Elevated ammonium (NH-N) contents in groundwater are a global concern, yet the mobilization and enrichment mechanisms controlling NH-N within riverside aquifers (RAS) remain poorly understood. RAS are important zones for nitrogen cycling and play a vital role in regulating groundwater NH-N contents. This study conducted an integrated assessment of a hydrochemistry dataset using a combination of hydrochemical analyses and multivariate geostatistical methods to identify hydrochemical compositions and NH-N distribution in the riverside aquifer within Central Yangtze River Basin, ultimately elucidating potential NH-N sources and factors controlling NH-N enrichment in groundwater ammonium hotspots. Compared to rivers, these hotspots exhibited extremely high levels of NH-N (5.26 mg/L on average), which were mainly geogenic in origin. The results indicated that N-containing organic matter (OM) mineralization, strong reducing condition in groundwater and release of exchangeable NH-N in sediment are main factors controlling these high concentrations of NH-N. The Eh representing redox state was the dominant variable affecting NH-N contents (50.17 % feature importance), with Fe and dissolved organic carbon (DOC) representing OM mineralization as secondary but important variables (26 % and 5.11 % feature importance, respectively). This study proposes a possible causative mechanism for the formation of these groundwater ammonium hotspots in RAS. Larger NH-N sources through OM mineralization and greater NH-N storage under strong reducing condition collectively drive NH-N enrichment in the riverside aquifer. The evolution of depositional environment driven by palaeoclimate and the unique local environment within the RAS likely play vital roles in this process.
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http://dx.doi.org/10.1016/j.scitotenv.2024.176094 | DOI Listing |
Front Genet
December 2024
Agricultural Research Council, Biotechnology Platform, Pretoria, South Africa.
Indigenous chickens are an important Farm Animal Genetic Resource (FAnGR) in South Africa as they alleviate poverty and are a source of protein. Climate change and market demand for high-performing exotic breeds threaten and undermine locally adapted village chickens. The current study explored the risk status and signatures of adaptation of village-based indigenous chickens from two provinces and mapped their environmental suitability across the country.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
December 2024
Department of Chemistry, National Institute of Technology-Tiruchirappalli, Tamil Nadu 620015, India. Electronic address:
R - C(S) - NH - N = CH - R [R = o-OCHCH & R = CHN (2-EBP), R = o-OCHCH & R = CHNO (2-EBM), R = p-OCHCH & R = CHN (4-EBP), and R = p-OCHCH & R = CHNO (4-EBM)] have been synthesized. The ligands have been verified via various spectroscopic methods such as IR, NMR, etc. Single-crystal X-ray diffraction methods were applied to identify the structure of 4-EBP.
View Article and Find Full Text PDFLang Cogn Neurosci
June 2024
Department of Psychological & Brain Sciences, Department of Communication Sciences & Disorders, Department of Otolaryngology - Head and Neck Surgery, Department of Linguistics, University of Iowa.
During word recognition, listeners must quickly map sounds to meaning, while suppressing similar sounding competitors. It remains an open question whether domain-general inhibitory control is recruited for resolving lexical competition. Cochlear implant (CI) users present a unique population for addressing this question because they are consistently confronted with degraded auditory input, and therefore may need to rely on domain-general mechanisms to compensate.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Chemistry, Wayne State University, Detroit, Michigan 48202, United States.
The development of small-molecule catalysts that can effectively activate both reacting partners simultaneously represents a pivotal pursuit in advancing the field of stereoselective glycosylation reactions. We report herein the development of the singly protonated form of readily available phenanthroline as an effective cooperative catalyst that facilitates the coupling of a wide variety of aliphatic alcohols, phenols, and aromatic amines with α-glycosyl trichloroacetimidate donors. The glycosylation reaction likely proceeds via an S2-like mechanism, generating β-selective glycoside products.
View Article and Find Full Text PDFJ Chem Phys
November 2024
Departamento de Física de la Materia Condensada, GIyA, CAC-CNEA, 1650 San Martín, Buenos Aires, Argentina, Instituto de Nanociencia y Nanotecnología, CNEA-CONICET, Buenos Aires, Argentina.
In this study, we present results from path integral molecular dynamics simulations that describe the characteristics of the quantum spatial delocalizations of protons participating in OH bonds in (MeOH)2H+ and in (MeOH)3H+. The characterization was carried out by examining the overall structures of the corresponding isomorphic polymers. To introduce full flexibility in the force treatment, we have adopted a neural network fitting procedure based on second-order Møller-Plesset perturbation theory predictions.
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