Apparent Capacity Research Articles

Relationships among soil test potassium forms influenced by clay mineralogy

AbstractPotassium fertilizer recommendations for optimal crop production may be improved by considering the ratio between expanding 2:1 layer silicates (smectite) with non‐expanding 2:1 layer silicates (illite). However, the interactive effects between clay mineralogy and various soil tests are not well understood. This study evaluated the relationships among soil test K (STK), water‐soluble K, HNO3‐extractable K, pH, apparent cation exchange capacity (CECa), soil organic matter, clay content, and smectite:illite ratios. Soil samples (0–15 cm) were collected from 41 locations in central and eastern South Dakota, with textures ranging from sandy loam to clay. Data were partitioned into soils with smectite:illite ratios < 1 (illitic), ≥1 but ≤4.5 (smectitic), and > 4.5 (highly smectitic). Mean pH and CECa were lowest in illitic soils, higher in smectitic soils, and highest in highly smectitic soils, whereas STK and water‐soluble K were lowest in highly smectitic soils relative to illitic and smectitic. Correlation analysis also showed that STK decreased with increasing smectite:illite ratio. These results suggest that exchangeable and water‐soluble K forms are reduced when the proportion of smectite increases. There was a strong, positive relationship between STK and HNO3‐extractable K across all three smectite:illite ratio groups. For soil pH, however, the relationship with STK was positive for illitic and smectitic soil groups, but negative for highly smectitic soils. Overall, these results suggest that the smectite:illite ratio influences the relationship among soil parameters and STK. This improves our understanding of the influence of clay mineralogy on plant‐available K and the implications for K fertilizer recommendations.

On the Origin of Capacity Increase in Rechargeable Magnesium Batteries with Manganese Oxide Cathodes and Copper Metal Current Collectors.

Rechargeable magnesium batteries (RMBs), with Cu as positive electrode current collector (CC), typically display a gradual capacity increase with cycling. Whereas the origin of this was suggested in gradual active material electro-activation, the fact that this is prevalent in many positive electrode material systems remains unexplained. Herein, we elucidate the underlying mechanism through a series of multiscale joint operando X-ray characterizations, including operando synchrotron X-ray diffraction and imaging technology. We select a series of manganese oxides as benchmark positive electrodes and find that no magnesium ions are stored within the lattices of these materials, despite an apparent cell capacity increase with cycling. The origin of capacity increase is rooted in the gradual electrochemical corrosion of metallic Cu, release of Cu(I, II) species in electrolyte, and their subsequent redox activity, resulting in apparent electrode capacity gains. Furthermore, the shuttle and redox speciation of Cu ions trigger the irreversible depletion of both the Cu CC (or any other source) and the magnesium metal, ultimately leading to cell failure. Our work suggests the need to reconsider the appropriateness of using Cu as a positive electrode CC for RMBs.

On the Origin of Capacity Increase in Rechargeable Magnesium Batteries with Manganese Oxide Cathodes and Copper Metal Current Collectors

Rechargeable magnesium batteries (RMBs), with Cu as positive electrode current collector (CC), typically display a gradual capacity increase with cycling. Whereas the origin of this was suggested in gradual active material electro‐activation, the fact that this is prevalent in many positive electrode material systems remains unexplained. Herein, we elucidate the underlying mechanism through a series of multiscale joint operando X‐ray characterizations, including operando synchrotron X‐ray diffraction and imaging technology. We select a series of manganese oxides as benchmark positive electrodes and find that no magnesium ions are stored within the lattices of these materials, despite an apparent cell capacity increase with cycling. The origin of capacity increase is rooted in the gradual electrochemical corrosion of metallic Cu, release of Cu(I, II) species in electrolyte, and their subsequent redox activity, resulting in apparent electrode capacity gains. Furthermore, the shuttle and redox speciation of Cu ions trigger the irreversible depletion of both the Cu CC (or any other source) and the magnesium metal, ultimately leading to cell failure. Our work suggests the need to reconsider the appropriateness of using Cu as a positive electrode CC for RMBs.

