80 research outputs found
The influence of weathering and soil organic matter on Zn isotopes in soils
Zinc is an essential micronutrient that is ultimately released during mineral weathering. In soils, organic matter plays a key role in influencing Zn partitioning and therefore on Zn biogeochemical cycling. Soil organic matter is partitioned between carbon that is more readily available for decomposition by microorganisms, and more stable carbon transiently preserved from decomposition. The role of the stable pool of soil organic matter on Zn biogeochemical cycling remains poorly understood. The pool of stable carbon is controlled by combination with mineral constituents or is material that is intrinsically resistant to decomposition. The Zn stable isotopes are fractionated by interactions between Zn and soil mineral and organic constituents. This study reports the Zn isotope composition of five Icelandic soil profiles derived from the same parent basalt and characterized by contrasting degrees of weathering and organic matter content (δ66Zn = + 0.10 ± 0.05 to + 0.35 ± 0.02‰), the distribution of reactive mineral constituents available to form associations with soil organic matter, and the amount of stable organic carbon. Throughout these soils, the δ66Zn isotope variations are little influenced by mineral constituents, but rather by soil organic matter content. These data suggest that a combination of organic matter accumulation and Zn loss by leaching is required to explain the observed decrease in Zn concentration in soils and lighter soil δ66Zn with increasing organic carbon content. These results suggest that the presence of stable organic carbon in soils provides a pool of light Zn, attributed to the Zn isotope signature of organic matter partially preserved from decomposition. Crucially, this stable organic carbon pool may also contribute to the formation of the light Zn isotope sink reported in organic-rich marine sediments, a key output required to explain the oceanic mass balance of Zn isotopes
Redox transfer at subduction zones: insights from Fe isotopes in the Mariana forearc
Subduction zones are active sites of chemical exchange between the Earth’s surface and deep interior and play a fundamental role in regulating planet habitability. However, the mechanisms by which redox sensitive elements (e.g., iron, carbon and sulfur) are cycled during subduction remains unclear. Here we use Fe stable isotopes (δ56Fe), which are sensitive to redox-related processes, to examine forearc serpentinite clasts recovered from deep sea drilling of mud volcanoes formed above the Mariana subduction zone in the Western Pacific. We show that serpentinisation of the forearc by slab-derived fluids produces dramatic δ56Fe variation. Unexpected negative correlations between serpentinite bulk δ56Fe, fluid-mobile element concentrations (e.g., B, As) and Fe3+/ƩFe suggest a concomitant oxidation of the mantle wedge through the transfer of isotopically light iron by slab-derived fluids. This process must reflect the transfer of either sulfate- or carbonate-bearing fluids that preferentially complex isotopically light Fe
Black pitch, carved histories: radiocarbon dating, wood species identification and strontium isotope analysis of prehistoric wood carvings from Trinidad's Pitch Lake
We report on the results of a multi-disciplinary project (including wood identification, radiocarbon dating and strontium isotope analysis) focused on a collection of pre-Columbian wooden carvings and human remains from Pitch Lake, Trinidad. While the lake's unusual conditions are conducive to the survival of organic artefacts, they also present particular challenges for analysis. There is a loss of any contextual association beyond that of the lake, and specific methodologies are required to deal with pitch contamination. A surprising taxonomic range of woods was employed for the various utilitarian and ceremonial items recovered. The 14C results range from ca. 3200 BCE to ca. 700 CE, and include the earliest known wooden carvings in the entire Caribbean. The strontium isotope results - interpreted with the aid of an isoscape developed for the project, based on extensive samples of modern trees across Trinidad and Tobago - indicate that most carvings are consistent with the site's immediate environs; however, a ‘weaving tool’ came from a more radiogenic region that is unlikely to be found on Trinidad, suggesting links with the South American mainland
Shallow forearc mantle dynamics and geochemistry: New insights from IODP Expedition 366
The Mariana forearc is a unique setting on Earth where serpentinite mud volcanoes exhume clasts originating from depths of 15 km and more from the forearc mantle. These peridotite clasts are variably serpentinized by interaction with slab derived fluid, and provide a record of forearc mantle dynamics and changes in geochemistry with depth. During International Oceanic Discovery Program (IODP) Expedition 366, we recovered serpentinized ultramafic clasts contained within serpentinite muds of three different mud volcanoes located at increasing distance from the Mariana trench and at increasing depth to the slab/mantle interface: Yinazao (distance to the trench: 55 km / depth to the slab/mantle interface: 13 km), Fantangisña (62 km / 14 km) and Asùt Tesoru (72 km / 18 km). Four different types of ultramafic clasts were recovered: blue serpentinites, lizardite-serpentinites, antigorite/lizardite- and antigorite-serpentinites. Lizardite-serpentinites are primarily composed of orange serpentine, forming mesh and bastite textures. Raman and microprobe analyses revealed that these textures contain a mixture of Fe-rich brucite (XMg ~ 0.84) and lizardite/chrysotile. Antigorite/lizardite- and antigorite-serpentinites record the progressive recrystallization of mesh and bastite textures to antigorite, magnetite and pure Fe-poor brucite (XMg ~ 0.92). Oxygen isotope compositions of clasts and pore fluids showed that the transition from lizardite to antigorite is due to the increase in temperature from 200 °C to about 400 °C within the forearc area above the slab/mantle interface. Lizardite-, antigorite/lizardite- and antigorite-serpentinites displayed U-shaped chondrite normalized Rare Earth Element (REE) patterns and are characterized by high fluid mobile element concentrations (Cs, Li, Sr, As, Sb, B, Li) relative to abyssal peridotites and/or primitive mantle. The recrystallization of lizardite to antigorite is accompanied by a decrease in Cs, Li and Sr, and an increase in As and Sb concentrations in the bulk clasts, whereas B concentrations are relatively constant. Some clasts are overprinted by blue serpentine, often in association with sulfides. Most of these blue serpentinites were recovered at Yinazao and the uppermost units of Fantangisña and Asùt Tesoru suggesting alteration in the shallower portions of the forearc, possibly during exhumation of the clasts. This episode of alteration resulted in a flattening of REE spectra and an increase of Zn concentrations in serpentinites. Otherwise, no systematic changes of ultramafic clasts chemistry or mineralogy were observed with increasing depth to the slab. The samples document previously undescribed prograde metamorphic events in the shallow portions of the Mariana subduction zone, consistent with a continuous burial of the serpentinized forearc mantle during subduction. Similar processes, induced by the interaction with fluids released from the downgoing slab, likely occur in subduction zones worldwide. At greater depth, breakdown of brucite and antigorite will result in the massive transfer of fluids and fluid mobile elements, such as As, Sb and B, to the source of arc magmas
Episodic magmatism during the growth of a Neoproterozoic oceanic arc (AntiAtlas, Morocco)
peer reviewe
Corrigendum to "The 2014-15 eruption and the short-term geochemical evolution of the Fogo volcano (Cape Verde):Evidence for small-scale mantle heterogeneity" [Lithos 288-289 (2017) 91-107]
The authors regret that the legends of Figs. 8, 9 and 10 have been presented in a wrong sequence. For the caption of Fig. 8, see Fig.10 (Page 103). For the caption of Fig. 9, see Fig. 8 (Page 101). For the caption of Fig. 10, see Fig. 8 (Page 102). The authors would like to apologise for any inconvenience caused.SCOPUS: er.jinfo:eu-repo/semantics/publishe
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