Geology topics

David W. Graham

Publications and source records attributed to David W. Graham.

4 recordsLinked to original sources

USGS2019

Hydrogen isotopes in high 3He/4He submarine basalts: Primordial vs. recycled water and the veil of mantle enrichment

The hydrogen isotope value ( δ D) of water indigenous to the mantle is masked by the early degassing and recycling of surface water through Earth's history. High 3 He/ 4 He ratios in some ocean island basalts, however, provide a clear geochemical signature of deep, primordial mantle that has been isolated within the Earth's interior from melting, degassing, and convective mixing with the upper mantle. Hydrogen isotopes were measured in high 3 He/ 4 He submarine basalt glasses from the Southeast Indian Ridge (SEIR) at the Amsterdam–St. Paul (ASP) Plateau ( δ D = −51 to −90‰, 3 He/ 4 He = 7.6 to 14.1 R A ) and in submarine glasses from Loihi seamount south of the island of Hawaii ( δ D = −70 to −90‰, 3 He/ 4 He = 22.5 to 27.8 R A ). These results highlight two contrasting patterns of δ D for high 3 He/ 4 He lavas: one trend toward high δ D of approximately −50‰, and another converging at δ D = −75‰. These same patterns are evident in a global compilation of previously reported δ D and 3 He/ 4 He results. We suggest that the high δ D values result from water recycled during subduction that is carried into the source region of mantle plumes at the core–mantle boundary where it is mixed with primordial mantle, resulting in high δ D and moderately high 3 He/ 4 He. Conversely, lower δ D values of −75‰, in basalts from Loihi seamount and also trace element depleted mid-ocean ridge basalts, imply a primordial Earth hydrogen isotopic value of −75‰ or lower. δ D values down to −100‰ also occur in the most trace element-depleted mid-ocean ridge basalts, typically in association with 87 Sr/ 86 Sr ratios near 0.703. These lower δ D values may be a result of multi-stage melting history of the upper mantle where minor D/H fractionation could be associated with hydrogen retention in nominally anhydrous residual minerals. Collectively, the predominance of δ D around −75‰ in the majority of mid-ocean ridge basalts and in high 3 He/ 4 He Loihi basalts is consistent with an origin of water on Earth that was dominated by accretion of chondritic material.

Earth and Planetary Science Letters↗

USGS2016

Asthenosphere–lithosphere interactions in Western Saudi Arabia: Inferences from 3 He/ 4 He in xenoliths and lava flows from Harrat Hutaymah

Extensive volcanic fields on the western Arabian Plate have erupted intermittently over the last 30 Ma following emplacement of the Afar flood basalts in Ethiopia. In an effort to better understand the origin of this volcanism in western Saudi Arabia, we analyzed 3 He/ 4 He, and He, CO 2 and trace element concentrations in minerals separated from xenoliths and lava flows from Harrat Hutaymah, supplemented with reconnaissance He isotope data from several other volcanic fields (Harrat Al Birk, Harrat Al Kishb and Harrat Ithnayn). Harrat Hutaymah is young (< 850 ka) and the northeasternmost of the volcanic fields. There is a remarkable homogeneity of 3 He/ 4 He trapped within most xenoliths, with a weighted mean of 7.54 ± 0.03 R A (2σ, n = 20). This homogeneity occurs over at least eight different xenolith types (including spinel lherzolite, amphibole clinopyroxenite, olivine websterite, clinopyroxenite and garnet websterite), and encompasses ten different volcanic centers within an area of ~ 2500 km 2 . The homogeneity is caused by volatile equilibration between the xenoliths and fluids derived from their host magma, as fluid inclusions are annealed during the infiltration of vapor-saturated magmas along crystalline grain boundaries. The notable exceptions are the anhydrous spinel lherzolites, which have a lower weighted mean 3 He/ 4 He of 6.8 ± 0.3 R A (2σ, n = 2), contain lower concentrations of trapped He, and have a distinctly depleted light rare earth element signature. 3 He/ 4 He values of ~ 6.8 R A are also commonly found in spinel lherzolites from harrats Ithnayn, Al Birk, and from Zabargad Island in the Red Sea. Olivine from non-xenolith-bearing lava flows at Hutaymah spans the He isotope range of the xenoliths. The lower 3 He/ 4 He in the anhydrous spinel lherzolites appears to be tied to remnant Proterozoic lithosphere prior to metasomatic fluid overprinting. Elevated 3 He/ 4 He in the western harrats has been observed only at Rahat (up to 11.8 R A ; Murcia et al., 2013), a volcanic field situated above thinned lithosphere beneath the Makkah-Medinah-Nafud volcanic lineament. Previous work established that spinel lherzolites at Hutaymah are sourced near the lithosphere-asthenosphere boundary (LAB), while other xenolith types there are derived from shallower depths within the lithosphere itself (Thornber, 1992). Helium isotopes are consistent with melts originating near the LAB beneath many of the Arabian harrats, and any magma derived from the Afar mantle plume currently appears to be of minor importance.

LITHOS↗

USGS2014

Contrasting volcanism in Hawaiʻi and the Galápagos

The archipelagos of Hawai‘i and the Galápagos originated at mantle hotspots, yet the volcanoes that make up the island chains differ in most respects. Some of the most important differences include the dynamics of magma supply, characteristics of magma storage and transport, morphology, and compositional and structural evolution. Of particular significance in the Galápagos is the lack of well-developed rift zones, which may be related to higher rates of pre-eruptive inflation compared to Hawai‘i, and the absence of widespread flank instability—a common feature of Hawai‘i's volcanoes. The close proximity of the Galápagos to a mid-ocean-ridge system may account for many of the differences between Hawaiian and Galápagos volcanoes. The Galápagos archipelago is built on young, thin oceanic crust, which might allow for contemporaneous growth of numerous volcanoes, and its volcanoes are fed by a mix of plume and asthenospheric melt sources. Hawaiian volcanoes, in contrast, grew in the middle of the Pacific Plate on older, thicker crust, where localized changes in mantle and lithosphere structure and composition did not exert dominant control over volcano evolution.

Book chapter↗

USGS1999

Natural attenuation of chloroacetinilide herbicides in aquatic systems

Chloroacetanilide herbicides (e.g. alachlor and metolachlor) and their breakdown products are frequently found in agriculturally impacted and other natural waters. Although these compounds are usually present at low concentrations in aquatic systems, defining their fate and attenuation rate is important because they can be toxic at comparatively low exposure levels. This paper summarizes results from a four-year research program assessing factors that affect herbicide attenuation rates and breakdown product formation patterns in aquatic systems. Over 70 different field microcosms (11.3 m 3 cylindrical fiberglass tanks) were selectively manipulated (in replicate) to create nine unique aquatic ecosystems for this study. Alachlor and/or metolachlor were added to these units and transformations were observed over time. Alachlor half-lives ranged from 6.0 days to more than 100 days depending upon the temperature, oxygen conditions, and the nutrient conditions in the microcosm waters. The highest rates of alachlor decay were observed in warm, nutrient-rich, anaerobic water columns, whereas the lowest alachlor decay rates were observed under cooler, aerobic, oligotrophic water conditions. Similar relationships were observed for metolachlor, although metolachlor decay rates were about 40% slower. Our data suggest that herbicides will decay rapidly in waters that are high in nutrients possibly resulting from human activities. Alternately, low nutrient or pristine waters will have the lowest rates of herbicide decay. On a policy level, all efforts should be made to prevent exposure of comparatively pristine waters to herbicide inputs.

Conference Paper↗