Screening of Cation Exchange Membranes for an Anthraquinone‐Ferrocyanide Flow Battery

AbstractThe disodium salt of 9,10‐anthraquinone‐2,7‐disulphonic acid (2,7‐AQDS) is an interesting platform for developing anthraquinone derivative negolytes for aqueous organic flow batteries. Recently, ammonium sulphate supporting electrolytes have been considered for improved stability and solubility. This work advances the 2,7‐AQDS/ferrocyanide flow battery with an ammonium sulphate supporting electrolyte (pH 5) by studying the suitability of six commercially available cation exchange membranes: E‐620, NR‐212, FS‐930, F‐1075‐PK, F‐1850 and N‐115. Cell cycling under galvanostatic regime plus potential hold was performed to determine coulombic efficiency, energy efficiency and accessible capacity for each membrane as well as capacity fade rate for three selected membranes under extended operation. Cell cycling under galvanostatic control only was carried out to observe transient membrane behavior alongside accessible capacity and apparent capacity fade rate. It was found that the capacity set by the limiting negolyte is consistent with 1.5 electrons per 2,7‐AQDS molecule and that energy efficiency shows a simple direct relationship to membrane thickness, with one exception. Meanwhile, four membranes displayed similar apparent capacity fade rates at this laboratory scale irrespective of their thickness, with capacity loss explained in terms of crossover. The best overall performance was attained by the thinnest membranes, E‐620 and NR‐212.

Distribution of soil fertility indices in aggregate size fractions under different land-use types for coarse-textured soils of the derived savannah

The research investigated the distribution of soil fertility indices among aggregate-size fractions across three land-use types (forested, cultivated, and fallow lands) for loamy sand at Ede-Oballa, a derived savannah in southeastern Nigeria. Surface soil samples from these land-use types were air-dried and separated into <0.25 mm, 0.25-0.5 mm, 0.5-1.0 mm, 1.0-2.0 mm, 2.0-4.0 mm, and 4.0-8.0 mm aggregates before analyses. There were significant interaction effects of land-use type and aggregate-size fraction on the distribution of soil particle sizes (sand, silt, and clay) and contents of total nitrogen, available phosphorus, exchangeable bases (Mg2+ and Na+), and exchangeable acidity as well as apparent cation exchange capacity (CEC). Land-use type affected soil pH, K+, Ca+, and percent base saturation but not soil organic carbon (SOC), which was rather unevenly distributed among the aggregate-size fractions. The distribution of most fertility indices, those defining CEC, and SOC content favoured >2.0 mm (large), 0.25-0.5 mm and <0.25 mm (micro-) aggregates, respectively, under cultivated land. However, soil total nitrogen and exchangeable acidity contents were best improved in the largest (4.0-8.0 mm) aggregates under forested and fallow lands, respectively. The study highlights the potential of land-use types generally and arable-crop cultivation specifically to engender aggregates of different sizes with specific roles in improving soil quality and fertility.

Strong daily routinisation, weak energy flexibility: a survey study of the stability and adaptability of everyday energy practices

Fundamental changes in everyday consumption patterns are required to mitigate negative environmental impacts, and these include adapting the timing of consumption. For example, flexible energy demand becomes increasingly important in response to larger shares of fluctuating energy production while dynamic electricity pricing suggests there is a need to encourage staggered electricity use. In this paper, we explore the stability, adjustability and flexibility of everyday practices to critically address the potential for flexible household energy demand. Based on a survey questionnaire (N=1,470), the paper takes its empirical focus in the Nordic welfare state Denmark, which has a high share of wind power and little focus on energy justice. Across household groups, it seems that morning routines are strongly routinised, especially on weekdays, and that variations in these primarily involve adjustment to other household members. The analysis indicates that there are differences across household types, for example, households with children and households whose inhabitants are aged 41-60 tend to be associated with stable evening routines, women tend to agree more to adjusting routines to lifestyle and household, while being in employment seems to be associated with stronger dependence on time schedules determined by factors outside the household. The study suggests that socio-temporal rhythms of everyday practices strongly depend on societal rhythms and practices outside the home. It follows therefore that expectations of energy flexibility in household energy demand should initially focus on common temporal patterns and dependence on these rather than on individual households’ (apparent) capacity to consume energy flexibly.

Mechanistic Fatigue Performance Evaluation of Stone Mastic Asphalt Mixtures: Effect of Asphalt Performance Grade and Elastic Recovery.

