Water Concentration Research Articles

Effects of cadmium on the growth, muscle composition, digestion, gene expression of antioxidant and lipid metabolism in juvenile tilapia (Oreochromis niloticus)

Cadmium could induce various degrees of harm to aquatic organisms. A 30-day feeding trial was conducted to investigate the effects of cadmium on growth, muscle composition, digestive enzyme activity, gene expression of antioxidants and lipid metabolism in juvenile genetic improvement of farmed tilapia (GIFT, Oreochromis niloticus, Initial weight: 21.36 ± 0.24 g). Four cadmium concentrations of aquaculture water were designed: 0, 0.2, 0.4, and 0.6 mg/L Cd2+. The main results are as follows: Compared with the control group (0 mg/L Cd2+), the weight gain rate (WGR), specific growth rate (SGR), daily growth index (DGI), and spleen index (SI) of juvenile GIFT under cadmium stress were significantly decreased (p< 0.05). The contents of crude protein and crude lipid in muscle were significantly decreased (p< 0.05), and the ash was significantly increased (p< 0.05). The activities of trypsin, lipase, and α-amylase in the intestinal were significantly decreased (p< 0.05). The relative expression levels of carnitine palmityl transferase 1 (cpt-1), peroxisome proliferator-activated receptor α (pparα), pparγ, hormone-sensitive lipase (hsl), lipoprotein lipase (lpl), malate dehydrogenase (mdh), leptin (lep), fatty acid synthetase (fas), cholesterol response element binding protein 1 (srebp1), squalene cyclooxygenase (sqle), and stearoyl-CoA desaturase (scd) genes in liver were significantly decreased (p< 0.05). The relative expression levels of catalase (cat), superoxide dismutase (sod), glutathione S-transferase (gst), and glutathione peroxidase (gsh-px) genes in the liver were significantly decreased (p< 0.05). In conclusion, exposure to cadmium stress could impact growth, muscle composition, digestive enzyme activity, gene expression of antioxidant and lipid metabolism in juvenile GIFT.

Effect of salt stress on plant regeneration efficiency in primed and non-primed seed's calli of rice (Oryza sativa L.) variety Swarna.

This study leads with the primed seeds of rice (var. Swarna) with distilled water (D.W.) and various concentrations of Mg(NO3)2 (0-8mM)/Kinetin (0-5ppm) alone or in combination with screen out the regeneration medium induced tolerance level of NaCl. To fulfill the objective, the primed and non-primed rice seeds were inoculated in MS medium supplemented with 30gL-1 maltose + 1gL-1 casein hydrolysate and 2mgL-1 of 2,4-D for callus induction and cultured up to 45days in two sets: one set for regeneration purpose in NaCl-induced regeneration medium and another set was used to study the physiological potentiality of the callus. The 45-day-old calli were transferred into regeneration medium MSR (MS medium for regeneration) (BAP: NAA: Kinetin = 4:1:1) containing NaCl with a concentration range of 0 to 300mM. The number of regenerating calli and shoot regeneration percentage, number of plantlets obtained from one callus, recovery of plantlets from each concentration of NaCl and proline estimation from the leaf of the regenerated plantlets were determined from one set obtained after 45days. The calli obtained from another set after 45days, the frequencies of total and embryogenic calli induction percentage, fresh and dry weights, proline content, nitrate reductase and superoxide dismutase activities were measured. The calli obtained from 2.5ppm kinetin + 4mMMg(NO3)2 primed seeds were showed best result as compared to the other treatments for the above-mentioned parameters in different concentrations of NaCl-induced medium and survive up to 200mM concentrations of NaCl.

Push-Pull Fluorescent Dyes with Trifluoroacetyl Acceptor for High-Fidelity Sensing of Polarity and Heterogeneity of Lipid Droplets.

