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1.
The 1.0-1.2 b.y. old rocks of the southeastern Llano Uplift, Texas include a 7 km thick sequence of amphibolite-grade, stratified, mafic metasedimentary rock (Packsaddle Schist) which is intruded by a varied suite of syntectonic and late-kinematic intrusions. The metasediments contain large blocks of serpentinized peridotite (Coal Creek serpentinite) and coarse hornblendite and metagabbro. Prior to the end of maximum deformation, the sequence was intruded by low to medium-K2O tholeiitic basalts (0.40-0.72% K2O). Late-kinematic low-K2O tholeiitic basalts (0.38-0.40% K2O) were intruded as dikes into the folded rocks. The Coal Creek serpentinite contains both syntectonic and late-kinematic low-K2O tholeiitic metabasalts (0.13–0.36% K2O). The Llano metabasalts and metagabbros are characterized by low Cr (67–378 ppm) and Ni (36–170 ppm), variable Rb (1.5–14.7 ppm), Sr (140–1229 ppm), TiO2 (0.40–2.20%), P (568–2707 ppm), and Zr (18–230 ppm), and Y (16–45 ppm), Co (40–57 ppm), and Sc (36–49 ppm) similar to modern MORB. The metabasalts have La abundances from 7 to 39 times chondritic and exhibit light REE enrichment with ¦La/Sm¦N from 1.13 to 1.45 and ¦La/Yb¦N from 1.12 to 2.99. The metabasalts show a strong correlation of increasing Zr, Ti, and Y and decreasing Eu/Eu* (1.56–1.00), CaO/TiO2, Al2O3/TiO2, and MgO/ MgO+FeO* with increasing REE enrichment (LaN). The Llano metabasalts and metagabbros have initial 87Sr/86Sr=0.7029±0.0001. A likely petrogenetic model for these metabasalts is an island arc in which events from early arc development to final late-kinematic intrusion were dominated by tholeiitic volcanism and intrusion. The chemical systematics of the Llano mafic metaigneous rocks suggest they are products of fractionation of olivine, clinopyroxene, and plagioclase from more primitive basaltic magmas generated beneath the island arc complex.  相似文献   

2.
The Karoo volcanic sequence in the southern Lebombo monocline in Mozambique contains different silicic units in the form of pyroclastic rocks, and two different basalt types. The silicic units in the lower part of the Lebombo sequence are formed by a lower unit of dacites and rhyolites (67–80 wt.% SiO2) with high Ba (990–2500 ppm), Zr (800–1100 ppm) and Y (130–240 ppm), which are part of the Jozini–Mbuluzi Formation, followed by a second unit, interlayered with the Movene basalts, of high-SiO2 rhyolites (76–78 wt.%; the Sica Beds Formation), with low Sr (19–54 ppm), Zr (340–480 ppm) and Ba (330–850 ppm) plus rare quartz-trachytes (64–66 wt.% SiO2), with high Nb and Rb contents (240–250 and 370–381 ppm, respectively), and relatively low Zr (450–460 ppm). The mafic rocks found at the top of the sequence are basalts and ferrobasalts belonging to the Movene Formation. The basalts have roughly flat mantle-normalized incompatible element patterns, with abundances of the most incompatible elements not higher than 25 times primitive mantle. The ferrobasalt has TiO2  4.7 wt.%, Fe2O3t = 16 wt.%, and high Y (100 ppm), Zr (420 ppm) and Ba (1000 ppm). The Movene basalts have initial (at 180 Ma) 87Sr/86Sr = 0.7052–0.7054 and 143Nd/144Nd = 0.51232, and the Movene ferrobasalt has even lower 87Sr/86Sr (0.70377) and higher 143Nd/144Nd (0.51259). The silicic rocks show a modest range of initial Sr-(87Sr/86Sr = 0.70470–0.70648) and Nd-(143Nd/144Nd = 0.51223–0.51243) isotope ratios. The less evolved dacites could have been formed after crystal fractionation of oxide-rich gabbroic cumulates from mafic parental magmas, whereas the most silica-rich rhyolites could have been formed after fractional crystallization of feldspars, pyroxenes, oxides, zircon and apatite from a parental dacite magma. The composition of the Movene basalts imply different feeding systems from those of the underlying Sabie River basalts.  相似文献   