This study evaluates the crack performance of stone mastic asphalt (SMA) mixtures according to the performance of a modified asphalt binder, evaluated based on the asphalt performance grade (PG) and the elastic recovery of multiple stress creep and recovery (MSCR) according to AASHTO M 320 and T 350. The cracking performance of the mixture was evaluated using the asphalt mixture performance tester (AMPT) according to AASHTO T 378 and T 400 through dynamic modulus and direct tension cyclic fatigue tests. Furthermore, the recently developed viscoelastic continuum damage (VECD) theory was utilized to evaluate the cyclic fatigue index parameter (apparent damage capacity, Sapp) and the permissible heavy vehicle class. For performance evaluation, six modified asphalt mixtures were prepared and tested using SMA aggregate gradation with a nominal maximum aggregate size (NMAS) of 10 mm. The MSCR test results revealed that, of the six asphalt mixtures, the rubber-based PG76-28 exhibited the least initial strain and the highest elastic recovery. The dynamic modulus test results demonstrated that using a rubber-based modifier increased the elastic modulus at high temperatures and decreased it at low temperatures, thereby enhancing resistance to plastic deformation in the summer and reducing low-temperature cracking in the winter. Finally, the correlation between the Sapp performance index and the elastic recovery of modified asphalt and the number of direct tension cyclic loads until failure of the mixture was evaluated as 0.87 and 0.76, respectively.

A Data-Driven Approach for Predicting the Lifetime of Lithium-Metal Batteries

Lithium-metal batteries (LMBs) are promising candidates for accelerating the implementation of electric vehicles in our society. LMBs comprise of a lithium-metal anode that possesses the highest theoretical specific capacity (3860 mAh/g) and the lowest redox potential (-3.04V vs standard hydrogen electrode).1 LMBs undergo repeated plating and stripping of lithium ions on the anode surface. The non-homogenous stripping process leads to the isolation of metallic lithium from the anode surface, forming dead-lithium.2 The parasitic reaction between the lithium-metal anode and the electrolyte leads to the formation of the solid electrolyte interphase (SEI) layer. These phenomena lead to the reduction of available lithium and a rise in cell impedance, causing a rapid reduction of lifetime for these batteries.3 , 4 In this talk, we present a diverse dataset collected from different LMBs of different capacities and voltage ranges, that includes features from the initial formation cycle, rest voltages and CV charging during cycling. A data-driven model from the LMB cycling data is presented to predict the remaining useful lifetime (RUL) of these cells. Insights from the model can be used to determine the bad cells in a batch, improve the designs of the cells and derive optimal charging protocols for their implementation in the BMS. References Lin, D., Liu, Y. & Cui, Y. Reviving the lithium metal anode for high-energy batteries. Nat. Nanotechnol. 12, 194 (2017).Xu, S., Chen, K.-H., Dasgupta, N. P., Siegel, J. B. & Stefanopoulou, A. G. Evolution of Dead Lithium Growth in Lithium Metal Batteries: Experimentally Validated Model of the Apparent Capacity Loss. J. Electrochem. Soc. 166, A3456–A3463 (2019).Liu, G. & Lu, W. A Model of Concurrent Lithium Dendrite Growth, SEI Growth, SEI Penetration and Regrowth. J. Electrochem. Soc. 164, A1826–A1833 (2017).Gao, N. et al. Fast Diagnosis of Failure Mechanisms and Lifetime Prediction of Li Metal Batteries. Small Methods 5, 1–11 (2021).

A Comparative Study of Phase I and II Hepatic Microsomal Biotransformation of Phenol in Three Species of Salmonidae: Hydroquinone, Catechol, and Phenylglucuronide Formation.

The in vitro biotransformation of phenol at 11 °C was studied using pre-spawn adult rainbow (Oncorhynchus mykiss) (RBT), brook (Salvelinus fontinalis) (BKT), and lake trout (Salvelinus namaycush) (LKT) hepatic microsomal preparations. The incubations were optimized for time, cofactor concentration, pH, and microsomal protein concentration. Formation of Phase I ring-hydroxylation and Phase II glucuronidation metabolites was quantified using HPLC with dual-channel electrochemical and UV detection. The biotransformation of phenol over a range of substrate concentrations (1 to 180 mM) was quantified, and the Michaelis-Menten kinetics constants, Km and Vmax, for the formation of hydroquinone (HQ), catechol (CAT), and phenylglucuronide (PG) were calculated. Species differences were noted in the Km values for Phase I enzyme production of HQ and CAT, with the following rank order of apparent enzyme affinity for substrate: RBT > BKT = LKT. However, no apparent differences in the Km for Phase II metabolism of phenol to PG were detected. Conversely, while there were no apparent differences in Vmax between species for HQ or CAT formation, the apparent maximum capacity for PG formation was significantly less in LKT than that observed for RBT and BKT. These experiments provide a means to quantify metabolic activation and deactivation of xenobiotics in fish, to compare activation and deactivation reactions across species, and to act as a guide for future predictions of new chemical biotransformation pathways and rates in fish. These experiments provided the necessary rate and capacity (Km and Vmax) inputs that are required to parameterize a fish physiologically based toxicokinetic (PB-TK) model for a reactive chemical that is readily biotransformed, such as phenol. In the future, an extensive database of these rate and capacity parameters on important fish species for selected chemical structures will be needed to allow the effective use of predictive models for reactive, biotransformation chemicals in aquatic toxicology and environmental risk assessment.

