Search Results (335)

Extensive studies have established that ultrasonic micro-jets and acoustic cavitation selectively intensify interfacial interactions at multiphase boundaries, thereby enhancing the flotation of soluble salt minerals and oxide ores. Although a growing body of evidence shows that pulp-borne nanoparticles (i.e., nanosolids, colloids, and nanoscale gas nuclei) mediate these effects, their role in the flotation of ultrafine smithsonite after collector addition has not yet been systematically examined. To fill this gap, we compared the flotation response of ultrafine smithsonite under conventional stirring (SC) and ultrasonic conditioning (UC), using sodium oleate (NaOL) as the collector, and dissected the governing mechanisms across three pillars, mineral–NaOL interaction, particle aggregation, and frothability, with particular attention paid to how nanoparticles modulate each dimension. The flotation results show that flotation performance under UC is dictated by NaOL concentration. At low NaOL levels (i.e., below 4 × 10⁻⁴ M), UC depresses both recovery and kinetics relative to SC, while at high NaOL levels, the trend reverses and UC outperforms SC. Mechanistic analysis reveals that sonication erodes mineral surfaces and generates cavitation, flooding the pulp with various nanoparticles. When NaOL is scarce, zinc-containing components and zinc-rich nanosolids sequester the collector through non-selective adsorption and precipitation, leaving smithsonite poorly hydrophobized. Consequently, particle aggregation and pulp frothability are markedly inferior to those in the SC system, so the flotation recovery and kinetics remain lower. As the NaOL concentration rises, smithsonite becomes adequately hydrophobized, and the pulp fills with hydrophobic zinc-rich nanosolids, along with cavitation-induced gas nuclei or tiny bubbles. These nanoparticles now act as bridges, accelerating the aggregation of ultrafine smithsonite once sonication stops and agitation begins, while simultaneously improving frothability. Although the strong dispersive action of ultrasound still suppresses initial flotation kinetics, cumulative recovery ultimately surpasses that of SC. The findings delineate a nanoparticle-regulated flotation paradigm and establish a critical NaOL concentration window for effective UC in ultrafine smithsonite flotation. This framework is readily transferable to the beneficiation of other ultrafine, soluble oxidized minerals (rhodochrosite, dolomite, etc.). Full article

Gout is a chronic inflammatory disease characterized by the deposition of monosodium urate (MSU) crystals within joints, leading to recurrent acute flares and long-term tissue damage. While various hypotheses have been proposed to explain the self-limiting nature of acute gout attacks, we posit that aggregated neutrophil extracellular traps (aggNETs) play a central role in this process. This review focuses on the mechanisms underlying MSU crystal-induced formation of neutrophil extracellular traps (NETs) and explores their dual role in the clinical progression of gout. During the initial phase of acute flares, massive NET formation is accompanied by the release of preformed inflammatory mediators, which is a condition that amplifies inflammatory cascades. As neutrophil recruitment reaches a critical threshold, the NETs tend to form high-order aggregates (aggNETs). The latter encapsulate MSU crystals and further pro-inflammatory mediators within their three-dimensional scaffold. High concentrations of neutrophil serine proteases (NSPs) within the aggNETs facilitate the degradation of soluble inflammatory mediators and eventually promote the resolution of inflammation in a kind of negative inflammatory feedback loop. In advanced stages of gout, MSU crystal deposits are often visible via dual-energy computed tomography (DECT), and the formation of palpable tophi is frequently observed. Based on the mechanisms of resolution of inflammation and the clinical course of the disease, building on the traditional static model of “central crystal–peripheral fibrous encapsulation,” we have expanded the NETs component and refined the overall concept, proposing a more dynamic, multilayered, multicentric, and heterogeneous model of tophus maturation. Notably, in patients with late-stage gout, tophi exist in a stable state, referred to as “silent” tophi. However, during clinical tophus removal, the disruption of the structural or functional stability of “silent” tophi often leads to the explosive reactivation of inflammation. Considering these findings, we propose that future therapeutic strategies should focus on the precise modulation of NET dynamics, aiming to maintain immune equilibrium and prevent the recurrence of gout flares. Full article

