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Fenix Garcia-Tigreros

Publications and source records attributed to Fenix Garcia-Tigreros.

9 recordsLinked to original sources

Arctic-boreal lakes of interior Alaska dominated by contemporary carbon

Northern high-latitude lakes are critical sites for carbon processing and serve as potential conduits for the emission of permafrost-derived carbon and greenhouse gases. However, the fate and emission pathways of permafrost carbon in these systems remain uncertain. Here, we used the natural abundance of radiocarbon to identify and trace the predominant sources of methane, carbon dioxide, dissolved inorganic and organic carbon in nine lakes within the Yukon Flats National Wildlife Refuge in interior Alaska, a discontinuous permafrost region with high landscape heterogeneity and susceptibility to climate, permafrost, and hydrological changes. We find that although Yukon Flats lakes primarily process young carbon (modern to 1290 ± 60 years before present), permafrost-derived carbon is present in some of the sampled lakes and contributes, at most, 30 ± 10% of the dissolved carbon in lake surface waters. Apportionment of young carbon and legacy carbon (carbon with radiocarbon age ⩾5000 years before present) is decoupled among the dissolved inorganic and organic carbon species, with methane showing a stronger legacy signature. Our observations suggest that permafrost-thaw-related transport of carbon through Yukon Flats lacustrine ecosystems and into the atmosphere is small, and likely regulated by surficial sediments, permafrost distribution, wildfire occurrence, or masked by contemporary carbon processes. The heterogeneity of lakes across our study area and northern landscapes more broadly cautions against using any one region (e.g. Yedoma permafrost lakes) to upscale their contribution across the pan-Arctic.

Alaska

High voltage: The molecular properties of redox-active dissolved organic matter in northern high-latitude lakes

Redox-active functional groups in dissolved organic matter (DOM) are crucial for microbial electron transfer and methane emissions. However, the extent of aquatic DOM redox properties across northern high-latitude lakes and their relationships with DOM composition have not been thoroughly described. We quantified electron donating capacity (EDC) and electron accepting capacity (EAC) in lake DOM from Canada to Alaska and assessed their relationships with parameters from absorbance, fluorescence, and ultrahigh resolution mass spectrometry (FT-ICR MS) analyses. EDC and EAC are strongly tied to aromaticity and negatively related to aliphaticity and protein-like content. Redox-active formulae spanned a range of aromaticity, including highly unsaturated phenolic formulae, and correlated negatively with many aliphatic N and S-containing formulae. This distribution illustrates the compositional diversity of redox-sensitive functional groups and their sensitivity to ecosystem properties such as local hydrology and residence time. Finally, we developed a reducing index ( RI ) to predict EDC in aquatic DOM from FT-ICR MS spectra and assessed its robustness using riverine DOM. As the hydrology of the northern high-latitudes continues to change, we expect differences in the quantity and partitioning of EDC and EAC within these lakes, which have implications for local water quality and methane emissions.

Environmental Science & Technology

Quantification of wetland vegetation communities features with airborne AVIRIS-NG, UAVSAR, and UAV LiDAR data in Peace-Athabasca Delta

Arctic-boreal wetlands, important ecosystems for biodiversity and ecological services, are experiencing hydrological changes including permafrost thaw, earlier snowmelt, and increased wildfire susceptibility. These changes are affecting wetland productivity, species diversity, and biogeochemical cycles. However, given the diverse forms and structures of wetland vegetation communities, traditional wetland maps generated from lower spatial and spectral resolution satellite imagery lack community-level vegetation classification and miss spatially complex patterns. In this study, we built a cloud-based workflow to map wetland vegetation community of the Peace-Athabasca Delta (PAD), Canada, by leveraging high-resolution (5-m) airborne multi-sensor datasets, namely NASA's Airborne Visible/Infrared Imaging Spectrometer-Next Generation (AVIRIS-NG) and Uninhabited Aerial Vehicle Synthetic Aperture Radar (UAVSAR), and a historical LiDAR archive. Validation of our classifications using ground references indicates that classifications derived from AVIRIS-NG have higher accuracies (≥87.9%) than either UAVSAR (65.6%) or LiDAR (75.9%) for mapping wetland vegetation communities. We also show improved classification accuracy when combining information from multiple sensors. In particular, incorporating AVIRIS-NG and UAVSAR datasets substantially reduced omission errors of wet graminoid and wet shrub classes from 29.6% to 20.5% and from 10.8% to 7.5%, respectively. Combining AVIRIS-NG and LiDAR datasets further improves overall accuracy (+2.2%) for most classifications, especially emergent vegetation, wet graminoid, and wet shrub. The best performing model, using features derived from all three sensors, achieved an overall accuracy of 93.5%. The framework established here can be used to leverage extensive airborne AVIRIS-NG and UAVSAR datasets collected across Alaska and northwest Canada to understand the spatial distribution of Arctic-Boreal wetland vegetation communities.

