador Formation ES 53 ES 61 ES 66 ES 47 ES 48 ES 2 ES 44 ES 1 ES 4 ES 3 ES 5 ES 6 (Ahuac.) (Ahuac.) (Ahuac.) (San Miguel) (Conchagua) (Boquerón) (Izalco) (Boquerón) (Coatepeque) (Boquerón) (Ilopango) (Ilopango) SiO2 (wt.%) 60.30 TiO2 0.62 Al2 O3 17.03 Fe2 O3 1.73 FeO 4.62 MnO 0.14 MgO 2.17 CaO 5.56 Na2 O 3.95 K2 O 2.02 P2 O5 0.20 L.O.I. 0.65 65.09 0.51 15.72 1.93 2.67 0.11 1.26 3.30 4.71 2.76 0.12 0.55 69.47 0.13 14.34 0.41 1.82 0.11 0.36 1.47 3.66 4.79 0.04 3.91 49.74 0.95 19.68 4.05 6.10 0.16 4.14 10.50 2.46 0.72 0.18 0.48 51.19 0.83 19.09 3.53 6.49 0.18 4.58 9.15 2.70 0.78 0.18 0.64 52.30 1.12 18.33 2.31 7.90 0.19 3.68 8.81 3.18 1.18 0.23 0.53 52.60 1.06 18.08 4.59 4.99 0.17 3.64 7.98 3.24 1.83 0.31 0.63 53.37 1.23 16.39 3.82 7.03 0.21 3.26 7.37 3.54 1.42 0.28 0.52 54.09 0.82 19.73 2.97 4.88 0.14 2.51 8.01 3.23 1.77 0.24 0.66 57.71 1.17 15.15 0.17 9.27 0.22 2.16 5.45 3.89 2.22 0.38 0.55 68.59 0.35 15.29 1.18 1.87 0.11 0.84 3.08 4.13 2.26 0.12 2.07 70.83 0.33 15.11 1.36 1.29 0.11 0.69 2.54 4.43 2.27 0.11 0.51 Total 98.99 98.73 100.51 99.16 99.34 99.76 99.12 98.44 99.05 98.34 99.89 99.58 97 0 17 3 66 0 11 5 8 0 2 5 48 341 24 156 4 65 232 34 218 4 166 115 34 198 7 729 17 36 1046 14 32 782 34 64 Be (ppm) Sc V Cr Co Ni Cu Ga Rb Sr Y Zr Nb Cs Ba La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Hf Ta Tl Pb Th U See Table 1 for description and exact location of samples collected. See Appendix A for description of analytical procedures. Trace element values in italics are XRF data. Ahuac., Ahuachapán. L.O.I., loss on ignition. 386 S. Agostini et al. / Geothermics 35 (2006) 368–408 Table 4 Major and trace elements in rock samples from Berlı́n and Ahuachapán boreholes Berlı́n Sample TR 2 TR 2 TR 2 TR 2 TR 8A TR 5B TR 17 TR 17 Depth (m) 1250 1350 1600 1650 1779 n.a. 2000 2417 51.20 0.97 19.55 9.29 0.14 3.23 9.65 2.30 0.96 0.23 2.81 51.16 0.93 18.35 8.08 0.18 3.10 8.43 2.21 1.33 0.38 5.70 52.86 0.88 19.93 8.60 0.15 3.89 4.82 3.85 1.70 0.17 2.98 57.38 0.56 19.37 5.98 0.15 2.37 6.71 4.42 0.89 0.13 2.04 47.79 0.95 19.29 9.89 0.15 4.54 8.96 3.21 1.38 0.12 3.61 45.66 0.98 16.26 11.53 0.21 3.33 11.27 2.35 0.80 0.20 6.54 58.88 0.86 15.01 8.53 0.19 2.88 6.34 3.75 0.23 0.30 2.58 41.59 1.12 19.77 13.81 0.27 4.65 13.97 1.94 0.03 0.28 3.93 100.33 99.85 99.83 100.00 99.89 99.13 99.55 101.36 SiO2 (wt.%) TiO2 Al2 O3 Fe2 O3T a MnO MgO CaO Na2 O K2 O P2 O5 L.O.I. Total Nb (ppm) Zr Y Sr Rb Ce Ba La Ni Cr V Co Berlı́n Ahuachapán Sample TR 18 TR 2 TR 2 AH 34-2 AH 34-3 AH 8-1 TO 1 TO 1 Depth (m) 1053 1450 1502 n.a. n.a. n.a. 40 50 SiO2 (wt.%) TiO2 Al2 O3 Fe2 O3T a MnO MgO CaO Na2 O K2 O P2 O5 L.O.I. 53.78 0.74 18.15 7.96 0.17 2.85 7.46 4.36 1.88 0.23 2.14 52.40 0.77 16.71 9.65 0.18 2.75 7.78 2.73 0.77 0.23 5.30 55.54 0.70 16.82 8.41 0.18 3.11 6.55 2.84 1.04 0.20 3.54 56.34 0.80 16.84 8.27 0.15 3.40 6.54 2.32 1.62 0.13 2.85 56.81 0.61 17.74 8.04 0.15 2.87 5.32 3.47 1.20 0.19 2.54 60.71 0.80 16.72 6.35 0.11 2.04 3.18 1.73 1.76 0.17 5.21 62.58 0.77 16.83 10.84 0.12 3.44 2.46 1.62 1.17 0.17 – 65.81 0.81 19.08 7.16 0.09 2.79 1.88 0.90 1.41 0.08 – Total 99.72 99.27 98.93 99.26 98.94 98.78 98.78 98.78 Nb (ppm) Zr Y Sr Rb 7 178 31 200 28 7 190 52 175 39 S. Agostini et al. / Geothermics 35 (2006) 368–408 387 Table 4 (Continued) Berlı́n Ahuachapán Sample TR 18 TR 2 TR 2 AH 34-2 AH 34-3 AH 8-1 TO 1 TO 1 Depth (m) 1053 1450 1502 n.a. n.a. n.a. 40 50 33 582 13 3 0 123 21 37 635 17 8 3 188 29 Ce Ba La Ni Cr V Co Ahuachapán Sample TO 1 TO 1 TO 1 TO 1 TO 1 TO 1 TO 1 TO 1 TO 1 Depth (m) 55 225 230 375 380 400 441 700 1500 SiO2 (wt.%) TiO2 Al2 O3 Fe2 O3T a MnO MgO CaO Na2 O K2 O P2 O5 L.O.I. 69.23 0.72 19.81 5.49 0.06 1.57 1.28 0.99 0.77 0.08 – 60.18 0.91 16.94 7.36 0.16 2.92 6.18 3.83 1.29 0.22 – 60.55 0.85 16.79 6.57 0.14 2.95 6.04 3.82 2.06 0.23 – 59.60 0.71 17.86 6.36 0.13 3.06 7.01 3.46 1.64 0.16 – 59.06 0.73 16.90 6.58 0.15 4.38 7.02 3.09 1.90 0.18 – 57.54 0.79 18.23 6.73 0.13 3.79 7.56 3.25 1.81 0.17 – 60.91 0.74 17.29 6.68 0.13 2.54 5.49 3.99 2.06 0.17 – 54.53 0.85 16.51 10.20 0.18 5.17 8.44 2.78 1.14 0.18 – 54.13 0.86 16.75 10.48 0.20 5.12 8.34 2.84 1.10 0.19 – Total 98.78 98.78 98.78 98.78 98.78 98.78 98.78 98.78 98.78 Nb (ppm) Zr Y Sr Rb Ce Ba La Ni Cr V Co 6 209 50 162 35 39 813 14 8 7 281 34 5 158 29 392 47 35 684 17 7 47 141 19 3 148 29 381 36 29 652 12 5 5 130 18 2 133 24 403 31 32 725 13 5 12 135 18 2 133 25 385 36 25 745 15 5 6 141 20 3 109 20 440 33 18 631 10 7 4 176 18 3 147 26 347 42 28 745 15 4 2 142 19 2 116 25 407 11 18 587 10 9 16 226 31 3 115 27 406 11 18 585 10 9 18 231 33 n.a.: not available. TR, Tronador; AH, Ahuachapán; TO, Tortuguero; L.O.I., loss on ignition. See Appendix A for description of analytical procedures. Trace element values in italics are XRF data. a Fe O 2 3T is total iron expressed as Fe2 O3 . In Fig. 12 the rocks are plotted in the AFM diagram, which shows the boundary line between calc-alkaline and tholeiitic series (Irvine and Baragar, 1971). The rocks display modest Fe enrichment; some slightly evolved samples show relatively high FeO*/MgO ratios falling in the tholeiitic field, although their K2 O content is not typical of tholeiitic arc lavas (Fig. 11). The Berlı́n rocks (from basaltic andesites to dacites) do not show any Fe enrichment. High values of the FeO*/MgO ratio and a mildly tholeiitic affinity have also been observed in recent volcanics of 388 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 11. K2 O vs. SiO2 classification diagram (after Peccerillo and Taylor, 1976) for Ahuachapán, Berlı́n and other volcanic rocks from the El Salvador volcanic front. SS in parentheses indicates samples from Ahuachapán and Berlı́n geothermal areas belonging to the San Salvador Formation. Fig. 12. AFM (Alkali–FeO–MgO) diagram for Ahuachapán, Berlı́n and other volcanic rocks from El Salvador volcanic front; boundary line between calc-alkaline and tholeiitic series taken from Irvine and Baragar (1971). SS in parentheses indicates samples from Ahuachapán and Berlı́n geothermal areas belonging to the San Salvador Formation. S. Agostini et al. / Geothermics 35 (2006) 368–408 389 the Boquerón (Fairbrothers et al., 1978) and Chichontepeque Volcanoes (Rotolo and Castorina, 1998). 