Original scientific paper Received: June 29, 2015 Accepted: October 2, 2015 Compositional characteristics of the migmatite gneiss around Awo, southwestern Nigeria Značilnosti sestave migmatitnega gnajsa pri Awu v jugozahodni Nigeriji Mustapha T. Jimoh1*, Anthony T. Bolarinwa2, Oluwanifemi O. Ashaye1 department of Earth Sciences, Ladoke Akintola University of Technology, Ogbomosho, Oyo state, Nigeria 2Department of Geology, University of Ibadan, Nigeria Corresponding author. E-mail: mtjimoh@lautech.edu.ng Abstract Migmatite gneiss within the Precambrian basement rocks around Awo, southwestern Nigeria were studied with a view to determine origin and compositional relationship of the paleosomes and neosomes. Other rocks associated with the migmatite gneiss are biotite gneiss, banded gneiss, syenite, granite, pegmatite and aplite. X-Ray Fluorescence geochemical studies reveal minor variations in the bulk chemical composition of paleosomes and neosomes. The composition is dominated by silica (w « 62 %) and alumina (w « 15 %). The migmatite gneiss magma type was high K-calc-al-kaline to calc-alkaline. The Total Alkali Silica (TAS) plot shows the protolith of the migmatite gneiss to be dio-ritic and quartz-dioritic rocks while the xenoliths were originally gabbro. The migmatite gneisses are mostly of sedimentary parentage. Trace element data revealed high Ba content, indicating its concentration in felsic minerals. Large Ion Lithophile Elements (LILE) such as Ba, Rb and Sr generally exhibit positive anomaly while High Field Strength Elements (HFSE) notably Ta, Nb, Hf and Zr display weak anomaly. The REE geochemistry revealed strong enrichment of LREE (La, Ce, Pr and Nd) while HREE (Ho, Er, Tm, Yb and Lu) are weakly anomalous. The paleosomes and neosomes of the migmatite gneiss displayed marginal compositional variation which indicates their evolution from the same mag-matic source. Key words: Migmatite gneiss, Paleosomes, Neosomes, Geochemistry, Magmatic source Izvleček Migmatitni gnajs v predkambrijskih kamninah podlage v okolici Awa v jugozahodni Nigeriji smo preučevali z namenom opredelitve izvora in primerjave sestave komponent paleosoma in neosoma. Druge kamnine v povezavi z migmatitnim gnajsom so biotitni gnajs, pasoviti gnajs, sienit, granit, pegmatit in aplit. Rentgenska fluorescenčna preiskava razkriva manjša nihanja celotne kemične sestave paleosoma in neosoma. V sestavi prevladujeta silicijeva (w « 62 %) in aluminijska (w « 15 %) komponenta. Tip migmatitno gnajso-ve magme je bil visoko K-kalk-alkalni do kalk-alkalni. Diagram celotne alkalne silicije (TAS) nakazuje, da so bile protolit migmatitnega gnajsa dioritne in kremeno-vodioritne kamnine, medtem ko so ksenoliti prvotno gabrski. Migmatitni gnajsi so pretežno sedimentnega porekla. Podatki o sledeh razkrivajo visoko vsebnost Ba, očitno koncentriranega v felsičnih mineralih. Ve-likoionske litofilne prvine (LILE), kot so Ba, Rb in Sr, splošno izkazujejo pozitivno anomalijo, prvine visoke poljske jakosti (HFSE), in sicer Ta, Nb, Hf in Zr, pa šibko anomalijo. Geokemična sestava prvin redkih zemelj priča o znatni obogatitvi LREE (La, Ce, Pr in Nd), medtem ko so HREE (Ho, Er, Tm, Yb in Lu) šibko anomal-ne. Paleosomi in neosomi migmatitnega gnajsa kažejo zmerno variacijo sestave, ki priča o njihovem poreklu iz istega magmatskega vira. Ključne besede: migmatitni gnajs, paleosomi, neoso-mi, geokemija, magmatski izvor Introduction Migmatites are heterogeneous metamorphic rocks consisting of intermingled leucosomes, melanosomes and mesosomes [1,2]. They are also described as partially melted rocks of the continental crust which is made up of two components the neosomes and paleosomes [3]. Neosomes are crystallized products and residual materials from the melt whereas the paleo-somes are the unmelted rocks. The study area which occur within the Precambrian basement complex of south-western Nigeria is located around Awo within Latitude 7° 45' N and 7° 4' N and Longitude of 4° 23' E and 4° 27' E. Field investigations showed the occurrence of diverse granitic rocks with structural features consistent with regional trend of the Nigeria basement