versión On-line ISSN 2007-2902
Rev. mex. cienc. geol vol.29 no.1 México abr. 2012
Geochemistry of late Quaternary tephrasediment sequence from northeastern Basin of Mexico (Mexico): implications to tephrochronology, chemical weathering and provenance
Geoquímica de una secuencia tefrosedimentaria del Cuaternario Tardío del noreste de la cuenca de México (México): Implicaciones para la tefrocronología, intemperismo químico y proveniencia
Priyadarsi D. Roy1*, José Luis Arce1, Rufino Lozano1, M.P. Jonathan2, Elena Centeno1, and Socorro Lozano1
1 Instituto de Geología, Universidad Nacional Autónoma de México, Ciudad Universitaria, Del. Coyoacán, C.P. 04510, México D.F., Mexico.*firstname.lastname@example.org
2 Centro Interdisciplinario de Investigaciones y estudios sobre Medio Ambiente y Desarrollo, Instituto Politécnico Nacional, Del. Gustavo A. Madero, C.P. 07340, México D.F., Mexico.
Manuscript received: December 15, 2010
Corrected manuscript received: September 5, 2011
Manuscript accepted: September 7, 2011
A ca.30 m thick tephrasediment sequence from the northeastern Basin of Mexico (Pachuca subbasin, central Mexico) is investigated for stratigraphy and multielement geochemistry to understand the tephrochronology, provenance and conditions of chemical weathering duringLate Quaternary. Chemical compositions of tephra layers are compared with products from surrounding volcanic structures (ApanTezontepece, Acoculco, Huichapan, Sierra de las Cruces and Tláloc) in order to identify their sources. Basalt to basalticandesite tephra layers (Tr 1, Tr 6 and Tr 7) show similar composition with rocks from ApanTezontepec monogenetic volcanicfield aged between 1.50 and 0.47Ma. Felsic tephra layers have composition comparable to Acoculco volcanic sequence. The dacitic ash (Tr 2) and rhyolitic ash and pumice fall deposits (Tr 3, Tr 4, Tr 5 and Tr 8) might be representatives of different Plinian eruptive events at Acoculco caldera and possibly occurred during <1.50 Ma and >0.24 Ma. Ternary diagrams (ACNK, ACN and ACNKFM) and trace element concentrations suggest that some of the sediment layers are formed from the chemical weathering of the underlying tephra and the rest of the interbedded sediments are derived from the erosion of rocks exposed at the Pachuca volcanic range. Indices of chemical weathering such as CIA and PIA indicate varying degrees of chemical alteration for these sediments possibly related to fluctuating humidity and duration of exposure to different weathering agents during their transportation from the hinterland to the subbasin.
Key words: geochemistry, tephrochronology, provenance, chemical weathering, Quaternary, Basin of Mexico.
En el presente trabajo se estudia la estratigrafía y geoquímica de multielementos de una secuencia tefrosedimentaria localizada al noreste de la Cuenca de México (subcuenca de Pachuca, centro de México), con el fin de entender la tefrocronología, proveniencia y condiciones de intemperismo químico durante el Cuaternario Tardío. Se compara la composición química de las tefras con productos de estructuras volcánicas de los alrededores del área de estudio (ApanTezontepec, Acoculco, Huichapan, Sierra de las Cruces y Tláloc) con el fin de identificar su posible fuente. Las tefras de composición basáltica a andesitabasáltica (Tr 1, Tr 6 y Tr 7) muestran composiciones similares a las rocas del campo monogenético ApanTezontepec, con edades entre 1.50 y 0.47 Ma. Las tefras félsicas muestran composiciones químicas similares a las secuencias volcánicas de Acoculco. En particular, la ceniza dacítica (Tr 2), así como los depósitos de caída de pómez riolítica (Tr 3, Tr 4, Tr 5 y Tr 8) podrían representar diferentes erupciones de tipo pliniano de la caldera Acoculco, ocurridas entre <1.50 Ma y >0.24 Ma. Diagramas ternarios (ACNK, ACN y ACNKFM) y la concentración de elementos traza sugieren que algunos de los sedimentos intercalados son productos de alteración de las tefras y los restos de sedimentos en la secuencia provienen de la erosión de rocas que afloran en la sierra volcánica de Pachuca. Los índices de intemperismo químico como CIA y PIA indican variaciones en el grado de alteración química para estos sedimentos, posiblemente relacionado a fluctuaciones de la humedad y tiempo de su transporte desde el interior a la subcuenca.
Palabras clave: geoquímica, tefrocronología, proveniencia, intemperismo químico, Cuaternario, cuenca de México.
Geochronological information of the Late Quaternary paleoenvironmental research is mainly based on radiocarbon dating of organic matter and luminescence dating (OSL and TL) of quartz grains. However, tephrochronology or tephrostratigraphy provides an alternate method to achieve reliable chronological information for both archeological and paleoenvironmental research in arid to semiarid regions with abundant volcanic activity (Giaccio et al., 2008) and correlation of different sites within the same basin. This is because of some uncertainty and complexity involved with both radiocarbon and luminescence dating methods. Radiocarbon method is unable to constrain the paleoenvironmental information prior to 50 ka and most importantly, it fails in dating sediments from arid and semiarid regions that lack organic matter. In the absence of organic matter, luminescence dating (OSL and TL) is a useful method for Quaternary geochronology (Aitken, 1985). However, this methodology needs special sampling, preparation and measurement procedures. In a recent study, González et al. (2006) reported the difficulties in dating volcanic material as it suffered from significant fading and caused severe age underestimates (Bonde et al., 2001).
