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Isotope geochemistry of early Kilauea magmas from the submarine Hilina bench: The nature of the Hilina mantle component

Journal of Volcanology and Geothermal Research

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DOI: 10.1016/j.jvolgeores.2005.07.024

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Abstract

Submarine lavas recovered from the Hilina bench region, offshore Kilauea, Hawaii Island provide information on ancient Kilauea volcano and the geochemical components of the Hawaiian hotspot. Alkalic lavas, including nephelinite, basanite, hawaiite, and alkali basalt, dominate the earliest stage of Kilauea magmatism. Transitional basalt pillow lavas are an intermediate phase, preceding development of the voluminous tholeiitic subaerial shield and submarine Puna Ridge. Most alkalic through transitional lavas are quite uniform in Sr-Nd-Pb isotopes, supporting the interpretation that variable extent partial melting of a relatively homogeneous source was responsible for much of the geochemical diversity of early Kilauea magmas (Sisson et al., 2002). These samples are among the highest 206Pb/204Pb known from Hawaii and may represent melts from a distinct geochemical and isotopic end-member involved in the generation of most Hawaiian tholeiites. This end-member is similar to the postulated literature Kea component, but we propose that it should be renamed Hilina, to avoid confusion with the geographically defined Kea-trend volcanoes. Isotopic compositions of some shield-stage Kilauea tholeiites overlap the Hilina end-member but most deviate far into the interior of the isotopic field defined by magmas from other Hawaiian volcanoes, reflecting the introduction of melt contributions from both "Koolau" (high 87Sr/86Sr, low 206Pb/204Pb) and depleted (low 87Sr/86Sr, intermediate 206Pb/204Pb) source materials. This shift in isotopic character from nearly uniform, end-member, and alkalic, to diverse and tholeiitic corresponds with the major increase in Kilauea's magmatic productivity. Two popular geodynamic models can account for these relations: (1) The upwelling mantle source could be concentrically zoned in both chemical/isotopic composition, and in speed/extent of upwelling, with Hilina (and Loihi) components situated in the weakly ascending margins and the Koolau component in the interior. The depleted component could be refractory and spread throughout or scavenged from the overlying lithosphere. (2) The Hilina (and Loihi) components could be a more fertile material (lower melting temperature) spread irregularly throughout the Hawaiian source in a matrix of more refractory depleted and Koolau compositions. Modest upwelling along the leading hotspot margin melts the fertile domains predominantly, while the refractory matrix also partially melts in the more vigorously upwelling hotspot interior, diluting the Hilina and Loihi components and yielding voluminous isotopically diverse tholeiitic magmas. ?? 2005 Elsevier B.V. All rights reserved.

Additional Publication Details

Publication type:
Article
Publication Subtype:
Journal Article
Title:
Isotope geochemistry of early Kilauea magmas from the submarine Hilina bench: The nature of the Hilina mantle component
Series title:
Journal of Volcanology and Geothermal Research
DOI:
10.1016/j.jvolgeores.2005.07.024
Volume
151
Issue:
1-3
Year Published:
2006
Language:
English
Larger Work Type:
Article
Larger Work Subtype:
Journal Article
Larger Work Title:
Journal of Volcanology and Geothermal Research
First page:
51
Last page:
72
Number of Pages:
22