5.2. Petrography Basalts are relatively abundant in the Ahuachapán area and in the products of the Bálsamo Formation, but are missing in the Berlı́n volcanic system where basaltic andesites are the most primitive rocks. Petrographically, the basalts and basaltic andesites have porphyritic to subaphyric textures. The basalts usually exhibit a phenocryst assemblage made up of abundant augitic clinopyroxene (cpx) and plagioclase (pl; up to 2–3 cm in size), and smaller olivine (ol). Only sample ES 55 (Ahuachapán) exhibits Mg-rich olivine (Fo86–77 ) as unique phenocryst, with augitic cpx present as microphenocryst and in the groundmass. The basalts typically have modal cpx > ol; the pyroxene is Mg-rich and displays Mg# [that is, Mg/(Mg + Fe2+ ) ratio] in the range 83–71, greater than the Mg# of olivine (Fo70–60 ), suggesting an earlier segregation of augite with respect to olivine. The plagioclases are generally zoned, with Ca-rich cores (An90–82 ) and rims, usually reaching labradoritic composition (An ≈ 60). Ore minerals are present in the groundmass, together with pl + cpx ± ol ± glass, and are essentially represented by Ti–magnetite (mt); there are rare needles of ilmenite (ilm). In the basaltic andesites, as well as the cpx + ol + pl assemblage, orthopyroxene may be present, with compositions ranging from En65 to En50 . Augite is weakly zoned, with slight Fe-enrichment in the rims; again their Mg# is much greater than the Fo content of zoned olivine (Fo67–53 ). Plagioclases are usually labradoritic, and may show oscillatory zoning. The matrices are generally crystalline for the most part, with abundant glass in a few samples; the groundmass mineral phases include plagioclase, two pyroxenes and Ti–magnetite. Intermediate rocks are represented by two-pyroxene andesites with predominant plagioclase, ranging in composition from Ca-rich bytownite (cores) to labradorite (rims). Embayed olivine may be present, mainly in low-silica andesites (e.g. ES 8, Berlı́n). Scattered opacitized amphibole occurs as megacrysts in sample ES 50 (Bálsamo Formation). Opaques are represented mainly by microphenocrysts of Ti–magnetite and ilmenite in very minor amounts. The evolved rocks consist of dacites and rhyolites, occurring either as lava flows or pyroclastics (ignimbrites and fall-out deposits). The dacites are slightly porphyritic, often with abundant glass in the matrix. The phenocryst assemblage is formed by andesinic plagioclase, ortho- and clinopyroxene with opx/cpx ratio > 1. Quartz and sanidine are sporadically present. In addition to quartz, feldspars (plagioclase and sanidine) and orthopyroxene, amphibole and/or biotite are sometimes found in the rhyolites. 5.3. Geothermal boreholes In the Berlı́n area, the borehole samples came from the El Tronador wells (TR 2–TR 18). The samples exhibit widespread alteration with parageneses that include mainly quartz-calciteclay minerals, along with diffuse albite, epidote, titanite, pyrite and, rarely, adularia. Zeolites, represented mainly by wairakite, are often present in veins together with calcite and phyllosilicates. In the Ahuachapán area, the Tortuguero field samples (well TO 1) show the occurrence of a widespread zeolite alteration zone in the upper part of the well (down to ≈400 m depth): the zeolites are represented by heulandite-clinoptinolite and stilbite-epistilbite; wairakite also occurs sporadically. The middle and lower part of this well is characterized by an association of quartz, 390 S. Agostini et al. / Geothermics 35 (2006) 368–408 clay minerals (mainly chlorite) and variable amounts of calcite. Epidote is observed at depth only sporadically in the calc-alumina-silicate zone. By contrast, the rocks from other Ahuachapán boreholes (wells AH) present extensive epidote-wairakite-actinolite alteration, as also observed in the nearby Chipilapa wells (Aumento et al., 1982). 5.4. Major element chemistry The data points display a good negative correlation of CaO, FeOtot , MgO and, to a lesser extent, TiO2 with silica (Fig. 13). Positive correlations are observed for Na2 O and K2 O, although a relative dispersion is present in the alkali abundances of the less evolved samples. A negative correlation between MgO and silica is observed, plotting as a convex curve. The most primitive Bálsamo and Ahuachapán basalts (MgO 6–9%) plot along a steeper curve, whereas, from the more evolved basalts (MgO < 5%) up to the most SiO2 -rich samples, the correlation flattens out and is almost linear. The Al2 O3 –SiO2 plot shows a wide dispersion for the basaltic rocks; at the same silica content (≈50%), alumina ranges from 16.6 to 21.0%, whereas a well-defined negative trend appears in the basaltic andesites-rhyolites range. As a whole, major element variations are compatible with a crystal fractionation process involving the mineral phases forming the observed parageneses. However, plagioclase and mafic minerals may play different roles during the fractionation process, as evidenced by the Al2 O3 versus MgO diagram (Fig. 14). In the most basic rocks, MgO and alumina are negatively correlated (up to ≈5% MgO), whilst in the more evolved products these two elements coherently decrease. These variations suggest that the first stages of crystallization involved mainly mafic phases (clinopyroxene ± olivine), whereas plagioclase becomes the dominant removed phase during successive stages of rock evolution. At about 3–5% MgO, the maximum Al2 O3 contents indicate the presence of plagioclase-cumulus phenomena, as evidenced by the strongly plagioclase-phyric textures. Borehole samples from Berlı́n and Ahuachapán exhibit basically the same geochemical and petrographic characters and largely overlap the variation range of the outcropping rocks (Fig. 13). The borehole samples from Berlı́n are generally less evolved than the exposed rocks, being mainly basalts and basaltic andesites. The samples most affected by hydrothermal alteration are depleted in Na2 O and enriched in Al2 O3 (Fig. 13). 