skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Puhahonu: Earth’s biggest and hottest shield volcano
New bathymetric and gravity mapping, refined volume calculations and petrologic analyses show that the Hawaiian volcano P¯uh¯ahonu is the largest and hottest shield volcano on Earth. This ∼12.5-14.1 Ma volcano in the northwest Hawaiian Ridge (NWHR) is twice the size of Mauna Loa volcano (148 ±29 vs. 74.0 ×103km3), which was assumed to be not only the largest Hawaiian volcano but also the largest known shield volcano. We considered four testable mechanisms to increase magma production, including 1) thinner lithosphere, 2) slower propagation rate, 3) more fertile source, and 4) hotter mantle. The first three of these have been ruled out. The lithosphere was old (∼88 Myrs) when P¯uh¯ahonu was formed, and thus, too thick and cold to allow for greater extents of partial melting. The propagation rate was relatively fast when it erupted (87 km/Myr), so this is another unlikely reason. Source fertility was Kea-like and no more fertile than for other much smaller NWHR volcanoes. A hotter mantle remains the best mechanism to produce the large magma volumes and is consistent with the high forsteritic olivine phenocryst compositions (up to 91.8%) and the calculated high percent of melting (24%). Thus, the gargantuan size of P¯uh¯ahonu reflects its high melting temperature, the highest reported for any Cenozoic basalt. A solitary wave within the Hawaiian plume is the probable cause of P¯uh¯ahonu’s higher melting temperature and the resulting increased volume flux given the absence of a more fertile source for P¯uh¯ahonu basalts, as found for many basalts from the Hawaiian Islands.  more » « less
Award ID(s):
1834758
PAR ID:
10283332
Author(s) / Creator(s):
; ; ;
Date Published:
Journal Name:
Chemical geology
Volume:
542
ISSN:
0168-9622
Page Range / eLocation ID:
116296
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    Oceanic island basalts are targeted for geochemical study because they provide a direct window into mantle composition and a wealth of information on the dynamics and timescales associated with Earth mixing. Previous studies mainly focused on the shield volcanic stage of oceanic islands and the more fusible, enriched mantle components that are easily distinguished in those basalts. Mantle depleted compositions are typically more difficult to resolve unless large amounts of this material participated in mantle melting (e.g., mid-ocean ridges), or unique processes allow for their compositions to be erupted undiluted, such as very small degrees of melting of a source with minimal fusible enriched components (e.g., rejuvenated basalts) or as xenoliths (e.g., abyssal peridotites). Mantle depleted components, defined here as material with low time-integrated Rb/Sr (low 87Sr/86Sr) and high time-integrated Sm/Nd and Lu/Hf ratios (high 143Nd/144Nd and 176Hf/177Hf) relative to primitive mantle, derive from a potentially very large volume reservoir (up to 80% of the mantle), and therefore need adequate characterization in order estimate the composition of the Earth and mantle-derived melts. This review focuses on mantle depleted compositions in oceanic island basalts using the Hawaiian-Emperor chain as a case study. The Hawaiian-Emperor chain is the ∼6000 km long geological record of the deeply sourced Hawaiian mantle plume, active for>81 Myr. Hawaiian volcanism evolves through four volcanic stages as a volcano traverses the Hawaiian plume: alkalic preshield, tholeiitic shield (80–90% volcano volume), alkalic postshield (∼1%), and silica undersaturated rejuvenated (< 0.1%). We report Pb-Sr-Nd-Hf isotope compositions and trace element concentrations of three rejuvenated Northwest Hawaiian Ridge basalts and compare them to an exhaustive compiled dataset of basalts from the Hawaiian Islands to the Emperor Seamounts. The Northwest Hawaiian Ridge (NWHR) includes 51 volcanoes spanning ∼42 m.y. between the bend in the Hawaiian-Emperor chain and the Hawaiian Islands where there is no high-precision isotopic data published on the rejuvenated-stage over ∼47% of the chain. NWHR and Hawaiian Island rejuvenated basalts are geochemically similar, indicating a consistent source for rejuvenated volcanism over ∼12.5 million years. In contrast, shield-stage basalts from the oldest Emperor Seamounts are more depleted in isotopic composition (i.e., higher 176Hf/177Hf, and 143Nd/144Nd with lower 87Sr/86Sr and 208Pb*/206Pb*) and trace element concentrations (i.e., much lower concentrations of highly incompatible elements) than all other depleted Hawaiian basalts younger than the bend, including NWHR rejuvenated basalts. The strongly depleted source for the oldest Emperor Seamounts (> 70 Ma) was likely related to interaction with the Kula-Pacific-Izanagi mid-ocean ridge spreading system active near the Hawaiian plume in the Late Cretaceous. In contrast, the incompatible trace element ratios of NWHR rejuvenated basalts require a distinct source in the Hawaiian mantle plume that was imprinted by ancient (> 1 Ga) partial melting, likely ancient recycled oceanic lithosphere. This review of the geochemistry of Hawaiian depleted components documents the need for the sampling of multiple distinctive depleted compositions, each preferentially melted during specific periods of Hawaiian plume activity. This suggests that the composition of depleted components can evolve during the lifetime of the mantle plume, as observed for enriched components in the Hawaiian mantle plume. Changes in the composition of depleted components are dominantly controlled by the upper mantle tectonic configurations at the time of eruption (i.e., proximity to a mid-ocean ridge), as this effect overwhelms the signal imparted by potentially sampling different lower mantle components through time. 
