Mineralizações magmatogénicas sulfuretadas de Ni-Cu no compartimento oeste da Sequência Gabróica Bandada de Beja Magmatic, Ni-Cu sulphide mineralization in the western compartment of the Beja Layered Gabbroic Sequence A. P. Jesus(1), A. Mateus(1), J. Munhá(1), J.M.C. Branco(2), V.H. Araújo(2) (1) Dep. Geologia, CREMINER / Centro de Geologia, Fac. Ciências Univ. Lisboa, Ed. C6, Piso 4, 1749-016 Lisboa (2) Rio Narcea Gold Mines SA, Rua Circular Poente, Bloco 36 R/c, Loja 1 – P.I.T.E., 7000-171 Évora ana.jesus@fc.ul.pt; amateus@fc.ul.pt; jmunha@fc.ul.pt; jmc.branco@rngm.pt; victor.araujo@rngm.pt SUMÁRIO No compartimento oeste da Sequência Gabróica Bandada de Beja (LGS), alguns cumulados piroxeníticos hospedam sulfuretos maciços intercumulus contendo até 0.89 wt% Ni e 0.93 wt% Cu. Os magmas que fraccionaram as fácies gabróicas relacionadas com estas mineralizações têm potencial para segregar líquidos sulfuretados com [Ni]5 wt%. Mas a possibilidade de gerar líquidos niquelíferos (máx. 12 wt% em 100% sulfuretos) durante os estádios iniciais da evolução do LGS é alta, valorizando o potencial da faixa gabróica sob cobertura Cenozóica. Palavras-chave: Complexo Ígneo de Beja, Minérios sulfuretados magmatogénicos de Ni-Cu SUMMARY In the western compartment of the Beja Layered Gabbroic Sequence (LGS), some pyroxene cumulates host intercummulus massive sulphides that show up to 0.89 wt% Ni and 0.96 wt% Cu. Magmas from which the gabbroic facies related to these ores were fractionated have potential to segregate sulphide melts containing up to 5 wt% Ni. But the possibility of generate Ni-rich melts (max. 12 wt% in 100% sulphide) during the early steps of LGS evolution is high, thus turning in a very promising target the belt underneath the Cenozoic cover. Key-words: Beja Igneous Complex, Magmatic Ni-Cu sulphide ores 1. Introduction The metallogenic potential of the Beja Layered Gabbroic Sequence (LGS) has been systematically assessed since 1999, taken advantage of early exploration surveys carried out by the Serviço de Fomento Mineiro [e.g. 1, 2]. Accordingly, the LGS western compartment (from W Torrão to Beringel) emerged as a very promising target and several studies were performed in order to: (i) unravel the internal architecture of the igneous complex [3-5]; (ii) evaluate the spatial distribution of oxide and sulphide enrichments (Fig. 1); and (iii) characterize the recognized oxide and sulphide accumulations. Available data for the Torrão-Ferreira do Alentejo sector allow grouping into five Series the outcropping LGS gab- broic succession, which, from NE to SW, were labelled Soberanas I and II, and Odivelas I, II and III [2-5]. Massive Fe-Ti-V oxide accumulations (type I mineralization) are hosted in olivine leucogabbros and cumulates of the Odivelas I lower section [2, 4, 6, 7]. Anastomosed veins of Po + Cpy Py (type II mineralization) are related to late metasomatic haloes and pegmatite dykes that affect gabbroic rocks in the upper section of Odivelas III [2, 8]. In the Ferreira do Alentejo-Beringel sector two other rhythmic Series were put in evidence (Beringel I and II – BRG I and II), the latter hosting intercummulus massive Ni-Cu-Co sulphides (type III mineralization) [9]. The major goal of this work is to report and discuss 1 Fig.1: Spatial distribution (qualitative estimation) of oxide and sulphide enrichments for the LGS western sector. Grid coordinates according with the international Gauss-ellipsoid, Lisbon datum. Details on geological features can be found in [5]. the geochemical features of type III mineralization and its gabbroic envelope. Additionally several lines of evidence will be examined in order to deduce significant geochemical guides for Ni-Cu exploration in LGS. 2. Type III mineralization The most important occurrence of this type so far identified is located at the Figueirinha quarry, close to the contact between BRG II and the Border Group (see Fig. 1 and [5]). As reported in [9], the intercummulus sulphides here observed are massive and mostly composed of Pen + Po + Cpy + linnaeite group minerals (Linn. s.l.) + Py. Pyroxenites hosting intercummulus sulphides comprise mainly randomly oriented, subhedral Cpx with typical adcumulate texture. Tiny blebs of Po with Pen-Cpy exsolutions occur as inclusions within coarser Cpx grains, forming graphic intergrowths. As sulphide modal proportion increases, Cpx grains are disrupted, displaying abundant corrosion gulfs but only mild retrograding effects. Rare Pl occurs interstitially or included within the Cpx-sulphide framework being slightly altered to a fine- grained mixture of chloriteprehnite. Minor magnetite and ilmenite coexist with Pen-Po-Cpy