Nd and Sr isotope signatures of the Khibina and Lovozero agpaitic centres, Kola Alkaline province, Russia

Nd and Sr compositions of the highly evolved agpaitic nepheline syenites and associated ijolites and carbonatites from the Khibina and the Lovozero alkaline centres define three magma sources. Isotopes of the voluminous nepheline syenites and ijolites of Khibina intrusions III, IV, V, VI and VII as well as of nepheline syenites of Lovozero lie on the Kola Carbonatite Mixing Line which is close to the “mantle array” defined by the components “bulk earth” and “prema” on a Sr---Nd plot. The Khibina carbonatites and associated silicate rocks of intrusion VIII, which have more radiogenic Sr, did not evolve from the same parent magma as the nepheline syenites.

Isotopic constraints exclude a pre-enrichment of Rb, Sr, Sm and Nd in the lithospheric mantle below Kola over more than 10 Ma prior to the crystallization of the magmas. A formation of the melts involving major participation of the Precambrian crust of the Baltic Shield is also excluded.

The lack of significant Eu anomalies in the Lovozero nepheline syenites gives evidence that the agpaitic magmas in the Kola region did not form from basaltic liquids by fractional crystallization of plagioclase or anorthoclase at crustal levels. A formation from nephelinite or nepheline benmoreite magmas at mantle pressures is more likely, possibly by dynamic flow crystallization.

Enrichment factors suggest that large-ion lithophile and high field-strength elements as Ta, La, Nb and Zr, which are highly concentrated in the agpaites, were scavenged from mantle volumes of some 100,000 km³. An enrichment of these elements prior to magma formation may have been performed by volatile transfer.

The well-defined whole-rock isochrons of the Khibina III–VII and the Lovozero agpaites of c. 370 Ma date the magma separation for the different intrusion, if these melts are cogenetic and formed by fractional crystallization in a Khibina and a Lovozero magma chamber. If, however, Rb and Sr were collected by a process of volatile transfer, and the initial Sr isotopic compositions of the two distinguished agpaite suites are, therefore, averages of the sampled mantle volumes, the Rb---Sr whole-rock isochron ages of c. 370 Ma would date this process of element collection. The concordance of the whole-rock ages with the mineral ages of Khibina and Lovozero samples is then further evidence for the short period between magma genesis, intrusion and crystallization.     

Basin hydrogeological characterization using remote sensing,hydrogeochemical and isotope methods (the case of Baro-Akobo,Eastern Nile,Ethiopia)

Hydrogeochemical and isotopic signatures of the waters of the Baro-Akobo River Basin show deviation from signatures in other Ethiopian river basins. In this study, hydrogeochemical and isotope methods were employed to determine regional and local hydrogeology and characteristics of the basin. Optical, thermal and radar remote sensing products were used to update geological and structural maps of the basin and determine sampling points using the judgment sampling method. A total of 363 samples from wells, springs, rivers, lakes, swamps and rain were collected for this study, and an additional 270 water quality data sets were added from previous studies. These data were analyzed for their hydrogeochemical characteristics and isotope signatures. Analysis of the oxygen, deuterium and tritium isotopes shows the groundwater of the basin is modern water. Among all basins in Ethiopia, the Baro-Akobo Basin shows the highest enrichment. This indicates the proximity of the rainfall sources, which presumably are the Sudd and other wetlands in South Sudan. The hydrochemical properties of the waters show evapotranspiration is the dominant hydrologic process in the basin and explains the large amount of water that is lost in the lowland plain. Analysis of radon-222 shows no significant groundwater flux over the wetlands, which are part of Machar Marshes. This shows evaporation to be dominant hydrologic process in this zone. Results from all analyses help explain the limited holding capacity of the aquifers in the recharge zone and their vulnerability to anthropogenic impacts and climate variability. There is a trend of decreasing surface flow and rainfall and increasing water soil erosion.     