3.
The Serra Geral (Paraná) continental flood basalt (SG-CFB) province in Brazil is associated with the Jurassic-Cretaceous breakup of Gondwanaland and the transition of continental to oceanic magmatism during the opening of the South Atlantic Ocean. A suite of 24 samples representative of the SG-CFB in Rio Grande do Sul, southern Brazil, shows a compositional continuum from basalt (50–53 wt% SiO2, Mg# 60-45), to basaltic andesite, to andesite, rhyodacite, and rhyolite (73 wt% SiO2). Certain compositional aspects of the mafic rocks (e.g., TiO2, K2O, CaO, Zr/Nb, Zr/Y, Ti/Zr) resemble those of basaltic dikes and flows associated with the opening of the North Atlantic Ocean.Fractionation trends are apparent in MgO variation diagrams and calculations show that basalt-basaltic andesite continuums are largely due to removal of plagioclase and clinopyroxene. These mafic rocks can be categorized as (i) having higher or lower incompatible-element contents (e.g. K2O 0.6–1.5 wt%; Rb 12–43 ppm; Ba 125–240 ppm) due to incorporation of Brazilian Archean crust or rhyolitic magma by basalt from a particular source material or to partial-melting differences of that source, and (ii) as having higher or lower TiO2, Sr, Ba, and P contents due to source heterogeneities. Crustal components are obvious in certain basaltic samples, as where K2O > 1 wt%, SiO2 > 51%, and TiO2 1%, but are insignificant in others (e.g., compositions close to those of South Atlantic basin basalts). Calculations indicate origins for intermediate and silicic rocks by removal of pl, cpx, and Ti-magnetite from basaltic andesite, but crust and magma-mixing affecting basaltic-andesite fractionates were likely also involved. Where contamination is insignificant, Zr, Nb, and Y abundances indicate T-type MORE source material like that for certain S. Atlantic Ocean basalts. Source material was essentially a 91 hybrid of N-type and P-type MORB components. N-type MORB lithosphere followed SG-CFB because decompression due to rifting crust enabled partial melting of uppermost (depleted) mantle.  相似文献   

4.
This paper documents the timing, geochemistry and possible origin of sodium enrichment associated with Proterozoic iron formation-hosted copper-gold ore lenses at the Starra deposit, Australia. The ore lenses are immediately underlain by variably sheared albitemagnetite-hematite-pyrite-bearing rocks, and overlain by mainly unaltered, less-sheared, meta-sediments. Evidence indicating that albite was abundant prior to deformation, and also prior to the main hydrothermal addition of Fe, S, Cu and Au, includes (1) regional albite development at this stratigraphic level; (2) alteration of albite by ore-related sericite; and (3) inclusion of unfoliated inclusions of albite and hematite in ore-related pyrite. Nevertheless, albite also developed around dolerites and within hangingwall shears during metamorphism and deformation. Least altered albite footwall rocks have SiO2 (67.31–73.13 wt.%), Al2O3(9.89–12.51 wt.%), total alkali elements (6.40–9.43 wt.%) and HFS elements (e.g., Zr = 179–275 ppm; Ti/Zr = 7.6–14.1) comparable with felsic volcanics, but have high relative Na2O contents (5.08–5.81 wt. %), and variable to high Na2O/K2O ratios (0.05–68.37). An episode of alkali alteration by high-Na fluids prior to the ore-related alteration is postulated to account for sodic compositions, after chemical consideration of the alternatives (1) arkosic sediments; (2) trondhjemitic volcaniclastics; and (3) Na-metasomatism of Staveley Formation sediments. During the most intense ore-alteration, isocon analysis indicates a density increase of 23% compared to the least altered albitised hostrocks. Cu, Fe, Au, Sn, W, Zn, K, Ba and Rb were enriched during the mineralising process, whereas Mn, Ca, Si, Nb and Zr were lost, and Al, Ti and Y were not changed (and were used to define the isocon). The loss of some high field strength elements during this alteration indicates that igneous rock classification diagrams based on immobile element ratios should be used with caution for albitemuscovite magnetite-pyrite assemblages associated with iron formation-hosted copper-gold deposits. Zircon was partially soluble, whereas titanium oxides were probably stable in the saline, high temperature (260°–380 °C), acid (pH = 3.9–6.0) fluids envisaged for ore-related alteration.  相似文献   

5.
Eocene igneous rocks from the Abrolhos Islands and surroundingsedimentary platform, offshore Brazil, 18?S, are largely Ti-richbasalt and diabase (4–6 wt.% TiO2), and cumulate rockssuch as wehrlite. Despite high Ti, incompatible-element abundancesare relatively low (e.g., K2O {small tilde} 1 wt.%; P2O5 0.5%; Zr 225 ppm; Rb 23 ppm; Ba 275 ppm); LREE enrichment yieldsLa/YbN {small tilde}8. Compared to other mafic rocks of theSouth Atlantic region, such as Mesozoic high-Ti dikes ({smalltilde}5 wt.% TiO2) and basalts (3–4 wt.% TiO2) of theSerra Geral (Paran?, southern Brazil) province, and high-Tibasalts ({small tilde}4 wt% TiO2) of some South Atlantic features(Walvis, southwest Indian ridge), Abrolhos basalts differ bylower incompatible-element concentrations and/or by isotopiccompositions that emphasize depleted characteristics (Sr–12;Nd 3) relative to bulk earth. Abrolhos isotopic compositionsdo, however, match those of some S. Atlantic islands (e.g.,Pb like those of nearby Trindade), and conform generally toDupal anomaly contours. Abrolhos high-Ti basalts can be modeled as liquids from about90% crystallization of parent picritic liquid emplaced nearthe base of the Brazilian crustal margin; no mantle geochemicalanomaly or special metasomatism are needed to account for theTi contents. Isotopic and trace-clement compositions (e.g.,Zr, Nb, Y) of the Abrolhos province suggest parentage in a mantlerepresenting a plume of bulk earth or ‘enriched’composition that interacted with overlying depleted mantle.  相似文献   

