Water Constituents Research Articles

Scene-cGAN: A GAN for underwater restoration and scene depth estimation

Despite their wide scope of application, the development of underwater models for image restoration and scene depth estimation is not a straightforward task due to the limited size and quality of underwater datasets, as well as variations in water colours resulting from attenuation, absorption and scattering phenomena in the water column. To address these challenges, we present an all-in-one conditional generative adversarial network (cGAN) called Scene-cGAN. Our cGAN is a physics-based multi-domain model designed for image dewatering, restoration and depth estimation. It comprises three generators and one discriminator. To train our Scene-cGAN, we use a multi-term loss function based on uni-directional cycle-consistency and a novel dataset. This dataset is constructed from RGB-D in-air images using spectral data and concentrations of water constituents obtained from real-world water quality surveys. This approach allows us to produce imagery consistent with the radiance and veiling light corresponding to representative water types. Additionally, we compare Scene-cGAN with current state-of-the-art methods using various datasets. Results demonstrate its competitiveness in terms of colour restoration and its effectiveness in estimating the depth information for complex underwater scenes.

The Effect of Salinity on the Dielectric Permittivity of Nanoconfined Geofluids.

Nanoporosity is a characteristic feature of geological formations that provides potential pathways for geofluids to meander and interact with minerals. Confinement of water within nanopores leads to unique phenomena. The dielectric constant of water becomes anisotropic and adopts tensorial properties rather than remaining a scalar value. In such nanoconfinement, it has been found that the permittivity of water decreases perpendicularly and increases parallel to the interface. As geofluids are rarely pure water in nature, being a water-salt(-gas) mixture within the Earth, it becomes pivotal to examine how these additional constituents of water affect the permittivity of fluids confined within the nanopores of rocks. In this study, we present the calculation of the permittivity of saline water in calcite slit nanopores using molecular dynamics simulations under low-pressure-temperature conditions. The dielectric properties are weakly dependent on salinity for both the perpendicular and parallel dielectric permittivity components. We analyzed the atomic charge and polarization density of the fluid perpendicular to the nanochannel walls and the orientation of water molecules' dipole inside the nanochannel. From our analysis, most of these factors were generally not altered significantly in the presence of salinity. These findings are significant because they enable us to use well-studied pure water properties under nanoconfinement to determine the geochemical behavior of fluids within natural nanoporous systems.

Seasonal and Spatial Variability of Absorption Properties in Cartagena Bay’s Complex Waters

Characterizing inherent optical properties (IOPs) of water constituents is crucial for remote sensing applications. Remote sensing in Cartagena Bay is particularly challenging due to significant variations in constituent concentrations caused by the seasonal and annual variability of discharges from the Canal del Dique. This article presents the variability in absorption coefficients of phytoplankton, chromophoric dissolved organic matter (aCDOM), and non-algal particles (aNAP) in Cartagena Bay. Absorption coefficients were measured in the laboratory across multiple monitoring campaigns, with seasonal analyses conducted to establish relationships between absorption properties and biogeochemical parameters such as chlorophyll-a, salinity, and turbidity. Results indicate that at 440 nm, aCDOM and aNAP primarily dominate absorption during the rainy season, while aNAP dominates during the dry season. This variation is influenced by inflows from the Canal del Dique. Lower CDOM absorption in 440 nm (aCDOM440), and higher CDOM absorption slope (SCDOM275–295) and higher salinity values were observed during the dry season, which is consistent with the reduced fluvial influx. Spatial variability shows that higher CDOM values prevail in the river plume area during both seasons, with particularly higher values in the rainy season. Median values of aNAP were similar in both seasons, with a strong relationship found between all aNAP data and turbidity (rp = 0.785). Compared to other estuaries, Cartagena Bay exhibits optical characteristics typical of a coastal water body subjected to river discharges, including the elevated turbidity and the high dissolved organic matter influenced by significant inflow from the Canal del Dique. These features highlight the bay’s dynamic interactions with terrestrial inputs. This study provides invaluable information on the optical characteristics of Cartagena Bay, which is crucial for improving the accuracy and effectiveness of remote sensing models for optically active parameters such as turbidity, suspended solids, CDOM, and chlorophyll-a.