5.5. Trace elements and isotope geochemistry Trace element data are presented in Table 3 and selected trace elements versus silica are plotted in Fig. 15. The abundances of compatible elements (e.g. V, Fig. 15; Co, Ni and Cr, not shown) are generally low, with the exception of the most primitive samples from the Ahuachapán area, e.g. ES 55 and ES 57, with 100 < Ni < 150 ppm. Taking into account all the samples, Ni and Cr display a negative hyperbolic correlation with silica, whereas V and Co exhibit a good negative linear correlation with r2 = 0.88 and 0.75, respectively. The large ion lithophile elements (LILE) show a generally positive correlation with an increase in evolution degree; a noteworthy exception is Sr (Fig. 15), which decreases with increasing silica. High field-strength elements (HFSE: Zr, Fig. 15; Nb and Y, not shown) are positively correlated with silica, although the data points are more scattered. Overall, the scattering of trace element abundances is generally greater in the most primitive rocks, matching the behaviour of major elements. Trace-element distribution in the primordial mantle-normalized, multi-element patterns (Fig. 16) shows the typical features of volcanic arc rocks, with high LILE/HFSE ratios, markedly S. Agostini et al. / Geothermics 35 (2006) 368–408 391 Fig. 13. Major element (anhydrous) variation diagrams plotted against SiO2 for Ahuachapán, Berlı́n and other volcanic rocks from El Salvador volcanic front (all units in wt.%). SS in parentheses indicates samples from Ahuachapán and Berlı́n geothermal areas belonging to the San Salvador Formation. 392 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 14. Al2 O3 vs. MgO variation diagram for Ahuachapán, Berlı́n and other volcanic rocks from El Salvador volcanic front. Thick grey lines delineate the path of crystal fractionation starting from basalt ES 42 to dacites, through high-Al basalts and andesites. ol, olivine; px, pyroxene; pl, plagioclase. The negative trend results from the removal of a solid assemblage in which mafic minerals plagioclase; conversely, plagioclase dominates fractionation in the final part of the trend, producing a positive correlation. SS in parentheses indicates samples from Ahuachapán and Berlı́n geothermal areas belonging to the San Salvador Formation. negative Nb, Ta, Ti and, to a lesser extent P, anomalies along with positive spikes of Ba, K and Sr; the latter are particularly evident in the Ahuachapán rocks (e.g. ES 42), where negative Hf and Zr anomalies are also observed. Rare earth elements (REE) are variably fractionated, with La/YbN ranging from ≈1.5 to 4. The Berlı́n samples in particular show higher REE contents, in agreement with their higher degree of evolution and patterns of a similar trend; a significant Eu negative anomaly is also observed (Eu/Eu* ≈ 0.7–0.8; Fig. 16). By contrast, the Bálsamo samples from Berlı́n show a large variability of LREE contents and patterns with variable slope. Basalt ES 42 from Ahuachapán is characterized by the lowest LREE/HREE ratio measured in the data set. A significant Ce negative anomaly is observed for the whole analyzed samples; this could be related with the involvement a slab-derived component depleted in cerium. Strontium and neodymium isotope ratios are reported in Table 5 and Fig. 17: Nd isotope ratios are close to a value of 0.5130 and show very small variations, between 0.51297 and 0.51301. On the other hand, the Sr isotopic composition ranges between 0.70357 and 0.70390. In the classic Sr–Nd diagram there is a shift toward higher Sr isotopic composition with respect to the mantle array (inset of Fig. 17). The 87 Sr/86 Sr and 143 Nd/144 Nd ratios in the Berlı́n borehole samples are very close to those of surface lavas, suggesting that water–rock interaction processes did not significantly modify their isotope features. The isotope composition of the drilled and outcropping rocks does not change from the surface down to bottomhole depth (2500 m), indicating a marked homogeneity S. Agostini et al. / Geothermics 35 (2006) 368–408 393 Fig. 15. Trace element (Rb, Sr, Zr and V) variation diagrams plotted against wt.% SiO2 (anhydrous) for Ahuachapán, Berlı́n and other volcanic rocks from the El Salvador volcanic front. Symbols as in Fig. 14. for the whole volcanic sequence, including its local volcanic basement. Ahuachapán boreholes have higher 87 Sr/86 Sr values than those measured in outcropping rocks; it is not clear from these data alone whether this difference is due to water–rock alteration processes or to intrinsic isotopic heterogeneities between basement and more recent rocks. 