Engineering and microstructural properties of environmentally friendly alkali-activated composites containing clinker aggregate: heat-curing regime and elevated-temperature effect

The common wisdom in the literature about clinker aggregate (CA) is that it improves the performance properties of mortar or concrete to some extent. The current study, in this context, investigated the physical characteristics and mechanical performances of alkali-activated composites (AACs) made entirely with CA. The CA was used in three particle sizes of 0–2 mm (named No.10), 2–4 mm (named No.5), and 4–8 mm (named medium). To examine the impact of the fine CA-size fraction on the characteristics of AAC, No.10 CA was partially replaced by No.5 CA up to 50%, while the content of the medium CA was kept constant in all AAC mixtures. Moreover, to evaluate the influence of the 8-h curing temperature on the performance of the AACs, different temperature-based curing strategies (ambient, 45, and 75 °C) were applied to the AACs. In the production of AACs, granulated blast furnace slag was employed as an aluminosilicate-rich raw material, and a sodium silicate and sodium hydroxide combination was used as an alkaline activator. Physical properties (flowability, water absorption, capillary water absorption, and dry unit weight), and 8-h strength performances (flexural and compressive) were determined. Furthermore, to monitor the influence of high temperatures on the characteristics of the AAC, the mixtures were exposed to elevated temperatures (200, 500, and 800 °C). In SEM image analysis, it was determined that spherical CSH gels were formed in the heat-cured AACs. It has been observed that the geopolymerization products decompose in AACs exposed to 800 °C. To evaluate statistically the experimental results, a multi-factor analysis of variance (ANOVA) was also applied. The results revealed that increasing the coarser fine aggregate fraction led to higher water absorption and apparent porosity capacities and lower unit weight. Besides, strength performance was improved by applying a heat-curing strategy to the AAC, whereas a decrease was observed by increasing the No.5 CA fraction. There was a remarkable reduction in compressive strength and considerable loss of mass when the AAC mixes were exposed to high temperatures.

15-epi-lipoxin A5 promotes neutrophil exit from exudates for clearance by splenic macrophages.

Specialized proresolving mediators (SPMs) promote local macrophage efferocytosis but excess leukocytes early in inflammation require additional leukocyte clearance mechanism for resolution. Here, neutrophil clearance mechanisms from localized acute inflammation were investigated in mouse dorsal air pouches. 15-HEPE (15-hydroxy-5Z,8Z,11Z,13E,17Z-eicosapentaenoic acid) levels were increased in the exudates. Activated human neutrophils converted 15-HEPE to lipoxin A5 (5S,6R,15S-trihydroxy-7E,9E,11Z,13E,17Z-eicosapentaenoic acid), 15-epi-lipoxin A5 (5S,6R,15R-trihydroxy-7E,9E,11Z,13E,17Z-eicosapentaenoic acid), and resolvin E4 (RvE4; 5S,15S-dihydroxy-6E,8Z,11Z,13E,17Z-eicosapentaenoic acid). Exogenous 15-epi-lipoxin A5, 15-epi-lipoxin A4 and a structural lipoxin mimetic significantly decreased exudate neutrophils and increased local tissue macrophage efferocytosis, with comparison to naproxen. 15-epi-lipoxin A5 also cleared exudate neutrophils faster than the apparent local capacity for stimulated macrophage efferocytosis, so the fate of exudate neutrophils was tracked with CD45.1 variant neutrophils. 15-epi-lipoxin A5 augmented the exit of adoptively transferred neutrophils from the pouch exudate to the spleen, and significantly increased splenic SIRPa+ and MARCO+ macrophage efferocytosis. Together, these findings demonstrate new systemic resolution mechanisms for 15-epi-lipoxin A5 and RvE4 in localized tissue inflammation, which distally engage the spleen to activate macrophage efferocytosis for the clearance of tissue exudate neutrophils.