Metal ions-mediated concerted electron-proton transfer enables catalytic oxidation of phenolic contaminants by permanganate

Permanganate has been extensively applied in water treatment due to its ease of handling and high stability. However, the impact of common water constituents, especially metal ions, on permanganate oxidation is poorly understood. Here, we report that many redox-inactive metal ions, such as Ca2+, Mg2+, Zn2+, Cu2+, and Al3+, can enhance the reactivity of permanganate with phenolic compounds. Moreover, the enhancing effects of metal ions are highly pH-dependent with the largest promotion effect obtained at the pH close to phenols’ pKa. Experimental and computational analysis revealed that the oxidation of protonated phenols by permanganate underwent proton-coupled electron transfer (PCET) pathways, regardless of the presence of metal ions. Nonetheless, metal ions could catalyze the concerted electron-proton transfer (CEPT) but exhibited negligible effect on ETPT (electron transfer followed by proton transfer) and PTET (proton transfer followed by electron transfer) reactions, accounting for the pH-dependent effects of metal ions. Correlation between CEPT rate constants and the complexing capability of metal ions with phenols suggested that the co-existing metal ions may coordinate to phenolic O–H group and thus facilitate the CEPT reaction of phenols. This study could shed light on the application of permanganate in real practice and the modulation of CEPT reactions.

Earth observation reveals the shifting patterns of China's lake colour driven by climate change and land cover

Water colour has been recognized as one of the most important Essential Climate Variables of the lake ecosystem, as it is directly related to changes in water constituents and almost all of the lake's ecological changes could alter water colour. Given the high retrieval accuracy from existing Earth observation satellite data, water colour, in terms of Forel Ule Index (FUI), can be a realistic indicator to track the long-term changes in the lake ecosystem and further explore the lake response to environmental changes. This paper aims to comprehensively investigate the spatiotemporal variation patterns of FUI in 159 large lakes (≥25 km2) across China during 2000–2022 based on the MODIS data and detect the climatic and anthropogenic driving forces of these changes. The 23 years of MODIS records revealed an overall downward trend of lake FUI across China, indicating the lakes in China shifted to bluer colour during the past two decades. Through driving factor analyses, the complicated interplay among lake colour, lake morphology, regional climate shifts and human interference dynamics was uncovered. In the long term, it was found the pronounced change in lake colour in the western lake zones was primarily attributed to climate warming and humidification, whereas that in the eastern lake zones was mainly related to the alterations in regional land cover during the past two decades. Seasonally, lake basin's air temperature was identified as the main factor impacting the seasonal patterns of lake colour, followed by wind speed and runoff. Spatially, there was high spatial variability in lake colour across China, which was mainly associated with lake elevation and lake basin's precipitation rate, although the factors exhibited considerable divergence across different zones. Based upon the above findings, the implications for lake environment protection and management in different regions of China were further discussed.