6.
Compositions of basaltic samples from the southeastern Brazil passive margin (18°–24° S) depict the change from continental to oceanic lithosphere during the opening of the South Atlantic Ocean. Samples studied range from 138 to 105 m.y. old and are from 12 Petrobrás drill cores recovered from the coastline to about 150 km offshore in the Espirito Santo, Campos, and Santos basins. Compositions vary, ranging, for example, from 49–54 wt.% SiO2, 0.5–3.0 wt.% TiO2, 0.6–5.0 FeO*/MgO, and 1-6 La/ Yb(n), but can be grouped: (i) basalts enriched in incompatible elements, such as K (some K2O>2.0 wt.%), Rb (>18 ppm), Zr (>120 ppm), and LREE (some FeO* 16 wt.%; most with SiO2 51–54 wt.%), and resembling Serra Geral continental flood basalts (SG-CFB) of southern Brazil; (ii) basalts less enriched, or transitional, in incompatible elements, having K2O <0.40 wt.% and flat REE patterns, and resemble N. Atlantic diabases and FAMOUS basalts; and (iii) one depleted sample, Ce/Yb(n)=0.7, where Ce(n)=4. Expressed in oceanic-basalt terminology and Zr-Nb-Y abundances, enriched samples are P- and T-type MORB (e.g., Zr/Nb 4–25), transitional samples are T-type (Zr/ Nb 8–27), and the depleted sample is N-type MORB (Zr/Nb>30).Trace-element ratios (e.g., Zr/Nb, Zr/Y) link the Brazil margin basalts to a heterogeneous mantle (attributed to metasomatic veining) of variably proportioned mixtures of depleted-mantle (N-MORB) and plume (P-MORB, e.g., Tristan hotspot) materials. The various compositions therefore reflect, in part, different zones of melting during the separation of Gondwanaland, where gradual decompression during rifting enabled concurrent melting of upper, more depleted (non- or sparsely-veined) mantle and enriched (densely-veined) mantle. Within the time represented, melting produced enriched, transitional, and depleted magmas that were emplaced subaerially, hypabyssally, and subaqueously; they mark the transition from CFB before rifting and separation (from deeper, enriched mantle) to N-MORB in the S. Atlantic afterwards (from non- or sparsely-veined upper mantle). While P-type mantle components account for the enriched compositions of some basalts (Zr/Nb<8), continental crust is largely responsible for that of others (e.g., Ti/Zr 40–57; La/Yb(n) 5–6, and 18O+12.2 in one sample). Some may be contaminated expressions of otherwise T-type basalts free of crustal components. This study identifies CFB to be from sources similar to those for T- and P-type oceanic rocks, where individual CFB magmas may or may not have acquired crustal signatures.  相似文献   

7.
Palaeoproterozoic basaltic rocks in the Halls Creek Orogen form part of two stratigraphic sequences on either side of a major structure, the Angelo‐Halls Creek‐Osmond Fault System. The two sequences have contrasting geological histories and probably formed in different tectonostratigraphic terranes. To the east, basalts of the Biscay Formation, which are part of the Halls Creek Group, were erupted at ca 1880 Ma and deformed and metamorphosed first at low grade between ca 1845 and ca 1820 Ma. To the west, basalts of the Tickalara Metamorphics were deposited after 1865 Ma, and were metamorphosed at medium to high grade and intruded by tonalite and leucogranite sheets at 1850 to 1845 Ma. Two groups of metabasalts are identified in the Biscay Formation. Group 1 samples have compositions similar to enriched (E‐)MORB. Group 2 samples have lower TiO2, P2O5, Cr, Y, Nb and Zr contents, and trace‐element ratios (e.g. Ti/V and Zr/Nb), similar to low‐TiO2 continental flood basalts. Metabasalts from the Tickalara Metamorphics consist of depleted and enriched types. The depleted samples have high field strength element (HFSE) and rare‐earth element (REE) abundances similar to oceanic island arc/backarc basin tholeiites. The enriched samples have compositions similar to E‐MORB, and are similarto group 1 samples from the Biscay Formation. Basalts of the Biscay Formation were erupted on a passive continental margin, whereas those of the Tickalara Metamorphics formed in an oceanic island arc/backarc basin or ensialic marginal basin, the two terranes being brought together by ca 1820 Ma. This is consistent with the evolution of the Halls Creek Orogen during the Palaeoproterozoic by plate‐tectonic processes similar to those operating in the Phanerozoic.  相似文献   

