Lithium is a moderately incompatible trace element in magmatic systems. High precision analyses for lithium conducted on well characterized suites of MORB and ocean island basalts suggest a bulk distribution coefficient of 0.25−0.35 and behavior which is similar to Yb during low pressure fractionation and V during melting, as long as garnet is not an important residual phase. Data for peridotites and basalts suggest a mantle lithium content of about 1.9 ppm and show that significant concentrations of lithium reside in olivine and orthopyroxene, resulting in unusual inter-mineral partitioning of Li and complex relationships between lithium and other incompatible trace elements. The lithium abundances of arc basalts are similar to those of MORB, but their Li/Yb ratios are considerably higher. The high Li/Yb suggests the addition of a Li-rich component to arc sources; relatively low Yb abundances are consistent with the derivation of some arc magmas by larger extents of melting or from a more depleted source than MORB. Although Li is enriched at arcs, K is enriched more, leading to elevated K/Li ratios in arc volcanics. The high K/Li and relatively low La/Yb of primitive arc basalts requires either incorporation of altered ocean crust into arc magma sources, or selective removal of K and Li from subducted sediments. Bulk incorporation of sediments alone does not explain the Li systematics. Data from primitive MORB indicate a relatively low (3–4 ppm) Li content for new oceanic crust. Thus, the Li flux from the ocean crust is probably \u3c1 × 1011 g/yr, and the oceanic crust may not be an important net source in the oceanic budget of lithium
Lavas from transects across the Kurile Islands arc showed geochemical variations related to changes in the compositions of fluids derived from the subducting slab. Enrichment factors for boron, cesium, arsenic, and antimony, all elements with strong affinities for water, decreased across the arc. This decrease is presumably related to losses of water-rich fluids during the dehydration of the subducting plate. Enrichments of potassium, barium, beryllium-10, and the light rare earth elements remained constant; these species may move in silica-rich fluids liberated from the slab at greater depths.
Boron behaves as a highly incompatible trace element in oceanic settings, while in arcs it shows unique systematics indicative of fluid-rock interactions. Boron analyses conducted on well-characterized mid-ocean ridge basalt (MORB) suites show that B approximates K most closely in its solid/ melt distribution behavior, with inferred bulk distribution coefficients of 0.004-0.009 during melting in the mantle and up to 0.07 during low-pressure crystallization. During differentiation processes in volcanic arc lavas B and K also vary similarly, but the B enrichments in basalts from different arc volcanoes are highly heterogeneous relative to those of K, Be, or other incompatibles. Boron shows strong affinities for fluids such as are liberated during the devolatilization of subducting slabs. Boron enrichments correlate directly with extents of melting in arc basalts, and inversely with the enrichments of most other lithophile trace elements. Boron enrichments at arcs are lower in those volcanoes that sample deeper portions of the slab, becoming indistinguishable from MORBs in the rearmost volcanic centers. That such B depletions are evident in lavas entails that magmatic processes and other transport mechanisms efficiently flush B through the mantle wedge and return it to surface reservoirs. The great mobility of boron apparent from the arc data precludes any long-term B enrichment in the sub-arc mantle and requires the existence of strong return fluxes for B in addition to arc volcanism