PREDIKSI PASANG SURUT PERAIRAN SEKITAR KOTA BITUNG DENGAN PENAMBAHAN KONSTANTA HARMONIK PERAIRAN DANGKAL

Bitung is a city with the most intensive marine space utilization activities in North Sulawesi Province. Therefore, information regarding oceanographic conditions is very important in relation to development in this city. One of the important information regarding oceanographic conditions is tides. This study was conducted with the aim of assessing the accuracy of tidal prediction with the addition of shallow water harmonic constituents and examining the amplitude fluctuations of the main harmonic component due to the addition of the shallow water constituents. The least squares method was used to calculate the amplitude and phase of tidal harmonic constituents, followed by data prediction. The data used is the measurement data of BMKG Bitung City tidal station in January, February and March 2024. The results obtained are the addition of shallow water harmonic constituents to the tidal analysis around Bitung City increases the accuracy of the prediction data. The best RMSE value for January data is 3.8323 cm; February 4.1902 cm; and March 4.2558 cm. The correlation coefficient increases and the percentage of predicted data with differences < 3 cm and < 6 cm with the observation data becomes larger. It is also found that when processing with few harmonic constituents, the amplitudes of constants M2, S2, K1, and O1 fluctuate. The addition of harmonic constituents in the analysis results in more constant amplitudes of constituents M2, S2, K1, and O1.

Assessing excimer far-UVC (222 nm) irradiation for advanced oxidation processes: Oxidants photochemistry and micropollutants degradation

The KrCl* excimer lamp (UV222) is a promising alternative of low-pressure mercury lamp (UV254) for UV-based advanced oxidation processes (UV-AOPs), because it is mercury-free and has high photon energy. But there lacks a comprehensive assessment of UV222-AOPs based on different radicals. Herein, the properties (e.g., oxidant decay and innate radical quantum yield), and micropollutant degradation, were comprehensively studied for representative oxidants (i.e., hydrogen peroxide, persulfate (PDS), monochloramine, and free active chlorine (FAC)) under UV222 irradiation. UV222 outperformed UV254 for the activation of oxidants with 2.6–14.4 times fluence-based kinetic constant (kF). The main reason of enhanced activation varied with oxidants: higher UV absorbance for H2O2, higher innate quantum yield for monochloramine and FAC, and both reasons for PDS. Overall, PDS was the optimum oxidant under UV222 for the degradation of 8 representative micropollutants because of effective promotion of radical formation, as confirmed by radical competitive kinetics and modeling simulations. In real water, UV222/PDS still show advantages than UV254/PDS in terms of micropollutant elimination efficacy (3.2–5.3 times) and energy consumption (33.9 %-57.6 % lower) though it was more inhibited by water constituents via competing for UV222 photons. This study fills gaps in photochemistry knowledge and will facilitate engineering practice of UV222-AOPs.

GC-MS Analysis of Chemical Constituents in Water and Methanol Crude Extracts of Red Sea Soft Coral Xenia macrospiculata Gohar, 1940

Soft corals are marine invertebrates known to be a prolific source of marine natural products. The genus Xenia is a rich source of bioactive compounds including terpenoids, steroids, saturated, unsaturated and poly unsaturated fatty acids. The water and methanol solvent extracts of soft coral Xenia macrospiculata Gohar, 1940 (X. macrospiculata) were screened for the novel chemical constituents using gas chromatography–mass spectroscopy (GC-MS). In the water extracts, seventeen compounds were identified including monounsaturated fatty acids (35.29%), saturated fatty acids (23.52%) followed by unsaturated fatty acids (5.88%), poly unsaturated fatty acid (5.88%), sesquiterpenoids (5.88%), aromatic compounds (5.88%), Alcohols (5.88%), thio compounds (5.88%) and pleuromutilin derivatives (5.88%). In methanol extract thirty compounds were identified, among which 30% are the poly unsaturated fatty acids (PUFA) followed by monounsaturated fatty acids (13.33%), unsaturated fatty acids (13.33%), saturated fatty acids (13.3%), sesquiterpenoids (10%), alcohols (6.66%), oxygenated heterocyclic compounds (3.33%), steroid (3.33%), organo-fluro compounds (3.33%) and aldehyde derivatives (3.33%). The GC-MS screening of water and methanol extracts of X. macrospiculata revealed the presence of several novel bioactive compounds. Fatty acids are potential nutraceutical compounds playing vital role in preventing the risk of cardiovascular disorders and fatty liver. In addition, these compounds also showed potential antioxidant activity, antimicrobial, antineoplastic, ichthyotoxic, cytotoxic, HIV-inhibitory, anti-inflammatory activity and 5α reductase inhibitory activity.