8.
N. Hald  C. Tegner   《Lithos》2000,54(3-4):207-233
The Paleozoic–Mesozoic Jameson Land Basin (East Greenland) is intruded by a sill complex and by a swarm of ESE trending dykes. Together with dykes of the inner Scoresby Sund fjord, they form a regional Early Tertiary intrusive complex located 200–400 km inland of the East Greenland rifted continental margin. Most of the intrusive rocks in the Jameson Land Basin are geochemically coherent and consist of evolved plagioclase–augite–olivine saturated, uncontaminated high-Ti basalt with 48.5–50.2 wt.% SiO2, 2.2–3.2 wt.% TiO2, 5.1–7.4 wt.% MgO, 9–17 ppm Nb and La/YbN=2.8–3.6. Minor tholeiitic rock types are: (a) low-Ti basalt (49.7 wt.% SiO2, 1.7 wt.% TiO2, 6.8 wt.% MgO, 2.6 ppm Nb and La/YbN=0.5) akin to oceanic basalts; (b) very-high-Ti basalt (48.6 wt.% SiO2, 4.1 wt.% TiO2, 5.1 wt.% MgO and 21 ppm Nb); and (c) plagioclase ultraphyric basalt. The tholeiitic dolerites are cut by alkali basalt (43.7–47.3 wt.% SiO2, 4.1–5.1 wt.% TiO2, 4.9–6.2 wt.% MgO, 29–46 ppm Nb and La/YbN=16–17) sills and dykes.Modelling of high-field-strength and rare-earth elements indicate that the high-Ti basalts formed from 6–10% melting of approximately equal proportions of garnet- and spinel-bearing mantle of slightly depleted composition beneath thick continental lithosphere. Conversely, dolerite intrusions and flood basalts of similar compositional kindred from adjacent but more rift-proximal occurrences in Northeast Greenland formed from shallower melting of dominantly spinel-bearing mantle beneath extended and thinned continental lithosphere. These variations in lithospheric thickness suggest the continent–ocean transition of the East Greenland rifted volcanic margin is sharp and narrow.40Ar–39Ar dating and paleomagnetism show that the high-Ti dolerites were emplaced at 53–52 Ma (most likely during C23r) and hence surprisingly postdate the main flood volcanism by 2–5 Ma and the inception of seafloor spreading between Greenland and Europe by 1–2 Ma. The formation of tholeiitic and alkaline magmas emplaced into the Jameson Land Basin corroborates to the importance of post-breakup magmatism along the East Greenland volcanic rifted margin. Upwelling of the ancestral Iceland mantle plume under central Greenland at 53–52 Ma (rather than under the active rift), perhaps accompanied by a failed attempt to shift the rift zone westward towards the plume axis, may have triggered post-breakup continental magmatism of the Jameson Land Basin and the inner Scoresby Sund region, along preexisting structural lineaments.  相似文献   

9.
The Betts Cove ophiolite, Newfoundland, consists of cumulate ultramafics, gabbro/clinopyroxenites, sheeted dikes and pillow lavas. The pillow lavas are divisible into three compositional groups: lower lavas (<0.25 wt.% TiO2), intermediate lavas (0.25–0.50 wt.% TiO2) and upper lavas (>0.7 wt.% TiO2). The lower and intermediate lavas are very depleted in Ti, Zr, Y, P, and REE and have high Al2O3/TiO2 ratios relative to normal oceanic tholeiite. The extreme depletion of these lavas and their dike equivalents (diabase and picrites) suggests they were derived by melting a severely depleted lherzolite. Conversely, the upper lavas, a volumetrically small part of the ophiolite, are compositionally similar to fractionated oceanic tholeiite and thus, their source material may be like that postulated for modern ocean floor basalts. Whereas the majority of basalts in the Betts Cove ophiolite are depleted in incompatible elements, most dikes and lavas from the Blow-MeDown ophiolite, western Newfoundland, are not and have incompatible element concentrations similar to modern oceanic tholeiite. The chemical differences between the two ophiolite massifs are related to melting of ultramafic source materials which are in different states of depletion brought about by previous melting episodes.  相似文献   

10.
For the first time occurrence of Ti rich Al depleted ultramafic cumulates having komatiitic signature in the northwestern fringe of Chotanagpur Gneissic Complex is presented. These rocks exhibit intrusive relationship with metasedimentary rocks and metaultramafites. Geochemically they are characterized by Mg# 79.1–91.60, high TiO2 (1.29–1.54 wt%), significantly low Al2O3/TiO2 and (Gd/Yb)n >1. Major oxides, trace and REE content suggest low degree of fractional crystallization and lesser degree of partial melting. These Al depleted komatiites are characterized by high concentration of incompatible elements than most suites of Barberton type komatiites. High Ti content suggests less degree of majorite garnet melting, leaving behind garnet in the restite. The rock shows higher Ti/Sc (190),Ti/V (22), Zr/Y (3), Zr/Sc (4), V/Sc (8), Zr/Sm (28) and Zr/Hf (47) ratios than primitive mantle and REE distribution pattern shows gentle slope from LREE to HREE in most samples pointing towards mantle metasomatism and crustal contamination during emplacement. The observed chemical characteristics indicate derivation of komatiite from an enriched mantle source and represent plume activity in an extensional tectonic regime of intracratonic setting.  相似文献   

