Heavy metal induced shifts in microbial community composition and interactions with dissolved organic matter in coastal sediments.

Heavy metals can impact the structure and function of coastal sediment. The dissolved organic matter (DOM) pool plays an important role in determining both the heavy metal toxicity and microbial community composition in coastal sediments. However, how heavy metals affect the interactions between microbial communities and DOM remains unclear. Here, we investigated the influence of heavy metals on the microbial community structure (including bacteria and archaea) and DOM composition in surface sediments of Beibu Gulf, China. Our results revealed firstly that chromium, zinc, cadmium, and lead were the heavy metals contributing to pollution in our studied area. Furthermore, the DOM chemical composition was distinctly different in the contaminated area from the uncontaminated area, characterized by a higher average O/C ratio and increased prevalence of carboxyl-rich alicyclic molecules (CRAM) and highly unsaturated compounds (HUC). This indicates that DOM in the contaminated area was more recalcitrant compared to the uncontaminated area. Except for differences in archaeal diversity between the two areas, there were no significant variations observed in the structure of archaea and bacteria, as well as the diversity of bacteria, across the two areas. Nevertheless, our co-occurrence network analysis revealed that the B2M28 and Euryarchaeota, dominating bacterial and archaeal groups in the contaminated area were strongly related to CRAM. The network analysis also unveiled correlations between active bacteria and elevated proportions of nitrogen-containing DOM molecules. In contrast, the archaea-DOM network exhibited strong associations with nitrogen- and sulfur-containing molecules. Collectively, these findings suggest that heavy metals indeed influence the interaction between microbial communities and DOM, potentially affecting the accumulation of recalcitrant compounds in coastal sediments.

Study of crosslinker size on the rheological properties of borate crosslinked guar gum.

Borate crosslinked guar gum gels have played a vital role in stimulating oil and gas wells for many years; however, the high dosage of guar gum in the existing fracturing fluid will increase the cost and cause more damage to the reservoir and ultimately affect the effect of stimulation. In this study, borate esters are modified onto polyethyleneimine (PEI) of different molecular weights, affording organic borate crosslinkers of different sizes. By analyzing the effect of crosslinker size on gel rheology, sand-carrying properties, and microstructure, it is observed that the crosslinking efficiency is most significantly enhanced when the crosslinker size is similar to the diameter of the guar gum molecules. This makes it possible for the gel to maintain good performance at low polymer concentrations and meet the performance requirements of fracturing, which provides new ideas for developing the next generation of economical, clean, and green fracturing fluids.

Unexpected high retention of 15 N-labeled nitrogen in a tropical legume forest under long-term nitrogen enrichment.

The responses of forests to nitrogen (N) deposition largely depend on the fates of deposited N within the ecosystem. Nitrogen-fixing legume trees widely occur in terrestrial forests, but the fates of deposited N in legume-dominated forests remain unclear, which limit a global evaluation of N deposition impacts and feedbacks on carbon sequestration. Here, we performed the first ecosystem-scale 15 N labeling experiment in a typical legume-dominated forest as well as in a nearby non-legume forest to determine the fates of N deposition between two different forest types and to explore their underlying mechanisms. The 15 N was sprayed bimonthly for 1 year to the forest floor in control and N addition (50 kg N ha-1  year-1 for 10 years) plots in both forests. We unexpectedly found a strong capacity of the legume forest to retain deposited N, with 75 ± 5% labeled N recovered in plants and soils, which was higher than that in the non-legume forest (56 ± 4%). The higher 15 N recovery in legume forest was mainly driven by uptake by the legume trees, in which 15 N recovery was approximately 15% more than that in the nearby non-legume trees. This indicates higher N-demand by the legume than non-legume trees. Mineral soil was the major sink for deposited N, with 39 ± 4% and 34 ± 3% labeled N retained in the legume and non-legume forests, respectively. Moreover, N addition did not significantly change the 15 N recovery patterns of both forests. Overall, these findings indicate that legume-dominated forests act as a strong sink for deposited N regardless of high soil N availability under long-term atmospheric N deposition, which suggest a necessity to incorporate legume-dominated forests into N-cycling models of Earth systems to improve the understanding and prediction of terrestrial N budgets and the global N deposition effects.