Soil biological and physical measurements did not improve the predictability of corn response to phosphorus fertilization

AbstractIncluding soil health and physical measurements with traditional soil fertility measurements has the potential to improve corn (Zea mays L.) P fertilizer recommendations. The objectives for this study were to (1) evaluate the accuracy of current South Dakota corn P recommendations in predicting yield increases and (2) determine if the predictability of yield response to P fertilization improves by including selected soil biological, physical, and chemical measurements. This project was conducted in central and eastern South Dakota from 2019 to 2022 at 117 experimental sites that varied in management, landform, and soil type. A treatment of 48.9 kg P2O5‐P ha−1 was compared to a control with no P fertilizer. Soil samples (0–15 cm) collected before fertilization were analyzed for selected soil physical, chemical, and biological parameters. Analysis suggested that the current critical P value of 16 mg Olsen‐P kg−1 was still accurate as it was still within the 68% confidence interval for the linear (12–19 mg kg−1) and quadratic plateau (16–26 mg kg−1) models. Using the critical value of 16 mg Olsen‐P kg−1, we correctly predicted P responsiveness 70% of the time. The accuracy of predicting P responsiveness was not further improved by considering selected enzymes, permanganate oxidizable C, soil respiration, total C, or total N, but was improved by considering pH, soil organic matter, and apparent cation exchange capacity. Therefore, the use of typical soil fertility measurements without soil physical and biological measurements is currently the best option for predicting the responsiveness of corn to P fertilization in South Dakota.

Drought in the middle growing season inhibited carbon uptake more critical in an anthropogenic shrub ecosystem of Northwest China

Large-scale ecological restoration efforts of the degraded desert steppe ecosystem in northwestern China have effectively combated desertification but have also resulted in the encroachment of shrubs. However, the function of the anthropogenic shrub ecosystem is still unknown under climate change, especially the response of carbon fluxes to drought, which hinders our further understanding of its sustainability in the future. Hence, based on the eddy covariance and environment sensors, continuous carbon and water fluxes and biophysical factors were monitored during 2019–2022 to investigate the characteristics of carbon fluxes and their response to seasonal drought in an anthropogenic shrub ecosystem dominated by Caragana liouana in the southern Mu Us sandy land, northwestern China. The results showed the shrub ecosystem was a stable carbon sink over the 4 years despite large interannual variability, with annual net ecosystem production (NEP) ranging from 54.37 to 150.35 g C·m−2·y−1. Interannual variability in NEP was mainly due to variation in gross primary productivity (GPP), which is driven by the fact that interannual variability in GPP was higher than interannual variability in ecosystem respiration (Reco). While drought inhibited GPP more than Reco, thus weakening the carbon sequestration ability of the ecosystem during the middle growing season, and thereby carbon fluxes in the shrub ecosystem were significantly suppressed by drought in the middle growing season but slightly in the early growing season. Furthermore, the magnitude and variation of carbon fluxes were determined by the maximum apparent photosynthetic capacity of the canopy (Pmax), leaf area index (LAI), and canopy conductance (gc), all of which are limited by water stress during drought. The work suggests that to keep the carbon sink of anthropogenic shrub ecosystems in arid and semi-arid areas, managers should focus on drought-relief measures in the middle growing season that are better adapted to future climate change.

Separation of ethylene glycol from propylene glycol via selective adsorption with basic anion-exchange resin

Ethylene glycol (EG) is a common impurity in bio-derived 1,2-propylene glycol (PG). EG was isolated from PG via selective adsorption on basic ion-exchange resin. A small amount of moisture improved the porosity of resin, thereby reinforcing the intraparticle diffusion and adsorption performance. The adsorption equilibrium could be reached within 1 min, indicating that EG can be instantly removed. The real adsorption capacity for PG was much lower than that for EG, and the selectivity was up to 5.5 at 60 °C due to the susceptibility of PG adsorption to temperature. The PG content was increased from 90 to 95.7 wt% in a continuous-flow process with low bed pressure drop. The EG adsorption process agreed with the Langmuir isotherm model, and the apparent EG adsorption capacity reached 250.6 mg/g at 60 °C, while real PG adsorption capacity was negligible. The different interactions between diols and OH− ions were proven by UV and surface-tension measurements, and the stronger acidity of hydroxyl group in EG contributed to its stronger acid-base interaction with basic materials. The resin adsorbent could be reused and completely regenerated without leaching via elution with 20 wt% NaOH. Based on the acidity of EG, this work presents an unprecedented cost-effective strategy to separate diols.