Imaging and sensing of lipid droplets (LDs) attracted significant attention due to growing evidence for their important role in cell life. Solvatochromic dyes are promising tools to probe LDs' local polarity, but this analysis is biased by their non-negligible emission from intracellular membranes and capacity to emit from both the apolar core and polar interface of LDs. Here, we developed two push-pull solvatochromic dyes based on naphthalene and fluorene cores bearing an exceptionally strong electron acceptor, the trifluoroacetyl group. The latter was found to boost the optical properties of the dyes by shifting their absorption and emission to red and increasing their extinction coefficient, photostability, and sensitivity to solvent polarity (solvatochromism). In contrast to classical solvatochromic dyes, such as parent aldehydes and reference Nile Red, the new dyes exhibited strong fluorescence quenching by millimolar water concentrations in organic solvents. In live cells, the trifluoroacetyl dyes exhibited high specificity to LDs, whereas the parent aldehydes and Nile Red showed a detectable backgrounds from intracellular membranes. Experiments in model lipid membranes and nanoemulsion droplets confirmed the high selectivity of new probes to LDs in contrast to classical solvatochromic dyes. Moreover, the new probes were found to be selective to the LDs oil core, where they can sense lipid unsaturation and chain length. Their ratiometric imaging in cells revealed strong heterogeneity in polarity within LDs, which covered the range of polarities of unsaturated triglyceride oils, whereas Nile Red failed to properly estimate the local polarity of LDs. Finally, the probes revealed that LDs core polarity can be altered by fatty acid diets, which correlates with their chain length and unsaturation.

Evaluation of heavy metal contamination in selected rivers of Kakheti

Water pollution is a significant ecotoxicological problem for the environment. Various toxic compounds discharged into water bodies disrupt the ecosystem's balance, reduce or completely destroy the self-cleaning ability of rivers, and decrease biodiversity. Priority pollutants include heavy metals, whose increased presence in the environment is particularly dangerous to human health. The paper presents the ecochemical condition of two rivers in Georgia: the Turdo River and the Didkhevi River. Water analyses were performed using modern methods and equipment that meet European standards. Based on the results of hydrochemical analyses, it was concluded that the levels of heavy metals—specifically cadmium and copper—have increased to their maximum permissible concentrations in these natural waters. The Didkhevi River was found to be more polluted, with recorded cadmium levels at 0.005 mg/l and copper levels at 4.01 mg/l. In comparison, the Turdo River had slightly lower levels of these pollutants, with cadmium content observed at 0.0023 mg/l and copper at 2.15 mg/l.

Controls of Cross‐Shore Planktonic Ecosystem Structure in an Idealized Eastern Boundary Upwelling System

AbstractEastern boundary upwelling systems (EBUSs) are among the most productive regions in the ocean because deep, nutrient‐rich waters are brought up to the surface. Previous studies have identified winds, mesoscale eddies and offshore nutrient distributions as key influences on the net primary production in EBUSs. However uncertainties remain regarding their roles in setting cross‐shore primary productivity and ecosystem diversity. Here, we use a quasi‐two‐dimensional (2D) model that combines ocean circulation with a spectrum of planktonic sizes to investigate the impact of winds, eddies, and offshore nutrient distributions in shaping EBUS ecosystems. A key finding is that variations in the strength of the wind stress and the nutrient concentration in the upwelled waters control the distribution and characteristics of the planktonic ecosystem. Specifically, a strengthening of the wind stress maximum, driving upwelling, increases the average planktonic size in the coastal upwelling zone, whereas the planktonic ecosystem is relatively insensitive to variations in the wind stress curl. Likewise, a deepening nutricline shifts the location of phytoplankton blooms shore‐ward, shoals the deep chlorophyll maximum offshore, and supports larger phytoplankton across the entire domain. Additionally, increased eddy stirring of nutrients suppresses coastal primary productivity via “eddy quenching,” whereas increased eddy restratification has relatively little impact on the coastal nutrient supply. These findings identify the wind stress maximum, isopycnal eddy diffusion, and nutricline depth as particularly influential on the coastal ecosystem, suggesting that variations in these quantities could help explain the observed differences between EBUSs, and influence the responses of EBUS ecosystems to climate shifts.