Lignin reinforced hydrogels with multi-functional sensing and moist-electric generating applications.

Hydrogels, including PVA hydrogels, have numerous applications in many fields; however, their poor mechanical strength limits their utilization potential. Lignin, the most abundant aromatic biopolymer in nature from lignocellulosic biomass, is presently under-utilized. Herein, we used lignin to improve strength and impart pH-responsive properties of PVA hydrogel. The lignin reinforced PVA (LRP) hydrogel has a maximum storage modulus of 83.1 kPa, which is much higher than the PVA hydrogel. The LRP hydrogel exhibits great ionic conductivity, mechanical properties, and strain-sensitivity even at -30 °C. The LRP hydrogel is subsequently applied for a moisture-induced electric generator, which delivers a voltage output of 226.6 mV from moisture flow. The eco-friendly, pH responsive, high antifreezing, ionic conductive, strain sensitive, and moist-electric generating hydrogels have potential applications in many fields, including biomedicine, flexible electrodes, pH-responsive switch, strain sensor, and next-generation self-powered device systems.

Experimental Study on High-Performers Quaternary Copolymer Based on Host-Guest Effect.

A quaternary polymer (HGP) was prepared by the free-radical polymerization of acrylamide, acrylic acid, maleic anhydride functionalized ß-cyclodextrin (MAH-ß-CD), and N-(3-methacrylamidopropyl)-N, N-dimethylnaphthalen-1-aminium chloride (NAP). It was found that host-guest behavior occurred most effectively at a molar rate of NAP and CD with 1:1, which exhibited better solubility than hydrophobically associative polymer. Moreover, the as-prepared polymer has superior salt tolerance, shear resistance, and viscoelasticity due to host-guest strategy. More importantly, the HGP solution simulates the distribution of formation water in the Bohai SZ1-1 oilfield has good rheological properties at 120 °C. All results show that the proposed polymer could be a competitive candidate in oilfield applications such as fracturing fluids, displacement fluids, and drilling fluids.

Synthesis and Anticancer Properties of Functionalized 1,6-Naphthyridines.

The burgeoning interest in synthesis and biological applications of 1,6-naphthyridines reflects the importance of 1,6-naphthyridines in the synthetic as well as medicinal chemistry fields. Specially, 1,6-naphthyridines are pharmacologically active, with variety of applications such as anticancer, anti-human immunodeficiency virus (HIV), anti-microbial, analgesic, anti-inflammatory and anti-oxidant activities. Although collective recent synthetic developments have paved a path to a wide range of functionalized 1,6-naphthyridines, a complete correlation of synthesis with biological activity remains elusive. The current review focuses on recent synthetic developments from the last decade and a thorough study of the anticancer activity of 1,6-naphthyridines on different cancer cell lines. Anticancer activity has been correlated to 1,6-naphthyridines using the literature on the structure-activity relationship (SAR) along with molecular modeling studies. Exceptionally, at the end of this review, the utility of 1,6-naphthyridines displaying activities other than anticancer has also been included as a glimmering extension.

Carbon burial over the last four millennia is regulated by both climatic and land use change.

Carbon sequestration by sediments and vegetated marine systems contributes to atmospheric carbon drawdown, but little empirical evidence is available to help separate the effects of climate change and other anthropogenic activities on carbon burial over centennial timescales. We used marine sediment organic carbon to determine the role of historic climate variability and human habitation in carbon burial over the past 5,071 years. There was centennial-scale sensitivity of carbon supply and burial to climatic variability, with Little Ice Age cooling causing an abrupt ecosystem shift and an increase in marine carbon contributions compared to terrestrial carbon. Although land use changes during the late 1800s did not cause marked alteration in average carbon burial, they did lead to marked increases in the spatial variability of carbon burial. Thus, while carbon burial by vegetated systems is expected to increase with projected climate warming over the coming century, ecosystem restructuring caused by abrupt climate change may produce unexpected change in carbon burial whose variability is also modulated by land use change.

Application of a Zwitterionic Hydrophobic Associating Polymer with High Salt and Heat Tolerance in Brine-Based Fracturing Fluid.

