Geology topics

Hilary G. Close

Publications and source records attributed to Hilary G. Close.

5 recordsLinked to original sources

USGS2026

Organic and isotopic indicators for sorting of sedimentary organic matter along a marginal submarine canyon

Submarine canyons are incised features of many continental margins that can have significant influence on the hydrodynamic distribution of sediments and organic matter eroded and deposited from the continents. Baltimore Canyon, on the mid-Atlantic margin of the United States, contains a complex set of sedimentary processes that simultaneously create unique benthic habitats and control the deposition of organic matter. Along the canyon axis, loci of net erosion, net deposition, and intense winnowing each host diverse faunal assemblages and varying mixtures of sedimentary organic matter derived both from production in the overlying water column and from mobilized sediments. Bioavailable components of this deposited organic matter sustain benthic communities, while recalcitrant components can contribute to long-term carbon burial in the deep sea. However, commonly employed bulk geochemical analyses provide little information about the relative bioavailability or depositional history of sedimentary organic matter. Here we employ a range of organic and isotopic analyses to explore in more detail how canyon-specific sediment dynamics determine the sorting of organic matter from shelf to open ocean. In combination with bulk geochemical characteristics, we subjected surface sediments from water depths of ∼200–1200 m in Baltimore Canyon to a sequential extraction procedure, isolating nonpolar and polar lipid classes, an acid-soluble fraction, and an acid-insoluble fraction. Each class was analyzed for carbon and nitrogen quantities and stable isotope ratios, and radiocarbon content where possible, along with compound-specific carbon and nitrogen isotope analysis of individual amino acids in the acid-hydrolysed fraction. We find different organic matter sources and depositional history recorded in the properties of younger, bioavailable organic matter components (polar lipids, amino acids) in comparison to the older, more recalcitrant components (nonpolar lipids, acid-insoluble fraction). These differences in source and bioavailability of organic matter vary along the canyon, correlating with grain size and erosion/deposition dynamics, and may help shape the benthic faunal assemblages. Additionally, our results suggest that determining the relative concentrations of acid-soluble and acid-insoluble organic matter may provide an easily accessible method to improve our understanding of the nutritional quality of sediments for benthic fauna than more commonly used bulk carbon or nitrogen concentrations.

Delaware, New Jersey↗

USGS2024

Design, development, and implementation of IsoBank: A centralized repository for isotopic data

Stable isotope data have made pivotal contributions to nearly every discipline of the physical and natural sciences. As the generation and application of stable isotope data continues to grow exponentially, so does the need for a unifying data repository to improve accessibility and promote collaborative engagement. This paper provides an overview of the design, development, and implementation of IsoBank , a community-driven initiative to create an open-access repository for stable isotope data implemented online in 2021. A central goal of IsoBank is to provide a web-accessible database supporting interdisciplinary stable isotope research and educational opportunities. To achieve this goal, we convened a multi-disciplinary group of over 40 analytical experts, stable isotope researchers, database managers, and web developers to collaboratively design the database. This paper outlines the main features of IsoBank and provides a focused description of the core metadata structure. We present plans for future database and tool development and engagement across the scientific community. These efforts will help facilitate interdisciplinary collaboration among the many users of stable isotopic data while also offering useful data resources and standardization of metadata reporting across eco-geoinformatics landscapes.

PLoS ONE↗

USGS2021

New geochemical tools for investigating resource and energy functions at deep-sea cold seeps using amino-acid δ15N in chemosymbiotic mussels (Bathymodiolus childressi)