5.6. Estimates of magmatic intensive parameters Different geothermometers were used to estimate crystallization temperatures in the studied rocks. In basalts, where clinopyroxene phenocrysts coexist with olivine, the olivine–augite Fe–Mg-exchange geothermometer of Loucks (1996) was applied; the standard error in this case is ±6 ◦ C. Just one basalt sample (ES 55, Ahuachapán) contains olivine phenocrysts only: the crystallization temperature in this rock was thus assessed through the Fe–Mg partition between olivine and whole rock (Beattie et al., 1991). In more evolved rocks, where two pyroxenes occur, the temperature of crystallization of the phenocryst assemblage was calculated by equilibrium enstatite–augite pairs (Wells, 1977). Oxygen fugacity was calculated by the QUILF code (Andersen et al., 1993, updated in 1995). Most of 394 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 16. Primitive Mantle (PM)-normalized trace-element variation diagrams (left side) and chondrite-normalized Rare Earth Element (REE) diagrams for volcanic rocks from Ahuachapán and Berlı́n geothermal areas. Normalization values from McDonough and Sun (1995). Bas And, Basaltic Andesite. the rocks display Ti–magnetite as microphenocrysts; ilmenite is generally confined to the groundmass as needles that are too small to be analyzed with any reliability. In only three samples it was possible to use ilmenite–magnetite pairs (ES 55, ES 46 and ES 10); for the other rocks the temperature was constrained by mafic assemblage equilibria. S. Agostini et al. / Geothermics 35 (2006) 368–408 395 Table 5 Sr and Nd isotope data of the Berlı́n and Ahuachapán geothermal areas Sample 87 Sr/86 Sr 2σ 143 Nd/144 Nd 2σ Berlı́n ES 7 (Bálsamo) ES 45 (Bálsamo) ES 10 ES 28 0.703850 0.703805 0.703867 0.703898 ±6 ±7 ±7 ± 10 0.512999 0.512999 0.512997 0.513002 ±7 ±6 ±7 ±8 Ahuachapán ES 50 (Bálsamo) ES 42 ES 61 0.703582 0.703666 0.703574 ±8 ±8 ±7 0.512997 0.513013 0.512997 ±8 ±8 ± 10 Borehole Berlı́n TR 8A 1779 TR 17 2000 TR 17 2417 0.703915 0.703872 0.703881 ± 17 ± 12 ±7 0.512999 0.512988 0.512990 ± 10 ±9 ±8 Borehole Ahuachapán TO 1 700 TO 1 1500 0.703778 0.703829 ±7 ± 10 0.512986 0.512993 ± 11 ± 12 The bulk samples were leached with hot HCl 6.6N. Sr and Nd isotope compositions were determined using a Finnigan MAT 262V multi-collector mass spectrometer following separation of Sr and Nd using conventional ion-exchange procedures. Measured 87 Sr/86 Sr ratios have been normalized to 86 Sr/88 Sr = 0.1194. During collection of isotopic data, 14 replicate analyses of SRM-NIST 987 (SrCO3 ) standard gave an average value of 0.710243 ± 0.000011 (2 standard deviations). Measured 143 Nd/144 Nd ratios have been normalized to 146 Nd/144 Nd = 0.7219. Replicate analyses of La Jolla standard gave an average 143 Nd/144 Nd of 0.511847 ± 0.000007 (2 standard deviations). Crystallization pressure (i.e. depth) was estimated using the thermobarometer of Putirka et al. (2003), which assesses temperature and pressure on the basis of equilibrium between clinopyroxene and liquid. Equilibrium is evaluated assuming a value of the Fe–Mg partition coefficient cpx-lq cpx-lq cpx lq lq cpx between cpx and liquid, KD (Fe–Mg) = 0.27 (KD (Fe–Mg)) = (XFe /XFe )(XMg /XMg ), where XFe and XMg are cation fractions of Fe and Mg in the superscripted phases, respectively; the liquid equilibrium composition was evaluated by readjusting the whole-rock chemistry, adding equilibrium olivine and clinopyroxene in cotectic proportions to reach the pre-defined KD value. This calculation was performed by a code described in Armienti et al. (in press). The results are reported in Table 6. The temperature of crystallization of mafic phenocrysts in basalts ranges between 1200 and 1050 ◦ C irrespective of the geothermometer applied. Overall, a negative correlation is observed between silica content and temperature, shifting from basalts to dacites. The temperatures of the groundmasses are generally 100–150 ◦ C lower than in the phenocrysts, except for sample ES 8 (andesite from Berlı́n) for which an anomalous high groundmass temperature was obtained; in this sample the mt–ilm equilibrium was probably not preserved. The values of fO2 are usually between +1 and +2 ΔFMQ ; no significant variations are observed with respect to the degree of evolution. The clinopyroxene crystallization depth varies from shallow level (pressure < 0.1 GPa) to levels corresponding to the intermediate crust (pressure ≈ 0.5 GPa). It is worth noting that the variations detected in basalt ES 42 (Ahuachapán), one of the most primitive rocks of the studied data set, show a good P–T correlation (r2 = 0.97). The continuous variations of pressure between 0.49 and 0.28 GPa suggest an uninterrupted segregation of pyroxene during magma ascent, starting from the middle crust where magma ponding probably occurred for the first time. 396 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 17. 143 N144 Nd vs. 87 Sr/86 Sr diagram for volcanic rocks from Ahuachapán and Berlı́n geothermal areas. The inset reports the “Mantle Array” and literature data for Central America volcanics (http://www.rci. rutgers.edu/∼carr/index.html). Dashed field encloses samples from Berlı́n area. SS in parentheses indicates samples from Ahuachapán and Berlı́n geothermal areas belonging to the San Salvador Formation. DMM, depleted MORB mantle; BSE, bulk silicate earth. Estimates of the water content of the magmas were constrained by applying two procedures to the more primitive and evolved rocks. In the basalts and basaltic andesites, the sequence of crystal precipitation, suggested from petrographic observations, is cpx ⇒ mt ⇒ ol ⇒ plg; this anhydrous assemblage and the crystallization sequence can be reproduced at a pressure between 0.3 and 0.5 GPa, with an H2 O content of around 3% if we consider the phase diagram for the basalt ES 42, produced by the MELT code (Ghiorso et al., 2002). In the dacitic rocks, water abundance was assessed by the experimental geohygrometer of Merzbacher and Eggler (1984), following the calculations of projection parameters proposed by Schmitt and De Silva (2000). The results are plotted in Fig. 18, where the data points generally fall along the line of 4% H2 O content. Only three glass-rich dacites (ES 54 and ES 62 from the Bálsamo Formation, and ES 10 from Berlı́n) fall outside the main trend, showing higher water contents, and within the field of amphibole stability, in spite of the anhydrous paragenesis of the phenocrysts. The basalt-dacite transition through crystal fractionation implies the removal of about 80% of solids (see below). The amount of water in the dacitic magma should therefore be very S. Agostini et al. / Geothermics 35 (2006) 368–408 397 Table 6 Estimate of intensive parameters of Ahuachapán and Berlı́n rocks Sample Rock type ES 55 ES 42 Basalt Groundmass Basalt T (◦ C) T (◦ C) cpx/lq P (GPa) cpx/lq TQ (◦ C) log fO2 ΔFMQ 981 0.1 1025 (a) −7 ± 0.8 −9.8 ± 3.5 +1.3 +0.7 1111 1101 1098 1092 1083 1078 1068 0.49 0.44 0.41 0.36 0.34 0.31 0.28 −7.2 +2.4 1076 1068 1059 0.07 0.14 0.02 −7.06 +2.1 1123 0.29 963 ± 41 −8.5 ± 0.3 −9.5 ± 0.7 +1.8 +2.0 1205 ± 10 −7.23 +0.96 1200 (ol–lq) 1206–1092 (ol–cpx) 1166–1123 (ol–cpx) ES 43 Basalt BER 3 Basalt ES 28 Basaltic andesite Groundmass 1179–1040 (ol–cpx) ES 50 Andesite 1041–1022 (ol–cpx) ES 8 Andesite Groundmass 1077–980 (ol–cpx) ES 46 Andesite Groundmass 1055–956 (opx–cpx) ES 10 Dacite Groundmass 1214 (opx–cpx) 773 ± 84 (a) −13.7 ± 1 +1.4 823 ± 35 (a) −13.5 ± 0.4 +0.7 Notes: ol–lq after Beattie et al. (1991); ol–cpx after Loucks (1996); opx–cpx after Wells (1977); cpx–lq after Putirka et al. (2003). TQ indicates estimates using the QUILF code (Andersen et al., 1993). (a) Ilmenite–magnetite pairs. ΔFMQ is oxygen fugacity expressed as the difference between estimated log fO2 and log fO2 of fayalite–magnetite–quartz buffer at TQ . ol, olivine; lq, liquid; cpx, clinopyroxene; opx, orthopyroxene. high (>10%) if the process occurred in a closed system. The estimated average H2 O content of around 4% suggests that the magmas suffered a significant water loss during magmatic differentiation. 6. Discussion 6.1. Magmatic constraints The volcanic products erupted along the El Salvador volcanic front constitute a typical calcalkaline association, ranging in composition from basalts to rhyolites. A small-scale geochemical variability is observed in the most primitive samples, where two groups of rocks can be distinguished on the basis of differences in 87 Sr/86 Sr (≈0.7036 and ≈0.70385, respectively), along with distinct LILE contents and LILE/HFSE ratios (Table 5; Fig. 19). In the Berlı́n volcanic system all the samples belong to the most 87 Sr-enriched group; Ahuachapán area samples are less 87 Sr-enriched, and, despite their limited number, are more 398 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 18. Whole-rock andesites and dacites plotted in the plagioclase (pl)–orthopyroxene (opx)–quartz + orthoclase (Q + or) system using the Schmitt and De Silva (2000) projection scheme. Lines represent pl–opx cotectic lines for water content of 2 and 4 wt.%. Grey area is the field of amphibole stability (Merzbacher and Eggler, 1984). variable. In contrast to the Sr isotopes, the 143 Nd/144 Nd ratios have almost constant values (0.51299–0.51301). The isotopic and geochemical variability observed in the studied rocks could mirror source heterogeneity and/or magma interaction with shallow crustal material. The lack of any cor- Fig. 19. 87 Sr/86 Sr vs. SiO2 (a) and Ba/Zr (b) for volcanic rocks from Ahuachapán and Berlı́n geothermal areas. Dashed fields enclose samples from Berlı́n area. S. Agostini et al. / Geothermics 35 (2006) 368–408 399 relation between evolution degree (e.g. SiO2 content; Fig. 19) and 87 Sr/86 Sr ratios, coupled with the occurrence of the relatively high isotope and geochemical variability in the basaltic rocks, strongly suggest that contamination processes played a minor role in the petrogenesis of this volcanic association. Hence, the geochemistry of the basaltic rocks is considered to be linked to the geochemical variability of the source. It is generally acknowledged that, in a subduction context, mantle characteristics reflect the addition of subduction-related components, different in their amounts and/or geochemical signatures (e.g. Tatsumi and Eggins, 1995). Many authors have described this mechanism for the Central America front lavas using trace elements and isotope features (e.g. Carr et al., 2004; Eiler et al., 2005). Considering our data set, the subduction component cannot be strictly constrained. However, the relative enrichment in 87 Sr and fluid mobile elements such as Rb, Ba, Cs, Sr and, to a lesser extent, LREEs, does suggest that the metasomatic agent was a hydrous fluid derived from the dehydration of the subducting oceanic lithosphere. Furthermore, the high uniform 143 Nd/144 Nd ratios (≈0.51300) indicate that the magma source, before the addition of the subduction component, had an Sm/Nd ratio close to the value observed in Mid-Ocean Ridge Basalts (MORB) sources. The variation of major and trace elements suggests that the main process occurring in the rock association was fractional crystallization, without significant interaction with crustal material. In order to evaluate this process we modeled, by major element mass balance calculations (Stormer and Nicholls, 1978), the transition basalt-andesite-dacite and basaltic andesite-dacite in the Ahuachapán and Berlı́n rocks, respectively. The results are reported in Table 7; the low values of the sum of square residuals between calculated and observed compositions suggest that removal of gabbroic assemblages is a viable mechanism to produce the studied rocks. To further check the model, we applied the Rayleigh equation for trace element crystal fractionation, using the amount and modal composition of removed solid as derived from major element mass balance calculations. The difference between calculated and measured contents is generally lower than 25% (Table 8), suggesting that the model is consistent. In some cases, however, the discrepancies reached 50%, mainly for compatible elements, which may be a consequence of the uncertainty with regard to their solid/liquid partition coefficients. In the transition basalt-andesite in Ahuachapán, the strong enrichment in Rb of the andesite (ES 60) cannot be explained by the model. 