Mantle processes during ocean formation：Petrologic records in peridotites from the Alpine－Apennine ophiolites

Mantle peridotites were early exposed at the sea-floor of the Jurassic Tethys derived from the subcontinental mantle of the Europe-Adria system. During continental rifting and oceanic spreading, these lithospheric peri-dotites were percolated via diffuse reactive porous flowby melt fractions produced by near-fractional melting of the upwelling asthenosphere. Ascending melts inter-acted with the lower lithosphere, dissolving pyroxenes and precipitating olivine, and crystallized at shallower levels in the mantle column causing melt impregnation.Subsequent focused porous flow formed replacive dunitechannels, cutting the impregnated oeridotites, which were conduits for upward migration of MORB-type liq-uids. Melt migration produced depletionlrefertilization and significant heating of the percolatedlimpregnated mantle, i.e the thermochemical erosion of the litho-sphere. Impregnated and thermally modified lithos-pheric mantle was cooled by conductive heat loss dur-ing progressive lithosphere thinning and was intrudeaby MORB magmas, which formed Mg-rich and Fe-richgabbroic dykes and bodies. Alpine-Apennine ophiolitic peridotites record the deep-seated migration of melts which changed their compositions and dynamics during the rift evolution. The thermochemical erosion of the lithospheric mantle by the ascending asthenospheric melts, which induces significant compositional and rhe-ological changes in the lower lithosphere, is a major process in the evolution of the continent-ocean transi-tion towards a slow spreading oceanic system.     

Trace element and isotope geochemistry of depleted peridotites from an N-MORB type ophiolite (Internal Liguride,N. Italy)

 Mantle peridotites of the Internal Liguride (IL) units (Northern Apennines) constitute a rare example of the depleted lithosphere of the Jurassic Ligurian Tethys. Detailed chemical (ICP-MS and SIMS techniques) and isotopic investigations on very fresh samples have been performed with the major aim to constrain the timing and mechanism of their evolution and to furnish new data for the geodynamic interpretation. The data are also useful to discuss some general geochemical aspects of oceanic-type mantle. The studied samples consist of clinopyroxene-poor spinel lherzolites, showing incipient re-equilibration in the plagioclase-facies stability field. The spinel-facies assemblage records high (asthenospheric) equilibration temperatures (1150–1250° C). Whole rocks, and constituent clinopyroxenes, show a decoupling between severe depletion in highly incompatible elements [light rare earth elements (LREE), Sr, Zr, Na, Ti] and less pronounced depletion in moderate incompatible elements (Ca, Al, Sc, V). Bulk rocks also display a relatively strong M(middle)REE/H(heavy)REE fractionation. These compositional features indicate low-degree (<10%) fractional melting, which presumably started in the garnet stability field, as the most suitable depletion mechanism. In this respect, the IL ultramafics show strong similarity to abyssal peridotites. The Sr and Nd isotopic compositions, determined on carefully handpicked clinopyroxene separates, indicate an extremely depleted signature (⁸⁷Sr/⁸⁶Sr=0.702203–0.702285; ¹⁴³Nd/¹⁴⁴Nd=0.513619–0.513775). The Sm/Nd model ages suggest that the IL peridotites melted most likely during Permian times. They could record, therefore, the early upwelling and melting of mid ocean ridge basalt (MORB) type asthenosphere, in response to the onset of extensional mechanisms which led to the opening of the Western Tethys. They subsequently cooled and experienced a composite subsolidus evolution testified by multiple episodes of gabbroic intrusions and HT-LP retrograde metamorphic re-equilibration, prior to their emplacement on the sea floor. The trace element chemistry of IL peridotites also provides useful information about the composition of oceanic-type mantle. The most important feature concerns the occurrence of Sr and Zr negative anomalies (relative to “adjacent” REE) in both clinopyroxenes and bulk rocks. We suggest that such anomalies reflect changes in the relative magnitude of Sr, Zr and REE partition coefficients, depending on the specific melting conditions. Received: 15 February 1995/Accepted: 4 August 1995     