The Basin of Mexico is a topographically closed and high altitude sedimentary basin located in the centraleastern part of the TransMexican Volcanic Belt (TMVB) in central Mexico (Figure 1a). Based on radiocarbon dates, the lacustrine sediments of the southern and central part of the basin (Figure 1b) were studied extensively for pollen, diatoms, mineral magnetism and sediment geochemistry to decipher the PleistoceneHolocene paleoenvironmental information (LozanoGarcía et al., 1993; Caballero, 1997; Caballero and OrtegaGuerrero, 1998; LozanoGarcía and OrtegaGuerrero, 1998; Caballero et al., 1999; Metcalfe et al., 2000). Similarly, González et al. (2006) and Lamb et al. (2009) studied the evidence of human impact on environmental conditions in the basin. However, relatively less is known from the northern part of the basin (Roy et al., 2008, 2009, 2010). Sedimentary records from different parts of the basin show the presence of Late Quaternary tephra layers. These tephra layers are products of volcanic activity from the surrounding monogenetic volcanoes and stratovolcanoes, and have potential to be used as time markers for the intrabasin paleoenvironmental research, especially for correlating the arid northern part of the basin that lacks organic matter with the relatively humid southcentral part. OrtegaGuerrero and Newton (1998) and Newton and Metcalfe (1999) attempted to establish tephrochronology as the basis of a geochronological framework for paleoenvironmental research in central Mexico, but no substantial work has been done afterwards.
In this paper, we present geochemical data of a Late Quaternary tephrasediment sequence from the Pachuca subbasin to understand the past volcanic activity and strengthen the tephrochronological information from the northeastern part of the basin. Additionally, we focus on the geochemical characterization of the sediments to understand their provenance and possible environmental conditions during their deposition using ACNK, (AK)CN and ACNKFM ternary diagrams and different indices of chemical weathering.
The Basin of Mexico is a high altitude (ca. 2240 m asl) sedimentary basin (Figure 1a) and receives varying average annual precipitation (600700 mm/yr at northeast and 7001000 mm/yr at southwest). The basin is limited to the north by the Pachuca volcanic range, to the southeast by the Sierra Nevada (Popocatépetl, Iztaccíhuatl, Telapón, and Tláloc volcanoes), to the south by Chichinautzin monogenetic volcanic field and to the west by Sierra de las Cruces volcanic range (Figure 1b). Though intense volcanic activity has occurred in the TMVB since the Oligocene epoch (OrtegaGuerrero and Newton, 1998), the topographically closed nature of the Basin of Mexico is associated with the formation of the Chichinautzin volcanic field in the Late Quaternary (0.78 Ma) (Mooser et al., 1974; Urrutia and Martín del Pozzo, 1993). Presently, the basin hosts a number of relict sedimentary subbasins: Xochimilco and Chalco in the south, Texcoco in the centre, Zumpango and Xaltocan in the north, and Tecocomulco and Pachuca in the northeast (Figure 1b).
The subbasin of Pachuca is located in the centraleastern sector of the TMVB where volcanism started during 3020 Ma (Mooser et al., 1974; Cantagrel and Robin, 1979) and is surrounded by a number of monogenetic and polygenetic volcanoes (Figure 1c). The ApanTezontepec monogenetic volcanic field (ATVF) is represented by at least 295 volcanic structures (scoria cones, shield volcanoes and domes) with basalt to basalticandesite lava flow, ash and scoria fallouts (GarcíaPalomo et al., 2002) constrained between 1.50 and 0.47 Ma (Cantagrel and Robin, 1979; LópezHernández and CastilloHernández, 1997; GarcíaPalomo et al., 2002). These mafic eruptions might have obstructed the existing drainage and formed the endorreic Pachuca subbasin.
The semirectangular caldera of Huichapan with a ca. 10 km wide depression is located at a distance of 87 km to the west of Pachuca. Two important caldera related eruptions of andesitic to trachydacitic pyroclastic flows and rhyolitic tuffs are dated to 5.0 and 4.2 Ma, respectively (AguirreDíaz and LópezMartínez, 2009). The semicircular Acoculco caldera is located at a distance of 33 km to the southeast (LópezHernández et al., 2009) and has an intense eruptive history ranging in composition between basalticandesite and rhyolite during 3.00.24 Ma (LópezHernández and CastilloHernández, 1997). One of the biggest eruptions responsible for the collapse of the structure took place at ca. 1.4 Ma and deposited a rhyolitic tuff (LópezHernández, 2009). Tláloc is a stratovolcano and forms the northernmost part of the Sierra Nevada volcanic chain. It is present at a distance of 74 km towards south of the study area. The main structure of the volcano is of Pliocene in age (GarcíaPalomo et al., 2002) with pumice flows and fallout deposits continuing during Pleistocene, with the recent eruptions at ca. 44 and ca. 31 ka 14C BP, respectively (Rueda et al., 2006, 2007). Chemical compositions of Tláloc products display a continuous range of silica contents, i.e. andesite, dacite and rhyolite.
