Self-similarity and vanishing diffusion in fluvial landscapes.

Complex topographies exhibit universal properties when fluvial erosion dominates landscape evolution over other geomorphological processes. Similarly, we show that the solutions of a minimalist landscape evolution model display invariant behavior as the impact of soil diffusion diminishes compared to fluvial erosion at the landscape scale, yielding complete self-similarity with respect to a dimensionless channelization index. Approaching its zero limit, soil diffusion becomes confined to a region of vanishing area and large concavity or convexity, corresponding to the locus of the ridge and valley network. We demonstrate these results using one dimensional analytical solutions and two dimensional numerical simulations, supported by real-world topographic observations. Our findings on the landscape self-similarity and the localized diffusion resemble the self-similarity of turbulent flows and the role of viscous dissipation. Topographic singularities in the vanishing diffusion limit are suggestive of shock waves and singularities observed in nonlinear complex systems.

Minimizing the impacts of the ammonia economy on the nitrogen cycle and climate.

Ammonia (NH3) is an attractive low-carbon fuel and hydrogen carrier. However, losses and inefficiencies across the value chain could result in reactive nitrogen emissions (NH3, NOx, and N2O), negatively impacting air quality, the environment, human health, and climate. A relatively robust ammonia economy (30 EJ/y) could perturb the global nitrogen cycle by up to 65 Mt/y with a 5% nitrogen loss rate, equivalent to 50% of the current global perturbation caused by fertilizers. Moreover, the emission rate of nitrous oxide (N2O), a potent greenhouse gas and ozone-depleting molecule, determines whether ammonia combustion has a greenhouse footprint comparable to renewable energy sources or higher than coal (100 to 1,400 gCO2e/kWh). The success of the ammonia economy hence hinges on adopting optimal practices and technologies that minimize reactive nitrogen emissions. We discuss how this constraint should be included in the ongoing broad engineering research to reduce environmental concerns and prevent the lock-in of high-leakage practices.

Nano- to Global-Scale Uncertainties in Terrestrial Enhanced Weathering.

Enhanced weathering (EW) is one of the most promising negative emissions technologies urgently needed to limit global warming to at least below 2 °C, a goal recently reaffirmed at the UN Global Climate Change conference (i.e., COP26). EW relies on the accelerated dissolution of crushed silicate rocks applied to soils and is considered a sustainable solution requiring limited technology. While EW has a high theoretical potential of sequestering CO2, research is still needed to provide accurate estimates of carbon (C) sequestration when applying different silicate materials across distinct climates and major soil types in combination with a variety of plants. Here we elaborate on fundamental advances that must be addressed before EW can be extensively adopted. These include identifying the most suitable environmental conditions, improving estimates of field dissolution rates and efficacy of CO2 removal, and identifying alternative sources of silicate materials to meet future EW demands. We conclude with considerations on the necessity of integrated modeling-experimental approaches to better coordinate future field experiments and measurements of CO2 removal, as well as on the importance of seamlessly coordinating EW with cropland and forest management.

The Carbon-Capture Efficiency of Natural Water Alkalinization: Implications For Enhanced weathering.

Enhanced weathering (EW) is a promising negative-emission technology that artificially accelerates the dissolution of natural minerals, promotes biomass growth, and alleviates the acidification of soils and natural waters. EW aims to increase the alkalinity of natural waters (alkalinization) to promote a transfer of CO2 from the atmosphere to the water. Here we provide a quantification of the alkalinization carbon-capture efficiency (ACE) as a function of the water chemistry. ACE can be used for any alkaline mineral in various natural waters. We show that ACE strongly depends on the water pH, with a sharp transition from minimum to maximum in a narrow interval of pH values. We also quantify ACE in three compartments of the land-to-ocean aquatic continuum: the world topsoils, the lakes of an acid-sensitive area, and the global surface ocean. The results reveal that the efficiency of terrestrial EW varies markedly, from 0 to 100 %, with a significant trade-off in acidic conditions between carbon-capture efficiency and enhanced chemical dissolution. The efficiency is more stable in the ocean, with a typical value of around 80 % and a latitudinal pattern driven by differences in seawater temperature and salinity. Our results point to the importance of an integrated hydrological and biogeochemical theory to assess the fate of the weathering products across the aquatic continuum from land to ocean.

Risk of the hydrogen economy for atmospheric methane.

Hydrogen (H2) is expected to play a crucial role in reducing greenhouse gas emissions. However, hydrogen losses to the atmosphere impact atmospheric chemistry, including positive feedback on methane (CH4), the second most important greenhouse gas. Here we investigate through a minimalist model the response of atmospheric methane to fossil fuel displacement by hydrogen. We find that CH4 concentration may increase or decrease depending on the amount of hydrogen lost to the atmosphere and the methane emissions associated with hydrogen production. Green H2 can mitigate atmospheric methane if hydrogen losses throughout the value chain are below 9 ± 3%. Blue H2 can reduce methane emissions only if methane losses are below 1%. We address and discuss the main uncertainties in our results and the implications for the decarbonization of the energy sector.

Concentration Fluctuations from Localized Atmospheric Releases.

We review the efforts made by the scientific community in more than seventy years to elucidate the behaviour of concentration fluctuations arising from localized atmospheric releases of dynamically passive and non-reactive scalars. Concentration fluctuations are relevant in many fields including the evaluation of toxicity, flammability, and odour nuisance. Characterizing concentration fluctuations requires not just the mean concentration but also at least the variance of the concentration in the location of interest. However, for most purposes the characterization of the concentration fluctuations requires knowledge of the concentration probability density function (PDF) in the point of interest and even the time evolution of the concentration. We firstly review the experimental works made both in the field and in the laboratory, and cover both point sources and line sources. Regarding modelling approaches, we cover analytical, semi-analytical, and numerical methods. For clarity of presentation we subdivide the models in two groups, models linked to a transport equation, which usually require a numerical resolution, and models mainly based on phenomenological aspects of dispersion, often providing analytical or semi-analytical relations. The former group includes: large-eddy simulations, Reynolds-averaged Navier-Stokes methods, two-particle Lagrangian stochastic models, PDF transport equation methods, and heuristic Lagrangian single-particle methods. The latter group includes: fluctuating plume models, semi-empirical models for the concentration moments, analytical models for the concentration PDF, and concentration time-series models. We close the review with a brief discussion highlighting possible useful additions to experiments and improvements to models.