Halogens in the mantle beneath the North Atlantic

F, Cl and Br contents of tholeiitic volcanic glasses dredged along the Mid-Atlantic Ridge from 53° to 28° N, including the transect over the Azores Plateau, are reported. The halogen variations parallel those of 87 Sr/ 86 Sr, La/Sm or other incompatible elements of varying volatility. The latitudinal halogen variation pattern is not obliterated if only Mg-rich lavas are considered. Variations in extent of low-pressure fractional crystallization or partial melting conditions do not appear to be the primary cause of the halogen variations. Instead, mantle-derived heterogeneities in halogens, with major enrichments in the mantle beneath the Azores, are suggested. The Azores platform is not only a ‘hotspot’ but also a ‘wetspot’, which may explain the unusually intense Azores volcanic activity. The magnitude of the halogen and incompatible element enrichments beneath the Azores appear strongly dependent on the size of these anions and cations, but independent of relative volatility at low pressure. The large anions Cl and Br behave similarly to large cations Rb, Cs and Ba, and the smaller anion F similarly to Sr and P. Processes involving crystal and liquid (fluid and/or melt), CO 2 rather than H 2 O dominated, seem to have produced these largescale mantle heterogeneities. Geochemical ‘anomalies’ beneath the Azores are no longer apparent for coherent element pair ratios of similar ionic size. Values of such ‘unfractionated’ coherent trace element ratios provide an indication of the mantle composition and its nature before fractionation event (s) which produced the inferred isotopic and trace element heterogeneities apparently present beneath the North Atlantic. The relative trace element composition of this precursor mantle does not resemble that of carbonaceous chondrites except for refractory trace element pairs of similar ionic size. It is strongly depleted in halogens, and to a lesser extent in large alkali ions Rb and Cs relative to refractory Ba. These relative depletions are comparable within a factor of 5 to Ganapathy & Anders’s estimates for the bulk Earth, with the exception of Cs. There is also evidence for removal of phosphorus into the iron core during its formation. With the exception of San Miguel, alkali basalts from the Azores Islands appear to have been derived from the same mantle source as tholeiitic basalts from the ridge transect over the Azores Platform but by half as much degree of partial melting. The Azores subaerial basalts seem to have been partly degassed in Cl, Br and F, in decreasing order of intensity. A working model involving metasomatism from release of fluids at phase transformation during convective mantle overturns is proposed to explain the formation of mantle plumes or diapirs enriched in larger relative to smaller halogen and other incompatible trace elements. The model is ad hoc and needs testing. However, any other dynamical model accounting for the 400 -1000 km long gradients in incompatible trace elements, halogens and radiogenic isotopes along the Mid-Atlantic Ridge should, at some stage, require either (1) some variable extent of mixing or (2) differential migration of liquid relative to crystals followed by re-equilibration (or both), as a diffusion controlled mechanism over such large distances is clearly ruled out, given the age of the Earth.

1975 ◽  
Vol 12 (3) ◽  
pp. 361-370 ◽  
Author(s):  
Jackson M. Barton Jr. ◽  
Erika S. Barton

The Snyder breccia is composed of angular to subrounded xenoliths of migmatites and amphibolites in a very fine grained matrix. It is apparently intrusive into the metasediments of the Snyder Group exposed at Snyder Bay, Labrador. The Snyder Group unconformably overlies a migmatitic and amphibolitic basement complex and is intruded by the Kiglapait layered intrusion. K–Ar ages indicate that the basement complex is Archean in age (> 2600 m.y. old) and that the Kiglapait layered intrusion was emplaced prior to 1280 m.y. ago. Major and trace element analyses of the matrix of the Snyder breccia indicate that while it was originally of tonalitic composition, later it locally underwent alteration characterized by loss of sodium and strontium and gain of potassium, rubidium and barium. Rb–Sr isotopic analyses show that this alteration occurred about 1842 m.y. ago, most probably contemporaneously with emplacement of the breccia. The Snyder Group thus was deposited sometime between 2600 and 1842 m.y. ago and may be correlative with other Aphebian successions preserved on the North Atlantic Archean craton.