This study investigates the self-assembly and host–guest complexation behaviour of novel resveratrol-based lipophenols (LipoResv)—resveratrol-4′-linoleate (Resv-4′-LA) and resveratrol-4′-docosahexaenoate (Resv-4′-DHA)—with hydroxypropyl-β-cyclodextrins (HP-β-CDs). These amphiphilic molecules display surfactant-like properties, forming micellar aggregates in aqueous media. Fluorescence spectroscopy was used to determine the critical micelle concentration (CMC), revealing that LipoResv exhibit significantly lower CMC values than their free fatty acids, indicating higher hydrophobicity. The formation of inclusion complexes with HP-β-CDs was evaluated based on changes in CMC values and further confirmed by dynamic light scattering (DLS) and molecular modelling analyses. Resv-4′-LA formed 1:1 complexes (Kc = 720 M⁻¹), while Resv-4′-DHA demonstrated a 1:2 stoichiometry with lower affinity constants (K₁ = 17 M⁻¹, K₂ = 0.18 M⁻¹). Environmental parameters (pH, temperature, and ionic strength) significantly modulated CMC and binding constants. Computational docking and molecular dynamics simulations supported the experimental findings by revealing the key structural determinants of the host–guest affinity and micelle stabilization. Ligand efficiency (LE) analysis further aligned with the experimental data, favouring the unmodified fatty acids. These results highlight the versatile encapsulation capacity of HP-β-CDs for bioactive amphiphile molecules and support their potential applications in drug delivery and functional food systems. Full article

In marine engineering applications, substituting conventional crushed stone coarse aggregates with coral aggregates offers dual advantages: reduced terrestrial quarrying operations and minimized construction material transportation costs. However, the inherent characteristics of coral aggregates—low bulk density, high porosity, and elevated water absorption capacity—adversely influence concrete workability and mechanical performance. To address these limitations, this investigation employed microbial-induced carbonate precipitation (MICP) for aggregate modification. The experimental design systematically evaluated the impacts of substrate concentration (1 mol/L) and mineralization period (14 days) on three critical parameters, mass gain percentage, water absorption reduction, and apparent density enhancement, across distinct particle size fractions (4.75–9.5 mm, 9.5–20 mm) and density classifications. Subsequent application trials assessed the performance of MICP-treated aggregates in marine concrete formulations. Results indicated that under a substrate concentration of 1 mol/L and mineralization period of 14 days, lightweight coral aggregates and coral aggregates within the 4.75–9.5 mm size fraction exhibited favorable modification effects. Specifically, their mass gain rates reached 11.75% and 11.22%, respectively, while their water absorption rates decreased by 32.22% and 34.75%, respectively. Apparent density increased from initial values of 1764 kg/m³ and 1930 kg/m³ to 2050 kg/m³ and 2207 kg/m³. Concrete mixtures incorporating modified aggregates exhibited enhanced workability and strength improvement at all curing ages. The 28-day compressive strengths reached 62.1 MPa (11.69% increment), 46.2 MPa (6.94% increment), and 60.1 MPa (14.91% increment) for the 4.75–9.5 mm, 9.5–20 mm, and continuous grading groups, respectively, compared to untreated counterparts. Full article