11.
The Wadi Dabr intrusive complex, west of Mersa-Alam, Eastern Desert, Egypt ranges in composition from gabbro to diorite, quartz diorite and tonalite. The gabbroic rocks include pyroxene-horn blend e gabbro, hornblende gabbro, quartz-hornblende gabbro, metagabbro and amphibolite. Mineral chemistry data for the gabbroic rocks indicate that the composition of clinopyroxenes ranges from diopside to augite and the corresponding magma is equivalent to a volcanic-arc basalt. Plagioclase cores range from An75 to An34 for the gabbroic varieties, except for the metagabbro which has An 11–18. The brown amphiboles are primary phases and classified as calcic amphiboles, which range from tschermakitic hornblende to magnesiohornblende. Green hornblende and actinolite are secondary phases. Hornblende barometry and hornblende-plagioclase themometry for the gabbroic rocks estimate crystallisation conditions of 2–5 kb and 885–716°C.The intrusive rocks cover an extensive silica range (47.86–72.54 wt%) and do not exhibit simple straight-line variation on Harker diagrams for many elements (e.g. TiO2, Al2O3, FeO*, MgP, CaO, P2O5, Cr, Ni, V, Sr, Zr and Y). Most of these elements exhibit two geochemical trends suggesting two magma sources.The gabbroic rocks are relatively enriched in large ion lithophile elements (K, Rb, Sr and Ba) and depleted in high field strength elements (Nb, Zr, Ti and Y) which suggest subduction-related magma. Rare earth element (REE) data demonstrate that the gabbroic rocks have a slight enrichment of light REE [(La/Yb)N=2.67−3.91] and depletion of heavy REE ((Tb/Yb)N=1.42−1.47], which suggest the parent magma was of relatively primitive mantle source.The diorites and tonalites are clearly calc-alkaline and have negative anomalies of Nb, Zr, and Y which also suggest subduction-related magma. They are related to continental trondhjemites in terms of Rb---Sr, K---Na---Ca, and to volcanic-arc granites in terms of Rb---and Nb---Y.The Wadi Dabr intrusive complex is analogous to intrusions emplaced in immature ensimatic island-arcs and represents a mixture of mantle (gabbroic rocks) and crustal fusion products (diorites and tonalites) modified by fractional processes.  相似文献   

12.
Geochemical investigations of Wai sub-group volcanic flows (in and around Mahabaleshwar) have been undertaken to determine the petrogenetic processes involved in the formation of volcanic flows. In comparison to the Ambenali Formation, Mahabaleshwar Formation flows were affected more by crustal materials, which left a signature consisting of enriched levels of K, Rb, Ba, Ti and P. Ratios of Nb/Zr and Ba/Y were sensitive to fractional crystallization; Mahabaleshwar formation flows showed the highest Nb/Zr ratios. Ba was noted as a boundary marker element between the Ambenali (47.3 to 63.9 ppm Ba) and Mahabaleshwar (83.1 to 180 ppm) formations. The general trend of incompatible element concentrations increasing from lower Poladpur to upper Mahabaleshwar flows with increasing Zr and the linear array on the plot are consistent with the fractionation of olivine and clinopyroxene. MgO ranged from 4.8 to 7.1 wt%, TiO2 from 1.8 to 4.6 wt%, SiO2 from 47 to 52 wt% and Al2O3 from 12 to15.5 wt%. The Mg number (Mg#) was much lower, ranging from 36 to 50. The K2O/ P2O5 ratio showed the role of assimilation in the basaltic flows. TiO2, Y, Zr, Nb and Mg# were used to determine fractional crystallization, whereas Ba, Rb, K2O and SiO2 were used for monitoring the fractional crystallization effects of crustal contamination. The range of Zr/Y and TiO2 > 1.8 wt% appears to have been generated by fractional crystallization starting from enriched mafic precursors.  相似文献   

13.
The Central African Belt in the Nkambe area, northwestern Cameroon represents a collisional zone between the Saharan metacraton and the Congo craton during the Pan-African orogeny, and exposes a variety of granitoids including foliated and massive biotite monzogranites in syn- and post-kinematic settings. Foliated and massive biotite monzogranites have almost identical high-K calc-alkaline compositions, with 73–67 wt.% SiO2, 17–13 wt.% Al2O3, 2.1–0.9 wt.% CaO, 4.4–2.7 wt.% Na2O and 6.3–4.4 wt.% K2O. High concentrations of Rb (264–96 ppm), Sr (976–117 ppm), Ba (3680–490 ppm) and Zr (494–99 ppm), with low concentrations of Y (mostly< 20 ppm with a range 54–6) and Nb (up to 24 ppm) suggest that the monzogranites intruded in collisional and post-collisional settings. The Sr/Y ratio ranges from 25 to 89. K, Rb and Ba resided in a single major phase such as K-feldspar in the source. Garnet was present in the source and remained as restite at the site of magma generation. This high K2O and Sr/Y granitic magma was generated by partial melting of a granitic protolith under high-pressure and H2O undersaturated conditions where garnet coexists with K-feldspar, albitic plagioclase. CHIME (chemical Th–U-total Pb isochron method) dating of zircon yields ages of 569 ± 12–558 ± 24 Ma for the foliated biotite monzogranite and 533 ± 12–524 ± 28 Ma for the massive biotite monzogranite indicating that the collision forming the Central African Belt continued in to Ediacaran (ca 560 Ma).  相似文献   