Tuning the morphology of argan shells-based activated carbon towards applications as an anode for lithium-ion battery

The application of carbonaceous materials other than graphite as an anode for lithium-ion batteries can generate significant advantages, mainly in terms of cost and sustainability while achieving high specific capacities. In this work, we successfully managed to tune the morphology of activated carbon prepared from argan shells to be used as an electrode material for lithium-ion batteries. Both Nanosphere-AC and Honeycomb-AC are obtained from the same precursor. The AC samples were comprehensively characterized using sorption isotherms, scanning electron microscopy, X-ray diffraction and Fourier-transforming infrared spectroscopy. Both materials were tested as anodes for lithium-ion batteries. It was found that Nanosphere-AC permitted great specific capacity (700 mAh.g−1at 50 mAh.g−1) and long-term cycling, showing no apparent capacity fade even after 200 cycles, offering promising application potential. Whereas Honeycomb-AC only achieved 220 mAh.g−1 at 50 mAh.g−1, but still exhibited great long-term cycling performance after 200 cycles and rate capability properties.

Job Loss Due to COVID-19: A Longitudinal Study of Mental Health, Protective and Risk Factors.

The COVID-19 pandemic had a devastating impact on unemployment, which-compounded by the additional stressors associated with the pandemic-had considerable mental health impact. The current study examined the trajectory of mental health amongst those experiencing pandemic-related job loss, alongside the impact of risk and protective factors. Data were obtained from 374 Australian participants who were allocated to a waitlist control arm of a randomised control trial. The outcome variables assessed at baseline and six-month follow-up consisted of depression, anxiety, and suicidality. The assessed risk and protective factors were age, gender, relationship status, education, exercise frequency, COVID-related stress, dispositional resilience, and coping self-efficacy. Re-employment by follow-up was used as a covariate. Overall, there were decreases in depression and anxiety symptoms, and partial evidence of decreased suicidality, demonstrating an apparent capacity for individuals to better cope with their circumstances over time. Demographics and exercise had no effect on changes in mental health. Those with high COVID-related stress, low resilience, and low coping self-efficacy had worse mental health at baseline, although exhibited significantly greater improvements in mental health over time. Obtaining re-employment by follow-up did not predict changes in mental health. The present results offer an optimistic picture of recovery for those experiencing pandemic-related job loss, even for those with the most substantial risk and severity. The likely protective role played by Australian social welfare policies over the course of the study is explored. Stress around one's broader sociocultural or economic circumstances, perceived resilience, and coping self-efficacy are valuable targets for intervention.

A cryptic syngameon within Betula shrubs revealed: Implications for conservation in changing subarctic environments.

Arctic and subarctic ecosystems are rapidly transforming due to global warming, emphasizing the need to understand the genetic diversity and adaptive strategies of northern plant species for effective conservation. This study focuses on Betula glandulosa, a native North American tundra shrub known as dwarf birch, which demonstrates an apparent capacity to adapt to changing climate conditions. To address the taxonomic challenges associated with shrub birches and logistical complexities of sampling in the northernmost areas where species' ranges overlap, we adopted a multicriteria approach. Incorporating molecular data, ploidy level assessment and leaf morphology, we aimed to distinguish B. glandulosa individuals from other shrub birch species sampled. Our results revealed three distinct species and their hybrids within the 537 collected samples, suggesting the existence of a shrub birch syngameon, a reproductive network of interconnected species. Additionally, we identified two discrete genetic clusters within the core species, B. glandulosa, that likely correspond to two different glacial lineages. A comparison between the nuclear and chloroplast SNP data emphasizes a long history of gene exchange between different birch species and genetic clusters. Furthermore, our results highlight the significance of incorporating interfertile congeneric species in conservation strategies and underscores the need for a holistic approach to conservation in the context of climate change, considering the complex dynamics of species interactions. While further research will be needed to describe this shrub birches syngameon and its constituents, this study is a first step in recognizing its existence and disseminating awareness among ecologists and conservation practitioners. This biological phenomenon, which offers evolutionary flexibility and resilience beyond what its constituent species can achieve individually, may have significant ecological implications.