Photo-reductive decomposition of perfluorooctane sulfonate (PFOS) and its common alternatives by UV/VUV/sulfite process: Mechanism, kinetic modeling, and water matrix effects

The present study investigated the photo-reduction of perfluorooctane sulfonate (PFOS) and its alternatives, focusing on decomposition mechanisms, active species involvement, the influence of background water constituents, and kinetic model development. The decomposition and defluorination rates followed the order of PFOS > PFHxS > 6:2 FTSA > PFBS, with shorter chains and CH2 linkers enhancing the resistance of PFOS alternatives against the attack of hydrated electrons (eaq−). Two primary pathways were identified during the photodegradation of PFAS: (i) H/F exchange at CF bonds with the lowest bond dissociation energies (BDEs) and (ii) functional group cleavage followed by short-chain PFCAs formation, with OH playing a crucial role in transforming intermediates. Adding iodide and elevated temperatures demonstrated a synergistic effect on PFBS decomposition and defluorination, with high temperatures promoting functional group cleavage as the preferred defluorination pathway. The study examined the impact of background water constituents in different aqueous environments, from surface waters to wastewater streams and ion-exchange brine concentrates. Chloride exhibited a concentration-based dual impact on the UV/VUV/sulfite process: promotive effects at low dosages (1–10 mM) by acting as a secondary eaq− mediator, and adverse effects at high dosages (20–500 mM) due to the scavenging effect of generated chlorine radicals (Cl). High ionic strength adversely affected eaq− quantum efficiency. Additionally, bicarbonate and natural organic matter (NOM) had opposing effects on PFOS photo-reduction, primarily through eaq− scavenging and pH alteration. Kinetic modeling revealed reaction rate constants of the studied PFAS with eaq− ranging from 1.8 × 106 to 1.3 × 109 M−1 s−1, corroborating the concentration profiles of active species and highlighting the reductive nature of sulfite-mediated processes.

Tourmaline triggered biofilm transformation: Boosting ultrafiltration efficiency and fouling resistance

Ultralow pressure filtration system, which integrates the dual functionalities of biofilm degradation and membrane filtration, has gained significant attention in water treatment due to its superior contaminant removal efficiency. However, it is a challenge to mitigate membrane biofouling while maintaining the high activity of biofilm. This study presents a novel ceramic-based ultrafiltration membrane functionalized with tourmaline nanoparticles to address this challenge. The incorporation of tourmaline nanoparticles enables the release of nutrient elements and the generation of an electric field, which enhances the biofilm activity on the membrane surface and simultaneously alleviates intrapore biofouling. The tourmaline-modified ceramic membrane (TCM) demonstrated a significant antifouling effect, with a substantial increase in water flux by 60 %. Additionally, the TCM achieved high removal efficiencies for contaminants (48.78 % in TOC, 22.28 % in UV254, and 24.42 % in TN) after 30 days of continuous operation. The fouling resistance by various constituents in natural water was individually analyzed using model compounds. The TCM with improved electronegativity and hydrophilicity exhibited superior resistance to irreversible fouling through increased electrostatic repulsion and reduced adhesion to foulants. Comprehensive characterizations and analyses, including interfacial interaction energies, redox reaction processes, and biofilm evolutions, demonstrated that the TCM can release nutrient elements to facilitate the development of functional microbial community within the biofilm, and generate reactive oxygen species (ROS) on the membrane surface to the degrade contaminants and mitigate membrane biofouling. The electric field generated by tourmaline nanoparticles can promote electron transfer in the Fe(III)/Fe(II) cycle, ensuring a stable and sustainable generation of ROS and bactericidal negative ions. These synergistic functions enhance contaminant removal and reduce irreversible fouling of the TCM. This study provides fundamental insights into the role of tourmaline-modified surfaces in enhancing membrane filtration performance and fouling resistance, inspiring the development of high-performance, anti-fouling membranes.