Isotope geochemical (Sr,Nd)-peculiarities and sources of Mesozoic magmatic associations of the Umlekano-Ogodzhinskii belt (Amur Area)

Doklady Earth Sciences -     

Early Devonian volcanics of southeastern Gorny Altai: Geochemistry,isotope (Sr,Nd, and O) composition,and petrogenesis (Aksai complex)

Geological, geochemical, and isotope (Sr, Nd, and O) parameters of Early Devonian (405 Ma) volcanics of southeastern Gorny Altai (Aksai and Kalguty volcanotectonic structures) are discussed. The studied igneous rock association comprises magnesian andesitoids, Nb-enriched andesite basalts, and A-type peraluminous silicic rocks (dacites, rhyolites, granites, and leucogranites). Magnesian andesitoids (mg# > 50) are characterized by a predominance of Na among alkalies (K₂O/Na₂O ≈ 0.1-0.7), medium contents of TiO₂ (~ 0.8-1.3 wt.%) and Al₂O₃ (~ 12-15 wt.%), enrichment in Cr (up to 216 ppm), and low Sr/Y ratios (4-15). The Nb-enriched (Nb = 10-17 ppm) andesite basalts have high contents of TiO₂ (1.7-2.7 wt.%) and P₂O₅ (0.4-1.4 wt.%). The A-type granitoids are characterized by high contents of K(K₂O/Na₂O ≤ 60) and alumina (ASI ≤ 2.9) and depletion in Ba, Sr, P, and Ti. The magnesian andesitoids and Nb-enriched andesite basalts are products of melts generated in the metasomatized lithospheric mantle; silicic magmas were formed through the melting of Cambrian-Ordovician metaturbidites of the Gorny Altai Group and, partly, Early-Middle Cambrian island-arc metabasites. The above rock association might have resulted from a plume impact on the lithospheric substrates of the continental paleomargin during the evolution of the Altai-Sayan rift system.     

Post-collisional melting of crustal sources: constraints from geochronology,petrology and Sr,Nd isotope geochemistry of the Variscan Sichevita and Poniasca granitoid plutons (South Carpathians,Romania)

The Sichevita and Poniasca plutons belong to an alignment of granites cutting across the metamorphic basement of the Getic Nappe in the South Carpathians. The present work provides SHRIMP age data for the zircon population from a Poniasca biotite diorite and geochemical analyses (major and trace elements, Sr–Nd isotopes) of representative rock types from the two intrusions grading from biotite diorite to biotite K-feldspar porphyritic monzogranite. U–Pb zircon data yielded 311 ± 2 Ma for the intrusion of the biotite diorite. Granites are mostly high-K leucogranites, and biotite diorites are magnesian, and calcic to calc-alkaline. Sr, and Nd isotope and trace element data (REE, Th, Ta, Cr, Ba and Rb) permit distinguishing five different groups of rocks corresponding to several magma batches: the Poniasca biotite diorite (P₁) shows a clear crustal character while the Poniasca granite (P₂) is more juvenile. Conversely, Sichevita biotite diorite (S₁), and a granite (S₂*) are more juvenile than the other Sichevita granites (S₂). Geochemical modelling of major elements and REE suggests that fractional crystallization can account for variations within P₁ and S₁ groups. Dehydration melting of a number of protoliths may be the source of these magma batches. The Variscan basement, a subduction accretion wedge, could correspond to such a heterogeneous source. The intrusion of the Sichevita–Poniasca plutons took place in the final stages of the Variscan orogeny, as is the case for a series of European granites around 310 Ma ago, especially in Bulgaria and in Iberia, no Alleghenian granitoids (late Carboniferous—early Permian times) being known in the Getic nappe. The geodynamical environment of Sichevita–Poniasca was typically post-collisional of the Variscan orogenic phase.     

Metal sources of the Navan carbonate-hosted base metal deposit, Ireland: Nd and Sr isotope evidence for deep hydrothermal convection