complex. The various geological units identified around the study area are migmatite gneiss, banded gneiss, biotite gneiss, quartzite, syenite, granite and pegmatite (Figure 1). The migmatite gneiss is located towards the central portion and the southwestern part of the study area (Figure 1). Field description revealed the migmatite gneiss as a massive outcrop. Xenoliths occur as fine grained mafic inclusions within the gneissic bodies. These inclusions are of various sizes and shapes. The shapes vary from angular, sub-angular, rounded, sub-rounded, lenticular to irregular pods (Figure 3). Odeyemi and Rahaman [4] postulated that the migmatite-gneiss of the basement complex and the meta-supracrustal rocks mark the termination of Precambrian activity in southwestern Nigeria. Migmatite gneiss complex is the oldest, most widespread and abundant rock type in the basement complex [4]. The migmatite gneiss is grayish in color and medium grained in texture, with alternation of mafic and felsic bands set in a medium to coarse grained ground mass. In some locations, pegmatite veins of variable dimensions are intruded into the gneissic bodies. These veins maintain various forms and relationship which are concordant, discordant, cross cutting and contorted with the foliation plane of the gneissic rock. The focus of this study is to investigate the migmatite gneiss with a view to highlighting the compositional characteristics of the pa-leosomal and neosomal components. r-■■■ FlA/li И| Ricilypes I □ BTBS*» Sui I «t- си-«* □ □ pe.^« 3 "rUff»*» □ .... S Эт. _I Figure 1: Geological map of the study area. Geological Settings and Field Characteristics Various geological units associated with the migmatite gneiss are banded gneiss, biotite gneiss, granite, syenite and pegmatite. Of all the rock types occurring in the study area, migmatite gneiss and biotite gneiss appear to be predominant while banded gneiss, syenite, granite and pegmatites occur in subordinate proportion. Migmatite gneisses are the oldest and most widespread lithology within the study area. They form the country rock in which all other rocks intrude. They are well exposed with mostly flat lying outcrop. They also cut across river and stream channels as highly weathered rocks. The migmatite gneisses are not treated as a single lithological unit they were segregated into paleosomes and neosomes. Neosomes are further segregated into leucosomes and melanosomes. (Table 1). The leucosomes are quartzofeldspathic in composition. Quartz appears dominant in the mode (> 70 %). The melanosomes contain varying amount of ferromagnesian minerals like platy biotite, prismatic hornblendes and equant pyroxene. Melanosomes are also identified as xenoliths. The presence of pyroxene confers a greenish tint on the rock body. The composite fabrics of paleosomes and neosomes are folded on mesoscopic scale. The paleosomes and leucosomes are concurrently folded and terminate abruptly into what appears as an enclave or tight isoclinal fold (Figure 2). The trends of the fold axis are mostly east- west. Lineation plunges usually to the north, reflecting ductile deformation. Deformations are mainly ductile. Fragments of enclaves or raft structure (competent materials) are enveloped within less competent components. The enclaves are mainly mafic subordinately felsic. These enclaves are of various shapes and sizes. Large number of shear planes was recognized in the study area, shearing was identified due to fabrics of the tectonically deformed rocks. Shearing had led to formation of various structural features like reorientation due to rotation, boudins and lenses (Figure 2). Enclaves are rock fragments that resisted migmatisation (resisters) or residual materials from which mobile materials have been extracted [5, 6]. Materials and Methods Geological mapping of Awo area was conducted on a scale of 1 : 50 000. Particular attention was taken for the location, physical characteristics, mineral constituents, structural elements and associated rocks of the migmatite gneiss. Sampling was done to preserve various structures within the migmatite gneiss for future studies. A