ZID16PM, a zwitterionic hydrophobic associating polymer, has equivalent positive and negative charges and some hydrophobic monomers with twin-tailed long hydrophobic chains. It exhibits a great heat resistance and salt tolerance to the common salt in formation brine (MgCl2, CaCl2, NaCl, and KCl), which is attributed to its anti-polyelectrolyte effect and strong association force. High-salinity water (seawater or formation water) can be prepared as a fracturing fluid directly. In this paper, the formation water of the West Sichuan Gas Field is directly prepared into fracturing fluid with a concentration of 0.3% ZID16PM (Fluid-1), and the seawater of the Gulf of Mexico is directly prepared into fracturing fluid with a concentration of 0.3% ZID16PM (Fluid-2). Finally, rheological measurements, proppant suspension tests, and core matrix permeability damage rate tests for the Fluid-1 and Fluid-2 are conducted. Results show that after 120 min of shearing at 140 and 160 °C, respectively, the viscosity of Fluid-1 remains in the range of 50-85 mPa‧s, and the viscosity of Fluid-2 remains in the range of 60-95 mPa‧s. And the wastewater produced by an oilfield in Shaanxi, Xinjiang, and Jiangsu are also prepared into fracturing fluids with a concentration of 0.3% ZID16PM, the viscosity of these fracturing fluids can remain 32, 42, and 45 mPa‧s, respectively, after 120 min of shearing at 160 °C. All results demonstrate that the polymer ZID16PM displays prominent performance in fracturing fluids.

Preparation of a Hydrophobic-Associating Polymer with Ultra-High Salt Resistance Using Synergistic Effect.

Polymer, SRP-2-1, was synthesized by micellar polymerization and characterized by ¹H NMR. Salt tolerance and viscoelasticity tests verified that the salt resistance of SRP-2-1 was promoted by the synergistic effects of oxyethylene groups, sulfonate, and hydrophobic chains. It is suggested that the structure of SRP-2-1 became more compact with increasing salinity. Furthermore, a mechanism is proposed as to why SRP-2-1 solution has excellent salt-resistance properties. The experimental results indicate that, because of the good shear resistance properties, the polymer SRP-2-1 could be used as an alternative in many fields, for instance in fracturing fluids, enhanced oil recovery, and sewage treatment.

Preparation of a novel fracturing fluid with good heat and shear resistance.

A new terpolymer (MAS-1) was created by copolymerizing acrylamide (AM), acrylic acid (AA), and 4-isopropenylcarbamoyl-benzene sulfonic acid (AMBS). Thermogravimetric analysis (TGA) suggested that MAS-1 has better heat resistance and meets the requirements for a fracturing fluid at 200 °C. X-ray diffraction (XRD), and conductivity tests showed that MAS-1 has good water solubility. The viscosity of the fracturing fluids containing MAS-1 was found to be about 135 mPa s after 120 min at 170 s-1 and 150 °C. SEM images and the determination of viscoelasticity showed that MAS-1 has a dense and robust spatial network structure in the fracturing fluid. The sedimentation velocity of the proppant was 0.0528 cm min-1 at 90 °C. When enough ammonium persulfate was added to yield approximately 0.10 wt%, the viscosity of the broken fluid was 4.5 mPa s, and the gel broken fluid was transparent without visible residue. In addition, the fracturing fluid did little damage to the reservoir. The drag reduction rate of MAS-1 was always higher than KYPAM-6A and HPAM with the shear rate ranging from 1000 s-1 to 7000 s-1. Therefore, this fracturing fluid could be an alternative for low permeability reservoir stimulation.

Evidence of two distinct dynamical freezing processes in single-layered perovskite La(0.7)Sr(1.3)CoO4.

The static and dynamic features of magnetization have been investigated in terms of dc magnetization, ac susceptibility, and memory effects on single-layered perovskite La(0.7)Sr(1.3)CoO(4). The results indicate that short-range ferromagnetic clusters coexist with the glassy magnetic state, i.e., a cluster-glass phase between T(f) and T(G) and a spin-glass-like phase below T(f). The clear evidence of memory effects in the dc magnetization is also observed below T(f) and T(G), respectively. These two glassy states with cooperative relaxation processes may derive from the different interaction processes among nanoscale ferromagnetic clusters mediated by the matrix, which is influenced by changing the spin state of Co(3+) ions in spontaneously phase-separated cobaltite.