    more » « less
  2. Abstract Maunaloa—the largest active volcano on Earth—erupted in 2022 after its longest known repose period (~38 years) and two decades of volcanic unrest. This eruptive hiatus at Maunaloa encompasses most of the ~35-year-long Puʻuʻōʻō eruption of neighboring Kīlauea, which ended in 2018 with a collapse of the summit caldera and an unusually voluminous (~1 km3) rift eruption. A long-term pattern of such anticorrelated eruptive behavior suggests that a magmatic connection exists between these volcanoes within the asthenospheric mantle source and melting region, the lithospheric mantle, and/or the volcanic edifice. The exact nature of this connection is enigmatic. In the past, the distinct compositions of lavas from Kīlauea and Maunaloa were thought to require completely separate magma pathways from the mantle source of each volcano to the surface. Here, we use a nearly 200-yr record of lava chemistry from both volcanoes to demonstrate that melt from a shared mantle source within the Hawaiian plume may be transported alternately to Kīlauea or Maunaloa on a timescale of decades. This process led to a correlated temporal variation in 206Pb/204Pb and 87Sr/86Sr at these volcanoes since the early 19th century with each becoming more active when it received melt from the shared source. Ratios of highly over moderately incompatible trace elements (e.g. Nb/Y) at Kīlauea reached a minimum from ~2000 to 2010, which coincides with an increase in seismicity and inflation at the summit of Maunaloa. Thereafter, a reversal in Nb/Y at Kīlauea signals a decline in the degree of mantle partial melting at this volcano and suggests that melt from the shared source is now being diverted from Kīlauea to Maunaloa for the first time since the early to mid-20th century. These observations link a mantle-related shift in melt generation and transport at Kīlauea to the awakening of Maunaloa in 2002 and its eruption in 2022. Monitoring of lava chemistry is a potential tool that may be used to forecast the behavior (e.g. eruption rate and frequency) of these adjacent volcanoes on a timescale of decades. A future increase in eruptive activity at Maunaloa is likely if the temporal increase in Nb/Y continues at Kīlauea. 
    more » « less
  3. Rejuvenated volcanism is a worldwide phenomena occurring on many volcanic oceanic islands in all of the major ocean basins (e.g., Samoa, Madeira, Mauritius). This plume-related volcanism follows the main edifice-building stage after a hiatus of variable duration (e.g., 0.6–2 Myrs in Hawai‘i). Hawaiian rejuvenated basalts typically have high MgO contents (>10 wt%) and carry upper mantle xenoliths. Thus, these magmas are assumed to have ascended rapidly through the crust. The basalts erupted along the Koko Rift in Honolulu, Hawai‘i are unusual in their large range in MgO (5.4–11.4 wt%), absence of mantle xenoliths and history of magma mixing. The Koko Rift is the youngest area of rejuvenated volcanism in Hawai‘i (67 ± 2 ka) and its best developed rejuvenation-stage rift system (15-km long rift with 12 major and several minor subaerial and submarine eruptive centers). Here we report on the first systematic petrologic investigation of the Koko Rift basalts to better understand this most recent example of Hawaiian rejuvenated volcanism. New textural and mineral chemical evidence indicates magma was stored along the rift and later mixed to produce the subaerial lavas with 10–11 wt% MgO. The lower MgO (5–6 wt%) subaerial lavas were probably byproducts of the initial hybrid magma, subsequent crystal fractionation and then a second magma mixing event. The absence of mantle xenoliths in Koko Rift lavas and the relatively moderate forsterite contents (84–85%) in the higher MgO lavas may be related to the development of a crustal magma system within the rift. The record of crustal magma storage and crystal fractionation, and two magma mixing episodes in the Koko Rift lavas is unique among Hawaiian rejuvenated volcanism. 
    more » « less
  4. Abstract The trondhjemite-tonalite-granodiorite (TTG) suite of rocks prominent in Earth’s Archean continents is thought to form by melting of hydrated basalt, but the specific tectonic settings of formation are unclear. Models for TTG genesis range from melting of downgoing mafic crust during subduction into a hotter mantle to melting at the base of a thick crustal plateau; while neither uniquely defines a global tectonic regime, the former is consistent with mobile lid tectonics and the latter a stagnant lid. One major problem for a subduction model is slabs sinking too quickly and steeply in a hotter mantle to melt downgoing crust. I show, however, that grain size reduction in the lithosphere leads to relatively strong plate boundaries on the early Earth, which slow slab sinking. During this “sluggish subduction,” sinking plates can heat up enough to melt when the mantle temperature is ≳1600 °C. Crustal melting via sluggish subduction can thus explain TTG formation during the Archean due to elevated mantle temperatures and the paucity of TTG production since due to mantle cooling. 
    more » « less
  5. Abstract Temporal variations in lava chemistry at active submarine volcanoes are difficult to decipher due to the challenges of dating their eruptions. Here, we use high-precision measurements of 226Ra-230Th disequilibria in basalts from Kama‘ehuakanaloa (formerly Lō‘ihi) to estimate model ages for recent eruptions of this submarine Hawaiian pre-shield volcano. The ages range from ca. 0 to 2300 yr (excluding two much older samples) with at least five eruptions in the past ∼150 yr. Two snapshots of the magmatic evolution of Kama‘ehuakanaloa (or “Kama‘ehu”) are revealed. First, a long-term transition from alkalic to tholeiitic volcanism was nearly complete by ca. 2 ka. Second, a systematic short-term fluctuation in ratios of incompatible elements (e.g., Th/Yb) for summit lavas occurred on a time scale of ∼1200 yr. This is much longer than the ∼200-yr-long historical cycle in lava chemistry at the neighboring subaerial volcano, Kīlauea. The slower pace of the variation in lava chemistry at Kama‘ehu is most likely controlled by sluggish mantle upwelling on the margin of the Hawaiian plume. 
    more » « less