few samples were collected from each rock body for geochemical analysis. Various field measurements were used during the mapping. Global Positioning System (GPS) was used for geographical positioning with respect to various outcrops available in the study area. Measurement of strike, dip, plunge of structures such as foliation, lineation and fold axis were made. Field descriptions and observation were adequately recorded in a field notebook. Samples collected were properly labeled and stored prior to analyses. Representative rock samples were pulverized at Geochemistry Laboratory, Department of Geology of the University of Ibadan and analyzed at ACME Laboratory, Ontario, Canada using X-Ray Fluorescence (XRF) methods. Geochemical data were processed using Petrographic software package for different geochemical variation and discrimination diagrams. Table 1: Chemical composition of the Migmatite gneiss of Awo NEOSOME PALEOSOME Major element concentration in mass fractions, w/% Analyte RS1 RS2 RS3 RS4 RS5 Mean Range RS6 RS7 RS8 RS9 Mean Range SiO2 44.5 55.5 58.7 61.5 61.5 56.34 61.5-44.5 65.1 63.8 65.3 74.2 67.1 74.2-63.8 Al2O3 12.54 14.77 14.93 14.49 15.16 14.38 15.16-12.54 14.96 14.39 14.43 15.50 14.82 15.50-14.39 Fe2°3 18.10 8.47 11.29 5.72 9.34 10.60 18.10-5.72 6.22 7.80 7.34 0.39 5.44 7.80-0.39 CaO 6.31 7.36 2.26 4.67 2.50 4.62 7.36-2.50 3.09 2.92 2.00 0.43 2.11 3.09-0.43 MgO 7.65 6.63 3.94 5.40 3.35 5.40 7.65-3.35 2.23 2.86 2.55 0.08 1.93 2.86-0.08 N^O 0.52 2.69 2.35 2.95 2.82 2.27 2.95-0.52 3.46 2.94 3.42 7.14 4.24 7.14-2.94 K2O 5.32 2.20 4.15 3.15 3.66 3.70 5.32-2.20 2.57 3.03 3.15 1.90 2.66 3.15-1.90 MnO 0.39 0.17 0.21 0.16 0.15 0.22 0.39-0.15 0.12 0.15 0.15 0.11 0.13 0.15-0.11 TiO2 2.43 2.08 1.77 0.74 1.32 1.47 2.43-0.74 1.00 1.30 1.22 0.04 0.89 1.30-0.04 P2O5 0.58 0.49 0.06 0.62 0.04 0.36 0.62-0.04 0.11 0.13 0.07 0.20 0.13 0.20-0.07 LOI 1.67 0.37 0.73 0.54 0.64 0.79 1.67-0.37 0.47 0.56 0.49 0.52 0.51 0.56-0.47 Total % 100.01 99.73 100.39 99.94 100.48 99.33 99.88 100.12 100.51 NEOSOME PALEOSOME Trace element concentration (x 10-6) Analyte RS1 RS2 RS3 RS4 RS5 Mean Range RS6 RS7 RS8 RS9 Mean Range Cu 20 10 70 10 10 24 70-10 20 10 10 10 13 20-10 Ni 270 110 100 40 90 122 270-40 10 40 30 10 11 40-10 Pb 10 10 10 10 10 10 10 10 10 10 10 10 10 Zn 250 110 160 120 110 150 250-110 10 110 110 40 68 110-10 Zr 161 186 425 189 231 238 231-161 251 307 367 24 242 367-24 Ba 706 478 992 871 638 737 992-478 647 891 667 42 562 891-42 Be 2 36 7 2 51 20 51-2 4 2 4 6 4 6-2 Co 38 32 32 27 23 30 38-23 18 18 20 1 14 20-1 Cs 4 20 4 3 30 12 30-3 2 2 3 4 3 4-2 Ga 26 19 21 21 20 54 54-19 18 20 19 22 20 22-18 Rb 187 166 159 137 245 179 245-137 94 116 141 158 127 158-94 Sn 6 4 1 2 3 3 6-1 1 1 6 11 5 11-1 Sr 68 277 297 393 356 267 356-68 303 299 247 10 215 303-10 V 261 182 203 188 78 182 261-78 100 135 125 10 93 135-101 Hf 5 5 12 5 6 7 12-5 8 11 10 1 8 11-1 Nb 40 30 30 26 37 31 40-26 15 16 26 20 19 20-15 Ta 2 6 1 1 11 4 11-1 1 1 1 1 1 1 Th 2 14 32 31 20 20 32-2 25 29 16 2 18 29-2 U 2 6 2 1 10 4 10-1 1 1 2 5 2 5-1 W 1 3 2 2 5 3 5-1 2 1 1 4 2 4-1 Y 62 30 24 20 24 32 62-20 23 25 13 6 17 25-6 Figure 2: Migmatite gneiss showing various structures: top left - basic dyke; top right - sheared boudins; middle left - rotated and folded metabasic rocks; middle right - symmetrical tail of leucosome around an enclave of melanosome; bottom left - randomly oriented raft structure of basic dykes embedded in matrix of leucosome; bottom right - tight folding of foliated paleosome, leucosome and melanosome. Results and Discussion Major Element Geochemistry Nine representative samples of the paleosomes and neosomes were selected to determine their major, trace and rare earth elements geochemistry. Five of the samples were taken from paleosomes and four from neosomes (Table 1). The xenolith expectedly has very low concentration of Na2O (w = 0.52 %), and much higher concentrations of K2O (w = 5.32 %) and a proportionately high concentration of Fe2O3 (w = 18.10 %) and MgO (w = 7.65 %) due to its mafic composition (Table 1). The paleosomes and neosomes of the migmatite gneisses are compositionally different in their mean values