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Research about Crater Lake, Mt. Mazama

Source-linked reports with geographic coverage including Crater Lake, Mt. Mazama.

2 recordsLinked to original sources

New insights into gas-driven phase segregation in andesitic enclaves from Mt. Mazama (Crater Lake), USA

A key process in active magmatic systems is the “recharge” of deep-sourced mafic magma into cooler, more evolved, and crystal-rich shallow reservoirs; recharge may be the cause of, or response to, eruptive activity. Although compositional evidence for recharge has been extensively documented, physical models of recharge are limited, particularly processes that separate exsolving volatiles and melts from rapidly growing crystals. To improve constraints on phase separation behaviors, we re-examine andesitic enclaves in silicic andesite lava flows of Mt. Mazama (Crater Lake), USA, that provided early evidence of gas-driven filter pressing (Bacon, 1986). 2D and 3D imaging shows that enclaves have a sample-spanning crystal framework that is disrupted by melt patches, indicating that initially deformable crystal networks were subject to early phase reorganization. Small enclaves are poorly vesicular and require early gas loss. Large enclaves have porous cores with angular (diktytaxitic) voids that are well-connected in 3D and denser rinds with isolated pores. Large enclave rinds have similar bulk compositions to small enclaves but their less evolved cores require ~ 20% melt removal. In the large enclave, diktytaxitic core textures and gas fingering structures at the core–rind boundary suggest relatively slow late-stage outward gas migration. Both scaling arguments and evidence of outward gas/melt migration require a resistant rind. Rind formation is best explained by differential cooling and demonstrates the importance of thermal gradients for gas-driven filter pressing. A corollary is a limited time scale of recharge, enclave formation, and vesiculation to produce diktytaxitic textures, suggesting that recharge was (near) synchronous with eruption.

Oregon

Stable isotope and petrologic evidence for open-system degassing during the climactic and pre-climactic eruptions of Mt. Mazama, Crater Lake, Oregon

Evaluation of the extent of volatile element recycling in convergent margin volcanism requires delineating likely source(s) of magmatic volatiles through stable isotopic characterization of sulfur, hydrogen and oxygen in erupted tephra with appropriate assessment of modification by degassing. The climactic eruption of Mt. Mazama ejected approximately 50 km 3 of rhyodacitic magma into the atmosphere and resulted in formation of a 10-km diameter caldera now occupied by Crater Lake, Oregon (lat. 43°N, long. 122°W). Isotopic compositions of whole-rocks, matrix glasses and minerals from Mt. Mazama climactic, pre-climactic and postcaldera tephra were determined to identify the likely source(s) of H 2 O and S. Integration of stable isotopic data with petrologic data from melt inclusions has allowed for estimation of pre-eruptive dissolved volatile concentrations and placed constraints on the extent, conditions and style of degassing. Sulfur isotope analyses of climactic rhyodacitic whole rocks yield δ 34 S values of 2.8–14.8‰ with corresponding matrix glass values of 2.4–13.2‰. δ 34 S tends to increase with stratigraphic height through climactic eruptive units, consistent with open-system degassing. Dissolved sulfur concentrations in melt inclusions (MIs) from pre-climactic and climactic rhyodacitic pumices varies from 80 to 330 ppm, with highest concentrations in inclusions with 4.8–5.2 wt% H 2 O (by FTIR). Up to 50% of the initial S may have been lost through pre-eruptive degassing at depths of 4–5 km. Ion microprobe analyses of pyrrhotite in climactic rhyodacitic tephra and andesitic scoria indicate a range in δ 34 S from −0.4‰ to 5.8‰ and from −0.1‰ to 3.5‰, respectively. Initial δ 34 S values of rhyodacitic and andesitic magmas were likely near the mantle value of 0‰. Hydrogen isotope (δD) and total H 2 O analyses of rhyodacitic obsidian (and vitrophyre) from the climactic fall deposit yielded values οf −103 to −53‰ and 0.23–1.74 wt%, respectively. Values of δD and wt% H 2 O of obsidian decrease towards the top of the fall deposit. Samples with depleted δD, and mantle δ 18 O values, have elevated δ 34 S values consistent with open-system degassing. These results imply that more mantle-derived sulfur is degassed to the Earth’s atmosphere/hydrosphere through convergent margin volcanism than previously attributed. Magmatic degassing can modify initial isotopic compositions of sulfur by >14‰ (to δ 34 S values of 14‰ or more here) and hydrogen isotopic compositions by 90‰ (to δD values of −127‰ in this case).

Oregon