Mechanism insight of sorption of Er(III) and Nd(III) ions onto Aluminium barium tungstate synthesized via streamlined sol–gel technique: Time-transient study

Aluminium barium tungstate powder (ABT) was chemically synthesized via streamlined sol–gel technique and exploited as a sorbent material for sorption of erbium and neodymium ions from aqueous solutions under simulated conditions using batch technique. The pH influence, time and temperature factors have been studied. The sorption of neodymium ions was found to be marginally higher than that of erbium ions and the apparent sorption capacity has a progressive influence with temperature. Thermodynamic parameters such as Gibbs free energy change (ΔG◦), enthalpy change (ΔH◦) and entropy change (ΔS◦) were calculated. The negative ΔG◦ values declines with an increase in temperature value, demonstrating that the sorption reaction for both studied ions was spontaneous and more promising at greater temperature. The positive ΔH◦ values affirm that the nature of the sorption processes is endothermic. The comparison of different time transient models applied to the sorption data was assessed for the pseudo first-order (PFO), the pseudo second-order, (PSO) and homogeneous particle diffusion (HPD) models. The results revealed that both PSO and HPD models were found to best correlate the experimental sorption rate data and a monolayer model was adopted as the best suitable model to explore the sorption mechanism for both studied ions. The attained particle diffusion coefficients and rate constant values were acquired from the graphical illustration of the anticipated models. Activation energy change (Ea) and activation entropy change (ΔS±) were also calculated from the linearized Arrhenius model and indicated that the binding process between the sorbent and the studied ions occurred through chemisorption and the sorption of both ions onto synthetic sorbent took place through associative mechanism.

Geologic Controls on Apparent Root‐Zone Storage Capacity

AbstractThe water storage capacity of the root zone can determine whether plants survive dry periods and control the partitioning of precipitation into streamflow and evapotranspiration. It is currently thought that top‐down, climatic factors are the primary control on this capacity via their interaction with plant rooting adaptations. However, it remains unclear to what extent bottom‐up, geologic factors can provide an additional constraint on storage capacity. Here we use a machine learning approach to identify regions with lower than climatically expected apparent storage capacity. We find that in seasonally dry California these regions overlap with particular geologic substrates. We hypothesize that these patterns reflect diverse mechanisms by which substrate can limit storage capacity, and highlight case studies consistent with limited weathered bedrock extent (melange in the Northern Coast Range), toxicity (ultramafic substrates in the Klamath‐Siskiyou region), nutrient limitation (phosphorus‐poor plutons in the southern Sierra Nevada), and low porosity capable of retaining water (volcanic formations in the southern Cascades). The observation that at regional scales climate alone does not “size” the root zone has implications for the parameterization of storage capacity in models of plant dynamics (and the interrelated carbon and water cycles), and also underscores the importance of geology in considerations of climate‐change induced biome migration and habitat suitability.

Understanding the Air‐Exposure Degradation Chemistry of the Sacrificial Cathode Additive Li5FeO4 for Li‐Ion Batteries

AbstractLi5FeO4 (LFO) is emerging as a promising prelithiation additive due to the high lithium donor capacity (>700 mAh g−1), cheap raw materials, good environmental adaptability, and reliable synthesis approach. However, LFO suffers from extremely poor air stability and the underlying mechanism remains elusive. Herein, LFO is subjected to different atmospheres (the main component of air) of O2, CO2, N2, and 30% humidity air to unravel its reaction mechanism with air and the interfacial chemistry. It is found that Li+ ions will escape from the LFO crystal lattice to construct Li2O, Li2CO3, and LiOH impurity phases with an obvious change of LFO surface morphology in contact with O2, CO2, and humidity air. These insulating species remarkedly inhibit Li+ ion diffusion from the material and thus lead to an increment of interfacial impedance and an apparent capacity degradation. Consequently, the initial charging capacity decays rapidly from 681.5 to 169.4 mAh g−1 (under O2) and to 54.8 mAh g−1 (under CO2), respectively. In this regard, a facile coating strategy is proposed on the surface of LFO to effectively improve its air stability.