Remote Sensing of Environment

Hydrologic and landscape controls on dissolved organic matter composition across western North American Arctic lakes

Northern high-latitude lakes are hotspots for cycling dissolved organic carbon (DOC) inputs from allochthonous sources to the atmosphere. However, the spatial distribution of lake dissolved organic matter (DOM) is largely unknown across Arctic-boreal regions with respect to the surrounding landscape. We expand on regional studies of northern high-latitude DOM composition by integrating DOC concentrations, optical properties, and molecular-level characterization from lakes spanning the Canadian Taiga to the Alaskan Tundra. Lakes were sampled during the summer from July to early September to capture the growing season. DOM became more optically processed and molecular-level aromaticity increased northward across the Canadian Shield to the southern Arctic and from interior Alaska to the Tundra, suggesting relatively greater DOM incorporation from allochthonous sources. Using water isotopes (δ 18 O-H 2 O), we report a weak overall trend of increasing DOC and decreasing aromaticity in lakes that were hydrologically isolated from the landscape and enriched in δ 18 O-H 2 O, while within-region trends were stronger and varied depending on the landscape. Finally, DOC correlated weakly with chromophoric dissolved organic matter (CDOM) across the study sites, suggesting that autochthonous and photobleached DOM were a major component of the DOC in these regions; however, some of the northernmost and wetland-dominated lakes followed pan-Arctic riverine DOC-CDOM relationships, indicating strong contributions from allochthonous inputs. As many lakes across the North American Arctic are experiencing changes in temperature and precipitation, we expect the proportions of allochthonous and autochthonous DOM to respond with aquatic optical browning with greater landscape connectivity and more internally produced DOM in hydrologically isolated lakes.

Global Biogeochemical Cycles

The importance of lake emergent aquatic vegetation for estimating Arctic-boreal methane emissions

Areas of lakes that support emergent aquatic vegetation emit disproportionately more methane than open water but are under-represented in upscaled estimates of lake greenhouse gas emissions. These shallow areas are typically less than ∼1.5 m deep and can be detected with synthetic aperture radar (SAR). To assess the importance of lake emergent vegetation (LEV) zones to landscape-scale methane emissions, we combine airborne SAR mapping with field measurements of vegetated and open-water methane flux. First, we use Uninhabited Aerial Vehicle SAR data from the NASA Arctic-Boreal Vulnerability Experiment to map LEV in 4,572 lakes across four Arctic-boreal study areas and find it comprises ∼16% of lake area, exceeding previous estimates, and exhibiting strong regional differences (averaging 59 [50–68]%, 22 [20–25]%, 1.0 [0.8–1.2]%, and 7.0 [5.0–12]% of lake areas in the Peace-Athabasca Delta, Yukon Flats, and northern and southern Canadian Shield, respectively). Next, we account for these vegetated areas through a simple upscaling exercise using paired methane fluxes from regions of open water and LEV. After excluding vegetated areas that could be accounted for as wetlands, we find that inclusion of LEV increases overall lake emissions by 21 [18–25]% relative to estimates that do not differentiate lake zones. While LEV zones are proportionately greater in small lakes, this relationship is weak and varies regionally, underscoring the need for methane-relevant remote sensing measurements of lake zones and a consistent criterion for distinguishing wetlands. Finally, Arctic-boreal lake methane upscaling estimates can be improved with more measurements from all lake zones.