14.
Summary Amphibole and mica lamprophyres and related dykes of Tertiary age from the Kreuzeck Mountains, Central Alps, Austria, have been investigated petrographically and geochemically. They intrude a sequence of early Palaeozoic metapelites, greenstones and amphibolites to the north of the Cretaceous Periadriatic Lineament, a major suture zone of 700 km E-W extent. The dykes are spatially associated with Sb, W, Hg, and Cu-Ag-Au deposits.Most lamprophyres are characterized by primitive chemistry (mg-numbers > 60 and Cr > 200 ppm) and have high contents of LIL elements (K, Rb, Sr and Ba). Geochemically, five different subgroups of calcalkaline/shoshonitic to alkaline affinity can be distinguished. These are: Group 1, amphibole-bearing shoshonitic lamprophyres (0.5–1.0 wt% Ti02, Zr < 150 ppm, Nb < 13 ppm, Ba/Rb < 10); Group 2, mica-bearing shoshonitic lamprophyres (1–1.5 wt% TiO2, Zr 180 ppm, Nb < 17 ppm, Ba/Rb > 20); Group 3, alkaline lamprophyres (1.5–2.1 wt% TiO2, Zr > 250 ppm, Nb > 30 ppm, Ba/Rb 10–25); Group 4, low-MgO alkaline lamprophyres ( 2.5 wt% TiO2, mg-number < 57, Nb 20 ppm, Ba/Rb 20); Group 5, calc-alkaline basaltic dykes ( 2.2 wt% TiO2, mg-number <55, Nb < 10 ppm, Ba/Rb < 10). Group 2,3 and 4 dykes have NE-SW orientations and are of Oligocene age (K-Ar age 27–32 Ma); Group 1 and 5 dykes are of Lower Oligocene age (K-Ar age 36 Ma) but have mostly E-W orientations.The Kreuzeck lamprophyres were generated in post-collisional magmatic events, which were probably linked to extensional tectonics following oblique continent-continent collision between the African and Eurasian Plates during the Eocene. Group 1, 2 and 5 dyke rocks have typical calc-alkaline geochemical signatures indicating that they represent partial melting products of subduction-modified lithosphere. Group 3 and 4 alkaline lamprophyres have geochemical features transitional between calc-alkaline and within-plate alkaline igneous rocks (e.g. Ba/Nb 30–70) indicating that their mantle source-region includes both subduction-modified lithospheric and OIB-type asthenospheric components.There is no apparent relationship between mineralization in the Kreuzeck region, thought to be of Ordovician-Devonian age, and much later lamprophyre intrusion. Alteration of the dykes by late-magmatic fluids has resulted in the formation of secondary minerals, and has occasionally led to increased Au and PGE values in the 10–35 ppb range particularly in close proximity to Cu-Ag-Au deposits.
Shoshonitische und alkalische Lamprophyre mit erhöhten Au- und PGE-Gehalten aus der Kreuzeckgruppe, Ostalpen, Österreich
Zusammenfassung Die vorliegende Arbeit untersucht die Petrographie und Geochemie tertiärer Lamprophyre und genetisch verwandter Ganggesteine aus der zentralalpinen Kreuzeckgruppe, nördlich des Periadriatischen Lineamentes, in Kärnten, Österreich. Die Ganggesteine durchschlagen die altpaläozoischen Metapelite, Grünsteine und Amphibolite des Altkristallins diskordant und stehen in räumlichem Zusammenhang mit Sb, W, Hg und Cu-Ag-Au Lagerstätten, die bereits seit dem Mittelalter abgebaut wurden.Die meisten Lamprophyre zeigen primitiven Charakter (Mg-Zahlen >60 und Cr > 200 ppm) und besitzen hohe Gehalte an LILE (K, Rb, Sr und Ba). Geochemisch lassen sich fünf verschiedeneGruppen mit kalkalkalisch/shoshonitischem bis alkalischem Charakter unterscheiden: Gruppe 1, Amphibol-führende shoshonitische Lamprophyre (0.5–1.0 Gew% TiO2, Zr < 150 ppm, Nb < 13 ppm, Ba/Rb < 10);Gruppe 2, Glimmer-führende shoshonitische Lamprophyre (1–1.5 Gew% TiO2, Zr 180 ppm, Nb < 17 ppm, Ba/Rb > 20); Gruppe 3, alkalische Lamprophyre (1.5–2.1 Gew% TiO2, Zr > 250 ppm, Nb > 30ppm, Ba/Rb 10–25); Gruppe 4, alkalische Lamprophyre mit geringen MgO-Anteil ( 2.5 Gew% TiO2, Mg-Zahl < 57, Nb 20 ppm, Ba/Rb 20); Gruppe 5, kalkalkalisch basaltische Ganggesteine ( 2.2 Gew% TiO2, Mg-Zahl < 55, Nb < 10 ppm, Ba/Rb < 10). Die Lamprophyre der Gruppen 2, 3 und 4 zeigen nordöstliches Streichen und oligozänes Intrusionsalter (K-Ar Alter 27–32 Ma), während die Ganggesteine der Gruppen 1 und 5 überwiegend östliches Streichen und UnterOligozänes Intrusionsalter (K-Ar Alter 36 Ma) aufweisen.Die Intrusionen erfolgten während einer tektonischen Dilatationsphaseim Oligozän nach der Kontinent-Kontinent Kollision zwischen derAfrikanischen und der Eurasischen Platte im unteren Eozän. Ganggesteine der Gruppen 1, 2 und 5 besitzen typisch kalkalkalischen Charakter und stellen vermutlich Produktevon aufgeschmolzener, subduzierter Lithosphäre dar. Die Geochemie der alkalischen Lamprophyre derGruppen 3 und 4 (e.g. Ba/Nb 30–70) deutet auf ihre genetische Zwischenstellung zwischen subduction-related und within-plate regime.Zwischen den tertiären Gangintrusionen und den vermutlich paläozoischen Vererzungen der Kreuzeckgruppe besteht kein genetischer Zusammenhang. Die Alteration der Ganggesteine durch postmagmatische Lösungen hat jedoch zur Bildung von sekundären Mineralen und teilweise zu überdurchschnittlich erhöhten Au und PGE Gehalten von bis zu 35 ppb geführt.