2006 ◽  
Vol 85 (2) ◽  
pp. 77-129 ◽  
Author(s):  
W. Sissingh

AbstractA review of the sequence stratigraphic development of the Tertiary basins of the North and West Alpine Foreland domains shows that their structural and depositional history was episodically affected by brief tectonic phases. These were associated with intermittent deformation events induced by the collisional convergence and compressional coupling of the Apulian and Iberian microplates with the European Plate. The plate kinematics-related episodicity was essentially isochronously recorded in the basin fills of the Alpine Foreland region. These are generally correlative with changes in eustatic sea level. The ensuing correlative successions of so-called Cenozoic Rift and Foredeep (CRF) sequences and phases can be traced throughout the European Cenozoic Rift System and Alpine Foreland Basin. Their temporal correlation indicates that, apparently, the changes in the plate collision-related stress regime of the Alpine Foreland were repeatedly accompanied by coeval changes in eustatic sea level. To test and substantiate the validity of this inferred causal relationship between intraplate deposition, plate kinematics and eustacy, the tectono-sedimentary evolution of the basins of the Mediterranean plate-boundary zone has been analysed in conjunction with a review of the plate-boundary events in the North Atlantic. Within the uncertainty range of available datings, synchroneity could thus be demonstrated for the punctuated tectonostratigraphic development of basins of the western Mediterranean (comprising the Liguro-Provençal Basin, Valencia Trough, Sardinia Rift and Tyrrhenian Basin), the Apenninic-Calabrian Arc, the Betic domain (including the Alboran Basin) and the North and West Alpine Foreland regions. Similar temporal correlations of plate tectonicsrelated events near the Mid-Atlantic Ridge in the North Atlantic and tectonostratigraphic sequences and phases of the Alpino-Pyrenean Foreland basins are further evidence of a common causal mechanism. The driving mechanisms appear to have been the northward drift of Africa and the resulting mechanical coupling of Apulia and Iberia with the southern passive margin of Europe, as well as the stepwise opening of the North Atlantic and accompanying episodic plate re-organisations of the Mid-Atlantic Ridge.


Studies of dredged and drilled samples from the North Atlantic ocean have revealed that basalts with a wide range of major and trace element compositions have been generated at the Mid-Atlantic Ridge (M.A.R.). Many of the basalts erupted between latitudes 30° and 70° N do not have the geochemical characteristics of normal mid-ocean ridge basalts (m.o.r.b.) depleted in the more-hygromagmatophile (hyg.) elements. Drilling along mantle flow lines transverse to the ridge has shown that different segments of the M.A.R. have produced basalts with a distinct compositional range for tens of millions of years. As more data have become available, the nature and scale of this variation have been established and tighter constraints can now be placed on the petrogenetic processes involved. The rare earth elements are used to test quantitatively the effects of open and closed system fractional crystallization, equilibrium partial melting (including continuous melting), zone refining and mantle mixing processes on basalt chemistry. When evaluated in terms of the more-hyg. elements, the results show that major heterogeneities must exist in the mantle sources feeding the M.A.R. Ratios of many of the more-hyg. elements remain consistent in space and time in basalts erupted at a particular ridge segment, but vary widely between different ridge segments. These ratios are not significantly modified by the processes of basalt generation. The hyg. element relations provide a major constraint on the nature of heterogeneity in the Earth’s mantle and the processes producing it. The mantle sources of anomalous ridge segments can be best explained in terms of variable veining of a hyg. element depleted host by a hyg. element enriched liquid or fluid generated by very small degrees of partial melting. Such incipient melting, as well as subduction zone processes, may be viable mechanisms for changing hyg. element ratios in the mantle source regions on the scale observed. These processes can be integrated into a model for mantle evolution which involves (1) upward migration of incipient melts to provide a hyg. element enriched source for alkali basalts and a hyg. element depleted source for normal m.o.r.b., and (2) extraction of continental crust and recycling of the depleted residue into the mantle at subduction zones. Also, some recycling of continental material into the mantle may be required to explain Pb isotope patterns.


The alkaline rocks of Carboniferous to Permian age in the Midland Valley province range in composition from hypersthene-normative, transitional basalts to strongly undersaturated basanitic and nephelinitic varieties. They were formed by varying degrees of equilibrium partial melting of a phlogopite peridotite mantle. Ba, Ce, Nb, P, Sr and Zr were strongly partitioned into the liquid during melting; K and Rb were retained by residual phlogopite for small degrees of melting only. The composition of the mantle source is inferred to have been broadly similar to that from which oceanic alkaline basalts are currently being generated. It was, however, heterogeneous as regards distribution of the incompatible trace elements, with up to fourfold variations in elemental abundances and ratios. The mantle beneath the province may be divisible into several areas, of some hundreds of square kilometres each, which retained a characteristic incompatible element chemistry for up to 50 Ma and which imparted a distinctive chemistry to all the basic magmas generated within them.


2020 ◽  
Vol 4 (11) ◽  
pp. 2185-2204
Author(s):  
Nolwenn Lemaitre ◽  
Hélène Planquette ◽  
Frank Dehairs ◽  
Frédéric Planchon ◽  
Géraldine Sarthou ◽  
...  

2005 ◽  
Vol 6 (1) ◽  
pp. n/a-n/a ◽  
Author(s):  
Janne Blichert-Toft ◽  
Arnaud Agranier ◽  
Magdalena Andres ◽  
Richard Kingsley ◽  
Jean-Guy Schilling ◽  
...  

1995 ◽  
Vol 100 (D1) ◽  
pp. 1199-1213 ◽  
Author(s):  
R. Arimoto ◽  
R. A. Duce ◽  
B. J. Ray ◽  
W. G. Ellis ◽  
J. D. Cullen ◽  
...  

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