6.2. Tectonic constraints The structural analyses carried out in our study lend support to the hypothesis that the active deformation resulting from oblique subduction of the Cocos Plate under the Caribbean Plate is accommodated within continental El Salvador by strike-slip movement along the E–W trending El Salvador Fault Zone (ESFZ). In particular, the kinematics and deformation rates of the major fault system, as well as the absence of large-scale compressional deformation, corroborate the model of strain partitioning between trench-orthogonal compression and trench-parallel transcurrent deformation at the Cocos-Caribbean plate boundary (Harlow and White, 1985; DeMets, 2001; Corti et al., 2005a). Analysis of the regional architecture of the ESFZ reveals the discontinuous nature of this fault system, with main segments separated by pull-apart structures (Fig. 20) (Corti et al., 2005a). The main fault segments contain active volcanism, which is more or less absent in the intervening pullapart basins. This coincidence between the segmentation of the ESFZ and that of the volcanic 400 Starting composition SiO2 (%) Total removed solids (%) SSR cpx ol mt pl opx Final composition SiO2 (%) Ahuachapán ES 42 Basalt ES 60 Andesite 48.32 59.96 −69.9 −30.4 0.42 0.34 −16.3 −0.6 −10.8 – −6.3 −2.9 −36.5 −21.5 – −5.4 ES 60 Andesite ES 61 Dacite 59.96 66.3 Berlı́n ES 28 Basaltic andesite 55.24 −47.7 0.05 −11.2 −4.6 −4.3 −27.7 – ES 10 Dacite 64.98 SSR, sum of square residuals; cpx, clinopyroxene; ol, olivine; mt, magnetite; opx, orthopyroxene. S. Agostini et al. / Geothermics 35 (2006) 368–408 Table 7 Differentiation fractionation model for Ahuachapán and Berlı́n rocks Table 8 Trace element fractionation model for Ahuachapán and Berlı́n rocks ES 28 Sc (ppm) V Cr Co Ni Rb Sr Y Zr Nb Ba La Ce 25 209 3.7 27 10.9 30.2 467 23.5 109 2.53 712 10.4 23.2 Ahuachapán Bulk KD 2.61 3.51 3.39 3.16 3.64 0.13 1.08 0.14 0.15 0.69 0.14 0.27 0.25 Model 8.6 40 0.8 6.6 1.9 53.3 443 41.2 191 3.10 1249 16.7 37.9 ES 10 ES 42 17 35 0.7 4.8 1.8 44.3 363 37.4 154 3.38 1135 14.4 32.8 45 343 25.8 46 23.2 6.0 393 21.6 56 1.30 309 5.6 12.4 Ahuachapán Bulk KD 1.55 1.86 4.02 1.78 2.17 0.10 1.08 0.60 0.15 0.23 0.21 0.25 0.28 Model 23.1 122 0.7 18.1 5.7 17.8 357 35.1 156 3.28 803 13.8 29.4 ES 60 ES 60 – 121 1.0 18.0 5.0 50.0 329 29.0 166 3.00 802 12.0 32.0 – 121 1.0 18.0 5.0 50.0 329 29.0 166 3.00 802 12.0 32.0 Bulk KD 0.71 3.04 2.90 2.74 1.44 0.15 2.03 0.17 0.05 0.03 0.27 0.25 0.26 Model – 59 0.5 9.7 4.3 67.8 227 39.0 233 4.25 1040 15.7 41.6 ES 61 – 66 – 11 5 65 232 34 218 4 1046 14 32 S. Agostini et al. / Geothermics 35 (2006) 368–408 Berlı́n Bulk KD for rocks derived from Kd of mineral phases; Kd values for minerals involved in the crystal fractionation process are taken from http://earthref.org. The amount of removed phases corresponds to the results of the model reported in Table 7. 401 402 S. Agostini et al. / Geothermics 35 (2006) 368–408 Fig. 20. Schematic hypothetical regional segmentation of El Salvador Fault Zone (ESFZ). Grey elliptic areas indicate the segments of the volcanic front; large black dots represent some of the main active volcanoes located at the boundaries of the volcanic segments close to the pull-apart basins. Dashed lines represent main segments of the ESFZ. A, Ahuachapán; B, Berlı́n. front suggests a genetic relationship between the two processes of faulting (lithospheric-scale deformation) and volcanism; the strike-slip fault system in particular acts as a preferential pathway for magma to ascend to the surface. However, more detailed analyses are needed to better define these relationships and to explain the absence of volcanic activity within pull-apart basins, where extensional tectonics is normally considered to favor volcanism. One important finding of our study is the difference in structural setting between the Berlı́n and Ahuachapán geothermal fields. The first field is located in correspondence to an important segment of the ESFZ. The major and minor structures affecting the Berlı́n area are presumably related to a transcurrent stress field, with a NNW-directed axis of maximum compression and an ENE-directed axis of maximum extension. Interaction of this stress field with the volcanic edifices has given rise to a local dominance of NNW- to NW-directed extensional structures within the Berlı́n geothermal area. Conversely, the Ahuachapán area is structurally less straightforward, being characterised by different groups of structures that cannot be so easily attributed to a dominant regional stress field. In this case, the complex fault arrangement possibly results from the interaction between three stress fields. Indeed, the E–W and NW–SE trending faults may be related to the transcurrent stress field associated with the El Salvador Fault Zone. The N–S dilatational joints and normal faults are presumably the result of the intraplate extension of the Caribbean Plate, whereas the influence of the Motagua fault system is possibly expressed by the NE–SW directed normal faults west of Ahuachapán. 