Water quality in New Zealand rivers: current state and trends

River water quality, particularly in lowland catchments, is a matter of concern to the New Zealand public. We assessed river water quality and biological state and trends using data from more than 900 monitoring sites. Parallel state and trend analyses were carried out using all sites and a subset of lowland river sites. Median water-quality state in urban and pastoral land-cover classes was poorer than in exotic forest and natural land-cover classes, and lowland sites in the urban and pastoral classes had the poorest water quality. Nutrient and Escherichia coli concentrations increased and visual clarity and Macroinvertebrate Community Index scores decreased as proportions of catchments in high-intensity agricultural and urban land cover increased. Ten-year trends (2004–2013) indicated recent improvements in ammoniacal nitrogen, dissolved reactive phosphorus and total phosphorus in the pastoral and urban classes, possibly reflecting improved land management. In contrast, trends in nitrate-nitrogen in the exotic forest and cool-dry/pastoral classes indicated worsening conditions.     

Experimental models of extension of continental lithosphere weakened by percolation of asthenospheric melts

Analogue models are used to investigate extension of a continental lithosphere weakened by asthenospheric melts percolating through the upper mantle, a process that has been hypothesised to control the opening of the Ligurian Tethys. Models were performed in a centrifuge apparatus and reproduced, by using materials such as sand and viscous mixtures, extension of 60-km thick, three-layer continental lithosphere floating above the asthenosphere. The percolated lithospheric mantle was assumed to be characterised by a rheological behaviour similar to that of the asthenosphere. Two sets of experiments investigated the influence on deformation of (1) the thickness of the percolated mantle and the associated strength contrast between the normal and weakened lithosphere, and (2) the lateral width of the weakened zone. Model results suggest that mantle percolation by asthenospheric melts is able to promote strong localised thinning of the continental lithosphere, provided that a significant thickness of the lithospheric mantle is weakened by migrating melts within a narrow region. Strain localisation is maximised for percolation of the whole lithospheric mantle and strong strength contrast between the normal and weakened lithosphere. Under these conditions, the thickness of the lithosphere may be reduced to less than 12 km in 3 Ma of extension. Conversely, localised thinning is strongly reduced if the thickness of the percolated zone is ≤1/3 of the thickness of the whole lithospheric mantle and/or the lithosphere is weakened over wide regions. Overall, model results support the working hypothesis that mantle percolation by asthenospheric melts is a controlling factor in the transition from distributed continental deformation to localised oceanic spreading.     

Subsolidus reactions monitored by trace element partitioning: the spinel- to plagioclase-facies transition in mantle peridotites

Mantle peridotites of the External Liguride (EL) Units (Northern Apennines) mainly consist of fertile spinel-lherzolites partially recrystallized to plagioclase-facies assemblages, and are consequently appropriate to investigate the interphase element partitioning related to the transition from spinel- to plagioclase-facies stability field. Evidence for the development of the plagioclase-facies assemblage is mainly given by: (1) large exsolution lamellae of orthopyroxene and plagioclase within spinel-facies clinopyroxene; (2) plagioclase rims around spinel; (3) granoblastic domains made up of olivine+plagioclase±clino-and orthopyroxene. In situ major and trace [REE (rare-earth elements), Ti, Sc, V, Cr, Sr, Y, Zr and Ba] element mineral analyses have been performed, by electron and ion probe, on selected samples which show the progressive development of the plagioclase-bearing assemblage. The main compositional variations observed during the change from spinel- to plagioclase-facies minerals are as follows: (1) clinopyroxenes decrease in Al, Na, Sr, Eu/Eu^* and increase in Y, V, Sc, Cr, Zr and Ti; (2) amphiboles decrease in Eu/Eu^*, Sr, Ba and increase in Zr and V; (3) spinels decrease in Al and increase in Cr and Ti. The most striking feature is the decoupling in the behaviour of similarly incompatible elements (D about 0.1) in clinopyroxene, e.g. Sr decrease is mirrored by Zr increase. Massbalance calculations indicate that the trace element interphase redistribution documented in the EL peridotites occurred in a closed system and in response to the metamorphic reaction governing the transition from the spinel- to the plagioclase-facies stability field. The observed element partitioning reveals, moreover, that subsolidus re-equilibration processes in the upper mantle produce HFSE (high-field-strength element)/REE fractionation in minerals, which must be evaluated for a reliable determination of mineral-melt distribution coefficients. The results of this study furnish evidence for subsolidus metamorphic evolution during decompression, without concomitant partial melting processes. This is consistent with the interpretation that the EL peridotites represent subcontinental lithospheric mantle emplaced at the surface in response to lithospheric thinning and tectonic denudation mechanisms related to the Triassic-Jurassic rifting of the Ligure-Piedmontese basin.     