blebs suggesting O2 conditions of late stage (~620 ºC) crystallization close to the QFM buffer. Table 1 illustrates the most relevant (major and trace) metal and sulphur contents for representative samples of type III mineralization. The concentra- tions obtained clearly reflect the chemical signature showed by the (i) sulphide mineralogy (mainly S, Fe, Ni, Cu, Co) and the (ii) accessory oxide assemblage (which incorporates minor amounts of Cr and Mn, besides Fe, Ti and V) [9]. Trace amounts of other base metals, like Pb and Zn, are also preferentially incorporated in sulphides (mainly in Cu-rich phases and Po), their scarcity reflecting the ultramafic nature of the parental melt. The whole-rock contents obtained for Sc, Se and Sr are, as expected, quite low and sometimes just slightly above the detection limit of the analytical method used; sulphides (chiefly Pen) can incorporate trace amounts of these elements, namely of Se and Sr (as confirmed by means of Micro-PIXE analysis). Tab.1: Summary of whole-rock chemical data for mineralised samples (Figueirinha quarry) S (%) Ni (%) Cu (%) Co (ppm) Cr (ppm) Mn (ppm) Ti (ppm) V (ppm) Pb (ppm) Zn (ppm) Sc (ppm) Se (ppm) Sr (ppm) FG-6A 6.17 0.31 0.93 413 201 246 1898 85 4 32 16 16 7 FG-6B 8.22 0.89 0.71 1194 121 216 741 43 6 27 5 27 23 FG-6 8.23 0.46 0.96 531 171 197 1592 66 4 28 12 18 5 2 3. Geochemistry of the gabbroic envelope A general overview concerning the gabbroic facies succession in BRG II and their main mineralogical features can be found in [5]. In order to fully characterize the chemical signature of these facies, thirty samples were collected along four, sub-parallel profiles. The obtained results will not be completely discussed here, but just those that help to unravel the Ni-Cu ore-forming process. A first inspection of Mg and Ni co-variation along sampling profiles (Fig. 2) suggest that Ni is preferentially included in olivine. Both plots enable, additionally, an evaluation of the general BRG II evolution, being clear that rocks of the Basal Group fractionated from the most primitive magma. The trend observed between rocks of the Basal Group and troctolites also supports the hypothesis that they represent products of the LGS primordial magmas. It should be noted that whole-rock contents reflect mostly the bulk result of accumulation processes, therefore providing an image of the mineralogical assemblage actually present. These plots also put in evidence the rhythmic nature of the Series, confirming the inferences discussed in [5]. Fig. 3: (A) log Ni/Cu and (B) log Cu versus log S contents for gabbroic rocks and mineralised samples of BRG II. Since there is a correlation between metal ratios (Ni/Cu) and increasing sulphidation, it could be suggested that most Ni and Cu are related to sulphides (Fig. 3A). The strong positive correlation between Cu and S contents (Fig. 3B) clearly demonstrates that significant dissemination of Cpy occurs in these rocks, as observed. Moreover, the log[Cu]– log[S] co-variance suggests that both (CliqS/CliqCu)initial and (Ds/liqS – Ds/liqCu) are roughly constant, thus allowing to deduce a self-similar behaviour for the distribution. Note, however, that this behaviour could be simply self-affine (statistically self-similar) if the clustering/dispersion obtained for (log[Cu], log[S]) values around (100, 1000) reflect an intrinsic property of the Cu-S distribution that implies rescaling by different factors (presently unknown). Nonetheless, and independently of the mathematical descriptor used to characterize the contents distribution, it is clear that the log[Cu]log[S] co-variance reflects an important geochemical feature that can be used as an exploration guide for type III mineralization, i.e. it records appropriate conditions for the segregation of sulphide melts. Fig.2: (A) Mg and (B) Ni content variations for BRG II Groups, excluding the mineralised samples. 4. Ni content variation in olivine Using the approach reported in [10] and assuming that Figueirinha sulphides were segregated before magma reached Ni depletion due to extensive olivine fractionation, an estimation of the olivine Ni content at the time of sulphide deposition can be performed. The calculations make use of the average 3 measured metal contents in Pen and Cpy and presume that all the analyzed Ni and Cu are incorporated in these sulphides, respectively; no correction for the presence of olivine is needed because no olivine is present in these samples. The only minerals that could induce some uncertainty in calculations are Pen or Linn. s.l.. The effect of Py in S estimation is for sure negligible given its relative scarcity; Linn. s.l. presents roughly