The northern end of Sierra de las Cruces volcanic range is represented by the La Bufa volcano (GarcíaPalomo et al., 2008), located at a distance of 100 km to the southwest. This is a complex structure dated at 3.7 Ma (Osete et al., 2000). Available geochemical analyses from La Bufa and the northern sector of Sierra de las Cruces show compositions ranging between andesite and dacite (RodríguezSaavedra, 2007). Apart from the Quaternary volcanoes and their products, Tertiary extrusive igneous rocks are exposed in different formations in the Pachuca volcanic range (Geyne et al., 1963). The rocks of San Cristóbal Fm. comprise basalticandesite, whereas the rocks from Corteza, Pachuca, Real del Monte, Santa Gertrudis, Vizcaína and Zumate Fms. consist of andesites. The volcanic deposits of Santiago and Tezuantle Fm. contain rhyolites and deposits of Cerezo Fm. are dacitic in nature.
Tephrochronological information of the basin
Tephra layers were studied in detail from the southern and central part of the TMVB and Basin of Mexico. OrtegaGuerrero and Newton (1998) reported the geochemical compositions of tephra layers ranging in age from 34 ka 14C BP to 2.6 ka 14C yr BP in the Chalco and Texcoco lakes. The 34 ka 14C BP basalticandesite Tláhuac tephra, 1514.4 ka 14C BP andesiterhyolite tephra and 14.3 ka 14C BP basalticandesite tephra layers were sourced from Popocatéptl volcano. The 1112 ka 14C BP rhyolitic pumice from the Nevado de Toluca is also identified in the deposits of Chalco (Bloomfield et al., 1977; Newton and Metcalfe, 1999). Gonzalez and Huddart (2007) and Lamb et al. (2009) reported the geochemistry of tephra layers from Tocuila and Tepexpan paleoindian sites (adjacent to Texcoco lake) and suggested that most of the tephra were reworked and the ca. 0.5 ka 14C BP basalticandesite and andesite tephra layer could be from one of the adjacent monogenetic cinder cones.
Information on tephrochronology from the northeastern part is relatively scarce, except for the geochemical characterization of two distinct tephra layers present in the Tecocomulco lake (Roy et al., 2008, 2009), a mafic tephra layer at Pachuca subbasin (Roy et al., 2010) and volcanic deposits of the Apan region (GarcíaPalomo et al., 2002). The ca. 50 ka 14C BP daciterhyolite tephra and ca. 31 ka 14C BP rhyolitic tephra from the lacustrine deposits of the Tecocomulco lake were sourced from the Acoculco caldera and Tláloc volcano, respectively. Additional information on tephrochronology comes from the Toluca basin, located to the south of Basin of Mexico. These tephra layers range between ca. 25 and 8.5 ka 14C BP (Newton and Metcalfe, 1999).
MATERIAL AND METHODS
A ca. 30 m thick tephrasediment sequence exposed in different parts of a mine in the Pachuca subbasin (Figure 1c) was studied for sediment stratigraphy and multielement geochemistry. For the geochemical analyses, 44 samples (26 samples from tephra layers and 18 samples from interbedded sediments) were collected and subjected to oven drying at 40°C, homogenized and grinded to 200 mesh (<0.074 mm) sizes using an agate mortar. Multielement concentrations (major elements in weight % and trace elements in ppm) were measured in a Siemens SRS 3000 wavelength dispersive Xray fluorescence (XRF) spectrometer after the methods of Guevara et al. (2005) and Lozano and Bernal (2005) at the Instituto de Geología, Universidad Nacional Autónoma de México. Major element oxides (SiO2, Al2O3, TiO2, Fe2O3, CaO, MgO, Na2O, K2O, MnO and P2O5) were measured in fused discs after determining the lost on ignition (LoI) by heating the sample up to 1000°C; trace elements were measured in the pressed pellets. The accuracy and precision of the analytical methods were established using international standards (QLO1 and JA2) and inhouse reference material (BCU3). XRF measurements have precisions up to 1.5 % for major elements and 6 % for trace elements. The accuracy for major and trace elements are 2 % and 9.5 %, respectively. Geochemical compositions of the volcanic rocks exposed in the Pachuca volcanic range are taken from Geyne et al. (1963). Bulk rock chemical analyses from Huichapan, Acoculco, Tláloc, Sierra de las Cruces, and ATVF are taken from several authors (GarcíaPalomo et al., 2002; Meier, 2007; RodríguezSaavedra, 2007; QuintanillaGarza, 2008; AguirreDíaz and LópezMartínez, 2009; LópezHernández, 2009; Roy et al., 2009).
The sequence (Figure 2) consists of at least eight different tephra layers (Tr 1 to Tr 8 from bottom to top) and interbedded sediments (S 1 to S 6 from bottom to top). The bottommost tephra layer (Tr 1) has a thickness of 2.8 m and consists of blackbrown multilayered lapilli to coarse ash scoria fallout deposits. It is characterized by granulometrically fining upward sequences. Each sequence begins with coarse grained and dark colored lapilli and terminates with coarse ash. Tr 1 has an erosive contact with the overlying sediments, i.e. S 1. S 1 consists of massive palebrown sandysilt and partly indurate fine sand. A massive beige color 3 m thick finemedium volcanic ash deposit (Tr 2) overlies S 1 with a sharp contact. The overlying massive palebrown sediment (S 2) has a gradual contact with Tr 2 and has a thickness of 2 m.
