Melt aggregation within the crust beneath the Mid-Atlantic Ridge: evidence from plagioclase and clinopyroxene major and trace element compositions

2000 ◽  
Vol 176 (2) ◽  
pp. 245-257 ◽  
Author(s):  
Laurence A. Coogan ◽  
Pamela D. Kempton ◽  
Andrew D. Saunders ◽  
Michael J. Norry

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.


2002 ◽  
Vol 203 (1) ◽  
pp. 479-498 ◽  
Author(s):  
P.J le Roux ◽  
A.P le Roex ◽  
J.-G Schilling ◽  
N Shimizu ◽  
W.W Perkins ◽  
...  

Clay Minerals ◽  
1983 ◽  
Vol 18 (1) ◽  
pp. 65-75 ◽  
Author(s):  
F. Grousset ◽  
C. Latouche ◽  
N. Maillet

AbstractClay mineral and trace element data indicate that sediments in the vicinity of the North Mid-Atlantic Ridge derive from material of both Icelandic and Canadian origin. These sources agree with the marine and atmospheric circulation patterns observed in this area.


2020 ◽  
Author(s):  
Emma Elizabeth McCully

Observations of seafloor bathymetry and gravity surveys indicate that magma focuses in the center of slow spreading Mid-Ocean Ridge (MOR) segments, however; it is not well constrained how magma is generated, stored, and transported to the segment ends. There are two end-member models for magma transport: 1) a focused magma model wherein the magma upwells beneath the entire ridge axis, is focused and pools beneath the center of the segment, and is then transported towards the segment ends via lateral diking in the shallow crust and 2) a distributed magma model wherein magma vertically upwells and is erupted on the seafloor along the entire segment, but there is enhanced focusing in the segment center. (Figure 1). Both models are supported by the bathymetric and geophysical observations but have different implications for the chemistry of lavas erupted along the segment. To test how lava chemistries vary along a slow-spreading MOR, we systematically sampled a segment of the Mid-Atlantic Ridge. The segment (~14°N) (Figure 2) is known to host Popping Rocks, gas-rich basalts which, upon reaching surface pressures, explode. Two expeditions to this region in 2016 and 2018 collected both ship-based bathymetry (75 m gridded resolution) aboard the R/V Atlantis and high-resolution bathymetry (1 m) from the Autonomous Underwater Vehicle (AUV) Sentry. 27 dives from the Human Occupied Vehicle (HOV) Alvin collected 382 lavas all of which have been analyzed for major element contents, and 162 have been analyzed for trace element contents. During these expeditions, samples were collected both along and across axis from the magmatically robust segment center, through a transition region, to a sparsely magmatic region. Analytical results show that there is significant chemical variability along this segment. For example, there is less variability at the segment center (K/Ti ratios from 0.24 to 0.46 and La/Sm from 2.58 to 3.59) compared to the sparsely magmatic region (K/Ti values from 0.06 to 0.42 and La/Sm). This suggests that magmas erupted at the segment center are more homogeneous compared to lavas erupting in the sparsely magmatic region. Major element contents in each region vary, but on average, become more mafic moving southward away from the magmatically robust segment center towards the sparsely magmatic region. Petrologic modeling of fractional crystallization and trace element contents show that fractional crystallization dominates the chemical variability in the sparsely magmatic region, while either extent of melting or differing mantle sources dominates the variability in the transition regions and the sparsely magmatic region. Reconciling these data with both physical and geophysical observations of a slow spreading ridge, we present a model of magma generation, storage, and transport that is a hybrid of the two proposed models.


Minerals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 743 ◽  
Author(s):  
Irina Melekestseva ◽  
Valery Maslennikov ◽  
Gennady Tret’yakov ◽  
Svetlana Maslennikova ◽  
Leonid Danyushevsky ◽  
...  

The trace element (TS) composition of isocubanite, chalcopyrite, pyrite, bornite, and covellite from oxidized Cu-rich massive sulfides of the Ashadze-2 hydrothermal field (12°58′ N, Mid-Atlantic Ridge) is studied using LA-ICP-MS. The understanding of TE behavior, which depends on the formation conditions and the mode of TE occurrence, in sulfides is important, since they are potential sources for byproduct TEs. Isocubanite has the highest Co contents). Chalcopyrite concentrates most Au. Bornite has the highest amounts of Se, Sn, and Te. Crystalline pyrite is a main carrier of Mn. Covellite after isocubanite is a host to the highest Sr, Ag, and Bi contents. Covellite after pyrite accumulates V, Ga and In. The isocubanite+chalcopyrite aggregates in altered gabrro contain the highest amounts of Ni, Zn, As, Mo, Cd, Sb (166 ppm), Tl, and Pb. The trace element geochemistry of sulfides is mainly controlled by local formation conditions. Submarine oxidation results in the formation of covellite and its enrichment in most trace elements relative to primary sulfides. This is a result of incorporation of seawater-derived elements and seawater-affected dissolution of accessory minerals (native gold, galena and clausthalite).


2006 ◽  
Vol 7 (12) ◽  
pp. n/a-n/a ◽  
Author(s):  
Christophe Hémond ◽  
Albrecht W. Hofmann ◽  
Ivan Vlastélic ◽  
François Nauret

Sign in / Sign up

Export Citation Format

Share Document