Petrogenesis of some Ligurian peridotites—I. Mineral and bulk-rock chemistry

Bulk-rock and mineral compositions of eleven lherzolitic specimens have been determined. Eight samples are from the Erro-Tobbio thrust sheet of the Gruppo di Voltri, western Liguria; three samples are from allochthonous eastern Ligurian masses within the External Ligurides. All specimens consist of spinel (±plagioclase) in addition to ol + opx + cpx, and have been derived from mantle portions of the South Alpine-Apennine lithospheric plate.Electron microprobe analyses of 11 olivines, 17 orthopyroxenes, 13 clinopyroxenes, eight spinels and one plagioclase have been performed. Except for Ca-rich and Ca-poor lamellae in some pyroxenes, and iron-enriched rims in a few spinels, the analyzed phases are remarkably homogeneous. Mineral compositions vary insignificantly from rock to rock. Consideration of major element partitioning in coexisting opx + cpx pairs, combined with the petrogenetic grid for aluminous lherzolite bulk compositions, yield the following provisional P-Tequilibration conditions: Erro-Tobbio complex, 1150 ± 50°C, 16 ± 6 kbar; External Ligurides, 1000 ± 50°C, 14 ± 6 kbar. Evidently the western Ligurian peridotites equilibrated at higher temperatures and possibly at slightly greater depths with the upper mantle than those from eastern Liguria.The lherzolite samples have nearly identical bulk-rock major element compositions. Comparisons with estimated compositions for the upper mantle, and for model pyrolite indicate that these Ligurian peridotites are primitive or only very slightly depleted in basaltic constituents. Thus, based on major element chemistry, the Ligurian peridotites cannot be regarded as residua left after extensive partial fusion, hence evidently cannot have produced large proportions of oceanic tholeiite liquid; on the other hand, they seem to represent a fertile mantle source for such melts.Relics of garnet have not been found, and apparent temperatures for both Erro-Tobbio and eastern Ligurian ultramafic suites exceed the classical intraplate oceanic geotherm; accordingly, these bodies may represent rising mantle material that recrystallized during ascent in the general vicinity of a spreading center, without having undergone extensive partial melting.     

Clinopyroxene-orthopyroxene major and rare earth elements partitioning in spinel peridotite xenoliths from Assab (Ethiopia)

Major element and rare earth element (REE) partitioning among coexisting clinopyroxene-orthopyroxene pairs from mantle xenoliths of the Assab Range (Ethiopia) are discussed in terms of crystal-chemistry.Major element partitioning indicates relatively uniform conditions of subsolidus equilibration over a narrow range of temperatures (mean value about 1100 C) in the spinel peridotite stability field. Major element distributions and correlations, moreover, seem to indicate that the mantle material studied underwent slightly different depletions prior to the metamorphic equilibration.In spite of the rather homogeneous major element compositions for both cpx and opx, clinopyroxenes show chondrite-normalized REE patterns which are widely variable both in shape and absolute values, whereas orthopyroxenes exhibit more restricted ranges and concordant profiles.REE activity ratios have been investigated by applying Iiyama's (Bull. Soc. fr. Minéral. Christallogr.97, 143–151) thermodynamic model: the estimated activity patterns exhibit a good coherence for the different pyroxene pairs, in spite of the contrasting features of their REE concentration ratios. The wide ranges in the measured partition values for the same rare earth element in different pyroxene pairs have been related to coupled substitutions involving A1 in the Z site and REE in the M₂ site of clinopyroxene.     