The mesoscopic-scale discrete element method (DEM) modeling approach demonstrated high compatibility with macroporous recycled concrete (MRC). However, existing DEM models failed to adequately balance modeling accuracy and computational efficiency for recycled aggregate (RA), replicate the three distinct interfacial transition zone (ITZ) types and pore structure of MRC, or establish a systematic calibration methodology. In this study, PFC 3D was employed to establish a randomly polyhedral RA composite model and an MRC model. A systematic methodology for parameter testing and calibration was proposed, and compressive test simulations were conducted on the MRC model. The model incorporated all components of MRC, including three types of ITZs, achieving an aggregate volume fraction of 57.7%. Errors in simulating compressive strength and elastic modulus were 3.8% and 18.2%, respectively. Compared to conventional concrete, MRC exhibits larger strain and a steeper post-peak descending portion in stress–strain curves. At peak stress, stress is concentrated in the central region and the surrounding arc-shaped zones. After peak stress, significant localized residual stress persists within specimens; both toughness and toughness retention capacity increase with rising porosity and declining compressive strength. Failure of MRC is dominated by tension rather than shear, with critical bonds determining strength accounting for only 1.4% of the total. The influence ranking of components on compressive strength is as follows: ITZ (new paste–old paste) > ITZ (new paste–natural aggregates) > new paste > old paste > ITZ (old paste–natural aggregates). The Poisson’s ratio of MRC (0.12–0.17) demonstrates a negative correlation with porosity. Predictive formulas for peak strain and elastic modulus of MRC were established, with errors of 2.6% and 3.9%, respectively. Full article

This study examined the eco-friendly synthesis of zinc oxide (ZnO) nanoparticles using Cladophora glomerata extracts as reducing and stabilizing agents, comparing zinc acetate and zinc chloride precursors for biomedical and environmental applications. Zinc acetate-synthesized ZnO nanoparticles showed a significant absorption peak around 320–330 nm, indicating stable, quasi-spherical ZnO nanoparticles with a narrow size distribution, primarily around 100 nm. Zeta potential measurements revealed a value of −25 mV for these particles, suggesting moderate colloidal stability. XRD analysis confirmed a highly crystalline hexagonal wurtzite structure for zinc acetate-derived ZnO, and SEM images supported a proper microstructure with approximately 2 µm particle size. FTIR analysis indicated higher-quality ZnO from zinc acetate due to the absence of moisture and hydroxyl groups. Conversely, zinc chloride-derived ZnO particles displayed a broader absorption spectrum around 370 nm, indicative of significant aggregation. Their narrower zeta potential distribution around +10 mV suggested diminished colloidal stability and a heightened aggregation tendency. While a peak around 100 nm was observed, many particles exceeded 1000 nm, reaching up to 10,000 nm. XRD results showed that zinc chloride adversely affected crystallinity, and SEM analysis indicated smaller particles (approx. 1 µm). FTIR analysis demonstrated that zinc chloride samples retained hydroxyl groups. Both zinc acetate- and zinc chloride-derived ZnO nanoparticles produced notable inhibitory zones against Gram-positive (L. monocytogenes, S. aureus) and specific Gram-negative bacteria (E. coli, K. pneumoniae). Zinc acetate-derived ZnO showed a 21 mm inhibitory zone against P. vulgaris, while zinc chloride-derived ZnO showed a 10.1 mm inhibitory zone against C. albicans. Notably, zinc chloride-derived ZnO exhibited broad-spectrum antimicrobial activity. MIC readings indicated that zinc acetate-derived ZnO had better antibacterial properties at lower concentrations, such as 3.125 µg/mL against L. monocytogenes. These findings emphasize that the precursor material selection critically influences particle characteristics, including optical properties, surface charge, and colloidal stability. Full article