In order to reconstruct the ecosystem structure of chemosynthetic environments in the fossil record, geochemical proxies must be developed. Here, we present a suite of novel compound-specific isotope parameters for tracing chemosynthetic production with a focus on understanding nitrogen dynamics in deep-sea cold seep environments. We examined the chemosymbiotic bivalve Bathymodiolus childressi from three geographically distinct seep sites on the NE Atlantic Margin and compared isotope data to non-chemosynthetic littoral mussels to test whether water depth, seep activity, and/or mussel bed size are linked to differences in chemosynthetic production. The bulk isotope analysis of carbon (δ 13 C) and nitrogen (δ 15 N), and δ 15 N values of individual amino acids (δ 15 N AA ) in both gill and muscle tissues, as well as δ 15 N AA- derived parameters including trophic level (TL), baseline δ 15 N value (δ 15 N Phe ), and a microbial resynthesis index (Σ V ), were used to investigate specific geochemical signatures of chemosynthesis. Our results show that δ 15 N AA values provide a number of new proxies for relative reliance on chemosynthesis, including TL, ∑V, and both δ 15 N values and molar percentages (Gly/Glu mol% index) of specific AA. Together, these parameters suggested that relative chemoautotrophy is linked to both degree of venting from seeps and mussel bed size. Finally, we tested a Bayesian mixing model using diagnostic AA δ 15 N values, showing that percent contribution of chemoautotrophic versus heterotrophic production to seep mussel nutrition can be directly estimated from δ 15 N AA values. Our results demonstrate that δ 15 N AA analysis can provide a new set of geochemical tools to better understand mixotrophic ecosystem function and energetics, and suggest extension to the study of ancient chemosynthetic environments in the fossil record.

Geobiology↗

USGS2020

Molecular indicators of methane metabolisms at cold seeps along the United States Atlantic margin

A lipid biomarker study was undertaken to determine the microbial composition and variability in authigenic carbonates and associated soft bottom habitats from the Norfolk and the Baltimore Canyon seep fields along the US mid-Atlantic margin. Results from this study capture a distinct molecular signal from methane oxidizing archaea, including archaeol (I), sn-2-hydroxyarchaeol, pentamethylicosane (PMI), and crocetane. These consortia of methane-oxidizing Archaea have been identified as carrying out anaerobic oxidation of methane (AOM), thereby favoring the precipitation of methane derived authigneic carbonates. The carbon isotope (δ13C) values of AOM-related lipids were strongly depleted in 13C, (i.e., archaeol: -91.64 ‰, sn-2-hydroxyarchaeol: -129.18 ‰, pentamethylicosane (PMI); -131.36 ‰, and crocetane: -70.94 ‰), confirming the dominance of methane as the dominant carbon source for the Archaea during AOM fractionation. The presence of terminally branched fatty acids such as the antesio- and iso-C15:0 components, diagnostic of sulfate-reducing bacteria (SRB), and their depleted δ13C signature (-107.6 ‰), supports syntrophy of SRB with methane-oxidizing archaea. While lipid biomarker profiles of authigenic carbonates biomarker are similar to those found in the seep sediment, suggesting a similar microbial assemblage within the seep-microbiome, a range in lipid composition, distribution, and isotopic signature between seep sites and matrix type suggests AOM is performed by multiple archaeal sources, instead of a single archaeal species.

Atlantic margin↗

USGS2017

Perspectives on chemical oceanography in the 21st century: Participants of the COME ABOARD Meeting examine aspects of the field in the context of 40 years of DISCO

The questions that chemical oceanographers prioritize over the coming decades, and the methods we use to address these questions, will define our field's contribution to 21st century science. In recognition of this, the U.S. National Science Foundation and National Oceanic and Atmospheric Administration galvanized a community effort (the Chemical Oceanography MEeting: A BOttom-up Approach to Research Directions, or COME ABOARD) to synthesize bottom-up perspectives on selected areas of research in Chemical Oceanography. Representing only a small subset of the community, COME ABOARD participants did not attempt to identify targeted research directions for the field. Instead, we focused on how best to foster diverse research in Chemical Oceanography, placing emphasis on the following themes: strengthening our core chemical skillset; expanding our tools through collaboration with chemists, engineers, and computer scientists; considering new roles for large programs; enhancing interface research through interdisciplinary collaboration; and expanding ocean literacy by engaging with the public. For each theme, COME ABOARD participants reflected on the present state of Chemical Oceanography, where the community hopes to go and why, and actionable pathways to get there. A unifying concept among the discussions was that dissimilar funding structures and metrics of success may be required to accommodate the various levels of readiness and stages of knowledge development found throughout our community. In addition to the science, participants of the concurrent Dissertations Symposium in Chemical Oceanography (DISCO) XXV, a meeting of recent and forthcoming Ph.D. graduates in Chemical Oceanography, provided perspectives on how our field could show leadership in addressing long-standing diversity and early-career challenges that are pervasive throughout science. Here we summarize the COME ABOARD Meeting discussions, providing a synthesis of reflections and perspectives on the field.

Marine Chemistry↗