Journal of Geophysical Research: Biogeosciences

Estimating the impact of seep methane oxidation on ocean pH and dissolved inorganic radiocarbon along the U.S. mid‐Atlantic Bight

Ongoing ocean warming can release methane (CH 4 ) currently stored in ocean sediments as free gas and gas hydrates. Once dissolved in ocean waters, this CH 4 can be oxidized to carbon dioxide (CO 2 ). While it has been hypothesized that the CO 2 produced from aerobic CH 4 oxidation could enhance ocean acidification, a previous study conducted in Hudson Canyon shows that CH 4 oxidation has a small short‐term influence on ocean pH and dissolved inorganic radiocarbon. Here we expand upon that investigation to assess the impact of widespread CH 4 seepage on CO 2 chemistry and possible accumulation of this carbon injection along 234 km of the U.S. Mid‐Atlantic Bight. Consistent with the estimates from Hudson Canyon, we demonstrate that a small fraction of ancient CH 4 ‐derived carbon is being assimilated into the dissolved inorganic radiocarbon (mean fraction of 0.5 ± 0.4 %). The areas with the highest fractions of ancient carbon coincide with elevated CH 4 concentration and active gas seepage. This suggests that aerobic CH 4 oxidation has a greater influence on the dissolved inorganic pool in areas where CH 4 concentrations are locally elevated, instead of displaying a cumulative effect downcurrent from widespread groupings of CH 4 seeps. An upper limit approximation of the input rate of ancient‐derived DIC into the waters overlying the northern U. S Mid‐Atlantic Bight further suggests that oxidation of ancient CH 4 ‐derived carbon is not negligible on the global scale and could contribute to deep‐water acidification over longer time scales.

Journal of Geophysical Research- Biogeosciences

Limited contribution of ancient methane to surface waters of the U.S. Beaufort Sea shelf

In response to warming climate, methane can be released to Arctic Ocean sediment and waters from thawing subsea permafrost and decomposing methane hydrates. However, it is unknown whether methane derived from this sediment storehouse of frozen ancient carbon reaches the atmosphere. We quantified the fraction of methane derived from ancient sources in shelf waters of the U.S. Beaufort Sea, a region that has both permafrost and methane hydrates and is experiencing significant warming. Although the radiocarbon-methane analyses indicate that ancient carbon is being mobilized and emitted as methane into shelf bottom waters, surprisingly, we find that methane in surface waters is principally derived from modern-aged carbon. We report that at and beyond approximately the 30-m isobath, ancient sources that dominate in deep waters contribute, at most, 10 ± 3% of the surface water methane. These results suggest that even if there is a heightened liberation of ancient carbon–sourced methane as climate change proceeds, oceanic oxidation and dispersion processes can strongly limit its emission to the atmosphere.

Science Advances

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

Enhanced transfer of terrestrially derived carbon to the atmosphere in a flooding event

Rising CO 2 concentration in the atmosphere, global climate change, and the sustainability of the Earth's biosphere are great societal concerns for the 21st century. Global climate change has, in part, resulted in a higher frequency of flooding events, which allow for greater exchange between soil/plant litter and aquatic carbon pools. Here we demonstrate that the summer 2011 flood in the Mississippi River basin, caused by extreme precipitation events, resulted in a “flushing” of terrestrially derived dissolved organic carbon (TDOC) to the northern Gulf of Mexico. Data from the lower Atchafalaya and Mississippi rivers showed that the DOC flux to the northern Gulf of Mexico during this flood was significantly higher than in previous years. We also show that consumption of radiocarbon-modern TDOC by bacteria in floodwaters in the lower Atchafalaya River and along the adjacent shelf contributed to northern Gulf shelf waters changing from a net sink to a net source of CO 2 to the atmosphere in June and August 2011. This work shows that enhanced flooding, which may or may not be caused by climate change, can result in rapid losses of stored carbon in soils to the atmosphere via processes in aquatic ecosystems.

Geophysical Research Letters