Nd and Sr isotope analyses are presented for gangue mineral samples from the giant carbonate-hosted Navan Zn–Pb deposit, Ireland, and for rocks from which Navan metals may have been derived. Analysis of gangue minerals spanning the Navan paragenetic sequence reveals systematic evolution in the composition of the mineralising fluid. Early fluid represented by replacive dolomite exhibits the lowest initial ⁸⁷Sr/⁸⁶Sr ratio (0.7083–0.7086), closest to that of the host limestone and to Lower Carboniferous seawater, and the highest ¹⁴³Nd/¹⁴⁴Nd ratio (0.51161–0.51176). Later generations of dolomite, barite and calcite, which encompass sulphide precipitation, have higher initial ⁸⁷Sr/⁸⁶Sr ratios (maximum 0.7105) and lower initial ¹⁴³Nd/¹⁴⁴Nd ratios (minimum 0.51157). All samples have initial Nd isotope ratios that are too low to have been acquired only from the host limestone. Drill core samples of presumed Ordovician volcanic and sedimentary rocks from beneath the Navan orebody have ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr ratios at the time of mineralisation of 0.51184–0.51217 and 0.7086–0.7138, respectively. The data are interpreted to indicate mixing of sulphide-rich, limestone-buffered brine, with a metal-bearing hydrothermal fluid, which had passed through sub-Carboniferous rocks, consistent with published fluid inclusion and S isotope data. The ¹⁴³Nd/¹⁴⁴Nd ratio of this basement-derived fluid is too low to have been imparted by flow through the Devonian Old Red Sandstone, as required in models of regional fluid flow in response to Hercynian uplift. Irrespective of whether such regional fluid flow occurred, the hydrothermal Nd must have been derived from sub-Devonian rocks. These conclusions broadly support the hydrothermal convection cell model in which brines, ultimately of surface origin, penetrated to a depth of several kilometres, leaching metals from the rocks through which they passed. The data also support increasing depth of penetration of convection cells with time. Metals were subsequently precipitated in carbonate rocks at sites of mixing with cooler, sulphide-rich fluids. However, comparison of the Navan hydrothermal gangue Nd–Sr isotope data with data from Lower Palaeozoic rocks strongly suggests that the latter cannot alone account for the “basement” signature. As the Navan deposit lies immediately north of the Iapetus Suture, this suggests that the Laurentian margin includes Precambrian basement.     

Sr and Nd isotopes as tracers of clastic sources in Lake Le Bourget sediment (NW Alps, France) during the Little Ice Age: Palaeohydrology implications

Geochemical methods (major elements and Sr, Nd isotopes) have been used to (1) characterize Lake Le Bourget sediments in the French Alps, (2) identify the current sources of the clastic sediments and estimate the source variability over the last 600 years. Major element results indicate that Lake Le Bourget sediments consist of 45% clastic component and 55% endogenic calcite. In addition, several individual flood levels have been identified during the Little Ice Age (LIA) on the basis of their higher clastic content (> 70%).Potential sources of Lake Le Bourget clastic sediments have been investigated from Sr and Nd isotope compositions. The sediments from the Sierroz River and Leysse River which are mainly derived from the Mesozoic Calcareous Massifs are characterised by lower ⁸⁷Sr/⁸⁶Sr ratios and slightly lower ?_Nd(0) ratios than the Arve River sediments which are derived from the Palaeozoic Mont-Blanc External Crystalline Massifs. The Rhône River appears to have been the main source of clastic sediments into the lake for the last 600 years, as evidenced by a similar Sr and Nd isotopic compositions analyzed in core B16 sediments (⁸⁷Sr/⁸⁶Sr = 0.719, ?_Nd(0) = − 10) and in the sediments of the Rhône River (⁸⁷Sr/⁸⁶Sr = 0.719, ?_Nd(0) = − 9.6).The isotopic signatures of flood events and background samples from core B16 in Lake Le Bourget are also similar. This indicates that prior to ∼ 1800, the inputs into the lake have remained relatively homogeneous with the proportion of clastic component mainly being a function of the palaeohydrology of the Rhone River. Early human modification (deforestation and agriculture) of the lake catchment before the 1800s appears to have had little influence on the source of clastic sediments.     

Sr and Nd isotope geochronology,geologic history,and origin of the Adirondack Anorthosite

We have analyzed samples from the Adirondack Marcy massif for Rb-Sr and Sm-Nd isotopes in an attempt to determine directly the primary crystallization age of a Proterozoic massif-type anorthosite rock suite. The oldest age obtained (1288 ± 36Ma) is from a 4 point Sm-Nd isochron defined by igneous-textured whole-rock and mineral separate data from a local layered sequence gradational from oxiderich pyroxenite to leuconorite. This age is older than Silver's (1969) 1113 Ma zircon age of associated charnockites, but is within the window of permissible anorthosite ages based on previous geochronology and field relationships. As such, 1288 Ma may represent the time of crystallization of the massif. For the most part, however, both Sm-Nd and Rb-Sr isotopic systems did not survive granulite facies metamorphism. Internal isochrons based on whole rocks and minerals yield ages between 995 and 919 Ma. These isotopic data suggest that the granulite fades metamorphism experienced by the massif was a prograde event that occurred a minimum of 100 Ma and as much as 350 Ma after crystallization of the massif. The relatively large range in Rb abundance, and in calculated initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ (0.7039–0.7050) and ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratios among anorthosite suite rocks, particularly those at or near the contacts of the Marcy massif is explicable by variable contamination with “crustal” materials and/or fluids, derived from surrounding acidic metaplutonic rocks, paragneisses, and marbles. Despite uncertainies caused by crustal contamination and metamorphic resetting of primary ages, Marcy samples have epsilon Nd values between +0.44 and +5.08, implying a source for the massif with long-term depletion in light rare earth elements. A probable source material would be depleted mantle.     