With 6 Figures  相似文献   

15.
Geochemical and isotopic (Nd, Sr) data are reported on Paleoproterozoic (1904–1864 Ma), maficintermediate (<63% SiO2), arc metavolcanic rocks from the Flin Flon greenstone belt, Manitoba and Saskatchewan. Major element criteria permit subdivision of the rocks into tholeiitic (TH), calc-alkaline (CA), alkaline, and boninitic (BO) magma series. Subaqueously erupted, TH and related CA basalt-basaltic andesite, and rare high-Ca boninites dominated between 1904 Ma and 1890 Ma. The TH rocks are similar to modern island are tholeiites, having low high-field-strength element (HFSE) and rare earth element (REE) abundances, and chondrite-normalized light REE depletion to slight enrichment. The boninites have even lower HFSE and REE abundances (1–2X chondrites). Along with their extreme ratios of refractory incompatible elements (e.g., high Al/Ti, Ti/Zr, low Ti/V, Zr/Y), these features indicate that the arc mantle source was strongly depleted, probably residual after MORB or back-arc basin basalt extraction. Elevated Th/Yb, Ba/La, La/Nb values, and the spread in Nd isotopic compositions (initial Nd=–0.4 to +4.8) suggest recycling of small amounts (0–8%) of Archean and possibly older Proterozoic crust via sediment subduction and, locally, intracrustal contamination. Calcalkaline andesite-rhyolite and rare shoshonite and trachyandesite, erupted between 1890 Ma and 1864 Ma, are more strongly light REE enriched and have comparatively higher HFSE abundances, and higher Zr/Y and Nb/Y values. The rocks have strong arc trace element signatures (e.g., high Th/Nb, La/Nb), and initial Nd values (+2.3 to +4.6) indicate that depleted mantle contributions to the magmas continued to be dominant. The geochemistry and geology of these younger volcanic rocks suggest a mature island arc setting in which the arc lithosphere was thicker than in the previous period, and a more fertile sub-arc mantle source was tapped. The pre-1890 Ma volcanism occurred in one or more separate arcs, probably characterized by rapid subduction of oceanic lithosphere, relatively thin, tholeiitic arc crust, and extensive backarc basin formation. In contrast, post-1890 Ma volcanism is dominantly calc-alkaline to (rarely) alkaline, and is interpreted to reflect crustal thickening due to longterm growth of arc edifice(s) and tectonic thickening associated with intraoceanic arc-arc (>1870 Ma) collision and subsequent intra-arc deformation.  相似文献   

16.
Mineral chemistry, major and trace elements, and 87Sr/86Sr ratios are presented for 29 igneous rocks dredged from the northern portion of the Izu-Ogasawara arc. These rocks are compositionally bimodal. Basement gabbro and trondhjemite from the arc are extremely poor in K2O (0.05–0.19%) and Rb (0.48–0.62 ppm), and their REE patterns and Sr isotope ratios indicate that there are island arc tholeiites. Quaternary volcanic rocks from the present volcanic front (Shichito Ridge; active arc), back-arc seamounts (east side; inactive arc) and Torishima knoll between the two back-arc depressions (incipient back-arc basins) behind the active arc have the same geochemical characteristics as the above plutonic rocks though they are not as depleted in K and Rb. Rhyolite pumice from the backarc depression is also the depleted island arc tholeiite, whereas basalts from the depression have compositions that are transitional between MORB and island arc tholeiites in trace element (Ti, Ni, Cr, V, Y and Zr) and mineral chemistries. The back-arc depression basalts have relatively high BaN/CeN(0.66–1.24), Cen/YbN(1.1–1.9) and K/Ba(45–105) and low 87Sr/86Sr (0.70302–0.70332) and Ba/Sr (0.1–0.2), which are similar to other back-arc basin basalts and E-type MORB, but are quite unlike the depleted island arc tholeiites. The diverse trace element and Sr isotope compositions of basalt-andesite from the back-arc depressions imply the interplay between E-type MORB and island arc tholeiite. These chemical characteristics and the relationships of (Ce/Yb)N vs (Ba/Ce)N and (Ce/Yb)N vs 87Sr/86Sr suggest that the back-arc depression magmas are generated by mixing of E-type MORB and depleted island arc tholeiite magmas. Geochemical characters of the associated rhyolite from the depression are compatible with partial melting of lower crust.  相似文献   