Tr 3 has a thickness of 0.6 m and is a whitebeige color, massive finemedium ash fall deposit. This is overlain by ca. 4.8 m thick palebrown sandysilt and siltyclay intercalations (S 3) with an abrupt contact. Both Tr 4 (1.2 m thick) and Tr 5 (0.8 m thick) are light gray in color and consist of grain supported pumice rich, lapilli size fall deposits. They are separated by a pale brown massive siltysand (S 4) showing an abrupt contact with Tr 4. Unlike Tr 5 which is massive, Tr 4 shows stratified base and massive top. Tr 5 is overlain by a 2 m thick massive sandysilt (S 5). Both Tr 6 and Tr 7 have similar characteristics and comprise of dark colored coarse to fine ash fall deposits. Both are separated by a brown massive sandysilt sediment layer (S 6) showing an abrupt contact with Tr 6. A massive 2 m thick, grain supported, lapilli sized pumice fall deposit (Tr 8) overlies ca. 1m thick reddish siltysand (could not be sampled). This is capped by a >5 m thick sequence consisting of altered tephra, sandysilt and silt intercalations.
Geochemistry of tephra layers
Chemical composition. Tephra layers range in composition from basalt to rhyolite (Figure 3a) and are subalkaline (Figure 3b) in nature. Based on their major element compositions, tephra layers are divided into three different groups. The first group (I) consists of basalt to basalticandesite Tr 1, Tr 6 and Tr 7. The second group (II) has Tr 2 that ranges between andesite to rhyolite with majority of the samples falling within the dacite field. The third group (III) comprises rhyolitic Tr 3, Tr 4, Tr 5 and Tr 8.
The basalt to basalticandesite tephra layers have SiO2 concentrations of 49.5457.15 wt. % and total alkalis (Na2O+K2O) concentrations of 2.324.32 wt. %. The rhyolitic tephra layers have SiO2 contents of 69.0371.87 wt. % and 8.4410.18 wt. % of total alkalis. The andesite to rhyolite tephra (Tr 2) has an intermediate chemical composition (SiO2: 62.7370.52 wt. % and Na2O+K2O: 5.017.73 wt. %) compared to both the above mentioned groups. Figures 3c to 3f show the bivariate plot of SiO2 vs. Al2O3 SiO2 vs. CaO, SiO2 vs. MgO, and SiO2 vs. TiO2 of the tephra layers and products of the surrounding volcanoes. Basalt to basalticandesite tephra layers (Tr 1, Tr 6 and Tr 7) have CaO, Al2O3, SiO2 and TiO2 concentrations comparable to volcanic products from ATVF. Similarly, basalticandesite Tr 7 has MgO concentrations similar to rocks from Sierra de la Cruces. Both Tr 2 and Tr 3 have Al2O3 contents similar to Acoculco volcanic products, whereas Tr 4, Tr 5 and Tr 8 have Al2O3 values comparable to products from both Huichapan and Acoculco. Dacite to rhyolitic tephra layers (Tr 2, Tr 3, Tr 4 and Tr 5) have CaO and TiO2 concentrations comparable to Tlaloc, Acoculco and Huichapan volcanic products.
Table 1 presents the average major and trace element concentrations of the tephra layers and volcanic products from ATVF, Huichapan, Acoculco, Sierra de las Cruces and Tláloc. Mafic tephra layers with composition varying between basalt and basalticandesite show higher concentrations of Sr, V, Cr, Co, Ni and Cu, whereas felsic tephra layers with composition varying between dacite and rhyolite have higher abundance of Rb, Y, Zr, Nb, Zn, Th and Pb.
ACNK diagram The molar proportions of Al2O3, CaO*+Na2O and K2O in the tephra layers are presented in the ACNK triangle (Figure 4a) (Al2O3 plotted as top apex (A), CaO*+Na2O at the bottom left (CN) and K2O at the bottom right (K)) of Nesbitt and Young (1984, 1989) to understand their weathering trends and mineralogical compositions. CaO* is the concentration of CaO in silicates and corrected for apatite and carbonate contents (Fedo et al., 1995). A quantitative estimation of the degree of chemical alteration of the tephra layers are obtained by calculating the Chemical Index of Alteration (CIA = [Al2O3 / (Al2O3+CaO*+Na2O+K2O)] x 100) as suggested by Nesbitt and Young (1982). The CIA values are indicated by the height of the sample above the baseline of the triangular diagram (Figure 4a).
CIA provides a dimensionless number that estimates the ratio of secondary aluminous minerals (clay minerals) to feldspars. Most unaltered rocks and primary minerals (feldspars and biotite) plot on or close to the feldspar join (5050 line in the ACNK triangle) and have CIA values near 50. However, mafic and ultramafic rocks and minerals like amphiboles and pyroxenes have lower CIA values and plot much below the feldspar join (Young, 2001). By contrast, the secondary products have CIA values of 7085 for smectite and illite and 100 for kaolinite group minerals and chlorite (Nesbitt and Wilson, 1992). The samples with CIA < 60 suggest lower weathering, 6080 moderate weathering and > 80 extreme weathering (Fedo et al., 1995). In the ACNK diagram, both parent material and their altered products fall along the same linear trend and the projection of this linear trend onto the feldspar join suggests the chemical composition and mineralogical association of the possible parental material.