7. Conclusions The tectonic and petrologic study of the El Salvador active volcanic front and its local volcanic basement has evidenced a strong link between active deformation and volcanic activity. In continental El Salvador, strike-slip deformation gives rise to a major dextral transcurrent fault system, the El Salvador Fault Zone, which is laterally discontinuous, being subdivided into different major en-echelon segments that partially overlap to form pull-apart structures. The present-day volcanic activity is more or less confined to the fault segments and is practically non-existent in the intervening pull-apart basins. The studied volcanic rocks were erupted during the Quaternary. The most recent composite volcanoes grew on a local volcanic basement with no recognizable temporal gap: indeed, the top of the Bálsamo Formation reaches the upper Pleistocene. No significant geochemical or petrological differences were found between the volcanics of the Bálsamo Formation and the most recent products. S. Agostini et al. / Geothermics 35 (2006) 368–408 403 Our study reveals the important volcano-structural and petrologic differences between the eastern (Berlı́n) and western (Ahuachapán) areas of El Salvador. The marked geochemical and isotopic homogeneity found in Berlı́n, where basalts are lacking, points to the presence of a single magmatic system. By contrast, the Ahuachapán rocks show significant variations in both Sr isotopes and the LILE/HFSE ratios. The multiple volcanic centres characterizing this area were fed by magma batches with different Sr isotopes and trace-element contents, inherited from their mantle source. The relative abundance of basaltic products reveals that in Ahuachapán most of the rising magmas were not intercepted by the shallow reservoirs linked to the small volcanic centres that erupted more evolved products. The geochemical homogeneity in the Berlı́n products reflects the “simple” tectonic framework of the area whose active deformation is controlled by the regional transcurrent stress field, resulting in the development of systems of right-lateral E–W-trending strike-slip faults and associated secondary Riedel and tensional shears. Conversely, the structural setting of the Ahuachapán area is more complex, characterized by different fault systems that may reflect an interaction among the ESFZ-dominated stress field, the sinistral Motagua transform fault, and the active E–W extension responsible for the intraplate deformation of the Caribbean Plate; the more complex and pervasive fault pattern of the Ahuachapán area facilitated the development of multiple smaller magma chambers, and the creation of pathways for the ascent of basaltic magma. Considering the different settings of the two areas, further geothermal exploration at Berlı́n and Ahuachapán may take different approaches. At Berlı́n, for example, prospecting should account for the existence of a regional geothermal anomaly magnified by the presence of a shallow magma chamber. On the other hand, at Ahuachapán the geothermal system appears more complex, and linked to local magma ponds that are probably limited in volume, as inferred by the small volcanic centres. This volcanological framework, coupled with the widespread and complex faulting pattern, has probably led to the occurrence of small-scale shallow geothermal anomalies. Overall, the results of this study show that a combined tectonic and petrological–geochemical approach may prove an important tool for selecting potential areas of geothermal interest, before proceeding with further more expensive geothermal exploration work. Acknowledgments The authors would like to thank ENEL and LaGeo for their support during the fieldwork, laboratory investigations and scientific discussions. They are indebted to Armando Ceccarelli and Marvyn O. Garcia for the stimulating discussions in the field. Reviews by R.M. Prol-Ledesma and M.J. Carr, as well as editorial comments by M.J. Lippmann, have significantly improved the quality of the manuscript. Appendix A. 40 Ar–39 Ar dating of selected samples A.1. Experimental procedures Six volcanic rock samples (ES 8, ES 27, ES 35, ES 39, ES 43, and ES 46) were selected for incremental laser-heating analyses. The groundmass was concentrated from the 250 to 300 m grain size using standard separation techniques and purified by hand-picking under a binocular microscope. The groundmass separates were further cleaned by acid leaching in an ultrasonic bath (1 h at ∼50 ◦ C in 3.5N HCl and 1N HNO3 ). The final product was wrapped in aluminum foil and irradiated for 2 h in the TRIGA reactor (University of Pavia, Italy) along 40 Ar–39 Ar 404 S. Agostini et al. / Geothermics 35 (2006) 368–408 with the dating standard FCT-3 biotite (age 27.95 Ma; Baksi et al., 1996). After irradiation, the samples (∼40 mg) were loaded into the 9-mm diameter holes of a copper holder, placed in an ultra high-vacuum laser port and baked overnight at ∼200 ◦ C. Incremental laser-heating experiments were carried out using an infrared laser beam generated by a diode-pumped CW Nd–YAG laser (maximum power 15 W), which was defocussed to ∼2 mm spot. The laser beam was homogenized by passing it through a lens that produces a flat-power distribution. Homogenous heating was achieved by slowly rastering the laser beam by a computercontrolled x–y stage. The heating steps were carried out at increasing laser powers until complete melting occurred. The gas extracted was purified by two SAES AP10 getters (at 400 ◦ C) and one SAES GP50 getter (at room temperature) and, after 15 min (including ∼6 min of laser heating), equilibrated via automated valves into an MAP215-50 noble gas mass-spectrometer fitted with a Balzers SEV 217 secondary electron multiplier. The data (Table A1) were corrected for postirradiation decay, mass