Comparison of surface freshwater PFAS sampling methods to evaluate potential for bias due to PFAS enrichment in the surface microlayer.

Per- and polyfluoroalkyl substances (PFAS) accumulate at the air-water interface of the surface microlayer (SML) on marine and freshwater bodies. In order to determine if including the SML when sampling bulk surface water leads to a high bias in measured PFAS concentrations, a pilot study and a full field study were conducted. The pilot study conducted at two sites was aimed at determining the analytical precision and small-scale (~1 m) spatial variability in concentrations of PFAS in bulk water and the SML. The full field study was performed at 11 sites, where three commonly used bulk surface water sampling methods were compared: (1) a peristaltic pump with tubing that excludes the SML, (2) a fully submerged sample bottle that excludes the SML, and (3) a partially submerged sample bottle that allows inclusion of the SML. The SML was sampled using the glass plate method. The samples were analyzed by liquid chromatography tandem mass spectrometry. The pilot study indicated that sampling variation was greater than analytical variation (although Levene's tests indicated that the differences were not statistically significant) and that relatively small differences in the mean concentration among sampling methods could be detected. The full investigation indicated that there was no evidence of high bias of PFAS concentrations in bulk surface water resulting from inclusion of SML using the partially submerged bottle sampling method. Unexpectedly, there was evidence that samples collected using the partially submerged bottle had slightly lower PFAS concentrations, particularly for less hydrophobic PFAS, than bulk water samples that excluded the SML. Additionally, the PFAS enrichment factor in the SML increased with increasing retention time, although the increase was not evident at all sampling sites for all PFAS. Integr Environ Assess Manag 2024;1-12. © 2024 SETAC.

Subsurface Drainage and Nitrogen Fertilizer Management Affect Fertilizer Fate in Claypan Soils

Sustainable nitrogen (N) fertilizer management practices in the Midwest U.S. strive to optimize crop production while minimizing N gas emission losses and nitrate-N (NO3-N) losses in subsurface drainage water. A replicated site in upstate Missouri from 2018 to 2020 investigated the influence of different N fertilizer management practices on nutrient concentrations in drainage water, nitrous oxide (N2O) emissions, and ammonia (NH3) volatilization losses in a corn (Zea mays, 2018, 2020)–soybean (Glyince max, 2019) rotation. Four N treatments applied to corn included fall anhydrous ammonia with nitrapyrin (fall AA + NI), spring anhydrous ammonia (spring AA), top dressed SuperU and ESN as a 25:75% granular blend (TD urea), and non-treated control (NTC). All treatments were applied to subsurface-drained (SD) and non-drained (ND) replicated plots, except TD urea, which was only applied with SD. Across the years, NO3-N concentration in subsurface drainage water was similar for fall AA + NI and spring AA treatments. The NO3-N concentration in subsurface drainage water was statistically (p < 0.0001) lower with TD urea (9.1 mg L−1) and NTC (8.9 mg L−1) compared to fall AA + NI (14.6 mg L−1) and spring AA (13.8 mg L−1) in corn growing years. During corn years (2018 and 2020), cumulative N2O emissions were significantly (p < 0.05) higher with spring AA compared to other fertilizer treatments with SD and ND. Reduced corn growth and plant N uptake in 2018 caused greater N2O loss with TD urea and spring AA compared to the NTC and fall AA + NI in 2019. Cumulative NH3 volatilization was ranked as TD urea > spring AA > fall AA + NI. Due to seasonal variability in soil moisture and temperature, gas losses were higher in 2018 compared to 2020. There were no environmental benefits to applying AA in the spring compared to AA + NI in the fall on claypan soils. Fall AA with a nitrification inhibitor is a viable alternative to spring AA, which maintains flexible N application timings for farmers.