The CIA values of tephra layers are presented in Table 1 and Figure 4a. Except for Tr 2, tephra layers have CIA values between 42 and 51 suggesting their unweathered nature. CIA of Tr 2 ranges between 51 and 62 and suggests lower chemical alteration. In the ACNK triangle, the tephra samples fall in different linear arrays subparallel to the ACN join (solid line with arrow) and the projection of these linear trends onto the feldspar join suggest their feldspar assemblage. The first linear array (1) consists of basalt to basalticandesite Tr 1, Tr 6 and Tr 7 and its projection onto the feldspar join suggests presence of abundant plagioclase and possible absence of Kfeldspar. Compared to Tr 6 and Tr 7, Tr 1 plots more towards the CaO*+Na2O apex below the feldspar join. This could be due to higher abundance of other CaNabearing silicates, e.g. amphiboles and pyroxenes. The dacitic Tr 2 constitutes the second linear array (2) and consist of plagioclase>Kfeldspar. The rhyolitic Tr 3, Tr 4, Tr 5 and Tr 8 have higher abundance of Kfeldspar (array 3). The Kfeldspar content in Tr 3 is lower compared to the rest. Compared to Tr 8, both Tr 4 and Tr 5 are plotted towards CN apex.
ACN diagram. Molar proportions of Al2O3 (minus Al associated with K), CaO* and Na2O are plotted in the ACN triangle (Figure 4b) (Al2O3K2O at upper apex, CaO* at left bottom and Na2O at right bottom) of Fedo et al. (1995) to understand trends of plagioclase weathering in tephra layers. Quantitative estimation of the plagioclase weathering is measured by calculating the Plagioclase Index of Alteration (PIA= [(Al2O3K2O) / (Al2O3+CaO*+Na2OK2O)] x 100) of Fedo et al. (1995) and presented in Table 1.
Both the PIA and CIA values are comparable. Basalt to basalticandesite tephra layers (Tr 1, Tr 6 and Tr 7) show PIA values between 43 and 51, whereas dacitic tephra layers (Tr 2) have PIA values of 5166. Rhyolitic tephra layers (Tr 3, Tr 4, Tr 5 and Tr 8) have lower PIA values (2952) compared to the rest. The plagioclase weathering trends suggest enrichment of anorthite in the mafic tephra layers and albite in the felsic tephra layers (Figure 4b). With increasing PIA, mafic tephra layers are depleted in CaO* and felsic tephra layers in Na2O. This suggests that with gradual increase in chemical weathering, the tephra layers are depleted in both anorthite and albite and enriched in secondary aluminous clay minerals. The relatively higher CaO* in Tr 1 compared to both Tr 6 and Tr 7 suggest that the amphiboles and pyroxenes in Tr 1 are Cabearing. Similarly, the higher Na2O in Tr 4 (PIA=29) and Tr 5 (PIA=36) suggest presence of some other Nabearing constituent, e.g. glass fragments.
ACNKFM diagram. Figure 4c shows the molar proportions of Al2O2 (A), CaO*+Na2O+K2O (CNK) and Fe2O3 + MgO (FM) in the ternary diagram of Nesbitt and Wilson (1992). Except for Tr 2, all the tephra layers fall long the linear array joining Feldspars (Fs) with FM apex. However, the mafic tephra layers (Tr 1, Tr 6 and Tr 7) plot away from the feldspars suggesting higher abundance of mafic minerals, e.g. olivine, pyroxene and amphibole. Rhyolitic tephra layers (Tr 4 and Tr 5) plot towards the CNK apex and suggest higher abundance of CaO*, Na2O and K2O. The relatively weathered dacitic tephra (Tr 2) plots within the feldspars (Fs), kaolinite (Ka) and smectite (Sm) compositional triangle. Except for few samples, they lie much closer to feldspars along the FsSm join. This suggests that feldspars and smectite are more abundant than kaolinite. Few samples of Tr 2 plot above the FsSm line and suggest presence of kaolinite (< 20 %).
Geochemistry of sediments
Chemical composition. Based on their major and trace element compositions, the sediments are divided into three different groups. The first group consists of S 2 and S 5 with higher concentrations of SiO2, K2O, Rb, Y, Zr, Zn, Th and Pb. Second group comprises S 4 and S 6 and show higher abundance of Al2O3, TiO2, Fe2O3, MgO, CaO, P2O5, Sr, Cu,
Cr and Ni. Except for few samples of S 2, both the groups have comparable MnO and Na2O concentrations. Ba does not show any significant pattern. The third group consists of S 1 and S 3 and show large variation in the concentrations of both major and trace elements. The concentration range covers the concentrations of both the above mentioned groups. Table 2 presents the average composition of the sediments and the rocks exposed in the Pachuca volcanic range.
ACNK diagram. The CIA values of sediments are presented in Table 2. Except for S 5, CIA of sediments vary between 53 and 77 suggesting low to intermediate chemical alteration of the parent material. The CIA value of S 5 (CIA=45) suggests absence of chemical alteration. In the ACNK ternary space (Figure 4a), the sediments fall along different linear arrays. S 5 plots below the feldspar join towards the CaO*+Na2O apex suggesting its higher abundance of amphiboles and pyroxenes. S 4, S 6 and some samples of S 1 and S 3 show higher abundance of plagioclase, whereas S 2 and some samples from S 1 and S 3 are characterized by presence of both Kfeldspar and plagioclase.
