Energy Sciences

Chronic groundwater overdraft threatens agricultural sustainability in California's Central Valley. Diverting flood flows onto farmland for groundwater recharge offers an opportunity to help address this challenge. We studied the infiltration rate of floodwater diverted from the Kings River at a turnout upstream of the James Weir onto adjoining cropland; and calculated how much land would be necessary to capture the available floodwater, how much recharge of groundwater might be achieved, and the costs. The 1,000-acre pilot study included fields growing tomatoes, wine grapes, alfalfa and pistachios. Flood flows diverted onto vineyards infiltrated at an average rate of 2.5 inches per day under sustained flooding. At that relatively high infiltration rate, 10 acres are needed to capture one CFS of diverted flood flow. We considered these findings in the context of regional expansion. Based upon a 30-year record of Kings Basin surplus flood flows, we estimate 30,000 acres operated for on-farm flood recharge would have had the capacity to capture 80% of available flood flows and potentially offset overdraft rates in the Kings Basin. Costs of on-farm flood capture for this study were estimated at $36 per acre-foot, less than the cost for surface water storage and dedicated recharge basins.

Field research and grower interviews were used to evaluate the potential of minimum tillage for California rice systems. We found that by tilling only in the fall (instead of both the fall and spring), rice farmers can control herbicide-resistant weeds when combined with a stale rice seedbed, which entails spring flooding to germinate weeds followed by a glyphosate application to kill them. Our results indicated that yield potentials are comparable between water-seeded minimum- and conventional-till systems. We also found that rice growers can reduce fuel costs and plant early. However, minimum tillage may require more nitrogen fertilizer to achieve these yields.

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New gene editing technologies give us the potential ability to bring back extinct species, help control the spread of invasive ones, and genetically modify those that spread diseases. They allows us to not only influence the evolutionary path of entire species, but entire ecosystems as well. Furthermore, gene editing has the potential to help us live healthier and longer lives. We have moved past rudimentary macroscopic methods of DNA manipulation and can now remove individual genes from a strand of DNA. However, due to the complexity of this technology, and given that there are few who can use it to its full effect, people have largely failed to respond to its development, particularly regulators. It is not within the scope of this paper to explore the full implications of these various emerging technologies, so instead I will focus on CRISPR, a specific new gene editing complex first used in 2012, and the major developments that have taken place since then.

Single-crystal X-ray diffraction and electron paramagnetic resonance (EPR) spectroscopic experiments, complemented by quantum chemical DFT calculations, were carried out on the copper-doped metal-organic hybrid and Tutton salt analogue zinc creatininium sulfate to determine its crystal structure, to characterize the electronic structure of the doped Cu(II) binding site, and to propose a pathway for an excited-state, proton-coupled electron transfer (PCET) process in UV-exposed crystals. The crystal structure is isomorphous to that of cadmium creatininium sulfate, which has the transition ion, not in direct coordination with the creatinine, but forming a hexahydrate complex, which is bridged to a creatininium through an intervening sulfate ion. The EPR g (2.446, 2.112, 2.082) and copper hyperfine (A^Cu: -327, -59.6, 10.8 MHz) tensor parameters are consistent with doped copper replacing host zinc in the metal-hexahydrate complex. These parameters are similar to those observed for copper hexahydrate in doped Tutton salt systems at low temperature, where the unpaired electron occupies mainly the copper 3d_x²-y² orbital. At room temperature in the Tutton systems, vibration couplings stemming from a dynamic Jahn-Teller effect cause tensor averaging which results in a reduction in their maximum g-tensor and hyperfine tensor values. However, like for the doped isomorphous Cd creatinine crystal, the Cu(II) EPR exhibits little, or no room temperature averaging compared to its low temperature pattern. Samples exposed to 254 nm UV light generate a carbon-centered free radical species, characterized by an isotropic g-tensor (g = 2.0029) and an alpha-proton hyperfine coupling (-24 -14 +4 G). These parameters identify it as a creatinine radical cation formed by the oxidative release of one of its C2 methylene hydrogens. DFT calculations confirm the unpaired electronic structures of both the Cu(II) site and free radical. The growth in radical concentration with an increase in the UV exposure time coincides with a decrease in the copper EPR signal, indicating a coupled light-induced oxidation reduction process. A comparison of the crystal structure with the EPR parameters and DFT results provides evidence for a UV-induced PCET.

Emergent magnetic phenomena at interfaces represent a frontier in materials science, pivotal for advancing technologies in spintronics and magnetic storage. In this Letter, we utilize a suite of advanced X-ray spectroscopic and scattering techniques to investigate emergent interfacial ferromagnetism in oxide superlattices composed of antiferromagnetic CaMnO₃ and paramagnetic CaRuO₃. Our findings demonstrate that ferromagnetism exhibits an asymmetric profile and may extend beyond the interfacial layer into multiple unit cells of CaMnO₃. Complementary density functional calculations reveal that the interfacial ferromagnetism is driven by the double exchange mechanism, facilitated by charge transfer from Ru to Mn ions. Additionally, defect chemistry, particularly the presence of oxygen vacancies, can play a crucial role in modifying the magnetic moments at the interface, possibly leading to the observed asymmetry between the top and bottom CaMnO₃ interfacial magnetic layers. Our findings underscore the potential of manipulating interfacial ferromagnetism through point defect engineering.

Topological surface states, protected by the global symmetry of the materials, are the keys to understanding various novel electrical, magnetic, and optical properties. TaSb2 is a newly discovered topological material with unique transport phenomena, including negative magnetoresistance and resistivity plateau, whose microscopic understanding is yet to be reached. In this study, we investigate the electronic band structure of TaSb2 using angle-resolved photoemission spectroscopy and density functional theory. Our analyses reveal distinct bulk and surface states in TaSb2, providing direct evidence of its topological nature. Notably, surface states predominate the electronic contribution near the Fermi level, while bulk bands are mostly located at higher binding energies. Our study underlines the importance of systematic investigations into the electronic structures of topological materials, offering insights into their fundamental properties and potential applications in future technologies.