Unlocking the nutraceutical potential of Corylus avellana L. shells: microwave-assisted extraction of phytochemicals with antiradical and anti-diabetic properties.

In recent years, the demand for high-quality natural extracts to be included in nutraceutical formulations has increased sharply. Hazelnut (Corylus avellana L.) shells (HZS) are underrated agricultural by-products that could be exploited as a source of active ingredients with pro-healthy properties. In the present study, a fully green microwave-assisted extraction (MAE) method was established for the first time aiming to recover bioactive constituents from HZS with significant nutraceutical value. Key MAE parameters, including ethanol in water concentration, microwave power, irradiation time and solvent-to-powder ratio, were optimized through response surface methodology utilizing a Box-Behnken design to achieve the highest total phenolic content and antioxidant/antiradical activities in the final extract. The optimal MAE conditions (28% v/v ethanol/water, 270 s, 670 W, and 37 mL g-1) yielded an extract with significant scavenging capacity against reactive oxygen species and remarkable inhibitory activity towards both α-amylase (IC50 = 7.73 μg mL-1) and α-glucosidase (IC50 = 49.44 μg mL-1), demonstrating stronger hypoglycaemic properties than the anti-diabetic drug acarbose. Additionally, fluorescence spectroscopy results highlighted the ability of the optimized extract from HZS (OHS-E) to counteract advanced glycation end-product formation throughout the glycation cascade in a dose-dependent manner. Liquid chromatography/electrospray ionization-tandem mass spectrometry profiling unveiled the presence of fatty acids and phenolic compounds, including lignans, flavonoids, gallic acid derivatives and diarylheptanoids. Lastly, the biocompatibility of OHS-E was attested on HT29-MTX and Caco-2 intestinal cells. Altogether, these findings encourage the potential application of OHS-E as an effective nutraceutical component against type 2 diabetes mellitus and oxidative stress. © 2024 The Author(s). Journal of the Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Single modular flow-electrode capacitive deionization using modified Prussian blue analogues as cation intercalation electrode for continuous water desalination.

Ion back-diffusion hinders the practical application of conventional flow-electrode capacitive deionization (FCDI) under long-term operational conditions. To address this challenge, the present study integrated cation intercalation deionization (CID) with FCDI. A novel PFCDI-CID system was developed by utilizing a modified Prussian blue analogues owing to their enhanced rheological and electrochemical properties. The PFCDI-CID system achieved a high charge efficiency of 89.77% and an energy-normalized removal salt of 0.69 mol kJ-1 in single-cycle (SC) mode with the flow electrodes mass fraction of 2% and a desalinized water chamber-to-concentrated saline water chamber ratio of 2:1. Furthermore, under continuous operation for 12 h in SC mode, the PFCDI-CID system maintained stable desalination performance within the first 2 h. Over an extended duration, the average charge efficiency of the PFCDI-CID system was maintained at 88.44%, with an average energy-normalized removal salt of 0.65 mol kJ-1. The mechanism revealed that the desalination process involving the Prussian blue analogues primarily involves Na+ intercalation, accompanied by a small amount of electro-sorption process. This system exhibits the characteristics of conventional FCDI while enabling desalination and concentration of simulated saline water during brine discharge, thereby mitigating the impact of ion back-diffusion and broadening the application scope of FCDI.

How does particle size of spent coffee ground affect the physicochemical properties of isolated cellulose nanosphere?