In this cross-disciplinary investigation, we uncover a suite of previously unexamined factors and their intricate interplay that hold causal relationships with the distribution of Trachurus japonicus in the northern reaches of the South China Sea, thereby extending the existing research paradigms. Leveraging advanced machine learning algorithms and causal inference, our robust experimental design uncovered nine key global and regional factors affecting the distribution of T. japonicus density. A robust experimental design identified nine key factors significantly influencing this density: mean sea-level pressure (msl-0, msl-4), surface pressure (sp-0, sp-4), Summit ozone concentration (Ozone_sum), F10.7 solar flux index (F10.7_index), nitrate concentration at 20 m depth (N3M20), sonar-detected effective vertical range beneath the surface (Height), and survey month (Month). Crucially, stable causal relationships were identified among Ozone_sum, F10.7_index, Height, and N3M20. Variations in Ozone_sum likely impact surface UV radiation levels, influencing plankton dynamics (a primary food source) and potentially larval/juvenile fish survival. The F10.7_index, reflecting solar activity, may affect geomagnetic fields, potentially influencing the migration and orientation behavior of T. japonicus. N3M20 directly modulates primary productivity by limiting phytoplankton growth, thereby shaping the availability and distribution of prey organisms throughout the food web. Height defines the vertical habitat range acoustically detectable, intrinsically linking directly to the vertical distribution and availability of the fish stock itself. Surface pressures (msl-0/sp-0) and their lagged effects (msl-4/sp-4) significantly influence sea surface temperature profiles, ocean currents, and stratification, all critical determinants of suitable habitats and prey aggregation. The strong influence of Month predominantly reflects seasonal changes in water temperature, reproductive cycles, and associated shifts in nutrient supply and plankton blooms. Rigorous robustness checks (Data Subset and Random Common Cause Refutation) confirmed the reliability and consistency of these causal findings. This elucidation of the distinct biological and physical pathways linking these diverse factors leading to T. japonicus density provides a significantly improved foundation for predicting distribution patterns globally and offers concrete scientific insights for sustainable fishery management strategies. Full article

In this study, a methacrylic derivative of xylan (XYLMA) was synthesized through transesterification reactions, with the aim of evaluating its physicochemical behavior and its interaction with kaolinite particles. Structural characterization by FT-IR and NMR spectroscopy confirmed the incorporation of methacrylic groups into the xylan (XYL) structure, with a degree of substitution of 0.67. Thermal analyses (TGA and DSC) showed a decrease in melting temperature and enthalpy in XYLMA compared to XYL, attributed to a loss of structural rigidity. Thermal analyses (TGA and DSC) revealed a decrease in the melting temperature and enthalpy of XYLMA compared to XYL, which is attributed to a loss of structural rigidity and a reduction in the crystalline order of the biopolymer. Aggregation tests in solution revealed that XYLMA exhibits amphiphilic behavior, forming micellar structures at a critical aggregation concentration (CAC) of 62 mg L⁻¹. In adsorption studies on kaolinite, XYL showed greater affinity than XYLMA, especially at acidic pH, due to reduced electrostatic forces and a greater number of hydroxyl groups capable of forming hydrogen bonds with the mineral surface. In contrast, modification with methacrylic groups in XYLMA reduced its adsorption capacity, probably due to the formation of supramolecular aggregates. These results suggest that interactions between xylan and kaolinite clay are key to understanding the role that hemicelluloses play in increasing copper recovery when added to flotation cells during the processing of copper sulfide ores with high clay content. Full article