It is interesting to note that most of the sediments do not fall along the linear trend that contains their underlying tephra layer, except for S 6 (linear trends 1 in Figure 4a). These sediments and their underlying tephra layer fall in different linear arrays. S 6 shows higher CIA compared to Tr 6 (Tables 1 and 2) and this suggests that S 6 is possibly produced by the geochemical alteration of underlying tephra layer Tr 6.
In order to understand the provenance of rest of the sediments, both sediments and rocks exposed in the Pachuca volcanic range are presented in a different ACNK space (Figure 5a). The linear array (i) consisting of S 4 and parts of both S 1 and S 3 projects onto the feldspar join suggesting parent material comparable to andesites from Pachuca, Real de Monte, Zumate and Vizcaína Formations. The linear trend (ii) consisting of parts of samples from S 1, S 2 and S 3 intersects the feldspar join and suggests a parent material similar to rhyolites from Santiago and Tezuantle Formations. The linear array (iii) consisting of some samples from S 2 and S 3 suggest a parent material more felsic than dacites of Cerezo Formation.
ACN diagram. Except for S 5, sediments have PIA values between 51 and 80. S 5 exhibits a PIA value of 42. In the ACN ternary space (Figure 5b), S 4 and S 6 and some samples of S 1 and S 3 show the presence of anorthite and display a linear trend with parental material comparable to andesites of Pachuca volcanic range. Although present along the same trend, S5 show higher CaO* concentration compared to the andesites possibly associated with pyroxenes and amphiboles. With gradual increase in chemical alteration, they are enriched in Al2O3 at the expense of CaO*. Similarly, S 2 and some samples from S 1 and S 3 have higher abundance of albite and are present along a linear trend suggesting parental material with compositions intermediate to dacite and rhylites of Pachuca volcanic range. Table 2 presents the PIA values of rocks exposed in the Pachuca volcanic range and sediments of the studied profile.
ACNKFM diagram. Figure 4c shows the distribution of sediments and tephra layers in the ACNKFM ternary diagram and Figure 5c shows the distributions of sediments with respect to the rocks exposed in the Pachuca volcanic range in a different ACNKFM diagram. Except for the rhyolite of Tezuantle Fm., all the rocks are present along the linear array joining feldspars with FM apex. The basalticandesite and andesites fall away from the feldspar apex and suggest higher abundance of mafic minerals. The dacite and rhyolite plot close to the feldspar apex and indicate higher abundance of feldspars. S 4 and some of the samples from S 1 and S 2 also plot along the FsFM join. S 4 samples plot closer to the andesites, whereas the S1 and S2 samples plot close to dacite and rhyolite.
The relatively altered rhyolite (CIA=57, Table 2) of Tezuantle Fm. and most of the sediments plot within the feldsparkaolinitesmectite compositional space. Most of the sediments plots towards the feldspar apex along the FsSm join and some plot above the FsSm join and indicate presence of kaolinite.
Tephrostratigraphy and tephrochronology
Stratigraphy of the studied profile suggests at least eigth different events of volcanic eruption in the vicinity of the Pachuca subbasin ranging in composition from basalt to rhyolite. The tephra layers have different sedimentary and geochemical characteristics. Among the mafic tephra layers, the ca. 2.8 m thick basalt to basalticandesite Tr 1 is characterised by multilayered lapilli to coarse ash deposits, whereas 0.5 m thick deposits of basalticandesite Tr 6 and Tr 7 comprise of fine ash. Compared to both Tr 6 and Tr 7, Tr 1 has higher Cabearing pyroxenes and amphiboles and all of them have abundant anorthite (Figures 4a, 4b). The felsic tephra layers are characterised by both massive fine grained ash and grain supported lapilli size pumice fall deposits. Except for Tr 3, the rhyolitic tephra layers are grain supported lapilli size pumice deposits and some even show stratifications, e.g. Tr 4. The rhyolitic tephra layers (Tr 3, Tr 4, Tr 5 and Tr 8) have relatively higher abundance of Kfeldspar compared to the dacitic ash deposit (Tr 2). Among the rhyolitic tephra, both Tr 4 and Tr 5 have higher Na2O content compared to Tr 8 possibly related to the presence of glass fragments (Figure 4b).