Studying the effect of raw material particle size on the properties of isolated nanocellulose is crucial for enhancing material performance, optimizing processing techniques, and promoting sustainability in various industrial applications. Therefore, this study aims to extract and characterize nanocellulose from spent coffee ground (SCG) with different particles size (A: 850–1000, B: 500–850, C: 350–500 μm). For this purpose, SCGs were purified using alkaline and bleaching agents to extract cellulose, followed by acid hydrolysis (sulfuric acid 64 %, 45 °C, 1 h) combined with ultrasonication treatment to produce nanocellulose. The obtained nanocelluloses were characterized in terms of morphology, size distribution, sulfur content, ζ-potential, crystallinity, crystal size, thermal stability, and re-dispersibility in water. Atomic force microscopy confirmed the production of spherical nanocellulose (CNS) with diameter ranging from 65.21 nm in A-CNS to 49.31 and 48.06 nm in B and C-CNS, respectively. The ζ-potential of fresh dispersions decreased with particle size, from −44 mV for A-CNS to −41 mV and −40 mV for B and C-CNS, respectively. The sulfur content also decreased gradually from 214.30 (A-CNS) to 191.29 mmol/kg (C-CNS). All CNS were relatively thermally stable, with thermal analysis showing enhanced stability for A-CNS. The crystallinity index (64–69 %) and the crystal size (2.21–2.39 nm) of CNS were not affected by the particle sizes. In summary, the CNS dimensions, ζ-potential of fresh dispersions, sulfur content and thermal stability of CNS varied significantly among samples, depending on the particle size of SCG. Therefore, it is strongly recommended that researchers choose the optimum particle size for producing nanocellulose for the desired applications.

Validation of the method for determining priority phthalates by GC-MS at trace concentrations in surface water with a background pollution level

A methodology for determining priority phthalates (PP) at trace concentrations in surface waters with a background pollution level has been validated. Lake Baikal, the largest natural reservoir that retains up to 20% of the world’s fresh surface waters, was chosen as a natural model for the study. Baikal is characterized by a minimal content of suspended organic matter, a low degree of mineralization and a background level of organic pollutants. Four priority phthalates were found in Baikal water: dimethyl phthalate, diethyl phthalate di-n-butyl phthalate and di-(2-ethylhexyl) phthalate present in the concentration range from 0.01 to 0.66 μg/liter. The method for phthalate determination includes a single liquid-liquid extraction of phthalates (Vsample = 1 liter) and direct analysis of the extracts by GC-MS. Considering the minimum content of suspended particles in water and the use of high sensitivity of the mass spectrometry, the stages of sample filtration and concentration of extracts are excluded from the procedure. Deuterated phthalates are used as surrogate internal standards for the quantitative determination of priority phthalates. The laboratory background of phthalates was assessed using reagent-blank methods, exhaustive multiple extraction and subsequent exclusion of the resulting value from the determination result as a systematic error. The limits of phthalate determination (0.01 – 0.17 μg/liter) and the error of determination (±δ from 12 to 38%) were assessed in the concentration range from 0.01 to 0.66 μg/liter. The method was validated during monitoring of persistent organic pollutants in water of Lake Baikal for the period 2015 – 2023.

Impact of legacy and unintentionally produced polychlorinated biphenyls (PCBs) in effluents from two wastewater treatment plants in rivers near Barcelona, Spain

Polychlorinated biphenyls (PCBs) are a family of 209 congeners listed as Persistent Organic Pollutants in the Stockholm Convention. Although there has been a lot of focus on those congeners present in the Aroclor or Clophen technical mixtures commercialized in the past (legacy PCBs), other industrial processes such as paint and pigment production can generate other congeners as byproducts (Unintentionally Produced PCBs or UP-PCBs). The present study focuses on the analysis of 72 PCB congeners (including 42 UP-PCBs) in the two major rivers surrounding the city of Barcelona -Llobregat and Besós rivers-, and their levels in two wastewater treatment plants during the production of effluents and reclaimed water. It was observed that WWTP can efficiently remove PCBs from untreated water during sludge production where concentrations are six orders of magnitude higher than in water (in the ng g−1 and pg L−1 ranges, respectively). Although PCB levels in the effluent and reclaimed water replenishing the rivers are not negligible, these do not significantly increase the concentrations already found in the studied rivers, and in most cases PCB concentrations in river water are reduced after merging with the reclaimed water due to dilution effect. The presence of UP-PCB-11 (not present in the Aroclor technical mixtures) in the analyzed water and sludge samples is significant (ranging from 22 to 25 % of the total PCB amount in the Besós river), being often one of the most abundant PCB congeners.