Soil aggregates play critical roles in regulating the behavior of heavy metal in soils. To understand the distribution of cadmium (Cd) in aggregates of different soil types, as well as their roles in regulating the Cd bioavailability of bulk soils, four major arable soils, including acidic, neutral, and calcareous purple soils and calcareous yellow soil (APS, NPS, CPS, and CYS), were sampled from Chongqing, China, for aggregate separation and determination of the total Cd(T-Cd) distribution, fractionation, and extractability in various-sized aggregates. A pot experiment with ryegrass (Lolium perenne L.) was conducted to evaluate the Cd bioavailability in bulk soils as influenced by aggregates. The results show that the composition of soil aggregates varies a lot among soils: lower soil pH tends to increase the proportion of macroaggregates while decreasing that of smaller aggregates. The Cd distribution, HCl-extractability, and active fraction (AF, T-Cd/HCl-Cd) in aggregates are all soil type-dependent, with pH and particle size being the main determining factors; the distribution pattern of Cd concentrated in smaller aggregates is only found for CPS and CYS (pH > 7.5) upon exogenous Cd addition, though the finest aggregates (silt–clay, <0.053 mm) consistently exhibited the highest Cd enrichment for all tested soils. The Cd extractability and AF values in all aggregates show a sequence of APS > NPS > CPS > CYS, indicating the fundamental influence of soil pH on Cd availability. Higher AF values over bulk soils, either in silt–clay aggregates or in microaggregates (0.053–0.25 mm), whereas lower AF in macroaggregates (1–2 mm) are found for APS and NPS, which correspond to the relative portions of Ex-Cd and Fe/Mn oxide-bound Cd (Fe/Mn-Cd) in these aggregates. In contrast, less variation of AF values among aggregates is observed for CPS and CYS and for APS/NPS upon Cd addition. Pot experiments demonstrated strong positive correlations between ryegrass Cd uptake and HCl-Cd in silt–clay aggregates and T-Cd in microaggregates, while a negative correlation was observed with T-Cd in macroaggregates. These findings supply new insight into the mechanisms of aggregates in controlling Cd bioavailability in bulk soils and shed light on the development of new strategies for remediating Cd-polluted soils. Full article

Because of their potential “smart” applications, multifunctional stimuli-responsive polymers are gaining increasing scientific interest. The present work explores the possibility of developing such materials based on the hydrolytically stable N-3-dimethylamino propyl methacrylamide), DMAPMA. To this end, the properties in aqueous solution of the homopolymer PDMAPMA and copolymers P(DMAPMA-co-MMA_x) of DMAPMA with the hydrophobic monomer methyl methacrylate, MMA, were explored. Two copolymers were prepared with a molar content x = 20% and 35%, as determined by Proton Nuclear Magnetic Resonance (¹H NMR). Turbidimetry studies revealed that, in contrast to the homopolymer exhibiting a lower critical solution temperature (LCST) behavior only at pH 14 in the absence of salt, the LCST of the copolymers covers a wider pH range (pH > 8.5) and can be tuned within the whole temperature range studied (from room temperature up to ~70 °C) through the use of salt. The copolymers self-assemble in water above a critical aggregation Concentration (CAC), as determined by Nile Red probing, and form nanostructures with a size of ~15 nm (for P(DMAPMA-co-MMA₃₅)), as revealed by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The combination of turbidimetry with ¹H NMR and automatic total organic carbon/total nitrogen (TOC/TN) results revealed the potential of the copolymers as visual CO₂ sensors. Finally, the alkylation of the copolymers with dodecyl groups lead to cationic amphiphilic materials with an order of magnitude lower CAC (as compared to the unmodified precursor), effectively stabilized in water as larger aggregates (~200 nm) over a wide temperature range, due to their increased ζ potential (+15 mV). Such alkylated products show promising biocidal properties against microorganisms such as Escherichia coli and Staphylococcus aureus. Full article