In order to understand the source of these tephra layers, we compared the bulk rock geochemistry of the tephra layers with the volcanic products from ApanTezontepec monogenetic volcanic field (ATVF) (GarcíaPalomo et al., 2002), Acoculco caldera (LópezHernández, 2009), Huichapan caldera (AguirreDíaz and LópezMartínez, 2009), northern Sierra de las Cruces including La Bufa volcano (RodríguezSaavedra, 2007; QuintanillaGarza, 2008) and Tláloc volcano (Meier, 2007; Roy et al., 2009) located in the surroundings of the Pachuca subbasin (Table 1 and Figure 3). Both the tephra layers and products from surrounding volcanoes show low to intermediate chemical alteration (CIA < 65). This suggests that the major element geochemistry of both tephra layers and volcanic products represent their original concentrations and hence can be compared. The compositions of the mafic tephra layers (Tr 1, Tr 6 and Tr 7) are comparable to the rocks of ATVF (Figure 3) and because they are typical deposits of monogenetic volcanism (particularly for Stromboliantype eruptions). The rocks forming the ATVF are basalt to basalticandesites with aphanitic texture and phenocrysts of olivine and plagioclase (GarcíaPalomo et al., 2002). The position of the mafic tephra layers in the ACNK (Figure 4a) and ACNKFM (Figure 4c) ternary spaces suggest presence of dominant plagioclase and mafic minerals similar to the deposits of ATVF. The available K/Ar dates from ATVF are 1.50±0.07 Ma (Cantagrel and Robin, 1979), 0.80±0.2 Ma (LópezHernández and CastilloHernández, 1997), and 0.47±0.07 Ma (GarcíaPalomo et al., 2002). The tephra layers from the studied profile lack chronological information. As the above mentioned tephra layers are primary fall out deposits and do not have any sedimentological feature showing reworking, they could be correlated to the above mentioned three eruptive events at ATVF based on geochemistry and stratigraphical position. However, the available geochemical data from AVTF do not mention specific ages (GarcíaPalomo et al., 2002). So, we do not correlate the mafic tephra layers to any of the three above mentioned volcanic events, but put the basalt to basalticandesite tephra layers in the time interval between 1.5 Ma and 0.47 Ma and the overlying felsic tephra layers as <1.5 Ma.
The rhyolitic tephra layers (Tr 3, Tr 4, Tr 5 and Tr 8) are compared to felsic rocks from Acoculco, Huichapan and Tláloc volcanic structures (Table 1). The chemical compositions of rhyolitic tephra layers and volcanic products from Huichapan and Acoculco calderas are comparable (Figure 3). However, the Huichapan tuff has an older age (4.2±0.2 Ma) and show relatively higher SiO2 content (AguirreDíaz and LópezMatínez, 2009) compared to the rhyolitic tephra layers. So, Huichapan caldera as a possible source for any of the rhyolitic tephra layers is ruled out. The rocks of the Acoculco volcanic sequence ranges in compositions from basalt to andesite to rhyolite and were deposited during 3.00.24 Ma (GarcíaPalomo et al., 2002) and the felsic rocks (rhyolites) were deposited towards the later part. LópezHernández and CastilloHernández (1997) reported the K/Ar date from one of the rhyolites from Acoculco volcanic sequence as 1.7±0.4 Ma. This suggests that the rhyolitic tephra layers at the Pachuca subbasin are representative of four different volcanic eruptions from the Acoculco caldera that might have occurred after 1.50 Ma and before 0.24 Ma.
The dacitic ash layer (Tr 2) has chemical composition comparable to the products from Acoculco caldera, northern Sierra de las Cruces and Tláloc (Figures 3 a and 3b). The felsic deposits of Tláloc are very young (44 ka and 31 ka, respectively) and hence can not be considered as a possible source. There exists a mismatch between Tr 2 and products from Sierra de las Cruces in some of the bivariate scattered plots (Figures 3d and 3e). Compared to the products from Sierra de las Cruces, Tr 2 show lower concentrations of CaO and MgO. This can be explained by its CIA (5162) and PIA values (5166) showing relatively higher chemical alteration compared to products of Sierra de las Cruces (CIA = 4850). So the mobile and soluble elements like Ca and Mg are possibly removed during the alteration of primary minerals of Tr 2. The above mentioned interpretation is also supported by bivariate plots involving insoluble elements, i.e. Al2O3 and TiO2 (Figures 3c and 3f) and presence of clay minerals i.e. smectite and kaolinite in Tr 2 (Figure 4c). The available K/Ar date constrains the most recent eruption from the northern Sierra de las Cruces and La Bufa volcano at 3.70±0.40 Ma (Osete et al., 2000), which is much older compared to the tephra layers of the studied profile. Apart from that Sierra de la Cruces are located at a larger distance (ca. 100 km from the studied profile) compared to the Acoculco caldera (ca. 33 km). This suggests that Tr 2 could be the result of a Pliniantype eruption at Acoculco. However, the interpretations presented here are preliminary and a detailed analysis including geochemistry of individual glass shards and radiometric dates would be needed to improve our understanding of the volcanic history in the northern part of the Basin of Mexico.
Provenance of the interbedded sediments
The interbedded sediments are characterized by different chemical composition and mineralogical association. S 2 shows felsic constituents, i.e. Kfeldspar (Figure 5a), albite (Figure 5b) and relatively higher abundance of K2O, Zr, Y, Rb, Th and Pb (Table 2). Similarly, S 4 and S 6 contain dominant mafic constituents, i.e. anorthite (plagioclase) and higher abundances of TiO2, Fe2O3, CaO, MgO, Sr, Cr, Ni and Cu. S 5 is characterized by presence of Cabearing pyroxenes and amphiboles along with plagioclase and Kfeldspar. Both S 1 and S 3 are characterized by presence of felsic and mafic constituents.