Methane dynamics altered by reservoir operations in a typical tributary of the Three Gorges Reservoir

Substantial nutrient inputs from reservoir impoundment typically increase sedimentation rate and primary production. This can greatly enhance methane (CH4) production, making reservoirs potentially significant sources of atmospheric CH4. Consequently, elucidating CH4 emissions from reservoirs is crucial for assessing their role in the global methane budget. Reservoir operations can also influence hydrodynamic and biogeochemical processes, potentially leading to pronounced spatiotemporal heterogeneity, especially in reservoirs with complex tributaries, such as the Three Gorges Reservoir (TGR). Although several studies have investigated the spatial and temporal variations in CH4 emissions in the TGR and its tributaries, considerable uncertainties remain regarding the impact of reservoir operations on CH4 dynamics. These uncertainties primarily arise from the limited spatial and temporal resolutions of previous measurements and the complex underlying mechanisms of CH4 dynamics in reservoirs. In this study, we employed a fast-response automated gas equilibrator to measure the spatial distribution and seasonal variations of dissolved CH4 concentrations in XXB, a representative area significantly impacted by TGR operations and known for severe algal blooms. Additionally, we measured CH4 production rates in sediments and diffusive CH4 flux in the surface water. Our multiple campaigns suggest substantial spatial and temporal variability in CH4 concentrations across XXB. Specifically, dissolved CH4 concentrations were generally higher upstream than downstream and exhibited a vertical stratification, with greater concentrations in bottom water compared to surface water. The peak dissolved CH4 concentration was observed in May during the drained period. Our results suggest that the interplay between aquatic organic matter, which promotes CH4 production, and the dilution process caused by intrusion flows from the mainstream primarily drives this spatiotemporal variability. Importantly, our study indicates the feasibility of using strategic reservoir operations to regulate these factors and mitigate CH4 emissions. This eco-environmental approach could also be a pivotal management strategy to reduce greenhouse gas emissions from other reservoirs.

Evaluation of cartilage properties from NIR diffuse reflectance spectra: numerical simulation

Diseased conditions of articular cartilage such as osteoarthritis (OA) are accompanied by a change in the water concentration, together with a decrease in cartilage thickness. These parameters are important indicators of the normal joint functioning. Light scattering in a heterogeneous joint tissue is a complex process and it is important to supplement its study with understanding gained from modelling. In this work we employed Monte Carlo for analysis of the relationship between changes in cartilage parameters and calculated diffuse reflectance spectra. It has been shown that water absorption peak at 980 nm is determined by both water content and cartilage thickness, while changes in diffuse reflectance spectra at 1450 nm are mostly driven only by water content. Since independent assessment of these parameters is clinically relevant, several approaches for their determination were developed. A heuristic algorithm for cartilage thickness determination and its quality metrics (R 2 = 0.96) were obtained. Several regression models were developed using the amplitudes of diffuse reflectance spectra at different wavelengths and it was shown that the use of a wide range of wavelengths (850–1700 nm) allows to determine the cartilage water concentration and its thickness with the accuracy R 2 0.96 and 0.99 while measuring at different probe-detector distances.

Anthropogenic impact of rare earth elements on groundwater and surface water in the watershed of the largest freshwater lake in China