Advanced green capture of microplastics from different water matrices by surface-modified magnetic nanoparticles

The extensive production and application of plastic in recent decades has resulted in the presence of microplastics (MPs) in different water bodies. Considered as contaminants of emerging concern (CECs), MPs are accessible to a wide range of organisms and can act as vectors for the transport of other persistent organic pollutants. The existing technologies to remove microplastics from wastewaters and prevent their intrusion in nature, still present several limitations, resulting in an urgent need to develop novel, fast, cost-effective and greener alternatives. In this work, the magnetophoretic capture of MPs by their assembly with magnetic nanoparticles through either electrostatic interactions or molecular forces is investigated. For the experimental assessment, magnetic nanoparticles were synthesized by hydrothermal coprecipitation and solvothermal decomposition methods, while polyethylene (PE) microspheres were selected as model microplastic pollutants. As a noteworthy novelty, thermal decomposition and coprecipitation particles were functionalized with amino groups and sodium alginate (SA), respectively, resulting in a modification of their surface properties and enhanced electrostatic or molecular interactions with MPs. After preliminary experiments, a concentration of 1.3 g L-1 and a contact time of 20 min between magnetic nanoparticles and MPs, were selected as operating conditions to assess the influence of the functional groups on the capture performance. The influence of other variables in the process was also evaluated, including the magnetic nanoparticles synthesis method, the pH of the medium, varied in the range 4–8, and the water constituents that may be present in water bodies. Results demonstrated that the presence of different types of polar groups on the surface of the magnetic nanoparticles make them interact towards MPs through electrostatic attraction or molecular forces, considerably enhancing the capture performance of bare magnetic nanoparticles. This work represents a step forward in the development of new and reliable techniques for the environmentally friendly capture of microplastics from polluted waters.

Activation of peracetic acid by electrodes using biogenic electrons: A novel energy- and catalyst-free process to eliminate pharmaceuticals

Peracetic acid (PAA) has received increasing attention as an alternative oxidant for wastewater treatment. However, existing processes for PAA activation to generate reactive species typically require external energy input (e.g., electrically and UV-mediated activation) or catalysts (e.g., Co2+), inevitably increasing treatment costs or introducing potential new contaminants that necessitate additional removal. In this work, we developed a catalyst-free, self-sustaining bioelectrochemical approach within a two-chamber bioelectrochemical system (BES), where a cathode electrode in-situ activates PAA using renewable biogenic electrons generated by anodic exoelectrogens (e.g., Geobacter) degrading biodegradable organic matter (e.g., acetic acid) in wastewater at the anode. This innovative BES-PAA technique achieved 98 % and 81 % removal of 2 µM sulfamethoxazole (SMX) in two hours at pH 2 (cation exchange membrane) and pH 6 (bipolar membrane) using 100 μM PAA without external voltage. Mechanistic studies, including radical quenching, molecular probe validation, electron spin resonance (ESR) experiments, and density functional theory (DFT) calculations, revealed that SMX degradation was driven by reactive species generated via biogenic electron-mediated OO cleavage of PAA, with CH3C(O)OO• contributing 68.1 %, •OH of 18.4 %, and CH3C(O)O• of 9.4 %, where initial formation of •OH and CH3C(O)O• rapidly reacts with PAA to produce CH3C(O)OO•. The presence of common water constituents such as anions (e.g., Cl−, NO3−, and H2PO4−) and humic acid (HA) significantly hinders SMX removal via the BES-PAA technique, whereas CO32− and HCO3− ions have a comparatively minor impact. Additionally, the study investigated the removal of various pharmaceuticals present in secondary treated municipal wastewater, attributing differences in removal efficiency to the selective action of CH3C(O)OO•. This research demonstrates a novel PAA activation method that is ecologically benign, inexpensive, and capable of overcoming catalyst deactivation and secondary pollution issues.