as revealed by major oxide data presented in Table 1.The lowest mean value of SiO2 is w = 44.5 % which indicates the mafic nature of the paleosomes while the highest mean value of SiO2 is w = 74.2 % which as well reveal the felsic nature of the neosomes. Low range values of oxides such as Na2O (w = 2.95-0.52 %) and high range values of Fe2O3 and MgO (w = 18.10-5.72 % and w = 7.65-3.35 %) further affirm the mafic composition of the paleosomes. The overall trend for all major elements suggests that the paleosomes evolved from parent material which is intermediate between felsic and mafic sources. This is evident from the moderately high concentration of SiO2 in the range of w = 61.5-44.5 % while a range value of w = 74.2-63.8 % for neosomes clearly indicates its felsic precursor. High contents of Fe2O3 (w = 18.10-5.72 %) for paleosomes attest the basic nature of the parent materials, while low Fe content (w = 7.800.39 %) in neosome indicates its felsic parentage. The mean values of Na2O and K2O (Table 1) for the paleosomes and neosomes reflect the abundance of K-rich rock forming silicates like biotite and microcline [7]. The paleosome and neosome show slight variation in their sources. The paleosomes are derived from diorite and syenodiorite sources whereas the neosomes are mostly derived from quartz diorite and granite sources (Figure 3). The AFM diagrams [9, 10] were used to determine whether the rock samples are derived from tholeiitic or calc-al-kaline rock suite, the major element data were plotted on triangular diagram comprising of A (Na2O + K2O), F (FeO + Fe2O3) and M (MgO). The plot falls within calc- alkaline rock suite which is rich in Na2O, K2O and total Fe but low in MgO (Figure 3). The AFM diagrams were also employed to investigate the enrichments of the paleosomes and neosomes in Na2O, K2O, MgO and total Fe. The paleosomes are moderately enriched in MgO and total Fe while the neosomes are highly enriched in Na2O and K2O with low amount of total Fe (Figure 3). It is further confirmed by the plot of SiO2 versus Na2O + K2O [8] which revealed that the migmatite gneiss originates from dioritic rocks (Figure 3). SiO2 was plotted against K2O adopting the model of Pec-cerillo and Taylor [13] to further determine if the rock series is high or medium calc-alkaline (Figure 3). In term of tectonic setting, following the model of Pearce et al [17] where Rb was plotted against Y + Nb, the neosome plots in the field of Volcanic Arc Granite while the paleosome plots in Within Plate Granite (Figure 3). Both components are thus product of post-col-lisional tectonic setting. Most of the values plot within field of high-K calc- alkaline series. Furthermore, all the major oxides were plotted against SiO2 in Harker's diagram (Figure 4) because SiO2 is regarded as fractionation index for the evolution of magma and the most abundant oxide in igneous rocks that exhibit a wide variation in composition [11]. Al2O3 and Na2O are positively correlated with SiO2 which is an indication of possible separation of felsic minerals like sodic plagioclase during fractional crystallization [12]. Fe2O3, CaO, K2O and MgO versus SiO2 were negatively correlated and indicate a separation of ferromagnesian minerals during crystallization (Figure 4). Various models were used to determine the ancestry of the migmatite gneiss. Awo migmatite gneiss on the Na2O/Al2O3 vs K2O/Al2O3 plot was used to discriminate between igneous and sed-imentary/metasedimentary rocks [14]. Approximately 90 % of the plots fell within sedimenta-ry/metasedimentary field (Figure 5). Similarly, the K2O vs Na2O plot [8] showed an overwhelming 90 % of the values plotting within eugeo-synclinal sandstones field (Figure 5). Furthermore, in the TiO2 vs SiO2 diagram [16], the plot fell within sedimentary field which suggests that the protolith of the migmatite gneiss has been grossly affected by crustal contamination (Figure 5). Trace and Rare Earth Elements Geochemistry Trace element concentrations of the paleosome and neosome are presented in Table l.The concentrations of Large Ion Lithophile Elements (LILE] such as Ba, Rb and Sr for paleosomes and