discrimination effects, isotopes derived from interfering neutron reactions and blanks. Errors are given at 2σ. A.2. Results Data from the six samples are presented in the form of age spectra in Fig. A1 and the complete analytical results are listed in Table A1. Analysis of these samples was extremely difficult because of their young age, low potassium content and the material analyzed (groundmass), which resulted in severe contamination by atmospheric argon (radiogenic argon 10% in most cases; see Table A1). Results from regression calculations in an isochron plot (36 Ar/40 Ar versus 39 Ar/40 Ar diagram), and the total gas, plateau and preferred ages are summarized in Table 2. In samples ES 8, ES 27, and ES 39, the ages measured at each heating step are close to or overlap with the zero age (Table A1, Fig. A1). For these samples, the data only allow us to set a lower (older) age limit. From Table 2 it is evident that samples ES 8, ES 27 and ES 39 should be conservatively considered coeval and younger than ∼100 ka, whereas the remaining samples are older. Sample ES 35 yielded a weighted mean (plateau age) of 125 ± 19 ka, which is in agreement with that of total gas (129 ± 31 ka). In an isochron plot, all eight heating steps gave a linear array with an intercept age of 127 ± 20 ka and an initial 40 Ar/36 Ar ratio of 295.1 ± 3.0, which is indistinguishable from that of modern atmospheric argon (295.5). The 127 ± 20 ka estimate is considered the best for sample ES 35. Fig. A1. Age release spectra of groundmass samples. Table A1 40 Ar–39 Ar laser step-heating data Step 36 Ar(atm) 37 Ar(Ca) 38 Ar(Cl) Ar(K) 0.04054 1.153 1.980 3.095 3.518 2.451 1.700 1.517 1.830 3.035 2.821 40 2.264 37.42 48.12 56.14 47.65 29.95 21.37 18.67 21.02 31.23 37.12 380 37 11 79 121 41 97 16 72 33 62 11677 421 180 164 166 98 144 96 97 112 67 62 53 6.540 14.12 15.02 4.558 2.198 1.098 0.8103 0.9825 24 46 27 117 133 172 33 35 122 69 42 101 88 132 392 325 50 35 223 145 127 115 88 219 78 109 194 63 25 40 94 340 340 133 129 31 65.60 92.53 65.54 18.15 9.337 4.273 2.519 2.387 Total gas Groundmass ES 35 (35.0 mg), J = 0.0001876 ± 0.0000021 1 0.05993 0.7921 0.01312 2 0.04204 4.847 0.03042 3 0.02173 5.593 0.04009 4 0.03817 3.869 0.05572 5 0.09676 3.944 0.08869 6 0.06209 1.697 0.02416 7 0.1240 2.098 0.04467 8 0.4344 4.236 0.1278 Total gas 1.909 7.856 8.959 5.123 3.453 0.7308 1.122 3.706 18.97 15.80 9.791 13.02 29.49 18.82 36.90 129.6 40 Ar* % 2.0 0.3 0.1 1.3 2.7 1.0 2.3 0.4 1.9 0.9 1.4 0.7 2.1 1.8 8.7 9.3 13.1 3.1 4.2 6.6 21.3 34.2 13.3 3.0 2.5 0.7 0.9 39 Ar(K) % 0.2 5.0 8.6 13.4 15.2 10.6 7.3 6.6 7.9 13.1 12.2 14.4 31.2 33.1 10.1 4.8 2.4 1.8 2.2 5.8 23.9 27.3 15.6 10.5 2.2 3.4 11.3 Ca/K ±2σ 1.40 1.38 1.63 2.01 2.58 3.12 3.66 4.40 3.98 3.87 3.92 0.39 0.05 0.05 0.06 0.07 0.09 0.10 0.13 0.11 0.11 0.11 3.060 0.030 0.566 0.787 1.097 1.775 3.339 5.71 4.64 4.06 0.019 0.027 0.031 0.053 0.091 0.16 0.16 0.14 1.340 0.016 0.783 1.164 1.178 1.425 2.155 4.38 3.53 2.157 0.031 0.036 0.036 0.041 0.064 0.15 0.11 0.061 1.555 0.018 405 Age (ka) Total gas Groundmass ES 27 (39.3 mg), J = 0.0001860 ± 0.0000022 1 0.2204 1.963 0.6265 2 0.3066 5.891 1.399 3 0.2177 8.733 1.441 4 0.05606 4.289 0.4237 5 0.02866 3.890 0.2044 6 0.01256 3.324 0.1181 7 0.00826 1.992 0.07095 8 0.00774 2.112 0.08928 ±2σ Ar(Tot) S. Agostini et al. / Geothermics 35 (2006) 368–408 Groundmass ES 8 (37.4 mg), J = 0.0001849 ± 0.0000023 1 0.00751 0.03016 0.00234 2 0.1262 0.8402 0.07276 3 0.1626 1.713 0.11935 4 0.1875 3.291 0.1669 5 0.1569 4.816 0.1936 6 0.1003 4.052 0.1329 7 0.07063 3.297 0.08571 8 0.06291 3.538 0.07979 9 0.06979 3.857 0.1579 10 0.1047 6.232 0.2775 11 0.1239 5.864 0.2576 39 406 Table A1 (Continued) Step 36 Ar (atm) 37 Ar (Ca) 38 Ar (Cl) 40 Ar (Tot) 1.700 5.391 10.59 7.563 3.289 1.575 1.330 6.104 21.41 26.55 38.15 51.02 57.77 56.39 36.29 153.8 Total gas Groundmass ES 43 (39.7 mg), J = 0.0001889 ± 0.0000019 1 0.1616 1.234 0.2326 2 0.3652 7.435 0.8010 3 0.1763 9.608 0.3407 4 0.08561 5.695 0.07166 5 0.08543 8.209 0.0694 6 0.09474 13.22 0.1367 7 0.02208 3.122 0.04114 8 0.04880 8.174 0.1053 2.516 8.740 6.597 2.199 1.528 2.535 0.7300 1.655 49.90 114.5 57.12 26.25 26.56 29.43 7.126 15.58 Total gas Groundmass ES 46 (44.1 mg), J = 0.0001896 ± 0.0000019 1 0.05429 0.9434 0.01339 2 0.05514 4.140 0.02935 3 0.04230 11.48 0.04496 4 0.02147 6.399 0.03770 5 0.03877 4.062 0.05531 6 0.05428 4.116 0.07147 7 0.02194 2.429 0.04945 8 0.02700 4.384 0.09843 Total gas 1.165 3.585 9.935 5.389 3.274 2.308 1.345 2.500 17.25 21.14 24.70 12.67 15.32 18.76 8.038 10.96 ±2σ 40 Ar* 25 65 65 31 75 24 84 74 127 28 25 27 185 326 235 62 0.6 3.9 5.3 1.3 1.3 0.2 0.9 0.9 58 27 289 258 260 147 294 193 280 239 352 132 66 260 387 88 277 102 248 67 355 464 421 402 404 404 396 409 468 133 26 36 42 76 71 46 414 29 Age (ka) Argon isotope concentrations are expressed in ×10−15 mol. Errors are given as 2s. J, irradiation parameter. 4.3 5.8 8.8 3.6 5.0 4.9 8.4 7.4 7.0 22.9 49.2 49.7 25.1 14.5 19.3 27.2 % 39 Ar 4.5 14.4 28.2 20.1 8.8 4.2 3.5 16.3 9.5 33.0 24.9 8.3 5.8 9.6 2.8 6.2 3.9 12.2 33.7 18.3 11.1 7.8 4.6 8.5 (K) % Ca/K ±2σ 0.691 0.839 0.888 0.998 1.312 2.206 1.870 1.522 0.026 0.027 0.026 0.029 0.041 0.074 0.062 0.047 1.124 0.014 0.925 1.605 2.748 4.89 10.14 9.84 8.07 9.32 0.037 0.064 0.089 0.17 0.36 0.30 0.25 0.28 4.037 0.053 1.53 2.18 2.18 2.24 2.34 3.37 3.41 3.31 0.12 0.08 0.07 0.07 0.07 0.10 0.11 0.10 2.427 0.032 S. Agostini et al. / Geothermics 35 (2006) 368–408 Groundmass ES 39 (35.6 mg), J = 0.0001883 ± 0.0000019 1 0.07205 0.6223 0.03904 2 0.08633 2.398 0.1285 3 0.1223 4.982 0.2302 4 0.1703 3.999 0.2214 5 0.1930 2.286 0.1403 6 0.1905 1.842 0.08904 7 0.1217 1.318 0.07362 8 0.5162 4.924 0.3370 39 Ar (K) S. 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