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Arthur J. Gold

Publications and source records attributed to Arthur J. Gold.

4 recordsLinked to original sources

Influence of land use and hydrologic variability on seasonal dissolved organic carbon and nitrate export: Insights from a multi-year regional analysis for the northeastern USA

Land use/land cover (LULC) change has significant impacts on nutrient loading to aquatic systems and has been linked to deteriorating water quality globally. While many relationships between LULC and nutrient loading have been identified, characterization of the interaction between LULC, climate (specifically variable hydrologic forcing) and solute export across seasonal and interannual time scales is needed to understand the processes that determine nutrient loading and responses to change. Recent advances in high-frequency water quality sensors provide opportunities to assess these interannual relationships with sufficiently high temporal resolution to capture the unpredictable, short-term storm events that likely drive important export mechanisms for dissolved organic carbon (DOC) and nitrate (NO 3 − –N). We deployed a network of in situ sensors in forested, agricultural, and urban watersheds across the northeastern United States. Using 2 years of high-frequency sensor data, we provide a regional assessment of how LULC and hydrologic variability affected the timing and magnitude of dissolved organic carbon and nitrate export, and the status of watershed fluxes as either supply or transport controlled. Analysis of annual export dynamics revealed systematic differences in the timing and magnitude of DOC and NO 3 − –N delivery among different LULC classes, with distinct regional similarities in the timing of DOC and NO 3 − –N fluxes from forested and urban watersheds. Conversely, export dynamics at agricultural sites appeared to be highly site-specific, likely driven by local agricultural practices and regulations. Furthermore, the magnitude of solute fluxes across watersheds responded strongly to interannual variability in rainfall, suggesting a high degree of hydrologic control over nutrient loading across the region. Thus, there is strong potential for climate-driven changes in regional hydrologic cycles to drive variation in the magnitude of downstream nutrient fluxes, particularly in watersheds where solute supply and/or transport has been modified.

Delaware, Rhode Island, Vermont

A multiscale approach to balance trade-offs among dam infrastructure, river restoration, and cost

Aging infrastructure and growing interests in river restoration have led to a substantial rise in dam removals in the U.S. However, the decision to remove a dam involves many complex trade-offs. The benefits of dam removal for hazard reduction and ecological restoration are potentially offset by the loss of hydroelectricity production, water supply, and other important services. We use a multi-objective approach to examine a wide array of trade-offs and synergies involved with strategic dam removal at three spatial scales in New England. We find that increasing the scale of decision-making improves the efficiency of trade-offs among ecosystem services, river safety, and economic costs resulting from dam removal, but this may lead to heterogeneous and less equitable local-scale outcomes. Our model may help facilitate multilateral funding, policy, and stakeholder agreements by analyzing the trade-offs of coordinated dam decisions, including net benefit alternatives to dam removal, at scales that satisfy these agreements.

New England

Watershed ‘chemical cocktails’: forming novel elemental combinations in Anthropocene fresh waters

In the Anthropocene, watershed chemical transport is increasingly dominated by novel combinations of elements, which are hydrologically linked together as ‘chemical cocktails.’ Chemical cocktails are novel because human activities greatly enhance elemental concentrations and their probability for biogeochemical interactions and shared transport along hydrologic flowpaths. A new chemical cocktail approach advances our ability to: trace contaminant mixtures in watersheds, develop chemical proxies with high-resolution sensor data, and manage multiple water quality problems. We explore the following questions: (1) Can we classify elemental transport in watersheds as chemical cocktails using a new approach? (2) What is the role of climate and land use in enhancing the formation and transport of chemical cocktails in watersheds? To address these questions, we first analyze trends in concentrations of carbon, nutrients, metals, and salts in fresh waters over 100 years. Next, we explore how climate and land use enhance the probability of formation of chemical cocktails of carbon, nutrients, metals, and salts. Ultimately, we classify transport of chemical cocktails based on solubility, mobility, reactivity, and dominant phases: (1) sieved chemical cocktails (e.g., particulate forms of nutrients, metals and organic matter); (2) filtered chemical cocktails (e.g., dissolved organic matter and associated metal complexes); (3) chromatographic chemical cocktails (e.g., ions eluted from soil exchange sites); and (4) reactive chemical cocktails (e.g., limiting nutrients and redox sensitive elements). Typically, contaminants are regulated and managed one element at a time, even though combinations of elements interact to influence many water quality problems such as toxicity to life, eutrophication, infrastructure corrosion, and water treatment. A chemical cocktail approach significantly expands evaluations of water quality signatures and impacts beyond single elements to mixtures. High-frequency sensor data (pH, specific conductance, turbidity, etc.) can serve as proxies for chemical cocktails and improve real-time analyses of water quality violations, identify regulatory needs, and track water quality recovery following storms and extreme climate events. Ultimately, a watershed chemical cocktail approach is necessary for effectively co-managing groups of contaminants and provides a more holistic approach for studying, monitoring, and managing water quality in the Anthropocene.

Biogeochemistry