neosomes are enriched, but the mean values are slightly higher in paleosome than neosome (Table 1). The concentrations of High Field Strength Elements (HFSE] like Ta, Nb and Hf are generally depleted; neosomes are more depleted in HFSE than paleosomes. However Zr is moderately enriched compared to other HFSE (Table 1). For trace elements, high content of Ba with mean values of 737 x 10-6 and 562 x 10-6 for paleosome and neosome respectively (Table 1] are conspicuously discernible which indicates its concentration in felsic minerals. This attests to granitic origin of the rock samples. The assertion is further corroborated by moderate amount of Rb (179 x 10-6 and 127 x 10-6 ] and Zr (238 x 10-6 and 242 x 10-6) for paleosomes and neosomes respectively which are concentrated in rocks of acidic or intermediate composition. The LILE such as Ba, Rb and Sr generally exhibit positive anomaly, while HFSE such as Ta, Nb, Hf and Zr display weak anomaly (Figure 6]. 35 40 45 50 55 65 70 75 X= SÌ02 Y= (No20+K20) 10"0 10-1 10"2 10"3 10"4 Figure 3: Top left - AFM diagrams (after Irvine and Baragar[ЮЗ); middle left - (after Kuno[9]); top right - Plot of Na2O Kp versus SiO2 (after Cox et al[83); middle right - Kp versus Sp2plot (after Peccerillo and Taylor n3]); bottom - Rb versus Y+Nb tectonic discrimination diagram (after Pearce et alП7!). Figure 4: Harker's variation plot of SiO2 versus other major elements 0.4 Nn..ü/Л .О KEY X Paleosome Igneous • Neosome * .... • X ■..... x • • Sedimentary and Metasedimentary « 0.2KjO/AI/J3 0.3 0.4 0.5 Figure 5: Top - TiO2 versus SiO2 plot (after Tarney"6'); middle - K2O vs Na2O plot (afterMiddlemost1151); bottom - Na2O/Al2O3 versus K2O/Al2O3 diagram (after Garrels and Mackenzie1141). Rb Ba Th U K Nb La Ce Sr Nd P HI Zi Sm Ti Tb V Tm Vb Hb Ba Th U V. Nb La Cs S, Nd P HI Z, Sm Ti Tb Y Trn Yb Figure 6: Left - Mantle normalized pattern of trace elements for Paleosome and neosome (after Wood et al"81); right - Chondrite normalized pattern of rare earth elements for paleosomes and neosomes after Haskin et al1'91). The enrichment in LILE and depletion in HFSE reflect geotectonic setting from which the rocks originated. The setting suggests the rocks to evolve in a process of subduction. REE concentrations of the paleosomes and neosomes as presented in Table 1 reveal strong positive anomaly for LREE such as La, Ce, Pr and Nd while HREE like Ho, Er, Tm, Yb, and Lu show weak anomaly. Source materials of the migma-tite gneiss can be inferred from trace and rare earth element patterns [12]. The moderately enriched LREE and weakly negative Eu anomaly possibly suggest the melt to have been derived from rocks of intermediate composition like diorite and quartz diorite (Figures 5 and 6]. Conclusion The study area occurs within metamorphic terrane of the south western basement complex of Nigeria. Formation of different rock types around the area is probably connected to post-collisional events that influenced the structural and textural features of the various geological units. The available geochemical data from the study area suggest the paleosomes and neosomes to be mostly of sedimentary parentage with minor input from igneous protolith (Figure 5]. The paleosome and neosome bear compositional similarities. However, minor pe-trological differences exist between each component. The differences are associated with the composition of their sources and crustal contamination during the transportation of the melted materials. The migmatite gneiss is derived from rocks of dioritic composition belonging to calc-alkaline series. Negative correlation between SiO2 and major elements like Fe2O3, CaO, K2O and MgO indicate a pronounced effect of fractional crystallization during the formation of the dioritic rocks. Large Ion Litho-phile Elements (LILE] such as Ba, Rb and Sr generally exhibit positive anomaly while High Field Strength Elements (HFSE] notably Ta, Nb, Hf and Zr display negative anomaly. The REE geochemistry revealed strong positive anomaly for LREE (La, Ce, Pr and Nd] while HREE (Ho, Er, Tm, Yb and Lu] are weakly anomalous. 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