Impact of mineral reactions and surface complexation on the transport of dissolved species in a subterranean estuary: Application of a comprehensive reactive transport modeling approach

Subterranean estuaries (STE) are hotspots of biogeochemical reactions. Here, dissolved constituents in waters of terrestrial and marine origin are transformed before they discharge to the coastal oceans. The involved biogeochemical reactions are complex and non-linear, calling for the application of numerical reactive transport modeling (RTM) to improve the process understanding. The aim of this study was to assess the roles of organic matter degradation and coupled secondary mineral reactions for the fate of dissolved species in STEs of sandy beaches. A comprehensive RTM approach was applied for this purpose, accounting for the effects of ion activities, pH, pe, redox reactions, mineral equilibria (calcite, goethite, siderite, iron sulfide, hydroxyapatite and vivianite) as well as surface complexation. Results show that the STE biogeochemistry and associated species fluxes are very sensitive to the assumed reaction network. For example, inorganic carbon and pH were largely controlled by calcite and siderite dynamics, and dissolved Fe2+ and HS- were precipitated as goethite, siderite and/or iron sulfides. Moreover, PO43- concentrations were affected by both the formation of vivianite or hydroxyapatite as well as surface complexation. This work helped to establish the relative importance of some of the major biogeochemical processes in the STE. However, further field studies are needed to understand which processes play a role in real-world STEs, including an exploration of the deep subsurface of STEs. Such field-based observations will improve our conceptual process understanding, which is key to developing well-constrained RTMs.

A metal-free Z-scheme PPy/MCN heterojunction for antibiotic removal via synergism of photocatalysis and peroxymonosulfate activation

Developing an active and synergistic system based on photocatalysis and peroxymonosulfate (PMS) activation is considered an effective strategy for efficient removal of antibiotics. However, photocatalytic heterojunctions generally comprise metallic catalysts that can cause metal leaching and secondary pollution, and a clear understanding of the synergy between photocatalysis and PMS activation is still missing. Herein, a metal-free Z-scheme polypyrrole (PPy)/melamine-derived graphitic carbon nitride (MCN) heterojunction photocatalyst was synthesized via calcination and in-situ loading for catalyzing the degradation of ciprofloxacin (CIP) and other emerging pollutants in a visible light-emitting diode (LED)/PMS synergistic system, which showed a significantly higher activity than the single LED and PMS systems. The optimal 0.5 %PPy/MCN (0.5 % is the mass ratio of PPy in the mixture of PPy/MCN) performed well under a wide pH range (3–11), while exhibiting superior anti-interference for common water constituents and outstanding reusability and stability. The 0.5 %PPy/MCN/LED/PMS synergistic system showed the highest kinetic constant (0.0643 1/min), which increased 3.00, 6.77 and 2.91-fold over the 0.5 %PPy/MCN/PMS, 0.5 %PPy/MCN/LED, and MCN/LED/PMS system, respectively. Mechanistic investigation and theoretical calculations revealed that PPy, with its high conductivity and strong light absorption ability, facilitated the generation and separation of e−/h+ in the 0.5 %PPy/MCN/LED/PMS system and activated PMS for generating reactive species such as 1O2, which degraded cCIP together with h+. Furthermore, electron transfer pathway (ETP) was elucidated using electrochemical characterizations. CIP was degraded via ring opening, cleavage hydroxylation, ammonia oxidation and elimination reactions, which substantially reduced the toxicity of CIP. Overall, this study may help the rational design of metal-free catalysts and provide a deep insight for the LED/PMS synergistic mechanisms.