Comparable concentrations of insoluble major and trace elements (Ti, Zr and Y, Tables 1 and 2) and their position along the same linear trend (Fig 4a) suggest that S 6 could be an altered product of its underlying tephra layer, i.e. Tr 6. This is also supported by the fact that CIA value of S 6 is higher compared to its source Tr 6. Similarly, both S 2 and underlying Tr 2 fall along the same linear array and some samples of S 1 and Tr 1 are present along the same linear trend. However, S 1 has an erosive contact with underlying Tr 1 and S 2 shows relatively lower chemical alteration compared to its source, i.e. Tr 2. Apart from that the sediments and their underlying tephra layers have different concentrations of trace elements (Rb, Sr, Y, Zr, Nb, V, Cr, Cu, Th and Pb). This rules out that both these sediment layers were derived from chemical alteration of their underlying tephra layers.
The position of rest of the sediments (S 1, S 3, S 4 and S 5) and their underlying tephra layers along different linear trends in the ACNK diagram. (Figure 4a) indicate that these sediments are not produced by the chemical weathering of their underlying tephra layers. Presence of all these sediments along different linear trends containing volcanic rocks from Pachuca range (Figures 5a and 5b) suggests that these sediments are possibly derived by the erosion of basalticandesite, andesite, dacite and rhyolites exposed along the Pachuca volcanic range.
However, dissimilarity in trace element concentrations between tephra and sediments could also be due to their different geochemical behavior. Immobile elements are enriched and soluble elements are leached away and hence depleted in the sediments during weathering and pedogenesis. So we consider the possibility that some more S layers could be alteration products of underlying tephra layers, without excluding the observation that some have produced as a result of erosion from the surrounding rocks and pedogenesis of the derived material.
Chemical weathering of the interbedded sediments
Except for S 5 (CIA and PIA < 50), the sediments show CIA values varying between 53 and 77 and PIA values ranging between 51 and 80. The varying values of indices of alteration are interpreted as indicators of major element changes due to chemical weathering and soil formation that led to conversion of primary feldspars, volcanic glass and mafic minerals to secondary clay minerals (kaolinite, smectite, etc.) and can be used as indicators of chemical weathering at the source terrain. The degree of chemical weathering and composition of siliciclastic sediments are controlled by both climate and tectonism. In S 5, the absence of chemical weathering and preservation of easily weatherable pyroxenes and amphiboles might have been the result of either a very cool or arid climate or some combination of both. Similarly, the lower to intermediate chemical weathering during deposition of rest of the sediments suggest relatively humid and varying climatic conditions at the source terrains. This is also supported by the presence of smectite and kaolinite in some of the sediments and their absence in others (Figures 5c). On the other hand, lower chemical weathering can also be the result of a tectonically active hinterland (upliftment of igneous rocks) causing its erosion at a higher rate (Andersson et al., 2004). The short time span of exposure to weathering (possibly enhanced by erosion or burial of younger sediments) might have led to lower alteration of the deposited sediments at Pachuca subbasin. In addition, there are various glacial and interglacial periods registered in high resolution late Quaternary paleoclimatic registers during the time span that cover the studied stratigraphy (last 1.50 Ma). However, it is difficult to propose a paleoclimatic reconstruction in the absence of any precise chronological constraint of the studied profile.
Compared to the southern and central Basin of Mexico, the northern part is relatively less studied. Stratigraphy and multielement geochemistry of a ca. 30 m thick tephrasediment sequence from the Pachuca subbasin gives preliminary but important information regarding tephrostratigraphy, tephrochronology, provenance and environmental conditions of the last ca. 1.50 Ma from the northern Basin of Mexico. More specifically:
(i) The mafic (basalt to basalticandesite) tephra layers represent three distinct eruptions from ApanTezontepec monogenetic volcanoes during 1.500.47 Ma. Tr 1 with multilayered lapilli to coarse ash scoria fall deposit could be sourced from a nearer structure, while Tr 6 and Tr 7 with coarse to fine ash fall deposits could be from a structure located at a higher distance.
(ii) The felsic tephra layers represent volcanic events during <1.50 >0.24 Ma at Acoculco caldera. The dacitic Tr 2 and rhyolitic Tr 3 comprises of fine ash deposits, whereas rhyolitic Tr 4, Tr 5 and Tr 8 are characterised by grain supported pumice rich lapilli fall deposits. The lapilli grain size and thicknesses (> 1 m) suggest that some of the volcanic events were of large magnitude (probably Pliniantype eruptions).
(iii) The compositions of the sediments with respect to their tephra layers and rocks exposed in the Pachuca volcanic range in the ternary diagrams suggest that some of them are weathering products of underlying tephra layers and rest of the sediments are possibly derived from the erosion of parental materials comparable to the rocks (basalticandesite, andesite, dacite and rhyolite) exposed in the Pachuca range. The varying indices of chemical weathering could be indicative of varying humidity or duration of exposure to different weathering agents during their transportation and deposition in the Pachuca subbasin.
PDR and MPJ acknowledge SNICONACyT. This work is financially supported by PROMEPSEP (PROMEP/103.5/05/1919) and CONACyT Ciencias Básicas (83800). Satellite image of the study area was downloaded from the Global Land Cover Facility, University of Maryland (http://glcf.umiacs.umd.edu/index.shtml) and then processed by L. Capra. We are thankful to both the anonymous reviewers and Jesús MartínezFrías for their critical comments. This is the 51st contribution from Earth System Science Group, Chennai, India.
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