Limited knowledge exists regarding the potential risks associated with anthropogenic release of rare earth elements (REEs) in the environment. This study aimed to investigate REE signatures in the watershed Poyang Lake, the largest freshwater lake in China. Samples of surface water, wastewater, and groundwater were collected from five rivers discharging into the lake. Results revealed wastewater from wastewater treatment plants contained total REE concentrations from 231 to 904 μg/L, exceeding those found in surface water (0.4 to 1.3 μg/L) and groundwater (0.5 to 416 μg/L). Samples with elevated REE were found in Ca-Mg-Cl/SO4 type waters and exhibited an 18OD deviation from local meteoric water line. Wastewater exhibited a higher positive Gd anomaly compared to surface water and groundwater, attributed to anthropogenic input of Gd (Gdanth). The determined Gdanth concentration ranged from 0.04 to 0.21 μg/L, and from 0.06 to 0.37 μg/L, accounting for 4 % to 21 % and 49 % to 84 % of total Gd concentrations in groundwater and surface water, respectively. Gdanth concentration in wastewater (0.19 to 0.43 μg/L) remained constant in effluent after wastewater treatment. Surface water displayed relatively complex normalized REE patterns influenced by anthropogenic activities and natural processes (weathering and complexation), while groundwater exhibited heavy REEs enrichment, due to carbonate solution complexation. Additionally, Gdanth concentration showed a positive correlation with ΣREE, Pb, Ni, and Co concentrations in groundwater, indicating a good pollution tracing potential. Health risk assessment using the hazard quotient (HQ) suggested higher HQGd values in groundwater compared to surface water. Residents in the eastern part of Poyang Lake were found to face higher risks associated with Gd in groundwater compared to the western part, with infants and children at greater risk than adult males and females. These findings offer valuable insights into environmental behavior and health risks of REEs in aquatic systems impacted by human activities.

Monitoring of neoadjuvant chemotherapy through time domain diffuse optics: breast tissue composition changes and collagen discriminative potential

The purpose of this clinical study is to test a broad spectral range (635-1060 nm) time-domain diffuse optical spectroscopy in monitoring the response of breast cancer patients to neoadjuvant chemotherapy (NAC). The broadband operation allows us to fully analyze tissue composition in terms of hemoglobin, water, lipids and collagen concentration, which has never been systematically studied until now during the course of therapy. Patients are subjected to multiple breast optical imaging sessions, each one performed at different stages of NAC, both on tumor-bearing and contralateral healthy breasts. We correlate the optical results with conventional imaging techniques and pathological response. Preliminary outcomes on 10 patients’ data show an average significant reduction in the concentrations of oxy-hemoglobin (-53%, p = 0.0020), collagen (-36%, p = 0.0039) and water (-15%, p = 0.0195), and increase in lipids (+39%, p = 0.0137) from baseline to the end of therapy in the tumor-bearing breast of patients who responded to therapy at least partially. With respect to scattering, the scattering amplitude, a, increases slightly (+15%, p = 0.0039) by the end of the therapy compared to the baseline, while the scattering slope, b, shows no significant change (+4%, p = 0.9219). Some change in the constituents’ concentrations was also noticed in the contralateral healthy breast, even though it was significant only for oxy-hemoglobin concentration. We observed that collagen seems to be the only component distinguishing between complete and partial responders by the end of 2-3 weeks from the baseline. In the complete responder group, collagen significantly decreased after 2-3 weeks with respect to baseline (p = 0.0423). While the partial responder group also showed a decrease, it did not reach statistical significance (p = 0.1012). This suggests that collagen could serve as a potential biomarker to measure NAC effectiveness early during treatment. Even though obtained on a small group of patients, these initial results are consistent with those of standard medical modalities and highlight the sensitivity of the technique to changes that occur in breast composition during NAC.

Spatiotemporal dynamics, bioaccumulation, and critical influencing factors of antibiotics in tilapia aquaculture: A study on source identification and environmental fate within typical farming systems