Distribution of trace elements during breakdown of mantle garnet: an example from Zabargad

Ion probe investigations on mineral phases forming the Al-Di pyroxenites from the Zabargad peridotite body indicate that porphyroclastic pyroxenes in composite mafic layers record an unusual HREE, Zr, Sc enrichment not registered by pyroxenes in spinel websterites. Orthopyroxene in the opx+sp clusters forming the inner, cpx-free zone of layered pyroxenites shows strongly fractionated REE patterns (HREE_N/LREE_N>1000; Yb>100xch) and very high Zr, Sc and Y abundances (up to 30,672 and 60ppm, respectively). In the outer, cpx-rich zone porphyroclastic clinopyroxene is strongly HREE enriched (HREE_N/LREE_N29; Yb 269xch) and displays very high Sc and Zr abundances (up to 819 and 164 ppm, respectively). It is suggested that the unusual trace element abundances are inherited from a precursor garnet. Composite pyroxenite layers are interpreted as former garnet clinopyroxenites characterized by gnt/cpx modal zoning. The sp+opx(cpx-free) assemblage in the inner part is a product of the break-down reaction of garnet upon decompression, with Ca of the original garnet completely entering the enstatite solid solution. The temperature at which the breakdown reaction occurred is estimated to be higher than 1000°C (P in the range 20–30 kbar). In the outer part, decompression caused the garnet to form a sp+opx assemblage; however, the grossularite component participated in the formation of new clinopyroxene which reacted with the clinopyroxene present in the original mode before the decompression reaction, thus forming a cpx₂+sp+opx assemblage. As a result of garnet breakdown, pyroxenes have peculiar HFSE anomalies. Progressive upwelling during the Red Sea rifting produced incomplete reaction under pl-facies conditions. The geochemical signatures of precursor garnet in pyroxenes were partially crased during the recrystallization from granular spincl-bearing to granoblastic plagioclase-bearing assemblages, being preserved only in a few porphyroclast relies. The finding of pyroxenes with trace element characteristics of precursor garnet has important geodynamic and geochemical implications. Al-Di pyroxenite layers had a long history within the mantle, before the continental lithosphere rifting and thinning took place in the region. It is suggested that Al-Di pyroxenites were formed by deep-seated tholeiitic magmatism unrelated to the Red Sea evolution, thus representing the earliest event in the Zabargad upper mantle. Garnet breakdown significantly preceded the metasomatism induced by hydrous fluids (crystallization of Ti-rich pargasite) and the later intrusion of hydrous (Cr-Di) pyroxenite dykes. During the stages of mantle evolution, the HFSE anomalies in pyroxenes varied significantly. We note that the study of HFSE anomalies in mineral phases reveals complex geochemical histories which are not recorded by the whole-rock system.     

Preliminary investigations on volcanism of the Sadah region (Yemen Arabic Republic)

Petrographic, geochemical and geochronological data on the volcanic sequences of the Sadah region (Yemen Arabic Republic — Y.A.R.) are presented and discussed. Two main volcanic units have been recognized in this area. The older unit (Trap Series) is characterized by alkaline and transitional basalts with minor differentiates. K/Ar age determinations on these rocks give values ranging from 30 to 22 m.y.B.P. The dominance of poorly evolved rock types indicates a fairly rapid ascent of the magmas. The feeding fissures are thought to be NNW-SSE trending fractures. This is deduced by the occurrence of many dykes cutting through the underlying basament which are comparable in both chemical composition and age range to those of the Trap Series. The younger unit (Al Harf Series) is made up of alkaline basalts whose K/Ar ages are around 10 m.y.B.P. and outcrops in a tectonic depression defined by NNW-SSE trending normal faults. The volcanism in the northern Y.A.R. extends from late Oligocene to late Miocene, and follows regional structures parallel to the present-day spreading axis of the Red Sea.