Holistic optical water type classification for ocean, coastal, and inland waters

AbstractWater constituents exhibit diverse optical properties across ocean, coastal, and inland waters, which alter their remote‐sensing reflectance obtained via satellites. Optical water type (OWT) classifications utilized in satellite data processing aim to mitigate optical complexity by identifying fitting ocean color algorithms tailored to each water type. This facilitates comprehension of biogeochemical cycles ranging from local to global scales. Previous OWT frameworks have focused narrowly on either oceanic or inland waters and have relied too heavily on specific data collections. We propose a novel holistic OWT framework applicable to all natural waters, based on state‐of‐the‐art bio‐geo‐optical modeling and radiative transfer simulations that encompass different phytoplankton groups. This framework employs a “knowledge‐driven” paradigm, combining domain knowledge and insights from previous studies to simulate the reflectance spectrum from water constituent concentrations and inherent optical properties. Our method extracts optical variables to represent the full spectrum of reflectance, consolidating both spectral shape and magnitude. We apply the framework utilizing diverse in situ, synthetic, and satellite data (Sentinel‐3 OLCI) and demonstrate its better classifiability than other frameworks. This framework lays the foundation for comprehensive global monitoring of natural waters.

MgO-loaded tubular ceramic membrane with spatial nanoconfinement for enhanced catalytic ozonation in refractory wastewater treatment

Heterogeneous catalytic ozonation (HCO) enables the destruction of organic pollutants in wastewater via oxidation by powerful hydroxyl radicals (·OH). However, the availability of short‐lived ·OH in aqueous bulk is low in practical treatment scenarios due to mass transfer limitations and quenching of water constituents. Herein, we overcome these challenges by loading MgO catalysts inside the pores of a tubular ceramic membrane (denoted as CCM) to confine ·OH within the nanopores and achieve efficient pollutant removal. When the pore size of the membrane was reduced from 1000 to 50 nm, the removal of ibuprofen (IBU) by CCM was increased from 49.6 % to 90.2 % due to the enhancement of ·OH enrichment in the nanospace. In addition, the CCM exhibited high catalytic activity in the presence of co-existing ions and over a wide pH range, as well as good self-cleaning ability in treating secondary wastewater. The experimental results revealed that ·OH were the dominant reactive oxygen species (ROS) in pollutant degradation, while surface hydroxyl groups were active sites for the generation of ·OH via ozone decomposition. This work provides a promising strategy to enhance the utilization of ·OH in HCO for the efficient degradation of organic pollutants in wastewater under spatial confinement.

Photo-transformation of ofloxacin in natural aquatic conditions: Impact of indirect photolysis on the product profile and transformation mechanism

The natural phototransformation of organic pollutants in the environment depends on several water constituents, including inorganic ions, humic substances, and pH. However, the literature information concerning the influence of various water components on the amount of phototransformation and their impact on the development of various transformation products (TPs) is minimal. This study investigated the phototransformation of ofloxacin (OFL), a fluoroquinolone antibiotic, in the presence of various water components such as cations (K+, Na+, Ca2+, NH4+, Mg2+), anions (NO3−, SO42−, HCO3−, CO32−, PO43−), pH, and humic substances when exposed to natural sunlight. The study reveals that neutral pH levels (0.39374 min⁻1) enhance the phototransformation of OFL in aquatic environments. Carbonate, among anions, shows the highest rate constant (2.89966 min⁻1), significantly influencing OFL phototransformation, while all anions exhibit a notable impact. In aquatic environments, indirect phototransformation of OFL, driven by increased reactive oxygen species, expedites light-induced reactions, potentially enhancing OFL phototransformation. A clear difference was visible in the type of transformation products (TPs) formed during direct and indirect photolysis. The impact of indirect photolysis in the product profile was evaluated by examining the unique properties of TPs in direct and indirect photolysis. The primary transformation products were generated by oxidation and cleavage processes directed towards the ofloxacin piperazinyl, oxazine, and carboxyl groups. The toxicity assessment of TPs derived from OFL revealed that among the 26 identified TPs, TP3 (demethylated product), TP7 and TP8 (decarboxylated products), and TP15 (piperazine ring cleaved product) could potentially have some toxicological effects. These findings suggest that the phototransformation of OFL in the presence of various water components is necessary when assessing this antibiotic's environmental fate.