Italy supplies about one-seventh of the European Union’s total glass production, and the sector’s sizeable resource demands make it a linchpin of national industrial strategy. With growing environmental regulations and the push for resource efficiency, Material Flow Accounting has become essential for companies to stay compliant and advance sustainability. The investigation concentrates on Italy’s glass industry to clarify its material requirements, ecological footprint, and overall sustainability performance. STAN software v2, combined with an Economy-Wide Material Flow Accounting (EW-MFA) framework, models the national economy as a single integrated input–output system. By tracking each material stream from initial extraction to end-of-life, the analysis delivers a cradle-to-grave picture of the sector’s environmental impacts. During the 2021 production year, Italy’s glass makers drew on a total of 10.5 million tonnes (Mt) of material inputs, supplied 76% (7.9 Mt) from domestic quarries, and 24% (2.6 Mt) via imports. Outbound trade in finished glass removed 1.0 Mt, leaving 9.5 Mt recorded as Domestic Material Consumption (DMC). Within that balance, 6.6 Mt (63%) was locked into long-lived stock, whereas 2.9 Mt (28%) left the system as waste streams and airborne releases, including roughly 2.1 Mt of CO₂. At present, the post-consumer cult substitutes only one-third of the furnace batch, signalling considerable scope for improved circularity. When benchmarked against EU-27 aggregates for 2021, Italy registers a NAS/DMI ratio of 0.63 (EU median 0.55) and a DPO/DMI ratio of 0.28 (EU 0.31), indicating a higher share of material retained in stock and slightly lower waste generated per ton of input. A detailed analysis of glass production identifies critical stages, environmental challenges, and areas for improvement. Quantitative data on material use, waste generation, and recycling rates reveal the industry’s environmental footprint. The findings emphasise Economy-Wide Material Flow Accounting’s value in evaluating and improving sustainability efforts, offering insights for policymakers and industry leaders to drive resource efficiency and sustainable resource management. Results help scholars and policymakers in the analysis of the Italian glass industry context, supporting in the data gathering, while also in the use of this methodology for other sectors. Full article

Oily wastewater is extensively generated during the petroleum extraction and refining processes, as crude oil production water and from the effluent systems in petrochemical enterprises. The discharge standards for such wastewater are stringent, with the Oslo–Paris Convention stipulating that the oil content must be below 30 mg/L for permissible discharge. Flotation, a conventional oil–water separation method, relies on the collision and adhesion of rising bubbles with oil droplets in water to form low-density aggregates that float to the surface for separation. The collision and adhesion mechanisms between bubbles and oil droplets are fundamental to this process. However, systematic studies on their interactions remain scarce. This study employs the extended Derjaguin–Landau–Verwey–Overbeek theory to analyze the three mechanical interactions during the collision–adhesion process theoretically and investigates the heterogeneous interaction dynamics experimentally. Furthermore, given the diverse liquid-phase environments of oily wastewater, the effects of salinity, pH, and surfactant concentration are decoupled and individually explored to clarify their underlying mechanisms. Finally, a solution is proposed to enhance the flotation efficiency fundamentally. This work systematically elucidates the influence of liquid-phase environments on the adhesion behavior for the first time through the unification of theoretical and experimental approaches. The findings provide critical insights for advancing flotation theory and guiding the development of novel coagulants. Full article

In the context of China’s ecosystem facing a high intensity of nitrogen loads, carbon–nitrogen interactions are receiving increasing attention. Physical protection by soil aggregates is critical for soil carbon and nitrogen sequestration in terrestrial ecosystems; however, there is currently limited information on how nitrogen addition influences carbon and nitrogen dynamics across different stages of forest ageing. Herein, a field nitrogen manipulation experiment over 6 years was established in subtropical forests (46, 78, and about 200 years old) in China. Aggregate fractions and stable isotope analyses were used to assess the effects of nitrogen addition. The results show that forest soil was dominated by macroaggregates, and these increased with forest ageing (p > 0.05). The macroaggregates’ carbon content decreased with forest ageing (p > 0.05), while the macroaggregates’ nitrogen content was highest in the 200-year-old forest. Nitrogen addition increased the aggregates’ carbon and nitrogen concentrations in the 46- and 200-year-old forests. The macroaggregates, under nitrogen addition in the 78- and 200-year-old forests, were relatively weak, while forest age and nitrogen addition mainly affected macroaggregate carbon and nitrogen concentrations to promote their carbon and nitrogen storage, and the macroaggregates were the main storage unit for fixing and protecting new carbon in soils. Nitrogen addition increased the macroaggregates’ δ¹³C abundance in the 78- and 200-year-old forests and decreased it in the 46-year-old forest (p > 0.05); significantly increased the macroaggregates’ δ¹⁵N in the 46-year-old forest (p < 0.05), and decreased the macroaggregates’ δ¹⁵N in the 200-year-old forest (p > 0.05). Considering the distribution of δ¹³C and δ¹⁵N in the aggregates, the effect of nitrogen addition on the dynamic mechanism of soil aggregate carbon and nitrogen fractions varied based on forest age and aggregate size. Correlation analysis further revealed that soil total phosphorus, NH₄⁺-N, NO₃⁻-N, dissolved organic nitrogen, pH, texture, etc., were the primary predictors explaining most of the variation in aggregate fractions and their δ¹³C distribution. In summary, the effect of nitrogen deposition on the carbon and nitrogen stability of soil aggregates in broad-leaved forests depends on forest age. Full article