This study investigated the spatiotemporal dynamics, bioaccumulation, and critical influencing factors of antibiotics in tilapia aquaculture, focusing on source identification and environmental fate within typical farming systems. The results revealed a progressive increase in antibiotic concentrations in pond water and sediments over the cultivation period, with suspended solids and chemical oxygen demand identified as significant environmental factors influencing the distribution and dissemination of antibiotics. The aquaculture water source was the primary contributor of antibiotics in the farming system. Furthermore, the bioaccumulation factor (BAF) calculations indicated varying degrees of antibiotic enrichment in tilapia tissues, with sulfadimethoxine exhibiting the highest BAFs. Correlation analyses, redundancy analysis, and multivariate linear regression analysis provided insights into the relationship between environmental factors and antibiotics, identifying key antibiotics and influencing factors. The study highlighted the importance of managing and treating water sources to reduce the inflow of antibiotics into aquaculture systems and emphasized the need for non-antibiotic aquaculture practices to minimize the impact on the environment and public health. In conclusion, this research contributes valuable information for the development of effective management strategies and policies aimed at curbing antibiotic pollution in aquaculture environments, ensuring the sustainability of the aquaculture industry, and protecting ecosystem and consumer health.

Stability Analysis of Pure Oil-Water Emulsion in Gravity-Based Separators

Abstract The purpose of this work is to investigate the stability of pure (emulsifier-free) oil-water emulsion in a gravity-based separator as a function of various parameters such as mixing speed, water volume concentration, temperature, and appearance. Only simple fluids (ExxsolTMD110 and distilled water) were used to form the dispersion in a separator of operational volume 200 ml and internal diameter of 60 mm. Data were gathered from a portable dispersion characterization rig where videos of liquid phase separation can be saved and scanned. The study considered a wide range of mixing speeds between 600 rpm and 2500 rpm, with elevated temperatures of 60 °C and 80 °C. Both types (oil-in-water (O/W) and water-in-oil (W/O)) of pure emulsion were studied. In addition, two volumetric water concentrations (WCs) were considered for each type to investigate its stability under the parameters tested (i.e., 25% and 50% WC for W/O emulsion and 75% and 90% WC for O/W emulsion). The stability of the emulsion was examined in terms of the separation profiles of the water and oil phase, oil/water mixture volume, initiation time of free phase separation and/or the final time of separation. Mixing speed was shown to drastically impact the stability of O/W emulsion, from a few minutes to over 4 h. Conversely, insignificant effects of mixing speed were seen for W/O emulsion as the emulsions overall separated in a few seconds. Although temperature accelerated the oil separation rates of 75% WC emulsions, it delayed the initiation time of water separation.

Enhanced Removal of Brine From Porous Structures by Supercritical CO2.

Supercritical CO2 (sCO2) removes water from brine held in pumice stone at levels well above the solubility of water in sCO2. The higher water removal results from a combination of passive emulsification of water in sCO2 and viscous fingering of sCO2 through the saturated pumice. This leads to higher levels of salt deposition than that expected from solubility considerations alone. These deposits could impact the injectivity of sCO2 as well as its movement in the subsurface. The finding that the water concentration in sCO2 is not necessarily capped at the solubility limit should influence the parametrization of injection models.

Microplastics and metals: Microplastics generated from biodegradable polylactic acid mulch reduce bioaccumulation of cadmium in earthworms compared to those generated from polyethylene

Biodegradable polylactic acid (PLA) mulch has been developed to replace conventional polyethylene (PE) mulch in agriculture as a response to growing concerns about recalcitrant plastic pollution and the accumulation of microplastics (MPs) in soil. Cadmium is a significant soil pollutant in China. MPs have been shown to adsorb metals. In this study the earthworm Lumbricus terrestris was exposed to either Cd (1.0–100 mg / kg) or MPs (PE and PLA, 0.1–3 % w / w), or a combination of the two, for 28 days. Cd bioavailability significantly decreased in the presence of MPs. In particular, at the end of the experiment, PLA treatments had lower measured Cd concentrations in both earthworms (2.127–29.24 mg / kg) and pore water (below detection limits - 0.1384 mg /L) relative to PE treatments (2.720–33.77 mg / kg and below detection limits - 0.2489 mg / L). In our adsorption experiment PLA MPs adsorbed significantly more Cd than PE MPs with maximum adsorption capacities of 126.0 and 23.2 mg / kg respectively. These results suggest that the PLA MPs reduce earthworm exposure to Cd relative to PE by removing it from solution and reducing its bioavailability.