the same (Ni,Co):Fe ratio of Pen and if its development is ascribed to low temperature sulphide transformation the bulk Ni:S ratio should be kept essentially the same. The estimated Ni contents were subsequently plotted in a diagram that relates the Ni content in 100% sulphide with the Ni-content of olivine that would fractionate from the same melt. The same procedure was further applied to samples of type II mineralization and all the LGS gabbroic Series [5], using in the latter the maximum Ni-Ol content. Fig. 4 summarizes the results obtained, and it is clear that the estimated Ni concentration for sulphide melts lies above 4.7 wt%, therefore comparable with values usually reported for economic Ni-Cu ore-forming systems. Fig.4: Empirical relation between Ni in Ol and Ni in 2500 2000 ppm Ni in Ol Border G Troct SB I ODV I ODV II ODV III BRG I BRG II Figueirinha Ventoso 1500 1000 500 0 15 10 5 0 wt% Ni in 100% sulfide sulphide melt that would segregate from a magma [10]. 5. Conclusions Following [5], Border Group troctolites and their equivalents in Soberanas I Series should represent the LGS primordial U-type magmas. Additionally, type III mineralization so far identified is confined to the SW limit of LGS, quite near to the contact between the Lower Group rocks of BRG II and the Border Group. Considering these features together, the possibility of having adequate conditions to segregate Ni-rich sulphide melts (maximum estimate 12.1 wt % Ni in 100% sulphide) is high, the sulphide accumulation occurring mostly at the transition from the feeder zone (from SW) to the magma chamber. This interpretation opens for the first time a sustained hypothesis that (primitive) LGS rocks underneath the Cenozoic sedimentary cover (between Torrão and Ferreira do Alentejo villages) include NiCu(-PGE?) sulphide mineralization. Furthermore, it fully justifies the exploration efforts recently per- formed in BRG II, which have potential to segregate sulphide melts containing up to 4.7 wt% Ni. Acknowledgements A. Mateus and J. Munhá appreciated the logistic support of CREMINER and Centro de Geologia (POCA-PETROLOG, UI : 263; POCTI / FEDER ) FCUL. A. Jesus acknowledges a PhD Grant SFRH/BD/6355/2001. Referências Bibliográficas [1] Jesus, A., Mateus, A., Oliveira, V., Munhá, J. (2003) Ore-forming systems in the layered gabbroic sequence of the Beja Igneous Complex (Ossa-Morena Zone, Portugal); state of the art and future perspectives. SGA Meeting, Athens, D.G. Eliopoulos et al., eds., Millpress, Rotterdam, vol. 1, pp. 591-594. [2] Jesus, A., Mateus, A., Gonçalves, M.A., Oliveira, V. (2003) Cu anomaly separation by multifractal modelling of soil geochemistry data from Ferreira do Alentejo to Serpa (Alentejo, Portugal). IV Cong. Ibérico Geoq., Coimbra, pp. 205-207. [3] Jesus, A.P. (2002) Mineralizações de Fe-Ti-V e ocorrências sulfuretadas em rochas gabróicas do Complexo Ígneo de Beja (Odivelas-Ferreira do Alentejo). MSc Thesis, Fac. Ciências, Univ. Lisboa, Lisboa. [4] Jesus A.P., Munhá, J. & Mateus, A. (2005). Critical features controlling the evolution of the Beja Layered Gabbroic Sequence; implications to ore-forming processes. VII Cong. Geoq. dos Países de Língua Portuguesa – XIV Sem. Geoq., Aveiro, pp. 305-310. [5] Jesus, A.P., Munhá, J., Mateus (2006) The western compartment of the Beja Layered Gabbroic Sequence: internal architecture and main petrogenetic features. VII Cong. Nac. Geol., Estremoz (this volume). [6] Mateus, A., Jesus, A.P., Oliveira, V., Gonçalves, M.A., Rosa, C. (2000) Vanadiferous iron-titanium ores in Gabbroic Series of the Beja Igneous Complex (Odivelas, Portugal); remarks on their possible economic interest. Est., Notas e Trab., IGM, Lisboa, 43, pp. 3-16. [7] Jesus, A.P., Mateus, A., Waerenborgh, J.C., Figueiras, J., Cerqueira, L. & Oliveira, V. (2003) Hypogene titanian, vanadian maghemite in reworked oxide cumulates in the Beja Layered Gabbro Complex, Odivelas, Southeastern Portugal. Canad. Min., 41, pp. 1105-1124. [8] Mateus, A., Jesus, A.P., Conceição, P., Oliveira, V., Rosa, C. (2001) Natureza mineralógica e geoquímica das mineralizações sulfuretadas em gabros do Complexo Ígneo de Beja: algumas questões relativas à sua génese. VI Cong. Ibérico de Geoq. – XII Sem. Geoq., Faro, pp. 125129. [9] Jesus, A., Mateus, A., Munhá, J., Pinto, A. (2005) Intercummulus massive Ni-Cu-Co, PGE-bearing sulphides in pyroxenite: a new mineralization type in the Layered Gabbroic Sequence of the Beja Igneous Complex (Portugal). SGA Meeting, Beijing, J. Mao and F.P. Bierlein eds., Springer Verlag, pp. 405-407. [10] Naldrett A.J. (2004). Magmatic sulfide deposits; geology, geochemistry and exploration. Springer Verlag, Berlin. 4