Geochemistry and isotope (Sr, Nd, O) study of Al–Mg granulites from the In Ouzzal Archaean block (Hoggar, Algeria)

The In Ouzzal Al–Mg granulites are found within sedimentary units deposited after 2.7 Ga, the whole association being metamorphosed under extreme temperature conditions (c. 1000 °C) at 2 Ga. The Al–Mg granulites are interlayered with other metasediments, including metapelites, quartzites and magnetite-bearing quartzites, forsterite-spinel marbles, and a few meta-igneous rocks (mainly pyroxenites). They do not occur at a specific position in the sedimentary suite, and they do not reflect any particular structural control. The major and trace element compositions of Al–Mg granulites (especially the high Cr, Ni, Co contents) show that their peculiar ‘refractory’ chemistry is more compatible with premetamorphic sedimentary characteristics rather than with metasomatic, metamorphic or partial melting processes. Sedimentary admixtures of a common mature detrital component coming from the weathering of the local acidic igneous crustal protoliths (normal pelitic component) with an extremely immature component derived from reworking of basic/ultrabasic lithologies (Al–Mg–Cr–Co–Ni–rich chloritic component) is consistent with the geochemistry of such rocks. As in other instances, the quartz-garnet oxygen isotopic thermometer here records an apparent temperature close to the peak metamorphism (c. 1000 °C). Although the persistence of pre-existing δ¹⁸O variations on a small scale during the metamorphism does not support a major pervasive fluid flow during metamorphism, it does not rule out the presence of syn- to post-metamorphic CO₂. The low δ¹⁸O (c.+ 5 to + 6‰) of the most typical Al–Mg granulites indicate that the ‘chloritic component’ in these rocks was derived from hydrothermally altered mafic/ultramafic protoliths rather than dominantly from palaeosols. It is suggested that the presence of such Al–Mg–Cr–Co–Ni–rich sediments is indirect evidence for the presence of greenstone belts in the local crust of the In Ouzzal at 2.6–2.7 Ga.     

Sr and Nd isotope data from the fluorspar district of Asturias, northern Spain

The origin and age of the hydrothermal fluids related to the precipitation of fluorite, barite and calcite in the Villabona, La Collada and Berbes localities (Asturias fluorspar district, N Spain) have been evaluated from Sr and Nd radiogenic isotopes. Sr isotope data (⁸⁷Sr / ⁸⁶Sr = 0.7081 to 0.7096) are compatible with mixing between seawater and a more evolved groundwater that interacted with the basement. From Nd isotopes in fluorite, an isochron age of 185 ± 29 Ma (Lower Jurassic) was obtained, consistent with other hydrothermal events in the Iberian Peninsula and Europe. These constraints are essential to proceed with a quantitative model for the genesis of the mineralization that includes fluid and heat flow together with reactive transport of solutes.     

德兴斑岩铜矿成矿过程的氧、锶、钕同位素证据

为探讨德兴铜厂斑岩铜矿床成矿热液流体的来源、作用范围、时空演化及Cu在热液流体中的行为和迁移方向等重要问题，对采集于该矿床南部不同蚀变程度的岩石进行了氧、锶、钕同位素分析，结果表明，虽然与铜三斑岩铜矿成矿过程有关的热液流体至少有3种，包括高温岩浆流体、来自深部围岩的非岩浆流体和大气降水，但是起主导作用的是岩浆流体，钕、锶同位素在空间上的变化表明，在成矿流体形成及演化过程中，锶同位素值由斑岩体内部向围岩接触带有规律地升高（0.705→0.711），指示了矿床是因热液流体将成矿元素从岩体内部迁移到接触带附近富集而成的，它符合斑岩铜矿的正岩浆模式，而钕同位素则相对稳定，可作为蚀变侵入体岩浆起源的示踪剂。     