Understanding the interplay between climate change, landscape patterns, and carbon sequestration is critical for sustainable ecosystem management. This study investigates the spatiotemporal evolution of vegetation Net Primary Productivity (NPP) and landscape patterns in Inner Mongolia, China, from 2000 to 2020, and evaluates their implications for carbon sink capacity under climate change. Using remote sensing data, meteorological records, and landscape metrics (CONTAG, SPLIT, IJI), we quantified the relationships between vegetation productivity, landscape connectivity, and fragmentation. Results reveal a northeast-to-southwest gradient in NPP, with high values concentrated in forested regions of the Greater Khingan Range and low values in arid western deserts. Over two decades, NPP increased by 73% in high-productivity zones, driven by rising temperatures and ecological restoration policies. Landscape aggregation (CONTAG) and patch connectivity showed strong positive correlations with NPP, while higher fragmentation values (SPLIT, IJI) negatively impacted carbon sequestration. Climate factors, particularly precipitation variability, emerged as critical drivers of NPP fluctuations, with human activities amplifying regional disparities. We propose targeted strategies—enhancing landscape connectivity, regional differentiation management, and optimizing patch structure—to bolster climate-resilient carbon sinks. These findings underscore the necessity of integrating climate-adaptive landscape planning into regional carbon neutrality frameworks, offering feasible alternatives for mitigating climate impacts in ecologically vulnerable regions. Full article

As emerging contaminants increasingly detected in aquatic and terrestrial ecosystems, environmental estrogens (EEs) pose significant ecological risks to marine ecosystems, particularly affecting photosynthetic microorganisms occupying fundamental roles in marine food webs. This review summarizes the current knowledge on the toxicological effects of EEs in marine microalgae through a systematic analysis of dose-dependent physiological, biochemical, and molecular responses. Experimental evidence reveals a biphasic response pattern characterized by growth promotion and photosynthetic enhancement in microalgae under low-concentration EE exposure (0.1–10 μg/L), while marked inhibition of both growth and photosynthetic activity was observed at elevated EE concentrations (>50 μg/L). Notably, sustained EE exposure induces metabolic reprogramming, manifested through reduced protein and polysaccharide biosynthesis concurrent with accelerated lipid accumulation. Cellular stress responses include significant ultrastructural alterations such as chloroplast membrane disruption, cell wall thickening, and the formation of multicellular aggregates. The study further elucidates the concentration-dependent modulation of toxin metabolism, with sublethal doses stimulating intracellular microcystin synthesis (1.5–2.3-fold increase), while acute exposure triggers toxin release through membrane permeabilization. At molecular levels, transcriptomic analyses identify the up-regulation of heat shock proteins (HSP70/90) and the differential expression of genes governing cell cycle progression (cyclin-D), apoptotic pathways (caspase-3), photosynthetic electron transport (psbA), and oxidative stress responses (SOD, CAT). These findings demonstrate that EEs exert multilevel impacts on microalgal physiology through interference with fundamental metabolic processes, potentially disrupting marine primary productivity and biogeochemical cycles. The identified response mechanisms provide critical insights for environmental risk assessment and establish a conceptual framework for investigating estrogenic pollutant effects in aquatic ecosystems. Full article