Temporal Transcriptomic Profiling Reveals Dynamic Changes in Gene Expression of Giant Freshwater Prawn upon Acute Saline-Alkaline Stresses.

Bicarbonate and sulfate are among two primary ion constituents of saline-alkaline water, with excessive levels potentially causing metabolic disorders in crustaceans, affecting their molting and interrupting development. As an economically important crustacean species, the molecular adaptive mechanism of giant freshwater prawn Macrobrachium rosenbergii in response to the stress of bicarbonate and sulfate remains unexplored. To investigate the mechanism underlying NaHCO3, Na2SO4, and mixed NaHCO3, Na2SO4 stresses, M. rosenbergii larvae were exposed to the above three stress conditions, followed by total RNA extraction and high-throughput sequencing at eight distinct time points (0, 4, 8, 12, 24, 48, 72, and 96h). Subsequent analysis revealed 13, 16, and 13 consistently identified differentially expressed genes (DEGs) across eight time points under three stress conditions. These consistently identified DEGs were significantly involved in the Gene Ontology (GO) terms of chitin-based cuticle development, protein-carbohydrate complex, structural constituent of cuticle, carnitine biosynthetic process, extracellular matrix, and polysaccharide catabolic process, indicating that alkaline stresses might potentially impact the energy metabolism, growth, and molting of M. rosenbergii larvae. Particularly, the transcriptome data revealed that DEGs associated with energy metabolism, immunity, and amino acid metabolism were enriched across multiple time points under three stress conditions. These DEGs are linked to Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, including glycolysis/glucogenesis, amino sugar and nucleotide sugar metabolism, and lysine degradation. Consistent enrichment findings across the three stress conditions support conclusions above. Together, these insights are instrumental in enhancing our understanding of the molecular mechanisms underlying the alkaline response in M. rosenbergii larvae. Additionally, they offer valuable perspectives on the regulatory mechanisms of freshwater crustaceans amid saline-alkaline water development.

UV Transmission in Prebiotic Environments on Early Earth.

Ultraviolet (UV) light is likely to have played important roles in surficial origins of life scenarios, potentially as a productive source of energy and molecular activation, as a selective means to remove unwanted side products, or as a destructive mechanism resulting in loss of molecules/biomolecules over time. The transmission of UV light through prebiotic waters depends upon the chemical constituents of such waters, but constraints on this transmission are limited. Here, we experimentally measure the molar decadic extinction coefficients for a number of small molecules used in various prebiotic synthetic schemes. We find that many small feedstock molecules absorb most at short (∼200 nm) wavelengths, with decreasing UV absorption at longer wavelengths. For comparison, we also measured the nucleobase adenine and found that adenine absorbs significantly more than the simpler molecules often invoked in prebiotic synthesis. Our results enable the calculation of UV photon penetration under varying chemical scenarios and allow further constraints on plausibility and self-consistency of such scenarios. While the precise path that prebiotic chemistry took remains elusive, improved understanding of the UV environment in prebiotically plausible waters can help constrain both the chemistry and the environmental conditions that may allow such chemistry to occur.

Potential Health Impacts of Hard Water: A Review of Literature

Abstract: Over the past five decades, accumulating evidence suggests that the hardness of drinking water, particularly its magnesium and calcium content, may influence mortality, especially cardiovascular mortality. Epidemiological studies have linked hard water to various health issues like cardiovascular disease, growth retardation, and reproductive failure. Additionally, the acidity of water affects the reabsorption of calcium and magnesium in the kidneys. Other constituents in water also impact different aspects of health. The review aims to explore these health effects, emphasizing the need for quality and quantitative assessment of drinking water to ensure its safety, especially considering that water with a total dissolved solid greater than 500 ppm may pose health risks upon prolonged consumption.