17.
《Gondwana Research》2001,4(3):509-518
The Proterozoic Bandal mafic rocks, exposed in Kullu-Rampur window, Lesser Himalaya, Himachal Pradesh, indicate two distinct (high-Ti and low-Ti) magma types. The high-Ti basalts are characterised by high-TiO2 (> 2 wt%), Ti/Y, Ti/Zr, TiO2/K2O and low Rb/Sr ratios. They are enriched in high field strength (HFS) elements (Nb, Zr, Ti) relative to low field strength (LFS) incompatible elements (K, Rb). The low-Ti basalts are charactersied by low TiO2 (< 2 wt%), Ti/Y, Ti/Zr and high Rb/Sr and Rb/Ba ratios. Quartz-normative composition, continental tholeiite characteristics with Nb/La less than 1 are some of the common factors of the two groups of the Bandal mafic rocks. The trace element concentrations and their ratios of the two groups of the basalts indicate that they have been derived from the asthenosphere at different depths, low-Ti at shallow and high-Ti at deeper levels. Some of the chemical features like low Mg #, Cr, Ni, high incompatible element concentrations (especially Ba), light rare earth element (LREE) enriched patterns point towards assimilation and fractional crystallisation (AFC) process which may have played a significant role in the generation of these basalts.Furthermore, the Bandal mafic rocks, apart from field settings, are geochemically similar to other Proterozoic mafic bodies like the Rampur volcanics, Mandi-Darla volcanics, Garhwal volcanics and Bhimtal-Bhowlai volcanics of the Lesser Himalaya. This widespread Proterozoic continental tholeiitic magmatism over an area of 170,000 km2 in the Lesser Himalaya provides an evidence of plume activity in the region.  相似文献   

18.
The clinopyroxenes and garnets from garnet lherzolite nodules in kimberlites were analyzed for the major and trace elements (Sc, Ti, V, Cr, Mn, Co, Sr, and Zr) with the secondary ion mass spectrometry (SIMS) techniques using an ion-microprobe. The concentration ranges for clinopyroxenes are: 12–90 ppm Sc, 60–2540 ppm Ti, 110–350 ppm V, 2400 ppm-1.68% Cr, 470–1100 ppm Mn, 18–70 ppm Co, 85–710 ppm Sr, and 6.3–120 ppm Zr. Those for garnets are: 71–180 ppm Sc, 140–6200 ppm Ti, 220–450 ppm V, 1.05–6.24% Cr, 1600–5220 ppm Mn, 33–92 ppm Co, and 66–250 ppm Zr.These data were used to assess a possible use of distribution of transition elements between clinopyroxene and garnet for geothermometry/geobarometry. The distribution coefficients of V and Mn show good correlations with (Ca/Ca+Mg+Fe)CPX, suggesting their potential usefulness.The abundances of these elements in minerals (and estimated whole-rocks) suggest that garnet lherzolite nodules in kimberlites can be classified into three groups. It is suggested that one of the groups (Group I) could be close to the pristine mantle on the basis of Ti and Zr abundances as well as REE systematics. Arguments on Ti/Zr ratios among different nodule types suggest that abundant granular garnet lherzolites could be cumulates crystallized from a residual liquid after ilmenite was extracted.IPG Contribution No. 281  相似文献   

19.
New chemical analyses and a review of published data show that there is a compositional diversity between volcanics of basaltic composition found in the M.A.R. rift valley, M.A.R. transform faults and aseismic ridges. The basaltic rocks from the M.A.R. transform faults are less mafic (depleted in olivine content) than those from the M.A.R. rift valley. The transform fault basalts have a higher range of TiO2 content (1–4%), of Fe2O3+FeO content (8–14%) and a lower range of Cr content (50–500 ppm) and Ni content (50–300 ppm). The volcanics from aseismic ridges around the world are considered to be the more felsic types of the two provinces. They have a higher range of variation for their TiO2 and Fe2O3+FeO (1.6–5%; 9–15%; respectively) and a lower range of variability for their Cr and Ni (<250 and 100 ppm respectively) than both the M.A.R. rift valley and transform fault volcanics.It is suggested that transform faults have, by faulting, exposed more fractionated types of basaltic rocks (may be as intrusives) than the rift valley volcanics. While aseismic ridges have undergone a greater degree of differentiation than both transform faults and rift valley volcanics.Contribution n 475 du Département Scientifique, Centre Océanologique de Bretagne Contribution No. 3803 of Woods Hole Oceanographic Institution (USA)  相似文献   

20.
Evidence is available that some elements, notably Zr, TiO2, Y, Sc, Ce and Nb are largely immobile during the alteration of volcanic rocks owing to metamorphism, hydrothermal events and weathering (e.g. Floyd and Winchester, 1978). However, it is shown, by reference to analyses of rocks from the environment of five volcanogenic massive sulphide bodies, that while Zr, TiO2 (and Ce?) are mostly immobile even during intense hydrothermal alteration, Y and particularly Sc and Nb may be extremely mobile. When elements are removed by solution in a hydrothermal fluid it seems that reaction rates are such that these elements are almost totally removed from the rock. Therefore, of the so-called immobile trace elements, only Zr and TiO2 may be used with any reliability to identify the degree of magmatic differentiation in an hydrothermally altered rock. However, if an element has been mobile it is usually readily identified as having moved.  相似文献   

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