Sm–Nd and Sr isotope systematics of scheelite from the giant Au(–W) deposit Muruntau (Uzbekistan): implications for the age and sources of Au mineralization

The application of the Sm-Nd isotope system of scheelite to dating of low-sulfide, quartz-vein hosted Au mineralization is still under discussion. In the present work, new Sm-Nd and Rb-Sr data for scheelite from the giant Muruntau/Myutenbai Au deposit (Kyzylkum, Western Uzbekistan) are discussed. Based on the geological relationship, mineralogical properties, and trace element characteristics, two types of scheelite can be distinguished within the deposit. The first one is represented by early bluish luminescent and weakly coloured scheelite (generation 1) found within strongly deformed flat quartz veins. The apparent isochron defined by this scheelite (351ᆪ Ma) is interpreted as a mixing line. Typically brownish to orange and yellowish luminescent scheelite from steeply dipping veins (generation 2) defines a Sm-Nd isochron age of 279ᆦ Ma ()_Nd=-9.5ǂ.3; MSWD: 1.5). No evidence for mixing or disturbance by late alteration were found for these scheelites. This Sm-Nd isochron age agrees with the Rb-Sr and K-Ar age range for wall rock alteration in this deposit reported previously. The age of 280 Ma is interpreted to date the high-grade ore formation in the Muruntau deposit. There are currently no reliable age data available on the magmatic events in the Muruntau region. Probably, there is some overlap in time of the Hercynian gold deposition with the intrusion of lamprophyric dykes. The Nd and Sr isotopic signatures of scheelite define the wall rocks (mainly metasiltstones and metasandstones) as the most probable sources for these elements in scheelite.     

Sr and Sr/Sr in the Yamuna River System in the Himalaya: sources, fluxes, and controls on sr isotope composition

Sr and ⁸⁷Sr/⁸⁶Sr have been measured in the Yamuna river headwaters and many of its tributaries (YRS) in the Himalaya. These results, with those available for major ions in YRS rivers and in various lithologies of their basin, have been used to determine their contributions to riverine Sr and its isotopic budget. Sr in the YRS ranges from 120 to 13,400 nM, and ⁸⁷Sr/⁸⁶Sr from 0.7142 to 0.7932. Streams in the upper reaches, draining predominantly silicates, have low Sr and high ⁸⁷Sr/⁸⁶Sr whereas those draining the lower reaches exhibit the opposite resulting from differences in drainage lithology. ⁸⁷Sr/⁸⁶Sr shows significant co-variation with SiO₂/TDS and (Na^* + K)/TZ⁺ (indices of silicate weathering) in YRS waters, suggesting the dominant role of silicate weathering in contributing to high radiogenic Sr. This is also consistent with the observation that streams draining largely silicate terrains have the highest ⁸⁷Sr/⁸⁶Sr, analogous to that reported for the Ganga headwaters. Evaluation of the significance of other sources such as calc-silicates and trace calcites in regulating Sr budget of these rivers and their high ⁸⁷Sr/⁸⁶Sr needs detailed work on their Sr and ⁸⁷Sr/⁸⁶Sr. Preliminary calculations, however, indicate that they can be a significant source to some of the rivers.It is estimated that on an average, ∼25% of Sr in the YRS is derived from silicate weathering. In the lower reaches, the streams receive ∼15% of their Sr from carbonate weathering whereas in the upper reaches, calc-silicates can contribute significantly (∼50%) to the Sr budget of rivers. These calculations reveal the need for additional sources for rivers in the lower reaches to balance their Sr budget. Evaporites and phosphorites are potential candidates as judged from their occurrence in the drainage basin. In general, Precambrian carbonates, evaporites, and phosphorites “dilute” the high ⁸⁷Sr/⁸⁶Sr supplied by silicates, thus making Sr isotope distribution in YRS an overall two end member mixing. Major constraints in quantifying contributions of Sr and ⁸⁷Sr/⁸⁶Sr from different sources to YRS rivers are the wide range in Sr and ⁸⁷Sr/⁸⁶Sr of major lithologies, limited data on Sr and ⁸⁷Sr/⁸⁶Sr in minor phases and on the behavior of Sr, Na, and Ca during weathering and transport.The Ganga and the Yamuna together transport ∼0.1% of the global Sr flux at the foothills of the Himalaya which is in the same proportion as their contribution to global water discharge. Dissolved Sr flux from the Yamuna and its mobilization rate in the YRS basin is higher than those in the Ganga basin in the Himalaya, a result consistent with higher physical and chemical erosion rates in the YRS.     

Tracing diffuse anthropogenic Pb sources in rural soils by means of Pb isotope analysis

Knowledge of the cause and source of Pb pollution is important to abate environmental Pb pollution by taking source-related actions. Lead isotope analysis is a potentially powerful tool to identify anthropogenic Pb and its sources in the environment. Spatial information on the variation of anthropogenic Pb content and anthropogenic Pb sources in rural topsoils is remarkably limited. This study presents results of a survey of approximately 350 topsoil samples from rural locations covering the entire Netherlands, for which the bulk geochemical and Pb isotope compositions were determined. The specific aim of this study is to determine the anthropogenic Pb sources in the topsoils from rural areas in The Netherlands. The spatial distribution of anthropogenic Pb in soils in The Netherlands will be explained in terms of land use and pollution sources.Nearly all studied topsoils display Pb contents that exceed the amount expected based on the soil lithology. The range in Pb isotope ratios of the additional Pb fraction in rural Dutch topsoils is established at 1.056–1.199, 2.336–2.486 and 0.452–0.490 for ²⁰⁶Pb/²⁰⁷Pb, ²⁰⁷Pb/²⁰⁸Pb and ²⁰⁶Pb/²⁰⁸Pb, respectively. Five land use types are distinguished (forest, open nature, moor, arable land and grassland) with distinct isotopic compositions for added Pb. Additional Pb in soils of natural areas (forest, open nature and moor) has on average lower ²⁰⁶Pb/²⁰⁷Pb, ²⁰⁸Pb/²⁰⁷Pb and ²⁰⁶Pb/²⁰⁸Pb ratios than the agricultural soils (arable land and grassland). Additional Pb in both natural area soils and agricultural soils is interpreted to be of anthropogenic origin: most likely a mixture of coal/galena, incinerator ashes and gasoline Pb. The dominant sources of additional Pb in the topsoil of open nature areas are most likely incinerator ash and gasoline Pb. In contrast, the on average higher ²⁰⁶Pb/²⁰⁷Pb, ²⁰⁸Pb/²⁰⁷Pb and ²⁰⁶Pb/²⁰⁸Pb ratios of additional Pb in agricultural soils are most likely caused by the presence of animal manure and N–P fertilizers.Several areas are observed with notably high additional Pb contents (26–211 mg/kg on an organic matter-free basis) in the topsoil. The largest area is the Randstad area, which has the highest population and traffic density, and hosts a considerable fraction of the Dutch chemical industry. Two other areas with high additional Pb contents in the topsoil are located near the Dutch borders and are most likely influenced by German and Belgian chemical industries. The topsoils in the coastal dunes and southern, central and northern forests are characterized by relatively low additional Pb contents (<10 mg/kg on an organic matter-free basis). The population, traffic and chemical industry density is low in these areas and no fertilizers are applied.     

Pb, Sr and Nd isotope study of two co-existing magmas in the Nízke Tatry Mountains, Western Carpathians (Slovakia)

Summary Two co-existing plutonic rocks (diorite and granodiorite) were studied from an intrusion of Variscan age in the Raztocna Valley – Nízke Tatry Mountains, Western Carpathians. Geochemical analyses of major and trace elements constrain a volcanic arc as emplacement environment and give the first hints of a mixture of two magmatic end-members: the so-called Prasivá granodiorite and the Raztocna diorite. The ⁸⁷Sr/⁸⁶Sr₍₀₎ ratios vary between 0.7075 and 0.7118, the ε Nd₍₀₎ values range from −1.4 to −5.0. Common Pb isotopes reveal a dominant crustal source with minor influences from a mantle and a lower crustal source. Modelling based on Sr and Nd isotope data and using three component mixing calculations indicates that mixing of 2/3 of upper mantle material with 1/3 upper crustal material can produce the isotopic composition of the Raztocna diorite. Very minor amounts of lower crust were incorporated in the diorite. For the Prasivá granodiorite, the mixing ratio of upper mantle and upper crust is similar, but a lower crustal reservoir contributed about 5–10% of the source material.